Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: SO_0000340
sequence version: NC_000021.8
sequence length: 48129895
sequence fasta: http://www.ncbi.nlm.nih.gov/nuccore/NC_000021.8
type: SO_0000987
sequence date: 2013-08-13
label: NC_000021.8
SIO_000068: refseq
dblink: PRJNA168
location: 1..48129895
location: region:1-48129895:1
organism: Homo sapiens
mol type: genomic DNA
chromosome: 21

GI:224589813
SIO_000068: ncbigi

PRJNA168
type: Entry

15496913
SIO_000068: pubmed

11237011
SIO_000068: pubmed

10830953
SIO_000068: pubmed

position:1:1
position: 1
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:48129895:1
position: 48129895
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

9606
SIO_000068: taxonomy

assembly_gap
type: SO_0000730
estimated length: 10000
gap type: telomere
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 1..10000
location: region:1-10000:1

position:10000:1
position: 10000
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 5201193
gap type: short_arm
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 10001..5211193
location: region:10001-5211193:1

position:10001:1
position: 10001
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:5211193:1
position: 5211193
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 4200000
gap type: between scaffolds
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 5211194..9411193
location: region:5211194-9411193:1

position:5211194:1
position: 5211194
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9411193:1
position: 9411193
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 50000
gap type: between scaffolds
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9595549..9645548
location: region:9595549-9645548:1

position:9595549:1
position: 9595549
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9645548:1
position: 9645548
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 50000
gap type: between scaffolds
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9775438..9825437
location: region:9775438-9825437:1

position:9775438:1
position: 9775438
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9825437:1
position: 9825437
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 50000
gap type: between scaffolds
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 10034921..10084920
location: region:10034921-10084920:1

position:10034921:1
position: 10034921
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:10084920:1
position: 10084920
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 150000
gap type: between scaffolds
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 10215977..10365976
location: region:10215977-10365976:1

position:10215977:1
position: 10215977
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:10365976:1
position: 10365976
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 50000
gap type: between scaffolds
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 10647897..10697896
location: region:10647897-10697896:1

position:10647897:1
position: 10647897
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:10697896:1
position: 10697896
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 50000
gap type: between scaffolds
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 11188130..11238129
location: region:11188130-11238129:1

position:11188130:1
position: 11188130
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:11238129:1
position: 11238129
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 50000
gap type: heterochromatin
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 11238130..11288129
location: region:11238130-11288129:1

position:11238130:1
position: 11238130
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:11288129:1
position: 11288129
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 3000000
gap type: centromere
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 11288130..14288129
location: region:11288130-14288129:1

position:11288130:1
position: 11288130
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14288129:1
position: 14288129
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 50000
gap type: between scaffolds
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 14288130..14338129
location: region:14288130-14338129:1

position:14288130:1
position: 14288130
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14338129:1
position: 14338129
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 50000
gap type: between scaffolds
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 42955560..43005559
location: region:42955560-43005559:1

position:42955560:1
position: 42955560
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:43005559:1
position: 43005559
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

assembly_gap
type: SO_0000730
estimated length: 10000
gap type: telomere
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 48119896..48129895
location: region:48119896-48129895:1

position:48119896:1
position: 48119896
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC100996520
type: SO_0000704
gene: LOC100996520
note: Derived by automated computational analysis using gene prediction method: Gnomon.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9492292..9492823
location: region:9492292-9492823:1
SIO_010080: LOC100996520

100996520
SIO_000068: ncbigene

position:9492292:1
position: 9492292
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9492823:1
position: 9492823
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC100996520
type: SO_0000147
gene: LOC100996520
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
number: 1
pseudo: true
so part of: LOC100996520
location: 9492292..9492823
location: region:9492292-9492823:1

LOC101927425
type: SO_0000704
gene: LOC101927425
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9663781..9677575
location: region:9663781-9677575:1
SIO_010080: LOC101927425

101927425
SIO_000068: ncbigene

position:9663781:1
position: 9663781
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9677575:1
position: 9677575
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927425
type: SO_0000673
gene: LOC101927425
product: uncharacterized LOC101927425
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 22% coverage by RNAseq alignments
transcript id: XR_246984.1
so part of: LOC101927425
location: join(9663781..9666088,9670442..9670451,9676600..9676714,9677506..9677575)
location: region:9663781-9677575:1

GI:530427717
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:9663781-9666088:1/exon

position:9666088:1
position: 9666088
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:9670442-9670451:1/exon

position:9670442:1
position: 9670442
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9670451:1
position: 9670451
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:9676600-9676714:1/exon

position:9676600:1
position: 9676600
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9676714:1
position: 9676714
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:9677506-9677575:1/exon

position:9677506:1
position: 9677506
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

SNX18P10
type: SO_0000704
gene: SNX18P10
note: sorting nexin 18 pseudogene 10; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(9689973..9690726)
location: region:9689973-9690726:-1

100419040
SIO_000068: ncbigene

39618
SIO_000068: hgnc

position:9689973:-1
position: 9689973
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:9690726:-1
position: 9690726
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MTCO1P1
type: SO_0000704
gene: MTCO1P1
note: MT-CO1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9734540..9735381
location: region:9734540-9735381:1

56167
SIO_000068: ncbigene

7420
SIO_000068: hgnc

position:9734540:1
position: 9734540
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9735381:1
position: 9735381
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ASNSP2
type: SO_0000704
alternative label: ASNSL2
gene: ASNSP2
gene synonym: ASNSL2
note: asparagine synthetase pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9742188..9742343
location: region:9742188-9742343:1

442
SIO_000068: ncbigene

755
SIO_000068: hgnc

position:9742188:1
position: 9742188
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9742343:1
position: 9742343
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ANKRD20A16P
type: SO_0000704
gene: ANKRD20A16P
note: ankyrin repeat domain 20 family, member A16, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9765961..9769809
location: region:9765961-9769809:1

100421427
SIO_000068: ncbigene

43607
SIO_000068: hgnc

position:9765961:1
position: 9765961
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9769809:1
position: 9769809
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR3648
type: SO_0000704
gene: MIR3648
note: microRNA 3648; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9825832..9826011
location: region:9825832-9826011:1
SIO_010080: MIR3648

100500862
SIO_000068: ncbigene

38941
SIO_000068: hgnc

MI0016048
SIO_000068: mirbase

position:9825832:1
position: 9825832
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9826011:1
position: 9826011
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR3648
type: SO_0000185
gene: MIR3648
product: microRNA 3648
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_037421.1
so part of: MIR3648
location: 9825832..9826011
location: region:9825832-9826011:1

GI:312147431
SIO_000068: ncbigi

MIR3648
type: SO_0000655
gene: MIR3648
nc RNA class: miRNA
product: hsa-miR-3648
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR3648
location: 9825859..9825879
location: region:9825859-9825879:1

MIMAT0018068
SIO_000068: mirbase

position:9825859:1
position: 9825859
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9825879:1
position: 9825879
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR3687
type: SO_0000704
gene: MIR3687
note: microRNA 3687; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9826203..9826263
location: region:9826203-9826263:1
SIO_010080: MIR3687

100500815
SIO_000068: ncbigene

38946
SIO_000068: hgnc

MI0016088
SIO_000068: mirbase

position:9826203:1
position: 9826203
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9826263:1
position: 9826263
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR3687
type: SO_0000185
gene: MIR3687
product: microRNA 3687
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_037458.1
so part of: MIR3687
location: 9826203..9826263
location: region:9826203-9826263:1

GI:312147056
SIO_000068: ncbigi

MIR3687
type: SO_0000655
gene: MIR3687
nc RNA class: miRNA
product: hsa-miR-3687
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR3687
location: 9826237..9826260
location: region:9826237-9826260:1

MIMAT0018115
SIO_000068: mirbase

position:9826237:1
position: 9826237
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9826260:1
position: 9826260
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927615
type: SO_0000704
gene: LOC101927615
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9891959..9897911
location: region:9891959-9897911:1
SIO_010080: LOC101927615

101927615
SIO_000068: ncbigene

position:9891959:1
position: 9891959
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9897911:1
position: 9897911
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927615
type: SO_0000673
gene: LOC101927615
product: uncharacterized LOC101927615
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage by RNAseq alignments
transcript id: XR_246985.1
so part of: LOC101927615
location: join(9891959..9892226,9895546..9895636,9897656..9897911)
location: region:9891959-9897911:1

GI:530418754
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:9891959-9892226:1/exon

position:9892226:1
position: 9892226
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:9895546-9895636:1/exon

position:9895546:1
position: 9895546
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9895636:1
position: 9895636
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:9897656-9897911:1/exon

position:9897656:1
position: 9897656
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

TEKT4P2
type: SO_0000704
alternative label: MAFIPL
alternative label: TEKT4P
gene: TEKT4P2
gene synonym: MAFIPL; TEKT4P
note: tektin 4 pseudogene 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(<9907189..9968593)
location: region:9907189-9968593:-1
SIO_010080: TEKT4P2

100132288
SIO_000068: ncbigene

40046
SIO_000068: hgnc

position:9907189:-1
position: 9907189
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: FuzzyPosition

position:9968593:-1
position: 9968593
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

TEKT4P2
type: SO_0000673
alternative label: MAFIPL
alternative label: TEKT4P
gene: TEKT4P2
gene synonym: MAFIPL; TEKT4P
product: tektin 4 pseudogene 2, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
transcript id: NR_038328.1
so part of: TEKT4P2
location: complement(join(<9907189..9907492,9909047..9909277,9966322..9966380,9968516..9968593))
location: region:9907189-9968593:-1

GI:334191703
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:9968516-9968593:-1/exon

position:9968516:-1
position: 9968516
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:9966322-9966380:-1/exon

position:9966322:-1
position: 9966322
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:9966380:-1
position: 9966380
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:9909047-9909277:-1/exon

position:9909047:-1
position: 9909047
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:9909277:-1
position: 9909277
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:9907189-9907492:-1/exon

position:9907492:-1
position: 9907492
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

TEKT4P2
type: SO_0000673
alternative label: MAFIPL
alternative label: TEKT4P
gene: TEKT4P2
gene synonym: MAFIPL; TEKT4P
product: tektin 4 pseudogene 2, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
transcript id: NR_038327.1
so part of: TEKT4P2
location: complement(join(<9907189..9908432,9909047..9909277,9966322..9966380,9968516..9968593))
location: region:9907189-9968593:-1

GI:334191702
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:9968516-9968593:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:9966322-9966380:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:9909047-9909277:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:9907189-9908432:-1/exon

position:9908432:-1
position: 9908432
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

TEKT4P2
type: SO_0000673
alternative label: MAFIPL
alternative label: TEKT4P
gene: TEKT4P2
gene synonym: MAFIPL; TEKT4P
product: tektin 4 pseudogene 2, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
transcript id: NR_038329.1
so part of: TEKT4P2
location: complement(join(<9915250..9916547,9966322..9966380,9968516..9968593))
location: region:9915250-9968593:-1

GI:334191704
SIO_000068: ncbigi

position:9915250:-1
position: 9915250
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: FuzzyPosition

urn:…
SIO_000300: 1
SIO_000628: feature:9968516-9968593:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:9966322-9966380:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:9915250-9916547:-1/exon

position:9916547:-1
position: 9916547
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100419957
type: SO_0000704
gene: LOC100419957
note: ankyrin repeat domain 57 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(9921434..9922742)
location: region:9921434-9922742:-1

100419957
SIO_000068: ncbigene

position:9921434:-1
position: 9921434
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:9922742:-1
position: 9922742
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

SNX18P11
type: SO_0000704
gene: SNX18P11
note: sorting nexin 18 pseudogene 11; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 9931701..9932442
location: region:9931701-9932442:1

100419043
SIO_000068: ncbigene

39619
SIO_000068: hgnc

position:9931701:1
position: 9931701
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:9932442:1
position: 9932442
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

SNX18P12
type: SO_0000704
gene: SNX18P12
note: sorting nexin 18 pseudogene 12; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(10203291..10204871)
location: region:10203291-10204871:-1

100419041
SIO_000068: ncbigene

39620
SIO_000068: hgnc

position:10203291:-1
position: 10203291
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10204871:-1
position: 10204871
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101927345
type: SO_0000704
gene: LOC101927345
note: Derived by automated computational analysis using gene prediction method: Gnomon.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(10207468..10215925)
location: region:10207468-10215925:-1
SIO_010080: LOC101927345

101927345
SIO_000068: ncbigene

position:10207468:-1
position: 10207468
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10215925:-1
position: 10215925
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101927345
type: SO_0000673
gene: LOC101927345
product: putative uncharacterized protein ENSP00000344348-like
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 93% coverage by RNAseq alignments, including 2 samples with support for all introns
pseudo: true
transcript id: XR_246983.1
so part of: LOC101927345
location: complement(join(10207468..10208159,10212780..10213000,10214339..10214552,10215185..10215925))
location: region:10207468-10215925:-1

GI:530427716
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:10215185-10215925:-1/exon

position:10215185:-1
position: 10215185
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:10214339-10214552:-1/exon

position:10214339:-1
position: 10214339
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10214552:-1
position: 10214552
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:10212780-10213000:-1/exon

position:10212780:-1
position: 10212780
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10213000:-1
position: 10213000
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:10207468-10208159:-1/exon

position:10208159:-1
position: 10208159
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100420925
type: SO_0000704
gene: LOC100420925
note: chromosome 2 open reading frame 27A pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 10614447..10615032
location: region:10614447-10615032:1

100420925
SIO_000068: ncbigene

position:10614447:1
position: 10614447
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:10615032:1
position: 10615032
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

IGHV1OR21-1
type: SO_0000704
gene: IGHV1OR21-1
note: immunoglobulin heavy variable 1/OR21-1 (non-functional); Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 10862622..10863067
location: region:10862622-10863067:1

390530
SIO_000068: ncbigene

38040
SIO_000068: hgnc

position:10862622:1
position: 10862622
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:10863067:1
position: 10863067
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

SLC25A15P4
type: SO_0000704
gene: SLC25A15P4
note: solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 pseudogene 4; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 10899078..10900002
location: region:10899078-10900002:1

100422636
SIO_000068: ncbigene

39845
SIO_000068: hgnc

position:10899078:1
position: 10899078
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:10900002:1
position: 10900002
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

TPTE
type: SO_0000704
alternative label: CT44
alternative label: PTEN2
gene: TPTE
gene synonym: CT44; PTEN2
note: transmembrane phosphatase with tensin homology; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(10906741..10990920)
location: region:10906741-10990920:-1
SIO_010080: TPTE

7179
SIO_000068: ncbigene

12023
SIO_000068: hgnc

604336
SIO_000068: omim

position:10906741:-1
position: 10906741
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10990920:-1
position: 10990920
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

TPTE
type: SO_0000234
alternative label: CT44
alternative label: PTEN2
gene: TPTE
gene synonym: CT44; PTEN2
product: transmembrane phosphatase with tensin homology, transcript variant 3
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_199260.2
exception: annotated by transcript or proteomic data
note: The RefSeq transcript has 2 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_199260.2
so part of: TPTE
location: complement(join(10906741..10907040,10908825..10908895,10910307..10910399,10914363..10914442,10916370..10916475,10920084..10920164,10921934..10921995,10933852..10933940,10934039..10934120,10934937..10934997,10941908..10941972,10942711..10942774,10942921..10943020,10944668..10944787,10951266..10951427,10952913..10952963,10970009..10970062,10971292..10971345,10973723..10973776,10985045..10985102,10987769..10987877,10990763..10990920))
location: region:10906741-10990920:-1

GI:109689709
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:10990763-10990920:-1/exon

position:10990763:-1
position: 10990763
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:10987769-10987877:-1/exon

position:10987769:-1
position: 10987769
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10987877:-1
position: 10987877
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:10985045-10985102:-1/exon

position:10985045:-1
position: 10985045
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10985102:-1
position: 10985102
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:10973723-10973776:-1/exon

position:10973723:-1
position: 10973723
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10973776:-1
position: 10973776
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:10971292-10971345:-1/exon

position:10971292:-1
position: 10971292
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10971345:-1
position: 10971345
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:10970009-10970062:-1/exon

position:10970009:-1
position: 10970009
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10970062:-1
position: 10970062
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:10952913-10952963:-1/exon

position:10952913:-1
position: 10952913
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10952963:-1
position: 10952963
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:10951266-10951427:-1/exon

position:10951266:-1
position: 10951266
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10951427:-1
position: 10951427
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:10944668-10944787:-1/exon

position:10944668:-1
position: 10944668
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10944787:-1
position: 10944787
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:10942921-10943020:-1/exon

position:10942921:-1
position: 10942921
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10943020:-1
position: 10943020
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:10942711-10942774:-1/exon

position:10942711:-1
position: 10942711
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10942774:-1
position: 10942774
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:10941908-10941972:-1/exon

position:10941908:-1
position: 10941908
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10941972:-1
position: 10941972
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:10934937-10934997:-1/exon

position:10934937:-1
position: 10934937
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10934997:-1
position: 10934997
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:10934039-10934120:-1/exon

position:10934039:-1
position: 10934039
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10934120:-1
position: 10934120
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:10933852-10933940:-1/exon

position:10933852:-1
position: 10933852
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10933940:-1
position: 10933940
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:10921934-10921995:-1/exon

position:10921934:-1
position: 10921934
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10921995:-1
position: 10921995
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 17
SIO_000628: feature:10920084-10920164:-1/exon

position:10920084:-1
position: 10920084
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10920164:-1
position: 10920164
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 18
SIO_000628: feature:10916370-10916475:-1/exon

position:10916370:-1
position: 10916370
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10916475:-1
position: 10916475
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 19
SIO_000628: feature:10914363-10914442:-1/exon

position:10914363:-1
position: 10914363
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10914442:-1
position: 10914442
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 20
SIO_000628: feature:10910307-10910399:-1/exon

position:10910307:-1
position: 10910307
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10910399:-1
position: 10910399
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 21
SIO_000628: feature:10908825-10908895:-1/exon

position:10908825:-1
position: 10908825
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10908895:-1
position: 10908895
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 22
SIO_000628: feature:10906741-10907040:-1/exon

position:10907040:-1
position: 10907040
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

TPTE
type: SO_0000234
alternative label: CT44
alternative label: PTEN2
gene: TPTE
gene synonym: CT44; PTEN2
product: transmembrane phosphatase with tensin homology, transcript variant 2
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_199259.2
exception: annotated by transcript or proteomic data
note: The RefSeq transcript has 2 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_199259.2
so part of: TPTE
location: complement(join(10906741..10907040,10908825..10908895,10910307..10910399,10914363..10914442,10916370..10916475,10920084..10920164,10921934..10921995,10933852..10933940,10934039..10934120,10934937..10934997,10941908..10941972,10942711..10942774,10942921..10943020,10944668..10944787,10951266..10951427,10952913..10952963,10959741..10959800,10970009..10970062,10971292..10971345,10973723..10973776,10985045..10985102,10987769..10987877,10990763..10990920))
location: region:10906741-10990920:-1

GI:109689708
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:10990763-10990920:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:10987769-10987877:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:10985045-10985102:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:10973723-10973776:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:10971292-10971345:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:10970009-10970062:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:10959741-10959800:-1/exon

position:10959741:-1
position: 10959741
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10959800:-1
position: 10959800
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:10952913-10952963:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:10951266-10951427:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:10944668-10944787:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:10942921-10943020:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:10942711-10942774:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:10941908-10941972:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:10934937-10934997:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:10934039-10934120:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:10933852-10933940:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:10921934-10921995:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:10920084-10920164:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:10916370-10916475:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:10914363-10914442:-1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:10910307-10910399:-1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:10908825-10908895:-1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:10906741-10907040:-1/exon

TPTE
type: SO_0000234
alternative label: CT44
alternative label: PTEN2
gene: TPTE
gene synonym: CT44; PTEN2
product: transmembrane phosphatase with tensin homology, transcript variant 1
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_199261.2
exception: annotated by transcript or proteomic data
note: The RefSeq transcript has 2 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_199261.2
so part of: TPTE
location: complement(join(10906741..10907040,10908825..10908895,10910307..10910399,10914363..10914442,10916370..10916475,10920084..10920164,10921934..10921995,10933852..10933940,10934039..10934120,10934937..10934997,10941908..10941972,10942711..10942774,10942921..10943020,10944668..10944787,10951266..10951427,10952913..10952963,10959741..10959800,10969075..10969128,10970009..10970062,10971292..10971345,10973723..10973776,10985045..10985102,10987769..10987877,10990763..10990920))
location: region:10906741-10990920:-1

GI:109689706
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:10990763-10990920:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:10987769-10987877:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:10985045-10985102:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:10973723-10973776:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:10971292-10971345:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:10970009-10970062:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:10969075-10969128:-1/exon

position:10969075:-1
position: 10969075
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10969128:-1
position: 10969128
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:10959741-10959800:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:10952913-10952963:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:10951266-10951427:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:10944668-10944787:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:10942921-10943020:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:10942711-10942774:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:10941908-10941972:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:10934937-10934997:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:10934039-10934120:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:10933852-10933940:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:10921934-10921995:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:10920084-10920164:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:10916370-10916475:-1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:10914363-10914442:-1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:10910307-10910399:-1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:10908825-10908895:-1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:10906741-10907040:-1/exon

TPTE
type: SO_0000316
alternative label: CT44
alternative label: PTEN2
gene: TPTE
gene synonym: CT44; PTEN2
inference: similar to AA sequence (same species):RefSeq:NP_954869.1
exception: annotated by transcript or proteomic data
note: isoform gamma is encoded by transcript variant 3; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: putative tyrosine-protein phosphatase TPTE isoform gamma
translation: MNESPDPTDLAGVIIELGPNDSPQTSEFKGATEEAPAKESSKIKKIVHSIVSSFAFGLFGVFLVLLDVTLILADLIFTDSKLYIPLEYRSISLAIALFFLMDVLLRVFVERRQQYFSDLFNILDTAIIVILLLVDVVYIFFDIKLLRNIPRWTHLLRLLRLIILLRIFHLFHQKRQLEKLIRRRVSENKRRYTRDGFDLDLTYVTERIIAMSFPSSGRQSFYRNPIKEVVRFLDKKHRNHYRVYNLCSERAYDPKHFHNRVVRIMIDDHNVPTLHQMVVFTKEVNEWMAQDLENIVAIHCKGGTDRTGTMVCAFLIASEICSTAKESLYYFGERRTDKTHSEKFQGVETPSQKRYVAYFAQVKHLYNWNLPPRRILFIKHFIIYSIPRYVRDLKIQIEMEKKVVFSTISLGKCSVLDNITTDKILIDVFDGLPLYDDVKVQFFYSNLPTYYDNCSFYFWLHTSFIENNRLYLPKNELDNLHKQKARRIYPSDFAVEILFGEKMTSSDVVAGSD
so part of: TPTE
location: complement(join(10906905..10907040,10908825..10908895,10910307..10910399,10914363..10914442,10916370..10916475,10920084..10920164,10921934..10921995,10933852..10933940,10934039..10934120,10934937..10934997,10941908..10941972,10942711..10942774,10942921..10943020,10944668..10944787,10951266..10951427,10952913..10952963,10970009..10970062,10971292..10971345,10973723..10973733))
location: region:10906905-10973733:-1

NP_954869.1
SIO_000068: ncbiprotein

GI:40549435
SIO_000068: ncbigi

CCDS33511.1
SIO_000068: ccds

position:10906905:-1
position: 10906905
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10973733:-1
position: 10973733
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:10973723-10973733:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:10971292-10971345:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:10970009-10970062:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:10952913-10952963:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:10951266-10951427:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:10944668-10944787:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:10942921-10943020:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:10942711-10942774:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:10941908-10941972:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:10934937-10934997:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:10934039-10934120:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:10933852-10933940:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:10921934-10921995:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:10920084-10920164:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:10916370-10916475:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:10914363-10914442:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:10910307-10910399:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:10908825-10908895:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:10906905-10907040:-1/exon

TPTE
type: SO_0000316
alternative label: CT44
alternative label: PTEN2
gene: TPTE
gene synonym: CT44; PTEN2
inference: similar to AA sequence (same species):RefSeq:NP_954868.1
exception: annotated by transcript or proteomic data
note: isoform beta is encoded by transcript variant 2; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: putative tyrosine-protein phosphatase TPTE isoform beta
translation: MNESPDPTDLAGVIIELGPNDSPQTSEFKGATEEAPAKESVLARLSKFEVEDAENVASYDSKIKKIVHSIVSSFAFGLFGVFLVLLDVTLILADLIFTDSKLYIPLEYRSISLAIALFFLMDVLLRVFVERRQQYFSDLFNILDTAIIVILLLVDVVYIFFDIKLLRNIPRWTHLLRLLRLIILLRIFHLFHQKRQLEKLIRRRVSENKRRYTRDGFDLDLTYVTERIIAMSFPSSGRQSFYRNPIKEVVRFLDKKHRNHYRVYNLCSERAYDPKHFHNRVVRIMIDDHNVPTLHQMVVFTKEVNEWMAQDLENIVAIHCKGGTDRTGTMVCAFLIASEICSTAKESLYYFGERRTDKTHSEKFQGVETPSQKRYVAYFAQVKHLYNWNLPPRRILFIKHFIIYSIPRYVRDLKIQIEMEKKVVFSTISLGKCSVLDNITTDKILIDVFDGLPLYDDVKVQFFYSNLPTYYDNCSFYFWLHTSFIENNRLYLPKNELDNLHKQKARRIYPSDFAVEILFGEKMTSSDVVAGSD
so part of: TPTE
location: complement(join(10906905..10907040,10908825..10908895,10910307..10910399,10914363..10914442,10916370..10916475,10920084..10920164,10921934..10921995,10933852..10933940,10934039..10934120,10934937..10934997,10941908..10941972,10942711..10942774,10942921..10943020,10944668..10944787,10951266..10951427,10952913..10952963,10959741..10959800,10970009..10970062,10971292..10971345,10973723..10973733))
location: region:10906905-10973733:-1

NP_954868.1
SIO_000068: ncbiprotein

GI:40549433
SIO_000068: ncbigi

CCDS33512.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:10973723-10973733:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:10971292-10971345:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:10970009-10970062:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:10959741-10959800:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:10952913-10952963:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:10951266-10951427:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:10944668-10944787:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:10942921-10943020:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:10942711-10942774:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:10941908-10941972:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:10934937-10934997:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:10934039-10934120:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:10933852-10933940:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:10921934-10921995:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:10920084-10920164:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:10916370-10916475:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:10914363-10914442:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:10910307-10910399:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:10908825-10908895:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:10906905-10907040:-1/exon

TPTE
type: SO_0000316
alternative label: CT44
alternative label: PTEN2
gene: TPTE
gene synonym: CT44; PTEN2
inference: similar to AA sequence (same species):RefSeq:NP_954870.2
exception: annotated by transcript or proteomic data
note: isoform alpha is encoded by transcript variant 1; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: putative tyrosine-protein phosphatase TPTE isoform alpha
translation: MNESPDPTDLAGVIIELGPNDSPQTSEFKGATEEAPAKESPHTSEFKGAARVSPISESVLARLSKFEVEDAENVASYDSKIKKIVHSIVSSFAFGLFGVFLVLLDVTLILADLIFTDSKLYIPLEYRSISLAIALFFLMDVLLRVFVERRQQYFSDLFNILDTAIIVILLLVDVVYIFFDIKLLRNIPRWTHLLRLLRLIILLRIFHLFHQKRQLEKLIRRRVSENKRRYTRDGFDLDLTYVTERIIAMSFPSSGRQSFYRNPIKEVVRFLDKKHRNHYRVYNLCSERAYDPKHFHNRVVRIMIDDHNVPTLHQMVVFTKEVNEWMAQDLENIVAIHCKGGTDRTGTMVCAFLIASEICSTAKESLYYFGERRTDKTHSEKFQGVETPSQKRYVAYFAQVKHLYNWNLPPRRILFIKHFIIYSIPRYVRDLKIQIEMEKKVVFSTISLGKCSVLDNITTDKILIDVFDGLPLYDDVKVQFFYSNLPTYYDNCSFYFWLHTSFIENNRLYLPKNELDNLHKQKARRIYPSDFAVEILFGEKMTSSDVVAGSD
so part of: TPTE
location: complement(join(10906905..10907040,10908825..10908895,10910307..10910399,10914363..10914442,10916370..10916475,10920084..10920164,10921934..10921995,10933852..10933940,10934039..10934120,10934937..10934997,10941908..10941972,10942711..10942774,10942921..10943020,10944668..10944787,10951266..10951427,10952913..10952963,10959741..10959800,10969075..10969128,10970009..10970062,10971292..10971345,10973723..10973733))
location: region:10906905-10973733:-1

NP_954870.2
SIO_000068: ncbiprotein

GI:109689707
SIO_000068: ncbigi

CCDS13560.2
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:10973723-10973733:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:10971292-10971345:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:10970009-10970062:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:10969075-10969128:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:10959741-10959800:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:10952913-10952963:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:10951266-10951427:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:10944668-10944787:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:10942921-10943020:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:10942711-10942774:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:10941908-10941972:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:10934937-10934997:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:10934039-10934120:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:10933852-10933940:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:10921934-10921995:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:10920084-10920164:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:10916370-10916475:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:10914363-10914442:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:10910307-10910399:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:10908825-10908895:-1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:10906905-10907040:-1/exon

CYCSP41
type: SO_0000704
alternative label: CYC1LP4
alternative label: HCP41
gene: CYCSP41
gene synonym: CYC1LP4; HCP41
note: cytochrome c, somatic pseudogene 41; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(10935975..10936167)
location: region:10935975-10936167:-1

360186
SIO_000068: ncbigene

2580
SIO_000068: hgnc

position:10935975:-1
position: 10935975
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:10936167:-1
position: 10936167
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101926954
type: SO_0000704
gene: LOC101926954
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(11015038..11049525)
location: region:11015038-11049525:-1
SIO_010080: LOC101926954

101926954
SIO_000068: ncbigene

position:11015038:-1
position: 11015038
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11049525:-1
position: 11049525
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101926954
type: SO_0000234
gene: LOC101926954
product: histone-lysine N-methyltransferase 2C-like
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage by RNAseq alignments
transcript id: XM_005269267.1
so part of: LOC101926954
location: complement(join(11015038..11015102,11020813..11020917,11021110..11021211,11026723..11026839,11029598..11029717,11030491..11030527,11038784..11039429,11047481..11047595,11049450..11049525))
location: region:11015038-11049525:-1

GI:530427023
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:11049450-11049525:-1/exon

position:11049450:-1
position: 11049450
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:11047481-11047595:-1/exon

position:11047481:-1
position: 11047481
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11047595:-1
position: 11047595
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:11038784-11039429:-1/exon

position:11038784:-1
position: 11038784
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11039429:-1
position: 11039429
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:11030491-11030527:-1/exon

position:11030491:-1
position: 11030491
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11030527:-1
position: 11030527
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:11029598-11029717:-1/exon

position:11029598:-1
position: 11029598
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11029717:-1
position: 11029717
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:11026723-11026839:-1/exon

position:11026723:-1
position: 11026723
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11026839:-1
position: 11026839
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:11021110-11021211:-1/exon

position:11021110:-1
position: 11021110
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11021211:-1
position: 11021211
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:11020813-11020917:-1/exon

position:11020813:-1
position: 11020813
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11020917:-1
position: 11020917
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:11015038-11015102:-1/exon

position:11015102:-1
position: 11015102
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101926954
type: SO_0000316
gene: LOC101926954
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: histone-lysine N-methyltransferase 2C-like
translation: MQMNTELEKQISNEADSEEMKMSSEVKHICGEDQIEDKMEVTENIEVVTHQITVQQEQLQLLEEPKTVVSKEESRPPKFVIESVTLPLETLVSPHEESTSLCPEEQLVIERLQGEKEQKEDSELSTGLMDSEMTPTIEGCVKDVSYQGGKSIKLSSETESSFSLSADISKADVSSSPTPSSDLPSHDMLRNYPSALSSSAGNIMPTTYISVTPKNWHGLVQGIAECGCSEEAWSTHNTVSPPSWSPDISGGREIFKPRQLPGSAIWSIKVGHGSGFPRKRRPRGAGLSGRGGRGRSKLKSGIGAVVLPGVSTADISSNKDDEENSMHTTVVLFSSSDKFTLNQDMCVVCGSFGQGAEGRLLACSQCGQCYHPYCVSIKVCLVQTLWSNICRSKM
so part of: LOC101926954
location: complement(join(11015052..11015102,11020813..11020917,11021110..11021211,11026723..11026839,11029598..11029717,11030491..11030527,11038784..11039429,11047481..11047487))
location: region:11015052-11047487:-1

XP_005269324.1
SIO_000068: ncbiprotein

GI:530427024
SIO_000068: ncbigi

position:11015052:-1
position: 11015052
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11047487:-1
position: 11047487
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:11047481-11047487:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:11038784-11039429:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:11030491-11030527:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:11029598-11029717:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:11026723-11026839:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:11021110-11021211:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:11020813-11020917:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:11015052-11015102:-1/exon

BAGE2
type: SO_0000704
alternative label: CT2.2
gene: BAGE2
gene synonym: CT2.2
note: B melanoma antigen family, member 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(11020842..11098925)
location: region:11020842-11098925:-1
SIO_010080: BAGE2

85319
SIO_000068: ncbigene

15723
SIO_000068: hgnc

position:11020842:-1
position: 11020842
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11098925:-1
position: 11098925
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

BAGE2
type: SO_0000234
alternative label: CT2.2
gene: BAGE2
gene synonym: CT2.2
product: B melanoma antigen family, member 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_182482.2
so part of: BAGE2
location: complement(join(11020842..11020917,11021110..11021211,11026723..11026839,11029598..11029717,11038728..11039429,11047481..11047595,11049450..11049621,11058161..11058323,11097546..11097646,11098703..11098925))
location: region:11020842-11098925:-1

GI:154146182
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:11098703-11098925:-1/exon

position:11098703:-1
position: 11098703
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:11097546-11097646:-1/exon

position:11097546:-1
position: 11097546
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11097646:-1
position: 11097646
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:11058161-11058323:-1/exon

position:11058161:-1
position: 11058161
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11058323:-1
position: 11058323
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:11049450-11049621:-1/exon

position:11049621:-1
position: 11049621
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:11047481-11047595:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:11038728-11039429:-1/exon

position:11038728:-1
position: 11038728
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:11029598-11029717:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:11026723-11026839:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:11021110-11021211:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:11020842-11020917:-1/exon

BAGE2
type: SO_0000316
alternative label: CT2.2
gene: BAGE2
gene synonym: CT2.2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: B melanoma antigen 2 precursor
translation: MAAGVVFLALSAQLLQARLMKEESPVVSWRLEPEDGTALDVHFVSTLEPLSNAVKRNVPRCIIILVLQEPTPFRISVTSSCFVQNTLTKLLKDRRKMQTVQCATARETS
so part of: BAGE2
location: complement(join(11049571..11049621,11058161..11058323,11097546..11097646,11098703..11098717))
location: region:11049571-11098717:-1

NP_872288.2
SIO_000068: ncbiprotein

GI:154146183
SIO_000068: ncbigi

position:11049571:-1
position: 11049571
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11098717:-1
position: 11098717
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:11098703-11098717:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:11097546-11097646:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:11058161-11058323:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:11049571-11049621:-1/exon

VN1R7P
type: SO_0000704
alternative label: ORLP1
alternative label: PHB4C5
gene: VN1R7P
gene synonym: ORLP1; PHB4C5
note: vomeronasal 1 receptor 7 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(11153077..11154804)
location: region:11153077-11154804:-1

100132759
SIO_000068: ncbigene

8496
SIO_000068: hgnc

position:11153077:-1
position: 11153077
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11154804:-1
position: 11154804
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

EIF3FP1
type: SO_0000704
alternative label: EIF3FP
alternative label: EIF3S5P
gene: EIF3FP1
gene synonym: EIF3FP; EIF3S5P
note: eukaryotic translation initiation factor 3, subunit F pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(11180762..11181817)
location: region:11180762-11181817:-1
SIO_010080: EIF3FP1

54053
SIO_000068: ncbigene

3276
SIO_000068: hgnc

position:11180762:-1
position: 11180762
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:11181817:-1
position: 11181817
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

EIF3FP1
type: SO_0000147
alternative label: EIF3FP
alternative label: EIF3S5P
gene: EIF3FP1
gene synonym: EIF3FP; EIF3S5P
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: EIF3FP1
location: complement(11180762..11181817)
location: region:11180762-11181817:-1

ANKRD30BP2
type: SO_0000704
alternative label: C21orf99
alternative label: CT85
alternative label: CTSP-1
alternative label: CTSP1
gene: ANKRD30BP2
gene synonym: C21orf99; CT85; CTSP-1; CTSP1
note: ankyrin repeat domain 30B pseudogene 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 14410487..>14490572
location: region:14410487-14490572:1
SIO_010080: ANKRD30BP2

149992
SIO_000068: ncbigene

16620
SIO_000068: hgnc

position:14410487:1
position: 14410487
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14490572:1
position: 14490572
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: FuzzyPosition

ANKRD30BP2
type: SO_0000673
alternative label: C21orf99
alternative label: CT85
alternative label: CTSP-1
alternative label: CTSP1
gene: ANKRD30BP2
gene synonym: C21orf99; CT85; CTSP-1; CTSP1
product: ankyrin repeat domain 30B pseudogene 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
transcript id: NR_026916.1
so part of: ANKRD30BP2
location: join(14410487..14410745,14414823..14414937,14415100..14415273,14417484..14417591,14421286..14421350,14424117..14425023,14432787..14433204,14435161..14435279,14437496..14438020,14439173..14439369,14441496..14441613,14490159..>14490572)
location: region:14410487-14490572:1

GI:223941873
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:14410487-14410745:1/exon

position:14410745:1
position: 14410745
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:14414823-14414937:1/exon

position:14414823:1
position: 14414823
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14414937:1
position: 14414937
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:14415100-14415273:1/exon

position:14415100:1
position: 14415100
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14415273:1
position: 14415273
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:14417484-14417591:1/exon

position:14417484:1
position: 14417484
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14417591:1
position: 14417591
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:14421286-14421350:1/exon

position:14421286:1
position: 14421286
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14421350:1
position: 14421350
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:14424117-14425023:1/exon

position:14424117:1
position: 14424117
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14425023:1
position: 14425023
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:14432787-14433204:1/exon

position:14432787:1
position: 14432787
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14433204:1
position: 14433204
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:14435161-14435279:1/exon

position:14435161:1
position: 14435161
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14435279:1
position: 14435279
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:14437496-14438020:1/exon

position:14437496:1
position: 14437496
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14438020:1
position: 14438020
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:14439173-14439369:1/exon

position:14439173:1
position: 14439173
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14439369:1
position: 14439369
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:14441496-14441613:1/exon

position:14441496:1
position: 14441496
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14441613:1
position: 14441613
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:14490159-14490572:1/exon

position:14490159:1
position: 14490159
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

VN1R109P
type: SO_0000704
gene: VN1R109P
note: vomeronasal 1 receptor 109 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(14463937..14464410)
location: region:14463937-14464410:-1

100312851
SIO_000068: ncbigene

37434
SIO_000068: hgnc

position:14463937:-1
position: 14463937
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:14464410:-1
position: 14464410
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ZNF355P
type: SO_0000704
alternative label: PRED65
alternative label: ZNF834
gene: ZNF355P
gene synonym: PRED65; ZNF834
note: zinc finger protein 355, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(14468106..14529382)
location: region:14468106-14529382:-1

100505852
SIO_000068: ncbigene

17218
SIO_000068: hgnc

position:14468106:-1
position: 14468106
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:14529382:-1
position: 14529382
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101928467
type: SO_0000704
gene: LOC101928467
note: Derived by automated computational analysis using gene prediction method: Gnomon.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 14490806..14493128
location: region:14490806-14493128:1
SIO_010080: LOC101928467

101928467
SIO_000068: ncbigene

position:14490806:1
position: 14490806
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14493128:1
position: 14493128
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101928467
type: SO_0000147
gene: LOC101928467
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 24% coverage by RNAseq alignments
number: 1
pseudo: true
so part of: LOC101928467
location: 14490806..14490925
location: region:14490806-14490925:1

position:14490925:1
position: 14490925
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101928467
type: SO_0000147
gene: LOC101928467
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 24% coverage by RNAseq alignments
number: 2
pseudo: true
so part of: LOC101928467
location: 14492541..14493128
location: region:14492541-14493128:1

position:14492541:1
position: 14492541
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

FGF7P2
type: SO_0000704
alternative label: FGF7L
alternative label: PRED3
gene: FGF7P2
gene synonym: FGF7L; PRED3
note: fibroblast growth factor 7 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 14721586..14725781
location: region:14721586-14725781:1
SIO_010080: FGF7P2

394217
SIO_000068: ncbigene

17193
SIO_000068: hgnc

position:14721586:1
position: 14721586
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14725781:1
position: 14725781
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

FGF7P2
type: SO_0000147
alternative label: FGF7L
alternative label: PRED3
gene: FGF7P2
gene synonym: FGF7L; PRED3
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: FGF7P2
location: 14721586..14721689
location: region:14721586-14721689:1

position:14721689:1
position: 14721689
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ANKRD30BP1
type: SO_0000704
alternative label: ANKRD30BP
alternative label: C21orf110
alternative label: PRED4
gene: ANKRD30BP1
gene synonym: ANKRD30BP; C21orf110; PRED4
note: ankyrin repeat domain 30B pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(14756163..14800096)
location: region:14756163-14800096:-1

642460
SIO_000068: ncbigene

19722
SIO_000068: hgnc

position:14756163:-1
position: 14756163
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:14800096:-1
position: 14800096
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MIR3156-3
type: SO_0000704
gene: MIR3156-3
note: microRNA 3156-3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(14778705..14778781)
location: region:14778705-14778781:-1
SIO_010080: MIR3156-3

100423018
SIO_000068: ncbigene

38229
SIO_000068: hgnc

MI0014242
SIO_000068: mirbase

position:14778705:-1
position: 14778705
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:14778781:-1
position: 14778781
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MIR3156-3
type: SO_0000185
gene: MIR3156-3
product: microRNA 3156-3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_036164.1
so part of: MIR3156-3
location: complement(14778705..14778781)
location: region:14778705-14778781:-1

GI:302129674
SIO_000068: ncbigi

MIR3156-3
type: SO_0000655
gene: MIR3156-3
nc RNA class: miRNA
product: hsa-miR-3156-5p
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR3156-3
location: complement(14778752..14778773)
location: region:14778752-14778773:-1

MIMAT0015030
SIO_000068: mirbase

position:14778752:-1
position: 14778752
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:14778773:-1
position: 14778773
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

GTF2IP2
type: SO_0000704
gene: GTF2IP2
note: general transcription factor IIi, pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(14815675..14834792)
location: region:14815675-14834792:-1

338448
SIO_000068: ncbigene

16082
SIO_000068: hgnc

position:14815675:-1
position: 14815675
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:14834792:-1
position: 14834792
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

VN1R8P
type: SO_0000704
alternative label: ORLP2
gene: VN1R8P
gene synonym: ORLP2
note: vomeronasal 1 receptor 8 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 14848562..14849776
location: region:14848562-14849776:1

54041
SIO_000068: ncbigene

8497
SIO_000068: hgnc

position:14848562:1
position: 14848562
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14849776:1
position: 14849776
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

SNX19P1
type: SO_0000704
alternative label: SNX19P
gene: SNX19P1
gene synonym: SNX19P
note: sorting nexin 19 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 14897424..14902332
location: region:14897424-14902332:1
SIO_010080: SNX19P1

378810
SIO_000068: ncbigene

16765
SIO_000068: hgnc

position:14897424:1
position: 14897424
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14902332:1
position: 14902332
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

SNX19P1
type: SO_0000147
alternative label: SNX19P
gene: SNX19P1
gene synonym: SNX19P
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: SNX19P1
location: 14897424..14902332
location: region:14897424-14902332:1

OR4K11P
type: SO_0000704
alternative label: OR21-1
gene: OR4K11P
gene synonym: OR21-1
note: olfactory receptor, family 4, subfamily K, member 11 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(14916552..14917506)
location: region:14916552-14917506:-1

81079
SIO_000068: ncbigene

15402
SIO_000068: hgnc

position:14916552:-1
position: 14916552
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:14917506:-1
position: 14917506
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

OR4K12P
type: SO_0000704
alternative label: OR21-2
gene: OR4K12P
gene synonym: OR21-2
note: olfactory receptor, family 4, subfamily K, member 12 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(14953393..14954325)
location: region:14953393-14954325:-1

81078
SIO_000068: ncbigene

15403
SIO_000068: hgnc

position:14953393:-1
position: 14953393
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:14954325:-1
position: 14954325
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

POTED
type: SO_0000704
alternative label: A26B3
alternative label: ANKRD21
alternative label: CT104.1
alternative label: POTE
alternative label: POTE-21
alternative label: POTE21
gene: POTED
gene synonym: A26B3; ANKRD21; CT104.1; POTE; POTE-21; POTE21
note: POTE ankyrin domain family, member D; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 14982498..15013937
location: region:14982498-15013937:1
SIO_010080: POTED

317754
SIO_000068: ncbigene

23822
SIO_000068: hgnc

607549
SIO_000068: omim

position:14982498:1
position: 14982498
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15013937:1
position: 15013937
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

POTED
type: SO_0000234
alternative label: A26B3
alternative label: ANKRD21
alternative label: CT104.1
alternative label: POTE
alternative label: POTE-21
alternative label: POTE21
gene: POTED
gene synonym: A26B3; ANKRD21; CT104.1; POTE; POTE-21; POTE21
product: POTE ankyrin domain family, member D
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_174981.3
so part of: POTED
location: join(14982498..14983070,14987444..14987558,14987718..14987891,14990670..14990776,14992479..14992616,14995126..14995196,15000703..15000773,15002177..15002221,15003262..15003428,15011836..15011959,15013666..15013906)
location: region:14982498-15013906:1

GI:153792283
SIO_000068: ncbigi

position:15013906:1
position: 15013906
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:14982498-14983070:1/exon

position:14983070:1
position: 14983070
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:14987444-14987558:1/exon

position:14987444:1
position: 14987444
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14987558:1
position: 14987558
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:14987718-14987891:1/exon

position:14987718:1
position: 14987718
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14987891:1
position: 14987891
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:14990670-14990776:1/exon

position:14990670:1
position: 14990670
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14990776:1
position: 14990776
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:14992479-14992616:1/exon

position:14992479:1
position: 14992479
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14992616:1
position: 14992616
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:14995126-14995196:1/exon

position:14995126:1
position: 14995126
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:14995196:1
position: 14995196
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:15000703-15000773:1/exon

position:15000703:1
position: 15000703
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15000773:1
position: 15000773
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:15002177-15002221:1/exon

position:15002177:1
position: 15002177
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15002221:1
position: 15002221
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:15003262-15003428:1/exon

position:15003262:1
position: 15003262
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15003428:1
position: 15003428
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:15011836-15011959:1/exon

position:15011836:1
position: 15011836
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15011959:1
position: 15011959
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:15013666-15013906:1/exon

position:15013666:1
position: 15013666
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

POTED
type: SO_0000234
alternative label: A26B3
alternative label: ANKRD21
alternative label: CT104.1
alternative label: POTE
alternative label: POTE-21
alternative label: POTE21
gene: POTED
gene synonym: A26B3; ANKRD21; CT104.1; POTE; POTE-21; POTE21
product: POTE ankyrin domain family, member D, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 EST, 5 Proteins, and 92% coverage by RNAseq alignments
transcript id: XM_005260963.1
so part of: POTED
location: join(14982510..14982737,14982837..14983070,14987444..14987558,14987718..14987891,14990670..14990776,14992479..14992616,14995126..14995196,15000703..15000773,15002177..15002221,15003262..15003428,15011836..15011959,15013666..15013937)
location: region:14982510-15013937:1

GI:530418872
SIO_000068: ncbigi

position:14982510:1
position: 14982510
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:14982510-14982737:1/exon

position:14982737:1
position: 14982737
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:14982837-14983070:1/exon

position:14982837:1
position: 14982837
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:14987444-14987558:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:14987718-14987891:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:14990670-14990776:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:14992479-14992616:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:14995126-14995196:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15000703-15000773:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15002177-15002221:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15003262-15003428:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:15011836-15011959:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:15013666-15013937:1/exon

POTED
type: SO_0000316
alternative label: A26B3
alternative label: ANKRD21
alternative label: CT104.1
alternative label: POTE
alternative label: POTE-21
alternative label: POTE21
gene: POTED
gene synonym: A26B3; ANKRD21; CT104.1; POTE; POTE-21; POTE21
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: POTE ankyrin domain family member D
translation: MVAEVCSMPTASTVKKPFDLRSKMGKWCHHRFPCCRGSGKSNMGTSGDHDDSFMKMLRSKMGKCCRHCFPCCRGSGTSNVGTSGDHENSFMKMLRSKMGKWCCHCFPCCRGSGKSNVGAWGDYDHSAFMEPRYHIRREDLDKLHRAAWWGKVPRKDLIVMLRDTDMNKRDKEKRTALHLASANGNSEVVQLLLDRRCQLNVLDNKKRTALIKAIQCQEDECVLMLLEHGADRNIPDEYGNTALHYAIYNEDKLMAKALLLYGADIESKNKCGLTPLLLGVHEQKQQVVKFLIKKKANLNVLDRYGRTALILAVCCGSASIVNLLLEQNVDVSSQDLSGQTAREYAVSSHHHVICELLSDYKEKQMLKISSENSNPEQDLKLTSEEESQRLKVSENSQPEKMSQEPEINKDCDREVEEEIKKHGSNPVGLPENLTNGASAGNGDDGLIPQRRSRKPENQQFPDTENEEYHSDEQNDTRKQLSEEQNTGISQDEILTNKQKQIEVAEQKMNSELSLSHKKEEDLLRENSVLQEEIAMLRLELDETKHQNQLRENKILEEIESVKEKTDKLLRAMQLNEEALTKTNI
so part of: POTED
location: join(14982550..14983070,14987444..14987558,14987718..14987891,14990670..14990776,14992479..14992616,14995126..14995196,15000703..15000773,15002177..15002221,15003262..15003428,15011836..15011959,15013666..15013887)
location: region:14982550-15013887:1

NP_778146.2
SIO_000068: ncbiprotein

GI:153792284
SIO_000068: ncbigi

CCDS13562.1
SIO_000068: ccds

position:14982550:1
position: 14982550
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15013887:1
position: 15013887
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:14982550-14983070:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:14987444-14987558:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:14987718-14987891:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:14990670-14990776:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:14992479-14992616:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:14995126-14995196:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15000703-15000773:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15002177-15002221:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15003262-15003428:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15011836-15011959:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:15013666-15013887:1/exon

POTED
type: SO_0000316
alternative label: A26B3
alternative label: ANKRD21
alternative label: CT104.1
alternative label: POTE
alternative label: POTE-21
alternative label: POTE21
gene: POTED
gene synonym: A26B3; ANKRD21; CT104.1; POTE; POTE-21; POTE21
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: POTE ankyrin domain family member D isoform X1
translation: MVAEVCSMPTASTVKKPFDLRSKMGKWCHHRFPCCRGSGKSNMGTSGDHDDSFMKMLRSKMGNKMGKWCCHCFPCCRGSGKSNVGAWGDYDHSAFMEPRYHIRREDLDKLHRAAWWGKVPRKDLIVMLRDTDMNKRDKEKRTALHLASANGNSEVVQLLLDRRCQLNVLDNKKRTALIKAIQCQEDECVLMLLEHGADRNIPDEYGNTALHYAIYNEDKLMAKALLLYGADIESKNKCGLTPLLLGVHEQKQQVVKFLIKKKANLNVLDRYGRTALILAVCCGSASIVNLLLEQNVDVSSQDLSGQTAREYAVSSHHHVICELLSDYKEKQMLKISSENSNPEQDLKLTSEEESQRLKVSENSQPEKMSQEPEINKDCDREVEEEIKKHGSNPVGLPENLTNGASAGNGDDGLIPQRRSRKPENQQFPDTENEEYHSDEQNDTRKQLSEEQNTGISQDEILTNKQKQIEVAEQKMNSELSLSHKKEEDLLRENSVLQEEIAMLRLELDETKHQNQLRENKILEEIESVKEKTDKLLRAMQLNEEALTKTNI
so part of: POTED
location: join(14982550..14982737,14982837..14983070,14987444..14987558,14987718..14987891,14990670..14990776,14992479..14992616,14995126..14995196,15000703..15000773,15002177..15002221,15003262..15003428,15011836..15011959,15013666..15013887)
location: region:14982550-15013887:1

XP_005261020.1
SIO_000068: ncbiprotein

GI:530418873
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:14982550-14982737:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:14982837-14983070:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:14987444-14987558:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:14987718-14987891:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:14990670-14990776:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:14992479-14992616:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:14995126-14995196:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15000703-15000773:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15002177-15002221:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15003262-15003428:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:15011836-15011959:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:15013666-15013887:1/exon

MIR3118-5
type: SO_0000704
gene: MIR3118-5
note: microRNA 3118-5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15017096..15017171)
location: region:15017096-15017171:-1
SIO_010080: MIR3118-5

100422890
SIO_000068: ncbigene

38351
SIO_000068: hgnc

MI0014243
SIO_000068: mirbase

position:15017096:-1
position: 15017096
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15017171:-1
position: 15017171
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MIR3118-5
type: SO_0000185
gene: MIR3118-5
product: microRNA 3118-5
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_036165.1
so part of: MIR3118-5
location: complement(15017096..15017171)
location: region:15017096-15017171:-1

GI:301171791
SIO_000068: ncbigi

MIR3118-5
type: SO_0000655
gene: MIR3118-5
nc RNA class: miRNA
product: hsa-miR-3118
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR3118-5
location: complement(15017105..15017127)
location: region:15017105-15017127:-1

MIMAT0014980
SIO_000068: mirbase

position:15017105:-1
position: 15017105
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15017127:-1
position: 15017127
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100631252
type: SO_0000704
gene: LOC100631252
note: GRAM domain containing 4 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15038188..15039878)
location: region:15038188-15039878:-1

100631252
SIO_000068: ncbigene

position:15038188:-1
position: 15038188
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15039878:-1
position: 15039878
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

CXADRP1
type: SO_0000704
alternative label: CAR
alternative label: CXADRP
gene: CXADRP1
gene synonym: CAR; CXADRP
note: coxsackie virus and adenovirus receptor pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15048262..15050713
location: region:15048262-15050713:1

653108
SIO_000068: ncbigene

23770
SIO_000068: hgnc

position:15048262:1
position: 15048262
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15050713:1
position: 15050713
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC441956
type: SO_0000704
gene: LOC441956
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15051627..15053453)
location: region:15051627-15053453:-1
SIO_010080: LOC441956

441956
SIO_000068: ncbigene

position:15051627:-1
position: 15051627
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15053453:-1
position: 15053453
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC441956
type: SO_0000673
gene: LOC441956
product: uncharacterized LOC441956
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 7% coverage by RNAseq alignments
transcript id: XR_109656.2
so part of: LOC441956
location: complement(15051627..15053453)
location: region:15051627-15053453:-1

GI:530419142
SIO_000068: ncbigi

LOC101927669
type: SO_0000704
gene: LOC101927669
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15095912..15097393
location: region:15095912-15097393:1
SIO_010080: LOC101927669

101927669
SIO_000068: ncbigene

position:15095912:1
position: 15095912
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15097393:1
position: 15097393
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927669
type: SO_0000673
gene: LOC101927669
product: uncharacterized LOC101927669
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XR_244292.1
so part of: LOC101927669
location: join(15095912..15096040,15096377..15096555,15097378..15097393)
location: region:15095912-15097393:1

GI:530419143
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15095912-15096040:1/exon

position:15096040:1
position: 15096040
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15096377-15096555:1/exon

position:15096377:1
position: 15096377
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15096555:1
position: 15096555
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15097378-15097393:1/exon

position:15097378:1
position: 15097378
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

FEM1AP1
type: SO_0000704
alternative label: FEM1DP
gene: FEM1AP1
gene synonym: FEM1DP
note: fem-1 homolog a (C. elegans) pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15134659..15136650
location: region:15134659-15136650:1

441957
SIO_000068: ncbigene

17219
SIO_000068: hgnc

position:15134659:1
position: 15134659
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15136650:1
position: 15136650
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

TERF1P1
type: SO_0000704
alternative label: TERF1P
gene: TERF1P1
gene synonym: TERF1P
note: telomeric repeat binding factor (NIMA-interacting) 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15148407..15151133
location: region:15148407-15151133:1
SIO_010080: TERF1P1

348567
SIO_000068: ncbigene

16733
SIO_000068: hgnc

position:15148407:1
position: 15148407
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15151133:1
position: 15151133
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

TERF1P1
type: SO_0000147
alternative label: TERF1P
gene: TERF1P1
gene synonym: TERF1P
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: TERF1P1
location: 15148407..15151133
location: region:15148407-15151133:1

FAM207CP
type: SO_0000704
gene: FAM207CP
note: family with sequence similarity 207, member C; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15164956..15165459
location: region:15164956-15165459:1

727987
SIO_000068: ncbigene

42676
SIO_000068: hgnc

position:15164956:1
position: 15164956
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15165459:1
position: 15165459
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC654338
type: SO_0000704
gene: LOC654338
note: brain cytoplasmic RNA 1 (non-protein coding) pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15181878..15182080)
location: region:15181878-15182080:-1
SIO_010080: LOC654338

654338
SIO_000068: ncbigene

position:15181878:-1
position: 15181878
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15182080:-1
position: 15182080
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC654338
type: SO_0000147
gene: LOC654338
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: LOC654338
location: complement(15181878..15182080)
location: region:15181878-15182080:-1

GXYLT1P2
type: SO_0000704
gene: GXYLT1P2
note: glucoside xylosyltransferase 1 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15195992..15197975)
location: region:15195992-15197975:-1

441958
SIO_000068: ncbigene

39677
SIO_000068: hgnc

position:15195992:-1
position: 15195992
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15197975:-1
position: 15197975
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

CNN2P7
type: SO_0000704
gene: CNN2P7
note: calponin 2 pseudogene 7; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15199018..15199945
location: region:15199018-15199945:1

391266
SIO_000068: ncbigene

39532
SIO_000068: hgnc

position:15199018:1
position: 15199018
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15199945:1
position: 15199945
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ZNF114P1
type: SO_0000704
gene: ZNF114P1
note: zinc finger protein 114 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15211051..15212115
location: region:15211051-15212115:1

100132509
SIO_000068: ncbigene

23771
SIO_000068: hgnc

position:15211051:1
position: 15211051
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15212115:1
position: 15212115
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

C21orf15
type: SO_0000704
gene: C21orf15
note: chromosome 21 open reading frame 15; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(<15215454..15220685)
location: region:15215454-15220685:-1
SIO_010080: C21orf15

54094
SIO_000068: ncbigene

1257
SIO_000068: hgnc

position:15215454:-1
position: 15215454
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: FuzzyPosition

position:15220685:-1
position: 15220685
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C21orf15
type: SO_0000673
gene: C21orf15
product: chromosome 21 open reading frame 15
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_026755.1
so part of: C21orf15
location: complement(join(<15215454..15215753,15216343..15216456,15217326..15217595,15218334..15218462,15219080..15219270,15220411..15220685))
location: region:15215454-15220685:-1

GI:223029445
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15220411-15220685:-1/exon

position:15220411:-1
position: 15220411
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15219080-15219270:-1/exon

position:15219080:-1
position: 15219080
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15219270:-1
position: 15219270
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15218334-15218462:-1/exon

position:15218334:-1
position: 15218334
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15218462:-1
position: 15218462
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:15217326-15217595:-1/exon

position:15217326:-1
position: 15217326
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15217595:-1
position: 15217595
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:15216343-15216456:-1/exon

position:15216343:-1
position: 15216343
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15216456:-1
position: 15216456
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:15215454-15215753:-1/exon

position:15215753:-1
position: 15215753
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

CYP4F29P
type: SO_0000704
alternative label: C21orf15
alternative label: CYP4F3LP
gene: CYP4F29P
gene synonym: C21orf15; CYP4F3LP
note: cytochrome P450, family 4, subfamily F, polypeptide 29, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15218979..15220176)
location: region:15218979-15220176:-1

54055
SIO_000068: ncbigene

2647
SIO_000068: hgnc

position:15218979:-1
position: 15218979
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15220176:-1
position: 15220176
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

SNX18P13
type: SO_0000704
gene: SNX18P13
note: sorting nexin 18 pseudogene 13; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15278059..15279641)
location: region:15278059-15279641:-1

100419042
SIO_000068: ncbigene

39621
SIO_000068: hgnc

position:15278059:-1
position: 15278059
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15279641:-1
position: 15279641
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100996622
type: SO_0000704
gene: LOC100996622
note: Derived by automated computational analysis using gene prediction method: Gnomon.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15282752..15306238)
location: region:15282752-15306238:-1
SIO_010080: LOC100996622

100996622
SIO_000068: ncbigene

position:15282752:-1
position: 15282752
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15306238:-1
position: 15306238
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100996622
type: SO_0000147
gene: LOC100996622
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 92% coverage by RNAseq alignments
number: 8
pseudo: true
so part of: LOC100996622
location: complement(15282752..15282870)
location: region:15282752-15282870:-1

position:15282870:-1
position: 15282870
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100996622
type: SO_0000147
gene: LOC100996622
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 92% coverage by RNAseq alignments
number: 7
pseudo: true
so part of: LOC100996622
location: complement(15284039..15284084)
location: region:15284039-15284084:-1

position:15284039:-1
position: 15284039
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15284084:-1
position: 15284084
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100996622
type: SO_0000147
gene: LOC100996622
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 92% coverage by RNAseq alignments
number: 6
pseudo: true
so part of: LOC100996622
location: complement(15287508..15287730)
location: region:15287508-15287730:-1

position:15287508:-1
position: 15287508
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15287730:-1
position: 15287730
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100996622
type: SO_0000147
gene: LOC100996622
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 92% coverage by RNAseq alignments
number: 5
pseudo: true
so part of: LOC100996622
location: complement(15289068..15289279)
location: region:15289068-15289279:-1

position:15289068:-1
position: 15289068
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15289279:-1
position: 15289279
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100996622
type: SO_0000147
gene: LOC100996622
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 92% coverage by RNAseq alignments
number: 4
pseudo: true
so part of: LOC100996622
location: complement(15289876..15290157)
location: region:15289876-15290157:-1

position:15289876:-1
position: 15289876
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15290157:-1
position: 15290157
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100996622
type: SO_0000147
gene: LOC100996622
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 92% coverage by RNAseq alignments
number: 3
pseudo: true
so part of: LOC100996622
location: complement(15297485..15297614)
location: region:15297485-15297614:-1

position:15297485:-1
position: 15297485
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15297614:-1
position: 15297614
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100996622
type: SO_0000147
gene: LOC100996622
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 92% coverage by RNAseq alignments
number: 2
pseudo: true
so part of: LOC100996622
location: complement(15304549..15304695)
location: region:15304549-15304695:-1

position:15304549:-1
position: 15304549
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15304695:-1
position: 15304695
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100996622
type: SO_0000147
gene: LOC100996622
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 92% coverage by RNAseq alignments
number: 1
pseudo: true
so part of: LOC100996622
location: complement(15306159..15306238)
location: region:15306159-15306238:-1

position:15306159:-1
position: 15306159
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

RHOT1P2
type: SO_0000704
gene: RHOT1P2
note: ras homolog family member T1 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15309314..15309646)
location: region:15309314-15309646:-1

100462811
SIO_000068: ncbigene

37838
SIO_000068: hgnc

position:15309314:-1
position: 15309314
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15309646:-1
position: 15309646
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ANKRD20A11P
type: SO_0000704
alternative label: C21orf81
gene: ANKRD20A11P
gene synonym: C21orf81
note: ankyrin repeat domain 20 family, member A11, pseudogene; Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15316090..15352765)
location: region:15316090-15352765:-1
SIO_010080: ANKRD20A11P

391267
SIO_000068: ncbigene

42024
SIO_000068: hgnc

position:15316090:-1
position: 15316090
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15352765:-1
position: 15352765
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ANKRD20A11P
type: SO_0000673
alternative label: C21orf81
gene: ANKRD20A11P
gene synonym: C21orf81
product: ankyrin repeat domain 20 family, member A11, pseudogene
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
transcript id: NR_027270.1
so part of: ANKRD20A11P
location: complement(join(15316090..15316183,15317360..15317430,15323388..15323460,15323553..15323581,15326387..15326471,15352023..15352765))
location: region:15316090-15352765:-1

GI:224586828
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15352023-15352765:-1/exon

position:15352023:-1
position: 15352023
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15326387-15326471:-1/exon

position:15326387:-1
position: 15326387
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15326471:-1
position: 15326471
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15323553-15323581:-1/exon

position:15323553:-1
position: 15323553
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15323581:-1
position: 15323581
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:15323388-15323460:-1/exon

position:15323388:-1
position: 15323388
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15323460:-1
position: 15323460
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:15317360-15317430:-1/exon

position:15317360:-1
position: 15317360
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15317430:-1
position: 15317430
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:15316090-15316183:-1/exon

position:15316183:-1
position: 15316183
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

NF1P3
type: SO_0000704
alternative label: NF1L1
gene: NF1P3
gene synonym: NF1L1
note: neurofibromin 1 pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15373246..15377600
location: region:15373246-15377600:1

4764
SIO_000068: ncbigene

7766
SIO_000068: hgnc

position:15373246:1
position: 15373246
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15377600:1
position: 15377600
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

PPP6R2P1
type: SO_0000704
gene: PPP6R2P1
note: protein phosphatase 6, regulatory subunit 2 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15379456..15387163
location: region:15379456-15387163:1

100631381
SIO_000068: ncbigene

39605
SIO_000068: hgnc

position:15379456:1
position: 15379456
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15387163:1
position: 15387163
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ANKRD20A18P
type: SO_0000704
alternative label: C21orf126
gene: ANKRD20A18P
gene synonym: C21orf126
note: ankyrin repeat domain 20 family, member A18, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15436540..15441409
location: region:15436540-15441409:1

391269
SIO_000068: ncbigene

23756
SIO_000068: hgnc

position:15436540:1
position: 15436540
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15441409:1
position: 15441409
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

RNA5SP488
type: SO_0000704
alternative label: RN5S488
gene: RNA5SP488
gene synonym: RN5S488
note: RNA, 5S ribosomal pseudogene 488; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15443192..15443307
location: region:15443192-15443307:1

100873730
SIO_000068: ncbigene

43388
SIO_000068: hgnc

position:15443192:1
position: 15443192
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15443307:1
position: 15443307
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ERLEC1P1
type: SO_0000704
gene: ERLEC1P1
note: endoplasmic reticulum lectin 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15451295..15516788
location: region:15451295-15516788:1

100288870
SIO_000068: ncbigene

38012
SIO_000068: hgnc

position:15451295:1
position: 15451295
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15516788:1
position: 15516788
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LIPI
type: SO_0000704
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
note: lipase, member I; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15480784..15583361)
location: region:15480784-15583361:-1
SIO_010080: LIPI

149998
SIO_000068: ncbigene

18821
SIO_000068: hgnc

14193
SIO_000068: hprd

609252
SIO_000068: omim

position:15480784:-1
position: 15480784
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15583361:-1
position: 15583361
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LIPI
type: SO_0000234
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
product: lipase, member I, transcript variant X5
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 100% coverage by RNAseq alignments
transcript id: XM_005260924.1
so part of: LIPI
location: complement(join(15480784..15481401,15535740..15535844,15537544..15537711,15538683..15538772,15554079..15554180,15558282..15558390,15561355..15561740,15583121..15583361))
location: region:15480784-15583361:-1

GI:530418790
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15583121-15583361:-1/exon

position:15583121:-1
position: 15583121
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

position:15561355:-1
position: 15561355
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15561740:-1
position: 15561740
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

position:15558282:-1
position: 15558282
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15558390:-1
position: 15558390
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

position:15554079:-1
position: 15554079
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15554180:-1
position: 15554180
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:15538683-15538772:-1/exon

position:15538683:-1
position: 15538683
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15538772:-1
position: 15538772
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:15537544-15537711:-1/exon

position:15537544:-1
position: 15537544
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15537711:-1
position: 15537711
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:15535740-15535844:-1/exon

position:15535740:-1
position: 15535740
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15535844:-1
position: 15535844
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:15480784-15481401:-1/exon

position:15481401:-1
position: 15481401
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LIPI
type: SO_0000234
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
product: lipase, member I, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 ESTs, 1 Protein, and 100% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XM_005260922.1
so part of: LIPI
location: complement(join(15481134..15481401,15516944..15517120,15524894..15525005,15535740..15535844,15537544..15537711,15554079..15554180,15558282..15558390,15561355..15561740,15583121..15583361))
location: region:15481134-15583361:-1

GI:530418786
SIO_000068: ncbigi

position:15481134:-1
position: 15481134
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15583121-15583361:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15537544-15537711:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15535740-15535844:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15524894-15525005:-1/exon

position:15524894:-1
position: 15524894
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15525005:-1
position: 15525005
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:15516944-15517120:-1/exon

position:15516944:-1
position: 15516944
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15517120:-1
position: 15517120
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:15481134-15481401:-1/exon

LIPI
type: SO_0000234
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
product: lipase, member I, transcript variant X4
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 96% coverage by RNAseq alignments
transcript id: XM_005260923.1
so part of: LIPI
location: complement(join(15481134..15481401,15516944..15517120,15524894..15525005,15535740..15535844,15537544..15537606,15538683..15538772,15554079..15554180,15558282..15558390,15561355..15561740,15583121..15583361))
location: region:15481134-15583361:-1

GI:530418788
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15583121-15583361:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15538683-15538772:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15537544-15537606:-1/exon

position:15537606:-1
position: 15537606
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:15535740-15535844:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15524894-15525005:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15516944-15517120:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15481134-15481401:-1/exon

LIPI
type: SO_0000234
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
product: lipase, member I, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 100% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XM_005260921.1
so part of: LIPI
location: complement(join(15481134..15481401,15516944..15517120,15524894..15525005,15535758..15535844,15537544..15537711,15538683..15538772,15554079..15554180,15558282..15558390,15561355..15561740,15583121..15583361))
location: region:15481134-15583361:-1

GI:530418784
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15583121-15583361:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15538683-15538772:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15537544-15537711:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15535758-15535844:-1/exon

position:15535758:-1
position: 15535758
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:15524894-15525005:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15516944-15517120:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15481134-15481401:-1/exon

LIPI
type: SO_0000234
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
product: lipase, member I, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 ESTs, 2 Proteins, and 100% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XM_005260920.1
so part of: LIPI
location: complement(join(15481134..15481401,15516944..15517120,15524894..15525005,15535740..15535844,15537544..15537711,15538683..15538772,15554079..15554180,15558282..15558390,15561355..15561740,15583121..15583361))
location: region:15481134-15583361:-1

GI:530418782
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15583121-15583361:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15538683-15538772:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15537544-15537711:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15535740-15535844:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15524894-15525005:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15516944-15517120:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15481134-15481401:-1/exon

LIPI
type: SO_0000234
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
product: lipase, member I
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_198996.2
so part of: LIPI
location: complement(join(15481134..15481401,15516944..15517120,15524894..15525005,15535740..15535844,15537544..15537711,15538683..15538772,15554079..15554180,15558282..15558390,15561355..15561740,15579136..15579254))
location: region:15481134-15579254:-1

GI:61742625
SIO_000068: ncbigi

position:15579254:-1
position: 15579254
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15579136-15579254:-1/exon

position:15579136:-1
position: 15579136
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15538683-15538772:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15537544-15537711:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15535740-15535844:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15524894-15525005:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15516944-15517120:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15481134-15481401:-1/exon

LIPI
type: SO_0000316
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: lipase member I isoform X5
translation: MILPKRNLNELRNFLFGELSAVFAFLRFQMRVYIFLCLMCWVRSDNKRPCLEFSQLSVKDSFRDLFIPRIETILMMYTRNNLNCAEPLFEQNNSLNVNFNTQKKTVWLIHGYRPVGSIPLWLQNFVRILLNEEDMNVIVVDWSRGATTFIYNRAVKNTRKVAVSLSVHIKNLLKHGASLDNFHFIGVSLGAHISGFVGKIFHGQLGRITGLDPAGPRFSRKPPYSRLDYTDAKFVDVIHSDSNGLGIQEPLGHIDFYPNGGNKQPGCPKSIFSGIQFIKCNHQRAVHLFMASLETNCNFISFPCRSYKDYKTSLCVDCDCFKEKSCPRLGYQAKLFKGVLKERMEGRPLRTTVFLDTSGTYPFCNHHFAGIILYLKTERKCFLIQTHVHQRTHKMPSSIKCTCL
so part of: LIPI
location: complement(join(15481280..15481401,15535740..15535844,15537544..15537711,15538683..15538772,15554079..15554180,15558282..15558390,15561355..15561740,15583121..15583253))
location: region:15481280-15583253:-1

XP_005260981.1
SIO_000068: ncbiprotein

GI:530418791
SIO_000068: ncbigi

position:15481280:-1
position: 15481280
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15583253:-1
position: 15583253
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15583121-15583253:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15538683-15538772:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15537544-15537711:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15535740-15535844:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15481280-15481401:-1/exon

LIPI
type: SO_0000316
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: lipase member I isoform X3
translation: MILPKRNLNELRNFLFGELSAVFAFLRFQMRVYIFLCLMCWVRSDNKRPCLEFSQLSVKDSFRDLFIPRIETILMMYTRNNLNCAEPLFEQNNSLNVNFNTQKKTVWLIHGYRPVGSIPLWLQNFVRILLNEEDMNVIVVDWSRGATTFIYNRAVKNTRKVAVSLSVHIKNLLKHGASLDNFHFIGVSLGAHISGFVGKIFHGQLGRITGLDPAGPRFSRKPPYSRLDYTDAKFVDVIHSDSNGIQFIKCNHQRAVHLFMASLETNCNFISFPCRSYKDYKTSLCVDCDCFKEKSCPRLGYQAKLFKGVLKERMEGRPLRTTVFLDTSGTYPFCTYYFVLSIIVPDKTMMDGSFSFKLLNQLGMIEEPRLYEKNKPFYKLQEVKILAQFYNDFVNISSIGLTYFQSSNLQCSTCTYKIQRLMLKSLTYPERPPLCRYNIVLKDREEVFLNPNTCTPKNT
so part of: LIPI
location: complement(join(15481314..15481401,15516944..15517120,15524894..15525005,15535740..15535844,15537544..15537711,15554079..15554180,15558282..15558390,15561355..15561740,15583121..15583253))
location: region:15481314-15583253:-1

XP_005260979.1
SIO_000068: ncbiprotein

GI:530418787
SIO_000068: ncbigi

position:15481314:-1
position: 15481314
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15583121-15583253:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15537544-15537711:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15535740-15535844:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15524894-15525005:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15516944-15517120:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15481314-15481401:-1/exon

LIPI
type: SO_0000316
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: lipase member I isoform X4
translation: MILPKRNLNELRNFLFGELSAVFAFLRFQMRVYIFLCLMCWVRSDNKRPCLEFSQLSVKDSFRDLFIPRIETILMMYTRNNLNCAEPLFEQNNSLNVNFNTQKKTVWLIHGYRPVGSIPLWLQNFVRILLNEEDMNVIVVDWSRGATTFIYNRAVKNTRKVAVSLSVHIKNLLKHGASLDNFHFIGVSLGAHISGFVGKIFHGQLGRITGLDPAGPRFSRKPPYSRLDYTDAKFVDVIHSDSNGLGIQEPLGHIDFYPNGGNKQPGCPKSIFSDYKTSLCVDCDCFKEKSCPRLGYQAKLFKGVLKERMEGRPLRTTVFLDTSGTYPFCTYYFVLSIIVPDKTMMDGSFSFKLLNQLGMIEEPRLYEKNKPFYKLQEVKILAQFYNDFVNISSIGLTYFQSSNLQCSTCTYKIQRLMLKSLTYPERPPLCRYNIVLKDREEVFLNPNTCTPKNT
so part of: LIPI
location: complement(join(15481314..15481401,15516944..15517120,15524894..15525005,15535740..15535844,15537544..15537606,15538683..15538772,15554079..15554180,15558282..15558390,15561355..15561740,15583121..15583253))
location: region:15481314-15583253:-1

XP_005260980.1
SIO_000068: ncbiprotein

GI:530418789
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15583121-15583253:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15538683-15538772:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15537544-15537606:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15535740-15535844:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15524894-15525005:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15516944-15517120:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15481314-15481401:-1/exon

LIPI
type: SO_0000316
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: lipase member I isoform X2
translation: MILPKRNLNELRNFLFGELSAVFAFLRFQMRVYIFLCLMCWVRSDNKRPCLEFSQLSVKDSFRDLFIPRIETILMMYTRNNLNCAEPLFEQNNSLNVNFNTQKKTVWLIHGYRPVGSIPLWLQNFVRILLNEEDMNVIVVDWSRGATTFIYNRAVKNTRKVAVSLSVHIKNLLKHGASLDNFHFIGVSLGAHISGFVGKIFHGQLGRITGLDPAGPRFSRKPPYSRLDYTDAKFVDVIHSDSNGLGIQEPLGHIDFYPNGGNKQPGCPKSIFSGIQFIKCNHQRAVHLFMASLETNCNFISFPCRSYKDYKTSLCVDCDCFKEKSCPRLGYQAKLFKGVLKERMEGRPLRTTVFLDTSAYYFVLSIIVPDKTMMDGSFSFKLLNQLGMIEEPRLYEKNKPFYKLQEVKILAQFYNDFVNISSIGLTYFQSSNLQCSTCTYKIQRLMLKSLTYPERPPLCRYNIVLKDREEVFLNPNTCTPKNT
so part of: LIPI
location: complement(join(15481314..15481401,15516944..15517120,15524894..15525005,15535758..15535844,15537544..15537711,15538683..15538772,15554079..15554180,15558282..15558390,15561355..15561740,15583121..15583253))
location: region:15481314-15583253:-1

XP_005260978.1
SIO_000068: ncbiprotein

GI:530418785
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15583121-15583253:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15538683-15538772:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15537544-15537711:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15535758-15535844:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15524894-15525005:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15516944-15517120:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15481314-15481401:-1/exon

LIPI
type: SO_0000316
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: lipase member I isoform X1
translation: MILPKRNLNELRNFLFGELSAVFAFLRFQMRVYIFLCLMCWVRSDNKRPCLEFSQLSVKDSFRDLFIPRIETILMMYTRNNLNCAEPLFEQNNSLNVNFNTQKKTVWLIHGYRPVGSIPLWLQNFVRILLNEEDMNVIVVDWSRGATTFIYNRAVKNTRKVAVSLSVHIKNLLKHGASLDNFHFIGVSLGAHISGFVGKIFHGQLGRITGLDPAGPRFSRKPPYSRLDYTDAKFVDVIHSDSNGLGIQEPLGHIDFYPNGGNKQPGCPKSIFSGIQFIKCNHQRAVHLFMASLETNCNFISFPCRSYKDYKTSLCVDCDCFKEKSCPRLGYQAKLFKGVLKERMEGRPLRTTVFLDTSGTYPFCTYYFVLSIIVPDKTMMDGSFSFKLLNQLGMIEEPRLYEKNKPFYKLQEVKILAQFYNDFVNISSIGLTYFQSSNLQCSTCTYKIQRLMLKSLTYPERPPLCRYNIVLKDREEVFLNPNTCTPKNT
so part of: LIPI
location: complement(join(15481314..15481401,15516944..15517120,15524894..15525005,15535740..15535844,15537544..15537711,15538683..15538772,15554079..15554180,15558282..15558390,15561355..15561740,15583121..15583253))
location: region:15481314-15583253:-1

XP_005260977.1
SIO_000068: ncbiprotein

GI:530418783
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15583121-15583253:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15538683-15538772:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15537544-15537711:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15535740-15535844:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15524894-15525005:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15516944-15517120:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15481314-15481401:-1/exon

LIPI
type: SO_0000316
alternative label: CT17
alternative label: LPDL
alternative label: PLA1C
alternative label: PRED5
gene: LIPI
gene synonym: CT17; LPDL; PLA1C; PRED5
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: lipase member I
translation: MLLKCLHNNLCQKYSAHAFQFSPRNVLWLLVVCLRSDNKRPCLEFSQLSVKDSFRDLFIPRIETILMMYTRNNLNCAEPLFEQNNSLNVNFNTQKKTVWLIHGYRPVGSIPLWLQNFVRILLNEEDMNVIVVDWSRGATTFIYNRAVKNTRKVAVSLSVHIKNLLKHGASLDNFHFIGVSLGAHISGFVGKIFHGQLGRITGLDPAGPRFSRKPPYSRLDYTDAKFVDVIHSDSNGLGIQEPLGHIDFYPNGGNKQPGCPKSIFSGIQFIKCNHQRAVHLFMASLETNCNFISFPCRSYKDYKTSLCVDCDCFKEKSCPRLGYQAKLFKGVLKERMEGRPLRTTVFLDTSGTYPFCTYYFVLSIIVPDKTMMDGSFSFKLLNQLGMIEEPRLYEKNKPFYKLQEVKILAQFYNDFVNISSIGLTYFQSSNLQCSTCTYKIQRLMLKSLTYPERPPLCRYNIVLKDREEVFLNPNTCTPKNT
so part of: LIPI
location: complement(join(15481314..15481401,15516944..15517120,15524894..15525005,15535740..15535844,15537544..15537711,15538683..15538772,15554079..15554180,15558282..15558390,15561355..15561740,15579136..15579244))
location: region:15481314-15579244:-1

NP_945347.1
SIO_000068: ncbiprotein

GI:39752679
SIO_000068: ncbigi

CCDS13564.1
SIO_000068: ccds

position:15579244:-1
position: 15579244
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15579136-15579244:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15561355-15561740:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15558282-15558390:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15554079-15554180:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15538683-15538772:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15537544-15537711:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15535740-15535844:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15524894-15525005:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:15516944-15517120:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:15481314-15481401:-1/exon

RBM11
type: SO_0000704
gene: RBM11
note: RNA binding motif protein 11; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15588466..15600693
location: region:15588466-15600693:1
SIO_010080: RBM11

54033
SIO_000068: ncbigene

9897
SIO_000068: hgnc

position:15588466:1
position: 15588466
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15600693:1
position: 15600693
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

RBM11
type: SO_0000234
gene: RBM11
product: RNA binding motif protein 11
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_144770.3
so part of: RBM11
location: join(15588466..15588603,15591884..15592046,15593418..15593490,15596759..15596858,15599201..15600693)
location: region:15588466-15600693:1

GI:169234629
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15588466-15588603:1/exon

position:15588603:1
position: 15588603
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15591884-15592046:1/exon

position:15591884:1
position: 15591884
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15592046:1
position: 15592046
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15593418-15593490:1/exon

position:15593418:1
position: 15593418
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15593490:1
position: 15593490
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:15596759-15596858:1/exon

position:15596759:1
position: 15596759
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15596858:1
position: 15596858
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:15599201-15600693:1/exon

position:15599201:1
position: 15599201
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

RBM11
type: SO_0000234
gene: RBM11
product: RNA binding motif protein 11, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, and 100% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XM_005260997.1
so part of: RBM11
location: join(15588472..15588603,15591884..15592046,15593418..15593490,15596759..15596858,15599180..15599245,15599372..15600686)
location: region:15588472-15600686:1

GI:530418955
SIO_000068: ncbigi

position:15588472:1
position: 15588472
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15600686:1
position: 15600686
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15588472-15588603:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15591884-15592046:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15593418-15593490:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15596759-15596858:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15599180-15599245:1/exon

position:15599180:1
position: 15599180
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15599245:1
position: 15599245
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:15599372-15600686:1/exon

position:15599372:1
position: 15599372
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

RBM11
type: SO_0000234
gene: RBM11
product: RNA binding motif protein 11, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 100% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XM_005260996.1
so part of: RBM11
location: join(15588472..15588603,15591884..15592046,15593418..15593490,15596759..15596858,15599180..15600684)
location: region:15588472-15600684:1

GI:530418953
SIO_000068: ncbigi

position:15600684:1
position: 15600684
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15588472-15588603:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15591884-15592046:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15593418-15593490:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15596759-15596858:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15599180-15600684:1/exon

RBM11
type: SO_0000234
gene: RBM11
product: RNA binding motif protein 11, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 ESTs, 2 Proteins, and 100% coverage by RNAseq alignments, including 4 samples with support for all introns
transcript id: XM_005260998.1
so part of: RBM11
location: join(15588479..15588603,15591874..15592046,15593418..15593490,15596759..15596858,15599201..15600683)
location: region:15588479-15600683:1

GI:530418957
SIO_000068: ncbigi

position:15588479:1
position: 15588479
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15600683:1
position: 15600683
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15588479-15588603:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15591874-15592046:1/exon

position:15591874:1
position: 15591874
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15593418-15593490:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15596759-15596858:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15599201-15600683:1/exon

RBM11
type: SO_0000316
gene: RBM11
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: splicing regulator RBM11 isoform X1
translation: MFPAQEEADRTVFVGNLEARVREEILYELFLQAGPLTKVTICKDREGKPKSFGFVCFKHPESVSYAIALLNGIRLYGRPINVQYRFGSSRSSEPANQSFESCVKINSHNYRNEEMLVGRSSFPMQYFPINNTSLPQEYFLFQKMMNVLFSQQWHVYNPVLQLPYYEMTAPLPNSASVSSSLNHVPDLEAGPSSYKWTHQQPSDSDLYQMTAPLPNSASVSSSLNHVPDLEAGPSSYKWTHQQPSDSDLYQMNKRKRQKQTSDSDSSTDNNRGNECSQKFRKSKKKKRY
so part of: RBM11
location: join(15588508..15588603,15591884..15592046,15593418..15593490,15596759..15596858,15599180..15599614)
location: region:15588508-15599614:1

XP_005261053.1
SIO_000068: ncbiprotein

GI:530418954
SIO_000068: ncbigi

position:15588508:1
position: 15588508
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15599614:1
position: 15599614
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15588508-15588603:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15591884-15592046:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15593418-15593490:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15596759-15596858:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15599180-15599614:1/exon

RBM11
type: SO_0000316
gene: RBM11
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: splicing regulator RBM11 isoform X2
translation: MFPAQEEADRTVFVGNLEARVREEILYELFLQAGPLTKVTICKDREGKPKSFGFVCFKHPESVSYAIALLNGIRLYGRPINVQYRFGSSRSSEPANQSFESCVKINSHNYRNEEMLVGRSSFPMQYFPINNTSLPQEYFLFQKMMNVLFSQQWHVYNPVLQLPYYEMTAPLPNSASVSSSLNHVPDLEAGPSSYKWTHQQPSDSDLYQMNKRKRQKQTSDSDSSTDNNRGNECSQKFRKSKKKKRY
so part of: RBM11
location: join(15588508..15588603,15591884..15592046,15593418..15593490,15596759..15596858,15599180..15599245,15599372..15599614)
location: region:15588508-15599614:1

XP_005261054.1
SIO_000068: ncbiprotein

GI:530418956
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15588508-15588603:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15591884-15592046:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15593418-15593490:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15596759-15596858:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15599180-15599245:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15599372-15599614:1/exon

RBM11
type: SO_0000316
gene: RBM11
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: splicing regulator RBM11
translation: MFPAQEEADRTVFVGNLEARVREEILYELFLQAGPLTKVTICKDREGKPKSFGFVCFKHPESVSYAIALLNGIRLYGRPINVQYRFGSSRSSEPANQSFESCVKINSHNYRNEEMLVGRSSFPMQYFPINNTSLPQEYFLFQKMQWHVYNPVLQLPYYEMTAPLPNSASVSSSLNHVPDLEAGPSSYKWTHQQPSDSDLYQMTAPLPNSASVSSSLNHVPDLEAGPSSYKWTHQQPSDSDLYQMNKRKRQKQTSDSDSSTDNNRGNECSQKFRKSKKKKRY
so part of: RBM11
location: join(15588508..15588603,15591884..15592046,15593418..15593490,15596759..15596858,15599201..15599614)
location: region:15588508-15599614:1

NP_658983.3
SIO_000068: ncbiprotein

GI:169234630
SIO_000068: ncbigi

CCDS46635.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:15588508-15588603:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15591884-15592046:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15593418-15593490:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15596759-15596858:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15599201-15599614:1/exon

RBM11
type: SO_0000316
gene: RBM11
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: splicing regulator RBM11 isoform X3
translation: MLVGRSSFPMQYFPINNTSLPQEYFLFQKMQWHVYNPVLQLPYYEMTAPLPNSASVSSSLNHVPDLEAGPSSYKWTHQQPSDSDLYQMTAPLPNSASVSSSLNHVPDLEAGPSSYKWTHQQPSDSDLYQMNKRKRQKQTSDSDSSTDNNRGNECSQKFRKSKKKKRY
so part of: RBM11
location: join(15596769..15596858,15599201..15599614)
location: region:15596769-15599614:1

XP_005261055.1
SIO_000068: ncbiprotein

GI:530418958
SIO_000068: ncbigi

position:15596769:1
position: 15596769
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15596769-15596858:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15599201-15599614:1/exon

ABCC13
type: SO_0000704
alternative label: C21orf73
alternative label: PRED6
gene: ABCC13
gene synonym: C21orf73; PRED6
note: ATP-binding cassette, sub-family C (CFTR/MRP), member 13, pseudogene; Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15646120..15673707
location: region:15646120-15673707:1
SIO_010080: ABCC13

150000
SIO_000068: ncbigene

16022
SIO_000068: hgnc

608835
SIO_000068: omim

position:15646120:1
position: 15646120
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15673707:1
position: 15673707
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ABCC13
type: SO_0000673
alternative label: C21orf73
alternative label: PRED6
gene: ABCC13
gene synonym: C21orf73; PRED6
product: ATP-binding cassette, sub-family C (CFTR/MRP), member 13, pseudogene, transcript variant A
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
transcript id: NR_003087.1
so part of: ABCC13
location: join(15646120..15646478,15651917..15651978,15659871..15660018,15660725..15660867,15663891..15664068,15671759..15673707)
location: region:15646120-15673707:1

GI:108773779
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15646120-15646478:1/exon

position:15646478:1
position: 15646478
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15651917-15651978:1/exon

position:15651917:1
position: 15651917
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15651978:1
position: 15651978
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15659871-15660018:1/exon

position:15659871:1
position: 15659871
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15660018:1
position: 15660018
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:15660725-15660867:1/exon

position:15660725:1
position: 15660725
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15660867:1
position: 15660867
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:15663891-15664068:1/exon

position:15663891:1
position: 15663891
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15664068:1
position: 15664068
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:15671759-15673707:1/exon

position:15671759:1
position: 15671759
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ABCC13
type: SO_0000673
alternative label: C21orf73
alternative label: PRED6
gene: ABCC13
gene synonym: C21orf73; PRED6
product: ATP-binding cassette, sub-family C (CFTR/MRP), member 13, pseudogene, transcript variant D
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
transcript id: NR_003088.1
so part of: ABCC13
location: join(15646120..15646478,15651917..15651978,15659871..15660018,15660725..15660867,15663607..15663720)
location: region:15646120-15663720:1

GI:108773780
SIO_000068: ncbigi

position:15663720:1
position: 15663720
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15646120-15646478:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15651917-15651978:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15659871-15660018:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15660725-15660867:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15663607-15663720:1/exon

position:15663607:1
position: 15663607
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

HSPA13
type: SO_0000704
alternative label: STCH
gene: HSPA13
gene synonym: STCH
note: heat shock protein 70kDa family, member 13; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15743436..15755509)
location: region:15743436-15755509:-1
SIO_010080: HSPA13

6782
SIO_000068: ncbigene

11375
SIO_000068: hgnc

601100
SIO_000068: omim

position:15743436:-1
position: 15743436
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15755509:-1
position: 15755509
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

HSPA13
type: SO_0000234
alternative label: STCH
gene: HSPA13
gene synonym: STCH
product: heat shock protein 70kDa family, member 13
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_006948.4
so part of: HSPA13
location: complement(join(15743436..15746605,15747973..15748140,15750520..15750733,15753524..15753864,15755416..15755509))
location: region:15743436-15755509:-1

GI:48928055
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15755416-15755509:-1/exon

position:15755416:-1
position: 15755416
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15753524-15753864:-1/exon

position:15753524:-1
position: 15753524
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15753864:-1
position: 15753864
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15750520-15750733:-1/exon

position:15750520:-1
position: 15750520
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15750733:-1
position: 15750733
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:15747973-15748140:-1/exon

position:15747973:-1
position: 15747973
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15748140:-1
position: 15748140
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:15743436-15746605:-1/exon

position:15746605:-1
position: 15746605
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

HSPA13
type: SO_0000234
alternative label: STCH
gene: HSPA13
gene synonym: STCH
product: heat shock protein 70kDa family, member 13, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 33 ESTs, 2 Proteins, and 97% coverage by RNAseq alignments
transcript id: XM_005261036.1
so part of: HSPA13
location: complement(join(15743436..15746605,15747973..15748140,15753524..15753864,15755416..15755456))
location: region:15743436-15755456:-1

GI:530419041
SIO_000068: ncbigi

position:15755456:-1
position: 15755456
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15755416-15755456:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15753524-15753864:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15747973-15748140:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15743436-15746605:-1/exon

HSPA13
type: SO_0000316
alternative label: STCH
gene: HSPA13
gene synonym: STCH
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: heat shock 70 kDa protein 13 precursor
translation: MAREMTILGSAVLTLLLAGYLAQQYLPLPTPKVIGIDLGTTYCSVGVFFPGTGKVKVIPDENGHISIPSMVSFTDNDVYVGYESVELADSNPQNTIYDAKRFIGKIFTAEELEAEIGRYPFKVLNKNGMVEFSVTSNETITVSPEYVGSRLLLKLKEMAEAYLGMPVANAVISVPAEFDLKQRNSTIEAANLAGLKILRVINEPTAAAMAYGLHKADVFHVLVIDLGGGTLDVSLLNKQGGMFLTRAMSGNNKLGGQDFNQRLLQYLYKQIYQTYGFVPSRKEEIHRLRQAVEMVKLNLTLHQSAQLSVLLTVEEQDRKEPHSSDTELPKDKLSSADDHRVNSGFGRGLSDKKSGESQVLFETEISRKLFDTLNEDLFQKILVPIQQVLKEGHLEKTEIDEVVLVGGSTRIPRIRQVIQEFFGKDPNTSVDPDLAVVTGVAIQAGIDGGSWPLQVSALEIPNKHLQKTNFN
so part of: HSPA13
location: complement(join(15745938..15746605,15747973..15748140,15750520..15750733,15753524..15753864,15755416..15755440))
location: region:15745938-15755440:-1

NP_008879.3
SIO_000068: ncbiprotein

GI:48928056
SIO_000068: ncbigi

CCDS13567.1
SIO_000068: ccds

position:15745938:-1
position: 15745938
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15755440:-1
position: 15755440
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15755416-15755440:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15753524-15753864:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15750520-15750733:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15747973-15748140:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15745938-15746605:-1/exon

HSPA13
type: SO_0000316
alternative label: STCH
gene: HSPA13
gene synonym: STCH
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: heat shock 70 kDa protein 13 isoform X1
translation: MAYGLHKADVFHVLVIDLGGGTLDVSLLNKQGGMFLTRAMSGNNKLGGQDFNQRLLQYLYKQIYQTYGFVPSRKEEIHRLRQAVEMVKLNLTLHQSAQLSVLLTVEEQDRKEPHSSDTELPKDKLSSADDHRVNSGFGRGLSDKKSGESQVLFETEISRKLFDTLNEDLFQKILVPIQQVLKEGHLEKTEIDEVVLVGGSTRIPRIRQVIQEFFGKDPNTSVDPDLAVVTGVAIQAGIDGGSWPLQVSALEIPNKHLQKTNFN
so part of: HSPA13
location: complement(join(15745938..15746605,15747973..15748096))
location: region:15745938-15748096:-1

XP_005261093.1
SIO_000068: ncbiprotein

GI:530419042
SIO_000068: ncbigi

position:15748096:-1
position: 15748096
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15747973-15748096:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15745938-15746605:-1/exon

SAMSN1
type: SO_0000704
alternative label: HACS1
alternative label: NASH1
alternative label: SASH2
alternative label: SH3D6B
alternative label: SLy2
gene: SAMSN1
gene synonym: HACS1; NASH1; SASH2; SH3D6B; SLy2
note: SAM domain, SH3 domain and nuclear localization signals 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15857549..15955723)
location: region:15857549-15955723:-1
SIO_010080: SAMSN1

64092
SIO_000068: ncbigene

10528
SIO_000068: hgnc

607978
SIO_000068: omim

position:15857549:-1
position: 15857549
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15955723:-1
position: 15955723
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

SAMSN1
type: SO_0000234
alternative label: HACS1
alternative label: NASH1
alternative label: SASH2
alternative label: SH3D6B
alternative label: SLy2
gene: SAMSN1
gene synonym: HACS1; NASH1; SASH2; SH3D6B; SLy2
product: SAM domain, SH3 domain and nuclear localization signals 1, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001256370.1
so part of: SAMSN1
location: complement(join(15857549..15858435,15870763..15870913,15872850..15873056,15882631..15882782,15884765..15884894,15889213..15889362,15893471..15893542,15954457..15954809,15955641..15955723))
location: region:15857549-15955723:-1

GI:373838707
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15955641-15955723:-1/exon

position:15955641:-1
position: 15955641
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15954457-15954809:-1/exon

position:15954457:-1
position: 15954457
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15954809:-1
position: 15954809
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15893471-15893542:-1/exon

position:15893471:-1
position: 15893471
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15893542:-1
position: 15893542
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:15889213-15889362:-1/exon

position:15889213:-1
position: 15889213
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15889362:-1
position: 15889362
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:15884765-15884894:-1/exon

position:15884765:-1
position: 15884765
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15884894:-1
position: 15884894
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:15882631-15882782:-1/exon

position:15882631:-1
position: 15882631
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15882782:-1
position: 15882782
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:15872850-15873056:-1/exon

position:15872850:-1
position: 15872850
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15873056:-1
position: 15873056
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:15870763-15870913:-1/exon

position:15870763:-1
position: 15870763
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15870913:-1
position: 15870913
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:15857549-15858435:-1/exon

position:15858435:-1
position: 15858435
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

SAMSN1
type: SO_0000234
alternative label: HACS1
alternative label: NASH1
alternative label: SASH2
alternative label: SH3D6B
alternative label: SLy2
gene: SAMSN1
gene synonym: HACS1; NASH1; SASH2; SH3D6B; SLy2
product: SAM domain, SH3 domain and nuclear localization signals 1, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 ESTs, 1 Protein, and 97% coverage by RNAseq alignments
transcript id: XM_005261022.1
so part of: SAMSN1
location: complement(join(15857549..15858435,15870763..15870913,15872850..15873056,15918526..15918681))
location: region:15857549-15918681:-1

GI:530419011
SIO_000068: ncbigi

position:15918681:-1
position: 15918681
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15918526-15918681:-1/exon

position:15918526:-1
position: 15918526
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15872850-15873056:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15870763-15870913:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15857549-15858435:-1/exon

SAMSN1
type: SO_0000234
alternative label: HACS1
alternative label: NASH1
alternative label: SASH2
alternative label: SH3D6B
alternative label: SLy2
gene: SAMSN1
gene synonym: HACS1; NASH1; SASH2; SH3D6B; SLy2
product: SAM domain, SH3 domain and nuclear localization signals 1, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_022136.4
so part of: SAMSN1
location: complement(join(15857549..15858435,15870763..15870913,15872850..15873056,15882631..15882782,15884765..15884894,15889213..15889362,15893471..15893542,15918526..15918681))
location: region:15857549-15918681:-1

GI:373838706
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15918526-15918681:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15893471-15893542:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15889213-15889362:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15884765-15884894:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15882631-15882782:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15872850-15873056:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15870763-15870913:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15857549-15858435:-1/exon

SAMSN1
type: SO_0000316
alternative label: HACS1
alternative label: NASH1
alternative label: SASH2
alternative label: SH3D6B
alternative label: SLy2
gene: SAMSN1
gene synonym: HACS1; NASH1; SASH2; SH3D6B; SLy2
note: isoform 2 is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: SAM domain-containing protein SAMSN-1 isoform 2
translation: MEIRLDTLSASLGRSSTLNNCNLEDKLAWYEGEAYMWHHWKPFPENPLWTCLDFQIAQVGPWDHCSSCIRHTRLKSSCSDMDLLHSWRSSSFGNFDRFRNNSLSKPDDSTEAHEGDPTNGSGEQSKTSNNGGGLGKKMRAISWTMKKKVGKKYIKALSEEKDEEDGENAHPYRNSDPVIGTHTEKVSLKASDSMDSLYSGQSSSSGITSCSDGTSNRDSFRLDDDGPYSGPFCGRARVHTDFTPSPYDTDSLKIKKGDIIDIICKTPMGMWTGMLNNKVGNFKFIYVDVISEEEAAPKKIKANRRSNSKKSKTLQEFLERIHLQEYTSTLLLNGYETLEDLKDIKESHLIELNIENPDDRRRLLSAAENFLEEEIIQEQENEPEPLSLSSDISLNKSQLDDCPRDSGCYISSGNSDNGKEDLESENLSDMVHKIIITEPSD
so part of: SAMSN1
location: complement(join(15858233..15858435,15870763..15870913,15872850..15873056,15882631..15882782,15884765..15884894,15889213..15889362,15893471..15893542,15954457..15954717))
location: region:15858233-15954717:-1

NP_001243299.1
SIO_000068: ncbiprotein

GI:373838708
SIO_000068: ncbigi

CCDS58786.1
SIO_000068: ccds

position:15858233:-1
position: 15858233
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15954717:-1
position: 15954717
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15954457-15954717:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15893471-15893542:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15889213-15889362:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15884765-15884894:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15882631-15882782:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15872850-15873056:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15870763-15870913:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15858233-15858435:-1/exon

SAMSN1
type: SO_0000316
alternative label: HACS1
alternative label: NASH1
alternative label: SASH2
alternative label: SH3D6B
alternative label: SLy2
gene: SAMSN1
gene synonym: HACS1; NASH1; SASH2; SH3D6B; SLy2
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: SAM domain-containing protein SAMSN-1 isoform X1
translation: MLKRKPSNVSEKEKHQKPKKGDIIDIICKTPMGMWTGMLNNKVGNFKFIYVDVISEEEAAPKKIKANRRSNSKKSKTLQEFLERIHLQEYTSTLLLNGYETLEDLKDIKESHLIELNIENPDDRRRLLSAAENFLEEEIIQEQENEPEPLSLSSDISLNKSQLDDCPRDSGCYISSGNSDNGKEDLESENLSDMVHKIIITEPSD
so part of: SAMSN1
location: complement(join(15858233..15858435,15870763..15870913,15872850..15873056,15918526..15918582))
location: region:15858233-15918582:-1

XP_005261079.1
SIO_000068: ncbiprotein

GI:530419012
SIO_000068: ncbigi

position:15918582:-1
position: 15918582
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:15918526-15918582:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15872850-15873056:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15870763-15870913:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15858233-15858435:-1/exon

SAMSN1
type: SO_0000316
alternative label: HACS1
alternative label: NASH1
alternative label: SASH2
alternative label: SH3D6B
alternative label: SLy2
gene: SAMSN1
gene synonym: HACS1; NASH1; SASH2; SH3D6B; SLy2
note: isoform 1 is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: SAM domain-containing protein SAMSN-1 isoform 1
translation: MLKRKPSNVSEKEKHQKPKRSSSFGNFDRFRNNSLSKPDDSTEAHEGDPTNGSGEQSKTSNNGGGLGKKMRAISWTMKKKVGKKYIKALSEEKDEEDGENAHPYRNSDPVIGTHTEKVSLKASDSMDSLYSGQSSSSGITSCSDGTSNRDSFRLDDDGPYSGPFCGRARVHTDFTPSPYDTDSLKIKKGDIIDIICKTPMGMWTGMLNNKVGNFKFIYVDVISEEEAAPKKIKANRRSNSKKSKTLQEFLERIHLQEYTSTLLLNGYETLEDLKDIKESHLIELNIENPDDRRRLLSAAENFLEEEIIQEQENEPEPLSLSSDISLNKSQLDDCPRDSGCYISSGNSDNGKEDLESENLSDMVHKIIITEPSD
so part of: SAMSN1
location: complement(join(15858233..15858435,15870763..15870913,15872850..15873056,15882631..15882782,15884765..15884894,15889213..15889362,15893471..15893542,15918526..15918582))
location: region:15858233-15918582:-1

NP_071419.3
SIO_000068: ncbiprotein

GI:48762709
SIO_000068: ncbigi

CCDS42906.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:15918526-15918582:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15893471-15893542:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15889213-15889362:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15884765-15884894:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15882631-15882782:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15872850-15873056:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15870763-15870913:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:15858233-15858435:-1/exon

SAMSN1-AS1
type: SO_0000704
gene: SAMSN1-AS1
note: SAMSN1 antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 15954523..15970624
location: region:15954523-15970624:1
SIO_010080: SAMSN1-AS1

100874190
SIO_000068: ncbigene

39599
SIO_000068: hgnc

position:15954523:1
position: 15954523
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15970624:1
position: 15970624
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

SAMSN1-AS1
type: SO_0000673
gene: SAMSN1-AS1
product: SAMSN1 antisense RNA 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_046512.1
so part of: SAMSN1-AS1
location: join(15954523..15954612,15957683..15957859,15963643..15963789,15967015..15967061,15970246..15970624)
location: region:15954523-15970624:1

GI:390125169
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:15954523-15954612:1/exon

position:15954612:1
position: 15954612
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15957683-15957859:1/exon

position:15957683:1
position: 15957683
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15957859:1
position: 15957859
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15963643-15963789:1/exon

position:15963643:1
position: 15963643
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15963789:1
position: 15963789
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:15967015-15967061:1/exon

position:15967015:1
position: 15967015
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15967061:1
position: 15967061
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:15970246-15970624:1/exon

position:15970246:1
position: 15970246
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC388813
type: SO_0000704
gene: LOC388813
note: uncharacterized protein ENSP00000383407-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(15964484..16015428)
location: region:15964484-16015428:-1
SIO_010080: LOC388813

388813
SIO_000068: ncbigene

position:15964484:-1
position: 15964484
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:16015428:-1
position: 16015428
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC388813
type: SO_0000234
gene: LOC388813
product: uncharacterized protein ENSP00000383407-like
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001256579.1
so part of: LOC388813
location: complement(join(15964484..15964960,15966334..15966399,15974344..15974420,15981803..15981889,15985197..15985234,15988297..15988337,16015323..16015428))
location: region:15964484-16015428:-1

GI:375151594
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:16015323-16015428:-1/exon

position:16015323:-1
position: 16015323
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:15988297-15988337:-1/exon

position:15988297:-1
position: 15988297
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15988337:-1
position: 15988337
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:15985197-15985234:-1/exon

position:15985197:-1
position: 15985197
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15985234:-1
position: 15985234
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:15981803-15981889:-1/exon

position:15981803:-1
position: 15981803
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15981889:-1
position: 15981889
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:15974344-15974420:-1/exon

position:15974344:-1
position: 15974344
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15974420:-1
position: 15974420
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:15966334-15966399:-1/exon

position:15966334:-1
position: 15966334
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:15966399:-1
position: 15966399
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:15964484-15964960:-1/exon

position:15964960:-1
position: 15964960
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC388813
type: SO_0000316
gene: LOC388813
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: putative uncharacterized protein ENSP00000383407
translation: MSSRTDSPIPPFGESEQTPNNLFVGVSNLENAKPKKRKLFRRFMSENKIFEGKTVNDKIWQEHSKHKNDSHIRRPCQLKDLNENDFLSNNIHTYQGKTLQGTSYQVTSECWSPFHYQRHVETTVDELAQEFM
so part of: LOC388813
location: complement(join(15964943..15964960,15966334..15966399,15974344..15974420,15981803..15981889,15985197..15985234,15988297..15988337,16015323..16015394))
location: region:15964943-16015394:-1

NP_001243508.1
SIO_000068: ncbiprotein

GI:375151595
SIO_000068: ncbigi

position:15964943:-1
position: 15964943
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:16015394:-1
position: 16015394
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:16015323-16015394:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:15988297-15988337:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:15985197-15985234:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:15981803-15981889:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:15974344-15974420:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:15966334-15966399:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:15964943-15964960:-1/exon

POLR2CP
type: SO_0000704
gene: POLR2CP
note: polymerase (RNA) II (DNA directed) polypeptide C, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 16129879..16131542
location: region:16129879-16131542:1
SIO_010080: POLR2CP

54038
SIO_000068: ncbigene

9190
SIO_000068: hgnc

position:16129879:1
position: 16129879
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:16131542:1
position: 16131542
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

POLR2CP
type: SO_0000147
gene: POLR2CP
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: POLR2CP
location: 16129879..16131542
location: region:16129879-16131542:1

GAPDHP16
type: SO_0000704
alternative label: GAPDP16
gene: GAPDHP16
gene synonym: GAPDP16
note: glyceraldehyde-3-phosphate dehydrogenase pseudogene 16; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 16146624..16147801
location: region:16146624-16147801:1

387491
SIO_000068: ncbigene

23768
SIO_000068: hgnc

position:16146624:1
position: 16146624
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:16147801:1
position: 16147801
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

RBMX2P1
type: SO_0000704
gene: RBMX2P1
note: RNA binding motif protein, X-linked 2 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(16201470..16202310)
location: region:16201470-16202310:-1

100128341
SIO_000068: ncbigene

39923
SIO_000068: hgnc

position:16201470:-1
position: 16201470
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:16202310:-1
position: 16202310
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

NRIP1
type: SO_0000704
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
note: nuclear receptor interacting protein 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(16333556..16438224)
location: region:16333556-16438224:-1
SIO_010080: NRIP1

8204
SIO_000068: ncbigene

8001
SIO_000068: hgnc

602490
SIO_000068: omim

position:16333556:-1
position: 16333556
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:16438224:-1
position: 16438224
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

NRIP1
type: SO_0000234
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
product: nuclear receptor interacting protein 1, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 65 ESTs, 6 Proteins, and 99% coverage by RNAseq alignments
transcript id: XM_005261064.1
so part of: NRIP1
location: complement(join(16333556..16340847,16415816..16415895,16438046..16438224))
location: region:16333556-16438224:-1

GI:530419097
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:16438046-16438224:-1/exon

position:16438046:-1
position: 16438046
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:16415816-16415895:-1/exon

position:16415816:-1
position: 16415816
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:16415895:-1
position: 16415895
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:16333556-16340847:-1/exon

position:16340847:-1
position: 16340847
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

NRIP1
type: SO_0000234
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
product: nuclear receptor interacting protein 1, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 64 ESTs, 6 Proteins, and 99% coverage by RNAseq alignments
transcript id: XM_005261062.1
so part of: NRIP1
location: complement(join(16333556..16340847,16386665..16386787,16415816..16415895,16438046..16438224))
location: region:16333556-16438224:-1

GI:530419093
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:16438046-16438224:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:16415816-16415895:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:16386665-16386787:-1/exon

position:16386665:-1
position: 16386665
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:16386787:-1
position: 16386787
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:16333556-16340847:-1/exon

NRIP1
type: SO_0000234
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
product: nuclear receptor interacting protein 1, transcript variant X4
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 63 ESTs, 6 Proteins, and 100% coverage by RNAseq alignments, including 4 samples with support for all introns
transcript id: XM_005261065.1
so part of: NRIP1
location: complement(join(16333556..16340847,16437066..16437250))
location: region:16333556-16437250:-1

GI:530419099
SIO_000068: ncbigi

position:16437250:-1
position: 16437250
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:16437066-16437250:-1/exon

position:16437066:-1
position: 16437066
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:16333556-16340847:-1/exon

NRIP1
type: SO_0000234
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
product: nuclear receptor interacting protein 1, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 63 ESTs, 6 Proteins, and 100% coverage by RNAseq alignments, including 5 samples with support for all introns
transcript id: XM_005261063.1
so part of: NRIP1
location: complement(join(16333556..16340847,16415816..16415895,16437066..16437250))
location: region:16333556-16437250:-1

GI:530419095
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:16437066-16437250:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:16415816-16415895:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:16333556-16340847:-1/exon

NRIP1
type: SO_0000234
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
product: nuclear receptor interacting protein 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_003489.3
so part of: NRIP1
location: complement(join(16333556..16340847,16386665..16386787,16415816..16415895,16437066..16437126))
location: region:16333556-16437126:-1

GI:212274353
SIO_000068: ncbigi

position:16437126:-1
position: 16437126
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:16437066-16437126:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:16415816-16415895:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:16386665-16386787:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:16333556-16340847:-1/exon

NRIP1
type: SO_0000234
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
product: nuclear receptor interacting protein 1, transcript variant X5
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 63 ESTs, 6 Proteins, and 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005261066.1
so part of: NRIP1
location: complement(join(16333556..16340847,16351522..16352015))
location: region:16333556-16352015:-1

GI:530419101
SIO_000068: ncbigi

position:16352015:-1
position: 16352015
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:16351522-16352015:-1/exon

position:16351522:-1
position: 16351522
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:16333556-16340847:-1/exon

NRIP1
type: SO_0000316
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: nuclear receptor-interacting protein 1
translation: MTHGEELGSDVHQDSIVLTYLEGLLMHQAAGGSGTAVDKKSAGHNEEDQNFNISGSAFPTCQSNGPVLNTHTYQGSGMLHLKKARLLQSSEDWNAAKRKRLSDSIMNLNVKKEALLAGMVDSVPKGKQDSTLLASLLQSFSSRLQTVALSQQIRQSLKEQGYALSHDSLKVEKDLRCYGVASSHLKTLLKKSKVKDQKPDTNLPDVTKNLIRDRFAESPHHVGQSGTKVMSEPLSCAARLQAVASMVEKRASPATSPKPSVACSQLALLLSSEAHLQQYSREHALKTQNANQAASERLAAMARLQENGQKDVGSYQLPKGMSSHLNGQARTSSSKLMASKSSATVFQNPMGIIPSSPKNAGYKNSLERNNIKQAANNSLLLHLLKSQTIPKPMNGHSHSERGSIFEESSTPTTIDEYSDNNPSFTDDSSGDESSYSNCVPIDLSCKHRTEKSESDQPVSLDNFTQSLLNTWDPKVPDVDIKEDQDTSKNSKLNSHQKVTLLQLLLGHKNEENVEKNTSPQGVHNDVSKFNTQNYARTSVIESPSTNRTTPVSTPPLLTSSKAGSPINLSQHSLVIKWNSPPYVCSTQSEKLTNTASNHSMDLTKSKDPPGEKPAQNEGAQNSATFSASKLLQNLAQCGMQSSMSVEEQRPSKQLLTGNTDKPIGMIDRLNSPLLSNKTNAVEENKAFSSQPTGPEPGLSGSEIENLLERRTVLQLLLGNPNKGKSEKKEKTPLRDESTQEHSERALSEQILMVKIKSEPCDDLQIPNTNVHLSHDAKSAPFLGMAPAVQRSAPALPVSEDFKSEPVSPQDFSFSKNGLLSRLLRQNQDSYLADDSDRSHRNNEMALLESKNLCMVPKKRKLYTEPLENPFKKMKNNIVDAANNHSAPEVLYGSLLNQEELKFSRNDLEFKYPAGHGSASESEHRSWARESKSFNVLKQLLLSENCVRDLSPHRSNSVADSKKKGHKNNVTNSKPEFSISSLNGLMYSSTQPSSCMDNRTFSYPGVVKTPVSPTFPEHLGCAGSRPESGLLNGCSMPSEKGPIKWVITDAEKNEYEKDSPRLTKTNPILYYMLQKGGNSVTSRETQDKDIWREASSAESVSQVTAKEELLPTAETKASFFNLRSPYNSHMGNNASRPHSANGEVYGLLGSVLTIKKESE
so part of: NRIP1
location: complement(16337037..16340513)
location: region:16337037-16340513:-1

NP_003480.2
SIO_000068: ncbiprotein

GI:57232746
SIO_000068: ncbigi

CCDS13568.1
SIO_000068: ccds

position:16337037:-1
position: 16337037
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:16340513:-1
position: 16340513
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

NRIP1
type: SO_0000316
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: nuclear receptor-interacting protein 1 isoform X1
translation: MTHGEELGSDVHQDSIVLTYLEGLLMHQAAGGSGTAVDKKSAGHNEEDQNFNISGSAFPTCQSNGPVLNTHTYQGSGMLHLKKARLLQSSEDWNAAKRKRLSDSIMNLNVKKEALLAGMVDSVPKGKQDSTLLASLLQSFSSRLQTVALSQQIRQSLKEQGYALSHDSLKVEKDLRCYGVASSHLKTLLKKSKVKDQKPDTNLPDVTKNLIRDRFAESPHHVGQSGTKVMSEPLSCAARLQAVASMVEKRASPATSPKPSVACSQLALLLSSEAHLQQYSREHALKTQNANQAASERLAAMARLQENGQKDVGSYQLPKGMSSHLNGQARTSSSKLMASKSSATVFQNPMGIIPSSPKNAGYKNSLERNNIKQAANNSLLLHLLKSQTIPKPMNGHSHSERGSIFEESSTPTTIDEYSDNNPSFTDDSSGDESSYSNCVPIDLSCKHRTEKSESDQPVSLDNFTQSLLNTWDPKVPDVDIKEDQDTSKNSKLNSHQKVTLLQLLLGHKNEENVEKNTSPQGVHNDVSKFNTQNYARTSVIESPSTNRTTPVSTPPLLTSSKAGSPINLSQHSLVIKWNSPPYVCSTQSEKLTNTASNHSMDLTKSKDPPGEKPAQNEGAQNSATFSASKLLQNLAQCGMQSSMSVEEQRPSKQLLTGNTDKPIGMIDRLNSPLLSNKTNAVEENKAFSSQPTGPEPGLSGSEIENLLERRTVLQLLLGNPNKGKSEKKEKTPLRDESTQEHSERALSEQILMVKIKSEPCDDLQIPNTNVHLSHDAKSAPFLGMAPAVQRSAPALPVSEDFKSEPVSPQDFSFSKNGLLSRLLRQNQDSYLADDSDRSHRNNEMALLESKNLCMVPKKRKLYTEPLENPFKKMKNNIVDAANNHSAPEVLYGSLLNQEELKFSRNDLEFKYPAGHGSASESEHRSWARESKSFNVLKQLLLSENCVRDLSPHRSNSVADSKKKGHKNNVTNSKPEFSISSLNGLMYSSTQPSSCMDNRTFSYPGVVKTPVSPTFPEHLGCAGSRPESGLLNGCSMPSEKGPIKWVITDAEKNEYEKDSPRLTKTNPILYYMLQKGGNSVTSRETQDKDIWREASSAESVSQVTAKEELLPTAETKASFFNLRSPYNSHMGNNASRPHSANGEVYGLLGSVLTIKKESE
so part of: NRIP1
location: complement(16337037..16340513)
location: region:16337037-16340513:-1

XP_005261119.1
SIO_000068: ncbiprotein

GI:530419094
SIO_000068: ncbigi

NRIP1
type: SO_0000316
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: nuclear receptor-interacting protein 1 isoform X2
translation: MTHGEELGSDVHQDSIVLTYLEGLLMHQAAGGSGTAVDKKSAGHNEEDQNFNISGSAFPTCQSNGPVLNTHTYQGSGMLHLKKARLLQSSEDWNAAKRKRLSDSIMNLNVKKEALLAGMVDSVPKGKQDSTLLASLLQSFSSRLQTVALSQQIRQSLKEQGYALSHDSLKVEKDLRCYGVASSHLKTLLKKSKVKDQKPDTNLPDVTKNLIRDRFAESPHHVGQSGTKVMSEPLSCAARLQAVASMVEKRASPATSPKPSVACSQLALLLSSEAHLQQYSREHALKTQNANQAASERLAAMARLQENGQKDVGSYQLPKGMSSHLNGQARTSSSKLMASKSSATVFQNPMGIIPSSPKNAGYKNSLERNNIKQAANNSLLLHLLKSQTIPKPMNGHSHSERGSIFEESSTPTTIDEYSDNNPSFTDDSSGDESSYSNCVPIDLSCKHRTEKSESDQPVSLDNFTQSLLNTWDPKVPDVDIKEDQDTSKNSKLNSHQKVTLLQLLLGHKNEENVEKNTSPQGVHNDVSKFNTQNYARTSVIESPSTNRTTPVSTPPLLTSSKAGSPINLSQHSLVIKWNSPPYVCSTQSEKLTNTASNHSMDLTKSKDPPGEKPAQNEGAQNSATFSASKLLQNLAQCGMQSSMSVEEQRPSKQLLTGNTDKPIGMIDRLNSPLLSNKTNAVEENKAFSSQPTGPEPGLSGSEIENLLERRTVLQLLLGNPNKGKSEKKEKTPLRDESTQEHSERALSEQILMVKIKSEPCDDLQIPNTNVHLSHDAKSAPFLGMAPAVQRSAPALPVSEDFKSEPVSPQDFSFSKNGLLSRLLRQNQDSYLADDSDRSHRNNEMALLESKNLCMVPKKRKLYTEPLENPFKKMKNNIVDAANNHSAPEVLYGSLLNQEELKFSRNDLEFKYPAGHGSASESEHRSWARESKSFNVLKQLLLSENCVRDLSPHRSNSVADSKKKGHKNNVTNSKPEFSISSLNGLMYSSTQPSSCMDNRTFSYPGVVKTPVSPTFPEHLGCAGSRPESGLLNGCSMPSEKGPIKWVITDAEKNEYEKDSPRLTKTNPILYYMLQKGGNSVTSRETQDKDIWREASSAESVSQVTAKEELLPTAETKASFFNLRSPYNSHMGNNASRPHSANGEVYGLLGSVLTIKKESE
so part of: NRIP1
location: complement(16337037..16340513)
location: region:16337037-16340513:-1

XP_005261120.1
SIO_000068: ncbiprotein

GI:530419096
SIO_000068: ncbigi

NRIP1
type: SO_0000316
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: nuclear receptor-interacting protein 1 isoform X3
translation: MTHGEELGSDVHQDSIVLTYLEGLLMHQAAGGSGTAVDKKSAGHNEEDQNFNISGSAFPTCQSNGPVLNTHTYQGSGMLHLKKARLLQSSEDWNAAKRKRLSDSIMNLNVKKEALLAGMVDSVPKGKQDSTLLASLLQSFSSRLQTVALSQQIRQSLKEQGYALSHDSLKVEKDLRCYGVASSHLKTLLKKSKVKDQKPDTNLPDVTKNLIRDRFAESPHHVGQSGTKVMSEPLSCAARLQAVASMVEKRASPATSPKPSVACSQLALLLSSEAHLQQYSREHALKTQNANQAASERLAAMARLQENGQKDVGSYQLPKGMSSHLNGQARTSSSKLMASKSSATVFQNPMGIIPSSPKNAGYKNSLERNNIKQAANNSLLLHLLKSQTIPKPMNGHSHSERGSIFEESSTPTTIDEYSDNNPSFTDDSSGDESSYSNCVPIDLSCKHRTEKSESDQPVSLDNFTQSLLNTWDPKVPDVDIKEDQDTSKNSKLNSHQKVTLLQLLLGHKNEENVEKNTSPQGVHNDVSKFNTQNYARTSVIESPSTNRTTPVSTPPLLTSSKAGSPINLSQHSLVIKWNSPPYVCSTQSEKLTNTASNHSMDLTKSKDPPGEKPAQNEGAQNSATFSASKLLQNLAQCGMQSSMSVEEQRPSKQLLTGNTDKPIGMIDRLNSPLLSNKTNAVEENKAFSSQPTGPEPGLSGSEIENLLERRTVLQLLLGNPNKGKSEKKEKTPLRDESTQEHSERALSEQILMVKIKSEPCDDLQIPNTNVHLSHDAKSAPFLGMAPAVQRSAPALPVSEDFKSEPVSPQDFSFSKNGLLSRLLRQNQDSYLADDSDRSHRNNEMALLESKNLCMVPKKRKLYTEPLENPFKKMKNNIVDAANNHSAPEVLYGSLLNQEELKFSRNDLEFKYPAGHGSASESEHRSWARESKSFNVLKQLLLSENCVRDLSPHRSNSVADSKKKGHKNNVTNSKPEFSISSLNGLMYSSTQPSSCMDNRTFSYPGVVKTPVSPTFPEHLGCAGSRPESGLLNGCSMPSEKGPIKWVITDAEKNEYEKDSPRLTKTNPILYYMLQKGGNSVTSRETQDKDIWREASSAESVSQVTAKEELLPTAETKASFFNLRSPYNSHMGNNASRPHSANGEVYGLLGSVLTIKKESE
so part of: NRIP1
location: complement(16337037..16340513)
location: region:16337037-16340513:-1

XP_005261121.1
SIO_000068: ncbiprotein

GI:530419098
SIO_000068: ncbigi

NRIP1
type: SO_0000316
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: nuclear receptor-interacting protein 1 isoform X4
translation: MTHGEELGSDVHQDSIVLTYLEGLLMHQAAGGSGTAVDKKSAGHNEEDQNFNISGSAFPTCQSNGPVLNTHTYQGSGMLHLKKARLLQSSEDWNAAKRKRLSDSIMNLNVKKEALLAGMVDSVPKGKQDSTLLASLLQSFSSRLQTVALSQQIRQSLKEQGYALSHDSLKVEKDLRCYGVASSHLKTLLKKSKVKDQKPDTNLPDVTKNLIRDRFAESPHHVGQSGTKVMSEPLSCAARLQAVASMVEKRASPATSPKPSVACSQLALLLSSEAHLQQYSREHALKTQNANQAASERLAAMARLQENGQKDVGSYQLPKGMSSHLNGQARTSSSKLMASKSSATVFQNPMGIIPSSPKNAGYKNSLERNNIKQAANNSLLLHLLKSQTIPKPMNGHSHSERGSIFEESSTPTTIDEYSDNNPSFTDDSSGDESSYSNCVPIDLSCKHRTEKSESDQPVSLDNFTQSLLNTWDPKVPDVDIKEDQDTSKNSKLNSHQKVTLLQLLLGHKNEENVEKNTSPQGVHNDVSKFNTQNYARTSVIESPSTNRTTPVSTPPLLTSSKAGSPINLSQHSLVIKWNSPPYVCSTQSEKLTNTASNHSMDLTKSKDPPGEKPAQNEGAQNSATFSASKLLQNLAQCGMQSSMSVEEQRPSKQLLTGNTDKPIGMIDRLNSPLLSNKTNAVEENKAFSSQPTGPEPGLSGSEIENLLERRTVLQLLLGNPNKGKSEKKEKTPLRDESTQEHSERALSEQILMVKIKSEPCDDLQIPNTNVHLSHDAKSAPFLGMAPAVQRSAPALPVSEDFKSEPVSPQDFSFSKNGLLSRLLRQNQDSYLADDSDRSHRNNEMALLESKNLCMVPKKRKLYTEPLENPFKKMKNNIVDAANNHSAPEVLYGSLLNQEELKFSRNDLEFKYPAGHGSASESEHRSWARESKSFNVLKQLLLSENCVRDLSPHRSNSVADSKKKGHKNNVTNSKPEFSISSLNGLMYSSTQPSSCMDNRTFSYPGVVKTPVSPTFPEHLGCAGSRPESGLLNGCSMPSEKGPIKWVITDAEKNEYEKDSPRLTKTNPILYYMLQKGGNSVTSRETQDKDIWREASSAESVSQVTAKEELLPTAETKASFFNLRSPYNSHMGNNASRPHSANGEVYGLLGSVLTIKKESE
so part of: NRIP1
location: complement(16337037..16340513)
location: region:16337037-16340513:-1

XP_005261122.1
SIO_000068: ncbiprotein

GI:530419100
SIO_000068: ncbigi

NRIP1
type: SO_0000316
alternative label: RIP140
gene: NRIP1
gene synonym: RIP140
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: nuclear receptor-interacting protein 1 isoform X5
translation: MTHGEELGSDVHQDSIVLTYLEGLLMHQAAGGSGTAVDKKSAGHNEEDQNFNISGSAFPTCQSNGPVLNTHTYQGSGMLHLKKARLLQSSEDWNAAKRKRLSDSIMNLNVKKEALLAGMVDSVPKGKQDSTLLASLLQSFSSRLQTVALSQQIRQSLKEQGYALSHDSLKVEKDLRCYGVASSHLKTLLKKSKVKDQKPDTNLPDVTKNLIRDRFAESPHHVGQSGTKVMSEPLSCAARLQAVASMVEKRASPATSPKPSVACSQLALLLSSEAHLQQYSREHALKTQNANQAASERLAAMARLQENGQKDVGSYQLPKGMSSHLNGQARTSSSKLMASKSSATVFQNPMGIIPSSPKNAGYKNSLERNNIKQAANNSLLLHLLKSQTIPKPMNGHSHSERGSIFEESSTPTTIDEYSDNNPSFTDDSSGDESSYSNCVPIDLSCKHRTEKSESDQPVSLDNFTQSLLNTWDPKVPDVDIKEDQDTSKNSKLNSHQKVTLLQLLLGHKNEENVEKNTSPQGVHNDVSKFNTQNYARTSVIESPSTNRTTPVSTPPLLTSSKAGSPINLSQHSLVIKWNSPPYVCSTQSEKLTNTASNHSMDLTKSKDPPGEKPAQNEGAQNSATFSASKLLQNLAQCGMQSSMSVEEQRPSKQLLTGNTDKPIGMIDRLNSPLLSNKTNAVEENKAFSSQPTGPEPGLSGSEIENLLERRTVLQLLLGNPNKGKSEKKEKTPLRDESTQEHSERALSEQILMVKIKSEPCDDLQIPNTNVHLSHDAKSAPFLGMAPAVQRSAPALPVSEDFKSEPVSPQDFSFSKNGLLSRLLRQNQDSYLADDSDRSHRNNEMALLESKNLCMVPKKRKLYTEPLENPFKKMKNNIVDAANNHSAPEVLYGSLLNQEELKFSRNDLEFKYPAGHGSASESEHRSWARESKSFNVLKQLLLSENCVRDLSPHRSNSVADSKKKGHKNNVTNSKPEFSISSLNGLMYSSTQPSSCMDNRTFSYPGVVKTPVSPTFPEHLGCAGSRPESGLLNGCSMPSEKGPIKWVITDAEKNEYEKDSPRLTKTNPILYYMLQKGGNSVTSRETQDKDIWREASSAESVSQVTAKEELLPTAETKASFFNLRSPYNSHMGNNASRPHSANGEVYGLLGSVLTIKKESE
so part of: NRIP1
location: complement(16337037..16340513)
location: region:16337037-16340513:-1

XP_005261123.1
SIO_000068: ncbiprotein

GI:530419102
SIO_000068: ncbigi

LOC101927745
type: SO_0000704
gene: LOC101927745
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(16777246..16785242)
location: region:16777246-16785242:-1
SIO_010080: LOC101927745

101927745
SIO_000068: ncbigene

position:16777246:-1
position: 16777246
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:16785242:-1
position: 16785242
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101927745
type: SO_0000673
gene: LOC101927745
product: uncharacterized LOC101927745
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XR_244293.1
so part of: LOC101927745
location: complement(join(16777246..16778083,16778199..16778248,16784995..16785242))
location: region:16777246-16785242:-1

GI:530419144
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:16784995-16785242:-1/exon

position:16784995:-1
position: 16784995
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:16778199-16778248:-1/exon

position:16778199:-1
position: 16778199
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:16778248:-1
position: 16778248
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:16777246-16778083:-1/exon

position:16778083:-1
position: 16778083
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

CYCSP42
type: SO_0000704
alternative label: CYC1LP5
alternative label: HCP42
gene: CYCSP42
gene synonym: CYC1LP5; HCP42
note: cytochrome c, somatic pseudogene 42; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(16862843..16863101)
location: region:16862843-16863101:-1

343727
SIO_000068: ncbigene

2581
SIO_000068: hgnc

position:16862843:-1
position: 16862843
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:16863101:-1
position: 16863101
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

RAD23BLP
type: SO_0000704
gene: RAD23BLP
note: RAD23 homolog B-like (S. cerevisiae) pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(17066619..17068730)
location: region:17066619-17068730:-1

54034
SIO_000068: ncbigene

9814
SIO_000068: hgnc

position:17066619:-1
position: 17066619
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:17068730:-1
position: 17068730
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

USP25
type: SO_0000704
alternative label: USP21
gene: USP25
gene synonym: USP21
note: ubiquitin specific peptidase 25; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 17102327..17252377
location: region:17102327-17252377:1
SIO_010080: USP25

29761
SIO_000068: ncbigene

12624
SIO_000068: hgnc

604736
SIO_000068: omim

position:17102327:1
position: 17102327
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17252377:1
position: 17252377
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

USP25
type: SO_0000234
alternative label: USP21
gene: USP25
gene synonym: USP21
product: ubiquitin specific peptidase 25, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 65 ESTs, 1 Protein, and 100% coverage by RNAseq alignments, including 5 samples with support for all introns
transcript id: XM_005260946.1
so part of: USP25
location: join(17102327..17102757,17135210..17135287,17138316..17138460,17150223..17150346,17163821..17163983,17172076..17172162,17177440..17177577,17181128..17181204,17183456..17183529,17191017..17191165,17196358..17196485,17197285..17197380,17198523..17198684,17199296..17199522,17202850..17202920,17203720..17203948,17205667..17205867,17214717..17214859,17219982..17220095,17222096..17222191,17236587..17236765,17238585..17238663,17242387..17242466,17246722..17246845,17250115..17250310,17250622..17251230)
location: region:17102327-17251230:1

GI:530418836
SIO_000068: ncbigi

position:17251230:1
position: 17251230
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17102327-17102757:1/exon

position:17102757:1
position: 17102757
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:17135210-17135287:1/exon

position:17135210:1
position: 17135210
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17135287:1
position: 17135287
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:17138316-17138460:1/exon

position:17138316:1
position: 17138316
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17138460:1
position: 17138460
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:17150223-17150346:1/exon

position:17150223:1
position: 17150223
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17150346:1
position: 17150346
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:17163821-17163983:1/exon

position:17163821:1
position: 17163821
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17163983:1
position: 17163983
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:17172076-17172162:1/exon

position:17172076:1
position: 17172076
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17172162:1
position: 17172162
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:17177440-17177577:1/exon

position:17177440:1
position: 17177440
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17177577:1
position: 17177577
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:17181128-17181204:1/exon

position:17181128:1
position: 17181128
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17181204:1
position: 17181204
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:17183456-17183529:1/exon

position:17183456:1
position: 17183456
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17183529:1
position: 17183529
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:17191017-17191165:1/exon

position:17191017:1
position: 17191017
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17191165:1
position: 17191165
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:17196358-17196485:1/exon

position:17196358:1
position: 17196358
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17196485:1
position: 17196485
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:17197285-17197380:1/exon

position:17197285:1
position: 17197285
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17197380:1
position: 17197380
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:17198523-17198684:1/exon

position:17198523:1
position: 17198523
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17198684:1
position: 17198684
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:17199296-17199522:1/exon

position:17199296:1
position: 17199296
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17199522:1
position: 17199522
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:17202850-17202920:1/exon

position:17202850:1
position: 17202850
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17202920:1
position: 17202920
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:17203720-17203948:1/exon

position:17203720:1
position: 17203720
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17203948:1
position: 17203948
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 17
SIO_000628: feature:17205667-17205867:1/exon

position:17205667:1
position: 17205667
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17205867:1
position: 17205867
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 18
SIO_000628: feature:17214717-17214859:1/exon

position:17214717:1
position: 17214717
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17214859:1
position: 17214859
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 19
SIO_000628: feature:17219982-17220095:1/exon

position:17219982:1
position: 17219982
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17220095:1
position: 17220095
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 20
SIO_000628: feature:17222096-17222191:1/exon

position:17222096:1
position: 17222096
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17222191:1
position: 17222191
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 21
SIO_000628: feature:17236587-17236765:1/exon

position:17236587:1
position: 17236587
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17236765:1
position: 17236765
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 22
SIO_000628: feature:17238585-17238663:1/exon

position:17238585:1
position: 17238585
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17238663:1
position: 17238663
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 23
SIO_000628: feature:17242387-17242466:1/exon

position:17242387:1
position: 17242387
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17242466:1
position: 17242466
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 24
SIO_000628: feature:17246722-17246845:1/exon

position:17246722:1
position: 17246722
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17246845:1
position: 17246845
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 25
SIO_000628: feature:17250115-17250310:1/exon

position:17250115:1
position: 17250115
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17250310:1
position: 17250310
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 26
SIO_000628: feature:17250622-17251230:1/exon

position:17250622:1
position: 17250622
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

USP25
type: SO_0000234
alternative label: USP21
gene: USP25
gene synonym: USP21
product: ubiquitin specific peptidase 25, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 63 ESTs, and 100% coverage by RNAseq alignments, including 5 samples with support for all introns
transcript id: XM_005260947.1
so part of: USP25
location: join(17102328..17102757,17135210..17135287,17138316..17138460,17150223..17150346,17163821..17163983,17172076..17172162,17177440..17177577,17181128..17181204,17183456..17183529,17191017..17191165,17196358..17196485,17197285..17197380,17198523..17198684,17199296..17199522,17202850..17202920,17203720..17203948,17205667..17205867,17214717..17214859,17219982..17220095,17236587..17236765,17238585..17238663,17242387..17242466,17246722..17246845,17250115..17250310,17250622..17251230)
location: region:17102328-17251230:1

GI:530418838
SIO_000068: ncbigi

position:17102328:1
position: 17102328
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17102328-17102757:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17135210-17135287:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17138316-17138460:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17150223-17150346:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17163821-17163983:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17172076-17172162:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17177440-17177577:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:17181128-17181204:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:17183456-17183529:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:17191017-17191165:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:17196358-17196485:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:17197285-17197380:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:17198523-17198684:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:17199296-17199522:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:17202850-17202920:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:17203720-17203948:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:17205667-17205867:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:17214717-17214859:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:17219982-17220095:1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:17236587-17236765:1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:17238585-17238663:1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:17242387-17242466:1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:17246722-17246845:1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:17250115-17250310:1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:17250622-17251230:1/exon

USP25
type: SO_0000234
alternative label: USP21
gene: USP25
gene synonym: USP21
product: ubiquitin specific peptidase 25, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 63 ESTs, 1 Protein, and 100% coverage by RNAseq alignments, including 6 samples with support for all introns
transcript id: XM_005260948.1
so part of: USP25
location: join(17102328..17102757,17135210..17135287,17138316..17138460,17150223..17150346,17163821..17163983,17172076..17172162,17177440..17177577,17181128..17181204,17183456..17183529,17191017..17191165,17196358..17196485,17197285..17197380,17198523..17198684,17199296..17199522,17202850..17202920,17203720..17203948,17205667..17205867,17214717..17214859,17222096..17222191,17236587..17236765,17238585..17238663,17242387..17242466,17246722..17246845,17250115..17250310,17250622..17251230)
location: region:17102328-17251230:1

GI:530418840
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:17102328-17102757:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17135210-17135287:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17138316-17138460:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17150223-17150346:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17163821-17163983:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17172076-17172162:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17177440-17177577:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:17181128-17181204:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:17183456-17183529:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:17191017-17191165:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:17196358-17196485:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:17197285-17197380:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:17198523-17198684:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:17199296-17199522:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:17202850-17202920:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:17203720-17203948:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:17205667-17205867:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:17214717-17214859:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:17222096-17222191:1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:17236587-17236765:1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:17238585-17238663:1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:17242387-17242466:1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:17246722-17246845:1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:17250115-17250310:1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:17250622-17251230:1/exon

USP25
type: SO_0000234
alternative label: USP21
gene: USP25
gene synonym: USP21
product: ubiquitin specific peptidase 25
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_013396.3
so part of: USP25
location: join(17102496..17102757,17135210..17135287,17138316..17138460,17150223..17150346,17163821..17163983,17172076..17172162,17177440..17177577,17181128..17181204,17183456..17183529,17191017..17191165,17196358..17196485,17197285..17197380,17198523..17198684,17199296..17199522,17202850..17202920,17203720..17203948,17205667..17205867,17214717..17214859,17236587..17236765,17238585..17238663,17242387..17242466,17246722..17246845,17250115..17250310,17250622..17252377)
location: region:17102496-17252377:1

GI:50312665
SIO_000068: ncbigi

position:17102496:1
position: 17102496
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17102496-17102757:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17135210-17135287:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17138316-17138460:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17150223-17150346:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17163821-17163983:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17172076-17172162:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17177440-17177577:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:17181128-17181204:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:17183456-17183529:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:17191017-17191165:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:17196358-17196485:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:17197285-17197380:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:17198523-17198684:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:17199296-17199522:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:17202850-17202920:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:17203720-17203948:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:17205667-17205867:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:17214717-17214859:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:17236587-17236765:1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:17238585-17238663:1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:17242387-17242466:1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:17246722-17246845:1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:17250115-17250310:1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:17250622-17252377:1/exon

USP25
type: SO_0000316
alternative label: USP21
gene: USP25
gene synonym: USP21
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: ubiquitin carboxyl-terminal hydrolase 25 isoform X1
translation: MTVEQNVLQQSAAQKHQQTFLNQLREITGINDTQILQQALKDSNGNLELAVAFLTAKNAKTPQQEETTYYQTALPGNDRYISVGSQADTNVIDLTGDDKDDLQRAIALSLAESNRAFRETGITDEEQAISRVLEASIAENKACLKRTPTEVWRDSRNPYDRKRQDKAPVGLKNVGNTCWFSAVIQSLFNLLEFRRLVLNYKPPSNAQDLPRNQKEHRNLPFMRELRYLFALLVGTKRKYVDPSRAVEILKDAFKSNDSQQQDVSEFTHKLLDWLEDAFQMKAEEETDEEKPKNPMVELFYGRFLAVGVLEGKKFENTEMFGQYPLQVNGFKDLHECLEAAMIEGEIESLHSENSGKSGQEHWFTELPPVLTFELSRFEFNQALGRPEKIHNKLEFPQVLYLDRYMHRNREITRIKREEIKRLKDYLTVLQQRLERYLSYGSGPKRFPLVDVLQYALEFASSKPVCTSPVDDIDASSPPSGSIPSQTLPSTTEQQGALSSELPSTSPSSVAAISSRSVIHKPFTQSRIPPDLPMHPAPRHITEEELSVLESCLHRWRTEIENDTRDLQESISRIHRTIELMYSDKSMIQVPYRLHAVLVHEGQANAGHYWAYIFDHRESRWMKYNDIAVTKSSWEELVRDSFGGYRNASAYCLMYINDKAQFLIQEEFNKETGQPLVGIETLPPDLRDFVEEDNQRFEKELEEWDAQLAQKALQEKLLASQKLRESETSVTTAQAAGDPEYLEQPSRSDFSKHLKEETIQIITKASHEHEDKSPETVLQSKPENTTSQPLSNQRVVEVAIPHVGKFMIESKEGGYDDEIMMTPNMQGIIMAIGKSRSVYDRCGPEAGFFKAIKLEYARLVKLAQEDTPPETDYRLHHVVVYFIQNQAPKKIIEKTLLEQFGDRNLSFDERCHNIMKVAQAKLEMIKPEEVNLEEYEEWHQDYRKFRETTMYLIIGLENFQRESYIDSLLFLICAYQNNKELLSKGLYRGHDEELISHYRRECLLKLNEQAAELFESGEDREVNNGLIIMNEFIVPFLPLLLVDEMEEKDILAVEDMRNRWCSYLGQEMEPHLQEKLTDFLPKLLDCSMEIKSFHEPPKLPSYSTHELCERFARIMLSLSRTPADGR
so part of: USP25
location: join(17102713..17102757,17135210..17135287,17138316..17138460,17150223..17150346,17163821..17163983,17172076..17172162,17177440..17177577,17181128..17181204,17183456..17183529,17191017..17191165,17196358..17196485,17197285..17197380,17198523..17198684,17199296..17199522,17202850..17202920,17203720..17203948,17205667..17205867,17214717..17214859,17219982..17220095,17222096..17222191,17236587..17236765,17238585..17238663,17242387..17242466,17246722..17246845,17250115..17250310,17250622..17250794)
location: region:17102713-17250794:1

XP_005261003.1
SIO_000068: ncbiprotein

GI:530418837
SIO_000068: ncbigi

position:17102713:1
position: 17102713
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17250794:1
position: 17250794
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17102713-17102757:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17135210-17135287:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17138316-17138460:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17150223-17150346:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17163821-17163983:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17172076-17172162:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17177440-17177577:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:17181128-17181204:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:17183456-17183529:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:17191017-17191165:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:17196358-17196485:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:17197285-17197380:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:17198523-17198684:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:17199296-17199522:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:17202850-17202920:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:17203720-17203948:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:17205667-17205867:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:17214717-17214859:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:17219982-17220095:1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:17222096-17222191:1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:17236587-17236765:1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:17238585-17238663:1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:17242387-17242466:1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:17246722-17246845:1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:17250115-17250310:1/exon

urn:…
SIO_000300: 26
SIO_000628: feature:17250622-17250794:1/exon

USP25
type: SO_0000316
alternative label: USP21
gene: USP25
gene synonym: USP21
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: ubiquitin carboxyl-terminal hydrolase 25 isoform X2
translation: MTVEQNVLQQSAAQKHQQTFLNQLREITGINDTQILQQALKDSNGNLELAVAFLTAKNAKTPQQEETTYYQTALPGNDRYISVGSQADTNVIDLTGDDKDDLQRAIALSLAESNRAFRETGITDEEQAISRVLEASIAENKACLKRTPTEVWRDSRNPYDRKRQDKAPVGLKNVGNTCWFSAVIQSLFNLLEFRRLVLNYKPPSNAQDLPRNQKEHRNLPFMRELRYLFALLVGTKRKYVDPSRAVEILKDAFKSNDSQQQDVSEFTHKLLDWLEDAFQMKAEEETDEEKPKNPMVELFYGRFLAVGVLEGKKFENTEMFGQYPLQVNGFKDLHECLEAAMIEGEIESLHSENSGKSGQEHWFTELPPVLTFELSRFEFNQALGRPEKIHNKLEFPQVLYLDRYMHRNREITRIKREEIKRLKDYLTVLQQRLERYLSYGSGPKRFPLVDVLQYALEFASSKPVCTSPVDDIDASSPPSGSIPSQTLPSTTEQQGALSSELPSTSPSSVAAISSRSVIHKPFTQSRIPPDLPMHPAPRHITEEELSVLESCLHRWRTEIENDTRDLQESISRIHRTIELMYSDKSMIQVPYRLHAVLVHEGQANAGHYWAYIFDHRESRWMKYNDIAVTKSSWEELVRDSFGGYRNASAYCLMYINDKAQFLIQEEFNKETGQPLVGIETLPPDLRDFVEEDNQRFEKELEEWDAQLAQKALQEKLLASQKLRESETSVTTAQAAGDPEYLEQPSRSDFSKHLKEETIQIITKASHEHEDKSPETVLQSKPENTTSQPLSNQRVVEVAIPHVGKFMIESKEGGYDDEAIKLEYARLVKLAQEDTPPETDYRLHHVVVYFIQNQAPKKIIEKTLLEQFGDRNLSFDERCHNIMKVAQAKLEMIKPEEVNLEEYEEWHQDYRKFRETTMYLIIGLENFQRESYIDSLLFLICAYQNNKELLSKGLYRGHDEELISHYRRECLLKLNEQAAELFESGEDREVNNGLIIMNEFIVPFLPLLLVDEMEEKDILAVEDMRNRWCSYLGQEMEPHLQEKLTDFLPKLLDCSMEIKSFHEPPKLPSYSTHELCERFARIMLSLSRTPADGR
so part of: USP25
location: join(17102713..17102757,17135210..17135287,17138316..17138460,17150223..17150346,17163821..17163983,17172076..17172162,17177440..17177577,17181128..17181204,17183456..17183529,17191017..17191165,17196358..17196485,17197285..17197380,17198523..17198684,17199296..17199522,17202850..17202920,17203720..17203948,17205667..17205867,17214717..17214859,17219982..17220095,17236587..17236765,17238585..17238663,17242387..17242466,17246722..17246845,17250115..17250310,17250622..17250794)
location: region:17102713-17250794:1

XP_005261004.1
SIO_000068: ncbiprotein

GI:530418839
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:17102713-17102757:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17135210-17135287:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17138316-17138460:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17150223-17150346:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17163821-17163983:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17172076-17172162:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17177440-17177577:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:17181128-17181204:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:17183456-17183529:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:17191017-17191165:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:17196358-17196485:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:17197285-17197380:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:17198523-17198684:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:17199296-17199522:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:17202850-17202920:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:17203720-17203948:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:17205667-17205867:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:17214717-17214859:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:17219982-17220095:1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:17236587-17236765:1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:17238585-17238663:1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:17242387-17242466:1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:17246722-17246845:1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:17250115-17250310:1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:17250622-17250794:1/exon

USP25
type: SO_0000316
alternative label: USP21
gene: USP25
gene synonym: USP21
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: ubiquitin carboxyl-terminal hydrolase 25 isoform X3
translation: MTVEQNVLQQSAAQKHQQTFLNQLREITGINDTQILQQALKDSNGNLELAVAFLTAKNAKTPQQEETTYYQTALPGNDRYISVGSQADTNVIDLTGDDKDDLQRAIALSLAESNRAFRETGITDEEQAISRVLEASIAENKACLKRTPTEVWRDSRNPYDRKRQDKAPVGLKNVGNTCWFSAVIQSLFNLLEFRRLVLNYKPPSNAQDLPRNQKEHRNLPFMRELRYLFALLVGTKRKYVDPSRAVEILKDAFKSNDSQQQDVSEFTHKLLDWLEDAFQMKAEEETDEEKPKNPMVELFYGRFLAVGVLEGKKFENTEMFGQYPLQVNGFKDLHECLEAAMIEGEIESLHSENSGKSGQEHWFTELPPVLTFELSRFEFNQALGRPEKIHNKLEFPQVLYLDRYMHRNREITRIKREEIKRLKDYLTVLQQRLERYLSYGSGPKRFPLVDVLQYALEFASSKPVCTSPVDDIDASSPPSGSIPSQTLPSTTEQQGALSSELPSTSPSSVAAISSRSVIHKPFTQSRIPPDLPMHPAPRHITEEELSVLESCLHRWRTEIENDTRDLQESISRIHRTIELMYSDKSMIQVPYRLHAVLVHEGQANAGHYWAYIFDHRESRWMKYNDIAVTKSSWEELVRDSFGGYRNASAYCLMYINDKAQFLIQEEFNKETGQPLVGIETLPPDLRDFVEEDNQRFEKELEEWDAQLAQKALQEKLLASQKLRESETSVTTAQAAGDPEYLEQPSRSDFSKHLKEETIQIITKASHEHEDKSPETVLQSIMMTPNMQGIIMAIGKSRSVYDRCGPEAGFFKAIKLEYARLVKLAQEDTPPETDYRLHHVVVYFIQNQAPKKIIEKTLLEQFGDRNLSFDERCHNIMKVAQAKLEMIKPEEVNLEEYEEWHQDYRKFRETTMYLIIGLENFQRESYIDSLLFLICAYQNNKELLSKGLYRGHDEELISHYRRECLLKLNEQAAELFESGEDREVNNGLIIMNEFIVPFLPLLLVDEMEEKDILAVEDMRNRWCSYLGQEMEPHLQEKLTDFLPKLLDCSMEIKSFHEPPKLPSYSTHELCERFARIMLSLSRTPADGR
so part of: USP25
location: join(17102713..17102757,17135210..17135287,17138316..17138460,17150223..17150346,17163821..17163983,17172076..17172162,17177440..17177577,17181128..17181204,17183456..17183529,17191017..17191165,17196358..17196485,17197285..17197380,17198523..17198684,17199296..17199522,17202850..17202920,17203720..17203948,17205667..17205867,17214717..17214859,17222096..17222191,17236587..17236765,17238585..17238663,17242387..17242466,17246722..17246845,17250115..17250310,17250622..17250794)
location: region:17102713-17250794:1

XP_005261005.1
SIO_000068: ncbiprotein

GI:530418841
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:17102713-17102757:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17135210-17135287:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17138316-17138460:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17150223-17150346:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17163821-17163983:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17172076-17172162:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17177440-17177577:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:17181128-17181204:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:17183456-17183529:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:17191017-17191165:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:17196358-17196485:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:17197285-17197380:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:17198523-17198684:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:17199296-17199522:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:17202850-17202920:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:17203720-17203948:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:17205667-17205867:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:17214717-17214859:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:17222096-17222191:1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:17236587-17236765:1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:17238585-17238663:1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:17242387-17242466:1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:17246722-17246845:1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:17250115-17250310:1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:17250622-17250794:1/exon

USP25
type: SO_0000316
alternative label: USP21
gene: USP25
gene synonym: USP21
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: ubiquitin carboxyl-terminal hydrolase 25
translation: MTVEQNVLQQSAAQKHQQTFLNQLREITGINDTQILQQALKDSNGNLELAVAFLTAKNAKTPQQEETTYYQTALPGNDRYISVGSQADTNVIDLTGDDKDDLQRAIALSLAESNRAFRETGITDEEQAISRVLEASIAENKACLKRTPTEVWRDSRNPYDRKRQDKAPVGLKNVGNTCWFSAVIQSLFNLLEFRRLVLNYKPPSNAQDLPRNQKEHRNLPFMRELRYLFALLVGTKRKYVDPSRAVEILKDAFKSNDSQQQDVSEFTHKLLDWLEDAFQMKAEEETDEEKPKNPMVELFYGRFLAVGVLEGKKFENTEMFGQYPLQVNGFKDLHECLEAAMIEGEIESLHSENSGKSGQEHWFTELPPVLTFELSRFEFNQALGRPEKIHNKLEFPQVLYLDRYMHRNREITRIKREEIKRLKDYLTVLQQRLERYLSYGSGPKRFPLVDVLQYALEFASSKPVCTSPVDDIDASSPPSGSIPSQTLPSTTEQQGALSSELPSTSPSSVAAISSRSVIHKPFTQSRIPPDLPMHPAPRHITEEELSVLESCLHRWRTEIENDTRDLQESISRIHRTIELMYSDKSMIQVPYRLHAVLVHEGQANAGHYWAYIFDHRESRWMKYNDIAVTKSSWEELVRDSFGGYRNASAYCLMYINDKAQFLIQEEFNKETGQPLVGIETLPPDLRDFVEEDNQRFEKELEEWDAQLAQKALQEKLLASQKLRESETSVTTAQAAGDPEYLEQPSRSDFSKHLKEETIQIITKASHEHEDKSPETVLQSAIKLEYARLVKLAQEDTPPETDYRLHHVVVYFIQNQAPKKIIEKTLLEQFGDRNLSFDERCHNIMKVAQAKLEMIKPEEVNLEEYEEWHQDYRKFRETTMYLIIGLENFQRESYIDSLLFLICAYQNNKELLSKGLYRGHDEELISHYRRECLLKLNEQAAELFESGEDREVNNGLIIMNEFIVPFLPLLLVDEMEEKDILAVEDMRNRWCSYLGQEMEPHLQEKLTDFLPKLLDCSMEIKSFHEPPKLPSYSTHELCERFARIMLSLSRTPADGR
so part of: USP25
location: join(17102713..17102757,17135210..17135287,17138316..17138460,17150223..17150346,17163821..17163983,17172076..17172162,17177440..17177577,17181128..17181204,17183456..17183529,17191017..17191165,17196358..17196485,17197285..17197380,17198523..17198684,17199296..17199522,17202850..17202920,17203720..17203948,17205667..17205867,17214717..17214859,17236587..17236765,17238585..17238663,17242387..17242466,17246722..17246845,17250115..17250310,17250622..17250794)
location: region:17102713-17250794:1

NP_037528.3
SIO_000068: ncbiprotein

GI:50312666
SIO_000068: ncbigi

CCDS33515.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:17102713-17102757:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17135210-17135287:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17138316-17138460:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17150223-17150346:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17163821-17163983:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17172076-17172162:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17177440-17177577:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:17181128-17181204:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:17183456-17183529:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:17191017-17191165:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:17196358-17196485:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:17197285-17197380:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:17198523-17198684:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:17199296-17199522:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:17202850-17202920:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:17203720-17203948:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:17205667-17205867:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:17214717-17214859:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:17236587-17236765:1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:17238585-17238663:1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:17242387-17242466:1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:17246722-17246845:1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:17250115-17250310:1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:17250622-17250794:1/exon

RBPMSLP
type: SO_0000704
gene: RBPMSLP
note: RNA binding protein with multiple splicing-like pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(17116323..17116647)
location: region:17116323-17116647:-1

54032
SIO_000068: ncbigene

9923
SIO_000068: hgnc

position:17116323:-1
position: 17116323
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:17116647:-1
position: 17116647
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

USP25
type: SO_0000234
alternative label: USP21
gene: USP25
gene synonym: USP21
product: ubiquitin specific peptidase 25, transcript variant X4
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 44 ESTs, and 99% coverage by RNAseq alignments, including 4 samples with support for all introns
transcript id: XM_005260949.1
so part of: USP25
location: join(17191040..17191165,17197285..17197380,17198523..17198684,17199296..17199522,17202850..17202920,17203720..17203948,17205667..17205867,17214717..17214859,17219982..17220095,17222096..17222191,17236587..17236765,17238585..17238663,17242387..17242466,17246722..17246845,17250115..17250310,17250622..17252031)
location: region:17191040-17252031:1

GI:530418842
SIO_000068: ncbigi

position:17191040:1
position: 17191040
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17252031:1
position: 17252031
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17191040-17191165:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17197285-17197380:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17198523-17198684:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17199296-17199522:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17202850-17202920:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17203720-17203948:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17205667-17205867:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:17214717-17214859:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:17219982-17220095:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:17222096-17222191:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:17236587-17236765:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:17238585-17238663:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:17242387-17242466:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:17246722-17246845:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:17250115-17250310:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:17250622-17252031:1/exon

USP25
type: SO_0000316
alternative label: USP21
gene: USP25
gene synonym: USP21
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: ubiquitin carboxyl-terminal hydrolase 25 isoform X4
translation: MHRNREITRIKREEIKRLKDYLTVLQQRLERYLSYGSGPKRFPLVDVLQYALEFASSKPVCTSPVDDIDASSPPSGSIPSQTLPSTTEQQGALSSELPSTSPSSVAAISSRSVIHKPFTQSRIPPDLPMHPAPRHITEEELSVLESCLHRWRTEIENDTRDLQESISRIHRTIELMYSDKSMIQVPYRLHAVLVHEGQANAGHYWAYIFDHRESRWMKYNDIAVTKSSWEELVRDSFGGYRNASAYCLMYINDKAQFLIQEEFNKETGQPLVGIETLPPDLRDFVEEDNQRFEKELEEWDAQLAQKALQEKLLASQKLRESETSVTTAQAAGDPEYLEQPSRSDFSKHLKEETIQIITKASHEHEDKSPETVLQSKPENTTSQPLSNQRVVEVAIPHVGKFMIESKEGGYDDEIMMTPNMQGIIMAIGKSRSVYDRCGPEAGFFKAIKLEYARLVKLAQEDTPPETDYRLHHVVVYFIQNQAPKKIIEKTLLEQFGDRNLSFDERCHNIMKVAQAKLEMIKPEEVNLEEYEEWHQDYRKFRETTMYLIIGLENFQRESYIDSLLFLICAYQNNKELLSKGLYRGHDEELISHYRRECLLKLNEQAAELFESGEDREVNNGLIIMNEFIVPFLPLLLVDEMEEKDILAVEDMRNRWCSYLGQEMEPHLQEKLTDFLPKLLDCSMEIKSFHEPPKLPSYSTHELCERFARIMLSLSRTPADGR
so part of: USP25
location: join(17197289..17197380,17198523..17198684,17199296..17199522,17202850..17202920,17203720..17203948,17205667..17205867,17214717..17214859,17219982..17220095,17222096..17222191,17236587..17236765,17238585..17238663,17242387..17242466,17246722..17246845,17250115..17250310,17250622..17250794)
location: region:17197289-17250794:1

XP_005261006.1
SIO_000068: ncbiprotein

GI:530418843
SIO_000068: ncbigi

position:17197289:1
position: 17197289
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17197289-17197380:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17198523-17198684:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17199296-17199522:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17202850-17202920:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17203720-17203948:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17205667-17205867:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17214717-17214859:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:17219982-17220095:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:17222096-17222191:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:17236587-17236765:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:17238585-17238663:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:17242387-17242466:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:17246722-17246845:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:17250115-17250310:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:17250622-17250794:1/exon

LINC00478
type: SO_0000704
alternative label: C21orf34
alternative label: C21orf35
alternative label: FLJ38295
gene: LINC00478
gene synonym: C21orf34; C21orf35; FLJ38295
note: long intergenic non-protein coding RNA 478; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 17442842..17982094
location: region:17442842-17982094:1
SIO_010080: LINC00478

388815
SIO_000068: ncbigene

1274
SIO_000068: hgnc

position:17442842:1
position: 17442842
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17982094:1
position: 17982094
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LINC00478
type: SO_0000673
alternative label: C21orf34
alternative label: C21orf35
alternative label: FLJ38295
gene: LINC00478
gene synonym: C21orf34; C21orf35; FLJ38295
product: long intergenic non-protein coding RNA 478, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_027790.1
so part of: LINC00478
location: join(17442842..17442868,17443434..17443718,17553911..17554007,17603376..17603435,17859810..17859858,17909699..17909759,17966660..17966774,17979314..17982094)
location: region:17442842-17982094:1

GI:239937464
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:17442842-17442868:1/exon

position:17442868:1
position: 17442868
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:17443434-17443718:1/exon

position:17443434:1
position: 17443434
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17443718:1
position: 17443718
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:17553911-17554007:1/exon

position:17553911:1
position: 17553911
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17554007:1
position: 17554007
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:17603376-17603435:1/exon

position:17603376:1
position: 17603376
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17603435:1
position: 17603435
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:17859810-17859858:1/exon

position:17859810:1
position: 17859810
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17859858:1
position: 17859858
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:17909699-17909759:1/exon

position:17909699:1
position: 17909699
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17909759:1
position: 17909759
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:17966660-17966774:1/exon

position:17966660:1
position: 17966660
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17966774:1
position: 17966774
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:17979314-17982094:1/exon

position:17979314:1
position: 17979314
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

VDAC2P1
type: SO_0000704
alternative label: VDAC2P
gene: VDAC2P1
gene synonym: VDAC2P
note: voltage-dependent anion channel 2 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(17466509..17467792)
location: region:17466509-17467792:-1

54015
SIO_000068: ncbigene

12673
SIO_000068: hgnc

position:17466509:-1
position: 17466509
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:17467792:-1
position: 17467792
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

RPS26P5
type: SO_0000704
alternative label: RPS26_31_1718
gene: RPS26P5
gene synonym: RPS26_31_1718
note: ribosomal protein S26 pseudogene 5; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(17493563..17493985)
location: region:17493563-17493985:-1

387495
SIO_000068: ncbigene

23776
SIO_000068: hgnc

position:17493563:-1
position: 17493563
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:17493985:-1
position: 17493985
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00478
type: SO_0000673
alternative label: C21orf34
alternative label: C21orf35
alternative label: FLJ38295
gene: LINC00478
gene synonym: C21orf34; C21orf35; FLJ38295
product: long intergenic non-protein coding RNA 478, transcript variant X5
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 100% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XR_244279.1
so part of: LINC00478
location: join(17566582..17566953,17603376..17603435,17763934..17764005,17859810..17859858,17966660..17966774,17979314..17979461)
location: region:17566582-17979461:1

GI:530418909
SIO_000068: ncbigi

position:17566582:1
position: 17566582
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17979461:1
position: 17979461
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17566582-17566953:1/exon

position:17566953:1
position: 17566953
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:17603376-17603435:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17763934-17764005:1/exon

position:17763934:1
position: 17763934
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17764005:1
position: 17764005
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:17859810-17859858:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17966660-17966774:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17979314-17979461:1/exon

LINC00478
type: SO_0000673
alternative label: C21orf34
alternative label: C21orf35
alternative label: FLJ38295
gene: LINC00478
gene synonym: C21orf34; C21orf35; FLJ38295
product: long intergenic non-protein coding RNA 478, transcript variant X4
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XR_244278.1
so part of: LINC00478
location: join(17566585..17566953,17603376..17603435,17763934..17764005,17859810..17859858,17909699..17909759,17966660..17966774,17968705..17968722,17979314..17979461)
location: region:17566585-17979461:1

GI:530418908
SIO_000068: ncbigi

position:17566585:1
position: 17566585
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17566585-17566953:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17603376-17603435:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17763934-17764005:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17859810-17859858:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17909699-17909759:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17966660-17966774:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17968705-17968722:1/exon

position:17968705:1
position: 17968705
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17968722:1
position: 17968722
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:17979314-17979461:1/exon

LINC00478
type: SO_0000673
alternative label: C21orf34
alternative label: C21orf35
alternative label: FLJ38295
gene: LINC00478
gene synonym: C21orf34; C21orf35; FLJ38295
product: long intergenic non-protein coding RNA 478, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, and 100% coverage by RNAseq alignments, including 5 samples with support for all introns
transcript id: XR_244275.1
so part of: LINC00478
location: join(17566588..17566953,17603376..17603435,17763934..17764005,17859810..17859858,17909699..17909759,17966660..17966774,17979314..17979461)
location: region:17566588-17979461:1

GI:530418905
SIO_000068: ncbigi

position:17566588:1
position: 17566588
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17566588-17566953:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17603376-17603435:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17763934-17764005:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17859810-17859858:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17909699-17909759:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17966660-17966774:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:17979314-17979461:1/exon

LINC00478
type: SO_0000673
alternative label: C21orf34
alternative label: C21orf35
alternative label: FLJ38295
gene: LINC00478
gene synonym: C21orf34; C21orf35; FLJ38295
product: long intergenic non-protein coding RNA 478, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_027791.1
so part of: LINC00478
location: join(17566699..17566953,17603376..17603435,17763934..17764005,17859810..17859858,17909699..17909759,17979314..17982094)
location: region:17566699-17982094:1

GI:239937465
SIO_000068: ncbigi

position:17566699:1
position: 17566699
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17566699-17566953:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17603376-17603435:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17763934-17764005:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17859810-17859858:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17909699-17909759:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:17979314-17982094:1/exon

LINC00478
type: SO_0000673
alternative label: C21orf34
alternative label: C21orf35
alternative label: FLJ38295
gene: LINC00478
gene synonym: C21orf34; C21orf35; FLJ38295
product: long intergenic non-protein coding RNA 478, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 100% coverage by RNAseq alignments, including 10 samples with support for all introns
transcript id: XR_244277.1
so part of: LINC00478
location: join(17791561..17792061,17859810..17859858,17909699..17909759,17966660..17966774,17979314..17979461)
location: region:17791561-17979461:1

GI:530418907
SIO_000068: ncbigi

position:17791561:1
position: 17791561
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17791561-17792061:1/exon

position:17792061:1
position: 17792061
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:17859810-17859858:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17909699-17909759:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17966660-17966774:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:17979314-17979461:1/exon

LINC00478
type: SO_0000673
alternative label: C21orf34
alternative label: C21orf35
alternative label: FLJ38295
gene: LINC00478
gene synonym: C21orf34; C21orf35; FLJ38295
product: long intergenic non-protein coding RNA 478, transcript variant X7
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 100% coverage by RNAseq alignments, including 10 samples with support for all introns
transcript id: XR_244281.1
so part of: LINC00478
location: join(17791648..17792061,17859810..17859858,17979314..17979461)
location: region:17791648-17979461:1

GI:530418911
SIO_000068: ncbigi

position:17791648:1
position: 17791648
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17791648-17792061:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17859810-17859858:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17979314-17979461:1/exon

LINC00478
type: SO_0000673
alternative label: C21orf34
alternative label: C21orf35
alternative label: FLJ38295
gene: LINC00478
gene synonym: C21orf34; C21orf35; FLJ38295
product: long intergenic non-protein coding RNA 478, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, and 100% coverage by RNAseq alignments, including 14 samples with support for all introns
transcript id: XR_244276.1
so part of: LINC00478
location: join(17791722..17792061,17859810..17859858,17909699..17909759,17979314..17979461)
location: region:17791722-17979461:1

GI:530418906
SIO_000068: ncbigi

position:17791722:1
position: 17791722
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17791722-17792061:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:17859810-17859858:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17909699-17909759:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:17979314-17979461:1/exon

LINC00478
type: SO_0000673
alternative label: C21orf34
alternative label: C21orf35
alternative label: FLJ38295
gene: LINC00478
gene synonym: C21orf34; C21orf35; FLJ38295
product: long intergenic non-protein coding RNA 478, transcript variant X6
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage by RNAseq alignments, including 8 samples with support for all introns
transcript id: XR_244280.1
so part of: LINC00478
location: join(17907329..17908029,17909699..17909759,17979314..17979461)
location: region:17907329-17979461:1

GI:530418910
SIO_000068: ncbigi

position:17907329:1
position: 17907329
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:17907329-17908029:1/exon

position:17908029:1
position: 17908029
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:17909699-17909759:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:17979314-17979461:1/exon

MIR99A
type: SO_0000704
alternative label: MIRN99A
gene: MIR99A
gene synonym: MIRN99A
note: microRNA 99a; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 17911409..17911489
location: region:17911409-17911489:1
SIO_010080: MIR99A

407055
SIO_000068: ncbigene

31650
SIO_000068: hgnc

614509
SIO_000068: omim

MI0000101
SIO_000068: mirbase

position:17911409:1
position: 17911409
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17911489:1
position: 17911489
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR99A
type: SO_0000185
alternative label: MIRN99A
gene: MIR99A
gene synonym: MIRN99A
product: microRNA 99a
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_029514.1
so part of: MIR99A
location: 17911409..17911489
location: region:17911409-17911489:1

GI:262205756
SIO_000068: ncbigi

MIR99A
type: SO_0000655
alternative label: MIRN99A
gene: MIR99A
gene synonym: MIRN99A
nc RNA class: miRNA
product: hsa-miR-99a-5p
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR99A
location: 17911421..17911442
location: region:17911421-17911442:1

MIMAT0000097
SIO_000068: mirbase

position:17911421:1
position: 17911421
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17911442:1
position: 17911442
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR99A
type: SO_0000655
alternative label: MIRN99A
gene: MIR99A
gene synonym: MIRN99A
nc RNA class: miRNA
product: hsa-miR-99a-3p
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR99A
location: 17911458..17911479
location: region:17911458-17911479:1

MIMAT0004511
SIO_000068: mirbase

position:17911458:1
position: 17911458
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17911479:1
position: 17911479
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIRLET7C
type: SO_0000704
alternative label: hsa-let-7c
alternative label: let-7c
alternative label: LET7C
alternative label: MIRNLET7C
gene: MIRLET7C
gene synonym: hsa-let-7c; let-7c; LET7C; MIRNLET7C
note: microRNA let-7c; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 17912148..17912231
location: region:17912148-17912231:1
SIO_010080: MIRLET7C

406885
SIO_000068: ncbigene

31480
SIO_000068: hgnc

612144
SIO_000068: omim

MI0000064
SIO_000068: mirbase

position:17912148:1
position: 17912148
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17912231:1
position: 17912231
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIRLET7C
type: SO_0000185
alternative label: hsa-let-7c
alternative label: let-7c
alternative label: LET7C
alternative label: MIRNLET7C
gene: MIRLET7C
gene synonym: hsa-let-7c; let-7c; LET7C; MIRNLET7C
product: microRNA let-7c
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_029480.1
so part of: MIRLET7C
location: 17912148..17912231
location: region:17912148-17912231:1

GI:262205602
SIO_000068: ncbigi

MIRLET7C
type: SO_0000655
alternative label: hsa-let-7c
alternative label: let-7c
alternative label: LET7C
alternative label: MIRNLET7C
gene: MIRLET7C
gene synonym: hsa-let-7c; let-7c; LET7C; MIRNLET7C
nc RNA class: miRNA
product: hsa-let-7c
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIRLET7C
location: 17912158..17912179
location: region:17912158-17912179:1

MIMAT0000064
SIO_000068: mirbase

position:17912158:1
position: 17912158
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17912179:1
position: 17912179
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR125B2
type: SO_0000704
alternative label: MIRN125B2
gene: MIR125B2
gene synonym: MIRN125B2
note: microRNA 125b-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 17962557..17962645
location: region:17962557-17962645:1
SIO_010080: MIR125B2

406912
SIO_000068: ncbigene

31507
SIO_000068: hgnc

610105
SIO_000068: omim

MI0000470
SIO_000068: mirbase

position:17962557:1
position: 17962557
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17962645:1
position: 17962645
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR125B2
type: SO_0000185
alternative label: MIRN125B2
gene: MIR125B2
gene synonym: MIRN125B2
product: microRNA 125b-2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_029694.1
so part of: MIR125B2
location: 17962557..17962645
location: region:17962557-17962645:1

GI:262205364
SIO_000068: ncbigi

MIR125B2
type: SO_0000655
alternative label: MIRN125B2
gene: MIR125B2
gene synonym: MIRN125B2
nc RNA class: miRNA
product: hsa-miR-125b-5p
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR125B2
location: 17962573..17962594
location: region:17962573-17962594:1

MIMAT0000423
SIO_000068: mirbase

position:17962573:1
position: 17962573
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17962594:1
position: 17962594
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR125B2
type: SO_0000655
alternative label: MIRN125B2
gene: MIR125B2
gene synonym: MIRN125B2
nc RNA class: miRNA
product: hsa-miR-125b-2-3p
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR125B2
location: 17962610..17962631
location: region:17962610-17962631:1

MIMAT0004603
SIO_000068: mirbase

position:17962610:1
position: 17962610
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:17962631:1
position: 17962631
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927771
type: SO_0000704
gene: LOC101927771
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 18003271..18012654
location: region:18003271-18012654:1
SIO_010080: LOC101927771

101927771
SIO_000068: ncbigene

position:18003271:1
position: 18003271
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18012654:1
position: 18012654
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927771
type: SO_0000673
gene: LOC101927771
product: uncharacterized LOC101927771
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XR_244294.1
so part of: LOC101927771
location: join(18003271..18003291,18003760..18003808,18012549..18012654)
location: region:18003271-18012654:1

GI:530419145
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:18003271-18003291:1/exon

position:18003291:1
position: 18003291
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:18003760-18003808:1/exon

position:18003760:1
position: 18003760
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18003808:1
position: 18003808
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:18012549-18012654:1/exon

position:18012549:1
position: 18012549
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

NEK4P1
type: SO_0000704
gene: NEK4P1
note: NIMA-related kinase 4 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(18582786..18583674)
location: region:18582786-18583674:-1

100421718
SIO_000068: ncbigene

39649
SIO_000068: hgnc

position:18582786:-1
position: 18582786
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:18583674:-1
position: 18583674
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C21orf37
type: SO_0000704
gene: C21orf37
note: chromosome 21 open reading frame 37; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 18811208..>18821503
location: region:18811208-18821503:1
SIO_010080: C21orf37

100505929
SIO_000068: ncbigene

1277
SIO_000068: hgnc

position:18811208:1
position: 18811208
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18821503:1
position: 18821503
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: FuzzyPosition

C21orf37
type: SO_0000673
gene: C21orf37
product: chromosome 21 open reading frame 37, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_037585.1
so part of: C21orf37
location: join(18811208..18811315,18813992..18814161,18816401..18816518,18821183..>18821503)
location: region:18811208-18821503:1

GI:312284077
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:18811208-18811315:1/exon

position:18811315:1
position: 18811315
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:18813992-18814161:1/exon

position:18813992:1
position: 18813992
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18814161:1
position: 18814161
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:18816401-18816518:1/exon

position:18816401:1
position: 18816401
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18816518:1
position: 18816518
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:18821183-18821503:1/exon

position:18821183:1
position: 18821183
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

C21orf37
type: SO_0000673
gene: C21orf37
product: chromosome 21 open reading frame 37, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_037586.1
so part of: C21orf37
location: join(18811208..18811315,18813992..18814161,18816401..18816518,18821189..>18821503)
location: region:18811208-18821503:1

GI:312284078
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:18811208-18811315:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18813992-18814161:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18816401-18816518:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18821189-18821503:1/exon

position:18821189:1
position: 18821189
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

TRNAG27
type: SO_0000704
gene: TRNAG27
note: Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(18827107..18827177)
location: region:18827107-18827177:-1
SIO_010080: TRNAG27

100189284
SIO_000068: ncbigene

34850
SIO_000068: hgnc

position:18827107:-1
position: 18827107
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:18827177:-1
position: 18827177
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

TRNAG27
type: SO_0000253
gene: TRNAG27
product: tRNA-Gly
inference: COORDINATES: profile:tRNAscan-SE:1.23
note: transfer RNA glycine 27 (anticodon GCC); tRNA features were annotated by tRNAscan-SE; Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
anticodon: (pos:complement(18827143..18827145),aa:Gly, seq:gcc)
so part of: TRNAG27
location: complement(18827107..18827177)
location: region:18827107-18827177:-1

RPL39P40
type: SO_0000704
alternative label: RPL39_21_1719
gene: RPL39P40
gene synonym: RPL39_21_1719
note: ribosomal protein L39 pseudogene 40; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(18872997..18873116)
location: region:18872997-18873116:-1

100271531
SIO_000068: ncbigene

35823
SIO_000068: hgnc

position:18872997:-1
position: 18872997
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:18873116:-1
position: 18873116
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

CXADR
type: SO_0000704
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
note: coxsackie virus and adenovirus receptor; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 18885224..18965897
location: region:18885224-18965897:1
SIO_010080: CXADR

1525
SIO_000068: ncbigene

2559
SIO_000068: hgnc

11804
SIO_000068: hprd

602621
SIO_000068: omim

position:18885224:1
position: 18885224
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18965897:1
position: 18965897
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

CXADR
type: SO_0000234
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
product: coxsackie virus and adenovirus receptor, transcript variant 5
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001207066.1
so part of: CXADR
location: join(18885224..18885490,18919345..18919511,18924067..18924271,18931294..18931449,18933020..18933142,18933656..18933794,18937746..18937929,18965470..18965897)
location: region:18885224-18965897:1

GI:333470708
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:18885224-18885490:1/exon

position:18885490:1
position: 18885490
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

position:18919345:1
position: 18919345
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18919511:1
position: 18919511
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:18924067-18924271:1/exon

position:18924067:1
position: 18924067
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18924271:1
position: 18924271
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:18931294-18931449:1/exon

position:18931294:1
position: 18931294
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18931449:1
position: 18931449
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:18933020-18933142:1/exon

position:18933020:1
position: 18933020
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18933142:1
position: 18933142
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:18933656-18933794:1/exon

position:18933656:1
position: 18933656
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18933794:1
position: 18933794
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:18937746-18937929:1/exon

position:18937746:1
position: 18937746
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18937929:1
position: 18937929
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:18965470-18965897:1/exon

position:18965470:1
position: 18965470
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

CXADR
type: SO_0000234
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
product: coxsackie virus and adenovirus receptor, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001338.4
so part of: CXADR
location: join(18885224..18885490,18919345..18919511,18924067..18924271,18931294..18931449,18933020..18933142,18933656..18933794,18937746..18942429)
location: region:18885224-18942429:1

GI:333470701
SIO_000068: ncbigi

position:18942429:1
position: 18942429
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:18885224-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18924067-18924271:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18931294-18931449:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:18933020-18933142:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:18933656-18933794:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:18937746-18942429:1/exon

CXADR
type: SO_0000234
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
product: coxsackie virus and adenovirus receptor, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001207063.1
so part of: CXADR
location: join(18885224..18885490,18919345..18919511,18924067..18924271,18931294..18931449,18937746..18942429)
location: region:18885224-18942429:1

GI:333470702
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:18885224-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18924067-18924271:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18931294-18931449:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:18937746-18942429:1/exon

CXADR
type: SO_0000234
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
product: coxsackie virus and adenovirus receptor, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001207064.1
so part of: CXADR
location: join(18885224..18885490,18919345..18919511,18924067..18924271,18937746..18942429)
location: region:18885224-18942429:1

GI:333470706
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:18885224-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18924067-18924271:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18937746-18942429:1/exon

CXADR
type: SO_0000234
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
product: coxsackie virus and adenovirus receptor, transcript variant 4
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001207065.1
so part of: CXADR
location: join(18885224..18885490,18919345..18919511,18937746..18942429)
location: region:18885224-18942429:1

GI:333470704
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:18885224-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18937746-18942429:1/exon

CXADR
type: SO_0000234
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
product: coxsackie virus and adenovirus receptor, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 51 ESTs, 1 Protein, and 96% coverage by RNAseq alignments
transcript id: XM_005260928.1
so part of: CXADR
location: join(18885334..18885490,18919345..18919511,18924067..18924271,18931294..18931449,18933656..18933794,18937746..18942418)
location: region:18885334-18942418:1

GI:530418798
SIO_000068: ncbigi

position:18885334:1
position: 18885334
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18942418:1
position: 18942418
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:18885334-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18924067-18924271:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18931294-18931449:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:18933656-18933794:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:18937746-18942418:1/exon

CXADR
type: SO_0000316
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
note: isoform 5 precursor is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: coxsackievirus and adenovirus receptor isoform 5 precursor
translation: MALLLCFVLLCGVVDFARSLSITTPEEMIEKAKGETAYLPCKFTLSPEDQGPLDIEWLISPADNQKVDQVIILYSGDKIYDDYYPDLKGRVHFTSNDLKSGDASINVTNLQLSDIGTYQCKVKKAPGVANKKIHLVVLVKPSGARCYVDGSEEIGSDFKIKCEPKEGSLPLQYEWQKLSDSQKMPTSWLAEMTSSVISVKNASSEYSGTYSCTVRNRVGSDQCLLRLNVVPPSNKAGLIAGAIIGTLLALALIGLIIFCCRKKRREEKYEKEVHHDIREDVPPPKSRTSTARSYIGSNHSSLGSMSPSNMEGYSKTQYNQVPSEDFERTPQSPTLPPAKFKYPYKTDGITVV
so part of: CXADR
location: join(18885448..18885490,18919345..18919511,18924067..18924271,18931294..18931449,18933020..18933142,18933656..18933794,18937746..18937929,18965470..18965511)
location: region:18885448-18965511:1

NP_001193995.1
SIO_000068: ncbiprotein

GI:333470709
SIO_000068: ncbigi

CCDS56204.1
SIO_000068: ccds

position:18885448:1
position: 18885448
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18965511:1
position: 18965511
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:18885448-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18924067-18924271:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18931294-18931449:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:18933020-18933142:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:18933656-18933794:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:18937746-18937929:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:18965470-18965511:1/exon

CXADR
type: SO_0000316
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
note: isoform 1 precursor is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: coxsackievirus and adenovirus receptor isoform 1 precursor
translation: MALLLCFVLLCGVVDFARSLSITTPEEMIEKAKGETAYLPCKFTLSPEDQGPLDIEWLISPADNQKVDQVIILYSGDKIYDDYYPDLKGRVHFTSNDLKSGDASINVTNLQLSDIGTYQCKVKKAPGVANKKIHLVVLVKPSGARCYVDGSEEIGSDFKIKCEPKEGSLPLQYEWQKLSDSQKMPTSWLAEMTSSVISVKNASSEYSGTYSCTVRNRVGSDQCLLRLNVVPPSNKAGLIAGAIIGTLLALALIGLIIFCCRKKRREEKYEKEVHHDIREDVPPPKSRTSTARSYIGSNHSSLGSMSPSNMEGYSKTQYNQVPSEDFERTPQSPTLPPAKVAAPNLSRMGAIPVMIPAQSKDGSIV
so part of: CXADR
location: join(18885448..18885490,18919345..18919511,18924067..18924271,18931294..18931449,18933020..18933142,18933656..18933794,18937746..18938010)
location: region:18885448-18938010:1

NP_001329.1
SIO_000068: ncbiprotein

GI:4503173
SIO_000068: ncbigi

CCDS33519.1
SIO_000068: ccds

position:18938010:1
position: 18938010
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:18885448-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18924067-18924271:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18931294-18931449:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:18933020-18933142:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:18933656-18933794:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:18937746-18938010:1/exon

CXADR
type: SO_0000316
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: coxsackievirus and adenovirus receptor isoform X1
translation: MALLLCFVLLCGVVDFARSLSITTPEEMIEKAKGETAYLPCKFTLSPEDQGPLDIEWLISPADNQKVDQVIILYSGDKIYDDYYPDLKGRVHFTSNDLKSGDASINVTNLQLSDIGTYQCKVKKAPGVANKKIHLVVLVKPSGARCYVDGSEEIGSDFKIKCEPKEGSLPLQYEWQKLSDSQKMPTSWLAASNKAGLIAGAIIGTLLALALIGLIIFCCRKKRREEKYEKEVHHDIREDVPPPKSRTSTARSYIGSNHSSLGSMSPSNMEGYSKTQYNQVPSEDFERTPQSPTLPPAKVAAPNLSRMGAIPVMIPAQSKDGSIV
so part of: CXADR
location: join(18885448..18885490,18919345..18919511,18924067..18924271,18931294..18931449,18933656..18933794,18937746..18938010)
location: region:18885448-18938010:1

XP_005260985.1
SIO_000068: ncbiprotein

GI:530418799
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:18885448-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18924067-18924271:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18931294-18931449:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:18933656-18933794:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:18937746-18938010:1/exon

CXADR
type: SO_0000316
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
note: isoform 2 precursor is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: coxsackievirus and adenovirus receptor isoform 2 precursor
translation: MALLLCFVLLCGVVDFARSLSITTPEEMIEKAKGETAYLPCKFTLSPEDQGPLDIEWLISPADNQKVDQVIILYSGDKIYDDYYPDLKGRVHFTSNDLKSGDASINVTNLQLSDIGTYQCKVKKAPGVANKKIHLVVLVKPSGARCYVDGSEEIGSDFKIKCEPKEGSLPLQYEWQKLSDSQKMPTSWLAGKMCHLQRAVRPLPEATSAVIIHPWGPCLLPTWKDIPRLSITKYQVKTLNALLRVRLSHLLR
so part of: CXADR
location: join(18885448..18885490,18919345..18919511,18924067..18924271,18931294..18931449,18937746..18937933)
location: region:18885448-18937933:1

NP_001193992.1
SIO_000068: ncbiprotein

GI:333470703
SIO_000068: ncbigi

CCDS56205.1
SIO_000068: ccds

position:18937933:1
position: 18937933
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:18885448-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18924067-18924271:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18931294-18931449:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:18937746-18937933:1/exon

CXADR
type: SO_0000316
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
note: isoform 3 precursor is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: coxsackievirus and adenovirus receptor isoform 3 precursor
translation: MALLLCFVLLCGVVDFARSLSITTPEEMIEKAKGETAYLPCKFTLSPEDQGPLDIEWLISPADNQKVDQVIILYSGDKIYDDYYPDLKGRVHFTSNDLKSGDASINVTNLQLSDIGTYQCKVKKAPGVANKKIHLVVLGKMCHLQRAVRPLPEATSAVIIHPWGPCLLPTWKDIPRLSITKYQVKTLNALLRVRLSHLLR
so part of: CXADR
location: join(18885448..18885490,18919345..18919511,18924067..18924271,18937746..18937933)
location: region:18885448-18937933:1

NP_001193993.1
SIO_000068: ncbiprotein

GI:333470707
SIO_000068: ncbigi

CCDS56206.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:18885448-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18924067-18924271:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18937746-18937933:1/exon

CXADR
type: SO_0000316
alternative label: CAR
alternative label: CAR4/6
alternative label: HCAR
gene: CXADR
gene synonym: CAR; CAR4/6; HCAR
note: isoform 4 precursor is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: coxsackievirus and adenovirus receptor isoform 4 precursor
translation: MALLLCFVLLCGVVDFARSLSITTPEEMIEKAKGETAYLPCKFTLSPEDQGPLDIEWLISPADNQKVDQVGRCATSKEPYVHCQKLHRQ
so part of: CXADR
location: join(18885448..18885490,18919345..18919511,18937746..18937805)
location: region:18885448-18937805:1

NP_001193994.1
SIO_000068: ncbiprotein

GI:333470705
SIO_000068: ncbigi

CCDS56207.1
SIO_000068: ccds

position:18937805:1
position: 18937805
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:18885448-18885490:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18919345-18919511:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18937746-18937805:1/exon

BTF3L4P1
type: SO_0000704
gene: BTF3L4P1
note: basic transcription factor 3-like 4 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(18889252..18891379)
location: region:18889252-18891379:-1

100505945
SIO_000068: ncbigene

39645
SIO_000068: hgnc

position:18889252:-1
position: 18889252
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:18891379:-1
position: 18891379
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

BTG3
type: SO_0000704
alternative label: ANA
alternative label: TOB5
alternative label: TOB55
alternative label: TOFA
gene: BTG3
gene synonym: ANA; TOB5; TOB55; TOFA
note: BTG family, member 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(18965968..18985268)
location: region:18965968-18985268:-1
SIO_010080: BTG3

10950
SIO_000068: ncbigene

1132
SIO_000068: hgnc

10415
SIO_000068: hprd

605674
SIO_000068: omim

position:18965968:-1
position: 18965968
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:18985268:-1
position: 18985268
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

BTG3
type: SO_0000234
alternative label: ANA
alternative label: TOB5
alternative label: TOB55
alternative label: TOFA
gene: BTG3
gene synonym: ANA; TOB5; TOB55; TOFA
product: BTG family, member 3, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_006806.4
so part of: BTG3
location: complement(join(18965968..18966650,18970935..18971142,18977178..18977315,18981290..18981470,18985017..18985268))
location: region:18965968-18985268:-1

GI:195963404
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:18985017-18985268:-1/exon

position:18985017:-1
position: 18985017
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:18981290-18981470:-1/exon

position:18981290:-1
position: 18981290
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:18981470:-1
position: 18981470
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:18977178-18977315:-1/exon

position:18977178:-1
position: 18977178
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:18977315:-1
position: 18977315
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:18970935-18971142:-1/exon

position:18970935:-1
position: 18970935
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:18971142:-1
position: 18971142
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:18965968-18966650:-1/exon

position:18966650:-1
position: 18966650
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

BTG3
type: SO_0000234
alternative label: ANA
alternative label: TOB5
alternative label: TOB55
alternative label: TOFA
gene: BTG3
gene synonym: ANA; TOB5; TOB55; TOFA
product: BTG family, member 3, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001130914.1
so part of: BTG3
location: complement(join(18965968..18966650,18970935..18971142,18976463..18976594,18977178..18977315,18981290..18981470,18985017..18985268))
location: region:18965968-18985268:-1

GI:195963405
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:18985017-18985268:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18981290-18981470:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18977178-18977315:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18976463-18976594:-1/exon

position:18976463:-1
position: 18976463
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:18976594:-1
position: 18976594
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:18970935-18971142:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:18965968-18966650:-1/exon

BTG3
type: SO_0000316
alternative label: ANA
alternative label: TOB5
alternative label: TOB55
alternative label: TOFA
gene: BTG3
gene synonym: ANA; TOB5; TOB55; TOFA
note: isoform b is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: protein BTG3 isoform b
translation: MKNEIAAVVFFFTRLVRKHDKLKKEAVERFAEKLTLILQEKYKNHWYPEKPSKGQAYRCIRVNKFQRVDPDVLKACENSCILYSDLGLPKELTLWVDPCEVCCRYGEKNNAFIVASFENKDENKDEISRKVTRALDKVTSDYHSGSSSSDEETSKEMEVKPSSVTAAASPVYQISELIFPPLPMWHPLPRKKPGMYRGNGHQNHYPPPVPFGYPNQGRKNKPYRPIPVTWVPPPGMHCDRNHWINPHMLAPH
so part of: BTG3
location: complement(join(18966411..18966650,18970935..18971142,18977178..18977315,18981290..18981462))
location: region:18966411-18981462:-1

NP_006797.3
SIO_000068: ncbiprotein

GI:28872722
SIO_000068: ncbigi

CCDS13569.1
SIO_000068: ccds

position:18966411:-1
position: 18966411
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:18981462:-1
position: 18981462
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:18981290-18981462:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18977178-18977315:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18970935-18971142:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18966411-18966650:-1/exon

BTG3
type: SO_0000316
alternative label: ANA
alternative label: TOB5
alternative label: TOB55
alternative label: TOFA
gene: BTG3
gene synonym: ANA; TOB5; TOB55; TOFA
note: isoform a is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: protein BTG3 isoform a
translation: MKNEIAAVVFFFTRLVRKHDKLKKEAVERFAEKLTLILQEKYKNHWYPEKPSKGQAYRCIRVNKFQRVDPDVLKACENSCILYSDLGLPKELTLWVDPCEVCCRRDGVSPCWPDCSQTPDLVIRPPWPPKALDYRREPLRPASSFLIMYGEKNNAFIVASFENKDENKDEISRKVTRALDKVTSDYHSGSSSSDEETSKEMEVKPSSVTAAASPVYQISELIFPPLPMWHPLPRKKPGMYRGNGHQNHYPPPVPFGYPNQGRKNKPYRPIPVTWVPPPGMHCDRNHWINPHMLAPH
so part of: BTG3
location: complement(join(18966411..18966650,18970935..18971142,18976463..18976594,18977178..18977315,18981290..18981462))
location: region:18966411-18981462:-1

NP_001124386.1
SIO_000068: ncbiprotein

GI:195963406
SIO_000068: ncbigi

CCDS46636.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:18981290-18981462:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:18977178-18977315:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:18976463-18976594:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:18970935-18971142:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:18966411-18966650:-1/exon

C21orf91-OT1
type: SO_0000704
alternative label: D21S2089E
alternative label: NCRNA00285
gene: C21orf91-OT1
gene synonym: D21S2089E; NCRNA00285
note: C21orf91 overlapping transcript 1 (non-protein coding); Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(<19149721..19164826)
location: region:19149721-19164826:-1
SIO_010080: C21orf91-OT1

246312
SIO_000068: ncbigene

16729
SIO_000068: hgnc

position:19149721:-1
position: 19149721
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: FuzzyPosition

position:19164826:-1
position: 19164826
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C21orf91-OT1
type: SO_0000673
alternative label: D21S2089E
alternative label: NCRNA00285
gene: C21orf91-OT1
gene synonym: D21S2089E; NCRNA00285
product: C21orf91 overlapping transcript 1 (non-protein coding), transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_038870.1
so part of: C21orf91-OT1
location: complement(join(<19149721..19149936,19159345..19159527,19164794..19164826))
location: region:19149721-19164826:-1

GI:336455044
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19164794-19164826:-1/exon

position:19164794:-1
position: 19164794
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:19159345-19159527:-1/exon

position:19159345:-1
position: 19159345
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19159527:-1
position: 19159527
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:19149721-19149936:-1/exon

position:19149936:-1
position: 19149936
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C21orf91-OT1
type: SO_0000673
alternative label: D21S2089E
alternative label: NCRNA00285
gene: C21orf91-OT1
gene synonym: D21S2089E; NCRNA00285
product: C21orf91 overlapping transcript 1 (non-protein coding), transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_038871.1
so part of: C21orf91-OT1
location: complement(join(<19149721..19149936,19157865..19157929,19159345..19159527,19164794..19164826))
location: region:19149721-19164826:-1

GI:336455045
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19164794-19164826:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19159345-19159527:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19157865-19157929:-1/exon

position:19157865:-1
position: 19157865
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19157929:-1
position: 19157929
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:19149721-19149936:-1/exon

C21orf91
type: SO_0000704
alternative label: C21orf14
alternative label: C21orf38
alternative label: CSSG1
alternative label: EURL
alternative label: YG81
gene: C21orf91
gene synonym: C21orf14; C21orf38; CSSG1; EURL; YG81
note: chromosome 21 open reading frame 91; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(19161284..19191703)
location: region:19161284-19191703:-1
SIO_010080: C21orf91

54149
SIO_000068: ncbigene

16459
SIO_000068: hgnc

position:19161284:-1
position: 19161284
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19191703:-1
position: 19191703
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C21orf91
type: SO_0000234
alternative label: C21orf14
alternative label: C21orf38
alternative label: CSSG1
alternative label: EURL
alternative label: YG81
gene: C21orf91
gene synonym: C21orf14; C21orf38; CSSG1; EURL; YG81
product: chromosome 21 open reading frame 91, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001100421.1
so part of: C21orf91
location: complement(join(19161284..19165898,19168899..19169435,19190509..19190642,19191620..19191703))
location: region:19161284-19191703:-1

GI:154426269
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19191620-19191703:-1/exon

position:19191620:-1
position: 19191620
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:19190509-19190642:-1/exon

position:19190509:-1
position: 19190509
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19190642:-1
position: 19190642
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:19168899-19169435:-1/exon

position:19168899:-1
position: 19168899
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19169435:-1
position: 19169435
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:19161284-19165898:-1/exon

position:19165898:-1
position: 19165898
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C21orf91
type: SO_0000234
alternative label: C21orf14
alternative label: C21orf38
alternative label: CSSG1
alternative label: EURL
alternative label: YG81
gene: C21orf91
gene synonym: C21orf14; C21orf38; CSSG1; EURL; YG81
product: chromosome 21 open reading frame 91, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_017447.3
so part of: C21orf91
location: complement(join(19161284..19165895,19167525..19167587,19168899..19169435,19190509..19190642,19191620..19191703))
location: region:19161284-19191703:-1

GI:154426301
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19191620-19191703:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19190509-19190642:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19168899-19169435:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19167525-19167587:-1/exon

position:19167525:-1
position: 19167525
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19167587:-1
position: 19167587
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:19161284-19165895:-1/exon

position:19165895:-1
position: 19165895
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C21orf91
type: SO_0000234
alternative label: C21orf14
alternative label: C21orf38
alternative label: CSSG1
alternative label: EURL
alternative label: YG81
gene: C21orf91
gene synonym: C21orf14; C21orf38; CSSG1; EURL; YG81
product: chromosome 21 open reading frame 91, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001100420.1
so part of: C21orf91
location: complement(join(19161284..19165898,19167525..19167587,19168899..19169435,19190509..19190642,19191620..19191703))
location: region:19161284-19191703:-1

GI:154426330
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19191620-19191703:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19190509-19190642:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19168899-19169435:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19167525-19167587:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:19161284-19165898:-1/exon

C21orf91
type: SO_0000316
alternative label: C21orf14
alternative label: C21orf38
alternative label: CSSG1
alternative label: EURL
alternative label: YG81
gene: C21orf91
gene synonym: C21orf14; C21orf38; CSSG1; EURL; YG81
note: isoform 2 is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: protein EURL homolog isoform 2
translation: MNEEEQFVNIDLNDDNICSVCKLGTDKETLSFCHICFELNIEGVPKSDLLHTKSLRGHKDCFEKYHLIANQGCPRSKLSKSTYEEVKTILSKKINWIVQYAQNKDLDSDSECSKNPQHHLFNFRHKPEEKLLPQFDSQVPKYSAKWIDGSAGGISNCTQRILEQRENTDFGLSMLQDSGATLCRNSVLWPHSHNQAQKKEETISSPEANVQTQHPHYSREELNSMTLGEVEQLNAKLLQQIQVFEELTHQVQEKDSLASQLHVRHVAIEQLLKNCSKLPCLQVGRTGMKSHLPINN
so part of: C21orf91
location: complement(join(19165732..19165895,19167525..19167587,19168899..19169435,19190509..19190635))
location: region:19165732-19190635:-1

NP_059143.3
SIO_000068: ncbiprotein

GI:154426302
SIO_000068: ncbigi

CCDS42908.1
SIO_000068: ccds

position:19165732:-1
position: 19165732
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19190635:-1
position: 19190635
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:19190509-19190635:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19168899-19169435:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19167525-19167587:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19165732-19165895:-1/exon

C21orf91
type: SO_0000316
alternative label: C21orf14
alternative label: C21orf38
alternative label: CSSG1
alternative label: EURL
alternative label: YG81
gene: C21orf91
gene synonym: C21orf14; C21orf38; CSSG1; EURL; YG81
note: isoform 1 is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: protein EURL homolog isoform 1
translation: MNEEEQFVNIDLNDDNICSVCKLGTDKETLSFCHICFELNIEGVPKSDLLHTKSLRGHKDCFEKYHLIANQGCPRSKLSKSTYEEVKTILSKKINWIVQYAQNKDLDSDSECSKNPQHHLFNFRHKPEEKLLPQFDSQVPKYSAKWIDGSAGGISNCTQRILEQRENTDFGLSMLQDSGATLCRNSVLWPHSHNQAQKKEETISSPEANVQTQHPHYSREELNSMTLGEVEQLNAKLLQQIQEVFEELTHQVQEKDSLASQLHVRHVAIEQLLKNCSKLPCLQVGRTGMKSHLPINN
so part of: C21orf91
location: complement(join(19165732..19165898,19167525..19167587,19168899..19169435,19190509..19190635))
location: region:19165732-19190635:-1

NP_001093890.1
SIO_000068: ncbiprotein

GI:154426331
SIO_000068: ncbigi

CCDS42907.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:19190509-19190635:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19168899-19169435:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19167525-19167587:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19165732-19165898:-1/exon

C21orf91
type: SO_0000316
alternative label: C21orf14
alternative label: C21orf38
alternative label: CSSG1
alternative label: EURL
alternative label: YG81
gene: C21orf91
gene synonym: C21orf14; C21orf38; CSSG1; EURL; YG81
note: isoform 3 is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: protein EURL homolog isoform 3
translation: MNEEEQFVNIDLNDDNICSVCKLGTDKETLSFCHICFELNIEGVPKSDLLHTKSLRGHKDCFEKYHLIANQGCPRSKLSKSTYEEVKTILSKKINWIVQYAQNKDLDSDSECSKNPQHHLFNFRHKPEEKLLPQFDSQVPKYSAKWIDGSAGGISNCTQRILEQRENTDFGLSMLQDSGATLCRNSVLWPHSHNQAQKKEETISSPEANVQTQHPHYSREE
so part of: C21orf91
location: complement(join(19165897..19165898,19168899..19169435,19190509..19190635))
location: region:19165897-19190635:-1

NP_001093891.1
SIO_000068: ncbiprotein

GI:154426270
SIO_000068: ncbigi

CCDS42909.1
SIO_000068: ccds

position:19165897:-1
position: 19165897
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:19190509-19190635:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19168899-19169435:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19165897-19165898:-1/exon

CHODL-AS1
type: SO_0000704
alternative label: C21orf39
alternative label: NCRNA00157
gene: CHODL-AS1
gene synonym: C21orf39; NCRNA00157
note: CHODL antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(19207989..19257925)
location: region:19207989-19257925:-1
SIO_010080: CHODL-AS1

54075
SIO_000068: ncbigene

1279
SIO_000068: hgnc

position:19207989:-1
position: 19207989
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19257925:-1
position: 19257925
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

CHODL-AS1
type: SO_0000673
alternative label: C21orf39
alternative label: NCRNA00157
gene: CHODL-AS1
gene synonym: C21orf39; NCRNA00157
product: CHODL antisense RNA 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_024354.1
so part of: CHODL-AS1
location: complement(join(19207989..19208143,19212812..19212970,19257779..19257925))
location: region:19207989-19257925:-1

GI:211904175
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19257779-19257925:-1/exon

position:19257779:-1
position: 19257779
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:19212812-19212970:-1/exon

position:19212812:-1
position: 19212812
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19212970:-1
position: 19212970
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:19207989-19208143:-1/exon

position:19208143:-1
position: 19208143
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

RPL37P3
type: SO_0000704
alternative label: RL37P
alternative label: RPL37_13_1720
gene: RPL37P3
gene synonym: RL37P; RPL37_13_1720
note: ribosomal protein L37 pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(19266465..19266824)
location: region:19266465-19266824:-1

378818
SIO_000068: ncbigene

17238
SIO_000068: hgnc

position:19266465:-1
position: 19266465
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19266824:-1
position: 19266824
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

CHODL
type: SO_0000704
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
note: chondrolectin; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: <19400190..19639687
location: region:19400190-19639687:1
SIO_010080: CHODL

140578
SIO_000068: ncbigene

17807
SIO_000068: hgnc

06261
SIO_000068: hprd

607247
SIO_000068: omim

position:19400190:1
position: 19400190
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: FuzzyPosition

position:19639687:1
position: 19639687
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

CHODL
type: SO_0000234
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
product: chondrolectin, transcript variant 4
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_001204176.1
exception: annotated by transcript or proteomic data
note: The RefSeq transcript aligns at 97% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001204176.1
so part of: CHODL
location: join(<19400190..19400289,19628826..19629135,19629287..19629444,19632517..19632603,19635108..19635210,19638271..19639687)
location: region:19400190-19639687:1

GI:323510653
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19400190-19400289:1/exon

position:19400289:1
position: 19400289
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:19628826-19629135:1/exon

position:19628826:1
position: 19628826
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition
type: FuzzyPosition

position:19629135:1
position: 19629135
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:19629287-19629444:1/exon

position:19629287:1
position: 19629287
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:19629444:1
position: 19629444
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:19632517-19632603:1/exon

position:19632517:1
position: 19632517
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:19632603:1
position: 19632603
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:19635108-19635210:1/exon

position:19635108:1
position: 19635108
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:19635210:1
position: 19635210
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:19638271-19639687:1/exon

position:19638271:1
position: 19638271
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

CHODL
type: SO_0000234
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
product: chondrolectin, transcript variant 6
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_001204178.1
exception: annotated by transcript or proteomic data
note: The RefSeq transcript aligns at 97% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001204178.1
so part of: CHODL
location: join(<19400190..19400289,19628826..19629135,19629287..19629444,19632517..19632603,19638271..19639687)
location: region:19400190-19639687:1

GI:323510657
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19400190-19400289:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19628826-19629135:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:19638271-19639687:1/exon

CHODL
type: SO_0000234
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
product: chondrolectin, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_024944.2
so part of: CHODL
location: join(19617150..19617619,19628826..19629135,19629287..19629444,19632517..19632603,19635108..19635210,19638271..19639687)
location: region:19617150-19639687:1

GI:20127635
SIO_000068: ncbigi

position:19617150:1
position: 19617150
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:19617150-19617619:1/exon

position:19617619:1
position: 19617619
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:19628826-19629135:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:19635108-19635210:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:19638271-19639687:1/exon

CHODL
type: SO_0000316
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
note: isoform a precursor is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: chondrolectin isoform a precursor
translation: MSRVVSLLLGAALLCGHGAFCRRVVSGQKVCFADFKHPCYKMAYFHELSSRVSFQEARLACESEGGVLLSLENEAEQKLIESMLQNLTKPGTGISDGDFWIGLWRNGDGQTSGACPDLYQWSDGSNSQYRNWYTDEPSCGSEKCVVMYHQPTANPGLGGPYLYQWNDDRCNMKHNYICKYEPEINPTAPVEKPYLTNQPGDTHQNVVVTEAGIIPNLIYVVIPTIPLLLLILVAFGTCCFQMLHKSKGRTKTSPNQSTLWISKSTRKESGMEV
so part of: CHODL
location: join(19617541..19617619,19628826..19629135,19629287..19629444,19632517..19632603,19635108..19635210,19638271..19638355)
location: region:19617541-19638355:1

NP_079220.2
SIO_000068: ncbiprotein

GI:20127636
SIO_000068: ncbigi

CCDS13570.1
SIO_000068: ccds

position:19617541:1
position: 19617541
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:19638355:1
position: 19638355
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:19617541-19617619:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19628826-19629135:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:19635108-19635210:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:19638271-19638355:1/exon

CHODL
type: SO_0000234
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
product: chondrolectin, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001204174.1
so part of: CHODL
location: join(19618192..19618286,19628826..19629135,19629287..19629444,19632517..19632603,19635108..19635210,19638271..19639687)
location: region:19618192-19639687:1

GI:323510648
SIO_000068: ncbigi

position:19618192:1
position: 19618192
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:19618192-19618286:1/exon

position:19618286:1
position: 19618286
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:19628826-19629135:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:19635108-19635210:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:19638271-19639687:1/exon

CHODL
type: SO_0000316
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
note: isoform b is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: chondrolectin isoform b
translation: MTAGSAHSQKVCFADFKHPCYKMAYFHELSSRVSFQEARLACESEGGVLLSLENEAEQKLIESMLQNLTKPGTGISDGDFWIGLWRNGDGQTSGACPDLYQWSDGSNSQYRNWYTDEPSCGSEKCVVMYHQPTANPGLGGPYLYQWNDDRCNMKHNYICKYEPEINPTAPVEKPYLTNQPGDTHQNVVVTEAGIIPNLIYVVIPTIPLLLLILVAFGTCCFQMLHKSKGRTKTSPNQSTLWISKSTRKESGMEV
so part of: CHODL
location: join(19618265..19618286,19628826..19629135,19629287..19629444,19632517..19632603,19635108..19635210,19638271..19638355)
location: region:19618265-19638355:1

NP_001191103.1
SIO_000068: ncbiprotein

GI:323510649
SIO_000068: ncbigi

CCDS56208.1
SIO_000068: ccds

position:19618265:1
position: 19618265
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:19618265-19618286:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19628826-19629135:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:19635108-19635210:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:19638271-19638355:1/exon

CHODL
type: SO_0000234
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
product: chondrolectin, transcript variant 3
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_001204175.1
exception: annotated by transcript or proteomic data
note: The RefSeq transcript aligns at 97% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001204175.1
so part of: CHODL
location: join(<19628826..19629135,19629287..19629444,19632517..19632603,19635108..19635210,19638271..19639687)
location: region:19628826-19639687:1

GI:323510651
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19628826-19629135:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19635108-19635210:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:19638271-19639687:1/exon

CHODL
type: SO_0000234
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
product: chondrolectin, transcript variant 5
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_001204177.1
exception: annotated by transcript or proteomic data
note: The RefSeq transcript aligns at 96% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001204177.1
so part of: CHODL
location: join(<19628826..19629135,19629287..19629444,19632517..19632603,19638271..19639687)
location: region:19628826-19639687:1

GI:323510655
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19628826-19629135:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19638271-19639687:1/exon

CHODL
type: SO_0000316
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
note: isoform d is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: chondrolectin isoform d
translation: MAYFHELSSRVSFQEARLACESEGGVLLSLENEAEQKLIESMLQNLTKPGTGISDGDFWIGLWRNGDGQTSGACPDLYQWSDGSNSQYRNWYTDEPSCGSEKCVVMYHQPTANPGLGGPYLYQWNDDRCNMKHNYICKYEPEINPTAPVEKPYLTNQPGDTHQNVVVTEAVKEEQKLVQTSLHCGFQRVPEKKVAWKYNNSLTWFQNFVILDLYKEWHQNNSLEWLEITKDLQDEL
so part of: CHODL
location: join(19628870..19629135,19629287..19629444,19632517..19632603,19638271..19638470)
location: region:19628870-19638470:1

NP_001191106.1
SIO_000068: ncbiprotein

GI:323510656
SIO_000068: ncbigi

CCDS56210.1
SIO_000068: ccds

position:19628870:1
position: 19628870
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:19638470:1
position: 19638470
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:19628870-19629135:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19638271-19638470:1/exon

CHODL
type: SO_0000316
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
note: isoform d is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: chondrolectin isoform d
translation: MAYFHELSSRVSFQEARLACESEGGVLLSLENEAEQKLIESMLQNLTKPGTGISDGDFWIGLWRNGDGQTSGACPDLYQWSDGSNSQYRNWYTDEPSCGSEKCVVMYHQPTANPGLGGPYLYQWNDDRCNMKHNYICKYEPEINPTAPVEKPYLTNQPGDTHQNVVVTEAVKEEQKLVQTSLHCGFQRVPEKKVAWKYNNSLTWFQNFVILDLYKEWHQNNSLEWLEITKDLQDEL
so part of: CHODL
location: join(19628870..19629135,19629287..19629444,19632517..19632603,19638271..19638470)
location: region:19628870-19638470:1

NP_001191107.1
SIO_000068: ncbiprotein

GI:323510658
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19628870-19629135:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19638271-19638470:1/exon

CHODL
type: SO_0000316
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
note: isoform c is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: chondrolectin isoform c
translation: MAYFHELSSRVSFQEARLACESEGGVLLSLENEAEQKLIESMLQNLTKPGTGISDGDFWIGLWRNGDGQTSGACPDLYQWSDGSNSQYRNWYTDEPSCGSEKCVVMYHQPTANPGLGGPYLYQWNDDRCNMKHNYICKYEPEINPTAPVEKPYLTNQPGDTHQNVVVTEAGIIPNLIYVVIPTIPLLLLILVAFGTCCFQMLHKSKGRTKTSPNQSTLWISKSTRKESGMEV
so part of: CHODL
location: join(19628870..19629135,19629287..19629444,19632517..19632603,19635108..19635210,19638271..19638355)
location: region:19628870-19638355:1

NP_001191104.1
SIO_000068: ncbiprotein

GI:323510652
SIO_000068: ncbigi

CCDS56209.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:19628870-19629135:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19635108-19635210:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:19638271-19638355:1/exon

CHODL
type: SO_0000316
alternative label: C21orf68
alternative label: MT75
alternative label: PRED12
gene: CHODL
gene synonym: C21orf68; MT75; PRED12
note: isoform c is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: chondrolectin isoform c
translation: MAYFHELSSRVSFQEARLACESEGGVLLSLENEAEQKLIESMLQNLTKPGTGISDGDFWIGLWRNGDGQTSGACPDLYQWSDGSNSQYRNWYTDEPSCGSEKCVVMYHQPTANPGLGGPYLYQWNDDRCNMKHNYICKYEPEINPTAPVEKPYLTNQPGDTHQNVVVTEAGIIPNLIYVVIPTIPLLLLILVAFGTCCFQMLHKSKGRTKTSPNQSTLWISKSTRKESGMEV
so part of: CHODL
location: join(19628870..19629135,19629287..19629444,19632517..19632603,19635108..19635210,19638271..19638355)
location: region:19628870-19638355:1

NP_001191105.1
SIO_000068: ncbiprotein

GI:323510654
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19628870-19629135:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19629287-19629444:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19632517-19632603:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19635108-19635210:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:19638271-19638355:1/exon

TMPRSS15
type: SO_0000704
alternative label: ENTK
alternative label: PRSS7
gene: TMPRSS15
gene synonym: ENTK; PRSS7
note: transmembrane protease, serine 15; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(19641433..19775970)
location: region:19641433-19775970:-1
SIO_010080: TMPRSS15

5651
SIO_000068: ncbigene

9490
SIO_000068: hgnc

606635
SIO_000068: omim

position:19641433:-1
position: 19641433
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19775970:-1
position: 19775970
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

TMPRSS15
type: SO_0000234
alternative label: ENTK
alternative label: PRSS7
gene: TMPRSS15
gene synonym: ENTK; PRSS7
product: transmembrane protease, serine 15
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_002772.2
exception: annotated by transcript or proteomic data
note: The RefSeq transcript has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_002772.2
so part of: TMPRSS15
location: complement(join(19641433..19642441,19647514..19647653,19651281..19651376,19653357..19653538,19666587..19666761,19666920..19666969,19670051..19670146,19685262..19685394,19687463..19687573,19698749..19698889,19701486..19701611,19704401..19704490,19713730..19713865,19715823..19715973,19716272..19716377,19725220..19725369,19726040..19726180,19732074..19732180,19737457..19737565,19744510..19744641,19751600..19751635,19755944..19756095,19770196..19770263,19770516..19770646,19775795..19775970))
location: region:19641433-19775970:-1

GI:223942068
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:19775795-19775970:-1/exon

position:19775795:-1
position: 19775795
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:19770516-19770646:-1/exon

position:19770516:-1
position: 19770516
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19770646:-1
position: 19770646
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:19770196-19770263:-1/exon

position:19770196:-1
position: 19770196
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19770263:-1
position: 19770263
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:19755944-19756095:-1/exon

position:19755944:-1
position: 19755944
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19756095:-1
position: 19756095
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:19751600-19751635:-1/exon

position:19751600:-1
position: 19751600
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19751635:-1
position: 19751635
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:19744510-19744641:-1/exon

position:19744510:-1
position: 19744510
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19744641:-1
position: 19744641
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:19737457-19737565:-1/exon

position:19737457:-1
position: 19737457
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19737565:-1
position: 19737565
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:19732074-19732180:-1/exon

position:19732074:-1
position: 19732074
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19732180:-1
position: 19732180
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:19726040-19726180:-1/exon

position:19726040:-1
position: 19726040
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19726180:-1
position: 19726180
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:19725220-19725369:-1/exon

position:19725220:-1
position: 19725220
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19725369:-1
position: 19725369
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:19716272-19716377:-1/exon

position:19716272:-1
position: 19716272
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19716377:-1
position: 19716377
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:19715823-19715973:-1/exon

position:19715823:-1
position: 19715823
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19715973:-1
position: 19715973
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:19713730-19713865:-1/exon

position:19713730:-1
position: 19713730
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19713865:-1
position: 19713865
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:19704401-19704490:-1/exon

position:19704401:-1
position: 19704401
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19704490:-1
position: 19704490
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:19701486-19701611:-1/exon

position:19701486:-1
position: 19701486
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19701611:-1
position: 19701611
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:19698749-19698889:-1/exon

position:19698749:-1
position: 19698749
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19698889:-1
position: 19698889
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 17
SIO_000628: feature:19687463-19687573:-1/exon

position:19687463:-1
position: 19687463
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19687573:-1
position: 19687573
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 18
SIO_000628: feature:19685262-19685394:-1/exon

position:19685262:-1
position: 19685262
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19685394:-1
position: 19685394
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 19
SIO_000628: feature:19670051-19670146:-1/exon

position:19670051:-1
position: 19670051
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19670146:-1
position: 19670146
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 20
SIO_000628: feature:19666920-19666969:-1/exon

position:19666920:-1
position: 19666920
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19666969:-1
position: 19666969
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 21
SIO_000628: feature:19666587-19666761:-1/exon

position:19666587:-1
position: 19666587
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19666761:-1
position: 19666761
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 22
SIO_000628: feature:19653357-19653538:-1/exon

position:19653357:-1
position: 19653357
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19653538:-1
position: 19653538
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 23
SIO_000628: feature:19651281-19651376:-1/exon

position:19651281:-1
position: 19651281
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19651376:-1
position: 19651376
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 24
SIO_000628: feature:19647514-19647653:-1/exon

position:19647514:-1
position: 19647514
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19647653:-1
position: 19647653
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 25
SIO_000628: feature:19641433-19642441:-1/exon

position:19642441:-1
position: 19642441
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

TMPRSS15
type: SO_0000316
alternative label: ENTK
alternative label: PRSS7
gene: TMPRSS15
gene synonym: ENTK; PRSS7
inference: similar to AA sequence (same species):RefSeq:NP_002763.2
exception: annotated by transcript or proteomic data
note: The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: enteropeptidase precursor
translation: MGSKRGISSRHHSLSSYEIMFAALFAILVVLCAGLIAVSCLTIKESQRGAALGQSHEARATFKITSGVTYNPNLQDKLSVDFKVLAFDLQQMIDEIFLSSNLKNEYKNSRVLQFENGSIIVVFDLFFAQWVSDENVKEELIQGLEANKSSQLVTFHIDLNSVDILDKLTTTSHLATPGNVSIECLPGSSPCTDALTCIKADLFCDGEVNCPDGSDEDNKMCATVCDGRFLLTGSSGSFQATHYPKPSETSVVCQWIIRVNQGLSIKLSFDDFNTYYTDILDIYEGVGSSKILRASIWETNPGTIRIFSNQVTATFLIESDESDYVGFNATYTAFNSSELNNYEKINCNFEDGFCFWVQDLNDDNEWERIQGSTFSPFTGPNFDHTFGNASGFYISTPTGPGGRQERVGLLSLPLDPTLEPACLSFWYHMYGENVHKLSINISNDQNMEKTVFQKEGNYGDNWNYGQVTLNETVKFKVAFNAFKNKILSDIALDDISLTYGICNGSLYPEPTLVPTPPPELPTDCGGPFELWEPNTTFSSTNFPNSYPNLAFCVWILNAQKGKNIQLHFQEFDLENINDVVEIRDGEEADSLLLAVYTGPGPVKDVFSTTNRMTVLLITNDVLARGGFKANFTTGYHLGIPEPCKADHFQCKNGECVPLVNLCDGHLHCEDGSDEADCVRFFNGTTNNNGLVRFRIQSIWHTACAENWTTQISNDVCQLLGLGSGNSSKPIFSTDGGPFVKLNTAPDGHLILTPSQQCLQDSLIRLQCNHKSCGKKLAAQDITPKIVGGSNAKEGAWPWVVGLYYGGRLLCGASLVSSDWLVSAAHCVYGRNLEPSKWTAILGLHMKSNLTSPQTVPRLIDEIVINPHYNRRRKDNDIAMMHLEFKVNYTDYIQPICLPEENQVFPPGRNCSIAGWGTVVYQGTTANILQEADVPLLSNERCQQQMPEYNITENMICAGYEEGGIDSCQGDSGGPLMCQENNRWFLAGVTSFGYKCALPNRPGVYARVSRFTEWIQSFLH
so part of: TMPRSS15
location: complement(join(19642286..19642441,19647514..19647653,19651281..19651376,19653357..19653538,19666587..19666761,19666920..19666969,19670051..19670146,19685262..19685394,19687463..19687573,19698749..19698889,19701486..19701611,19704401..19704490,19713730..19713865,19715823..19715973,19716272..19716377,19725220..19725369,19726040..19726180,19732074..19732180,19737457..19737565,19744510..19744641,19751600..19751635,19755944..19756095,19770196..19770263,19770516..19770646,19775795..19775939))
location: region:19642286-19775939:-1

NP_002763.2
SIO_000068: ncbiprotein

GI:223942069
SIO_000068: ncbigi

CCDS13571.1
SIO_000068: ccds

position:19642286:-1
position: 19642286
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19775939:-1
position: 19775939
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:19775795-19775939:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:19770516-19770646:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:19770196-19770263:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:19755944-19756095:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:19751600-19751635:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:19744510-19744641:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:19737457-19737565:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:19732074-19732180:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:19726040-19726180:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:19725220-19725369:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:19716272-19716377:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:19715823-19715973:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:19713730-19713865:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:19704401-19704490:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:19701486-19701611:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:19698749-19698889:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:19687463-19687573:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:19685262-19685394:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:19670051-19670146:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:19666920-19666969:-1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:19666587-19666761:-1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:19653357-19653538:-1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:19651281-19651376:-1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:19647514-19647653:-1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:19642286-19642441:-1/exon

LOC101927797
type: SO_0000704
gene: LOC101927797
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(19933583..20132130)
location: region:19933583-20132130:-1
SIO_010080: LOC101927797

101927797
SIO_000068: ncbigene

position:19933583:-1
position: 19933583
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:20132130:-1
position: 20132130
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101927797
type: SO_0000673
gene: LOC101927797
product: uncharacterized LOC101927797
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST
transcript id: XR_244295.1
so part of: LOC101927797
location: complement(join(19933583..19934009,19961845..19961938,20110242..20110343,20132092..20132130))
location: region:19933583-20132130:-1

GI:530419146
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:20132092-20132130:-1/exon

position:20132092:-1
position: 20132092
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:20110242-20110343:-1/exon

position:20110242:-1
position: 20110242
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:20110343:-1
position: 20110343
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:19961845-19961938:-1/exon

position:19961845:-1
position: 19961845
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:19961938:-1
position: 19961938
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:19933583-19934009:-1/exon

position:19934009:-1
position: 19934009
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MIR548X
type: SO_0000704
gene: MIR548X
note: microRNA 548x; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(20058408..20058482)
location: region:20058408-20058482:-1
SIO_010080: MIR548X

100422920
SIO_000068: ncbigene

38248
SIO_000068: hgnc

MI0014244
SIO_000068: mirbase

position:20058408:-1
position: 20058408
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:20058482:-1
position: 20058482
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MIR548X
type: SO_0000185
gene: MIR548X
product: microRNA 548x
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_036166.1
so part of: MIR548X
location: complement(20058408..20058482)
location: region:20058408-20058482:-1

GI:301171799
SIO_000068: ncbigi

MIR548X
type: SO_0000655
gene: MIR548X
nc RNA class: miRNA
product: hsa-miR-548x-3p
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR548X
location: complement(20058418..20058437)
location: region:20058418-20058437:-1

MIMAT0015081
SIO_000068: mirbase

position:20058418:-1
position: 20058418
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:20058437:-1
position: 20058437
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MIR548X
type: SO_0000655
gene: MIR548X
nc RNA class: miRNA
product: hsa-miR-548x-5p
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR548X
location: complement(20058453..20058475)
location: region:20058453-20058475:-1

MIMAT0022733
SIO_000068: mirbase

position:20058453:-1
position: 20058453
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:20058475:-1
position: 20058475
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

PPIAP22
type: SO_0000704
alternative label: PPIA3L
alternative label: PPIAL3
gene: PPIAP22
gene synonym: PPIA3L; PPIAL3
note: peptidylprolyl isomerase A (cyclophilin A) pseudogene 22; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 20230097..20230594
location: region:20230097-20230594:1

653214
SIO_000068: ncbigene

17236
SIO_000068: hgnc

position:20230097:1
position: 20230097
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:20230594:1
position: 20230594
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

SLC6A6P1
type: SO_0000704
alternative label: SLC6A6P
gene: SLC6A6P1
gene synonym: SLC6A6P
note: solute carrier family 6, member 6 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 20616712..20618714
location: region:20616712-20618714:1

54019
SIO_000068: ncbigene

11053
SIO_000068: hgnc

position:20616712:1
position: 20616712
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:20618714:1
position: 20618714
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

RPL37P4
type: SO_0000704
alternative label: RL37P2
alternative label: RPL37_10_1721
gene: RPL37P4
gene synonym: RL37P2; RPL37_10_1721
note: ribosomal protein L37 pseudogene 4; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 20966021..20966585
location: region:20966021-20966585:1

378819
SIO_000068: ncbigene

17239
SIO_000068: hgnc

position:20966021:1
position: 20966021
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:20966585:1
position: 20966585
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

NIPA2P3
type: SO_0000704
gene: NIPA2P3
note: non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 20993066..21004088
location: region:20993066-21004088:1

100128057
SIO_000068: ncbigene

42043
SIO_000068: hgnc

position:20993066:1
position: 20993066
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:21004088:1
position: 21004088
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC100288151
type: SO_0000704
gene: LOC100288151
note: SREK1-interacting protein 1 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 21112023..21112461
location: region:21112023-21112461:1

100288151
SIO_000068: ncbigene

position:21112023:1
position: 21112023
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:21112461:1
position: 21112461
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

C1QBPP
type: SO_0000704
gene: C1QBPP
note: complement component 1, q subcomponent binding protein, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(21131434..21132441)
location: region:21131434-21132441:-1
SIO_010080: C1QBPP

54098
SIO_000068: ncbigene

1244
SIO_000068: hgnc

position:21131434:-1
position: 21131434
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:21132441:-1
position: 21132441
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C1QBPP
type: SO_0000147
gene: C1QBPP
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: C1QBPP
location: complement(21131434..21132441)
location: region:21131434-21132441:-1

FDPSP6
type: SO_0000704
alternative label: FDPSP
gene: FDPSP6
gene synonym: FDPSP
note: farnesyl diphosphate synthase pseudogene 6; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 21760493..21761253
location: region:21760493-21761253:1

54051
SIO_000068: ncbigene

3637
SIO_000068: hgnc

position:21760493:1
position: 21760493
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:21761253:1
position: 21761253
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

KRT18P2
type: SO_0000704
gene: KRT18P2
note: keratin 18 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(21797207..21798519)
location: region:21797207-21798519:-1
SIO_010080: KRT18P2

54044
SIO_000068: ncbigene

6435
SIO_000068: hgnc

position:21797207:-1
position: 21797207
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:21798519:-1
position: 21798519
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

KRT18P2
type: SO_0000147
gene: KRT18P2
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: KRT18P2
location: complement(21797207..21798519)
location: region:21797207-21798519:-1

RPS3AP1
type: SO_0000704
alternative label: RPS3AP
gene: RPS3AP1
gene synonym: RPS3AP
note: ribosomal protein S3A pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(21802712..21803074)
location: region:21802712-21803074:-1

101241875
SIO_000068: ncbigene

10422
SIO_000068: hgnc

position:21802712:-1
position: 21802712
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:21803074:-1
position: 21803074
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00320
type: SO_0000704
alternative label: C21orf131
alternative label: NCRNA00320
alternative label: PRED14
gene: LINC00320
gene synonym: C21orf131; NCRNA00320; PRED14
note: long intergenic non-protein coding RNA 320; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(22114863..22175569)
location: region:22114863-22175569:-1
SIO_010080: LINC00320

387486
SIO_000068: ncbigene

19690
SIO_000068: hgnc

position:22114863:-1
position: 22114863
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:22175569:-1
position: 22175569
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00320
type: SO_0000673
alternative label: C21orf131
alternative label: NCRNA00320
alternative label: PRED14
gene: LINC00320
gene synonym: C21orf131; NCRNA00320; PRED14
product: long intergenic non-protein coding RNA 320, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, and 75% coverage by RNAseq alignments
transcript id: XR_244274.1
so part of: LINC00320
location: complement(join(22114863..22116151,22150736..22150865,22153667..22153792,22153888..22153979,22154625..22154760,22158354..22158406,22175313..22175569))
location: region:22114863-22175569:-1

GI:530418904
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:22175313-22175569:-1/exon

position:22175313:-1
position: 22175313
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:22158354-22158406:-1/exon

position:22158354:-1
position: 22158354
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:22158406:-1
position: 22158406
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:22154625-22154760:-1/exon

position:22154625:-1
position: 22154625
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:22154760:-1
position: 22154760
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:22153888-22153979:-1/exon

position:22153888:-1
position: 22153888
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:22153979:-1
position: 22153979
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:22153667-22153792:-1/exon

position:22153667:-1
position: 22153667
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:22153792:-1
position: 22153792
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:22150736-22150865:-1/exon

position:22150736:-1
position: 22150736
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:22150865:-1
position: 22150865
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:22114863-22116151:-1/exon

position:22116151:-1
position: 22116151
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00320
type: SO_0000673
alternative label: C21orf131
alternative label: NCRNA00320
alternative label: PRED14
gene: LINC00320
gene synonym: C21orf131; NCRNA00320; PRED14
product: long intergenic non-protein coding RNA 320
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_024090.1
so part of: LINC00320
location: complement(join(22114913..22116151,22150736..22150865,22150961..22151080,22153667..22153792,22153888..22153979,22154625..22154764,22158354..22158406,22175313..22175426))
location: region:22114913-22175426:-1

GI:197116379
SIO_000068: ncbigi

position:22114913:-1
position: 22114913
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:22175426:-1
position: 22175426
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:22175313-22175426:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:22158354-22158406:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:22154625-22154764:-1/exon

position:22154764:-1
position: 22154764
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:22153888-22153979:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:22153667-22153792:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:22150961-22151080:-1/exon

position:22150961:-1
position: 22150961
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:22151080:-1
position: 22151080
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:22150736-22150865:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:22114913-22116151:-1/exon

LINC00320
type: SO_0000673
alternative label: C21orf131
alternative label: NCRNA00320
alternative label: PRED14
gene: LINC00320
gene synonym: C21orf131; NCRNA00320; PRED14
product: long intergenic non-protein coding RNA 320, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, and 65% coverage by RNAseq alignments
transcript id: XR_244272.1
so part of: LINC00320
location: complement(join(22115239..22116151,22129629..22129735,22150736..22150865,22150961..22151080,22153667..22153792,22153888..22153979,22154568..22154764,22175313..22175569))
location: region:22115239-22175569:-1

GI:530418902
SIO_000068: ncbigi

position:22115239:-1
position: 22115239
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:22175313-22175569:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:22154568-22154764:-1/exon

position:22154568:-1
position: 22154568
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:22153888-22153979:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:22153667-22153792:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:22150961-22151080:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:22150736-22150865:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:22129629-22129735:-1/exon

position:22129629:-1
position: 22129629
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:22129735:-1
position: 22129735
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:22115239-22116151:-1/exon

LINC00320
type: SO_0000673
alternative label: C21orf131
alternative label: NCRNA00320
alternative label: PRED14
gene: LINC00320
gene synonym: C21orf131; NCRNA00320; PRED14
product: long intergenic non-protein coding RNA 320, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, and 69% coverage by RNAseq alignments
transcript id: XR_244273.1
so part of: LINC00320
location: complement(join(22115239..22116151,22150736..22150865,22153667..22153792,22153888..22153979,22154568..22154764,22158354..22158406,22175313..22175569))
location: region:22115239-22175569:-1

GI:530418903
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:22175313-22175569:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:22158354-22158406:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:22154568-22154764:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:22153888-22153979:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:22153667-22153792:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:22150736-22150865:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:22115239-22116151:-1/exon

PPIAP1
type: SO_0000704
alternative label: PPIAP
gene: PPIAP1
gene synonym: PPIAP
note: peptidylprolyl isomerase A (cyclophilin A), pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(22200236..22200982)
location: region:22200236-22200982:-1

100288185
SIO_000068: ncbigene

9254
SIO_000068: hgnc

position:22200236:-1
position: 22200236
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:22200982:-1
position: 22200982
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

NCAM2
type: SO_0000704
alternative label: NCAM21
gene: NCAM2
gene synonym: NCAM21
note: neural cell adhesion molecule 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 22370633..22913892
location: region:22370633-22913892:1
SIO_010080: NCAM2

4685
SIO_000068: ncbigene

7657
SIO_000068: hgnc

03619
SIO_000068: hprd

602040
SIO_000068: omim

position:22370633:1
position: 22370633
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22913892:1
position: 22913892
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

NCAM2
type: SO_0000234
alternative label: NCAM21
gene: NCAM2
gene synonym: NCAM21
product: neural cell adhesion molecule 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_004540.3
so part of: NCAM2
location: join(22370633..22370936,22652898..22652972,22656514..22656720,22658589..22658732,22664424..22664561,22696703..22696820,22707825..22707985,22710709..22710854,22746183..22746333,22782594..22782781,22790793..22790889,22804428..22804601,22838927..22839046,22840983..22841104,22849612..22849792,22881172..22881376,22906858..22906977,22910167..22912517)
location: region:22370633-22912517:1

GI:316659209
SIO_000068: ncbigi

position:22912517:1
position: 22912517
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:22370633-22370936:1/exon

position:22370936:1
position: 22370936
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:22652898-22652972:1/exon

position:22652898:1
position: 22652898
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22652972:1
position: 22652972
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:22656514-22656720:1/exon

position:22656514:1
position: 22656514
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22656720:1
position: 22656720
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:22658589-22658732:1/exon

position:22658589:1
position: 22658589
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22658732:1
position: 22658732
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:22664424-22664561:1/exon

position:22664424:1
position: 22664424
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22664561:1
position: 22664561
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:22696703-22696820:1/exon

position:22696703:1
position: 22696703
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22696820:1
position: 22696820
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:22707825-22707985:1/exon

position:22707825:1
position: 22707825
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22707985:1
position: 22707985
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:22710709-22710854:1/exon

position:22710709:1
position: 22710709
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22710854:1
position: 22710854
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:22746183-22746333:1/exon

position:22746183:1
position: 22746183
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22746333:1
position: 22746333
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:22782594-22782781:1/exon

position:22782594:1
position: 22782594
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22782781:1
position: 22782781
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:22790793-22790889:1/exon

position:22790793:1
position: 22790793
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22790889:1
position: 22790889
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:22804428-22804601:1/exon

position:22804428:1
position: 22804428
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22804601:1
position: 22804601
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:22838927-22839046:1/exon

position:22838927:1
position: 22838927
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22839046:1
position: 22839046
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:22840983-22841104:1/exon

position:22840983:1
position: 22840983
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22841104:1
position: 22841104
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:22849612-22849792:1/exon

position:22849612:1
position: 22849612
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22849792:1
position: 22849792
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:22881172-22881376:1/exon

position:22881172:1
position: 22881172
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22881376:1
position: 22881376
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 17
SIO_000628: feature:22906858-22906977:1/exon

position:22906858:1
position: 22906858
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22906977:1
position: 22906977
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 18
SIO_000628: feature:22910167-22912517:1/exon

position:22910167:1
position: 22910167
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

NCAM2
type: SO_0000316
alternative label: NCAM21
gene: NCAM2
gene synonym: NCAM21
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: neural cell adhesion molecule 2 precursor
translation: MSLLLSFYLLGLLVSSGQALLQVTISLSKVELSVGESKFFTCTAIGEPESIDWYNPQGEKIISTQRVVVQKEGVRSRLTIYNANIEDAGIYRCQATDAKGQTQEATVVLEIYQKLTFREVVSPQEFKQGEDAEVVCRVSSSPAPAVSWLYHNEEVTTISDNRFAMLANNNLQILNINKSDEGIYRCEGRVEARGEIDFRDIIVIVNVPPAISMPQKSFNATAERGEEMTFSCRASGSPEPAISWFRNGKLIEENEKYILKGSNTELTVRNIINSDGGPYVCRATNKAGEDEKQAFLQVFVQPHIIQLKNETTYENGQVTLVCDAEGEPIPEITWKRAVDGFTFTEGDKSLDGRIEVKGQHGSSSLHIKDVKLSDSGRYDCEAASRIGGHQKSMYLDIEYAPKFISNQTIYYSWEGNPINISCDVKSNPPASIHWRRDKLVLPAKNTTNLKTYSTGRKMILEIAPTSDNDFGRYNCTATNHIGTRFQEYILALADVPSSPYGVKIIELSQTTAKVSFNKPDSHGGVPIHHYQVDVKEVASEIWKIVRSHGVQTMVVLNNLEPNTTYEIRVAAVNGKGQGDYSKIEIFQTLPVREPSPPSIHGQPSSGKSFKLSITKQDDGGAPILEYIVKYRSKDKEDQWLEKKVQGNKDHIILEHLQWTMGYEVQITAANRLGYSEPTVYEFSMPPKPNIIKDTLFNGLGLGAVIGLGVAALLLILVVTDVSCFFIRQCGLLMCITRRMCGKKSGSSGKSKELEEGKAAYLKDGSKEPIVEMRTEDERVTNHEDGSPVNEPNETTPLTEPEKLPLKEEDGKEALNPETIEIKVSNDIIQSKEDDSKA
so part of: NCAM2
location: join(22370882..22370936,22652898..22652972,22656514..22656720,22658589..22658732,22664424..22664561,22696703..22696820,22707825..22707985,22710709..22710854,22746183..22746333,22782594..22782781,22790793..22790889,22804428..22804601,22838927..22839046,22840983..22841104,22849612..22849792,22881172..22881376,22906858..22906977,22910167..22910278)
location: region:22370882-22910278:1

NP_004531.2
SIO_000068: ncbiprotein

GI:33519481
SIO_000068: ncbigi

CCDS42910.1
SIO_000068: ccds

position:22370882:1
position: 22370882
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22910278:1
position: 22910278
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:22370882-22370936:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:22652898-22652972:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:22656514-22656720:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:22658589-22658732:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:22664424-22664561:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:22696703-22696820:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:22707825-22707985:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:22710709-22710854:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:22746183-22746333:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:22782594-22782781:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:22790793-22790889:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:22804428-22804601:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:22838927-22839046:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:22840983-22841104:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:22849612-22849792:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:22881172-22881376:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:22906858-22906977:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:22910167-22910278:1/exon

NCAM2
type: SO_0000234
alternative label: NCAM21
gene: NCAM2
gene synonym: NCAM21
product: neural cell adhesion molecule 2, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 43 ESTs, 6 Proteins, and 96% coverage by RNAseq alignments
transcript id: XM_005260987.1
so part of: NCAM2
location: join(22519438..22519569,22582860..22583010,22652898..22652972,22656514..22656720,22658589..22658732,22664424..22664561,22696703..22696820,22707825..22707985,22710709..22710854,22746183..22746333,22782594..22782781,22790793..22790889,22804428..22804601,22838927..22839046,22840983..22841104,22849612..22849792,22881172..22881376,22906858..22906977,22910167..22913892)
location: region:22519438-22913892:1

GI:530418935
SIO_000068: ncbigi

position:22519438:1
position: 22519438
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:22519438-22519569:1/exon

position:22519569:1
position: 22519569
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:22582860-22583010:1/exon

position:22582860:1
position: 22582860
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:22583010:1
position: 22583010
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:22652898-22652972:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:22656514-22656720:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:22658589-22658732:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:22664424-22664561:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:22696703-22696820:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:22707825-22707985:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:22710709-22710854:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:22746183-22746333:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:22782594-22782781:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:22790793-22790889:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:22804428-22804601:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:22838927-22839046:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:22840983-22841104:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:22849612-22849792:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:22881172-22881376:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:22906858-22906977:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:22910167-22913892:1/exon

NCAM2
type: SO_0000234
alternative label: NCAM21
gene: NCAM2
gene synonym: NCAM21
product: neural cell adhesion molecule 2, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 ESTs, 1 Protein, and 86% coverage by RNAseq alignments
transcript id: XM_005260989.1
so part of: NCAM2
location: join(22519438..22519569,22582860..22583010,22652898..22652972,22656514..22656720,22658589..22658732,22664424..22664561,22696703..22696820,22707825..22707985,22710709..22710854,22746183..22746333,22757924..22758033)
location: region:22519438-22758033:1

GI:530418939
SIO_000068: ncbigi

position:22758033:1
position: 22758033
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:22519438-22519569:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:22582860-22583010:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:22652898-22652972:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:22656514-22656720:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:22658589-22658732:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:22664424-22664561:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:22696703-22696820:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:22707825-22707985:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:22710709-22710854:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:22746183-22746333:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:22757924-22758033:1/exon

position:22757924:1
position: 22757924
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

NCAM2
type: SO_0000316
alternative label: NCAM21
gene: NCAM2
gene synonym: NCAM21
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: neural cell adhesion molecule 2 isoform X1
translation: MVRSDSGGQVYLDYHNRQGLFVDWKYNEALYLEEGQPETYYRTALLQVTISLSKVELSVGESKFFTCTAIGEPESIDWYNPQGEKIISTQRVVVQKEGVRSRLTIYNANIEDAGIYRCQATDAKGQTQEATVVLEIYQKLTFREVVSPQEFKQGEDAEVVCRVSSSPAPAVSWLYHNEEVTTISDNRFAMLANNNLQILNINKSDEGIYRCEGRVEARGEIDFRDIIVIVNVPPAISMPQKSFNATAERGEEMTFSCRASGSPEPAISWFRNGKLIEENEKYILKGSNTELTVRNIINSDGGPYVCRATNKAGEDEKQAFLQVFVQPHIIQLKNETTYENGQVTLVCDAEGEPIPEITWKRAVDGFTFTEGDKSLDGRIEVKGQHGSSSLHIKDVKLSDSGRYDCEAASRIGGHQKSMYLDIEYAPKFISNQTIYYSWEGNPINISCDVKSNPPASIHWRRDKLVLPAKNTTNLKTYSTGRKMILEIAPTSDNDFGRYNCTATNHIGTRFQEYILALADVPSSPYGVKIIELSQTTAKVSFNKPDSHGGVPIHHYQVDVKEVASEIWKIVRSHGVQTMVVLNNLEPNTTYEIRVAAVNGKGQGDYSKIEIFQTLPVREPSPPSIHGQPSSGKSFKLSITKQDDGGAPILEYIVKYRSKDKEDQWLEKKVQGNKDHIILEHLQWTMGYEVQITAANRLGYSEPTVYEFSMPPKPNIIKDTLFNGLGLGAVIGLGVAALLLILVVTDVSCFFIRQCGLLMCITRRMCGKKSGSSGKSKELEEGKAAYLKDGSKEPIVEMRTEDERVTNHEDGSPVNEPNETTPLTEPEKLPLKEEDGKEALNPETIEIKVSNDIIQSKEDDSKA
so part of: NCAM2
location: join(22582881..22583010,22652898..22652972,22656514..22656720,22658589..22658732,22664424..22664561,22696703..22696820,22707825..22707985,22710709..22710854,22746183..22746333,22782594..22782781,22790793..22790889,22804428..22804601,22838927..22839046,22840983..22841104,22849612..22849792,22881172..22881376,22906858..22906977,22910167..22910278)
location: region:22582881-22910278:1

XP_005261044.1
SIO_000068: ncbiprotein

GI:530418936
SIO_000068: ncbigi

position:22582881:1
position: 22582881
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:22582881-22583010:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:22652898-22652972:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:22656514-22656720:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:22658589-22658732:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:22664424-22664561:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:22696703-22696820:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:22707825-22707985:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:22710709-22710854:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:22746183-22746333:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:22782594-22782781:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:22790793-22790889:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:22804428-22804601:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:22838927-22839046:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:22840983-22841104:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:22849612-22849792:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:22881172-22881376:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:22906858-22906977:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:22910167-22910278:1/exon

NCAM2
type: SO_0000316
alternative label: NCAM21
gene: NCAM2
gene synonym: NCAM21
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: neural cell adhesion molecule 2 isoform X3
translation: MVRSDSGGQVYLDYHNRQGLFVDWKYNEALYLEEGQPETYYRTALLQVTISLSKVELSVGESKFFTCTAIGEPESIDWYNPQGEKIISTQRVVVQKEGVRSRLTIYNANIEDAGIYRCQATDAKGQTQEATVVLEIYQKLTFREVVSPQEFKQGEDAEVVCRVSSSPAPAVSWLYHNEEVTTISDNRFAMLANNNLQILNINKSDEGIYRCEGRVEARGEIDFRDIIVIVNVPPAISMPQKSFNATAERGEEMTFSCRASGSPEPAISWFRNGKLIEENEKYILKGSNTELTVRNIINSDGGPYVCRATNKAGEDEKQAFLQVFVQPHIIQLKNETTYENGQVTLVCDAEGEPIPEITWKRAVDGFTFTEGDKSLDGRIEVKGQHGSSSLHIKDVKLSDSGRYDCEAASRIGGHQKSMYLDIES
so part of: NCAM2
location: join(22582881..22583010,22652898..22652972,22656514..22656720,22658589..22658732,22664424..22664561,22696703..22696820,22707825..22707985,22710709..22710854,22746183..22746333,22757924..22757928)
location: region:22582881-22757928:1

XP_005261046.1
SIO_000068: ncbiprotein

GI:530418940
SIO_000068: ncbigi

position:22757928:1
position: 22757928
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:22582881-22583010:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:22652898-22652972:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:22656514-22656720:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:22658589-22658732:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:22664424-22664561:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:22696703-22696820:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:22707825-22707985:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:22710709-22710854:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:22746183-22746333:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:22757924-22757928:1/exon

NCAM2
type: SO_0000234
alternative label: NCAM21
gene: NCAM2
gene synonym: NCAM21
product: neural cell adhesion molecule 2, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 37 ESTs, and 100% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XM_005260988.1
so part of: NCAM2
location: join(22658669..22658744,22664424..22664561,22696703..22696820,22707825..22707985,22710709..22710854,22746183..22746333,22782594..22782781,22790793..22790889,22804428..22804601,22838927..22839046,22840983..22841104,22849612..22849792,22881172..22881376,22906858..22906977,22910167..22913892)
location: region:22658669-22913892:1

GI:530418937
SIO_000068: ncbigi

position:22658669:1
position: 22658669
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:22658669-22658744:1/exon

position:22658744:1
position: 22658744
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:22664424-22664561:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:22696703-22696820:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:22707825-22707985:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:22710709-22710854:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:22746183-22746333:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:22782594-22782781:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:22790793-22790889:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:22804428-22804601:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:22838927-22839046:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:22840983-22841104:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:22849612-22849792:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:22881172-22881376:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:22906858-22906977:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:22910167-22913892:1/exon

NCAM2
type: SO_0000316
alternative label: NCAM21
gene: NCAM2
gene synonym: NCAM21
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: neural cell adhesion molecule 2 isoform X2
translation: MLANNNLQILNINKSDEGIYRCEGRVEARGEIDFRDIIVIVNVPPAISMPQKSFNATAERGEEMTFSCRASGSPEPAISWFRNGKLIEENEKYILKGSNTELTVRNIINSDGGPYVCRATNKAGEDEKQAFLQVFVQPHIIQLKNETTYENGQVTLVCDAEGEPIPEITWKRAVDGFTFTEGDKSLDGRIEVKGQHGSSSLHIKDVKLSDSGRYDCEAASRIGGHQKSMYLDIEYAPKFISNQTIYYSWEGNPINISCDVKSNPPASIHWRRDKLVLPAKNTTNLKTYSTGRKMILEIAPTSDNDFGRYNCTATNHIGTRFQEYILALADVPSSPYGVKIIELSQTTAKVSFNKPDSHGGVPIHHYQVDVKEVASEIWKIVRSHGVQTMVVLNNLEPNTTYEIRVAAVNGKGQGDYSKIEIFQTLPVREPSPPSIHGQPSSGKSFKLSITKQDDGGAPILEYIVKYRSKDKEDQWLEKKVQGNKDHIILEHLQWTMGYEVQITAANRLGYSEPTVYEFSMPPKPNIIKDTLFNGLGLGAVIGLGVAALLLILVVTDVSCFFIRQCGLLMCITRRMCGKKSGSSGKSKELEEGKAAYLKDGSKEPIVEMRTEDERVTNHEDGSPVNEPNETTPLTEPEKLPLKEEDGKEALNPETIEIKVSNDIIQSKEDDSKA
so part of: NCAM2
location: join(22664435..22664561,22696703..22696820,22707825..22707985,22710709..22710854,22746183..22746333,22782594..22782781,22790793..22790889,22804428..22804601,22838927..22839046,22840983..22841104,22849612..22849792,22881172..22881376,22906858..22906977,22910167..22910278)
location: region:22664435-22910278:1

XP_005261045.1
SIO_000068: ncbiprotein

GI:530418938
SIO_000068: ncbigi

position:22664435:1
position: 22664435
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:22664435-22664561:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:22696703-22696820:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:22707825-22707985:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:22710709-22710854:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:22746183-22746333:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:22782594-22782781:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:22790793-22790889:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:22804428-22804601:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:22838927-22839046:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:22840983-22841104:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:22849612-22849792:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:22881172-22881376:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:22906858-22906977:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:22910167-22910278:1/exon

LINC00317
type: SO_0000704
alternative label: C21orf117
alternative label: NCRNA00317
alternative label: PRED89
gene: LINC00317
gene synonym: C21orf117; NCRNA00317; PRED89
note: long intergenic non-protein coding RNA 317; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(<23095613..23109639)
location: region:23095613-23109639:-1
SIO_010080: LINC00317

378828
SIO_000068: ncbigene

23126
SIO_000068: hgnc

position:23095613:-1
position: 23095613
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: FuzzyPosition

position:23109639:-1
position: 23109639
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00317
type: SO_0000673
alternative label: C21orf117
alternative label: NCRNA00317
alternative label: PRED89
gene: LINC00317
gene synonym: C21orf117; NCRNA00317; PRED89
product: long intergenic non-protein coding RNA 317
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_038872.1
so part of: LINC00317
location: complement(join(<23095613..23096094,23099352..23099413,23109572..23109639))
location: region:23095613-23109639:-1

GI:336455047
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:23109572-23109639:-1/exon

position:23109572:-1
position: 23109572
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:23099352-23099413:-1/exon

position:23099352:-1
position: 23099352
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:23099413:-1
position: 23099413
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:23095613-23096094:-1/exon

position:23096094:-1
position: 23096094
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101927821
type: SO_0000704
gene: LOC101927821
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 23119305..23169735
location: region:23119305-23169735:1
SIO_010080: LOC101927821

101927821
SIO_000068: ncbigene

position:23119305:1
position: 23119305
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:23169735:1
position: 23169735
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927821
type: SO_0000673
gene: LOC101927821
product: uncharacterized LOC101927821
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 19% coverage by RNAseq alignments
transcript id: XR_244296.1
so part of: LOC101927821
location: join(23119305..23119363,23120715..23121004,23157293..23157373,23158619..23158711,23169499..23169735)
location: region:23119305-23169735:1

GI:530419147
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:23119305-23119363:1/exon

position:23119363:1
position: 23119363
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:23120715-23121004:1/exon

position:23120715:1
position: 23120715
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:23121004:1
position: 23121004
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:23157293-23157373:1/exon

position:23157293:1
position: 23157293
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:23157373:1
position: 23157373
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:23158619-23158711:1/exon

position:23158619:1
position: 23158619
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:23158711:1
position: 23158711
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:23169499-23169735:1/exon

position:23169499:1
position: 23169499
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927843
type: SO_0000704
gene: LOC101927843
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(23381477..23470778)
location: region:23381477-23470778:-1
SIO_010080: LOC101927843

101927843
SIO_000068: ncbigene

position:23381477:-1
position: 23381477
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:23470778:-1
position: 23470778
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101927843
type: SO_0000673
gene: LOC101927843
product: uncharacterized LOC101927843
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 5% coverage by RNAseq alignments
transcript id: XR_244297.1
so part of: LOC101927843
location: complement(join(23381477..23381677,23388619..23388729,23413539..23413754,23415264..23415427,23468848..23468905,23470632..23470778))
location: region:23381477-23470778:-1

GI:530419148
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:23470632-23470778:-1/exon

position:23470632:-1
position: 23470632
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:23468848-23468905:-1/exon

position:23468848:-1
position: 23468848
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:23468905:-1
position: 23468905
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:23415264-23415427:-1/exon

position:23415264:-1
position: 23415264
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:23415427:-1
position: 23415427
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:23413539-23413754:-1/exon

position:23413539:-1
position: 23413539
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:23413754:-1
position: 23413754
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:23388619-23388729:-1/exon

position:23388619:-1
position: 23388619
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:23388729:-1
position: 23388729
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:23381477-23381677:-1/exon

position:23381677:-1
position: 23381677
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00308
type: SO_0000704
alternative label: C21orf74
alternative label: NCRNA00308
alternative label: PRED16
gene: LINC00308
gene synonym: C21orf74; NCRNA00308; PRED16
note: long intergenic non-protein coding RNA 308; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 23470936..23488847
location: region:23470936-23488847:1
SIO_010080: LINC00308

54143
SIO_000068: ncbigene

16023
SIO_000068: hgnc

position:23470936:1
position: 23470936
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:23488847:1
position: 23488847
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LINC00308
type: SO_0000673
alternative label: C21orf74
alternative label: NCRNA00308
alternative label: PRED16
gene: LINC00308
gene synonym: C21orf74; NCRNA00308; PRED16
product: long intergenic non-protein coding RNA 308
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_038400.1
so part of: LINC00308
location: join(23470936..23471031,23481765..23481872,23484090..23484145,23487079..23487217,23487297..23487431,23488655..23488847)
location: region:23470936-23488847:1

GI:336020376
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:23470936-23471031:1/exon

position:23471031:1
position: 23471031
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:23481765-23481872:1/exon

position:23481765:1
position: 23481765
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:23481872:1
position: 23481872
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:23484090-23484145:1/exon

position:23484090:1
position: 23484090
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:23484145:1
position: 23484145
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:23487079-23487217:1/exon

position:23487079:1
position: 23487079
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:23487217:1
position: 23487217
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:23487297-23487431:1/exon

position:23487297:1
position: 23487297
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:23487431:1
position: 23487431
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:23488655-23488847:1/exon

position:23488655:1
position: 23488655
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC100420035
type: SO_0000704
gene: LOC100420035
note: phosphoglycerate kinase 1 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(23507895..23508455)
location: region:23507895-23508455:-1

100420035
SIO_000068: ncbigene

position:23507895:-1
position: 23507895
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:23508455:-1
position: 23508455
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MAPK6PS2
type: SO_0000704
gene: MAPK6PS2
note: mitogen-activated protein kinase 6 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(23807356..23811387)
location: region:23807356-23811387:-1
SIO_010080: MAPK6PS2

254664
SIO_000068: ncbigene

16756
SIO_000068: hgnc

position:23807356:-1
position: 23807356
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:23811387:-1
position: 23811387
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MAPK6PS2
type: SO_0000147
gene: MAPK6PS2
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: MAPK6PS2
location: complement(23807356..23811387)
location: region:23807356-23811387:-1

ZNF299P
type: SO_0000704
alternative label: ZNF299
alternative label: ZNF299P1
gene: ZNF299P
gene synonym: ZNF299; ZNF299P1
note: zinc finger protein 299, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(24462793..24464066)
location: region:24462793-24464066:-1

54012
SIO_000068: ncbigene

13088
SIO_000068: hgnc

position:24462793:-1
position: 24462793
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:24464066:-1
position: 24464066
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MSANTD2P1
type: SO_0000704
gene: MSANTD2P1
note: Myb/SANT-like DNA-binding domain containing 2 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 24473509..24475393
location: region:24473509-24475393:1

100130310
SIO_000068: ncbigene

39637
SIO_000068: hgnc

position:24473509:1
position: 24473509
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:24475393:1
position: 24475393
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

D21S2088E
type: SO_0000704
gene: D21S2088E
note: D21S2088E; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(<24733426..24757156)
location: region:24733426-24757156:-1
SIO_010080: D21S2088E

266917
SIO_000068: ncbigene

position:24733426:-1
position: 24733426
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: FuzzyPosition

position:24757156:-1
position: 24757156
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

D21S2088E
type: SO_0000673
gene: D21S2088E
product: D21S2088E
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_040254.1
so part of: D21S2088E
location: complement(join(<24733426..24734561,24736360..24736515,24744649..24744770,24745270..24745406,24757009..24757156))
location: region:24733426-24757156:-1

GI:339275877
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:24757009-24757156:-1/exon

position:24757009:-1
position: 24757009
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:24745270-24745406:-1/exon

position:24745270:-1
position: 24745270
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:24745406:-1
position: 24745406
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:24744649-24744770:-1/exon

position:24744649:-1
position: 24744649
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:24744770:-1
position: 24744770
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:24736360-24736515:-1/exon

position:24736360:-1
position: 24736360
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:24736515:-1
position: 24736515
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:24733426-24734561:-1/exon

position:24734561:-1
position: 24734561
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

EEF1A1P1
type: SO_0000704
alternative label: EEF1A1P
gene: EEF1A1P1
gene synonym: EEF1A1P
note: eukaryotic translation elongation factor 1 alpha 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 24762580..24763614
location: region:24762580-24763614:1

54054
SIO_000068: ncbigene

3191
SIO_000068: hgnc

position:24762580:1
position: 24762580
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:24763614:1
position: 24763614
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

TUBAP
type: SO_0000704
gene: TUBAP
note: tubulin, alpha pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(24779812..24781542)
location: region:24779812-24781542:-1

54016
SIO_000068: ncbigene

12411
SIO_000068: hgnc

position:24779812:-1
position: 24779812
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:24781542:-1
position: 24781542
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

VN2R20P
type: SO_0000704
gene: VN2R20P
note: vomeronasal 2 receptor 20 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 25282442..25282672
location: region:25282442-25282672:1

100033408
SIO_000068: ncbigene

33226
SIO_000068: hgnc

position:25282442:1
position: 25282442
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:25282672:1
position: 25282672
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927869
type: SO_0000704
gene: LOC101927869
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(25676863..25693690)
location: region:25676863-25693690:-1
SIO_010080: LOC101927869

101927869
SIO_000068: ncbigene

position:25676863:-1
position: 25676863
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:25693690:-1
position: 25693690
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101927869
type: SO_0000673
gene: LOC101927869
product: uncharacterized LOC101927869
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST
transcript id: XR_244298.1
so part of: LOC101927869
location: complement(join(25676863..25678482,25679932..25680072,25680529..25680646,25693563..25693690))
location: region:25676863-25693690:-1

GI:530419149
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:25693563-25693690:-1/exon

position:25693563:-1
position: 25693563
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:25680529-25680646:-1/exon

position:25680529:-1
position: 25680529
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:25680646:-1
position: 25680646
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:25679932-25680072:-1/exon

position:25679932:-1
position: 25679932
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:25680072:-1
position: 25680072
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:25676863-25678482:-1/exon

position:25678482:-1
position: 25678482
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC339622
type: SO_0000704
gene: LOC339622
note: uncharacterized LOC339622; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 26212864..26430059
location: region:26212864-26430059:1
SIO_010080: LOC339622

339622
SIO_000068: ncbigene

position:26212864:1
position: 26212864
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:26430059:1
position: 26430059
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC339622
type: SO_0000673
gene: LOC339622
product: uncharacterized LOC339622
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_046198.3
so part of: LOC339622
location: join(26212864..26213042,26217093..26217243,26402097..26402172,26427747..26430059)
location: region:26212864-26430059:1

GI:392953820
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:26212864-26213042:1/exon

position:26213042:1
position: 26213042
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:26217093-26217243:1/exon

position:26217093:1
position: 26217093
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:26217243:1
position: 26217243
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:26402097-26402172:1/exon

position:26402097:1
position: 26402097
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:26402172:1
position: 26402172
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:26427747-26430059:1/exon

position:26427747:1
position: 26427747
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC100419737
type: SO_0000704
gene: LOC100419737
note: CTAGE family, member 5 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(26403331..26404233)
location: region:26403331-26404233:-1

100419737
SIO_000068: ncbigene

position:26403331:-1
position: 26403331
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26404233:-1
position: 26404233
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

RNA5SP489
type: SO_0000704
alternative label: RN5S489
gene: RNA5SP489
gene synonym: RN5S489
note: RNA, 5S ribosomal pseudogene 489; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 26574521..26574629
location: region:26574521-26574629:1

100873731
SIO_000068: ncbigene

43389
SIO_000068: hgnc

position:26574521:1
position: 26574521
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:26574629:1
position: 26574629
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

RPL13AP7
type: SO_0000704
alternative label: RPL13A_12_1722
gene: RPL13AP7
gene synonym: RPL13A_12_1722
note: ribosomal protein L13a pseudogene 7; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 26734109..26735238
location: region:26734109-26735238:1
SIO_010080: RPL13AP7

284821
SIO_000068: ncbigene

23755
SIO_000068: hgnc

position:26734109:1
position: 26734109
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:26735238:1
position: 26735238
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

RPL13AP7
type: SO_0000147
alternative label: RPL13A_12_1722
gene: RPL13AP7
gene synonym: RPL13A_12_1722
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: RPL13AP7
location: 26734109..26735238
location: region:26734109-26735238:1

LINC00158
type: SO_0000704
alternative label: C21orf42
alternative label: NCRNA00158
gene: LINC00158
gene synonym: C21orf42; NCRNA00158
note: long intergenic non-protein coding RNA 158; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(<26758133..26804013)
location: region:26758133-26804013:-1
SIO_010080: LINC00158

54072
SIO_000068: ncbigene

1283
SIO_000068: hgnc

position:26758133:-1
position: 26758133
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: FuzzyPosition

position:26804013:-1
position: 26804013
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00158
type: SO_0000673
alternative label: C21orf42
alternative label: NCRNA00158
gene: LINC00158
gene synonym: C21orf42; NCRNA00158
product: long intergenic non-protein coding RNA 158
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_024027.2
so part of: LINC00158
location: complement(join(<26758133..26758651,26793020..26793112,26796866..26796961,26802078..26802321,26803490..26804013))
location: region:26758133-26804013:-1

GI:209862749
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:26803490-26804013:-1/exon

position:26803490:-1
position: 26803490
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:26802078-26802321:-1/exon

position:26802078:-1
position: 26802078
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26802321:-1
position: 26802321
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:26796866-26796961:-1/exon

position:26796866:-1
position: 26796866
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26796961:-1
position: 26796961
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:26793020-26793112:-1/exon

position:26793020:-1
position: 26793020
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26793112:-1
position: 26793112
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:26758133-26758651:-1/exon

position:26758651:-1
position: 26758651
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MIR155HG
type: SO_0000704
alternative label: BIC
alternative label: MIRHG2
alternative label: NCRNA00172
gene: MIR155HG
gene synonym: BIC; MIRHG2; NCRNA00172
note: MIR155 host gene (non-protein coding); Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 26934457..>26947480
location: region:26934457-26947480:1
SIO_010080: MIR155HG

114614
SIO_000068: ncbigene

35460
SIO_000068: hgnc

position:26934457:1
position: 26934457
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:26947480:1
position: 26947480
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: FuzzyPosition

MIR155HG
type: SO_0000673
alternative label: BIC
alternative label: MIRHG2
alternative label: NCRNA00172
gene: MIR155HG
gene synonym: BIC; MIRHG2; NCRNA00172
product: MIR155 host gene (non-protein coding)
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_001458.3
so part of: MIR155HG
location: join(26934457..26934569,26942149..26942233,26946205..>26947480)
location: region:26934457-26947480:1

GI:209862755
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:26934457-26934569:1/exon

position:26934569:1
position: 26934569
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:26942149-26942233:1/exon

position:26942149:1
position: 26942149
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:26942233:1
position: 26942233
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:26946205-26947480:1/exon

position:26946205:1
position: 26946205
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR155
type: SO_0000704
alternative label: MIRN155
alternative label: miRNA155
gene: MIR155
gene synonym: MIRN155; miRNA155
note: microRNA 155; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 26946292..26946356
location: region:26946292-26946356:1
SIO_010080: MIR155

406947
SIO_000068: ncbigene

31542
SIO_000068: hgnc

609337
SIO_000068: omim

MI0000681
SIO_000068: mirbase

position:26946292:1
position: 26946292
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:26946356:1
position: 26946356
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR155
type: SO_0000185
alternative label: MIRN155
alternative label: miRNA155
gene: MIR155
gene synonym: MIRN155; miRNA155
product: microRNA 155
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_030784.1
so part of: MIR155
location: 26946292..26946356
location: region:26946292-26946356:1

GI:269846817
SIO_000068: ncbigi

MIR155
type: SO_0000655
alternative label: MIRN155
alternative label: miRNA155
gene: MIR155
gene synonym: MIRN155; miRNA155
nc RNA class: miRNA
product: hsa-miR-155-5p
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR155
location: 26946295..26946317
location: region:26946295-26946317:1

MIMAT0000646
SIO_000068: mirbase

position:26946295:1
position: 26946295
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:26946317:1
position: 26946317
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MIR155
type: SO_0000655
alternative label: MIRN155
alternative label: miRNA155
gene: MIR155
gene synonym: MIRN155; miRNA155
nc RNA class: miRNA
product: hsa-miR-155-3p
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: MIR155
location: 26946334..26946355
location: region:26946334-26946355:1

MIMAT0004658
SIO_000068: mirbase

position:26946334:1
position: 26946334
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:26946355:1
position: 26946355
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LINC00515
type: SO_0000704
alternative label: C21orf71
alternative label: PRED21
gene: LINC00515
gene synonym: C21orf71; PRED21
note: long intergenic non-protein coding RNA 515; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(<26955087..26955536)
location: region:26955087-26955536:-1
SIO_010080: LINC00515

282566
SIO_000068: ncbigene

16019
SIO_000068: hgnc

position:26955087:-1
position: 26955087
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: FuzzyPosition

position:26955536:-1
position: 26955536
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00515
type: SO_0000673
alternative label: C21orf71
alternative label: PRED21
gene: LINC00515
gene synonym: C21orf71; PRED21
product: long intergenic non-protein coding RNA 515
inference: similar to RNA sequence (same species):RefSeq:NR_024092.1
exception: annotated by transcript or proteomic data
note: The RefSeq transcript has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_024092.1
so part of: LINC00515
location: complement(<26955087..26955536)
location: region:26955087-26955536:-1

GI:197116383
SIO_000068: ncbigi

MRPL39
type: SO_0000704
alternative label: C21orf92
alternative label: L39mt
alternative label: MRP-L5
alternative label: MRPL5
alternative label: MSTP003
alternative label: PRED22
alternative label: PRED66
alternative label: RPML5
gene: MRPL39
gene synonym: C21orf92; L39mt; MRP-L5; MRPL5; MSTP003; PRED22; PRED66; RPML5
note: mitochondrial ribosomal protein L39; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(26957968..26979801)
location: region:26957968-26979801:-1
SIO_010080: MRPL39

54148
SIO_000068: ncbigene

14027
SIO_000068: hgnc

11371
SIO_000068: hprd

611845
SIO_000068: omim

position:26957968:-1
position: 26957968
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26979801:-1
position: 26979801
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MRPL39
type: SO_0000234
alternative label: C21orf92
alternative label: L39mt
alternative label: MRP-L5
alternative label: MRPL5
alternative label: MSTP003
alternative label: PRED22
alternative label: PRED66
alternative label: RPML5
gene: MRPL39
gene synonym: C21orf92; L39mt; MRP-L5; MRPL5; MSTP003; PRED22; PRED66; RPML5
product: mitochondrial ribosomal protein L39, transcript variant 1
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_017446.3
exception: annotated by transcript or proteomic data
note: The RefSeq transcript has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_017446.3
so part of: MRPL39
location: complement(join(26957968..26958066,26961147..26961194,26965124..26965277,26966205..26966270,26969614..26969726,26972111..26972178,26973680..26973779,26976108..26976247,26978761..26978967,26979715..26979801))
location: region:26957968-26979801:-1

GI:110618246
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:26979715-26979801:-1/exon

position:26979715:-1
position: 26979715
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:26978761-26978967:-1/exon

position:26978761:-1
position: 26978761
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26978967:-1
position: 26978967
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:26976108-26976247:-1/exon

position:26976108:-1
position: 26976108
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26976247:-1
position: 26976247
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:26973680-26973779:-1/exon

position:26973680:-1
position: 26973680
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26973779:-1
position: 26973779
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:26972111-26972178:-1/exon

position:26972111:-1
position: 26972111
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26972178:-1
position: 26972178
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:26969614-26969726:-1/exon

position:26969614:-1
position: 26969614
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26969726:-1
position: 26969726
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:26966205-26966270:-1/exon

position:26966205:-1
position: 26966205
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26966270:-1
position: 26966270
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:26965124-26965277:-1/exon

position:26965124:-1
position: 26965124
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26965277:-1
position: 26965277
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:26961147-26961194:-1/exon

position:26961147:-1
position: 26961147
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26961194:-1
position: 26961194
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:26957968-26958066:-1/exon

position:26958066:-1
position: 26958066
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MRPL39
type: SO_0000234
alternative label: C21orf92
alternative label: L39mt
alternative label: MRP-L5
alternative label: MRPL5
alternative label: MSTP003
alternative label: PRED22
alternative label: PRED66
alternative label: RPML5
gene: MRPL39
gene synonym: C21orf92; L39mt; MRP-L5; MRPL5; MSTP003; PRED22; PRED66; RPML5
product: mitochondrial ribosomal protein L39, transcript variant 2
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_080794.3
exception: annotated by transcript or proteomic data
note: The RefSeq transcript has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_080794.3
so part of: MRPL39
location: complement(join(26957968..26958066,26960013..26960101,26961147..26961194,26965124..26965277,26966205..26966270,26969614..26969726,26972111..26972178,26973680..26973779,26976108..26976247,26978761..26978967,26979715..26979801))
location: region:26957968-26979801:-1

GI:110618245
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:26979715-26979801:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:26978761-26978967:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:26976108-26976247:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:26973680-26973779:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:26972111-26972178:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:26969614-26969726:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:26966205-26966270:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:26965124-26965277:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:26961147-26961194:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:26960013-26960101:-1/exon

position:26960013:-1
position: 26960013
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26960101:-1
position: 26960101
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:26957968-26958066:-1/exon

MRPL39
type: SO_0000316
alternative label: C21orf92
alternative label: L39mt
alternative label: MRP-L5
alternative label: MRPL5
alternative label: MSTP003
alternative label: PRED22
alternative label: PRED66
alternative label: RPML5
gene: MRPL39
gene synonym: C21orf92; L39mt; MRP-L5; MRPL5; MSTP003; PRED22; PRED66; RPML5
inference: similar to AA sequence (same species):RefSeq:NP_059142.2
exception: annotated by transcript or proteomic data
note: isoform a is encoded by transcript variant 1; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: 39S ribosomal protein L39, mitochondrial isoform a
translation: MEALAMGSRALRLWLVAPGGGIKWRFIATSPASQLSPTELTEMRNDLFNKEKARQLSLTPRTEKIEVKHVGKTDPGTVFVMNKNISTPYSCAMHLSEWYCRKSILALVDGQPWDMYKPLTKSCEIKFLTFKDCDPGEVNKAYWRSCAMMMGCVIERAFKDEYMVNLVRAPEVPVISGAFCYDVVLDSKLDEWMPTKENLRSFTKDAHALIYKDLPFETLEVEAKVALEIFQHSKYKVDFIEEKASQNPERIVKLHRIGDFIDVSEGPLIPRTSICFQYEVSAVHNLQPTQPSLIRRFQGVSLPVHLRAHFTIWDKLLERSRKMVTEDQSKATEECTST
so part of: MRPL39
location: complement(join(26958019..26958066,26961147..26961194,26965124..26965277,26966205..26966270,26969614..26969726,26972111..26972178,26973680..26973779,26976108..26976247,26978761..26978967,26979715..26979787))
location: region:26958019-26979787:-1

NP_059142.2
SIO_000068: ncbiprotein

GI:27886582
SIO_000068: ncbigi

CCDS13573.1
SIO_000068: ccds

position:26958019:-1
position: 26958019
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:26979787:-1
position: 26979787
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:26979715-26979787:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:26978761-26978967:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:26976108-26976247:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:26973680-26973779:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:26972111-26972178:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:26969614-26969726:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:26966205-26966270:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:26965124-26965277:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:26961147-26961194:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:26958019-26958066:-1/exon

MRPL39
type: SO_0000316
alternative label: C21orf92
alternative label: L39mt
alternative label: MRP-L5
alternative label: MRPL5
alternative label: MSTP003
alternative label: PRED22
alternative label: PRED66
alternative label: RPML5
gene: MRPL39
gene synonym: C21orf92; L39mt; MRP-L5; MRPL5; MSTP003; PRED22; PRED66; RPML5
inference: similar to AA sequence (same species):RefSeq:NP_542984.2
exception: annotated by transcript or proteomic data
note: isoform b is encoded by transcript variant 2; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: 39S ribosomal protein L39, mitochondrial isoform b
translation: MEALAMGSRALRLWLVAPGGGIKWRFIATSPASQLSPTELTEMRNDLFNKEKARQLSLTPRTEKIEVKHVGKTDPGTVFVMNKNISTPYSCAMHLSEWYCRKSILALVDGQPWDMYKPLTKSCEIKFLTFKDCDPGEVNKAYWRSCAMMMGCVIERAFKDEYMVNLVRAPEVPVISGAFCYDVVLDSKLDEWMPTKENLRSFTKDAHALIYKDLPFETLEVEAKVALEIFQHSKYKVDFIEEKASQNPERIVKLHRIGDFIDVSEGPLIPRTSICFQYEVSAVHNLQPTQPSLIRRFQGVSLPVHLRAHFTIWDKLLERSRKMTPFPILLLFTTQSFFTTSPESYLLHGTVSE
so part of: MRPL39
location: complement(join(26958063..26958066,26960013..26960101,26961147..26961194,26965124..26965277,26966205..26966270,26969614..26969726,26972111..26972178,26973680..26973779,26976108..26976247,26978761..26978967,26979715..26979787))
location: region:26958063-26979787:-1

NP_542984.2
SIO_000068: ncbiprotein

GI:27886570
SIO_000068: ncbigi

CCDS33522.1
SIO_000068: ccds

position:26958063:-1
position: 26958063
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:26979715-26979787:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:26978761-26978967:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:26976108-26976247:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:26973680-26973779:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:26972111-26972178:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:26969614-26969726:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:26966205-26966270:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:26965124-26965277:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:26961147-26961194:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:26960013-26960101:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:26958063-26958066:-1/exon

JAM2
type: SO_0000704
alternative label: C21orf43
alternative label: CD322
alternative label: JAM-B
alternative label: JAMB
alternative label: PRO245
alternative label: VE-JAM
alternative label: VEJAM
gene: JAM2
gene synonym: C21orf43; CD322; JAM-B; JAMB; PRO245; VE-JAM; VEJAM
note: junctional adhesion molecule 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 27011594..>27089874
location: region:27011594-27089874:1
SIO_010080: JAM2

58494
SIO_000068: ncbigene

14686
SIO_000068: hgnc

06041
SIO_000068: hprd

606870
SIO_000068: omim

position:27011594:1
position: 27011594
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27089874:1
position: 27089874
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: FuzzyPosition
type: ExactPosition

JAM2
type: SO_0000234
alternative label: C21orf43
alternative label: CD322
alternative label: JAM-B
alternative label: JAMB
alternative label: PRO245
alternative label: VE-JAM
alternative label: VEJAM
gene: JAM2
gene synonym: C21orf43; CD322; JAM-B; JAMB; PRO245; VE-JAM; VEJAM
product: junctional adhesion molecule 2, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_021219.3
so part of: JAM2
location: join(27011594..27012200,27056195..27056260,27062178..27062285,27066068..27066220,27070989..27071191,27074482..27074581,27078291..27078398,27081746..27081761,27084652..27084694,27086952..27089874)
location: region:27011594-27089874:1

GI:393715109
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27011594-27012200:1/exon

position:27012200:1
position: 27012200
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27056195-27056260:1/exon

position:27056195:1
position: 27056195
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27056260:1
position: 27056260
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:27062178-27062285:1/exon

position:27062178:1
position: 27062178
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27062285:1
position: 27062285
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:27066068-27066220:1/exon

position:27066068:1
position: 27066068
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27066220:1
position: 27066220
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:27070989-27071191:1/exon

position:27070989:1
position: 27070989
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27071191:1
position: 27071191
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:27074482-27074581:1/exon

position:27074482:1
position: 27074482
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27074581:1
position: 27074581
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:27078291-27078398:1/exon

position:27078291:1
position: 27078291
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27078398:1
position: 27078398
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:27081746-27081761:1/exon

position:27081746:1
position: 27081746
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27081761:1
position: 27081761
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:27084652-27084694:1/exon

position:27084652:1
position: 27084652
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27084694:1
position: 27084694
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:27086952-27089874:1/exon

position:27086952:1
position: 27086952
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

JAM2
type: SO_0000673
alternative label: C21orf43
alternative label: CD322
alternative label: JAM-B
alternative label: JAMB
alternative label: PRO245
alternative label: VE-JAM
alternative label: VEJAM
gene: JAM2
gene synonym: C21orf43; CD322; JAM-B; JAMB; PRO245; VE-JAM; VEJAM
product: junctional adhesion molecule 2, transcript variant 4
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_072999.1
so part of: JAM2
location: join(27011594..27012200,27056195..27056260,27062178..27062285,27066068..27066220,27070989..27071191,27074482..27074577,27078291..27078398,27081746..27081761,27084652..27084694,27086952..>27089874)
location: region:27011594-27089874:1

GI:393715114
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27011594-27012200:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27056195-27056260:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27062178-27062285:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27066068-27066220:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27070989-27071191:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27074482-27074577:1/exon

position:27074577:1
position: 27074577
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:27078291-27078398:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27081746-27081761:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27084652-27084694:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27086952-27089874:1/exon

JAM2
type: SO_0000234
alternative label: C21orf43
alternative label: CD322
alternative label: JAM-B
alternative label: JAMB
alternative label: PRO245
alternative label: VE-JAM
alternative label: VEJAM
gene: JAM2
gene synonym: C21orf43; CD322; JAM-B; JAMB; PRO245; VE-JAM; VEJAM
product: junctional adhesion molecule 2, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001270407.1
so part of: JAM2
location: join(27011594..27012200,27056195..27056260,27066068..27066220,27070989..27071191,27074482..27074581,27078291..27078398,27081746..27081761,27084652..27084694,27086952..27089874)
location: region:27011594-27089874:1

GI:393715110
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27011594-27012200:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27056195-27056260:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27066068-27066220:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27070989-27071191:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27074482-27074581:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27078291-27078398:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27081746-27081761:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27084652-27084694:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27086952-27089874:1/exon

JAM2
type: SO_0000234
alternative label: C21orf43
alternative label: CD322
alternative label: JAM-B
alternative label: JAMB
alternative label: PRO245
alternative label: VE-JAM
alternative label: VEJAM
gene: JAM2
gene synonym: C21orf43; CD322; JAM-B; JAMB; PRO245; VE-JAM; VEJAM
product: junctional adhesion molecule 2, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001270408.1
so part of: JAM2
location: join(27011594..27012200,27056195..27056260,27062178..27062285,27066068..27066220,27070989..27071191,27074482..27074581,27078291..27078398,27081746..27081761,27084652..27084694,27086543..27086885)
location: region:27011594-27086885:1

GI:393715112
SIO_000068: ncbigi

position:27086885:1
position: 27086885
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27011594-27012200:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27056195-27056260:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27062178-27062285:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27066068-27066220:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27070989-27071191:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27074482-27074581:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27078291-27078398:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27081746-27081761:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27084652-27084694:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27086543-27086885:1/exon

position:27086543:1
position: 27086543
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

JAM2
type: SO_0000316
alternative label: C21orf43
alternative label: CD322
alternative label: JAM-B
alternative label: JAMB
alternative label: PRO245
alternative label: VE-JAM
alternative label: VEJAM
gene: JAM2
gene synonym: C21orf43; CD322; JAM-B; JAMB; PRO245; VE-JAM; VEJAM
note: isoform 1 precursor is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: junctional adhesion molecule B isoform 1 precursor
translation: MARRSRHRLLLLLLRYLVVALGYHKAYGFSAPKDQQVVTAVEYQEAILACKTPKKTVSSRLEWKKLGRSVSFVYYQQTLQGDFKNRAEMIDFNIRIKNVTRSDAGKYRCEVSAPSEQGQNLEEDTVTLEVLVAPAVPSCEVPSSALSGTVVELRCQDKEGNPAPEYTWFKDGIRLLENPRLGSQSTNSSYTMNTKTGTLQFNTVSKLDTGEYSCEARNSVGYRRCPGKRMQVDDLNISGIIAAVVVVALVISVCGLGVCYAQRKGYFSKETSFQKSNSSSKATTMSENDFKHTKSFII
so part of: JAM2
location: join(27012134..27012200,27056195..27056260,27062178..27062285,27066068..27066220,27070989..27071191,27074482..27074581,27078291..27078398,27081746..27081761,27084652..27084694,27086952..27086984)
location: region:27012134-27086984:1

NP_067042.1
SIO_000068: ncbiprotein

GI:10864029
SIO_000068: ncbigi

CCDS42911.1
SIO_000068: ccds

position:27012134:1
position: 27012134
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27086984:1
position: 27086984
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27012134-27012200:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27056195-27056260:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27062178-27062285:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27066068-27066220:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27070989-27071191:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27074482-27074581:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27078291-27078398:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27081746-27081761:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27084652-27084694:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27086952-27086984:1/exon

JAM2
type: SO_0000316
alternative label: C21orf43
alternative label: CD322
alternative label: JAM-B
alternative label: JAMB
alternative label: PRO245
alternative label: VE-JAM
alternative label: VEJAM
gene: JAM2
gene synonym: C21orf43; CD322; JAM-B; JAMB; PRO245; VE-JAM; VEJAM
note: isoform 2 precursor is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: junctional adhesion molecule B isoform 2 precursor
translation: MARRSRHRLLLLLLRYLVVALGYHKAYGFSAPKDQQVVTAVEYQGDFKNRAEMIDFNIRIKNVTRSDAGKYRCEVSAPSEQGQNLEEDTVTLEVLVAPAVPSCEVPSSALSGTVVELRCQDKEGNPAPEYTWFKDGIRLLENPRLGSQSTNSSYTMNTKTGTLQFNTVSKLDTGEYSCEARNSVGYRRCPGKRMQVDDLNISGIIAAVVVVALVISVCGLGVCYAQRKGYFSKETSFQKSNSSSKATTMSENDFKHTKSFII
so part of: JAM2
location: join(27012134..27012200,27056195..27056260,27066068..27066220,27070989..27071191,27074482..27074581,27078291..27078398,27081746..27081761,27084652..27084694,27086952..27086984)
location: region:27012134-27086984:1

NP_001257336.1
SIO_000068: ncbiprotein

GI:393715111
SIO_000068: ncbigi

CCDS58788.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:27012134-27012200:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27056195-27056260:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27066068-27066220:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27070989-27071191:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27074482-27074581:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27078291-27078398:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27081746-27081761:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27084652-27084694:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27086952-27086984:1/exon

JAM2
type: SO_0000316
alternative label: C21orf43
alternative label: CD322
alternative label: JAM-B
alternative label: JAMB
alternative label: PRO245
alternative label: VE-JAM
alternative label: VEJAM
gene: JAM2
gene synonym: C21orf43; CD322; JAM-B; JAMB; PRO245; VE-JAM; VEJAM
note: isoform 3 precursor is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: junctional adhesion molecule B isoform 3 precursor
translation: MARRSRHRLLLLLLRYLVVALGYHKAYGFSAPKDQQVVTAVEYQEAILACKTPKKTVSSRLEWKKLGRSVSFVYYQQTLQGDFKNRAEMIDFNIRIKNVTRSDAGKYRCEVSAPSEQGQNLEEDTVTLEVLVAPAVPSCEVPSSALSGTVVELRCQDKEGNPAPEYTWFKDGIRLLENPRLGSQSTNSSYTMNTKTGTLQFNTVSKLDTGEYSCEARNSVGYRRCPGKRMQVDDLNISGIIAAVVVVALVISVCGLGVCYAQRKGYFSKETSFQKSNSSSKATTMSENVQWLTPVIPALWKAAAGGSRGQEF
so part of: JAM2
location: join(27012134..27012200,27056195..27056260,27062178..27062285,27066068..27066220,27070989..27071191,27074482..27074581,27078291..27078398,27081746..27081761,27084652..27084694,27086543..27086617)
location: region:27012134-27086617:1

NP_001257337.1
SIO_000068: ncbiprotein

GI:393715113
SIO_000068: ncbigi

CCDS58787.1
SIO_000068: ccds

position:27086617:1
position: 27086617
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27012134-27012200:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27056195-27056260:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27062178-27062285:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27066068-27066220:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27070989-27071191:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27074482-27074581:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27078291-27078398:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27081746-27081761:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27084652-27084694:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27086543-27086617:1/exon

RNGTTP1
type: SO_0000704
gene: RNGTTP1
note: RNA guanylyltransferase and 5'-phosphatase pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 27015857..27016531
location: region:27015857-27016531:1

100421428
SIO_000068: ncbigene

39652
SIO_000068: hgnc

position:27015857:1
position: 27015857
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27016531:1
position: 27016531
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

FDX1P2
type: SO_0000704
alternative label: FDXP2
gene: FDX1P2
gene synonym: FDXP2
note: ferredoxin 1 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 27064483..27065457
location: region:27064483-27065457:1

2216
SIO_000068: ncbigene

3641
SIO_000068: hgnc

position:27064483:1
position: 27064483
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27065457:1
position: 27065457
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ATP5J
type: SO_0000704
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
note: ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(27096791..27107965)
location: region:27096791-27107965:-1
SIO_010080: ATP5J

522
SIO_000068: ncbigene

847
SIO_000068: hgnc

04399
SIO_000068: hprd

603152
SIO_000068: omim

position:27096791:-1
position: 27096791
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27107965:-1
position: 27107965
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ATP5J
type: SO_0000234
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
product: ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant 4
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001003697.1
so part of: ATP5J
location: complement(join(27096791..27096988,27097537..27097661,27101942..27102112,27107798..27107965))
location: region:27096791-27107965:-1

GI:51479138
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27107798-27107965:-1/exon

position:27107798:-1
position: 27107798
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27101942-27102112:-1/exon

position:27101942:-1
position: 27101942
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27102112:-1
position: 27102112
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:27097537-27097661:-1/exon

position:27097537:-1
position: 27097537
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27097661:-1
position: 27097661
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:27096791-27096988:-1/exon

position:27096988:-1
position: 27096988
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ATP5J
type: SO_0000234
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
product: ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001003696.1
so part of: ATP5J
location: complement(join(27096791..27096988,27097537..27097661,27101942..27102112,27107626..27107965))
location: region:27096791-27107965:-1

GI:51479136
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27107626-27107965:-1/exon

position:27107626:-1
position: 27107626
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27101942-27102112:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27096791-27096988:-1/exon

ATP5J
type: SO_0000234
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
product: ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001685.4
so part of: ATP5J
location: complement(join(27096791..27096988,27097537..27097661,27101942..27102112,27107300..27107965))
location: region:27096791-27107965:-1

GI:51479133
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27107300-27107965:-1/exon

position:27107300:-1
position: 27107300
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27101942-27102112:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27096791-27096988:-1/exon

ATP5J
type: SO_0000234
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
product: ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant 5
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001003701.1
so part of: ATP5J
location: complement(join(27096791..27096988,27097537..27097661,27101942..27102112,27107250..27107965))
location: region:27096791-27107965:-1

GI:51479140
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27107250-27107965:-1/exon

position:27107250:-1
position: 27107250
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27101942-27102112:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27096791-27096988:-1/exon

ATP5J
type: SO_0000234
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
product: ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001003703.1
so part of: ATP5J
location: complement(join(27096791..27096988,27097537..27097661,27101942..27102112,27107164..27107965))
location: region:27096791-27107965:-1

GI:51479142
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27107164-27107965:-1/exon

position:27107164:-1
position: 27107164
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27101942-27102112:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27096791-27096988:-1/exon

ATP5J
type: SO_0000234
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
product: ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 24 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 15 samples with support for all introns
transcript id: XM_005260992.1
so part of: ATP5J
location: complement(join(27096811..27096988,27097537..27097661,27101942..27102112,27106644..27106686,27107164..27107216))
location: region:27096811-27107216:-1

GI:530418945
SIO_000068: ncbigi

position:27096811:-1
position: 27096811
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27107216:-1
position: 27107216
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27107164-27107216:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27106644-27106686:-1/exon

position:27106644:-1
position: 27106644
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27106686:-1
position: 27106686
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:27101942-27102112:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27096811-27096988:-1/exon

ATP5J
type: SO_0000316
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
note: isoform b precursor is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: ATP synthase-coupling factor 6, mitochondrial isoform b precursor
translation: MHCDGGISMILQRLFRFSSVIRSAVSVHLRRNIGVTAVAFNKELDPIQKLFVDKIREYKSKRQTSGGPVDASSEYQQELERELFKLKQMFGNADMNTFPTFKFEDPKFEVIEKPQA
so part of: ATP5J
location: complement(join(27096951..27096988,27097537..27097661,27101942..27102112,27107250..27107266))
location: region:27096951-27107266:-1

NP_001003701.1
SIO_000068: ncbiprotein

GI:51479141
SIO_000068: ncbigi

CCDS46637.1
SIO_000068: ccds

position:27096951:-1
position: 27096951
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27107266:-1
position: 27107266
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27107250-27107266:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27101942-27102112:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27096951-27096988:-1/exon

ATP5J
type: SO_0000316
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: ATP synthase-coupling factor 6, mitochondrial isoform X1
translation: MILQRLFRFSSVIRSAVSVHLRRNIGVTAVAFNKELDPIQKLFVDKIREYKSKRQTSGGPVDASSEYQQELERELFKLKQMFGNADMNTFPTFKFEDPKFEVIEKPQA
so part of: ATP5J
location: complement(join(27096951..27096988,27097537..27097661,27101942..27102105))
location: region:27096951-27102105:-1

XP_005261049.1
SIO_000068: ncbiprotein

GI:530418946
SIO_000068: ncbigi

position:27102105:-1
position: 27102105
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27101942-27102105:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27096951-27096988:-1/exon

ATP5J
type: SO_0000316
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
note: isoform a precursor is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: ATP synthase-coupling factor 6, mitochondrial isoform a precursor
translation: MILQRLFRFSSVIRSAVSVHLRRNIGVTAVAFNKELDPIQKLFVDKIREYKSKRQTSGGPVDASSEYQQELERELFKLKQMFGNADMNTFPTFKFEDPKFEVIEKPQA
so part of: ATP5J
location: complement(join(27096951..27096988,27097537..27097661,27101942..27102105))
location: region:27096951-27102105:-1

NP_001676.2
SIO_000068: ncbiprotein

GI:18644883
SIO_000068: ncbigi

CCDS13574.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:27101942-27102105:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27096951-27096988:-1/exon

ATP5J
type: SO_0000316
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
note: isoform a precursor is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: ATP synthase-coupling factor 6, mitochondrial isoform a precursor
translation: MILQRLFRFSSVIRSAVSVHLRRNIGVTAVAFNKELDPIQKLFVDKIREYKSKRQTSGGPVDASSEYQQELERELFKLKQMFGNADMNTFPTFKFEDPKFEVIEKPQA
so part of: ATP5J
location: complement(join(27096951..27096988,27097537..27097661,27101942..27102105))
location: region:27096951-27102105:-1

NP_001003696.1
SIO_000068: ncbiprotein

GI:51479137
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27101942-27102105:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27096951-27096988:-1/exon

ATP5J
type: SO_0000316
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
note: isoform a precursor is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: ATP synthase-coupling factor 6, mitochondrial isoform a precursor
translation: MILQRLFRFSSVIRSAVSVHLRRNIGVTAVAFNKELDPIQKLFVDKIREYKSKRQTSGGPVDASSEYQQELERELFKLKQMFGNADMNTFPTFKFEDPKFEVIEKPQA
so part of: ATP5J
location: complement(join(27096951..27096988,27097537..27097661,27101942..27102105))
location: region:27096951-27102105:-1

NP_001003697.1
SIO_000068: ncbiprotein

GI:51479139
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27101942-27102105:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27096951-27096988:-1/exon

ATP5J
type: SO_0000316
alternative label: ATP5
alternative label: ATP5A
alternative label: ATPM
alternative label: CF6
alternative label: F6
gene: ATP5J
gene synonym: ATP5; ATP5A; ATPM; CF6; F6
note: isoform a precursor is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: ATP synthase-coupling factor 6, mitochondrial isoform a precursor
translation: MILQRLFRFSSVIRSAVSVHLRRNIGVTAVAFNKELDPIQKLFVDKIREYKSKRQTSGGPVDASSEYQQELERELFKLKQMFGNADMNTFPTFKFEDPKFEVIEKPQA
so part of: ATP5J
location: complement(join(27096951..27096988,27097537..27097661,27101942..27102105))
location: region:27096951-27102105:-1

NP_001003703.1
SIO_000068: ncbiprotein

GI:51479143
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27101942-27102105:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27097537-27097661:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27096951-27096988:-1/exon

GABPA
type: SO_0000704
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
note: GA binding protein transcription factor, alpha subunit 60kDa; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: 27107258..27144771
location: region:27107258-27144771:1
SIO_010080: GABPA

2551
SIO_000068: ncbigene

4071
SIO_000068: hgnc

11793
SIO_000068: hprd

600609
SIO_000068: omim

position:27107258:1
position: 27107258
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27144771:1
position: 27144771
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

GABPA
type: SO_0000234
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
product: GA binding protein transcription factor, alpha subunit 60kDa, transcript variant 2
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_001197297.1
exception: annotated by transcript or proteomic data
note: The RefSeq transcript has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001197297.1
so part of: GABPA
location: join(27107258..27107381,27113884..27113986,27117521..27117665,27121347..27121431,27124300..27124545,27130321..27130515,27134623..27134676,27136521..27136661,27136906..27137098,27141315..27144771)
location: region:27107258-27144771:1

GI:308818208
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27107258-27107381:1/exon

position:27107381:1
position: 27107381
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27113884-27113986:1/exon

position:27113884:1
position: 27113884
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27113986:1
position: 27113986
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:27117521-27117665:1/exon

position:27117521:1
position: 27117521
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27117665:1
position: 27117665
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:27121347-27121431:1/exon

position:27121347:1
position: 27121347
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27121431:1
position: 27121431
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:27124300-27124545:1/exon

position:27124300:1
position: 27124300
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27124545:1
position: 27124545
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:27130321-27130515:1/exon

position:27130321:1
position: 27130321
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27130515:1
position: 27130515
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:27134623-27134676:1/exon

position:27134623:1
position: 27134623
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27134676:1
position: 27134676
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:27136521-27136661:1/exon

position:27136521:1
position: 27136521
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27136661:1
position: 27136661
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:27136906-27137098:1/exon

position:27136906:1
position: 27136906
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27137098:1
position: 27137098
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:27141315-27144771:1/exon

position:27141315:1
position: 27141315
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

GABPA
type: SO_0000234
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
product: GA binding protein transcription factor, alpha subunit 60kDa, transcript variant 1
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_002040.3
exception: annotated by transcript or proteomic data
note: The RefSeq transcript has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_002040.3
so part of: GABPA
location: join(27107329..27107889,27113884..27113986,27117521..27117665,27121347..27121431,27124300..27124545,27130321..27130515,27134623..27134676,27136521..27136661,27136906..27137098,27141315..27144771)
location: region:27107329-27144771:1

GI:163644305
SIO_000068: ncbigi

position:27107329:1
position: 27107329
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27107329-27107889:1/exon

position:27107889:1
position: 27107889
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27113884-27113986:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27117521-27117665:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27121347-27121431:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27124300-27124545:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27130321-27130515:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27134623-27134676:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27136521-27136661:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27136906-27137098:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27141315-27144771:1/exon

GABPA
type: SO_0000234
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
product: GA binding protein transcription factor, alpha subunit 60kDa, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 34 ESTs, 8 Proteins, and 100% coverage by RNAseq alignments, including 7 samples with support for all introns
transcript id: XM_005260938.1
so part of: GABPA
location: join(27107501..27107696,27113884..27113986,27117521..27117665,27121347..27121431,27124300..27124545,27130321..27130515,27134623..27134676,27136521..27136661,27136906..27137098,27141315..27144771)
location: region:27107501-27144771:1

GI:530418818
SIO_000068: ncbigi

position:27107501:1
position: 27107501
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27107501-27107696:1/exon

position:27107696:1
position: 27107696
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27113884-27113986:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27117521-27117665:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27121347-27121431:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27124300-27124545:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27130321-27130515:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27134623-27134676:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27136521-27136661:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27136906-27137098:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27141315-27144771:1/exon

GABPA
type: SO_0000234
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
product: GA binding protein transcription factor, alpha subunit 60kDa, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 32 ESTs, 8 Proteins, and 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005260939.1
so part of: GABPA
location: join(27112318..27112343,27113884..27113986,27117521..27117665,27121347..27121431,27124300..27124545,27130321..27130515,27134623..27134676,27136521..27136661,27136906..27137098,27141315..27144771)
location: region:27112318-27144771:1

GI:530418820
SIO_000068: ncbigi

position:27112318:1
position: 27112318
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27112318-27112343:1/exon

position:27112343:1
position: 27112343
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27113884-27113986:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27117521-27117665:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27121347-27121431:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27124300-27124545:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27130321-27130515:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27134623-27134676:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27136521-27136661:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27136906-27137098:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27141315-27144771:1/exon

GABPA
type: SO_0000234
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
product: GA binding protein transcription factor, alpha subunit 60kDa, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 32 ESTs, 8 Proteins, and 100% coverage by RNAseq alignments, including 4 samples with support for all introns
transcript id: XM_005260940.1
so part of: GABPA
location: join(27112732..27112798,27113884..27113986,27117521..27117665,27121347..27121431,27124300..27124545,27130321..27130515,27134623..27134676,27136521..27136661,27136906..27137098,27141315..27144771)
location: region:27112732-27144771:1

GI:530418822
SIO_000068: ncbigi

position:27112732:1
position: 27112732
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27112732-27112798:1/exon

position:27112798:1
position: 27112798
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27113884-27113986:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27117521-27117665:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27121347-27121431:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27124300-27124545:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27130321-27130515:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27134623-27134676:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27136521-27136661:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27136906-27137098:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27141315-27144771:1/exon

GABPA
type: SO_0000316
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: GA-binding protein alpha chain
translation: MTKREAEELIEIEIDGTEKAECTEESIVEQTYAPAECVSQAIDINEPIGNLKKLLEPRLQCSLDAHEICLQDIQLDPERSLFDQGVKTDGTVQLSVQVISYQGIEPKLNILEIVKPADTVEVVIDPDAHHAESEAHLVEEAQVITLDGTKHITTISDETSEQVTRWAAALEGYRKEQERLGIPYDPIQWSTDQVLHWVVWVMKEFSMTDIDLTTLNISGRELCSLNQEDFFQRVPRGEILWSHLELLRKYVLASQEQQMNEIVTIDQPVQIIPASVQSATPTTIKVINSSAKAAKVQRAPRISGEDRSSPGNRTGNNGQIQLWQFLLELLTDKDARDCISWVGDEGEFKLNQPELVAQKWGQRKNKPTMNYEKLSRALRYYYDGDMICKVQGKRFVYKFVCDLKTLIGYSAAELNRLVTECEQKKLAKMQLHGIAQPVTAVALATASLQTEKDN
so part of: GABPA
location: join(27113910..27113986,27117521..27117665,27121347..27121431,27124300..27124545,27130321..27130515,27134623..27134676,27136521..27136661,27136906..27137098,27141315..27141543)
location: region:27113910-27141543:1

NP_002031.2
SIO_000068: ncbiprotein

GI:34452721
SIO_000068: ncbigi

CCDS13575.1
SIO_000068: ccds

position:27113910:1
position: 27113910
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:27141543:1
position: 27141543
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27113910-27113986:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27117521-27117665:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27121347-27121431:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27124300-27124545:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27130321-27130515:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27134623-27134676:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27136521-27136661:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27136906-27137098:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27141315-27141543:1/exon

GABPA
type: SO_0000316
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: GA-binding protein alpha chain
translation: MTKREAEELIEIEIDGTEKAECTEESIVEQTYAPAECVSQAIDINEPIGNLKKLLEPRLQCSLDAHEICLQDIQLDPERSLFDQGVKTDGTVQLSVQVISYQGIEPKLNILEIVKPADTVEVVIDPDAHHAESEAHLVEEAQVITLDGTKHITTISDETSEQVTRWAAALEGYRKEQERLGIPYDPIQWSTDQVLHWVVWVMKEFSMTDIDLTTLNISGRELCSLNQEDFFQRVPRGEILWSHLELLRKYVLASQEQQMNEIVTIDQPVQIIPASVQSATPTTIKVINSSAKAAKVQRAPRISGEDRSSPGNRTGNNGQIQLWQFLLELLTDKDARDCISWVGDEGEFKLNQPELVAQKWGQRKNKPTMNYEKLSRALRYYYDGDMICKVQGKRFVYKFVCDLKTLIGYSAAELNRLVTECEQKKLAKMQLHGIAQPVTAVALATASLQTEKDN
so part of: GABPA
location: join(27113910..27113986,27117521..27117665,27121347..27121431,27124300..27124545,27130321..27130515,27134623..27134676,27136521..27136661,27136906..27137098,27141315..27141543)
location: region:27113910-27141543:1

NP_001184226.1
SIO_000068: ncbiprotein

GI:308818209
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27113910-27113986:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27117521-27117665:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27121347-27121431:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27124300-27124545:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27130321-27130515:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27134623-27134676:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27136521-27136661:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27136906-27137098:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27141315-27141543:1/exon

GABPA
type: SO_0000316
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: GA-binding protein alpha chain isoform X1
translation: MTKREAEELIEIEIDGTEKAECTEESIVEQTYAPAECVSQAIDINEPIGNLKKLLEPRLQCSLDAHEICLQDIQLDPERSLFDQGVKTDGTVQLSVQVISYQGIEPKLNILEIVKPADTVEVVIDPDAHHAESEAHLVEEAQVITLDGTKHITTISDETSEQVTRWAAALEGYRKEQERLGIPYDPIQWSTDQVLHWVVWVMKEFSMTDIDLTTLNISGRELCSLNQEDFFQRVPRGEILWSHLELLRKYVLASQEQQMNEIVTIDQPVQIIPASVQSATPTTIKVINSSAKAAKVQRAPRISGEDRSSPGNRTGNNGQIQLWQFLLELLTDKDARDCISWVGDEGEFKLNQPELVAQKWGQRKNKPTMNYEKLSRALRYYYDGDMICKVQGKRFVYKFVCDLKTLIGYSAAELNRLVTECEQKKLAKMQLHGIAQPVTAVALATASLQTEKDN
so part of: GABPA
location: join(27113910..27113986,27117521..27117665,27121347..27121431,27124300..27124545,27130321..27130515,27134623..27134676,27136521..27136661,27136906..27137098,27141315..27141543)
location: region:27113910-27141543:1

XP_005260995.1
SIO_000068: ncbiprotein

GI:530418819
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27113910-27113986:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27117521-27117665:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27121347-27121431:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27124300-27124545:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27130321-27130515:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27134623-27134676:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27136521-27136661:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27136906-27137098:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27141315-27141543:1/exon

GABPA
type: SO_0000316
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: GA-binding protein alpha chain isoform X2
translation: MTKREAEELIEIEIDGTEKAECTEESIVEQTYAPAECVSQAIDINEPIGNLKKLLEPRLQCSLDAHEICLQDIQLDPERSLFDQGVKTDGTVQLSVQVISYQGIEPKLNILEIVKPADTVEVVIDPDAHHAESEAHLVEEAQVITLDGTKHITTISDETSEQVTRWAAALEGYRKEQERLGIPYDPIQWSTDQVLHWVVWVMKEFSMTDIDLTTLNISGRELCSLNQEDFFQRVPRGEILWSHLELLRKYVLASQEQQMNEIVTIDQPVQIIPASVQSATPTTIKVINSSAKAAKVQRAPRISGEDRSSPGNRTGNNGQIQLWQFLLELLTDKDARDCISWVGDEGEFKLNQPELVAQKWGQRKNKPTMNYEKLSRALRYYYDGDMICKVQGKRFVYKFVCDLKTLIGYSAAELNRLVTECEQKKLAKMQLHGIAQPVTAVALATASLQTEKDN
so part of: GABPA
location: join(27113910..27113986,27117521..27117665,27121347..27121431,27124300..27124545,27130321..27130515,27134623..27134676,27136521..27136661,27136906..27137098,27141315..27141543)
location: region:27113910-27141543:1

XP_005260996.1
SIO_000068: ncbiprotein

GI:530418821
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27113910-27113986:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27117521-27117665:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27121347-27121431:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27124300-27124545:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27130321-27130515:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27134623-27134676:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27136521-27136661:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27136906-27137098:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27141315-27141543:1/exon

GABPA
type: SO_0000316
alternative label: E4TF1-60
alternative label: E4TF1A
alternative label: NFT2
alternative label: NRF2
alternative label: NRF2A
alternative label: RCH04A07
gene: GABPA
gene synonym: E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: GA-binding protein alpha chain isoform X3
translation: MTKREAEELIEIEIDGTEKAECTEESIVEQTYAPAECVSQAIDINEPIGNLKKLLEPRLQCSLDAHEICLQDIQLDPERSLFDQGVKTDGTVQLSVQVISYQGIEPKLNILEIVKPADTVEVVIDPDAHHAESEAHLVEEAQVITLDGTKHITTISDETSEQVTRWAAALEGYRKEQERLGIPYDPIQWSTDQVLHWVVWVMKEFSMTDIDLTTLNISGRELCSLNQEDFFQRVPRGEILWSHLELLRKYVLASQEQQMNEIVTIDQPVQIIPASVQSATPTTIKVINSSAKAAKVQRAPRISGEDRSSPGNRTGNNGQIQLWQFLLELLTDKDARDCISWVGDEGEFKLNQPELVAQKWGQRKNKPTMNYEKLSRALRYYYDGDMICKVQGKRFVYKFVCDLKTLIGYSAAELNRLVTECEQKKLAKMQLHGIAQPVTAVALATASLQTEKDN
so part of: GABPA
location: join(27113910..27113986,27117521..27117665,27121347..27121431,27124300..27124545,27130321..27130515,27134623..27134676,27136521..27136661,27136906..27137098,27141315..27141543)
location: region:27113910-27141543:1

XP_005260997.1
SIO_000068: ncbiprotein

GI:530418823
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27113910-27113986:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27117521-27117665:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27121347-27121431:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27124300-27124545:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27130321-27130515:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27134623-27134676:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27136521-27136661:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27136906-27137098:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27141315-27141543:1/exon

APP
type: SO_0000704
alternative label: AAA
alternative label: ABETA
alternative label: ABPP
alternative label: AD1
alternative label: APPI
alternative label: CTFgamma
alternative label: CVAP
alternative label: PN-II
alternative label: PN2
gene: APP
gene synonym: AAA; ABETA; ABPP; AD1; APPI; CTFgamma; CVAP; PN-II; PN2
note: amyloid beta (A4) precursor protein; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
location: complement(27252861..27543446)
location: region:27252861-27543446:-1
SIO_010080: APP
SIO_010080: feature:27252861-27543138:-1/mRNA:80
SIO_010080: feature:27252861-27543138:-1/mRNA:81
SIO_010080: feature:27252861-27512708:-1/mRNA:82
SIO_010080: feature:27253981-27542938:-1/CDS:73
SIO_010080: feature:27253981-27542938:-1/CDS:74
SIO_010080: feature:27253981-27542938:-1/CDS:75
SIO_010080: feature:27253981-27542938:-1/CDS:76
SIO_010080: feature:27253981-27542938:-1/CDS:77
SIO_010080: feature:27253981-27542938:-1/CDS:78
SIO_010080: feature:27253981-27542938:-1/CDS:79
SIO_010080: feature:27253981-27542938:-1/CDS:80
SIO_010080: feature:27253981-27512512:-1/CDS:81
SIO_010080: feature:27253981-27484415:-1/CDS:82

351
SIO_000068: ncbigene

620
SIO_000068: hgnc

104760
SIO_000068: omim

position:27252861:-1
position: 27252861
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27543446:-1
position: 27543446
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

APP
type: SO_0000234
alternative label: AAA
alternative label: ABETA
alternative label: ABPP
alternative label: AD1
alternative label: APPI
alternative label: CTFgamma
alternative label: CVAP
alternative label: PN-II
alternative label: PN2
gene: APP
gene synonym: AAA; ABETA; ABPP; AD1; APPI; CTFgamma; CVAP; PN-II; PN2
product: amyloid beta (A4) precursor protein, transcript variant 7
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001136131.2
so part of: APP
location: complement(join(27252861..27254082,27264034..27264180,27269885..27269985,27277336..27277389,27284053..27284274,27326904..27327003,27327941..27328069,27347383..27347541,27348267..27348341,27354657..27354790,27394156..27394358,27423316..27423509,27425552..27425664,27462259..27462388,27484296..27484463,27543303..27543446))
location: region:27252861-27543446:-1

GI:324021747
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27543303-27543446:-1/exon

position:27543303:-1
position: 27543303
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27484296-27484463:-1/exon

position:27484296:-1
position: 27484296
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27484463:-1
position: 27484463
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:27462259-27462388:-1/exon

position:27462259:-1
position: 27462259
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27462388:-1
position: 27462388
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:27425552-27425664:-1/exon

position:27425552:-1
position: 27425552
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27425664:-1
position: 27425664
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:27423316-27423509:-1/exon

position:27423316:-1
position: 27423316
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27423509:-1
position: 27423509
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:27394156-27394358:-1/exon

position:27394156:-1
position: 27394156
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27394358:-1
position: 27394358
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:27354657-27354790:-1/exon

position:27354657:-1
position: 27354657
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27354790:-1
position: 27354790
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:27348267-27348341:-1/exon

position:27348267:-1
position: 27348267
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27348341:-1
position: 27348341
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:27347383-27347541:-1/exon

position:27347383:-1
position: 27347383
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27347541:-1
position: 27347541
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:27327941-27328069:-1/exon

position:27327941:-1
position: 27327941
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27328069:-1
position: 27328069
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:27326904-27327003:-1/exon

position:27326904:-1
position: 27326904
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27327003:-1
position: 27327003
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:27284053-27284274:-1/exon

position:27284053:-1
position: 27284053
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27284274:-1
position: 27284274
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:27277336-27277389:-1/exon

position:27277336:-1
position: 27277336
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27277389:-1
position: 27277389
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:27269885-27269985:-1/exon

position:27269885:-1
position: 27269885
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27269985:-1
position: 27269985
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:27264034-27264180:-1/exon

position:27264034:-1
position: 27264034
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27264180:-1
position: 27264180
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:27252861-27254082:-1/exon

position:27254082:-1
position: 27254082
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

APP
type: SO_0000234
alternative label: AAA
alternative label: ABETA
alternative label: ABPP
alternative label: AD1
alternative label: APPI
alternative label: CTFgamma
alternative label: CVAP
alternative label: PN-II
alternative label: PN2
gene: APP
gene synonym: AAA; ABETA; ABPP; AD1; APPI; CTFgamma; CVAP; PN-II; PN2
product: amyloid beta (A4) precursor protein, transcript variant 5
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001136129.2
so part of: APP
location: complement(join(27252861..27254082,27264034..27264180,27269885..27269985,27277336..27277389,27284053..27284274,27326904..27327003,27327941..27328069,27347383..27347541,27348267..27348341,27354657..27354790,27394156..27394358,27423316..27423509,27425552..27425664,27462259..27462388,27542882..27543138))
location: region:27252861-27543138:-1

GI:228008402
SIO_000068: ncbigi

position:27543138:-1
position: 27543138
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:27542882-27543138:-1/exon

position:27542882:-1
position: 27542882
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:27462259-27462388:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27425552-27425664:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27423316-27423509:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27394156-27394358:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27354657-27354790:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27348267-27348341:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27347383-27347541:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27327941-27328069:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27326904-27327003:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:27284053-27284274:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:27277336-27277389:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:27269885-27269985:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:27264034-27264180:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:27252861-27254082:-1/exon

APP
type: SO_0000234
alternative label: AAA
alternative label: ABETA
alternative label: ABPP
alternative label: AD1
alternative label: APPI
alternative label: CTFgamma
alternative label: CVAP
alternative label: PN-II
alternative label: PN2
gene: APP
gene synonym: AAA; ABETA; ABPP; AD1; APPI; CTFgamma; CVAP; PN-II; PN2
product: amyloid beta (A4) precursor protein, transcript variant 6
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001136130.2
so part of: APP
location: complement(join(27252861..27254082,27264034..27264180,27269885..27269985,27277336..27277389,27284053..27284274,27326904..27327003,27327941..27328069,27347383..27347541,27348267..27348341,27354657..27354790,27369675..27369731,27372330..27372497,27394156..27394358,27423316..27423509,27425552..27425664,27462259..27462388,27542882..27543138))
location: region:27252861-27543138:-1

GI:228008401
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27542882-27543138:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27462259-27462388:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27425552-27425664:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27423316-27423509:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27394156-27394358:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27372330-27372497:-1/exon

position:27372330:-1
position: 27372330
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27372497:-1
position: 27372497
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:27369675-27369731:-1/exon

position:27369675:-1
position: 27369675
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:27369731:-1
position: 27369731
reference: Homo sapiens chromosome 21, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:27354657-27354790:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27348267-27348341:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27347383-27347541:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:27327941-27328069:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:27326904-27327003:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:27284053-27284274:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:27277336-27277389:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:27269885-27269985:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:27264034-27264180:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:27252861-27254082:-1/exon

APP
type: SO_0000234
alternative label: AAA
alternative label: ABETA
alternative label: ABPP
alternative label: AD1
alternative label: APPI
alternative label: CTFgamma
alternative label: CVAP
alternative label: PN-II
alternative label: PN2
gene: APP
gene synonym: AAA; ABETA; ABPP; AD1; APPI; CTFgamma; CVAP; PN-II; PN2
product: amyloid beta (A4) precursor protein, transcript variant 10
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001204303.1
so part of: APP
location: complement(join(27252861..27254082,27264034..27264180,27269885..27269985,27284053..27284274,27326904..27327003,27327941..27328069,27347383..27347541,27348267..27348341,27354657..27354790,27394156..27394358,27423316..27423509,27425552..27425664,27462259..27462388,27484296..27484463,27542882..27543138))
location: region:27252861-27543138:-1

GI:324021739
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27542882-27543138:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27484296-27484463:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27462259-27462388:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27425552-27425664:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27423316-27423509:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27394156-27394358:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27354657-27354790:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27348267-27348341:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27347383-27347541:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27327941-27328069:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:27326904-27327003:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:27284053-27284274:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:27269885-27269985:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:27264034-27264180:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:27252861-27254082:-1/exon

APP
type: SO_0000234
alternative label: AAA
alternative label: ABETA
alternative label: ABPP
alternative label: AD1
alternative label: APPI
alternative label: CTFgamma
alternative label: CVAP
alternative label: PN-II
alternative label: PN2
gene: APP
gene synonym: AAA; ABETA; ABPP; AD1; APPI; CTFgamma; CVAP; PN-II; PN2
product: amyloid beta (A4) precursor protein, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_201414.2
so part of: APP
location: complement(join(27252861..27254082,27264034..27264180,27269885..27269985,27277336..27277389,27284053..27284274,27326904..27327003,27327941..27328069,27347383..27347541,27348267..27348341,27354657..27354790,27394156..27394358,27423316..27423509,27425552..27425664,27462259..27462388,27484296..27484463,27542882..27543138))
location: region:27252861-27543138:-1

GI:228008405
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27542882-27543138:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27484296-27484463:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27462259-27462388:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27425552-27425664:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27423316-27423509:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27394156-27394358:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27354657-27354790:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27348267-27348341:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27347383-27347541:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27327941-27328069:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:27326904-27327003:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:27284053-27284274:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:27277336-27277389:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:27269885-27269985:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:27264034-27264180:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:27252861-27254082:-1/exon

APP
type: SO_0000234
alternative label: AAA
alternative label: ABETA
alternative label: ABPP
alternative label: AD1
alternative label: APPI
alternative label: CTFgamma
alternative label: CVAP
alternative label: PN-II
alternative label: PN2
gene: APP
gene synonym: AAA; ABETA; ABPP; AD1; APPI; CTFgamma; CVAP; PN-II; PN2
product: amyloid beta (A4) precursor protein, transcript variant 9
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001204302.1
so part of: APP
location: complement(join(27252861..27254082,27264034..27264180,27269885..27269985,27284053..27284274,27326904..27327003,27327941..27328069,27347383..27347541,27348267..27348341,27354657..27354790,27372330..27372497,27394156..27394358,27423316..27423509,27425552..27425664,27462259..27462388,27484296..27484463,27542882..27543138))
location: region:27252861-27543138:-1

GI:324021735
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27542882-27543138:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27484296-27484463:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:27462259-27462388:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:27425552-27425664:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:27423316-27423509:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:27394156-27394358:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:27372330-27372497:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:27354657-27354790:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:27348267-27348341:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:27347383-27347541:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:27327941-27328069:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:27326904-27327003:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:27284053-27284274:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:27269885-27269985:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:27264034-27264180:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:27252861-27254082:-1/exon

APP
type: SO_0000234
alternative label: AAA
alternative label: ABETA
alternative label: ABPP
alternative label: AD1
alternative label: APPI
alternative label: CTFgamma
alternative label: CVAP
alternative label: PN-II
alternative label: PN2
gene: APP
gene synonym: AAA; ABETA; ABPP; AD1; APPI; CTFgamma; CVAP; PN-II; PN2
product: amyloid beta (A4) precursor protein, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_201413.2
so part of: APP
location: complement(join(27252861..27254082,27264034..27264180,27269885..27269985,27277336..27277389,27284053..27284274,27326904..27327003,27327941..27328069,27347383..27347541,27348267..27348341,27354657..27354790,27372330..27372497,27394156..27394358,27423316..27423509,27425552..27425664,27462259..27462388,27484296..27484463,27542882..27543138))
location: region:27252861-27543138:-1

GI:228008404
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:27542882-27543138:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:27484296-27484463:-1/exon