Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: SO_0000340
sequence version: NC_000018.9
sequence length: 78077248
sequence fasta: http://www.ncbi.nlm.nih.gov/nuccore/NC_000018.9
type: SO_0000987
sequence date: 2013-08-13
label: NC_000018.9
SIO_000068: refseq
dblink: PRJNA168
location: 1..78077248
location: region:1-78077248:1
organism: Homo sapiens
mol type: genomic DNA
chromosome: 18

GI:224589809
SIO_000068: ncbigi

PRJNA168
type: Entry

16177791
SIO_000068: pubmed

15496913
SIO_000068: pubmed

11237011
SIO_000068: pubmed

position:1:1
position: 1
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:78077248:1
position: 78077248
reference: Homo sapiens chromosome 18, 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 18, GRCh37.p13 Primary Assembly.
location: 1..10000
location: region:1-10000:1

position:10000:1
position: 10000
reference: Homo sapiens chromosome 18, 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 18, GRCh37.p13 Primary Assembly.
location: 15410899..15460898
location: region:15410899-15460898:1

position:15410899:1
position: 15410899
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:15460898:1
position: 15460898
reference: Homo sapiens chromosome 18, 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 18, GRCh37.p13 Primary Assembly.
location: 15460899..18460898
location: region:15460899-18460898:1

position:15460899:1
position: 15460899
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18460898:1
position: 18460898
reference: Homo sapiens chromosome 18, 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 18, GRCh37.p13 Primary Assembly.
location: 18460899..18510898
location: region:18460899-18510898:1

position:18460899:1
position: 18460899
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:18510898:1
position: 18510898
reference: Homo sapiens chromosome 18, 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 18, GRCh37.p13 Primary Assembly.
location: 52059137..52209136
location: region:52059137-52209136:1

position:52059137:1
position: 52059137
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:52209136:1
position: 52209136
reference: Homo sapiens chromosome 18, 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 18, GRCh37.p13 Primary Assembly.
location: 78017249..78067248
location: region:78017249-78067248:1

position:78017249:1
position: 78017249
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:78067248:1
position: 78067248
reference: Homo sapiens chromosome 18, 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 18, GRCh37.p13 Primary Assembly.
location: 78067249..78077248
location: region:78067249-78077248:1

position:78067249:1
position: 78067249
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC260334
type: SO_0000704
gene: LOC260334
note: HSA18p11 beta-tubulin 4Q pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(47390..49557)
location: region:47390-49557:-1

260334
SIO_000068: ncbigene

position:47390:-1
position: 47390
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:49557:-1
position: 49557
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

IL9RP4
type: SO_0000704
gene: IL9RP4
note: interleukin 9 receptor pseudogene 4; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(79721..88561)
location: region:79721-88561:-1
SIO_010080: IL9RP4

100132166
SIO_000068: ncbigene

6034
SIO_000068: hgnc

position:79721:-1
position: 79721
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:88561:-1
position: 88561
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

IL9RP4
type: SO_0000147
gene: IL9RP4
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: IL9RP4
location: complement(88459..88561)
location: region:88459-88561:-1

position:88459:-1
position: 88459
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ROCK1P1
type: SO_0000704
gene: ROCK1P1
note: Rho-associated, coiled-coil containing protein kinase 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 109065..>122219
location: region:109065-122219:1
SIO_010080: ROCK1P1

727758
SIO_000068: ncbigene

37832
SIO_000068: hgnc

position:109065:1
position: 109065
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:122219:1
position: 122219
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: FuzzyPosition

ROCK1P1
type: SO_0000673
gene: ROCK1P1
product: Rho-associated, coiled-coil containing protein kinase 1 pseudogene 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
transcript id: NR_033770.1
so part of: ROCK1P1
location: join(109065..109453,116842..116920,117043..117304,118297..118504,120701..>122219)
location: region:109065-122219:1

GI:298566317
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:109065-109453:1/exon

position:109453:1
position: 109453
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:116842-116920:1/exon

position:116842:1
position: 116842
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:116920:1
position: 116920
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:117043-117304:1/exon

position:117043:1
position: 117043
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:117304:1
position: 117304
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:118297-118504:1/exon

position:118297:1
position: 118297
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:118504:1
position: 118504
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:120701-122219:1/exon

position:120701:1
position: 120701
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

USP14
type: SO_0000704
alternative label: TGT
gene: USP14
gene synonym: TGT
note: ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 158483..213739
location: region:158483-213739:1
SIO_010080: USP14

9097
SIO_000068: ncbigene

12612
SIO_000068: hgnc

607274
SIO_000068: omim

position:158483:1
position: 158483
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:213739:1
position: 213739
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

USP14
type: SO_0000234
alternative label: TGT
gene: USP14
gene synonym: TGT
product: ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase), transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_005151.3
so part of: USP14
location: join(158483..158714,163308..163453,166787..166819,178933..179037,180236..180339,192842..192900,196637..196767,197616..197696,198047..198132,199202..199316,202880..202945,203098..203190,204564..204692,209971..210031,210386..210493,211133..213739)
location: region:158483-213739:1

GI:82880646
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:158483-158714:1/exon

position:158714:1
position: 158714
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:163308-163453:1/exon

position:163308:1
position: 163308
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:163453:1
position: 163453
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:166787-166819:1/exon

position:166787:1
position: 166787
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:166819:1
position: 166819
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:178933-179037:1/exon

position:178933:1
position: 178933
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:179037:1
position: 179037
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:180236-180339:1/exon

position:180236:1
position: 180236
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:180339:1
position: 180339
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:192842-192900:1/exon

position:192842:1
position: 192842
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:192900:1
position: 192900
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:196637-196767:1/exon

position:196637:1
position: 196637
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:196767:1
position: 196767
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:197616-197696:1/exon

position:197616:1
position: 197616
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:197696:1
position: 197696
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:198047-198132:1/exon

position:198047:1
position: 198047
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:198132:1
position: 198132
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:199202-199316:1/exon

position:199202:1
position: 199202
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:199316:1
position: 199316
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:202880-202945:1/exon

position:202880:1
position: 202880
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:202945:1
position: 202945
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:203098-203190:1/exon

position:203098:1
position: 203098
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:203190:1
position: 203190
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:204564-204692:1/exon

position:204564:1
position: 204564
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:204692:1
position: 204692
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:209971-210031:1/exon

position:209971:1
position: 209971
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:210031:1
position: 210031
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:210386-210493:1/exon

position:210386:1
position: 210386
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:210493:1
position: 210493
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:211133-213739:1/exon

position:211133:1
position: 211133
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

USP14
type: SO_0000234
alternative label: TGT
gene: USP14
gene synonym: TGT
product: ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase), transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001037334.1
so part of: USP14
location: join(158483..158714,163308..163453,166787..166819,180236..180339,192842..192900,196637..196767,197616..197696,198047..198132,199202..199316,202880..202945,203098..203190,204564..204692,209971..210031,210386..210493,211133..213739)
location: region:158483-213739:1

GI:82880644
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:158483-158714:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:163308-163453:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:166787-166819:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:180236-180339:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:192842-192900:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:196637-196767:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:197616-197696:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:198047-198132:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:199202-199316:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:202880-202945:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:203098-203190:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:204564-204692:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:209971-210031:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:210386-210493:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:211133-213739:1/exon

USP14
type: SO_0000234
alternative label: TGT
gene: USP14
gene synonym: TGT
product: ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase), transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 72 ESTs, 1 Protein, and 98% coverage by RNAseq alignments
transcript id: XM_005258164.1
so part of: USP14
location: join(158559..158714,163308..163453,178933..179037,180236..180339,192842..192900,196637..196767,197616..197696,198047..198132,199202..199316,202880..202945,203098..203190,204564..204692,209971..210031,210386..210493,211133..212227)
location: region:158559-212227:1

GI:530424980
SIO_000068: ncbigi

position:158559:1
position: 158559
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:212227:1
position: 212227
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:158559-158714:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:163308-163453:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:178933-179037:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:180236-180339:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:192842-192900:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:196637-196767:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:197616-197696:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:198047-198132:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:199202-199316:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:202880-202945:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:203098-203190:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:204564-204692:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:209971-210031:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:210386-210493:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:211133-212227:1/exon

USP14
type: SO_0000316
alternative label: TGT
gene: USP14
gene synonym: TGT
note: isoform a is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: ubiquitin carboxyl-terminal hydrolase 14 isoform a
translation: MPLYSVTVKWGKEKFEGVELNTDEPPMVFKAQLFALTGVQPARQKVMVKGGTLKDDDWGNIKIKNGMTLLMMGSADALPEEPSAKTVFVEDMTEEQLASAMELPCGLTNLGNTCYMNATVQCIRSVPELKDALKRYAGALRASGEMASAQYITAALRDLFDSMDKTSSSIPPIILLQFLHMAFPQFAEKGEQGQYLQQDANECWIQMMRVLQQKLEAIEDDSVKETDSSSASAATPSKKKSLIDQFFGVEFETTMKCTESEEEEVTKGKENQLQLSCFINQEVKYLFTGLKLRLQEEITKQSPTLQRNALYIKSSKISRLPAYLTIQMVRFFYKEKESVNAKVLKDVKFPLMLDMYELCTPELQEKMVSFRSKFKDLEDKKVNQQPNTSDKKSSPQKEVKYEPFSFADDIGSNNCGYYDLQAVLTHQGRSSSSGHYVSWVKRKQDEWIKFDDDKVSIVTPEDILRLSGGGDWHIAYVLLYGPRRVEIMEEESEQ
so part of: USP14
location: join(158699..158714,163308..163453,166787..166819,178933..179037,180236..180339,192842..192900,196637..196767,197616..197696,198047..198132,199202..199316,202880..202945,203098..203190,204564..204692,209971..210031,210386..210493,211133..211284)
location: region:158699-211284:1

NP_005142.1
SIO_000068: ncbiprotein

GI:4827050
SIO_000068: ncbigi

CCDS32780.1
SIO_000068: ccds

position:158699:1
position: 158699
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:211284:1
position: 211284
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:158699-158714:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:163308-163453:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:166787-166819:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:178933-179037:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:180236-180339:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:192842-192900:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:196637-196767:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:197616-197696:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:198047-198132:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:199202-199316:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:202880-202945:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:203098-203190:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:204564-204692:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:209971-210031:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:210386-210493:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:211133-211284:1/exon

USP14
type: SO_0000316
alternative label: TGT
gene: USP14
gene synonym: TGT
note: isoform b is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: ubiquitin carboxyl-terminal hydrolase 14 isoform b
translation: MPLYSVTVKWGKEKFEGVELNTDEPPMVFKAQLFALTGVQPARQKVMVKGGTLKDDDWGNIKIKNMELPCGLTNLGNTCYMNATVQCIRSVPELKDALKRYAGALRASGEMASAQYITAALRDLFDSMDKTSSSIPPIILLQFLHMAFPQFAEKGEQGQYLQQDANECWIQMMRVLQQKLEAIEDDSVKETDSSSASAATPSKKKSLIDQFFGVEFETTMKCTESEEEEVTKGKENQLQLSCFINQEVKYLFTGLKLRLQEEITKQSPTLQRNALYIKSSKISRLPAYLTIQMVRFFYKEKESVNAKVLKDVKFPLMLDMYELCTPELQEKMVSFRSKFKDLEDKKVNQQPNTSDKKSSPQKEVKYEPFSFADDIGSNNCGYYDLQAVLTHQGRSSSSGHYVSWVKRKQDEWIKFDDDKVSIVTPEDILRLSGGGDWHIAYVLLYGPRRVEIMEEESEQ
so part of: USP14
location: join(158699..158714,163308..163453,166787..166819,180236..180339,192842..192900,196637..196767,197616..197696,198047..198132,199202..199316,202880..202945,203098..203190,204564..204692,209971..210031,210386..210493,211133..211284)
location: region:158699-211284:1

NP_001032411.1
SIO_000068: ncbiprotein

GI:82880645
SIO_000068: ncbigi

CCDS32781.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:158699-158714:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:163308-163453:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:166787-166819:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:180236-180339:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:192842-192900:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:196637-196767:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:197616-197696:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:198047-198132:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:199202-199316:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:202880-202945:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:203098-203190:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:204564-204692:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:209971-210031:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:210386-210493:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:211133-211284:1/exon

USP14
type: SO_0000316
alternative label: TGT
gene: USP14
gene synonym: TGT
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: ubiquitin carboxyl-terminal hydrolase 14 isoform X1
translation: MPLYSVTVKWGKEKFEGVELNTDEPPMVFKAQLFALTGVQPARQKVMVKGGTLKGMTLLMMGSADALPEEPSAKTVFVEDMTEEQLASAMELPCGLTNLGNTCYMNATVQCIRSVPELKDALKRYAGALRASGEMASAQYITAALRDLFDSMDKTSSSIPPIILLQFLHMAFPQFAEKGEQGQYLQQDANECWIQMMRVLQQKLEAIEDDSVKETDSSSASAATPSKKKSLIDQFFGVEFETTMKCTESEEEEVTKGKENQLQLSCFINQEVKYLFTGLKLRLQEEITKQSPTLQRNALYIKSSKISRLPAYLTIQMVRFFYKEKESVNAKVLKDVKFPLMLDMYELCTPELQEKMVSFRSKFKDLEDKKVNQQPNTSDKKSSPQKEVKYEPFSFADDIGSNNCGYYDLQAVLTHQGRSSSSGHYVSWVKRKQDEWIKFDDDKVSIVTPEDILRLSGGGDWHIAYVLLYGPRRVEIMEEESEQ
so part of: USP14
location: join(158699..158714,163308..163453,178933..179037,180236..180339,192842..192900,196637..196767,197616..197696,198047..198132,199202..199316,202880..202945,203098..203190,204564..204692,209971..210031,210386..210493,211133..211284)
location: region:158699-211284:1

XP_005258221.1
SIO_000068: ncbiprotein

GI:530424981
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:158699-158714:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:163308-163453:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:178933-179037:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:180236-180339:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:192842-192900:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:196637-196767:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:197616-197696:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:198047-198132:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:199202-199316:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:202880-202945:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:203098-203190:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:204564-204692:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:209971-210031:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:210386-210493:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:211133-211284:1/exon

THOC1
type: SO_0000704
alternative label: HPR1
alternative label: P84
alternative label: P84N5
gene: THOC1
gene synonym: HPR1; P84; P84N5
note: THO complex 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(214520..268059)
location: region:214520-268059:-1
SIO_010080: THOC1

9984
SIO_000068: ncbigene

19070
SIO_000068: hgnc

606930
SIO_000068: omim

position:214520:-1
position: 214520
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:268059:-1
position: 268059
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

THOC1
type: SO_0000234
alternative label: HPR1
alternative label: P84
alternative label: P84N5
gene: THOC1
gene synonym: HPR1; P84; P84N5
product: THO complex 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_005131.2
so part of: THOC1
location: complement(join(214520..214921,215429..215504,216486..216633,218886..218969,223440..223505,224084..224179,224924..224994,225089..225139,225337..225403,226801..226901,246324..246455,247849..247957,252539..252612,254273..254355,259180..259275,259682..259730,260186..260304,264026..264092,265303..265363,265457..265530,267966..268059))
location: region:214520-268059:-1

GI:154448889
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:267966-268059:-1/exon

position:267966:-1
position: 267966
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:265457-265530:-1/exon

position:265457:-1
position: 265457
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:265530:-1
position: 265530
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:265303-265363:-1/exon

position:265303:-1
position: 265303
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:265363:-1
position: 265363
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:264026-264092:-1/exon

position:264026:-1
position: 264026
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:264092:-1
position: 264092
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:260186-260304:-1/exon

position:260186:-1
position: 260186
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:260304:-1
position: 260304
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:259682-259730:-1/exon

position:259682:-1
position: 259682
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:259730:-1
position: 259730
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:259180-259275:-1/exon

position:259180:-1
position: 259180
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:259275:-1
position: 259275
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:254273-254355:-1/exon

position:254273:-1
position: 254273
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:254355:-1
position: 254355
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:252539-252612:-1/exon

position:252539:-1
position: 252539
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:252612:-1
position: 252612
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:247849-247957:-1/exon

position:247849:-1
position: 247849
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:247957:-1
position: 247957
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:246324-246455:-1/exon

position:246324:-1
position: 246324
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:246455:-1
position: 246455
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:226801-226901:-1/exon

position:226801:-1
position: 226801
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:226901:-1
position: 226901
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:225337-225403:-1/exon

position:225337:-1
position: 225337
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:225403:-1
position: 225403
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:225089-225139:-1/exon

position:225089:-1
position: 225089
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:225139:-1
position: 225139
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:224924-224994:-1/exon

position:224924:-1
position: 224924
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:224994:-1
position: 224994
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:224084-224179:-1/exon

position:224084:-1
position: 224084
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:224179:-1
position: 224179
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 17
SIO_000628: feature:223440-223505:-1/exon

position:223440:-1
position: 223440
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:223505:-1
position: 223505
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 18
SIO_000628: feature:218886-218969:-1/exon

position:218886:-1
position: 218886
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:218969:-1
position: 218969
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 19
SIO_000628: feature:216486-216633:-1/exon

position:216486:-1
position: 216486
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:216633:-1
position: 216633
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 20
SIO_000628: feature:215429-215504:-1/exon

position:215429:-1
position: 215429
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:215504:-1
position: 215504
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 21
SIO_000628: feature:214520-214921:-1/exon

position:214921:-1
position: 214921
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

THOC1
type: SO_0000316
alternative label: HPR1
alternative label: P84
alternative label: P84N5
gene: THOC1
gene synonym: HPR1; P84; P84N5
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: THO complex subunit 1
translation: MSPTPPLFSLPEARTRFTKSTREALNNKNIKPLLSTFSQVPGSENEKKCTLDQAFRGILEEEIINHSSCENVLAIISLAIGGVTEGICTASTPFVLLGDVLDCLPLDQCDTIFTFVEKNVATWKSNTFYSAGKNYLLRMCNDLLRRLSKSQNTVFCGRIQLFLARLFPLSEKSGLNLQSQFNLENVTVFNTNEQESTLGQKHTEDREEGMDVEEGEMGDEEAPTTCSIPIDYNLYRKFWSLQDYFRNPVQCYEKISWKTFLKYSEEVLAVFKSYKLDDTQASRKKMEELKTGGEHVYFAKFLTSEKLMDLQLSDSNFRRHILLQYLILFQYLKGQVKFKSSNYVLTDEQSLWIEDTTKSVYQLLSENPPDGERFSKMVEHILNTEENWNSWKNEGCPSFVKERTSDTKPTRIIRKRTAPEDFLGKGPTKKILMGNEELTRLWNLCPDNMEACKSETREHMPTLEEFFEEAIEQADPENMVENEYKAVNNSNYGWRALRLLARRSPHFFQPTNQQFKSLPEYLENMVIKLAKELPPPSEEIKTGEDEDEEDNDALLKENESPDVRRDKPVTGEQIEVFANKLGEQWKILAPYLEMKDSEIRQIECDSEDMKMRAKQLLVAWQDQEGVHATPENLINALNKSGLSDLAESLTNDNETNS
so part of: THOC1
location: complement(join(214626..214921,215429..215504,216486..216633,218886..218969,223440..223505,224084..224179,224924..224994,225089..225139,225337..225403,226801..226901,246324..246455,247849..247957,252539..252612,254273..254355,259180..259275,259682..259730,260186..260304,264026..264092,265303..265363,265457..265530,267966..268019))
location: region:214626-268019:-1

NP_005122.2
SIO_000068: ncbiprotein

GI:154448890
SIO_000068: ncbigi

CCDS45820.1
SIO_000068: ccds

position:214626:-1
position: 214626
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:268019:-1
position: 268019
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:267966-268019:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:265457-265530:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:265303-265363:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:264026-264092:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:260186-260304:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:259682-259730:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:259180-259275:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:254273-254355:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:252539-252612:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:247849-247957:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:246324-246455:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:226801-226901:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:225337-225403:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:225089-225139:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:224924-224994:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:224084-224179:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:223440-223505:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:218886-218969:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:216486-216633:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:215429-215504:-1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:214626-214921:-1/exon

COLEC12
type: SO_0000704
alternative label: CLP1
alternative label: NSR2
alternative label: SCARA4
alternative label: SRCL
gene: COLEC12
gene synonym: CLP1; NSR2; SCARA4; SRCL
note: collectin sub-family member 12; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(319355..500729)
location: region:319355-500729:-1
SIO_010080: COLEC12

81035
SIO_000068: ncbigene

16016
SIO_000068: hgnc

06358
SIO_000068: hprd

607621
SIO_000068: omim

position:319355:-1
position: 319355
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:500729:-1
position: 500729
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

COLEC12
type: SO_0000234
alternative label: CLP1
alternative label: NSR2
alternative label: SCARA4
alternative label: SRCL
gene: COLEC12
gene synonym: CLP1; NSR2; SCARA4; SRCL
product: collectin sub-family member 12
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_130386.2
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_130386.2
so part of: COLEC12
location: complement(join(319355..320064,321662..321807,331668..331777,333007..333143,334742..335230,346295..347341,348065..348163,357400..357522,480707..480757,500508..500729))
location: region:319355-500729:-1

GI:197245360
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:500508-500729:-1/exon

position:500508:-1
position: 500508
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:480707-480757:-1/exon

position:480707:-1
position: 480707
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:480757:-1
position: 480757
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:357400-357522:-1/exon

position:357400:-1
position: 357400
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:357522:-1
position: 357522
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:348065-348163:-1/exon

position:348065:-1
position: 348065
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:348163:-1
position: 348163
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:346295-347341:-1/exon

position:346295:-1
position: 346295
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:347341:-1
position: 347341
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:334742-335230:-1/exon

position:334742:-1
position: 334742
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:335230:-1
position: 335230
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:333007-333143:-1/exon

position:333007:-1
position: 333007
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:333143:-1
position: 333143
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:331668-331777:-1/exon

position:331668:-1
position: 331668
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:331777:-1
position: 331777
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:321662-321807:-1/exon

position:321662:-1
position: 321662
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:321807:-1
position: 321807
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:319355-320064:-1/exon

position:320064:-1
position: 320064
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

COLEC12
type: SO_0000316
alternative label: CLP1
alternative label: NSR2
alternative label: SCARA4
alternative label: SRCL
gene: COLEC12
gene synonym: CLP1; NSR2; SCARA4; SRCL
inference: similar to AA sequence (same species):RefSeq:NP_569057.1
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: collectin-12
translation: MKDDFAEEEEVQSFGYKRFGIQEGTQCTKCKNNWALKFSIILLYILCALLTITVAILGYKVVEKMDNVTGGMETSRQTYDDKLTAVESDLKKLGDQTGKKAISTNSELSTFRSDILDLRQQLREITEKTSKNKDTLEKLQASGDALVDRQSQLKETLENNSFLITTVNKTLQAYNGYVTNLQQDTSVLQGNLQNQMYSHNVVIMNLNNLNLTQVQQRNLITNLQRSVDDTSQAIQRIKNDFQNLQQVFLQAKKDTDWLKEKVQSLQTLAANNSALAKANNDTLEDMNSQLNSFTGQMENITTISQANEQNLKDLQDLHKDAENRTAIKFNQLEERFQLFETDIVNIISNISYTAHHLRTLTSNLNEVRTTCTDTLTKHTDDLTSLNNTLANIRLDSVSLRMQQDLMRSRLDTEVANLSVIMEEMKLVDSKHGQLIKNFTILQGPPGPRGPRGDRGSQGPPGPTGNKGQKGEKGEPGPPGPAGERGPIGPAGPPGERGGKGSKGSQGPKGSRGSPGKPGPQGPSGDPGPPGPPGKEGLPGPQGPPGFQGLQGTVGEPGVPGPRGLPGLPGVPGMPGPKGPPGPPGPSGAVVPLALQNEPTPAPEDNGCPPHWKNFTDKCYYFSVEKEIFEDAKLFCEDKSSHLVFINTREEQQWIKKQMVGRESHWIGLTDSERENEWKWLDGTSPDYKNWKAGQPDNWGHGHGPGEDCAGLIYAGQWNDFQCEDVNNFICEKDRETVLSSAL
so part of: COLEC12
location: complement(join(320045..320064,321662..321807,331668..331777,333007..333143,334742..335230,346295..347341,348065..348163,357400..357522,480707..480757,500508..500514))
location: region:320045-500514:-1

NP_569057.1
SIO_000068: ncbiprotein

GI:18641360
SIO_000068: ncbigi

CCDS32782.1
SIO_000068: ccds

position:320045:-1
position: 320045
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:500514:-1
position: 500514
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:500508-500514:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:480707-480757:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:357400-357522:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:348065-348163:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:346295-347341:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:334742-335230:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:333007-333143:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:331668-331777:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:321662-321807:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:320045-320064:-1/exon

CETN1
type: SO_0000704
alternative label: CEN1
alternative label: CETN
gene: CETN1
gene synonym: CEN1; CETN
note: centrin, EF-hand protein, 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 580369..581524
location: region:580369-581524:1
SIO_010080: CETN1

1068
SIO_000068: ncbigene

1866
SIO_000068: hgnc

04425
SIO_000068: hprd

603187
SIO_000068: omim

position:580369:1
position: 580369
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:581524:1
position: 581524
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

CETN1
type: SO_0000234
alternative label: CEN1
alternative label: CETN
gene: CETN1
gene synonym: CEN1; CETN
product: centrin, EF-hand protein, 1
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_004066.1
exception: annotated by transcript or proteomic data
note: The RefSeq transcript has 2 substitutions and 2 indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_004066.1
so part of: CETN1
location: 580369..581524
location: region:580369-581524:1

GI:4757973
SIO_000068: ncbigi

CETN1
type: SO_0000316
alternative label: CEN1
alternative label: CETN
gene: CETN1
gene synonym: CEN1; CETN
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: centrin-1
translation: MASGFKKPSAASTGQKRKVAPKPELTEDQKQEVREAFDLFDVDGSGTIDAKELKVAMRALGFEPRKEEMKKMISEVDREGTGKISFNDFLAVMTQKMSEKDTKEEILKAFRLFDDDETGKISFKNLKRVANELGENLTDEELQEMIDEADRDGDGEVNEEEFLRIMKKTSLY
so part of: CETN1
location: 580409..580927
location: region:580409-580927:1

NP_004057.1
SIO_000068: ncbiprotein

GI:4757974
SIO_000068: ncbigi

CCDS11820.1
SIO_000068: ccds

position:580409:1
position: 580409
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:580927:1
position: 580927
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

CLUL1
type: SO_0000704
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
note: clusterin-like 1 (retinal); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 596998..650298
location: region:596998-650298:1
SIO_010080: CLUL1

27098
SIO_000068: ncbigene

2096
SIO_000068: hgnc

16726
SIO_000068: hprd

position:596998:1
position: 596998
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:650298:1
position: 650298
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

CLUL1
type: SO_0000234
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
product: clusterin-like 1 (retinal), transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_014410.4
so part of: CLUL1
location: join(596998..597129,617988..618106,619213..619361,624865..625032,627097..627529,633298..633435,641327..641541,644910..645097,649898..650298)
location: region:596998-650298:1

GI:40316929
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:596998-597129:1/exon

position:597129:1
position: 597129
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:617988-618106:1/exon

position:617988:1
position: 617988
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:618106:1
position: 618106
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:619213-619361:1/exon

position:619213:1
position: 619213
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:619361:1
position: 619361
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:624865-625032:1/exon

position:624865:1
position: 624865
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:625032:1
position: 625032
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:627097-627529:1/exon

position:627097:1
position: 627097
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:627529:1
position: 627529
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:633298-633435:1/exon

position:633298:1
position: 633298
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:633435:1
position: 633435
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:641327-641541:1/exon

position:641327:1
position: 641327
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:641541:1
position: 641541
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:644910-645097:1/exon

position:644910:1
position: 644910
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:645097:1
position: 645097
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:649898-650298:1/exon

position:649898:1
position: 649898
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

CLUL1
type: SO_0000234
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
product: clusterin-like 1 (retinal), transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 14 ESTs, and 100% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XM_005258103.1
so part of: CLUL1
location: join(612768..612911,616660..616757,617988..618106,619213..619361,624865..625032,627097..627529,633298..633435,641327..641541,644910..645097,649898..650298)
location: region:612768-650298:1

GI:530424842
SIO_000068: ncbigi

position:612768:1
position: 612768
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:612768-612911:1/exon

position:612911:1
position: 612911
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:616660-616757:1/exon

position:616660:1
position: 616660
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:616757:1
position: 616757
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:617988-618106:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:619213-619361:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:624865-625032:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:627097-627529:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:633298-633435:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:641327-641541:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:644910-645097:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:649898-650298:1/exon

CLUL1
type: SO_0000234
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
product: clusterin-like 1 (retinal), transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 ESTs, and 100% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XM_005258105.1
so part of: CLUL1
location: join(612768..612911,617988..618106,619213..619361,624865..625032,627097..627529,633298..633435,641327..641541,644910..645097,649898..650290)
location: region:612768-650290:1

GI:530424846
SIO_000068: ncbigi

position:650290:1
position: 650290
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:612768-612911:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:617988-618106:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:619213-619361:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:624865-625032:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:627097-627529:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:633298-633435:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:641327-641541:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:644910-645097:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:649898-650290:1/exon

CLUL1
type: SO_0000316
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: clusterin-like protein 1 isoform X1
translation: MKIKAEKNEGPSRSWWQLHWGDIANNSGNMKPPLLVFIVCLLWLKDSHCAPTWKDKTAISENLKSFSEVGEIDADEEVKKALTGIKQMKIMMERKEKEHTNLMSTLKKCREEKQEALKLLNEVQEHLEEEERLCRESLADSWGECRSCLENNCMRIYTTCQPSWSSVKNKIERFFRKIYQFLFPFHEDNEKDLPISEKLIEEDAQLTQMEDVFSQLTVDVNSLFNRSFNVFRQMQQEFDQTFQSHFISDTDLTEPYFFPAFSKEPMTKADLEQCWDIPNFFQLFCNFSVSIYESVSETITKMLKAIEDLPKQDKAPDHGGLISKMLPGQDRGLCGELDQNLSRCFKFHEKCQKCQAHLSEDCPDVPALHTELDEAIRLVNVSNQQYGQILQMTRKHLEDTAYLVEKMRGQFGWVSELANQAPETEIIFNSIQVVPRIHEGNISKQDETMMTDLSILPSSNFTLKIPLEESAESSNFIGYVVAKALQHFKEHFKTW
so part of: CLUL1
location: join(616684..616757,617988..618106,619213..619361,624865..625032,627097..627529,633298..633435,641327..641541,644910..645097,649898..649901)
location: region:616684-649901:1

XP_005258160.1
SIO_000068: ncbiprotein

GI:530424843
SIO_000068: ncbigi

position:616684:1
position: 616684
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:649901:1
position: 649901
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:616684-616757:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:617988-618106:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:619213-619361:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:624865-625032:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:627097-627529:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:633298-633435:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:641327-641541:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:644910-645097:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:649898-649901:1/exon

CLUL1
type: SO_0000234
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
product: clusterin-like 1 (retinal), transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_199167.1
so part of: CLUL1
location: join(616700..616757,617988..618106,619213..619361,624865..625032,627097..627529,633298..633435,641327..641541,644910..645097,649898..650298)
location: region:616700-650298:1

GI:40316925
SIO_000068: ncbigi

position:616700:1
position: 616700
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:616700-616757:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:617988-618106:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:619213-619361:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:624865-625032:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:627097-627529:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:633298-633435:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:641327-641541:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:644910-645097:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:649898-650298:1/exon

CLUL1
type: SO_0000234
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
product: clusterin-like 1 (retinal), transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 12 ESTs, and 99% coverage by RNAseq alignments
transcript id: XM_005258104.1
so part of: CLUL1
location: join(616718..616764,617988..618106,619213..619361,624865..625032,627097..627529,633298..633435,641327..641541,644910..645097,649898..650290)
location: region:616718-650290:1

GI:530424844
SIO_000068: ncbigi

position:616718:1
position: 616718
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:616718-616764:1/exon

position:616764:1
position: 616764
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:617988-618106:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:619213-619361:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:624865-625032:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:627097-627529:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:633298-633435:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:641327-641541:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:644910-645097:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:649898-650290:1/exon

CLUL1
type: SO_0000316
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: clusterin-like protein 1 isoform X2
translation: MKPPLLVFIVCLLWLKDSHCAPTWKDKTAISENLKSFSEVGEIDADEEVKKALTGIKQMKIMMERKEKEHTNLMSTLKKCREEKQEALKLLNEVQEHLEEEERLCRESLADSWGECRSCLENNCMRIYTTCQPSWSSVKNKIERFFRKIYQFLFPFHEDNEKDLPISEKLIEEDAQLTQMEDVFSQLTVDVNSLFNRSFNVFRQMQQEFDQTFQSHFISDTDLTEPYFFPAFSKEPMTKADLEQCWDIPNFFQLFCNFSVSIYESVSETITKMLKAIEDLPKQDKAPDHGGLISKMLPGQDRGLCGELDQNLSRCFKFHEKCQKCQAHLSEDCPDVPALHTELDEAIRLVNVSNQQYGQILQMTRKHLEDTAYLVEKMRGQFGWVSELANQAPETEIIFNSIQVVPRIHEGNISKQDETMMTDLSILPSSNFTLKIPLEESAESSNFIGYVVAKALQHFKEHFKTW
so part of: CLUL1
location: join(618001..618106,619213..619361,624865..625032,627097..627529,633298..633435,641327..641541,644910..645097,649898..649901)
location: region:618001-649901:1

XP_005258161.1
SIO_000068: ncbiprotein

GI:530424845
SIO_000068: ncbigi

position:618001:1
position: 618001
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:618001-618106:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:619213-619361:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:624865-625032:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:627097-627529:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:633298-633435:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:641327-641541:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:644910-645097:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:649898-649901:1/exon

CLUL1
type: SO_0000316
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: clusterin-like protein 1 isoform X3
translation: MKPPLLVFIVCLLWLKDSHCAPTWKDKTAISENLKSFSEVGEIDADEEVKKALTGIKQMKIMMERKEKEHTNLMSTLKKCREEKQEALKLLNEVQEHLEEEERLCRESLADSWGECRSCLENNCMRIYTTCQPSWSSVKNKIERFFRKIYQFLFPFHEDNEKDLPISEKLIEEDAQLTQMEDVFSQLTVDVNSLFNRSFNVFRQMQQEFDQTFQSHFISDTDLTEPYFFPAFSKEPMTKADLEQCWDIPNFFQLFCNFSVSIYESVSETITKMLKAIEDLPKQDKAPDHGGLISKMLPGQDRGLCGELDQNLSRCFKFHEKCQKCQAHLSEDCPDVPALHTELDEAIRLVNVSNQQYGQILQMTRKHLEDTAYLVEKMRGQFGWVSELANQAPETEIIFNSIQVVPRIHEGNISKQDETMMTDLSILPSSNFTLKIPLEESAESSNFIGYVVAKALQHFKEHFKTW
so part of: CLUL1
location: join(618001..618106,619213..619361,624865..625032,627097..627529,633298..633435,641327..641541,644910..645097,649898..649901)
location: region:618001-649901:1

XP_005258162.1
SIO_000068: ncbiprotein

GI:530424847
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:618001-618106:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:619213-619361:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:624865-625032:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:627097-627529:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:633298-633435:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:641327-641541:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:644910-645097:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:649898-649901:1/exon

CLUL1
type: SO_0000316
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: clusterin-like protein 1 precursor
translation: MKPPLLVFIVCLLWLKDSHCAPTWKDKTAISENLKSFSEVGEIDADEEVKKALTGIKQMKIMMERKEKEHTNLMSTLKKCREEKQEALKLLNEVQEHLEEEERLCRESLADSWGECRSCLENNCMRIYTTCQPSWSSVKNKIERFFRKIYQFLFPFHEDNEKDLPISEKLIEEDAQLTQMEDVFSQLTVDVNSLFNRSFNVFRQMQQEFDQTFQSHFISDTDLTEPYFFPAFSKEPMTKADLEQCWDIPNFFQLFCNFSVSIYESVSETITKMLKAIEDLPKQDKAPDHGGLISKMLPGQDRGLCGELDQNLSRCFKFHEKCQKCQAHLSEDCPDVPALHTELDEAIRLVNVSNQQYGQILQMTRKHLEDTAYLVEKMRGQFGWVSELANQAPETEIIFNSIQVVPRIHEGNISKQDETMMTDLSILPSSNFTLKIPLEESAESSNFIGYVVAKALQHFKEHFKTW
so part of: CLUL1
location: join(618001..618106,619213..619361,624865..625032,627097..627529,633298..633435,641327..641541,644910..645097,649898..649901)
location: region:618001-649901:1

NP_954636.1
SIO_000068: ncbiprotein

GI:40316926
SIO_000068: ncbigi

CCDS42405.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:618001-618106:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:619213-619361:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:624865-625032:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:627097-627529:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:633298-633435:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:641327-641541:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:644910-645097:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:649898-649901:1/exon

CLUL1
type: SO_0000316
alternative label: RA337M
gene: CLUL1
gene synonym: RA337M
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: clusterin-like protein 1 precursor
translation: MKPPLLVFIVCLLWLKDSHCAPTWKDKTAISENLKSFSEVGEIDADEEVKKALTGIKQMKIMMERKEKEHTNLMSTLKKCREEKQEALKLLNEVQEHLEEEERLCRESLADSWGECRSCLENNCMRIYTTCQPSWSSVKNKIERFFRKIYQFLFPFHEDNEKDLPISEKLIEEDAQLTQMEDVFSQLTVDVNSLFNRSFNVFRQMQQEFDQTFQSHFISDTDLTEPYFFPAFSKEPMTKADLEQCWDIPNFFQLFCNFSVSIYESVSETITKMLKAIEDLPKQDKAPDHGGLISKMLPGQDRGLCGELDQNLSRCFKFHEKCQKCQAHLSEDCPDVPALHTELDEAIRLVNVSNQQYGQILQMTRKHLEDTAYLVEKMRGQFGWVSELANQAPETEIIFNSIQVVPRIHEGNISKQDETMMTDLSILPSSNFTLKIPLEESAESSNFIGYVVAKALQHFKEHFKTW
so part of: CLUL1
location: join(618001..618106,619213..619361,624865..625032,627097..627529,633298..633435,641327..641541,644910..645097,649898..649901)
location: region:618001-649901:1

NP_055225.1
SIO_000068: ncbiprotein

GI:7657490
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:618001-618106:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:619213-619361:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:624865-625032:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:627097-627529:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:633298-633435:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:641327-641541:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:644910-645097:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:649898-649901:1/exon

C18orf56
type: SO_0000704
gene: C18orf56
note: chromosome 18 open reading frame 56; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(649620..658340)
location: region:649620-658340:-1
SIO_010080: C18orf56

494514
SIO_000068: ncbigene

29553
SIO_000068: hgnc

position:649620:-1
position: 649620
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:658340:-1
position: 658340
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C18orf56
type: SO_0000234
gene: C18orf56
product: chromosome 18 open reading frame 56
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001012716.2
so part of: C18orf56
location: complement(join(649620..649964,657842..658340))
location: region:649620-658340:-1

GI:270265903
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:657842-658340:-1/exon

position:657842:-1
position: 657842
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:649620-649964:-1/exon

position:649964:-1
position: 649964
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

TYMS
type: SO_0000704
alternative label: HST422
alternative label: TMS
alternative label: TS
gene: TYMS
gene synonym: HST422; TMS; TS
note: thymidylate synthetase; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 657590..673499
location: region:657590-673499:1
SIO_010080: TYMS

7298
SIO_000068: ncbigene

12441
SIO_000068: hgnc

01774
SIO_000068: hprd

188350
SIO_000068: omim

position:657590:1
position: 657590
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:673499:1
position: 673499
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

TYMS
type: SO_0000234
alternative label: HST422
alternative label: TMS
alternative label: TS
gene: TYMS
gene synonym: HST422; TMS; TS
product: thymidylate synthetase, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 27 ESTs, 1 Protein, and 97% coverage by RNAseq alignments
transcript id: XM_005258137.1
so part of: TYMS
location: join(657590..657947,659641..659714,662146..662320,670692..670867,671380..671451,672860..673493)
location: region:657590-673493:1

GI:530424926
SIO_000068: ncbigi

position:673493:1
position: 673493
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:657590-657947:1/exon

position:657947:1
position: 657947
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:659641-659714:1/exon

position:659641:1
position: 659641
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:659714:1
position: 659714
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:662146-662320:1/exon

position:662146:1
position: 662146
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:662320:1
position: 662320
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:670692-670867:1/exon

position:670692:1
position: 670692
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:670867:1
position: 670867
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:671380-671451:1/exon

position:671380:1
position: 671380
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:671451:1
position: 671451
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:672860-673493:1/exon

position:672860:1
position: 672860
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

TYMS
type: SO_0000234
alternative label: HST422
alternative label: TMS
alternative label: TS
gene: TYMS
gene synonym: HST422; TMS; TS
product: thymidylate synthetase
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001071.2
so part of: TYMS
location: join(657604..657947,659641..659714,662146..662320,669072..669173,670692..670867,671380..671451,672860..673499)
location: region:657604-673499:1

GI:186972144
SIO_000068: ncbigi

position:657604:1
position: 657604
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:657604-657947:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:659641-659714:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:662146-662320:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:669072-669173:1/exon

position:669072:1
position: 669072
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:669173:1
position: 669173
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:670692-670867:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:671380-671451:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:672860-673499:1/exon

TYMS
type: SO_0000234
alternative label: HST422
alternative label: TMS
alternative label: TS
gene: TYMS
gene synonym: HST422; TMS; TS
product: thymidylate synthetase, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 26 ESTs, 1 Protein, and 97% coverage by RNAseq alignments
transcript id: XM_005258138.1
so part of: TYMS
location: join(657623..657947,669072..669173,670692..670867,671380..671451,672860..673493)
location: region:657623-673493:1

GI:530424928
SIO_000068: ncbigi

position:657623:1
position: 657623
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:657623-657947:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:669072-669173:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:670692-670867:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:671380-671451:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:672860-673493:1/exon

TYMS
type: SO_0000316
alternative label: HST422
alternative label: TMS
alternative label: TS
gene: TYMS
gene synonym: HST422; TMS; TS
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: thymidylate synthase
translation: MPVAGSELPRRPLPPAAQERDAEPRPPHGELQYLGQIQHILRCGVRKDDRTGTGTLSVFGMQARYSLRDEFPLLTTKRVFWKGVLEELLWFIKGSTNAKELSSKGVKIWDANGSRDFLDSLGFSTREEGDLGPVYGFQWRHFGAEYRDMESDYSGQGVDQLQRVIDTIKTNPDDRRIIMCAWNPRDLPLMALPPCHALCQFYVVNSELSCQLYQRSGDMGLGVPFNIASYALLTYMIAHITGLKPGDFIHTLGDAHIYLNHIEPLKIQLQREPRPFPKLRILRKVEKIDDFKAEDFQIEGYNPHPTIKMEMAV
so part of: TYMS
location: join(657743..657947,659641..659714,662146..662320,669072..669173,670692..670867,671380..671451,672860..672997)
location: region:657743-672997:1

NP_001062.1
SIO_000068: ncbiprotein

GI:4507751
SIO_000068: ncbigi

CCDS11821.1
SIO_000068: ccds

position:657743:1
position: 657743
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:672997:1
position: 672997
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:657743-657947:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:659641-659714:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:662146-662320:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:669072-669173:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:670692-670867:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:671380-671451:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:672860-672997:1/exon

TYMS
type: SO_0000316
alternative label: HST422
alternative label: TMS
alternative label: TS
gene: TYMS
gene synonym: HST422; TMS; TS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: thymidylate synthase isoform X1
translation: MPVAGSELPRRPLPPAAQERDAEPRPPHGELQYLGQIQHILRCGVRKDDRTGTGTLSVFGMQARYSLRDEFPLLTTKRVFWKGVLEELLWFIKGSTNAKELSSKGVKIWDANGSRDFLDSLGFSTREEGDLGPVYGFQWRHFGAEYRDMESDLPLMALPPCHALCQFYVVNSELSCQLYQRSGDMGLGVPFNIASYALLTYMIAHITGLKPGDFIHTLGDAHIYLNHIEPLKIQLQREPRPFPKLRILRKVEKIDDFKAEDFQIEGYNPHPTIKMEMAV
so part of: TYMS
location: join(657743..657947,659641..659714,662146..662320,670692..670867,671380..671451,672860..672997)
location: region:657743-672997:1

XP_005258194.1
SIO_000068: ncbiprotein

GI:530424927
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:657743-657947:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:659641-659714:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:662146-662320:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:670692-670867:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:671380-671451:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:672860-672997:1/exon

TYMS
type: SO_0000316
alternative label: HST422
alternative label: TMS
alternative label: TS
gene: TYMS
gene synonym: HST422; TMS; TS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: thymidylate synthase isoform X2
translation: MPVAGSELPRRPLPPAAQERDAEPRPPHGELQYLGQIQHILRCGVRKDDRTGTGTLSVFGMQARYSLRDYSGQGVDQLQRVIDTIKTNPDDRRIIMCAWNPRDLPLMALPPCHALCQFYVVNSELSCQLYQRSGDMGLGVPFNIASYALLTYMIAHITGLKPGDFIHTLGDAHIYLNHIEPLKIQLQREPRPFPKLRILRKVEKIDDFKAEDFQIEGYNPHPTIKMEMAV
so part of: TYMS
location: join(657743..657947,669072..669173,670692..670867,671380..671451,672860..672997)
location: region:657743-672997:1

XP_005258195.1
SIO_000068: ncbiprotein

GI:530424929
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:657743-657947:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:669072-669173:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:670692-670867:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:671380-671451:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:672860-672997:1/exon

C18orf56
type: SO_0000316
gene: C18orf56
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: putative uncharacterized protein C18orf56
translation: MTPASGATASLGRLRARPRSRWDAAYLPAVAAVCVARASHVPNGTLRFGVCKARRTMRPLPRRIEVRTKRGPQRPAAPERSPQPRLPPSRHPSRRGPRRHLSGCSAPACRIPTGCRCPCGRPS
so part of: C18orf56
location: complement(657876..658247)
location: region:657876-658247:-1

NP_001012734.2
SIO_000068: ncbiprotein

GI:270265904
SIO_000068: ncbigi

position:657876:-1
position: 657876
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:658247:-1
position: 658247
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ENOSF1
type: SO_0000704
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: enolase superfamily member 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(670324..712662)
location: region:670324-712662:-1
SIO_010080: ENOSF1

55556
SIO_000068: ncbigene

30365
SIO_000068: hgnc

607427
SIO_000068: omim

position:670324:-1
position: 670324
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:712662:-1
position: 712662
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001126123.3
so part of: ENOSF1
location: complement(join(670324..673076,674161..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,706470..706578,712504..712662))
location: region:670324-712662:-1

GI:315013565
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:712504-712662:-1/exon

position:712504:-1
position: 712504
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

position:706470:-1
position: 706470
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:706578:-1
position: 706578
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:694248-694334:-1/exon

position:694248:-1
position: 694248
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:694334:-1
position: 694334
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:693882-693908:-1/exon

position:693882:-1
position: 693882
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:693908:-1
position: 693908
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:691204-691276:-1/exon

position:691204:-1
position: 691204
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:691276:-1
position: 691276
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:691068-691106:-1/exon

position:691068:-1
position: 691068
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:691106:-1
position: 691106
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:690549-690631:-1/exon

position:690549:-1
position: 690549
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:690631:-1
position: 690631
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:688574-688608:-1/exon

position:688574:-1
position: 688574
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:688608:-1
position: 688608
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:685921-686008:-1/exon

position:685921:-1
position: 685921
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:686008:-1
position: 686008
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:683246-683380:-1/exon

position:683246:-1
position: 683246
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:683380:-1
position: 683380
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:678696-678737:-1/exon

position:678696:-1
position: 678696
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:678737:-1
position: 678737
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:677743-677872:-1/exon

position:677743:-1
position: 677743
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:677872:-1
position: 677872
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:677345-677444:-1/exon

position:677345:-1
position: 677345
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:677444:-1
position: 677444
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:675321-675402:-1/exon

position:675321:-1
position: 675321
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:675402:-1
position: 675402
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:674161-674406:-1/exon

position:674161:-1
position: 674161
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:674406:-1
position: 674406
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:670324-673076:-1/exon

position:673076:-1
position: 673076
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_017512.5
so part of: ENOSF1
location: complement(join(670324..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712504..712662))
location: region:670324-712662:-1

GI:315013566
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:712504-712662:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

position:697240:-1
position: 697240
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:697355:-1
position: 697355
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:670324-674406:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_202758.3
so part of: ENOSF1
location: complement(join(670324..674406,675321..675402,677345..677444,677743..677872,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712360..712517))
location: region:670324-712517:-1

GI:315013569
SIO_000068: ncbigi

position:712517:-1
position: 712517
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712517:-1/exon

position:712360:-1
position: 712360
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:670324-674406:-1/exon

ENOSF1
type: SO_0000673
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X12
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 47 ESTs, 7 Proteins, and 99% coverage by RNAseq alignments, including 10 samples with support for all introns
transcript id: XR_243811.1
so part of: ENOSF1
location: complement(join(672543..673076,674161..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712504..712648))
location: region:672543-712648:-1

GI:530424873
SIO_000068: ncbigi

position:672543:-1
position: 672543
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:712648:-1
position: 712648
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712504-712648:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:674161-674406:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:672543-673076:-1/exon

ENOSF1
type: SO_0000673
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X11
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 38 ESTs, 4 Proteins, and 99% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XR_243810.1
so part of: ENOSF1
location: complement(join(672543..673076,674161..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712360..712638))
location: region:672543-712638:-1

GI:530424872
SIO_000068: ncbigi

position:712638:-1
position: 712638
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712638:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:674161-674406:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:672543-673076:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 28 ESTs, 3 Proteins, and 98% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XM_005258113.1
so part of: ENOSF1
location: complement(join(673879..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,693882..693908,694248..694334,706470..706578,712360..712639))
location: region:673879-712639:-1

GI:530424876
SIO_000068: ncbigi

position:673879:-1
position: 673879
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:712639:-1
position: 712639
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712639:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:673879-674406:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 40 ESTs, 4 Proteins, and 99% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XM_005258111.1
so part of: ENOSF1
location: complement(join(673879..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712360..712638))
location: region:673879-712638:-1

GI:530424870
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712638:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:673879-674406:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X4
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 30 ESTs, 2 Proteins, and 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258114.1
so part of: ENOSF1
location: complement(join(673879..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,693882..693908,694248..694334,706470..706578,712504..712637))
location: region:673879-712637:-1

GI:530424878
SIO_000068: ncbigi

position:712637:-1
position: 712637
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712504-712637:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:673879-674406:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X6
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258116.1
so part of: ENOSF1
location: complement(join(673879..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,706470..706578,712486..712503))
location: region:673879-712503:-1

GI:530424882
SIO_000068: ncbigi

position:712503:-1
position: 712503
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712486-712503:-1/exon

position:712486:-1
position: 712486
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:673879-674406:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258112.1
so part of: ENOSF1
location: complement(join(673879..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712486..712497))
location: region:673879-712497:-1

GI:530424874
SIO_000068: ncbigi

position:712497:-1
position: 712497
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712486-712497:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:673879-674406:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X5
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XM_005258115.1
so part of: ENOSF1
location: complement(join(673879..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,706470..706578,712360..712420))
location: region:673879-712420:-1

GI:530424880
SIO_000068: ncbigi

position:712420:-1
position: 712420
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712420:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:673879-674406:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X8
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 30 ESTs, 2 Proteins, and 96% coverage by RNAseq alignments
transcript id: XM_005258118.1
so part of: ENOSF1
location: complement(join(673879..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690745,693882..693908,694248..694334,697240..697355,706470..706578))
location: region:673879-706578:-1

GI:530424887
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:690549-690745:-1/exon

position:690745:-1
position: 690745
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:673879-674406:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X7
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 ESTs, 2 Proteins, and 91% coverage by RNAseq alignments, including 6 samples with support for all introns
transcript id: XM_005258117.1
so part of: ENOSF1
location: complement(join(673879..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,692770..693755))
location: region:673879-693755:-1

GI:530424885
SIO_000068: ncbigi

position:693755:-1
position: 693755
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:692770-693755:-1/exon

position:692770:-1
position: 692770
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:673879-674406:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X10
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 ESTs, 1 Protein, and 95% coverage by RNAseq alignments, including 8 samples with support for all introns
transcript id: XM_005258120.1
so part of: ENOSF1
location: complement(join(673879..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688519..688608,690549..690631,691068..691106,691204..691221))
location: region:673879-691221:-1

GI:530424891
SIO_000068: ncbigi

position:691221:-1
position: 691221
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:691204-691221:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:688519-688608:-1/exon

position:688519:-1
position: 688519
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:673879-674406:-1/exon

ENOSF1
type: SO_0000673
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X13
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 1 Protein, and 98% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XR_243812.1
so part of: ENOSF1
location: complement(join(673881..674406,675321..675402,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712360..712639))
location: region:673881-712639:-1

GI:530424884
SIO_000068: ncbigi

position:673881:-1
position: 673881
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712639:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:673881-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform X4
translation: MVRGRISRLSVRDVRFPTSLGGHGADAMHTDPDYSAAYVVIETDAEDGIKGCGITFTLGKGTEVDWSRKGRGAPGDSGRPKRGVGLVGQAGGKACLEVTCGHEKQMLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,693882..693908,694248..694334,706470..706578,712504..712587))
location: region:674305-712587:-1

XP_005258171.1
SIO_000068: ncbiprotein

GI:530424879
SIO_000068: ncbigi

position:674305:-1
position: 674305
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:712587:-1
position: 712587
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712504-712587:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: isoform rTSbeta is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform rTSbeta
translation: MVRGRISRLSVRDVRFPTSLGGHGADAMHTDPDYSAAYVVIETDAEDGIKGCGITFTLGKGTEVVVCAVNALAHHVLNKDLKDIVGDFRGFYRQLTSDGQLRWIGPEKGVVHLATAAVLNAVWDLWAKQEGKPVWKLLVDMDPRMLVSCIDFRYITDVLTEEDALEILQKGQIGKKEREKQMLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712504..712587))
location: region:674305-712587:-1

NP_059982.2
SIO_000068: ncbiprotein

GI:42544119
SIO_000068: ncbigi

CCDS11822.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:712504-712587:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform X3
translation: MVRGRISRLSVRDVRFPTSLGGHGADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMHTDPDYSAAYVVIETDAEDGIKGCGITFTLGKGTEVDWSRKGRGAPGDSGRPKRGVGLVGQAGGKACLEVTCGHEKQMLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,693882..693908,694248..694334,706470..706578,712360..712587))
location: region:674305-712587:-1

XP_005258170.1
SIO_000068: ncbiprotein

GI:530424877
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712587:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform X1
translation: MVRGRISRLSVRDVRFPTSLGGHGADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMHTDPDYSAAYVVIETDAEDGIKGCGITFTLGKGTEVVVCAVNALAHHVLNKDLKDIVGDFRGFYRQLTSDGQLRWIGPEKGVVHLATAAVLNAVWDLWAKQEGKPVWKLLVDMDPRMLVSCIDFRYITDVLTEEDALEILQKGQIGKKEREKQMLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712360..712587))
location: region:674305-712587:-1

XP_005258168.1
SIO_000068: ncbiprotein

GI:530424871
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712587:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: isoform rTSgamma is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform rTSgamma
translation: MVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMHTDPDYSAAYVVIETDAEDGIKGCGITFTLGKGTEVVVCAVNALAHHVLNKDLKDIVGDFRGFYRQLTSDGQLRWIGPEKGVVHLATAAVLNAVWDLWAKQEGKPVWKLLVDMDPRMLVSCIDFRYITDVLTEEDALEILQKGQIGKKEREKQMLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712360..712506))
location: region:674305-712506:-1

NP_974487.1
SIO_000068: ncbiprotein

GI:42544117
SIO_000068: ncbigi

CCDS11823.1
SIO_000068: ccds

position:712506:-1
position: 712506
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712506:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform X2
translation: MHTDPDYSAAYVVIETDAEDGIKGCGITFTLGKGTEVVVCAVNALAHHVLNKDLKDIVGDFRGFYRQLTSDGQLRWIGPEKGVVHLATAAVLNAVWDLWAKQEGKPVWKLLVDMDPRMLVSCIDFRYITDVLTEEDALEILQKGQIGKKEREKQMLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712486..712488))
location: region:674305-712488:-1

XP_005258169.1
SIO_000068: ncbiprotein

GI:530424875
SIO_000068: ncbigi

position:712488:-1
position: 712488
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712486-712488:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform X5
translation: MQKMESRGVELPSLWEKALKLIGPEKGVVHLATAAVLNAVWDLWAKQEGKPVWKLLVDMDPRMLVSCIDFRYITDVLTEEDALEILQKGQIGKKEREKQMLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,706470..706532))
location: region:674305-706532:-1

XP_005258172.1
SIO_000068: ncbiprotein

GI:530424881
SIO_000068: ncbigi

position:706532:-1
position: 706532
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:706470-706532:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform X6
translation: MQKMESRGVELPSLWEKALKLIGPEKGVVHLATAAVLNAVWDLWAKQEGKPVWKLLVDMDPRMLVSCIDFRYITDVLTEEDALEILQKGQIGKKEREKQMLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,706470..706532))
location: region:674305-706532:-1

XP_005258173.1
SIO_000068: ncbiprotein

GI:530424883
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:706470-706532:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: isoform rTSalpha is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform rTSalpha
translation: MQKMESRGVELPSLWEKALKLIGPEKGVVHLATAAVLNAVWDLWAKQEGKPVWKLLVDMDPRMLVSCIDFRYITDVLTEEDALEILQKGQIGKKEREKQMLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691276,693882..693908,694248..694334,706470..706532))
location: region:674305-706532:-1

NP_001119595.1
SIO_000068: ncbiprotein

GI:186972148
SIO_000068: ncbigi

CCDS45821.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:706470-706532:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform X7
translation: MLVSCIDFRYITDVLTEEDALEILQKGQIGKKEREKQMLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690631,691068..691106,691204..691267))
location: region:674305-691267:-1

XP_005258174.1
SIO_000068: ncbiprotein

GI:530424886
SIO_000068: ncbigi

position:691267:-1
position: 691267
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:691204-691267:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:690549-690631:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform X8
translation: MLAQGYPAYTTSCAWLGYSDDTLKQLCAQALKDGWTRFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688574..688608,690549..690623))
location: region:674305-690623:-1

XP_005258175.1
SIO_000068: ncbiprotein

GI:530424888
SIO_000068: ncbigi

position:690623:-1
position: 690623
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:690549-690623:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:688574-688608:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform X10
translation: MAGPGECDDGPDFPSWRQERLRQFKVKVGADLQDDMRRCQIIRDMIGPEKTLMMDANQRWDVPEAVEWMSKLAKFKPLWIEEPTSPDDILGHATISKALVPLGIGIATGEQCHNRVIFKQLLQAKALQFLQIDSCRLGSVNENLSVLLMAKKFEIPVCPHAGGVGLCELVQHLIIFDYISVSASLENRVCEYVDHLHEHFKYPVMIQRASYMPPKDPGYSTEMKEESVKKHQYPDGEVWKKLLPAQEN
so part of: ENOSF1
location: complement(join(674305..674406,675321..675402,677345..677444,677743..677872,678696..678737,683246..683380,685921..686008,688519..688586))
location: region:674305-688586:-1

XP_005258177.1
SIO_000068: ncbiprotein

GI:530424892
SIO_000068: ncbigi

position:688586:-1
position: 688586
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:688519-688586:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:685921-686008:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:683246-683380:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:678696-678737:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:677743-677872:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:677345-677444:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:675321-675402:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:674305-674406:-1/exon

ENOSF1
type: SO_0000234
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
product: enolase superfamily member 1, transcript variant X9
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, 1 Protein, and 97% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258119.1
so part of: ENOSF1
location: complement(join(690639..690745,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712360..712639))
location: region:690639-712639:-1

GI:530424889
SIO_000068: ncbigi

position:690639:-1
position: 690639
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712639:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690639-690745:-1/exon

ENOSF1
type: SO_0000316
alternative label: HSRTSBETA
alternative label: RTS
alternative label: TYMSAS
gene: ENOSF1
gene synonym: HSRTSBETA; RTS; TYMSAS
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: mitochondrial enolase superfamily member 1 isoform X9
translation: MVRGRISRLSVRDVRFPTSLGGHGADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMVSADAMHTDPDYSAAYVVIETDAEDGIKGCGITFTLGKGTEVVVCAVNALAHHVLNKDLKDIVGDFRGFYRQLTSDGQLRWIGPEKGVVHLATAAVLNAVWDLWAKQEGKPVWKLLVDMDPRMLVSCIDFRYITDVLTEEDALEILQKGQIGKKERGPDQENSWTLQGKQLSYRHFQFRRALESAKC
so part of: ENOSF1
location: complement(join(690651..690745,691068..691106,691204..691276,693882..693908,694248..694334,697240..697355,706470..706578,712360..712587))
location: region:690651-712587:-1

XP_005258176.1
SIO_000068: ncbiprotein

GI:530424890
SIO_000068: ncbigi

position:690651:-1
position: 690651
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:712360-712587:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:706470-706578:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:697240-697355:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:694248-694334:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:693882-693908:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:691204-691276:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:691068-691106:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:690651-690745:-1/exon

YES1
type: SO_0000704
alternative label: c-yes
alternative label: HsT441
alternative label: P61-YES
alternative label: Yes
gene: YES1
gene synonym: c-yes; HsT441; P61-YES; Yes
note: v-yes-1 Yamaguchi sarcoma viral oncogene homolog 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(721592..812327)
location: region:721592-812327:-1
SIO_010080: YES1

7525
SIO_000068: ncbigene

12841
SIO_000068: hgnc

01285
SIO_000068: hprd

164880
SIO_000068: omim

position:721592:-1
position: 721592
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:812327:-1
position: 812327
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

YES1
type: SO_0000234
alternative label: c-yes
alternative label: HsT441
alternative label: P61-YES
alternative label: Yes
gene: YES1
gene synonym: c-yes; HsT441; P61-YES; Yes
product: v-yes-1 Yamaguchi sarcoma viral oncogene homolog 1
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_005433.3
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_005433.3
so part of: YES1
location: complement(join(721592..724632,732834..732965,736808..736961,739735..739811,742918..743097,743260..743415,745708..745857,745948..746051,747920..748018,751705..751804,756557..756835,812115..812327))
location: region:721592-812327:-1

GI:51702529
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:812115-812327:-1/exon

position:812115:-1
position: 812115
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:756557-756835:-1/exon

position:756557:-1
position: 756557
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:756835:-1
position: 756835
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:751705-751804:-1/exon

position:751705:-1
position: 751705
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:751804:-1
position: 751804
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:747920-748018:-1/exon

position:747920:-1
position: 747920
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:748018:-1
position: 748018
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:745948-746051:-1/exon

position:745948:-1
position: 745948
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:746051:-1
position: 746051
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:745708-745857:-1/exon

position:745708:-1
position: 745708
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:745857:-1
position: 745857
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:743260-743415:-1/exon

position:743260:-1
position: 743260
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:743415:-1
position: 743415
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:742918-743097:-1/exon

position:742918:-1
position: 742918
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:743097:-1
position: 743097
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:739735-739811:-1/exon

position:739735:-1
position: 739735
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:739811:-1
position: 739811
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:736808-736961:-1/exon

position:736808:-1
position: 736808
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:736961:-1
position: 736961
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:732834-732965:-1/exon

position:732834:-1
position: 732834
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:732965:-1
position: 732965
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:721592-724632:-1/exon

position:724632:-1
position: 724632
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

YES1
type: SO_0000234
alternative label: c-yes
alternative label: HsT441
alternative label: P61-YES
alternative label: Yes
gene: YES1
gene synonym: c-yes; HsT441; P61-YES; Yes
product: v-yes-1 Yamaguchi sarcoma viral oncogene homolog 1, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 ESTs, and 95% coverage by RNAseq alignments, including 6 samples with support for all introns
transcript id: XM_005258139.1
so part of: YES1
location: complement(join(721592..724632,736808..736961,739735..739811,742918..743097,743260..743415,745708..745857,745948..746051,747920..748018,751705..751804,756557..756835,812115..812272))
location: region:721592-812272:-1

GI:530424930
SIO_000068: ncbigi

position:812272:-1
position: 812272
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:812115-812272:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:756557-756835:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:751705-751804:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:747920-748018:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:745948-746051:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:745708-745857:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:743260-743415:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:742918-743097:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:739735-739811:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:736808-736961:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:721592-724632:-1/exon

YES1
type: SO_0000316
alternative label: c-yes
alternative label: HsT441
alternative label: P61-YES
alternative label: Yes
gene: YES1
gene synonym: c-yes; HsT441; P61-YES; Yes
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: tyrosine-protein kinase Yes isoform X1
translation: MGCIKSKENKSPAIKYRPENTPEPVSTSVSHYGAEPTTVSPCPSSSAKGTAVNFSSLSMTPFGGSSGVTPFGGASSSFSVVPSSYPAGLTGGVTIFVALYDYEARTTEDLSFKKGERFQIINNTEGDWWEARSIATGKNGYIPSNYVAPADSIQAEEWYFGKMGRKDAERLLLNPGNQRGIFLVRESETTKGAYSLSIRDWDEIRGDNVKHYKIRKLDNGGYYITTRAQFDTLQKLVKHYTEHADGLCHKLTTVCPTVKPQTQGLAKDAWEIPRESLRLEVKLGQGCFGEVWMGTWNGTTKVAIKTLKPGTMMPEAFLQEAQIMKKLRHDKLVPLYAVVSEEPIYIVTEFMSKGSLLDFLKEGDGKYLKLPQLVDMAAQIADGMAYIERMNYIHRDLRAANILVGENLVCKIADFGLARLIEDNEYTARQGMVNREVLEQVERGYRMPCPQGCPESLHELMNLCWKKDPDERPTFEYIQSFLEDYFTATEPQYQPGENL
so part of: YES1
location: complement(join(724424..724632,736808..736961,739735..739811,742918..743097,743260..743415,745708..745857,745948..746051,747920..748018,751705..751804,756557..756827))
location: region:724424-756827:-1

XP_005258196.1
SIO_000068: ncbiprotein

GI:530424931
SIO_000068: ncbigi

position:724424:-1
position: 724424
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:756827:-1
position: 756827
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:756557-756827:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:751705-751804:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:747920-748018:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:745948-746051:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:745708-745857:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:743260-743415:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:742918-743097:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:739735-739811:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:736808-736961:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:724424-724632:-1/exon

YES1
type: SO_0000316
alternative label: c-yes
alternative label: HsT441
alternative label: P61-YES
alternative label: Yes
gene: YES1
gene synonym: c-yes; HsT441; P61-YES; Yes
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: tyrosine-protein kinase Yes
translation: MGCIKSKENKSPAIKYRPENTPEPVSTSVSHYGAEPTTVSPCPSSSAKGTAVNFSSLSMTPFGGSSGVTPFGGASSSFSVVPSSYPAGLTGGVTIFVALYDYEARTTEDLSFKKGERFQIINNTEGDWWEARSIATGKNGYIPSNYVAPADSIQAEEWYFGKMGRKDAERLLLNPGNQRGIFLVRESETTKGAYSLSIRDWDEIRGDNVKHYKIRKLDNGGYYITTRAQFDTLQKLVKHYTEHADGLCHKLTTVCPTVKPQTQGLAKDAWEIPRESLRLEVKLGQGCFGEVWMGTWNGTTKVAIKTLKPGTMMPEAFLQEAQIMKKLRHDKLVPLYAVVSEEPIYIVTEFMSKGSLLDFLKEGDGKYLKLPQLVDMAAQIADGMAYIERMNYIHRDLRAANILVGENLVCKIADFGLARLIEDNEYTARQGAKFPIKWTAPEAALYGRFTIKSDVWSFGILQTELVTKGRVPYPGMVNREVLEQVERGYRMPCPQGCPESLHELMNLCWKKDPDERPTFEYIQSFLEDYFTATEPQYQPGENL
so part of: YES1
location: complement(join(724424..724632,732834..732965,736808..736961,739735..739811,742918..743097,743260..743415,745708..745857,745948..746051,747920..748018,751705..751804,756557..756827))
location: region:724424-756827:-1

NP_005424.1
SIO_000068: ncbiprotein

GI:4885661
SIO_000068: ncbigi

CCDS11824.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:756557-756827:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:751705-751804:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:747920-748018:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:745948-746051:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:745708-745857:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:743260-743415:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:742918-743097:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:739735-739811:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:736808-736961:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:732834-732965:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:724424-724632:-1/exon

LOC100652796
type: SO_0000704
gene: LOC100652796
note: bolA homolog 2B (E. coli) pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 832136..832470
location: region:832136-832470:1

100652796
SIO_000068: ncbigene

position:832136:1
position: 832136
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:832470:1
position: 832470
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC441806
type: SO_0000704
gene: LOC441806
note: proteasome (prosome, macropain) 26S subunit, non-ATPase, 8 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 856528..857422
location: region:856528-857422:1

441806
SIO_000068: ncbigene

position:856528:1
position: 856528
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:857422:1
position: 857422
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ADCYAP1
type: SO_0000704
alternative label: PACAP
gene: ADCYAP1
gene synonym: PACAP
note: adenylate cyclase activating polypeptide 1 (pituitary); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 904366..912173
location: region:904366-912173:1
SIO_010080: ADCYAP1

116
SIO_000068: ncbigene

241
SIO_000068: hgnc

102980
SIO_000068: omim

position:904366:1
position: 904366
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:912173:1
position: 912173
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ADCYAP1
type: SO_0000234
alternative label: PACAP
gene: ADCYAP1
gene synonym: PACAP
product: adenylate cyclase activating polypeptide 1 (pituitary), transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 19 ESTs, 5 Proteins, and 98% coverage by RNAseq alignments
transcript id: XM_005258081.1
so part of: ADCYAP1
location: join(904366..904559,904762..905061,905387..905497,907660..907791,908266..908364,909447..912173)
location: region:904366-912173:1

GI:530424798
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:904366-904559:1/exon

position:904559:1
position: 904559
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:904762-905061:1/exon

position:904762:1
position: 904762
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:905061:1
position: 905061
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:905387-905497:1/exon

position:905387:1
position: 905387
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:905497:1
position: 905497
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:907660-907791:1/exon

position:907660:1
position: 907660
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:907791:1
position: 907791
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:908266-908364:1/exon

position:908266:1
position: 908266
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:908364:1
position: 908364
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:909447-912173:1/exon

position:909447:1
position: 909447
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

ADCYAP1
type: SO_0000316
alternative label: PACAP
gene: ADCYAP1
gene synonym: PACAP
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: pituitary adenylate cyclase-activating polypeptide isoform X1
translation: MNKNRSATVQQNILYLKATGRQMLTKRALQKPCSDRFLRTAQINRSRRPVTSVTSGSSSRSRASPHRPLFLSSASLSAPPSLRVTLPPGSARLQTFEQNTSLGKRVPQLLLLLPLVPAASAQTPTPDGDASRVVTPAQELEEALCPPSYLAALLAAGGVEGMTMCSGARLALLVYGIIMHSSVYSSPAAAGLRFPGIRPEEEAYGEDGNPLPDFDGSEPPGAGSPASAPRAAAAWYRPAGRRDVAHGILNEAYRKVLDQLSAGKHLQSLVARGVGGSLGGGAGDDAEPLSKRHSDGIFTDSYSRYRKQMAVKKYLAAVLGKRYKQRVKNKGRRIAYL
so part of: ADCYAP1
location: join(904378..904559,904762..905061,905387..905497,907660..907791,908266..908364,909447..909636)
location: region:904378-909636:1

XP_005258138.1
SIO_000068: ncbiprotein

GI:530424799
SIO_000068: ncbigi

position:904378:1
position: 904378
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:909636:1
position: 909636
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:904378-904559:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:904762-905061:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:905387-905497:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:907660-907791:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:908266-908364:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:909447-909636:1/exon

ADCYAP1
type: SO_0000234
alternative label: PACAP
gene: ADCYAP1
gene synonym: PACAP
product: adenylate cyclase activating polypeptide 1 (pituitary), transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001099733.1
so part of: ADCYAP1
location: join(904944..905061,905387..905497,907660..907791,908266..908364,909447..912173)
location: region:904944-912173:1

GI:153266791
SIO_000068: ncbigi

position:904944:1
position: 904944
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:904944-905061:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:905387-905497:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:907660-907791:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:908266-908364:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:909447-912173:1/exon

ADCYAP1
type: SO_0000234
alternative label: PACAP
gene: ADCYAP1
gene synonym: PACAP
product: adenylate cyclase activating polypeptide 1 (pituitary), transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001117.4
so part of: ADCYAP1
location: join(905197..905497,907660..907791,908266..908364,909447..912173)
location: region:905197-912173:1

GI:452085176
SIO_000068: ncbigi

position:905197:1
position: 905197
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:905197-905497:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:907660-907791:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:908266-908364:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:909447-912173:1/exon

ADCYAP1
type: SO_0000316
alternative label: PACAP
gene: ADCYAP1
gene synonym: PACAP
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: pituitary adenylate cyclase-activating polypeptide preproprotein
translation: MTMCSGARLALLVYGIIMHSSVYSSPAAAGLRFPGIRPEEEAYGEDGNPLPDFDGSEPPGAGSPASAPRAAAAWYRPAGRRDVAHGILNEAYRKVLDQLSAGKHLQSLVARGVGGSLGGGAGDDAEPLSKRHSDGIFTDSYSRYRKQMAVKKYLAAVLGKRYKQRVKNKGRRIAYL
so part of: ADCYAP1
location: join(905388..905497,907660..907791,908266..908364,909447..909636)
location: region:905388-909636:1

NP_001093203.1
SIO_000068: ncbiprotein

GI:153266792
SIO_000068: ncbigi

CCDS11825.1
SIO_000068: ccds

position:905388:1
position: 905388
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:905388-905497:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:907660-907791:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:908266-908364:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:909447-909636:1/exon

ADCYAP1
type: SO_0000316
alternative label: PACAP
gene: ADCYAP1
gene synonym: PACAP
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: pituitary adenylate cyclase-activating polypeptide preproprotein
translation: MTMCSGARLALLVYGIIMHSSVYSSPAAAGLRFPGIRPEEEAYGEDGNPLPDFDGSEPPGAGSPASAPRAAAAWYRPAGRRDVAHGILNEAYRKVLDQLSAGKHLQSLVARGVGGSLGGGAGDDAEPLSKRHSDGIFTDSYSRYRKQMAVKKYLAAVLGKRYKQRVKNKGRRIAYL
so part of: ADCYAP1
location: join(905388..905497,907660..907791,908266..908364,909447..909636)
location: region:905388-909636:1

NP_001108.2
SIO_000068: ncbiprotein

GI:153266795
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:905388-905497:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:907660-907791:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:908266-908364:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:909447-909636:1/exon

LOC388456
type: SO_0000704
gene: LOC388456
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(926084..927994)
location: region:926084-927994:-1
SIO_010080: LOC388456

388456
SIO_000068: ncbigene

position:926084:-1
position: 926084
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:927994:-1
position: 927994
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC388456
type: SO_0000673
gene: LOC388456
product: uncharacterized LOC388456
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA
transcript id: XR_243815.1
so part of: LOC388456
location: complement(join(926084..926884,927935..927994))
location: region:926084-927994:-1

GI:530425013
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:927935-927994:-1/exon

position:927935:-1
position: 927935
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:926084-926884:-1/exon

position:926884:-1
position: 926884
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

SLC25A3P3
type: SO_0000704
gene: SLC25A3P3
note: solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(1159190..1159773)
location: region:1159190-1159773:-1

100422606
SIO_000068: ncbigene

43785
SIO_000068: hgnc

position:1159190:-1
position: 1159190
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:1159773:-1
position: 1159773
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

COX6CP3
type: SO_0000704
gene: COX6CP3
note: cytochrome c oxidase subunit VIc pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(1176651..1177073)
location: region:1176651-1177073:-1

100130247
SIO_000068: ncbigene

31721
SIO_000068: hgnc

position:1176651:-1
position: 1176651
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:1177073:-1
position: 1177073
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00470
type: SO_0000704
alternative label: C18orf2
gene: LINC00470
gene synonym: C18orf2
note: long intergenic non-protein coding RNA 470; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(1268312..1359630)
location: region:1268312-1359630:-1
SIO_010080: LINC00470

56651
SIO_000068: ncbigene

1225
SIO_000068: hgnc

position:1268312:-1
position: 1268312
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:1359630:-1
position: 1359630
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00470
type: SO_0000673
alternative label: C18orf2
gene: LINC00470
gene synonym: C18orf2
product: long intergenic non-protein coding RNA 470, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_023927.1
so part of: LINC00470
location: complement(join(1268312..1269853,1272443..1272512,1358727..1358761,1359388..1359630))
location: region:1268312-1359630:-1

GI:193083204
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:1359388-1359630:-1/exon

position:1359388:-1
position: 1359388
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:1358727-1358761:-1/exon

position:1358727:-1
position: 1358727
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:1358761:-1
position: 1358761
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:1272443-1272512:-1/exon

position:1272443:-1
position: 1272443
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:1272512:-1
position: 1272512
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:1268312-1269853:-1/exon

position:1269853:-1
position: 1269853
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00470
type: SO_0000673
alternative label: C18orf2
gene: LINC00470
gene synonym: C18orf2
product: long intergenic non-protein coding RNA 470, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_023926.1
so part of: LINC00470
location: complement(join(1268312..1269853,1272443..1272512,1273362..1273534,1275967..1276088,1358727..1358761,1359388..1359630))
location: region:1268312-1359630:-1

GI:193083201
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:1359388-1359630:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:1358727-1358761:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:1275967-1276088:-1/exon

position:1275967:-1
position: 1275967
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:1276088:-1
position: 1276088
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:1273362-1273534:-1/exon

position:1273362:-1
position: 1273362
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:1273534:-1
position: 1273534
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:1272443-1272512:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:1268312-1269853:-1/exon

LINC00470
type: SO_0000673
alternative label: C18orf2
gene: LINC00470
gene synonym: C18orf2
product: long intergenic non-protein coding RNA 470, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_023925.1
so part of: LINC00470
location: complement(join(1268312..1269853,1272443..1272512,1273362..1273534,1275967..1276078,1353408..1353463,1358727..1358761,1359388..1359630))
location: region:1268312-1359630:-1

GI:193083199
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:1359388-1359630:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:1358727-1358761:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:1353408-1353463:-1/exon

position:1353408:-1
position: 1353408
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:1353463:-1
position: 1353463
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:1275967-1276078:-1/exon

position:1276078:-1
position: 1276078
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:1273362-1273534:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:1272443-1272512:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:1268312-1269853:-1/exon

LOC100129774
type: SO_0000704
gene: LOC100129774
note: ATPase family, AAA domain containing 1 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(1362444..1363874)
location: region:1362444-1363874:-1

100129774
SIO_000068: ncbigene

position:1362444:-1
position: 1362444
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:1363874:-1
position: 1363874
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100128360
type: SO_0000704
gene: LOC100128360
note: axin interactor, dorsalization associated pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(1927727..1929088)
location: region:1927727-1929088:-1

100128360
SIO_000068: ncbigene

position:1927727:-1
position: 1927727
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:1929088:-1
position: 1929088
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101926997
type: SO_0000704
gene: LOC101926997
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(2517249..2519259)
location: region:2517249-2519259:-1
SIO_010080: LOC101926997

101926997
SIO_000068: ncbigene

position:2517249:-1
position: 2517249
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2519259:-1
position: 2519259
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101926997
type: SO_0000673
gene: LOC101926997
product: uncharacterized LOC101926997
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 17% coverage by RNAseq alignments
transcript id: XR_243816.1
so part of: LOC101926997
location: complement(join(2517249..2518436,2518502..2519259))
location: region:2517249-2519259:-1

GI:530425014
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:2518502-2519259:-1/exon

position:2518502:-1
position: 2518502
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2517249-2518436:-1/exon

position:2518436:-1
position: 2518436
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

METTL4
type: SO_0000704
alternative label: HsT661
gene: METTL4
gene synonym: HsT661
note: methyltransferase like 4; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(2537524..2571489)
location: region:2537524-2571489:-1
SIO_010080: METTL4

64863
SIO_000068: ncbigene

24726
SIO_000068: hgnc

position:2537524:-1
position: 2537524
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2571489:-1
position: 2571489
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

METTL4
type: SO_0000234
alternative label: HsT661
gene: METTL4
gene synonym: HsT661
product: methyltransferase like 4
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_022840.3
so part of: METTL4
location: complement(join(2537524..2539144,2544194..2544285,2544652..2544758,2547354..2547528,2552694..2552763,2554668..2555037,2563796..2563858,2566820..2567653,2571148..2571489))
location: region:2537524-2571489:-1

GI:145275205
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:2571148-2571489:-1/exon

position:2571148:-1
position: 2571148
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2566820-2567653:-1/exon

position:2566820:-1
position: 2566820
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2567653:-1
position: 2567653
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:2563796-2563858:-1/exon

position:2563796:-1
position: 2563796
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2563858:-1
position: 2563858
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:2554668-2555037:-1/exon

position:2554668:-1
position: 2554668
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2555037:-1
position: 2555037
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:2552694-2552763:-1/exon

position:2552694:-1
position: 2552694
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2552763:-1
position: 2552763
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:2547354-2547528:-1/exon

position:2547354:-1
position: 2547354
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2547528:-1
position: 2547528
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:2544652-2544758:-1/exon

position:2544652:-1
position: 2544652
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2544758:-1
position: 2544758
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:2544194-2544285:-1/exon

position:2544194:-1
position: 2544194
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2544285:-1
position: 2544285
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:2537524-2539144:-1/exon

position:2539144:-1
position: 2539144
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

METTL4
type: SO_0000234
alternative label: HsT661
gene: METTL4
gene synonym: HsT661
product: methyltransferase like 4, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 25 ESTs, and 89% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258132.1
so part of: METTL4
location: complement(join(2537529..2539144,2547354..2547528,2552694..2552763,2554668..2555037,2563796..2563858,2566820..2567653,2571148..2571265))
location: region:2537529-2571265:-1

GI:530424916
SIO_000068: ncbigi

position:2537529:-1
position: 2537529
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2571265:-1
position: 2571265
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2571148-2571265:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2566820-2567653:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2563796-2563858:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2554668-2555037:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2552694-2552763:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2547354-2547528:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2537529-2539144:-1/exon

METTL4
type: SO_0000234
alternative label: HsT661
gene: METTL4
gene synonym: HsT661
product: methyltransferase like 4, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 20 ESTs, and 87% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XM_005258133.1
so part of: METTL4
location: complement(join(2537529..2539144,2544194..2544285,2544652..2544758,2547354..2547528,2552694..2552763,2554668..2555037,2563796..2563858,2567511..2567653,2571148..2571232))
location: region:2537529-2571232:-1

GI:530424918
SIO_000068: ncbigi

position:2571232:-1
position: 2571232
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2571148-2571232:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2567511-2567653:-1/exon

position:2567511:-1
position: 2567511
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:2563796-2563858:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2554668-2555037:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2552694-2552763:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2547354-2547528:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2544652-2544758:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2544194-2544285:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2537529-2539144:-1/exon

METTL4
type: SO_0000316
alternative label: HsT661
gene: METTL4
gene synonym: HsT661
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: methyltransferase-like protein 4
translation: MSVVHQLSAGWLLDHLSFINKINYQLHQHHEPCCRKKEFTTSVHFESLQMDSVSSSGVCAAFIASDSSTKPENDDGGNYEMFTRKFVFRPELFDVTKPYITPAVHKECQQSNEKEDLMNGVKKEISISIIGKKRKRCVVFNQGELDAMEYHTKIRELILDGSLQLIQEGLKSGFLYPLFEKQDKGSKPITLPLDACSLSELCEMAKHLPSLNEMEHQTLQLVEEDTSVTEQDLFLRVVENNSSFTKVITLMGQKYLLPPKSSFLLSDISCMQPLLNYRKTFDVIVIDPPWQNKSVKRSNRYSYLSPLQIQQIPIPKLAAPNCLLVTWVTNRQKHLRFIKEELYPSWSVEVVAEWHWVKITNSGEFVFPLDSPHKKPYEGLILGRVQEKTALPLRNADVNVLPIPDHKLIVSVPCTLHSHKPPLAEVLKDYIKPDGEYLELFARNLQPGWTSWGNEVLKFQHVDYFIAVESGS
so part of: METTL4
location: complement(join(2538999..2539144,2544194..2544285,2544652..2544758,2547354..2547528,2552694..2552763,2554668..2555037,2563796..2563858,2566820..2567215))
location: region:2538999-2567215:-1

NP_073751.3
SIO_000068: ncbiprotein

GI:145275206
SIO_000068: ncbigi

CCDS11826.1
SIO_000068: ccds

position:2538999:-1
position: 2538999
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2567215:-1
position: 2567215
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2566820-2567215:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2563796-2563858:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2554668-2555037:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2552694-2552763:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2547354-2547528:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2544652-2544758:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2544194-2544285:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2538999-2539144:-1/exon

METTL4
type: SO_0000316
alternative label: HsT661
gene: METTL4
gene synonym: HsT661
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: methyltransferase like 4 isoform X3
translation: MEYHTKIRELILDGSLQLIQEGLKSGFLYPLFEKQDKGSKPITLPLDACSLSELCEMAKHLPSLNEMEHQTLQLVEEDTSVTEQDLFLRVVENNSSFTKVITLMGQKYLLPPKSSFLLSDISCMQPLLNYRKTFDVIVIDPPWQNKSVKRSNRYSYLSPLQIQQIPIPKLAAPNCLLVTWVTNRQKHLRFIKEELYPSWSVEVVAEWHWVKITNSGEFVFPLDSPHKKPYEGLILGRVQEKTALPLRNADVNVLPIPDHKLIVSVPCTLHSHKPPLAEVLKDYIKPDGEYLELFARNLQPGWTSWGNEVLKFQHVDYFIAVESGS
so part of: METTL4
location: complement(join(2538999..2539144,2544194..2544285,2544652..2544758,2547354..2547528,2552694..2552763,2554668..2555037,2563796..2563813))
location: region:2538999-2563813:-1

XP_005258190.1
SIO_000068: ncbiprotein

GI:530424919
SIO_000068: ncbigi

position:2563813:-1
position: 2563813
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2563796-2563813:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2554668-2555037:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2552694-2552763:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2547354-2547528:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2544652-2544758:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2544194-2544285:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2538999-2539144:-1/exon

METTL4
type: SO_0000673
alternative label: HsT661
gene: METTL4
gene synonym: HsT661
product: methyltransferase like 4, transcript variant X4
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, and 100% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XR_243813.1
so part of: METTL4
location: complement(join(2539083..2539144,2540666..2540860,2544194..2544285,2544652..2544758,2547354..2547528,2552694..2552763,2554668..2555037,2563796..2563858,2566820..2567653,2571148..2571265))
location: region:2539083-2571265:-1

GI:530424915
SIO_000068: ncbigi

position:2539083:-1
position: 2539083
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2571148-2571265:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2566820-2567653:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2563796-2563858:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2554668-2555037:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2552694-2552763:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2547354-2547528:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2544652-2544758:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2544194-2544285:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2540666-2540860:-1/exon

position:2540666:-1
position: 2540666
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2540860:-1
position: 2540860
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:2539083-2539144:-1/exon

METTL4
type: SO_0000316
alternative label: HsT661
gene: METTL4
gene synonym: HsT661
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: methyltransferase like 4 isoform X2
translation: MSVVHQLSAGWLLDHLSFINKINYQLHQHHEPCCRKKEFTTSVHFESLQMDSVSSSGVCAAFIASDSSTKPENDDGGNYEMFTRKFVFRPELFDVTKPYITPAVHKECQQSNEKEDLMNGVKKEISISIIGKKRKRCVVFNQGELDAMEYHTKIRELILDGSLQLIQEGLKSGFLYPLFEKQDKGSKPITLPLDACSLSELCEMAKHLPSLNEMEHQTLQLVEEDTSVTEQDLFLRVVENNSSFTKVITLMGQKYLLPPKSSFLLSDISCMQPLLNYRKTFDVIVIDPPWQNKSVKRSNRYSYLSPLQIQQIPIPKLAAPNCLLVTWVTNRQKHLRFIKEELYPSWSVEVVAEWHWVKRF
so part of: METTL4
location: complement(join(2539136..2539144,2547354..2547528,2552694..2552763,2554668..2555037,2563796..2563858,2566820..2567215))
location: region:2539136-2567215:-1

XP_005258189.1
SIO_000068: ncbiprotein

GI:530424917
SIO_000068: ncbigi

position:2539136:-1
position: 2539136
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2566820-2567215:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2563796-2563858:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2554668-2555037:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2552694-2552763:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2547354-2547528:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2539136-2539144:-1/exon

METTL4
type: SO_0000234
alternative label: HsT661
gene: METTL4
gene synonym: HsT661
product: methyltransferase like 4, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, and 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258131.1
so part of: METTL4
location: complement(join(2539778..2540860,2544194..2544285,2544652..2544758,2547354..2547528,2552694..2552763,2554668..2555037,2563796..2563858,2566820..2567653,2571148..2571265))
location: region:2539778-2571265:-1

GI:530424913
SIO_000068: ncbigi

position:2539778:-1
position: 2539778
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2571148-2571265:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2566820-2567653:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2563796-2563858:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2554668-2555037:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2552694-2552763:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2547354-2547528:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2544652-2544758:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2544194-2544285:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2539778-2540860:-1/exon

METTL4
type: SO_0000316
alternative label: HsT661
gene: METTL4
gene synonym: HsT661
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: methyltransferase like 4 isoform X1
translation: MSVVHQLSAGWLLDHLSFINKINYQLHQHHEPCCRKKEFTTSVHFESLQMDSVSSSGVCAAFIASDSSTKPENDDGGNYEMFTRKFVFRPELFDVTKPYITPAVHKECQQSNEKEDLMNGVKKEISISIIGKKRKRCVVFNQGELDAMEYHTKIRELILDGSLQLIQEGLKSGFLYPLFEKQDKGSKPITLPLDACSLSELCEMAKHLPSLNEMEHQTLQLVEEDTSVTEQDLFLRVVENNSSFTKVITLMGQKYLLPPKSSFLLSDISCMQPLLNYRKTFDVIVIDPPWQNKSVKRSNRYSYLSPLQIQQIPIPKLAAPNCLLVTWVTNRQKHLRFIKEELYPSWSVEVVAEWHWVKITNSGEFVFPLDSPHKKPYEGLILGRVQEKTALPLRNADVNVLPIPDHKLIVSVPCTLHSHKPPLAGLLTSSYQKSEQMKQKQTKPFFSVT
so part of: METTL4
location: complement(join(2540784..2540860,2544194..2544285,2544652..2544758,2547354..2547528,2552694..2552763,2554668..2555037,2563796..2563858,2566820..2567215))
location: region:2540784-2567215:-1

XP_005258188.1
SIO_000068: ncbiprotein

GI:530424914
SIO_000068: ncbigi

position:2540784:-1
position: 2540784
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2566820-2567215:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2563796-2563858:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2554668-2555037:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2552694-2552763:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2547354-2547528:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2544652-2544758:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2544194-2544285:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2540784-2540860:-1/exon

LOC100128926
type: SO_0000704
gene: LOC100128926
note: Derived by automated computational analysis using gene prediction method: Gnomon.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 2568389..2569121
location: region:2568389-2569121:1
SIO_010080: LOC100128926

100128926
SIO_000068: ncbigene

position:2568389:1
position: 2568389
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2569121:1
position: 2569121
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC100128926
type: SO_0000147
gene: LOC100128926
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: LOC100128926
location: 2568389..2568466
location: region:2568389-2568466:1

position:2568466:1
position: 2568466
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC100128926
type: SO_0000147
gene: LOC100128926
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
number: 2
pseudo: true
so part of: LOC100128926
location: 2568769..2568860
location: region:2568769-2568860:1

position:2568769:1
position: 2568769
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2568860:1
position: 2568860
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC100128926
type: SO_0000147
gene: LOC100128926
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
number: 3
pseudo: true
so part of: LOC100128926
location: 2568974..2569121
location: region:2568974-2569121:1

position:2568974:1
position: 2568974
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

NDC80
type: SO_0000704
alternative label: HEC
alternative label: HEC1
alternative label: HsHec1
alternative label: hsNDC80
alternative label: KNTC2
alternative label: TID3
gene: NDC80
gene synonym: HEC; HEC1; HsHec1; hsNDC80; KNTC2; TID3
note: NDC80 kinetochore complex component; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 2571510..2616634
location: region:2571510-2616634:1
SIO_010080: NDC80

10403
SIO_000068: ncbigene

16909
SIO_000068: hgnc

06277
SIO_000068: hprd

607272
SIO_000068: omim

position:2571510:1
position: 2571510
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2616634:1
position: 2616634
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

NDC80
type: SO_0000234
alternative label: HEC
alternative label: HEC1
alternative label: HsHec1
alternative label: hsNDC80
alternative label: KNTC2
alternative label: TID3
gene: NDC80
gene synonym: HEC; HEC1; HsHec1; hsNDC80; KNTC2; TID3
product: NDC80 kinetochore complex component
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_006101.2
so part of: NDC80
location: join(2571510..2571682,2572976..2573085,2574988..2575065,2577745..2577868,2577968..2578140,2578926..2579028,2585112..2585201,2587829..2587922,2589203..2589309,2590017..2590161,2595415..2595620,2599018..2599170,2601395..2601484,2606414..2606506,2608699..2608829,2610758..2610860,2616436..2616634)
location: region:2571510-2616634:1

GI:215820615
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:2571510-2571682:1/exon

position:2571682:1
position: 2571682
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2572976-2573085:1/exon

position:2572976:1
position: 2572976
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2573085:1
position: 2573085
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:2574988-2575065:1/exon

position:2574988:1
position: 2574988
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2575065:1
position: 2575065
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:2577745-2577868:1/exon

position:2577745:1
position: 2577745
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2577868:1
position: 2577868
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:2577968-2578140:1/exon

position:2577968:1
position: 2577968
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2578140:1
position: 2578140
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:2578926-2579028:1/exon

position:2578926:1
position: 2578926
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2579028:1
position: 2579028
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:2585112-2585201:1/exon

position:2585112:1
position: 2585112
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2585201:1
position: 2585201
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:2587829-2587922:1/exon

position:2587829:1
position: 2587829
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2587922:1
position: 2587922
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:2589203-2589309:1/exon

position:2589203:1
position: 2589203
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2589309:1
position: 2589309
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:2590017-2590161:1/exon

position:2590017:1
position: 2590017
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2590161:1
position: 2590161
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:2595415-2595620:1/exon

position:2595415:1
position: 2595415
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2595620:1
position: 2595620
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:2599018-2599170:1/exon

position:2599018:1
position: 2599018
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2599170:1
position: 2599170
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:2601395-2601484:1/exon

position:2601395:1
position: 2601395
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2601484:1
position: 2601484
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:2606414-2606506:1/exon

position:2606414:1
position: 2606414
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2606506:1
position: 2606506
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:2608699-2608829:1/exon

position:2608699:1
position: 2608699
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2608829:1
position: 2608829
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:2610758-2610860:1/exon

position:2610758:1
position: 2610758
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2610860:1
position: 2610860
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 17
SIO_000628: feature:2616436-2616634:1/exon

position:2616436:1
position: 2616436
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

NDC80
type: SO_0000316
alternative label: HEC
alternative label: HEC1
alternative label: HsHec1
alternative label: hsNDC80
alternative label: KNTC2
alternative label: TID3
gene: NDC80
gene synonym: HEC; HEC1; HsHec1; hsNDC80; KNTC2; TID3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: kinetochore protein NDC80 homolog
translation: MKRSSVSSGGAGRLSMQELRSQDVNKQGLYTPQTKEKPTFGKLSINKPTSERKVSLFGKRTSGHGSRNSQLGIFSSSEKIKDPRPLNDKAFIQQCIRQLCEFLTENGYAHNVSMKSLQAPSVKDFLKIFTFLYGFLCPSYELPDTKFEEEVPRIFKDLGYPFALSKSSMYTVGAPHTWPHIVAALVWLIDCIKIHTAMKESSPLFDDGQPWGEETEDGIMHNKLFLDYTIKCYESFMSGADSFDEMNAELQSKLKDLFNVDAFKLESLEAKNRALNEQIARLEQEREKEPNRLESLRKLKASLQGDVQKYQAYMSNLESHSAILDQKLNGLNEEIARVELECETIKQENTRLQNIIDNQKYSVADIERINHERNELQQTINKLTKDLEAEQQKLWNEELKYARGKEAIETQLAEYHKLARKLKLIPKGAENSKGYDFEIKFNPEAGANCLVKYRAQVYVPLKELLNETEEEINKALNKKMGLEDTLEQLNAMITESKRSVRTLKEEVQKLDDLYQQKIKEAEEEDEKCASELESLEKHKHLLESTVNQGLSEAMNELDAVQREYQLVVQTTTEERRKVGNNLQRLLEMVATHVGSVEKHLEEQIAKVDREYEECMSEDLSENIKEIRDKYEKKATLIKSSEE
so part of: NDC80
location: join(2572985..2573085,2574988..2575065,2577745..2577868,2577968..2578140,2578926..2579028,2585112..2585201,2587829..2587922,2589203..2589309,2590017..2590161,2595415..2595620,2599018..2599170,2601395..2601484,2606414..2606506,2608699..2608829,2610758..2610860,2616436..2616573)
location: region:2572985-2616573:1

NP_006092.1
SIO_000068: ncbiprotein

GI:5174457
SIO_000068: ncbigi

CCDS11827.1
SIO_000068: ccds

position:2572985:1
position: 2572985
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2616573:1
position: 2616573
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2572985-2573085:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2574988-2575065:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2577745-2577868:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2577968-2578140:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2578926-2579028:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2585112-2585201:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2587829-2587922:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2589203-2589309:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2590017-2590161:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2595415-2595620:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2599018-2599170:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2601395-2601484:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2606414-2606506:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2608699-2608829:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2610758-2610860:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2616436-2616573:1/exon

LOC100420946
type: SO_0000704
gene: LOC100420946
note: katanin p80 subunit B-like 1 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(2593673..2594912)
location: region:2593673-2594912:-1

100420946
SIO_000068: ncbigene

position:2593673:-1
position: 2593673
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2594912:-1
position: 2594912
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

CBX3P2
type: SO_0000704
gene: CBX3P2
note: chromobox homolog 3 pseudogene 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(2652169..2655394)
location: region:2652169-2655394:-1
SIO_010080: CBX3P2

645158
SIO_000068: ncbigene

42874
SIO_000068: hgnc

position:2652169:-1
position: 2652169
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2655394:-1
position: 2655394
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

CBX3P2
type: SO_0000673
gene: CBX3P2
product: chromobox homolog 3 pseudogene 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
transcript id: NR_033754.2
so part of: CBX3P2
location: complement(join(2652169..2653301,2655099..2655394))
location: region:2652169-2655394:-1

GI:338332400
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:2655099-2655394:-1/exon

position:2655099:-1
position: 2655099
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2652169-2653301:-1/exon

position:2653301:-1
position: 2653301
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

SMCHD1
type: SO_0000704
gene: SMCHD1
note: structural maintenance of chromosomes flexible hinge domain containing 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 2655886..2805015
location: region:2655886-2805015:1
SIO_010080: SMCHD1

23347
SIO_000068: ncbigene

29090
SIO_000068: hgnc

614982
SIO_000068: omim

position:2655886:1
position: 2655886
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2805015:1
position: 2805015
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

SMCHD1
type: SO_0000234
gene: SMCHD1
product: structural maintenance of chromosomes flexible hinge domain containing 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_015295.2
so part of: SMCHD1
location: join(2655886..2656260,2666156..2666231,2666869..2667030,2673280..2673362,2674014..2674144,2688392..2688506,2688626..2688745,2694525..2694691,2697030..2697120,2697829..2698039,2700537..2700657,2700733..2700916,2703690..2703884,2705692..2705805,2706362..2706468,2707561..2707643,2707805..2707918,2718156..2718233,2718313..2718432,2722517..2722661,2724897..2724993,2726450..2726522,2728455..2728594,2729273..2729407,2732263..2732490,2738395..2738543,2739430..2739518,2740701..2740819,2743759..2743926,2747520..2747645,2750041..2750120,2750348..2750505,2751276..2751391,2752486..2752550,2760650..2760737,2762103..2762234,2763635..2763787,2769692..2769818,2769987..2770106,2771531..2771616,2772248..2772370,2775732..2775922,2777804..2777913,2778167..2778237,2784448..2784619,2795947..2796105,2796405..2796519,2802526..2805015)
location: region:2655886-2805015:1

GI:148839304
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:2655886-2656260:1/exon

position:2656260:1
position: 2656260
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2666156-2666231:1/exon

position:2666156:1
position: 2666156
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2666231:1
position: 2666231
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:2666869-2667030:1/exon

position:2666869:1
position: 2666869
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2667030:1
position: 2667030
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:2673280-2673362:1/exon

position:2673280:1
position: 2673280
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2673362:1
position: 2673362
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:2674014-2674144:1/exon

position:2674014:1
position: 2674014
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2674144:1
position: 2674144
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:2688392-2688506:1/exon

position:2688392:1
position: 2688392
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2688506:1
position: 2688506
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:2688626-2688745:1/exon

position:2688626:1
position: 2688626
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2688745:1
position: 2688745
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:2694525-2694691:1/exon

position:2694525:1
position: 2694525
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2694691:1
position: 2694691
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:2697030-2697120:1/exon

position:2697030:1
position: 2697030
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2697120:1
position: 2697120
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:2697829-2698039:1/exon

position:2697829:1
position: 2697829
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2698039:1
position: 2698039
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:2700537-2700657:1/exon

position:2700537:1
position: 2700537
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2700657:1
position: 2700657
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:2700733-2700916:1/exon

position:2700733:1
position: 2700733
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2700916:1
position: 2700916
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:2703690-2703884:1/exon

position:2703690:1
position: 2703690
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2703884:1
position: 2703884
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:2705692-2705805:1/exon

position:2705692:1
position: 2705692
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2705805:1
position: 2705805
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:2706362-2706468:1/exon

position:2706362:1
position: 2706362
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2706468:1
position: 2706468
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:2707561-2707643:1/exon

position:2707561:1
position: 2707561
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2707643:1
position: 2707643
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 17
SIO_000628: feature:2707805-2707918:1/exon

position:2707805:1
position: 2707805
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2707918:1
position: 2707918
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 18
SIO_000628: feature:2718156-2718233:1/exon

position:2718156:1
position: 2718156
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2718233:1
position: 2718233
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 19
SIO_000628: feature:2718313-2718432:1/exon

position:2718313:1
position: 2718313
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2718432:1
position: 2718432
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 20
SIO_000628: feature:2722517-2722661:1/exon

position:2722517:1
position: 2722517
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2722661:1
position: 2722661
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 21
SIO_000628: feature:2724897-2724993:1/exon

position:2724897:1
position: 2724897
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2724993:1
position: 2724993
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 22
SIO_000628: feature:2726450-2726522:1/exon

position:2726450:1
position: 2726450
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2726522:1
position: 2726522
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 23
SIO_000628: feature:2728455-2728594:1/exon

position:2728455:1
position: 2728455
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2728594:1
position: 2728594
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 24
SIO_000628: feature:2729273-2729407:1/exon

position:2729273:1
position: 2729273
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2729407:1
position: 2729407
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 25
SIO_000628: feature:2732263-2732490:1/exon

position:2732263:1
position: 2732263
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2732490:1
position: 2732490
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 26
SIO_000628: feature:2738395-2738543:1/exon

position:2738395:1
position: 2738395
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2738543:1
position: 2738543
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 27
SIO_000628: feature:2739430-2739518:1/exon

position:2739430:1
position: 2739430
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2739518:1
position: 2739518
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 28
SIO_000628: feature:2740701-2740819:1/exon

position:2740701:1
position: 2740701
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2740819:1
position: 2740819
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 29
SIO_000628: feature:2743759-2743926:1/exon

position:2743759:1
position: 2743759
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2743926:1
position: 2743926
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 30
SIO_000628: feature:2747520-2747645:1/exon

position:2747520:1
position: 2747520
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2747645:1
position: 2747645
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 31
SIO_000628: feature:2750041-2750120:1/exon

position:2750041:1
position: 2750041
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2750120:1
position: 2750120
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 32
SIO_000628: feature:2750348-2750505:1/exon

position:2750348:1
position: 2750348
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2750505:1
position: 2750505
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 33
SIO_000628: feature:2751276-2751391:1/exon

position:2751276:1
position: 2751276
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2751391:1
position: 2751391
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 34
SIO_000628: feature:2752486-2752550:1/exon

position:2752486:1
position: 2752486
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2752550:1
position: 2752550
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 35
SIO_000628: feature:2760650-2760737:1/exon

position:2760650:1
position: 2760650
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2760737:1
position: 2760737
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 36
SIO_000628: feature:2762103-2762234:1/exon

position:2762103:1
position: 2762103
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2762234:1
position: 2762234
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 37
SIO_000628: feature:2763635-2763787:1/exon

position:2763635:1
position: 2763635
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2763787:1
position: 2763787
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 38
SIO_000628: feature:2769692-2769818:1/exon

position:2769692:1
position: 2769692
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2769818:1
position: 2769818
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 39
SIO_000628: feature:2769987-2770106:1/exon

position:2769987:1
position: 2769987
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2770106:1
position: 2770106
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 40
SIO_000628: feature:2771531-2771616:1/exon

position:2771531:1
position: 2771531
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2771616:1
position: 2771616
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 41
SIO_000628: feature:2772248-2772370:1/exon

position:2772248:1
position: 2772248
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2772370:1
position: 2772370
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 42
SIO_000628: feature:2775732-2775922:1/exon

position:2775732:1
position: 2775732
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2775922:1
position: 2775922
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 43
SIO_000628: feature:2777804-2777913:1/exon

position:2777804:1
position: 2777804
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2777913:1
position: 2777913
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 44
SIO_000628: feature:2778167-2778237:1/exon

position:2778167:1
position: 2778167
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2778237:1
position: 2778237
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 45
SIO_000628: feature:2784448-2784619:1/exon

position:2784448:1
position: 2784448
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2784619:1
position: 2784619
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 46
SIO_000628: feature:2795947-2796105:1/exon

position:2795947:1
position: 2795947
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2796105:1
position: 2796105
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 47
SIO_000628: feature:2796405-2796519:1/exon

position:2796405:1
position: 2796405
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2796519:1
position: 2796519
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 48
SIO_000628: feature:2802526-2805015:1/exon

position:2802526:1
position: 2802526
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

SMCHD1
type: SO_0000316
gene: SMCHD1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: structural maintenance of chromosomes flexible hinge domain-containing protein 1
translation: MAAADGGGPGGASVGTEEDGGGVGHRTVYLFDRREKESELGDRPLQVGERSDYAGFRACVCQTLGISPEEKFVITTTSRKEITCDNFDETVKDGVTLYLLQSVNQLLLTATKERIDFLPHYDTLVKSGMYEYYASEGQNPLPFALAELIDNSLSATSRNIGVRRIQIKLLFDETQGKPAVAVIDNGRGMTSKQLNNWAVYRLSKFTRQGDFESDHSGYVRPVPVPRSLNSDISYFGVGGKQAVFFVGQSARMISKPADSQDVHELVLSKEDFEKKEKNKEAIYSGYIRNRKPSDSVHITNDDERFLHHLIIEEKEKDSFTAVVITGVQPEHIQYLKNYFHLWTRQLAHIYHYYIHGPKGNEIRTSKEVEPFNNIDIEISMFEKGKVPKIVNLREIQDDMQTLYVNTAADSFEFKAHVEGDGVVEGIIRYHPFLYDRETYPDDPCFPSKLKDEDDEDDCFILEKAARGKRPIFECFWNGRLIPYTSVEDFDWCTPPKKRGLAPIECYNRISGALFTNDKFQVSTNKLTFMDLELKLKDKNTLFTRILNGQEQRMKIDREFALWLKDCHEKYDKQIKFTLFKGVITRPDLPSKKQGPWATYAAIEWDGKIYKAGQLVKTIKTLPLFYGSIVRFFLYGDHDGEVYATGGEVQIAMEPQALYDEVRTVPIAKLDRTVAEKAVKKYVEDEMARLPDRLSVTWPEGDELLPNEVRPAGTPIGALRIEILNKKGEAMQKLPGTSHGGSKKLLVELKVILHSSSGNKEIISHISQHGGKWPYWFKKMENIQKLGNYTLKLQVVLNESNADTYAGRPLPSKAIKFSVKEGKPEKFSFGLLDLPFRVGVPFNIPLEFQDEFGHTSQLVTDIQPVLEASGLSLHYEEITKGPNCVIRGVTAKGPVNSCQGKNYNLKVTLPGLKEDSQILKIRLLPGHPRRLKVKPDSEILVIENGTAFPFQVEVLDESDNITAQPKLIVHCKFSGAPNLPVYVVDCSSSGTSILTGSAIQVQNIKKDQTLKARIEIPSCKDVAPVEKTIKLLPSSHVARLQIFSVEGQKAIQIKHQDEVNWIAGDIMHNLIFQMYDEGEREINITSALAEKIKVNWTPEINKEHLLQGLLPDVQVPTSVKDMRYCQVSFQDDHVSLESAFTVRPLPDEPKHLKCEMKGGKTVQMGQELQGEVVIIITDQYGNQIQAFSPSSLSSLSIAGVGLDSSNLKTTFQENTQSISVRGIKFIPGPPGNKDLCFTWREFSDFIRVQLISGPPAKLLLIDWPELKESIPVINGRDLQNPIIVQLCDQWDNPAPVQHVKISLTKASNLKLMPSNQQHKTDEKGRANLGVFSVFAPRGEHTLQVKAIYNKSIIEGPIIKLMILPDPEKPVRLNVKYDKDASFLAGGLFTDFMISVISEDDSIIKNINPARISMKMWKLSTSGNRPPANAETFSCNKIKDNDKEDGCFYFRDKVIPNKVGTYCIQFGFMMDKTNILNSEQVIVEVLPNQPVKLVPKIKPPTPAVSNVRSVASRTLVRDLHLSITDDYDNHTGIDLVGTIIATIKGSNEEDTDTPLFIGKVRTLEFPFVNGSAEIMSLVLAESSPGRDSTEYFIVFEPRLPLLSRTLEPYILPFMFYNDVKKQQQMAALTKEKDQLSQSIVMYKSLFEASQQLLNEMKCQVEEARLKEAQLRNELKIHNIDIPTTQQVPHIEALLKRKLSEQEELKKKPRRSCTLPNYTKGSGDVLGKIAHLAQIEDDRAAMVISWHLASDMDCVVTLTTDAARRIYDETQGRQQVLPLDSIYKKTLPDWKRSLPHFRNGKLYFKPIGDPVFARDLLTFPDNVEHCETVFGMLLGDTIILDNLDAANHYRKEVVKITHCPTLLTRDGDRIRSNGKFGGLQNKAPPMDKLRGMVFGAPVPKQCLILGEQIDLLQQYRSAVCKLDSVNKDLNSQLEYLRTPDMRKKKQELDEHEKNLKLIEEKLGMTPIRKCNDSLRHSPKVETTDCPVPPKRMRREATRQNRII…
so part of: SMCHD1
location: join(2656075..2656260,2666156..2666231,2666869..2667030,2673280..2673362,2674014..2674144,2688392..2688506,2688626..2688745,2694525..2694691,2697030..2697120,2697829..2698039,2700537..2700657,2700733..2700916,2703690..2703884,2705692..2705805,2706362..2706468,2707561..2707643,2707805..2707918,2718156..2718233,2718313..2718432,2722517..2722661,2724897..2724993,2726450..2726522,2728455..2728594,2729273..2729407,2732263..2732490,2738395..2738543,2739430..2739518,2740701..2740819,2743759..2743926,2747520..2747645,2750041..2750120,2750348..2750505,2751276..2751391,2752486..2752550,2760650..2760737,2762103..2762234,2763635..2763787,2769692..2769818,2769987..2770106,2771531..2771616,2772248..2772370,2775732..2775922,2777804..2777913,2778167..2778237,2784448..2784619,2795947..2796105,2796405..2796519,2802526..2802550)
location: region:2656075-2802550:1

NP_056110.2
SIO_000068: ncbiprotein

GI:148839305
SIO_000068: ncbigi

CCDS45822.1
SIO_000068: ccds

position:2656075:1
position: 2656075
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2802550:1
position: 2802550
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2656075-2656260:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2666156-2666231:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2666869-2667030:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2673280-2673362:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2674014-2674144:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2688392-2688506:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2688626-2688745:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2694525-2694691:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2697030-2697120:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2697829-2698039:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2700537-2700657:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2700733-2700916:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2703690-2703884:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2705692-2705805:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2706362-2706468:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2707561-2707643:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:2707805-2707918:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:2718156-2718233:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:2718313-2718432:1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:2722517-2722661:1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:2724897-2724993:1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:2726450-2726522:1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:2728455-2728594:1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:2729273-2729407:1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:2732263-2732490:1/exon

urn:…
SIO_000300: 26
SIO_000628: feature:2738395-2738543:1/exon

urn:…
SIO_000300: 27
SIO_000628: feature:2739430-2739518:1/exon

urn:…
SIO_000300: 28
SIO_000628: feature:2740701-2740819:1/exon

urn:…
SIO_000300: 29
SIO_000628: feature:2743759-2743926:1/exon

urn:…
SIO_000300: 30
SIO_000628: feature:2747520-2747645:1/exon

urn:…
SIO_000300: 31
SIO_000628: feature:2750041-2750120:1/exon

urn:…
SIO_000300: 32
SIO_000628: feature:2750348-2750505:1/exon

urn:…
SIO_000300: 33
SIO_000628: feature:2751276-2751391:1/exon

urn:…
SIO_000300: 34
SIO_000628: feature:2752486-2752550:1/exon

urn:…
SIO_000300: 35
SIO_000628: feature:2760650-2760737:1/exon

urn:…
SIO_000300: 36
SIO_000628: feature:2762103-2762234:1/exon

urn:…
SIO_000300: 37
SIO_000628: feature:2763635-2763787:1/exon

urn:…
SIO_000300: 38
SIO_000628: feature:2769692-2769818:1/exon

urn:…
SIO_000300: 39
SIO_000628: feature:2769987-2770106:1/exon

urn:…
SIO_000300: 40
SIO_000628: feature:2771531-2771616:1/exon

urn:…
SIO_000300: 41
SIO_000628: feature:2772248-2772370:1/exon

urn:…
SIO_000300: 42
SIO_000628: feature:2775732-2775922:1/exon

urn:…
SIO_000300: 43
SIO_000628: feature:2777804-2777913:1/exon

urn:…
SIO_000300: 44
SIO_000628: feature:2778167-2778237:1/exon

urn:…
SIO_000300: 45
SIO_000628: feature:2784448-2784619:1/exon

urn:…
SIO_000300: 46
SIO_000628: feature:2795947-2796105:1/exon

urn:…
SIO_000300: 47
SIO_000628: feature:2796405-2796519:1/exon

urn:…
SIO_000300: 48
SIO_000628: feature:2802526-2802550:1/exon

SMCHD1
type: SO_0000234
gene: SMCHD1
product: structural maintenance of chromosomes flexible hinge domain containing 1, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 71 ESTs, 3 Proteins, and 98% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258102.1
so part of: SMCHD1
location: join(2673074..2673193,2673280..2673362,2674014..2674144,2688392..2688506,2688626..2688745,2694525..2694691,2697030..2697120,2697829..2698039,2700537..2700657,2700733..2700916,2703690..2703884,2705692..2705805,2706362..2706468,2707561..2707643,2707805..2707918,2718156..2718233,2718313..2718432,2722517..2722661,2724897..2724993,2726450..2726522,2728455..2728594,2729273..2729407,2732263..2732490,2738395..2738543,2739430..2739518,2740701..2740819,2743759..2743926,2747520..2747645,2750041..2750120,2750348..2750505,2751276..2751391,2752486..2752550,2760650..2760737,2762103..2762234,2763635..2763787,2769692..2769818,2769987..2770106,2771531..2771616,2772248..2772370,2775732..2775922,2777804..2777913,2778167..2778237,2784448..2784619,2795947..2796105,2796405..2796519,2802526..2805015)
location: region:2673074-2805015:1

GI:530424840
SIO_000068: ncbigi

position:2673074:1
position: 2673074
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2673074-2673193:1/exon

position:2673193:1
position: 2673193
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2673280-2673362:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2674014-2674144:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2688392-2688506:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2688626-2688745:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2694525-2694691:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2697030-2697120:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2697829-2698039:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2700537-2700657:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2700733-2700916:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2703690-2703884:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2705692-2705805:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2706362-2706468:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2707561-2707643:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2707805-2707918:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2718156-2718233:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:2718313-2718432:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:2722517-2722661:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:2724897-2724993:1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:2726450-2726522:1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:2728455-2728594:1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:2729273-2729407:1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:2732263-2732490:1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:2738395-2738543:1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:2739430-2739518:1/exon

urn:…
SIO_000300: 26
SIO_000628: feature:2740701-2740819:1/exon

urn:…
SIO_000300: 27
SIO_000628: feature:2743759-2743926:1/exon

urn:…
SIO_000300: 28
SIO_000628: feature:2747520-2747645:1/exon

urn:…
SIO_000300: 29
SIO_000628: feature:2750041-2750120:1/exon

urn:…
SIO_000300: 30
SIO_000628: feature:2750348-2750505:1/exon

urn:…
SIO_000300: 31
SIO_000628: feature:2751276-2751391:1/exon

urn:…
SIO_000300: 32
SIO_000628: feature:2752486-2752550:1/exon

urn:…
SIO_000300: 33
SIO_000628: feature:2760650-2760737:1/exon

urn:…
SIO_000300: 34
SIO_000628: feature:2762103-2762234:1/exon

urn:…
SIO_000300: 35
SIO_000628: feature:2763635-2763787:1/exon

urn:…
SIO_000300: 36
SIO_000628: feature:2769692-2769818:1/exon

urn:…
SIO_000300: 37
SIO_000628: feature:2769987-2770106:1/exon

urn:…
SIO_000300: 38
SIO_000628: feature:2771531-2771616:1/exon

urn:…
SIO_000300: 39
SIO_000628: feature:2772248-2772370:1/exon

urn:…
SIO_000300: 40
SIO_000628: feature:2775732-2775922:1/exon

urn:…
SIO_000300: 41
SIO_000628: feature:2777804-2777913:1/exon

urn:…
SIO_000300: 42
SIO_000628: feature:2778167-2778237:1/exon

urn:…
SIO_000300: 43
SIO_000628: feature:2784448-2784619:1/exon

urn:…
SIO_000300: 44
SIO_000628: feature:2795947-2796105:1/exon

urn:…
SIO_000300: 45
SIO_000628: feature:2796405-2796519:1/exon

urn:…
SIO_000300: 46
SIO_000628: feature:2802526-2805015:1/exon

SMCHD1
type: SO_0000316
gene: SMCHD1
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: structural maintenance of chromosomes flexible hinge domain-containing protein 1 isoform X1
translation: MTSKQLNNWAVYRLSKFTRQGDFESDHSGYVRPVPVPRSLNSDISYFGVGGKQAVFFVGQSARMISKPADSQDVHELVLSKEDFEKKEKNKEAIYSGYIRNRKPSDSVHITNDDERFLHHLIIEEKEKDSFTAVVITGVQPEHIQYLKNYFHLWTRQLAHIYHYYIHGPKGNEIRTSKEVEPFNNIDIEISMFEKGKVPKIVNLREIQDDMQTLYVNTAADSFEFKAHVEGDGVVEGIIRYHPFLYDRETYPDDPCFPSKLKDEDDEDDCFILEKAARGKRPIFECFWNGRLIPYTSVEDFDWCTPPKKRGLAPIECYNRISGALFTNDKFQVSTNKLTFMDLELKLKDKNTLFTRILNGQEQRMKIDREFALWLKDCHEKYDKQIKFTLFKGVITRPDLPSKKQGPWATYAAIEWDGKIYKAGQLVKTIKTLPLFYGSIVRFFLYGDHDGEVYATGGEVQIAMEPQALYDEVRTVPIAKLDRTVAEKAVKKYVEDEMARLPDRLSVTWPEGDELLPNEVRPAGTPIGALRIEILNKKGEAMQKLPGTSHGGSKKLLVELKVILHSSSGNKEIISHISQHGGKWPYWFKKMENIQKLGNYTLKLQVVLNESNADTYAGRPLPSKAIKFSVKEGKPEKFSFGLLDLPFRVGVPFNIPLEFQDEFGHTSQLVTDIQPVLEASGLSLHYEEITKGPNCVIRGVTAKGPVNSCQGKNYNLKVTLPGLKEDSQILKIRLLPGHPRRLKVKPDSEILVIENGTAFPFQVEVLDESDNITAQPKLIVHCKFSGAPNLPVYVVDCSSSGTSILTGSAIQVQNIKKDQTLKARIEIPSCKDVAPVEKTIKLLPSSHVARLQIFSVEGQKAIQIKHQDEVNWIAGDIMHNLIFQMYDEGEREINITSALAEKIKVNWTPEINKEHLLQGLLPDVQVPTSVKDMRYCQVSFQDDHVSLESAFTVRPLPDEPKHLKCEMKGGKTVQMGQELQGEVVIIITDQYGNQIQAFSPSSLSSLSIAGVGLDSSNLKTTFQENTQSISVRGIKFIPGPPGNKDLCFTWREFSDFIRVQLISGPPAKLLLIDWPELKESIPVINGRDLQNPIIVQLCDQWDNPAPVQHVKISLTKASNLKLMPSNQQHKTDEKGRANLGVFSVFAPRGEHTLQVKAIYNKSIIEGPIIKLMILPDPEKPVRLNVKYDKDASFLAGGLFTDFMISVISEDDSIIKNINPARISMKMWKLSTSGNRPPANAETFSCNKIKDNDKEDGCFYFRDKVIPNKVGTYCIQFGFMMDKTNILNSEQVIVEVLPNQPVKLVPKIKPPTPAVSNVRSVASRTLVRDLHLSITDDYDNHTGIDLVGTIIATIKGSNEEDTDTPLFIGKVRTLEFPFVNGSAEIMSLVLAESSPGRDSTEYFIVFEPRLPLLSRTLEPYILPFMFYNDVKKQQQMAALTKEKDQLSQSIVMYKSLFEASQQLLNEMKCQVEEARLKEAQLRNELKIHNIDIPTTQQVPHIEALLKRKLSEQEELKKKPRRSCTLPNYTKGSGDVLGKIAHLAQIEDDRAAMVISWHLASDMDCVVTLTTDAARRIYDETQGRQQVLPLDSIYKKTLPDWKRSLPHFRNGKLYFKPIGDPVFARDLLTFPDNVEHCETVFGMLLGDTIILDNLDAANHYRKEVVKITHCPTLLTRDGDRIRSNGKFGGLQNKAPPMDKLRGMVFGAPVPKQCLILGEQIDLLQQYRSAVCKLDSVNKDLNSQLEYLRTPDMRKKKQELDEHEKNLKLIEEKLGMTPIRKCNDSLRHSPKVETTDCPVPPKRMRREATRQNRIITKTDV
so part of: SMCHD1
location: join(2674071..2674144,2688392..2688506,2688626..2688745,2694525..2694691,2697030..2697120,2697829..2698039,2700537..2700657,2700733..2700916,2703690..2703884,2705692..2705805,2706362..2706468,2707561..2707643,2707805..2707918,2718156..2718233,2718313..2718432,2722517..2722661,2724897..2724993,2726450..2726522,2728455..2728594,2729273..2729407,2732263..2732490,2738395..2738543,2739430..2739518,2740701..2740819,2743759..2743926,2747520..2747645,2750041..2750120,2750348..2750505,2751276..2751391,2752486..2752550,2760650..2760737,2762103..2762234,2763635..2763787,2769692..2769818,2769987..2770106,2771531..2771616,2772248..2772370,2775732..2775922,2777804..2777913,2778167..2778237,2784448..2784619,2795947..2796105,2796405..2796519,2802526..2802550)
location: region:2674071-2802550:1

XP_005258159.1
SIO_000068: ncbiprotein

GI:530424841
SIO_000068: ncbigi

position:2674071:1
position: 2674071
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2674071-2674144:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2688392-2688506:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2688626-2688745:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2694525-2694691:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2697030-2697120:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2697829-2698039:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2700537-2700657:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2700733-2700916:1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2703690-2703884:1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2705692-2705805:1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2706362-2706468:1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2707561-2707643:1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2707805-2707918:1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2718156-2718233:1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2718313-2718432:1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2722517-2722661:1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:2724897-2724993:1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:2726450-2726522:1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:2728455-2728594:1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:2729273-2729407:1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:2732263-2732490:1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:2738395-2738543:1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:2739430-2739518:1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:2740701-2740819:1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:2743759-2743926:1/exon

urn:…
SIO_000300: 26
SIO_000628: feature:2747520-2747645:1/exon

urn:…
SIO_000300: 27
SIO_000628: feature:2750041-2750120:1/exon

urn:…
SIO_000300: 28
SIO_000628: feature:2750348-2750505:1/exon

urn:…
SIO_000300: 29
SIO_000628: feature:2751276-2751391:1/exon

urn:…
SIO_000300: 30
SIO_000628: feature:2752486-2752550:1/exon

urn:…
SIO_000300: 31
SIO_000628: feature:2760650-2760737:1/exon

urn:…
SIO_000300: 32
SIO_000628: feature:2762103-2762234:1/exon

urn:…
SIO_000300: 33
SIO_000628: feature:2763635-2763787:1/exon

urn:…
SIO_000300: 34
SIO_000628: feature:2769692-2769818:1/exon

urn:…
SIO_000300: 35
SIO_000628: feature:2769987-2770106:1/exon

urn:…
SIO_000300: 36
SIO_000628: feature:2771531-2771616:1/exon

urn:…
SIO_000300: 37
SIO_000628: feature:2772248-2772370:1/exon

urn:…
SIO_000300: 38
SIO_000628: feature:2775732-2775922:1/exon

urn:…
SIO_000300: 39
SIO_000628: feature:2777804-2777913:1/exon

urn:…
SIO_000300: 40
SIO_000628: feature:2778167-2778237:1/exon

urn:…
SIO_000300: 41
SIO_000628: feature:2784448-2784619:1/exon

urn:…
SIO_000300: 42
SIO_000628: feature:2795947-2796105:1/exon

urn:…
SIO_000300: 43
SIO_000628: feature:2796405-2796519:1/exon

urn:…
SIO_000300: 44
SIO_000628: feature:2802526-2802550:1/exon

EMILIN2
type: SO_0000704
alternative label: EMILIN-2
alternative label: FOAP-10
gene: EMILIN2
gene synonym: EMILIN-2; FOAP-10
note: elastin microfibril interfacer 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 2846786..2914090
location: region:2846786-2914090:1
SIO_010080: EMILIN2

84034
SIO_000068: ncbigene

19881
SIO_000068: hgnc

608928
SIO_000068: omim

position:2846786:1
position: 2846786
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2914090:1
position: 2914090
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

EMILIN2
type: SO_0000234
alternative label: EMILIN-2
alternative label: FOAP-10
gene: EMILIN2
gene synonym: EMILIN-2; FOAP-10
product: elastin microfibril interfacer 2, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 26 ESTs, 5 Proteins, and 100% coverage by RNAseq alignments, including 4 samples with support for all introns
transcript id: XM_005258154.1
so part of: EMILIN2
location: join(2846786..2846804,2847807..2847929,2884962..2885137,2890559..2892484,2906781..2907083,2908941..2908973,2909689..2909817,2913065..2914085)
location: region:2846786-2914085:1

GI:530424960
SIO_000068: ncbigi

position:2914085:1
position: 2914085
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2846786-2846804:1/exon

position:2846804:1
position: 2846804
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2847807-2847929:1/exon

position:2847807:1
position: 2847807
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2847929:1
position: 2847929
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:2884962-2885137:1/exon

position:2884962:1
position: 2884962
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2885137:1
position: 2885137
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:2890559-2892484:1/exon

position:2890559:1
position: 2890559
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2892484:1
position: 2892484
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:2906781-2907083:1/exon

position:2906781:1
position: 2906781
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2907083:1
position: 2907083
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:2908941-2908973:1/exon

position:2908941:1
position: 2908941
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2908973:1
position: 2908973
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:2909689-2909817:1/exon

position:2909689:1
position: 2909689
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2909817:1
position: 2909817
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:2913065-2914085:1/exon

position:2913065:1
position: 2913065
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

EMILIN2
type: SO_0000316
alternative label: EMILIN-2
alternative label: FOAP-10
gene: EMILIN2
gene synonym: EMILIN-2; FOAP-10
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: EMILIN-2 isoform X1
translation: MLNWCAYIVNKNVSCSVLEGSESFIQAQYNCAWNQMPCPSALVYRVNFRPRYVTRYKTVTQLEWRCCPGFRGGDCQEGPKDPVKTLRPTPARPRNSLKKATDNEPSQFSEPRKTLSPTGTAQPSWGVDPKEGPQELQEKKIQVLEEKVLRLTRTVLDLQSSLAGVSENLKHATQDDASRTRAPGLSSQHPKPDTTVSGDTETGQSPGVFNTKESGMKDIKSELAEVKDTLKNKSDKLEELDGKVKGYEGQLRQLQEAAQGPTVTMTTNELYQAYVDSKIDALREELMEGMDRKLADLKNSCEYKLTGLQQQCDDYGSSYLGVIELIGEKETSLRKEINNLRARLQEPSAQANCCDSEKNGDIGQQIKTLDQKIERVAEATRMLNGRLDNEFDRLIVPEPDVDFDAKWNELDARINVTEKNAEEHCFYIEETLRGAINGEVGDLKQLVDQKIQSLEDRLGSVLLQMTNNTGAELSPPGAAALPGVSGSGDERVMMELNHLKDKVQVVEDICLLNIQGKPHGMEGALPNREDRAVRDSLHLLKSLNDTMHRKFQETEQTIQKLQQDFSFLYSQLNHTENDVTHLQKEMSNCRAGENAGMGRFTKVGEQERTVDTLPSPQHPVAHCCSQLEERWQRLQSQVISELDACKECTQGVQREVSMVEGRVSHMEKTCSKLDSISGNLQRIKEGLNKHVSSLWNCVRQMNGTLRSHSRDISGLKNSVQQFYSHVFQISTDLQDLVKFQPSAKAPSPPPPAEAPKEPLQPEPAPPRPSGPATAEDPGRRPVLPQRPPEERPPQPPGSTGVIAETGQAGPPAGAGVSGRGLPRGVDGQTGSGTVPGAEGFAGAPGYPKSPPVASPGAPVPSLVSFSAGLTQKPFPSDGGVVLFNKVLVNDGDVYNPSTGVFTAPYDGRYLITATLTPERDAYVEAVLSVSNASVAQLHTAGYRREFLEYHRPPGALHTCGGPGAFHLIVHLKAGDAVNVVVTGGKLAHTDFDEMYSTFSGVFLYPFLSHL
so part of: EMILIN2
location: join(2846800..2846804,2847807..2847929,2884962..2885137,2890559..2892484,2906781..2907083,2908941..2908973,2909689..2909817,2913065..2913402)
location: region:2846800-2913402:1

XP_005258211.1
SIO_000068: ncbiprotein

GI:530424961
SIO_000068: ncbigi

position:2846800:1
position: 2846800
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2913402:1
position: 2913402
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2846800-2846804:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2847807-2847929:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2884962-2885137:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2890559-2892484:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2906781-2907083:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2908941-2908973:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2909689-2909817:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2913065-2913402:1/exon

EMILIN2
type: SO_0000234
alternative label: EMILIN-2
alternative label: FOAP-10
gene: EMILIN2
gene synonym: EMILIN-2; FOAP-10
product: elastin microfibril interfacer 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_032048.2
so part of: EMILIN2
location: join(2847028..2847320,2847807..2847929,2884962..2885137,2890559..2892484,2906781..2907083,2908941..2908973,2909689..2909817,2913065..2914090)
location: region:2847028-2914090:1

GI:60498977
SIO_000068: ncbigi

position:2847028:1
position: 2847028
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2847028-2847320:1/exon

position:2847320:1
position: 2847320
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2847807-2847929:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2884962-2885137:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2890559-2892484:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2906781-2907083:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2908941-2908973:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2909689-2909817:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2913065-2914090:1/exon

EMILIN2
type: SO_0000316
alternative label: EMILIN-2
alternative label: FOAP-10
gene: EMILIN2
gene synonym: EMILIN-2; FOAP-10
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: EMILIN-2 precursor
translation: MWQPRRPWPRVPWRWALALLALVGAGLCHAGPQPGYPARPSARNKNWCAYIVNKNVSCSVLEGSESFIQAQYNCAWNQMPCPSALVYRVNFRPRYVTRYKTVTQLEWRCCPGFRGGDCQEGPKDPVKTLRPTPARPRNSLKKATDNEPSQFSEPRKTLSPTGTAQPSWGVDPKEGPQELQEKKIQVLEEKVLRLTRTVLDLQSSLAGVSENLKHATQDDASRTRAPGLSSQHPKPDTTVSGDTETGQSPGVFNTKESGMKDIKSELAEVKDTLKNKSDKLEELDGKVKGYEGQLRQLQEAAQGPTVTMTTNELYQAYVDSKIDALREELMEGMDRKLADLKNSCEYKLTGLQQQCDDYGSSYLGVIELIGEKETSLRKEINNLRARLQEPSAQANCCDSEKNGDIGQQIKTLDQKIERVAEATRMLNGRLDNEFDRLIVPEPDVDFDAKWNELDARINVTEKNAEEHCFYIEETLRGAINGEVGDLKQLVDQKIQSLEDRLGSVLLQMTNNTGAELSPPGAAALPGVSGSGDERVMMELNHLKDKVQVVEDICLLNIQGKPHGMEGALPNREDRAVRDSLHLLKSLNDTMHRKFQETEQTIQKLQQDFSFLYSQLNHTENDVTHLQKEMSNCRAGENAGMGRFTKVGEQERTVDTLPSPQHPVAHCCSQLEERWQRLQSQVISELDACKECTQGVQREVSMVEGRVSHMEKTCSKLDSISGNLQRIKEGLNKHVSSLWNCVRQMNGTLRSHSRDISGLKNSVQQFYSHVFQISTDLQDLVKFQPSAKAPSPPPPAEAPKEPLQPEPAPPRPSGPATAEDPGRRPVLPQRPPEERPPQPPGSTGVIAETGQAGPPAGAGVSGRGLPRGVDGQTGSGTVPGAEGFAGAPGYPKSPPVASPGAPVPSLVSFSAGLTQKPFPSDGGVVLFNKVLVNDGDVYNPSTGVFTAPYDGRYLITATLTPERDAYVEAVLSVSNASVAQLHTAGYRREFLEYHRPPGALHTCGGPGAFHLIVHLKAGDAVNVVVTGGKLAHTDFDEMYSTFSGVFLYPFLSHL
so part of: EMILIN2
location: join(2847187..2847320,2847807..2847929,2884962..2885137,2890559..2892484,2906781..2907083,2908941..2908973,2909689..2909817,2913065..2913402)
location: region:2847187-2913402:1

NP_114437.2
SIO_000068: ncbiprotein

GI:60498978
SIO_000068: ncbigi

CCDS11828.1
SIO_000068: ccds

position:2847187:1
position: 2847187
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2847187-2847320:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2847807-2847929:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2884962-2885137:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2890559-2892484:1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2906781-2907083:1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2908941-2908973:1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2909689-2909817:1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2913065-2913402:1/exon

LPIN2
type: SO_0000704
gene: LPIN2
note: lipin 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(2916992..3013313)
location: region:2916992-3013313:-1
SIO_010080: LPIN2

9663
SIO_000068: ncbigene

14450
SIO_000068: hgnc

16114
SIO_000068: hprd

605519
SIO_000068: omim

position:2916992:-1
position: 2916992
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3013313:-1
position: 3013313
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LPIN2
type: SO_0000234
gene: LPIN2
product: lipin 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_014646.2
so part of: LPIN2
location: complement(join(2916992..2920435,2920776..2920879,2921531..2921645,2922045..2922197,2923773..2923859,2924396..2924544,2925222..2925366,2926721..2926803,2927720..2927809,2928589..2928658,2929063..2929156,2931254..2931441,2934349..2934448,2937690..2938035,2939478..2939601,2940603..2940710,2951053..2951354,2954502..2954597,2960647..2960847,3011716..3011945))
location: region:2916992-3011945:-1

GI:22027649
SIO_000068: ncbigi

position:3011945:-1
position: 3011945
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3011716-3011945:-1/exon

position:3011716:-1
position: 3011716
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2960647-2960847:-1/exon

position:2960647:-1
position: 2960647
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2960847:-1
position: 2960847
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:2954502-2954597:-1/exon

position:2954502:-1
position: 2954502
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2954597:-1
position: 2954597
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:2951053-2951354:-1/exon

position:2951053:-1
position: 2951053
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2951354:-1
position: 2951354
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:2940603-2940710:-1/exon

position:2940603:-1
position: 2940603
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2940710:-1
position: 2940710
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:2939478-2939601:-1/exon

position:2939478:-1
position: 2939478
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2939601:-1
position: 2939601
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:2937690-2938035:-1/exon

position:2937690:-1
position: 2937690
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2938035:-1
position: 2938035
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:2934349-2934448:-1/exon

position:2934349:-1
position: 2934349
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2934448:-1
position: 2934448
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:2931254-2931441:-1/exon

position:2931254:-1
position: 2931254
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2931441:-1
position: 2931441
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:2929063-2929156:-1/exon

position:2929063:-1
position: 2929063
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2929156:-1
position: 2929156
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:2928589-2928658:-1/exon

position:2928589:-1
position: 2928589
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2928658:-1
position: 2928658
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:2927720-2927809:-1/exon

position:2927720:-1
position: 2927720
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2927809:-1
position: 2927809
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:2926721-2926803:-1/exon

position:2926721:-1
position: 2926721
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2926803:-1
position: 2926803
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:2925222-2925366:-1/exon

position:2925222:-1
position: 2925222
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2925366:-1
position: 2925366
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:2924396-2924544:-1/exon

position:2924396:-1
position: 2924396
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2924544:-1
position: 2924544
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:2923773-2923859:-1/exon

position:2923773:-1
position: 2923773
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2923859:-1
position: 2923859
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 17
SIO_000628: feature:2922045-2922197:-1/exon

position:2922045:-1
position: 2922045
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2922197:-1
position: 2922197
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 18
SIO_000628: feature:2921531-2921645:-1/exon

position:2921531:-1
position: 2921531
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2921645:-1
position: 2921645
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 19
SIO_000628: feature:2920776-2920879:-1/exon

position:2920776:-1
position: 2920776
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2920879:-1
position: 2920879
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 20
SIO_000628: feature:2916992-2920435:-1/exon

position:2920435:-1
position: 2920435
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LPIN2
type: SO_0000234
gene: LPIN2
product: lipin 2, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 64 ESTs, 19 Proteins, and 97% coverage by RNAseq alignments, including 6 samples with support for all introns
transcript id: XM_005258178.1
so part of: LPIN2
location: complement(join(2916997..2920435,2920776..2920879,2921531..2921645,2922045..2922197,2923773..2923859,2924396..2924544,2925222..2925366,2926721..2926803,2927720..2927809,2928589..2928658,2929063..2929156,2931254..2931441,2934349..2934448,2937690..2938035,2939478..2939601,2940603..2940710,2951053..2951354,2954502..2954597,2960647..2960847,3013085..3013313))
location: region:2916997-3013313:-1

GI:530425008
SIO_000068: ncbigi

position:2916997:-1
position: 2916997
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3013085-3013313:-1/exon

position:3013085:-1
position: 3013085
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2960647-2960847:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2954502-2954597:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2951053-2951354:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2940603-2940710:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2939478-2939601:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2937690-2938035:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2934349-2934448:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2931254-2931441:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2929063-2929156:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2928589-2928658:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2927720-2927809:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2926721-2926803:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2925222-2925366:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2924396-2924544:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2923773-2923859:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:2922045-2922197:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:2921531-2921645:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:2920776-2920879:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:2916997-2920435:-1/exon

LPIN2
type: SO_0000234
gene: LPIN2
product: lipin 2, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 61 ESTs, 19 Proteins, and 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258179.1
so part of: LPIN2
location: complement(join(2916997..2920435,2920776..2920879,2921531..2921645,2922045..2922197,2923773..2923859,2924396..2924544,2925222..2925366,2926721..2926803,2927720..2927809,2928589..2928658,2929063..2929156,2931254..2931441,2934349..2934448,2937690..2938035,2939478..2939601,2940603..2940710,2951053..2951354,2954502..2954597,2960647..2960847,3013035..3013158))
location: region:2916997-3013158:-1

GI:530425010
SIO_000068: ncbigi

position:3013158:-1
position: 3013158
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3013035-3013158:-1/exon

position:3013035:-1
position: 3013035
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2960647-2960847:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2954502-2954597:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2951053-2951354:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2940603-2940710:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2939478-2939601:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2937690-2938035:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2934349-2934448:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2931254-2931441:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2929063-2929156:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2928589-2928658:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2927720-2927809:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2926721-2926803:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2925222-2925366:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2924396-2924544:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2923773-2923859:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:2922045-2922197:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:2921531-2921645:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:2920776-2920879:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:2916997-2920435:-1/exon

LPIN2
type: SO_0000234
gene: LPIN2
product: lipin 2, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 61 ESTs, 19 Proteins, and 99% coverage by RNAseq alignments, including 6 samples with support for all introns
transcript id: XM_005258177.1
so part of: LPIN2
location: complement(join(2916997..2920435,2920776..2920879,2921531..2921645,2922045..2922197,2923773..2923859,2924396..2924544,2925222..2925366,2926721..2926803,2927720..2927809,2928589..2928658,2929063..2929156,2931254..2931441,2934349..2934448,2937690..2938035,2939478..2939601,2940603..2940710,2951053..2951354,2954502..2954597,2960647..2960847,2982666..2982896))
location: region:2916997-2982896:-1

GI:530425006
SIO_000068: ncbigi

position:2982896:-1
position: 2982896
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2982666-2982896:-1/exon

position:2982666:-1
position: 2982666
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:2960647-2960847:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2954502-2954597:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2951053-2951354:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2940603-2940710:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2939478-2939601:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2937690-2938035:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2934349-2934448:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2931254-2931441:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2929063-2929156:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2928589-2928658:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2927720-2927809:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2926721-2926803:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2925222-2925366:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2924396-2924544:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2923773-2923859:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:2922045-2922197:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:2921531-2921645:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:2920776-2920879:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:2916997-2920435:-1/exon

LPIN2
type: SO_0000316
gene: LPIN2
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: phosphatidate phosphatase LPIN2 isoform X1
translation: MFYLEDDKEDEVVCKGSLSKTQDVYHDKSPPGILSQTMNYVGQLAGQVIVTVKELYKGINQATLSGCIDVIVVQQQDGSYQCSPFHVRFGKLGVLRSKEKVIDIEINGSAVDLHMKLGDNGEAFFVEETEEEYEKLPAYLATSPIPTEDQFFKDIDTPLVKSGGDETPSQSSDISHVLETETIFTPSSVKKKKRRRKKYKQDSKKEEQAASAAAEDTCDVGVSSDDDKGAQAARGSSNASLKEEECKEPLLFHSGDHYPLSDGDWSPLETTYPQTACPKSDSELEVKPAESLLRSESHMEWTWGGFPESTKVSKRERSDHHPRTATITPSENTHFRVIPSEDNLISEVEKDASMEDTVCTIVKPKPRALGTQMSDPTSVAELLEPPLESTQISSMLDADHLPNAALAEAPSESKPAAKVDSPSKKKGVHKRSQHQGPDDIYLDDLKGLEPEVAALYFPKSESEPGSRQWPESDTLSGSQSPQSVGSAAADSGTECLSDSAMDLPDVTLSLCGGLSENGEISKEKFMEHIITYHEFAENPGLIDNPNLVIRIYNRYYNWALAAPMILSLQVFQKSLPKATVESWVKDKMPKKSGRWWFWRKRESMTKQLPESKEGKSEAPPASDLPSSSKEPAGARPAENDSSSDEGSQELEESITVDPIPTEPLSHGSTTSYKKSLRLSSDQIAKLKLHDGPNDVVFSITTQYQGTCRCAGTIYLWNWNDKIIISDIDGTITKSDALGQILPQLGKDWTHQGIAKLYHSINENGYKFLYCSARAIGMADMTRGYLHWVNDKGTILPRGPLMLSPSSLFSAFHREVIEKKPEKFKIECLNDIKNLFAPSKQPFYAAFGNRPNDVYAYTQVGVPDCRIFTVNPKGELIQERTKGNKSSYHRLSELVEHVFPLLSKEQNSAFPCPEFSSFCYWRDPIPEVDLDDLS
so part of: LPIN2
location: complement(join(2920291..2920435,2920776..2920879,2921531..2921645,2922045..2922197,2923773..2923859,2924396..2924544,2925222..2925366,2926721..2926803,2927720..2927809,2928589..2928658,2929063..2929156,2931254..2931441,2934349..2934448,2937690..2938035,2939478..2939601,2940603..2940710,2951053..2951354,2954502..2954597,2960647..2960847,2982666..2982767))
location: region:2920291-2982767:-1

XP_005258234.1
SIO_000068: ncbiprotein

GI:530425007
SIO_000068: ncbigi

position:2920291:-1
position: 2920291
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2982767:-1
position: 2982767
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2982666-2982767:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2960647-2960847:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2954502-2954597:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2951053-2951354:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2940603-2940710:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2939478-2939601:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2937690-2938035:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2934349-2934448:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2931254-2931441:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2929063-2929156:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2928589-2928658:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2927720-2927809:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2926721-2926803:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2925222-2925366:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2924396-2924544:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2923773-2923859:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:2922045-2922197:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:2921531-2921645:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:2920776-2920879:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:2920291-2920435:-1/exon

LPIN2
type: SO_0000316
gene: LPIN2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: phosphatidate phosphatase LPIN2
translation: MNYVGQLAGQVIVTVKELYKGINQATLSGCIDVIVVQQQDGSYQCSPFHVRFGKLGVLRSKEKVIDIEINGSAVDLHMKLGDNGEAFFVEETEEEYEKLPAYLATSPIPTEDQFFKDIDTPLVKSGGDETPSQSSDISHVLETETIFTPSSVKKKKRRRKKYKQDSKKEEQAASAAAEDTCDVGVSSDDDKGAQAARGSSNASLKEEECKEPLLFHSGDHYPLSDGDWSPLETTYPQTACPKSDSELEVKPAESLLRSESHMEWTWGGFPESTKVSKRERSDHHPRTATITPSENTHFRVIPSEDNLISEVEKDASMEDTVCTIVKPKPRALGTQMSDPTSVAELLEPPLESTQISSMLDADHLPNAALAEAPSESKPAAKVDSPSKKKGVHKRSQHQGPDDIYLDDLKGLEPEVAALYFPKSESEPGSRQWPESDTLSGSQSPQSVGSAAADSGTECLSDSAMDLPDVTLSLCGGLSENGEISKEKFMEHIITYHEFAENPGLIDNPNLVIRIYNRYYNWALAAPMILSLQVFQKSLPKATVESWVKDKMPKKSGRWWFWRKRESMTKQLPESKEGKSEAPPASDLPSSSKEPAGARPAENDSSSDEGSQELEESITVDPIPTEPLSHGSTTSYKKSLRLSSDQIAKLKLHDGPNDVVFSITTQYQGTCRCAGTIYLWNWNDKIIISDIDGTITKSDALGQILPQLGKDWTHQGIAKLYHSINENGYKFLYCSARAIGMADMTRGYLHWVNDKGTILPRGPLMLSPSSLFSAFHREVIEKKPEKFKIECLNDIKNLFAPSKQPFYAAFGNRPNDVYAYTQVGVPDCRIFTVNPKGELIQERTKGNKSSYHRLSELVEHVFPLLSKEQNSAFPCPEFSSFCYWRDPIPEVDLDDLS
so part of: LPIN2
location: complement(join(2920291..2920435,2920776..2920879,2921531..2921645,2922045..2922197,2923773..2923859,2924396..2924544,2925222..2925366,2926721..2926803,2927720..2927809,2928589..2928658,2929063..2929156,2931254..2931441,2934349..2934448,2937690..2938035,2939478..2939601,2940603..2940710,2951053..2951354,2954502..2954597,2960647..2960838))
location: region:2920291-2960838:-1

NP_055461.1
SIO_000068: ncbiprotein

GI:7662022
SIO_000068: ncbigi

CCDS11829.1
SIO_000068: ccds

position:2960838:-1
position: 2960838
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:2960647-2960838:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2954502-2954597:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2951053-2951354:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2940603-2940710:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2939478-2939601:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2937690-2938035:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2934349-2934448:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2931254-2931441:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2929063-2929156:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2928589-2928658:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2927720-2927809:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2926721-2926803:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2925222-2925366:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2924396-2924544:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2923773-2923859:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2922045-2922197:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:2921531-2921645:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:2920776-2920879:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:2920291-2920435:-1/exon

LPIN2
type: SO_0000316
gene: LPIN2
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: phosphatidate phosphatase LPIN2 isoform X2
translation: MNYVGQLAGQVIVTVKELYKGINQATLSGCIDVIVVQQQDGSYQCSPFHVRFGKLGVLRSKEKVIDIEINGSAVDLHMKLGDNGEAFFVEETEEEYEKLPAYLATSPIPTEDQFFKDIDTPLVKSGGDETPSQSSDISHVLETETIFTPSSVKKKKRRRKKYKQDSKKEEQAASAAAEDTCDVGVSSDDDKGAQAARGSSNASLKEEECKEPLLFHSGDHYPLSDGDWSPLETTYPQTACPKSDSELEVKPAESLLRSESHMEWTWGGFPESTKVSKRERSDHHPRTATITPSENTHFRVIPSEDNLISEVEKDASMEDTVCTIVKPKPRALGTQMSDPTSVAELLEPPLESTQISSMLDADHLPNAALAEAPSESKPAAKVDSPSKKKGVHKRSQHQGPDDIYLDDLKGLEPEVAALYFPKSESEPGSRQWPESDTLSGSQSPQSVGSAAADSGTECLSDSAMDLPDVTLSLCGGLSENGEISKEKFMEHIITYHEFAENPGLIDNPNLVIRIYNRYYNWALAAPMILSLQVFQKSLPKATVESWVKDKMPKKSGRWWFWRKRESMTKQLPESKEGKSEAPPASDLPSSSKEPAGARPAENDSSSDEGSQELEESITVDPIPTEPLSHGSTTSYKKSLRLSSDQIAKLKLHDGPNDVVFSITTQYQGTCRCAGTIYLWNWNDKIIISDIDGTITKSDALGQILPQLGKDWTHQGIAKLYHSINENGYKFLYCSARAIGMADMTRGYLHWVNDKGTILPRGPLMLSPSSLFSAFHREVIEKKPEKFKIECLNDIKNLFAPSKQPFYAAFGNRPNDVYAYTQVGVPDCRIFTVNPKGELIQERTKGNKSSYHRLSELVEHVFPLLSKEQNSAFPCPEFSSFCYWRDPIPEVDLDDLS
so part of: LPIN2
location: complement(join(2920291..2920435,2920776..2920879,2921531..2921645,2922045..2922197,2923773..2923859,2924396..2924544,2925222..2925366,2926721..2926803,2927720..2927809,2928589..2928658,2929063..2929156,2931254..2931441,2934349..2934448,2937690..2938035,2939478..2939601,2940603..2940710,2951053..2951354,2954502..2954597,2960647..2960838))
location: region:2920291-2960838:-1

XP_005258235.1
SIO_000068: ncbiprotein

GI:530425009
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:2960647-2960838:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2954502-2954597:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2951053-2951354:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2940603-2940710:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2939478-2939601:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2937690-2938035:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2934349-2934448:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2931254-2931441:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2929063-2929156:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2928589-2928658:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2927720-2927809:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2926721-2926803:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2925222-2925366:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2924396-2924544:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2923773-2923859:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2922045-2922197:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:2921531-2921645:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:2920776-2920879:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:2920291-2920435:-1/exon

LPIN2
type: SO_0000316
gene: LPIN2
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: phosphatidate phosphatase LPIN2 isoform X3
translation: MNYVGQLAGQVIVTVKELYKGINQATLSGCIDVIVVQQQDGSYQCSPFHVRFGKLGVLRSKEKVIDIEINGSAVDLHMKLGDNGEAFFVEETEEEYEKLPAYLATSPIPTEDQFFKDIDTPLVKSGGDETPSQSSDISHVLETETIFTPSSVKKKKRRRKKYKQDSKKEEQAASAAAEDTCDVGVSSDDDKGAQAARGSSNASLKEEECKEPLLFHSGDHYPLSDGDWSPLETTYPQTACPKSDSELEVKPAESLLRSESHMEWTWGGFPESTKVSKRERSDHHPRTATITPSENTHFRVIPSEDNLISEVEKDASMEDTVCTIVKPKPRALGTQMSDPTSVAELLEPPLESTQISSMLDADHLPNAALAEAPSESKPAAKVDSPSKKKGVHKRSQHQGPDDIYLDDLKGLEPEVAALYFPKSESEPGSRQWPESDTLSGSQSPQSVGSAAADSGTECLSDSAMDLPDVTLSLCGGLSENGEISKEKFMEHIITYHEFAENPGLIDNPNLVIRIYNRYYNWALAAPMILSLQVFQKSLPKATVESWVKDKMPKKSGRWWFWRKRESMTKQLPESKEGKSEAPPASDLPSSSKEPAGARPAENDSSSDEGSQELEESITVDPIPTEPLSHGSTTSYKKSLRLSSDQIAKLKLHDGPNDVVFSITTQYQGTCRCAGTIYLWNWNDKIIISDIDGTITKSDALGQILPQLGKDWTHQGIAKLYHSINENGYKFLYCSARAIGMADMTRGYLHWVNDKGTILPRGPLMLSPSSLFSAFHREVIEKKPEKFKIECLNDIKNLFAPSKQPFYAAFGNRPNDVYAYTQVGVPDCRIFTVNPKGELIQERTKGNKSSYHRLSELVEHVFPLLSKEQNSAFPCPEFSSFCYWRDPIPEVDLDDLS
so part of: LPIN2
location: complement(join(2920291..2920435,2920776..2920879,2921531..2921645,2922045..2922197,2923773..2923859,2924396..2924544,2925222..2925366,2926721..2926803,2927720..2927809,2928589..2928658,2929063..2929156,2931254..2931441,2934349..2934448,2937690..2938035,2939478..2939601,2940603..2940710,2951053..2951354,2954502..2954597,2960647..2960838))
location: region:2920291-2960838:-1

XP_005258236.1
SIO_000068: ncbiprotein

GI:530425011
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:2960647-2960838:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2954502-2954597:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2951053-2951354:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2940603-2940710:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2939478-2939601:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2937690-2938035:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2934349-2934448:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2931254-2931441:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2929063-2929156:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2928589-2928658:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2927720-2927809:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2926721-2926803:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:2925222-2925366:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:2924396-2924544:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:2923773-2923859:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:2922045-2922197:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:2921531-2921645:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:2920776-2920879:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:2920291-2920435:-1/exon

LPIN2
type: SO_0000673
gene: LPIN2
product: lipin 2, transcript variant X4
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 9 Proteins, and 98% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XR_243814.1
so part of: LPIN2
location: complement(join(2926721..2926803,2927720..2927809,2929063..2929156,2931254..2931441,2934349..2934448,2937690..2938035,2939478..2939601,2940603..2940710,2951053..2951354,2954502..2954597,2960647..2960847,2982666..2982896))
location: region:2926721-2982896:-1

GI:530425012
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:2982666-2982896:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:2960647-2960847:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:2954502-2954597:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:2951053-2951354:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:2940603-2940710:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:2939478-2939601:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:2937690-2938035:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:2934349-2934448:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:2931254-2931441:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:2929063-2929156:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:2927720-2927809:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:2926721-2926803:-1/exon

LOC727896
type: SO_0000704
gene: LOC727896
note: cysteine and histidine-rich domain (CHORD) containing 1 pseudogene; Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(2943210..2946621)
location: region:2943210-2946621:-1
SIO_010080: LOC727896

727896
SIO_000068: ncbigene

position:2943210:-1
position: 2943210
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:2946621:-1
position: 2946621
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC727896
type: SO_0000673
gene: LOC727896
product: cysteine and histidine-rich domain (CHORD) containing 1 pseudogene
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
pseudo: true
transcript id: NR_026659.1
so part of: LOC727896
location: complement(2943210..2946621)
location: region:2943210-2946621:-1

GI:221219005
SIO_000068: ncbigi

LOC100310848
type: SO_0000704
gene: LOC100310848
note: small nuclear ribonucleoprotein polypeptide C pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 2990648..2991310
location: region:2990648-2991310:1

100310848
SIO_000068: ncbigene

position:2990648:1
position: 2990648
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:2991310:1
position: 2991310
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MYOM1
type: SO_0000704
alternative label: SKELEMIN
gene: MYOM1
gene synonym: SKELEMIN
note: myomesin 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(3066805..3220106)
location: region:3066805-3220106:-1
SIO_010080: MYOM1

8736
SIO_000068: ncbigene

7613
SIO_000068: hgnc

603508
SIO_000068: omim

position:3066805:-1
position: 3066805
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3220106:-1
position: 3220106
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MYOM1
type: SO_0000234
alternative label: SKELEMIN
gene: MYOM1
gene synonym: SKELEMIN
product: myomesin 1, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_019856.1
so part of: MYOM1
location: complement(join(3066805..3067553,3071832..3071887,3075452..3075474,3075723..3075759,3079177..3079340,3083787..3083892,3083987..3084025,3085043..3085130,3086036..3086149,3089172..3089239,3089535..3089594,3090656..3090800,3094168..3094304,3100157..3100201,3100318..3100424,3102472..3102628,3112296..3112410,3116329..3116513,3119867..3119993,3126699..3126895,3131373..3131494,3134648..3134822,3135545..3135728,3141937..3142061,3149143..3149199,3151692..3151891,3154945..3155086,3164276..3164437,3168815..3168979,3173936..3173998,3174118..3174206,3176040..3176132,3187478..3187635,3188746..3189085,3193816..3193956,3214932..3215249,3219801..3220106))
location: region:3066805-3220106:-1

GI:140560916
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3219801-3220106:-1/exon

position:3219801:-1
position: 3219801
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3214932-3215249:-1/exon

position:3214932:-1
position: 3214932
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3215249:-1
position: 3215249
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3193816-3193956:-1/exon

position:3193816:-1
position: 3193816
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3193956:-1
position: 3193956
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:3188746-3189085:-1/exon

position:3188746:-1
position: 3188746
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3189085:-1
position: 3189085
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:3187478-3187635:-1/exon

position:3187478:-1
position: 3187478
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3187635:-1
position: 3187635
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:3176040-3176132:-1/exon

position:3176040:-1
position: 3176040
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3176132:-1
position: 3176132
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:3174118-3174206:-1/exon

position:3174118:-1
position: 3174118
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3174206:-1
position: 3174206
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:3173936-3173998:-1/exon

position:3173936:-1
position: 3173936
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3173998:-1
position: 3173998
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:3168815-3168979:-1/exon

position:3168815:-1
position: 3168815
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3168979:-1
position: 3168979
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:3164276-3164437:-1/exon

position:3164276:-1
position: 3164276
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3164437:-1
position: 3164437
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:3154945-3155086:-1/exon

position:3154945:-1
position: 3154945
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3155086:-1
position: 3155086
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:3151692-3151891:-1/exon

position:3151692:-1
position: 3151692
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3151891:-1
position: 3151891
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:3149143-3149199:-1/exon

position:3149143:-1
position: 3149143
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3149199:-1
position: 3149199
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:3141937-3142061:-1/exon

position:3141937:-1
position: 3141937
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3142061:-1
position: 3142061
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:3135545-3135728:-1/exon

position:3135545:-1
position: 3135545
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3135728:-1
position: 3135728
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:3134648-3134822:-1/exon

position:3134648:-1
position: 3134648
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3134822:-1
position: 3134822
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 17
SIO_000628: feature:3131373-3131494:-1/exon

position:3131373:-1
position: 3131373
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3131494:-1
position: 3131494
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 18
SIO_000628: feature:3126699-3126895:-1/exon

position:3126699:-1
position: 3126699
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3126895:-1
position: 3126895
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 19
SIO_000628: feature:3119867-3119993:-1/exon

position:3119867:-1
position: 3119867
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3119993:-1
position: 3119993
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 20
SIO_000628: feature:3116329-3116513:-1/exon

position:3116329:-1
position: 3116329
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3116513:-1
position: 3116513
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 21
SIO_000628: feature:3112296-3112410:-1/exon

position:3112296:-1
position: 3112296
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3112410:-1
position: 3112410
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 22
SIO_000628: feature:3102472-3102628:-1/exon

position:3102472:-1
position: 3102472
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3102628:-1
position: 3102628
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 23
SIO_000628: feature:3100318-3100424:-1/exon

position:3100318:-1
position: 3100318
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3100424:-1
position: 3100424
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 24
SIO_000628: feature:3100157-3100201:-1/exon

position:3100157:-1
position: 3100157
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3100201:-1
position: 3100201
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 25
SIO_000628: feature:3094168-3094304:-1/exon

position:3094168:-1
position: 3094168
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3094304:-1
position: 3094304
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 26
SIO_000628: feature:3090656-3090800:-1/exon

position:3090656:-1
position: 3090656
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3090800:-1
position: 3090800
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 27
SIO_000628: feature:3089535-3089594:-1/exon

position:3089535:-1
position: 3089535
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3089594:-1
position: 3089594
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 28
SIO_000628: feature:3089172-3089239:-1/exon

position:3089172:-1
position: 3089172
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3089239:-1
position: 3089239
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 29
SIO_000628: feature:3086036-3086149:-1/exon

position:3086036:-1
position: 3086036
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3086149:-1
position: 3086149
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 30
SIO_000628: feature:3085043-3085130:-1/exon

position:3085043:-1
position: 3085043
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3085130:-1
position: 3085130
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 31
SIO_000628: feature:3083987-3084025:-1/exon

position:3083987:-1
position: 3083987
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3084025:-1
position: 3084025
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 32
SIO_000628: feature:3083787-3083892:-1/exon

position:3083787:-1
position: 3083787
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3083892:-1
position: 3083892
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 33
SIO_000628: feature:3079177-3079340:-1/exon

position:3079177:-1
position: 3079177
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3079340:-1
position: 3079340
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 34
SIO_000628: feature:3075723-3075759:-1/exon

position:3075723:-1
position: 3075723
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3075759:-1
position: 3075759
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 35
SIO_000628: feature:3075452-3075474:-1/exon

position:3075452:-1
position: 3075452
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3075474:-1
position: 3075474
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 36
SIO_000628: feature:3071832-3071887:-1/exon

position:3071832:-1
position: 3071832
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3071887:-1
position: 3071887
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 37
SIO_000628: feature:3066805-3067553:-1/exon

position:3067553:-1
position: 3067553
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

MYOM1
type: SO_0000234
alternative label: SKELEMIN
gene: MYOM1
gene synonym: SKELEMIN
product: myomesin 1, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_003803.3
so part of: MYOM1
location: complement(join(3066805..3067553,3071832..3071887,3075452..3075474,3075723..3075759,3079177..3079340,3083787..3083892,3083987..3084025,3085043..3085130,3086036..3086149,3089172..3089239,3089535..3089594,3090656..3090800,3094168..3094304,3100157..3100201,3100318..3100424,3102472..3102628,3112296..3112410,3116329..3116513,3119867..3119993,3126699..3126895,3129230..3129517,3131373..3131494,3134648..3134822,3135545..3135728,3141937..3142061,3149143..3149199,3151692..3151891,3154945..3155086,3164276..3164437,3168815..3168979,3173936..3173998,3174118..3174206,3176040..3176132,3187478..3187635,3188746..3189085,3193816..3193956,3214932..3215249,3219801..3220106))
location: region:3066805-3220106:-1

GI:140560918
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3219801-3220106:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3214932-3215249:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3193816-3193956:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3188746-3189085:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3187478-3187635:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3176040-3176132:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3174118-3174206:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3173936-3173998:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3168815-3168979:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3164276-3164437:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3154945-3155086:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:3151692-3151891:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:3149143-3149199:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:3141937-3142061:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:3135545-3135728:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:3134648-3134822:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:3131373-3131494:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:3129230-3129517:-1/exon

position:3129230:-1
position: 3129230
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3129517:-1
position: 3129517
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 19
SIO_000628: feature:3126699-3126895:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:3119867-3119993:-1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:3116329-3116513:-1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:3112296-3112410:-1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:3102472-3102628:-1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:3100318-3100424:-1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:3100157-3100201:-1/exon

urn:…
SIO_000300: 26
SIO_000628: feature:3094168-3094304:-1/exon

urn:…
SIO_000300: 27
SIO_000628: feature:3090656-3090800:-1/exon

urn:…
SIO_000300: 28
SIO_000628: feature:3089535-3089594:-1/exon

urn:…
SIO_000300: 29
SIO_000628: feature:3089172-3089239:-1/exon

urn:…
SIO_000300: 30
SIO_000628: feature:3086036-3086149:-1/exon

urn:…
SIO_000300: 31
SIO_000628: feature:3085043-3085130:-1/exon

urn:…
SIO_000300: 32
SIO_000628: feature:3083987-3084025:-1/exon

urn:…
SIO_000300: 33
SIO_000628: feature:3083787-3083892:-1/exon

urn:…
SIO_000300: 34
SIO_000628: feature:3079177-3079340:-1/exon

urn:…
SIO_000300: 35
SIO_000628: feature:3075723-3075759:-1/exon

urn:…
SIO_000300: 36
SIO_000628: feature:3075452-3075474:-1/exon

urn:…
SIO_000300: 37
SIO_000628: feature:3071832-3071887:-1/exon

urn:…
SIO_000300: 38
SIO_000628: feature:3066805-3067553:-1/exon

MYOM1
type: SO_0000316
alternative label: SKELEMIN
gene: MYOM1
gene synonym: SKELEMIN
note: isoform b is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: myomesin-1 isoform b
translation: MSLPFYQRCHQHYDLSYRNKDVRSTVSHYQREKKRSAVYTQGSTAYSSRSSAAHRRESEAFRRASASSSQQQASQHALSSEVSRKAASAYDYGSSHGLTDSSLLLDDYSSKLSPKPKRAKHSLLSGEEKENLPSDYMVPIFSGRQKHVSGITDTEEERIKEAAAYIAQRNLLASEEGITTSKQSTASKQTTASKQSTASKQSTASKQSTASRQSTASRQSVVSKQATSALQQEETSEKKSRKVVIREKAERLSLRKTLEETETYHAKLNEDHLLHAPEFIIKPRSHTVWEKENVKLHCSIAGWPEPRVTWYKNQVPINVHANPGKYIIESRYGMHTLEINGCDFEDTAQYRASAMNVKGELSAYASVVVKRYKGEFDETRFHAGASTMPLSFGVTPYGYASRFEIHFDDKFDVSFGREGETMSLGCRVVITPEIKHFQPEIQWYRNGVPLSPSKWVQTLWSGERATLTFSHLNKEDEGLYTIRVRMGEYYEQYSAYVFVRDADAEIEGAPAAPLDVKCLEANKDYIIISWKQPAVDGGSPILGYFIDKCEVGTDSWSQCNDTPVKFARFPVTGLIEGRSYIFRVRAVNKMGIGFPSRVSEPVAALDPAEKARLKSRPSAPWTGQIIVTEEEPSEGIVPGPPTDLSVTEATRSYVVLSWKPPGQRGHEGIMYFVEKCEAGTENWQRVNTELPVKSPRFALFDLAEGKSYCFRVRCSNSAGVGEPSEATEVTVVGDKLDIPKAPGKIIPSRNTDTSVVVSWEESKDAKELVGYYIEASVAGSGKWEPCNNNPVKGSRFTCHGLVTGQSYIFRVRAVNAAGLSEYSQDSEAIEVKAAIAPPSPPCDITCLESFRDSMVLGWKQPDKIGGAEITGYYVNYREVIDGVPGKWREANVKAVSEEAYKISNLKENMVYQFQVAAMNMAGLGAPSAVSECFKCEEWTIAVPGPPHSLKCSEVRKDSLVLQWKPPVHSGRTPVTGYFVDLKEAKAKEDQWRGLNEAAIKNVYLKVRGLKEGVSYVFRVRAINQAGVGKPSDLAGPVVAETRPGTKEVVVNVDDDGVISLNFECDKMTPKSEFSWSKDYVSTEDSPRLEVESKGNKTKMTFKDLGMDDLGIYSCDVTDTDGIASSYLIDEEELKRLLALSHEHKFPTVPVKSELAVEILEKGQVRFWMQAEKLSGNAKVNYIFNEKEIFEGPKYKMHIDRNTGIIEMFMEKLQDEDEGTYTFQLQDGKATNHSTVVLVGDVFKKLQKEAEFQRQEWIRKQGPHFVEYLSWEVTGECNVLLKCKVANIKKETHIVWYKDEREISVDEKHDFKDGICTLLITEFSKKDAGIYEVILKDDRGKDKSRLKLVDEAFKELMMEVCKKIALSATDLKIQSTAEGIQLYSFVTYYVEDLKVNWSHNGSAIRYSDRVKTGVTGEQIWLQINEPTPNDKGKYVMELFDGKTGHQKTVDLSGQAYDEAYAEFQRLKQAAIAEKNRARVLGGLPDVVTIQEGKALNLTCNVWGDPPPEVSWLKNEKALASDDHCNLKFEAGRTAYFTINGVSTADSGKYGLVVKNKYGSETSDFTVSVFIPEEEARMAALESLKGGKKAK
so part of: MYOM1
location: complement(join(3067260..3067553,3071832..3071887,3075452..3075474,3075723..3075759,3079177..3079340,3083787..3083892,3083987..3084025,3085043..3085130,3086036..3086149,3089172..3089239,3089535..3089594,3090656..3090800,3094168..3094304,3100157..3100201,3100318..3100424,3102472..3102628,3112296..3112410,3116329..3116513,3119867..3119993,3126699..3126895,3131373..3131494,3134648..3134822,3135545..3135728,3141937..3142061,3149143..3149199,3151692..3151891,3154945..3155086,3164276..3164437,3168815..3168979,3173936..3173998,3174118..3174206,3176040..3176132,3187478..3187635,3188746..3189085,3193816..3193956,3214932..3215221))
location: region:3067260-3215221:-1

NP_062830.1
SIO_000068: ncbiprotein

GI:140560917
SIO_000068: ncbigi

CCDS45823.1
SIO_000068: ccds

position:3067260:-1
position: 3067260
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3215221:-1
position: 3215221
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3214932-3215221:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3193816-3193956:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3188746-3189085:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3187478-3187635:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3176040-3176132:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3174118-3174206:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3173936-3173998:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3168815-3168979:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3164276-3164437:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3154945-3155086:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3151692-3151891:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:3149143-3149199:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:3141937-3142061:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:3135545-3135728:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:3134648-3134822:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:3131373-3131494:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:3126699-3126895:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:3119867-3119993:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:3116329-3116513:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:3112296-3112410:-1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:3102472-3102628:-1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:3100318-3100424:-1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:3100157-3100201:-1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:3094168-3094304:-1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:3090656-3090800:-1/exon

urn:…
SIO_000300: 26
SIO_000628: feature:3089535-3089594:-1/exon

urn:…
SIO_000300: 27
SIO_000628: feature:3089172-3089239:-1/exon

urn:…
SIO_000300: 28
SIO_000628: feature:3086036-3086149:-1/exon

urn:…
SIO_000300: 29
SIO_000628: feature:3085043-3085130:-1/exon

urn:…
SIO_000300: 30
SIO_000628: feature:3083987-3084025:-1/exon

urn:…
SIO_000300: 31
SIO_000628: feature:3083787-3083892:-1/exon

urn:…
SIO_000300: 32
SIO_000628: feature:3079177-3079340:-1/exon

urn:…
SIO_000300: 33
SIO_000628: feature:3075723-3075759:-1/exon

urn:…
SIO_000300: 34
SIO_000628: feature:3075452-3075474:-1/exon

urn:…
SIO_000300: 35
SIO_000628: feature:3071832-3071887:-1/exon

urn:…
SIO_000300: 36
SIO_000628: feature:3067260-3067553:-1/exon

MYOM1
type: SO_0000316
alternative label: SKELEMIN
gene: MYOM1
gene synonym: SKELEMIN
note: isoform a is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: myomesin-1 isoform a
translation: MSLPFYQRCHQHYDLSYRNKDVRSTVSHYQREKKRSAVYTQGSTAYSSRSSAAHRRESEAFRRASASSSQQQASQHALSSEVSRKAASAYDYGSSHGLTDSSLLLDDYSSKLSPKPKRAKHSLLSGEEKENLPSDYMVPIFSGRQKHVSGITDTEEERIKEAAAYIAQRNLLASEEGITTSKQSTASKQTTASKQSTASKQSTASKQSTASRQSTASRQSVVSKQATSALQQEETSEKKSRKVVIREKAERLSLRKTLEETETYHAKLNEDHLLHAPEFIIKPRSHTVWEKENVKLHCSIAGWPEPRVTWYKNQVPINVHANPGKYIIESRYGMHTLEINGCDFEDTAQYRASAMNVKGELSAYASVVVKRYKGEFDETRFHAGASTMPLSFGVTPYGYASRFEIHFDDKFDVSFGREGETMSLGCRVVITPEIKHFQPEIQWYRNGVPLSPSKWVQTLWSGERATLTFSHLNKEDEGLYTIRVRMGEYYEQYSAYVFVRDADAEIEGAPAAPLDVKCLEANKDYIIISWKQPAVDGGSPILGYFIDKCEVGTDSWSQCNDTPVKFARFPVTGLIEGRSYIFRVRAVNKMGIGFPSRVSEPVAALDPAEKARLKSRPSAPWTGQIIVTEEEPSEGIVPGPPTDLSVTEATRSYVVLSWKPPGQRGHEGIMYFVEKCEAGTENWQRVNTELPVKSPRFALFDLAEGKSYCFRVRCSNSAGVGEPSEATEVTVVGDKLDIPKAPGKIIPSRNTDTSVVVSWEESKDAKELVGYYIEASVAGSGKWEPCNNNPVKGSRFTCHGLVTGQSYIFRVRAVNAAGLSEYSQDSEAIEVKAAIGGGVSPDVCPALSDEPGGLTASRGRVHEASPPTFQKDALLGSKPNKPSLPSSSQNLGQTEVSKVSETVQEELTPPPQKAAPQGKSKSDPLKKKTDRAPPSPPCDITCLESFRDSMVLGWKQPDKIGGAEITGYYVNYREVIDGVPGKWREANVKAVSEEAYKISNLKENMVYQFQVAAMNMAGLGAPSAVSECFKCEEWTIAVPGPPHSLKCSEVRKDSLVLQWKPPVHSGRTPVTGYFVDLKEAKAKEDQWRGLNEAAIKNVYLKVRGLKEGVSYVFRVRAINQAGVGKPSDLAGPVVAETRPGTKEVVVNVDDDGVISLNFECDKMTPKSEFSWSKDYVSTEDSPRLEVESKGNKTKMTFKDLGMDDLGIYSCDVTDTDGIASSYLIDEEELKRLLALSHEHKFPTVPVKSELAVEILEKGQVRFWMQAEKLSGNAKVNYIFNEKEIFEGPKYKMHIDRNTGIIEMFMEKLQDEDEGTYTFQLQDGKATNHSTVVLVGDVFKKLQKEAEFQRQEWIRKQGPHFVEYLSWEVTGECNVLLKCKVANIKKETHIVWYKDEREISVDEKHDFKDGICTLLITEFSKKDAGIYEVILKDDRGKDKSRLKLVDEAFKELMMEVCKKIALSATDLKIQSTAEGIQLYSFVTYYVEDLKVNWSHNGSAIRYSDRVKTGVTGEQIWLQINEPTPNDKGKYVMELFDGKTGHQKTVDLSGQAYDEAYAEFQRLKQAAIAEKNRARVLGGLPDVVTIQEGKALNLTCNVWGDPPPEVSWLKNEKALASDDHCNLKFEAGRTAYFTINGVSTADSGKYGLVVKNKYGSETSDFTVSVFIPEEEARMAALESLKGGKKAK
so part of: MYOM1
location: complement(join(3067260..3067553,3071832..3071887,3075452..3075474,3075723..3075759,3079177..3079340,3083787..3083892,3083987..3084025,3085043..3085130,3086036..3086149,3089172..3089239,3089535..3089594,3090656..3090800,3094168..3094304,3100157..3100201,3100318..3100424,3102472..3102628,3112296..3112410,3116329..3116513,3119867..3119993,3126699..3126895,3129230..3129517,3131373..3131494,3134648..3134822,3135545..3135728,3141937..3142061,3149143..3149199,3151692..3151891,3154945..3155086,3164276..3164437,3168815..3168979,3173936..3173998,3174118..3174206,3176040..3176132,3187478..3187635,3188746..3189085,3193816..3193956,3214932..3215221))
location: region:3067260-3215221:-1

NP_003794.3
SIO_000068: ncbiprotein

GI:140560919
SIO_000068: ncbigi

CCDS45824.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:3214932-3215221:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3193816-3193956:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3188746-3189085:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3187478-3187635:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3176040-3176132:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3174118-3174206:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3173936-3173998:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3168815-3168979:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3164276-3164437:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3154945-3155086:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3151692-3151891:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:3149143-3149199:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:3141937-3142061:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:3135545-3135728:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:3134648-3134822:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:3131373-3131494:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:3129230-3129517:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:3126699-3126895:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:3119867-3119993:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:3116329-3116513:-1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:3112296-3112410:-1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:3102472-3102628:-1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:3100318-3100424:-1/exon

urn:…
SIO_000300: 24
SIO_000628: feature:3100157-3100201:-1/exon

urn:…
SIO_000300: 25
SIO_000628: feature:3094168-3094304:-1/exon

urn:…
SIO_000300: 26
SIO_000628: feature:3090656-3090800:-1/exon

urn:…
SIO_000300: 27
SIO_000628: feature:3089535-3089594:-1/exon

urn:…
SIO_000300: 28
SIO_000628: feature:3089172-3089239:-1/exon

urn:…
SIO_000300: 29
SIO_000628: feature:3086036-3086149:-1/exon

urn:…
SIO_000300: 30
SIO_000628: feature:3085043-3085130:-1/exon

urn:…
SIO_000300: 31
SIO_000628: feature:3083987-3084025:-1/exon

urn:…
SIO_000300: 32
SIO_000628: feature:3083787-3083892:-1/exon

urn:…
SIO_000300: 33
SIO_000628: feature:3079177-3079340:-1/exon

urn:…
SIO_000300: 34
SIO_000628: feature:3075723-3075759:-1/exon

urn:…
SIO_000300: 35
SIO_000628: feature:3075452-3075474:-1/exon

urn:…
SIO_000300: 36
SIO_000628: feature:3071832-3071887:-1/exon

urn:…
SIO_000300: 37
SIO_000628: feature:3067260-3067553:-1/exon

RNU7-25P
type: SO_0000704
alternative label: U7.25
gene: RNU7-25P
gene synonym: U7.25
note: RNA, U7 small nuclear 25 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3093567..3093629
location: region:3093567-3093629:1
SIO_010080: RNU7-25P

100147812
SIO_000068: ncbigene

34121
SIO_000068: hgnc

position:3093567:1
position: 3093567
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3093629:1
position: 3093629
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

RNU7-25P
type: SO_0000147
alternative label: U7.25
gene: RNU7-25P
gene synonym: U7.25
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: RNU7-25P
location: 3093567..3093629
location: region:3093567-3093629:1

LOC101927044
type: SO_0000704
gene: LOC101927044
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3236439..3246499
location: region:3236439-3246499:1
SIO_010080: LOC101927044

101927044
SIO_000068: ncbigene

position:3236439:1
position: 3236439
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3246499:1
position: 3246499
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927044
type: SO_0000673
gene: LOC101927044
product: uncharacterized LOC101927044
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 ESTs, and 86% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XR_243817.1
so part of: LOC101927044
location: join(3236439..3236536,3245955..3246499)
location: region:3236439-3246499:1

GI:530425015
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3236439-3236536:1/exon

position:3236536:1
position: 3236536
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3245955-3246499:1/exon

position:3245955:1
position: 3245955
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MYL12A
type: SO_0000704
alternative label: MLCB
alternative label: MRCL3
alternative label: MRLC3
alternative label: MYL2B
gene: MYL12A
gene synonym: MLCB; MRCL3; MRLC3; MYL2B
note: myosin, light chain 12A, regulatory, non-sarcomeric; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3247472..3256234
location: region:3247472-3256234:1
SIO_010080: MYL12A

10627
SIO_000068: ncbigene

16701
SIO_000068: hgnc

14735
SIO_000068: hprd

position:3247472:1
position: 3247472
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3256234:1
position: 3256234
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MYL12A
type: SO_0000234
alternative label: MLCB
alternative label: MRCL3
alternative label: MRLC3
alternative label: MYL2B
gene: MYL12A
gene synonym: MLCB; MRCL3; MRLC3; MYL2B
product: myosin, light chain 12A, regulatory, non-sarcomeric, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 ESTs, 36 Proteins, and 100% coverage by RNAseq alignments, including 18 samples with support for all introns
transcript id: XM_005258076.1
so part of: MYL12A
location: join(3247472..3247585,3253231..3253426,3253887..3254048,3255744..3256234)
location: region:3247472-3256234:1

GI:530424788
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3247472-3247585:1/exon

position:3247585:1
position: 3247585
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3253231-3253426:1/exon

position:3253231:1
position: 3253231
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3253426:1
position: 3253426
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3253887-3254048:1/exon

position:3253887:1
position: 3253887
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3254048:1
position: 3254048
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:3255744-3256234:1/exon

position:3255744:1
position: 3255744
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MYL12A
type: SO_0000234
alternative label: MLCB
alternative label: MRCL3
alternative label: MRLC3
alternative label: MYL2B
gene: MYL12A
gene synonym: MLCB; MRCL3; MRLC3; MYL2B
product: myosin, light chain 12A, regulatory, non-sarcomeric
inference: similar to RNA sequence, mRNA (same species):RefSeq:NM_006471.2
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_006471.2
so part of: MYL12A
location: join(3247528..3247907,3253231..3253426,3253887..3254048,3255744..3256234)
location: region:3247528-3256234:1

GI:31543210
SIO_000068: ncbigi

position:3247528:1
position: 3247528
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3247528-3247907:1/exon

position:3247907:1
position: 3247907
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3253231-3253426:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3253887-3254048:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3255744-3256234:1/exon

MYL12A
type: SO_0000234
alternative label: MLCB
alternative label: MRCL3
alternative label: MRLC3
alternative label: MYL2B
gene: MYL12A
gene synonym: MLCB; MRCL3; MRLC3; MYL2B
product: myosin, light chain 12A, regulatory, non-sarcomeric, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 49 ESTs, 36 Proteins, and 100% coverage by RNAseq alignments, including 9 samples with support for all introns
transcript id: XM_005258077.1
so part of: MYL12A
location: join(3252214..3252323,3253231..3253426,3253887..3254048,3255744..3256234)
location: region:3252214-3256234:1

GI:530424790
SIO_000068: ncbigi

position:3252214:1
position: 3252214
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3252214-3252323:1/exon

position:3252323:1
position: 3252323
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3253231-3253426:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3253887-3254048:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3255744-3256234:1/exon

MYL12A
type: SO_0000234
alternative label: MLCB
alternative label: MRCL3
alternative label: MRLC3
alternative label: MYL2B
gene: MYL12A
gene synonym: MLCB; MRCL3; MRLC3; MYL2B
product: myosin, light chain 12A, regulatory, non-sarcomeric, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 ESTs, 35 Proteins, and 100% coverage by RNAseq alignments, including 6 samples with support for all introns
transcript id: XM_005258078.1
so part of: MYL12A
location: join(3252219..3252480,3253231..3253426,3253887..3254048,3255744..3256234)
location: region:3252219-3256234:1

GI:530424792
SIO_000068: ncbigi

position:3252219:1
position: 3252219
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3252219-3252480:1/exon

position:3252480:1
position: 3252480
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3253231-3253426:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3253887-3254048:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3255744-3256234:1/exon

MYL12A
type: SO_0000316
alternative label: MLCB
alternative label: MRCL3
alternative label: MRLC3
alternative label: MYL2B
gene: MYL12A
gene synonym: MLCB; MRCL3; MRLC3; MYL2B
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: myosin regulatory light chain 12A isoform X2
translation: MDLTTTMSSKRTKTKTKKRPQRATSNVFAMFDQSQIQEFKEAFNMIDQNRDGFIDKEDLHDMLASLGKNPTDEYLDAMMNEAPGPINFTMFLTMFGEKLNGTDPEDVIRNAFACFDEEATGTIQEDYLRELLTTMGDRFTDEEVDELYREAPIDKKGNFNYIEFTRILKHGAKDKDD
so part of: MYL12A
location: join(3252321..3252323,3253231..3253426,3253887..3254048,3255744..3255916)
location: region:3252321-3255916:1

XP_005258134.1
SIO_000068: ncbiprotein

GI:530424791
SIO_000068: ncbigi

position:3252321:1
position: 3252321
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3255916:1
position: 3255916
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3252321-3252323:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3253231-3253426:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3253887-3254048:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3255744-3255916:1/exon

MYL12A
type: SO_0000316
alternative label: MLCB
alternative label: MRCL3
alternative label: MRLC3
alternative label: MYL2B
gene: MYL12A
gene synonym: MLCB; MRCL3; MRLC3; MYL2B
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: myosin regulatory light chain 12A
translation: MSSKRTKTKTKKRPQRATSNVFAMFDQSQIQEFKEAFNMIDQNRDGFIDKEDLHDMLASLGKNPTDEYLDAMMNEAPGPINFTMFLTMFGEKLNGTDPEDVIRNAFACFDEEATGTIQEDYLRELLTTMGDRFTDEEVDELYREAPIDKKGNFNYIEFTRILKHGAKDKDD
so part of: MYL12A
location: join(3253246..3253426,3253887..3254048,3255744..3255916)
location: region:3253246-3255916:1

NP_006462.1
SIO_000068: ncbiprotein

GI:5453740
SIO_000068: ncbigi

CCDS11830.1
SIO_000068: ccds

position:3253246:1
position: 3253246
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3253246-3253426:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3253887-3254048:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3255744-3255916:1/exon

MYL12A
type: SO_0000316
alternative label: MLCB
alternative label: MRCL3
alternative label: MRLC3
alternative label: MYL2B
gene: MYL12A
gene synonym: MLCB; MRCL3; MRLC3; MYL2B
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: myosin regulatory light chain 12A isoform X1
translation: MSSKRTKTKTKKRPQRATSNVFAMFDQSQIQEFKEAFNMIDQNRDGFIDKEDLHDMLASLGKNPTDEYLDAMMNEAPGPINFTMFLTMFGEKLNGTDPEDVIRNAFACFDEEATGTIQEDYLRELLTTMGDRFTDEEVDELYREAPIDKKGNFNYIEFTRILKHGAKDKDD
so part of: MYL12A
location: join(3253246..3253426,3253887..3254048,3255744..3255916)
location: region:3253246-3255916:1

XP_005258133.1
SIO_000068: ncbiprotein

GI:530424789
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3253246-3253426:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3253887-3254048:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3255744-3255916:1/exon

MYL12A
type: SO_0000316
alternative label: MLCB
alternative label: MRCL3
alternative label: MRLC3
alternative label: MYL2B
gene: MYL12A
gene synonym: MLCB; MRCL3; MRLC3; MYL2B
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: myosin regulatory light chain 12A isoform X3
translation: MSSKRTKTKTKKRPQRATSNVFAMFDQSQIQEFKEAFNMIDQNRDGFIDKEDLHDMLASLGKNPTDEYLDAMMNEAPGPINFTMFLTMFGEKLNGTDPEDVIRNAFACFDEEATGTIQEDYLRELLTTMGDRFTDEEVDELYREAPIDKKGNFNYIEFTRILKHGAKDKDD
so part of: MYL12A
location: join(3253246..3253426,3253887..3254048,3255744..3255916)
location: region:3253246-3255916:1

XP_005258135.1
SIO_000068: ncbiprotein

GI:530424793
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3253246-3253426:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3253887-3254048:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3255744-3255916:1/exon

LOC101927061
type: SO_0000704
gene: LOC101927061
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(3255949..3261822)
location: region:3255949-3261822:-1
SIO_010080: LOC101927061

101927061
SIO_000068: ncbigene

position:3255949:-1
position: 3255949
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3261822:-1
position: 3261822
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101927061
type: SO_0000673
gene: LOC101927061
product: uncharacterized LOC101927061, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XR_243819.1
so part of: LOC101927061
location: complement(join(3255949..3256320,3261608..3261822))
location: region:3255949-3261822:-1

GI:530425017
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3261608-3261822:-1/exon

position:3261608:-1
position: 3261608
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3255949-3256320:-1/exon

position:3256320:-1
position: 3256320
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101927061
type: SO_0000673
gene: LOC101927061
product: uncharacterized LOC101927061, transcript variant X1
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_243818.1
so part of: LOC101927061
location: complement(join(3255962..3256320,3261270..3261328,3261608..3261822))
location: region:3255962-3261822:-1

GI:530425016
SIO_000068: ncbigi

position:3255962:-1
position: 3255962
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3261608-3261822:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3261270-3261328:-1/exon

position:3261270:-1
position: 3261270
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3261328:-1
position: 3261328
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3255962-3256320:-1/exon

MYL12B
type: SO_0000704
alternative label: MLC-B
alternative label: MRLC2
gene: MYL12B
gene synonym: MLC-B; MRLC2
note: myosin, light chain 12B, regulatory; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3262111..3278282
location: region:3262111-3278282:1
SIO_010080: MYL12B

103910
SIO_000068: ncbigene

29827
SIO_000068: hgnc

10095
SIO_000068: hprd

609211
SIO_000068: omim

position:3262111:1
position: 3262111
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3278282:1
position: 3278282
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MYL12B
type: SO_0000234
alternative label: MLC-B
alternative label: MRLC2
gene: MYL12B
gene synonym: MLC-B; MRLC2
product: myosin, light chain 12B, regulatory, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_033546.3
so part of: MYL12B
location: join(3262111..3262235,3272882..3273080,3277251..3277412,3277763..3278282)
location: region:3262111-3278282:1

GI:222144322
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3262111-3262235:1/exon

position:3262235:1
position: 3262235
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3272882-3273080:1/exon

position:3272882:1
position: 3272882
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3273080:1
position: 3273080
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3277251-3277412:1/exon

position:3277251:1
position: 3277251
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3277412:1
position: 3277412
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:3277763-3278282:1/exon

position:3277763:1
position: 3277763
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

MYL12B
type: SO_0000234
alternative label: MLC-B
alternative label: MRLC2
gene: MYL12B
gene synonym: MLC-B; MRLC2
product: myosin, light chain 12B, regulatory, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001144944.1
so part of: MYL12B
location: join(3262611..3262754,3272882..3273080,3277251..3277412,3277763..3278282)
location: region:3262611-3278282:1

GI:222144323
SIO_000068: ncbigi

position:3262611:1
position: 3262611
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3262611-3262754:1/exon

position:3262754:1
position: 3262754
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3272882-3273080:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3277251-3277412:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3277763-3278282:1/exon

MYL12B
type: SO_0000234
alternative label: MLC-B
alternative label: MRLC2
gene: MYL12B
gene synonym: MLC-B; MRLC2
product: myosin, light chain 12B, regulatory, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001144945.1
so part of: MYL12B
location: join(3262717..3262782,3272882..3273080,3277251..3277412,3277763..3278282)
location: region:3262717-3278282:1

GI:222144325
SIO_000068: ncbigi

position:3262717:1
position: 3262717
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3262717-3262782:1/exon

position:3262782:1
position: 3262782
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3272882-3273080:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3277251-3277412:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3277763-3278282:1/exon

MYL12B
type: SO_0000234
alternative label: MLC-B
alternative label: MRLC2
gene: MYL12B
gene synonym: MLC-B; MRLC2
product: myosin, light chain 12B, regulatory, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 ESTs, 35 Proteins, and 96% coverage by RNAseq alignments
transcript id: XM_005258075.1
so part of: MYL12B
location: join(3262959..3263136,3272882..3273080,3277251..3277412,3277763..3278205)
location: region:3262959-3278205:1

GI:530424786
SIO_000068: ncbigi

position:3262959:1
position: 3262959
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3278205:1
position: 3278205
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3262959-3263136:1/exon

position:3263136:1
position: 3263136
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3272882-3273080:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3277251-3277412:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3277763-3278205:1/exon

MYL12B
type: SO_0000316
alternative label: MLC-B
alternative label: MRLC2
gene: MYL12B
gene synonym: MLC-B; MRLC2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: myosin regulatory light chain 12B
translation: MSSKKAKTKTTKKRPQRATSNVFAMFDQSQIQEFKEAFNMIDQNRDGFIDKEDLHDMLASLGKNPTDAYLDAMMNEAPGPINFTMFLTMFGEKLNGTDPEDVIRNAFACFDEEATGTIQEDYLRELLTTMGDRFTDEEVDELYREAPIDKKGNFNYIEFTRILKHGAKDKDD
so part of: MYL12B
location: join(3272897..3273080,3277251..3277412,3277763..3277935)
location: region:3272897-3277935:1

NP_291024.1
SIO_000068: ncbiprotein

GI:15809016
SIO_000068: ncbigi

CCDS11831.1
SIO_000068: ccds

position:3272897:1
position: 3272897
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3277935:1
position: 3277935
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3272897-3273080:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3277251-3277412:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3277763-3277935:1/exon

MYL12B
type: SO_0000316
alternative label: MLC-B
alternative label: MRLC2
gene: MYL12B
gene synonym: MLC-B; MRLC2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: myosin regulatory light chain 12B
translation: MSSKKAKTKTTKKRPQRATSNVFAMFDQSQIQEFKEAFNMIDQNRDGFIDKEDLHDMLASLGKNPTDAYLDAMMNEAPGPINFTMFLTMFGEKLNGTDPEDVIRNAFACFDEEATGTIQEDYLRELLTTMGDRFTDEEVDELYREAPIDKKGNFNYIEFTRILKHGAKDKDD
so part of: MYL12B
location: join(3272897..3273080,3277251..3277412,3277763..3277935)
location: region:3272897-3277935:1

NP_001138416.1
SIO_000068: ncbiprotein

GI:222144324
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3272897-3273080:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3277251-3277412:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3277763-3277935:1/exon

MYL12B
type: SO_0000316
alternative label: MLC-B
alternative label: MRLC2
gene: MYL12B
gene synonym: MLC-B; MRLC2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: myosin regulatory light chain 12B
translation: MSSKKAKTKTTKKRPQRATSNVFAMFDQSQIQEFKEAFNMIDQNRDGFIDKEDLHDMLASLGKNPTDAYLDAMMNEAPGPINFTMFLTMFGEKLNGTDPEDVIRNAFACFDEEATGTIQEDYLRELLTTMGDRFTDEEVDELYREAPIDKKGNFNYIEFTRILKHGAKDKDD
so part of: MYL12B
location: join(3272897..3273080,3277251..3277412,3277763..3277935)
location: region:3272897-3277935:1

NP_001138417.1
SIO_000068: ncbiprotein

GI:222144326
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3272897-3273080:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3277251-3277412:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3277763-3277935:1/exon

MYL12B
type: SO_0000316
alternative label: MLC-B
alternative label: MRLC2
gene: MYL12B
gene synonym: MLC-B; MRLC2
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: myosin regulatory light chain 12B isoform X1
translation: MSSKKAKTKTTKKRPQRATSNVFAMFDQSQIQEFKEAFNMIDQNRDGFIDKEDLHDMLASLGKNPTDAYLDAMMNEAPGPINFTMFLTMFGEKLNGTDPEDVIRNAFACFDEEATGTIQEDYLRELLTTMGDRFTDEEVDELYREAPIDKKGNFNYIEFTRILKHGAKDKDD
so part of: MYL12B
location: join(3272897..3273080,3277251..3277412,3277763..3277935)
location: region:3272897-3277935:1

XP_005258132.1
SIO_000068: ncbiprotein

GI:530424787
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3272897-3273080:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3277251-3277412:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3277763-3277935:1/exon

RPL31P59
type: SO_0000704
alternative label: RPL31_23_1580
gene: RPL31P59
gene synonym: RPL31_23_1580
note: ribosomal protein L31 pseudogene 59; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(3377924..3378245)
location: region:3377924-3378245:-1

100271480
SIO_000068: ncbigene

36975
SIO_000068: hgnc

position:3377924:-1
position: 3377924
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3378245:-1
position: 3378245
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

IGLJCOR18
type: SO_0000704
alternative label: IGLJ-C/OR18
alternative label: IGLJ-COR18
gene: IGLJCOR18
gene synonym: IGLJ-C/OR18; IGLJ-COR18
note: immunoglobulin lambda joining-constant/OR18 (pseudogene); Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3394884..3395315
location: region:3394884-3395315:1

204777
SIO_000068: ncbigene

28614
SIO_000068: hgnc

position:3394884:1
position: 3394884
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3395315:1
position: 3395315
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

RPL21P127
type: SO_0000704
alternative label: RPL21_61_1581
gene: RPL21P127
gene synonym: RPL21_61_1581
note: ribosomal protein L21 pseudogene 127; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(3406308..3406856)
location: region:3406308-3406856:-1
SIO_010080: RPL21P127

100271452
SIO_000068: ncbigene

36099
SIO_000068: hgnc

position:3406308:-1
position: 3406308
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3406856:-1
position: 3406856
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

RPL21P127
type: SO_0000147
alternative label: RPL21_61_1581
gene: RPL21P127
gene synonym: RPL21_61_1581
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: RPL21P127
location: complement(3406308..3406856)
location: region:3406308-3406856:-1

TGIF1
type: SO_0000704
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: TGFB-induced factor homeobox 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3411925..3458409
location: region:3411925-3458409:1
SIO_010080: TGIF1

7050
SIO_000068: ncbigene

11776
SIO_000068: hgnc

04023
SIO_000068: hprd

602630
SIO_000068: omim

position:3411925:1
position: 3411925
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3458409:1
position: 3458409
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 8
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_174886.2
so part of: TGIF1
location: join(3411925..3412252,3418141..3418213,3456352..3456578,3457363..3458409)
location: region:3411925-3458409:1

GI:522838247
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3411925-3412252:1/exon

position:3412252:1
position: 3412252
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3418141-3418213:1/exon

position:3418141:1
position: 3418141
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3418213:1
position: 3418213
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3456352-3456578:1/exon

position:3456352:1
position: 3456352
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3456578:1
position: 3456578
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:3457363-3458409:1/exon

position:3457363:1
position: 3457363
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 11
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001278686.1
so part of: TGIF1
location: join(3412854..3413047,3418141..3418213,3456352..3456578,3457363..3458409)
location: region:3412854-3458409:1

GI:522838245
SIO_000068: ncbigi

position:3412854:1
position: 3412854
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3412854-3413047:1/exon

position:3413047:1
position: 3413047
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3418141-3418213:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3457363-3458409:1/exon

LOC100129468
type: SO_0000704
gene: LOC100129468
note: biorientation of chromosomes in cell division 1 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3415077..3416634
location: region:3415077-3416634:1

100129468
SIO_000068: ncbigene

position:3415077:1
position: 3415077
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3416634:1
position: 3416634
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC101927094
type: SO_0000704
gene: LOC101927094
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(3447004..3447517)
location: region:3447004-3447517:-1
SIO_010080: LOC101927094

101927094
SIO_000068: ncbigene

position:3447004:-1
position: 3447004
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3447517:-1
position: 3447517
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC101927094
type: SO_0000673
gene: LOC101927094
product: uncharacterized LOC101927094
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_243820.1
so part of: LOC101927094
location: complement(join(3447004..3447184,3447481..3447517))
location: region:3447004-3447517:-1

GI:530425018
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3447481-3447517:-1/exon

position:3447481:-1
position: 3447481
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3447004-3447184:-1/exon

position:3447184:-1
position: 3447184
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_173207.2
so part of: TGIF1
location: join(3447584..3447795,3456352..3456578,3457363..3458409)
location: region:3447584-3458409:1

GI:522838231
SIO_000068: ncbigi

position:3447584:1
position: 3447584
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3447584-3447795:1/exon

position:3447795:1
position: 3447795
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform b is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform b
translation: MTCSGKSCALARSSLTSSQGIVAASGSETEDEDSMDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3447738..3447795,3456352..3456578,3457363..3457938)
location: region:3447738-3457938:1

NP_775299.1
SIO_000068: ncbiprotein

GI:28178845
SIO_000068: ncbigi

CCDS11832.1
SIO_000068: ccds

position:3447738:1
position: 3447738
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3457938:1
position: 3457938
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3447738-3447795:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 24 ESTs, 2 Proteins, and 100% coverage by RNAseq alignments, including 5 samples with support for all introns
transcript id: XM_005258135.1
so part of: TGIF1
location: join(3448088..3448595,3456352..3456578,3457363..3458409)
location: region:3448088-3458409:1

GI:530424922
SIO_000068: ncbigi

position:3448088:1
position: 3448088
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3448088-3448595:1/exon

position:3448595:1
position: 3448595
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 9
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001278682.1
so part of: TGIF1
location: join(3449411..3449654,3456352..3456578,3457363..3458409)
location: region:3449411-3458409:1

GI:522838236
SIO_000068: ncbigi

position:3449411:1
position: 3449411
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3449411-3449654:1/exon

position:3449654:1
position: 3449654
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform e is encoded by transcript variant 9; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform e
translation: MAAAHSGRSIVAASGSETEDEDSMDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3449630..3449654,3456352..3456578,3457363..3457938)
location: region:3449630-3457938:1

NP_001265611.1
SIO_000068: ncbiprotein

GI:522838237
SIO_000068: ncbigi

position:3449630:1
position: 3449630
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3449630-3449654:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_173208.2
so part of: TGIF1
location: join(3449649..3450068,3450320..3450503,3456352..3456578,3457363..3458409)
location: region:3449649-3458409:1

GI:522838232
SIO_000068: ncbigi

position:3449649:1
position: 3449649
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3449649-3450068:1/exon

position:3450068:1
position: 3450068
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3450320-3450503:1/exon

position:3450320:1
position: 3450320
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3450503:1
position: 3450503
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 10
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001278684.1
so part of: TGIF1
location: join(3449649..3450068,3450323..3450503,3456352..3456578,3457363..3458409)
location: region:3449649-3458409:1

GI:522838241
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3449649-3450068:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3450323-3450503:1/exon

position:3450323:1
position: 3450323
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 5
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_173209.2
so part of: TGIF1
location: join(3449649..3450068,3456352..3456578,3457363..3458409)
location: region:3449649-3458409:1

GI:522838234
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3449649-3450068:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 32 ESTs, 11 Proteins, and 100% coverage by RNAseq alignments, including 5 samples with support for all introns
transcript id: XM_005258134.1
so part of: TGIF1
location: join(3449672..3450068,3450180..3450503,3456352..3456578,3457363..3458409)
location: region:3449672-3458409:1

GI:530424920
SIO_000068: ncbigi

position:3449672:1
position: 3449672
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3449672-3450068:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3450180-3450503:1/exon

position:3450180:1
position: 3450180
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 4
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_003244.3
so part of: TGIF1
location: join(3450170..3450503,3456352..3456578,3457363..3458409)
location: region:3450170-3458409:1

GI:522838233
SIO_000068: ncbigi

position:3450170:1
position: 3450170
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3450170-3450503:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: homeobox protein TGIF1 isoform X1
translation: MKGKKGIVAASGSETEDEDSMDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3450488..3450503,3456352..3456578,3457363..3457938)
location: region:3450488-3457938:1

XP_005258191.1
SIO_000068: ncbiprotein

GI:530424921
SIO_000068: ncbigi

position:3450488:1
position: 3450488
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3450488-3450503:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform c is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform c
translation: MKGKKGIVAASGSETEDEDSMDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3450488..3450503,3456352..3456578,3457363..3457938)
location: region:3450488-3457938:1

NP_775300.1
SIO_000068: ncbiprotein

GI:28178849
SIO_000068: ncbigi

CCDS11833.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:3450488-3450503:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform c is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform c
translation: MKGKKGIVAASGSETEDEDSMDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3450488..3450503,3456352..3456578,3457363..3457938)
location: region:3450488-3457938:1

NP_003235.1
SIO_000068: ncbiprotein

GI:4507473
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3450488-3450503:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform c is encoded by transcript variant 10; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform c
translation: MKGKKGIVAASGSETEDEDSMDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3450488..3450503,3456352..3456578,3457363..3457938)
location: region:3450488-3457938:1

NP_001265613.1
SIO_000068: ncbiprotein

GI:522838242
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3450488-3450503:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_170695.3
so part of: TGIF1
location: join(3451403..3452380,3456352..3456578,3457363..3458409)
location: region:3451403-3458409:1

GI:522838230
SIO_000068: ncbigi

position:3451403:1
position: 3451403
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3451403-3452380:1/exon

position:3452380:1
position: 3452380
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 6
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_173210.2
so part of: TGIF1
location: join(3451403..3451773,3456352..3456578,3457363..3458409)
location: region:3451403-3458409:1

GI:522838235
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3451403-3451773:1/exon

position:3451773:1
position: 3451773
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 4 samples with support for all introns
transcript id: XM_005258136.1
so part of: TGIF1
location: join(3451652..3451769,3456352..3456578,3457363..3458409)
location: region:3451652-3458409:1

GI:530424924
SIO_000068: ncbigi

position:3451652:1
position: 3451652
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3451652-3451769:1/exon

position:3451769:1
position: 3451769
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform a is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform a
translation: MVLAQSRVSAGVGSPHCSGSGGGGSDSFPWPASHPGNPQCSFSTAFLASPRLSRGTLAYLPPAPWSSLATPSALLGSSCAPPPPPARCPQPRALSPELGTKAGPRRPHRWELPRSPSQGAQGPAPRRRLLETMKGIVAASGSETEDEDSMDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3451978..3452380,3456352..3456578,3457363..3457938)
location: region:3451978-3457938:1

NP_733796.2
SIO_000068: ncbiprotein

GI:28178843
SIO_000068: ncbigi

CCDS11834.1
SIO_000068: ccds

position:3451978:1
position: 3451978
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3451978-3452380:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000234
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
product: TGFB-induced factor homeobox 1, transcript variant 7
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_173211.1
so part of: TGIF1
location: join(3453772..3453854,3456352..3456578,3457363..3458409)
location: region:3453772-3458409:1

GI:28178854
SIO_000068: ncbigi

position:3453772:1
position: 3453772
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3453772-3453854:1/exon

position:3453854:1
position: 3453854
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3456352-3456578:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3457363-3458409:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: homeobox protein TGIF1 isoform X2
translation: MDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3456396..3456578,3457363..3457938)
location: region:3456396-3457938:1

XP_005258192.1
SIO_000068: ncbiprotein

GI:530424923
SIO_000068: ncbigi

position:3456396:1
position: 3456396
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3456396-3456578:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: homeobox protein TGIF1 isoform X3
translation: MDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3456396..3456578,3457363..3457938)
location: region:3456396-3457938:1

XP_005258193.1
SIO_000068: ncbiprotein

GI:530424925
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3456396-3456578:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform d is encoded by transcript variant 7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform d
translation: MDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3456396..3456578,3457363..3457938)
location: region:3456396-3457938:1

NP_775303.1
SIO_000068: ncbiprotein

GI:28178855
SIO_000068: ncbigi

CCDS11835.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:3456396-3456578:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform d is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform d
translation: MDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3456396..3456578,3457363..3457938)
location: region:3456396-3457938:1

NP_775301.1
SIO_000068: ncbiprotein

GI:28178851
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3456396-3456578:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform d is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform d
translation: MDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3456396..3456578,3457363..3457938)
location: region:3456396-3457938:1

NP_775302.1
SIO_000068: ncbiprotein

GI:28178853
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3456396-3456578:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform d is encoded by transcript variant 11; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform d
translation: MDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3456396..3456578,3457363..3457938)
location: region:3456396-3457938:1

NP_001265615.1
SIO_000068: ncbiprotein

GI:522838246
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3456396-3456578:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3457363-3457938:1/exon

TGIF1
type: SO_0000316
alternative label: HPE4
alternative label: TGIF
gene: TGIF1
gene synonym: HPE4; TGIF
note: isoform d is encoded by transcript variant 8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: homeobox protein TGIF1 isoform d
translation: MDIPLDLSSSAGSGKRRRRGNLPKESVQILRDWLYEHRYNAYPSEQEKALLSQQTHLSTLQVCNWFINARRRLLPDMLRKDGKDPNQFTISRRGAKISETSSVESVMGIKNFMPALEETPFHSCTAGPNPTLGRPLSPKPSSPGSVLARPSVICHTTVTALKDVPFSLCQSVGVGQNTDIQQIAAKNFTDTSLMYPEDTCKSGPSTNTQSGLFNTPPPTPPDLNQDFSGFQLLVDVALKRAAEMELQAKLTA
so part of: TGIF1
location: join(3456396..3456578,3457363..3457938)
location: region:3456396-3457938:1

NP_777480.1
SIO_000068: ncbiprotein

GI:28178857
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3456396-3456578:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3457363-3457938:1/exon

LOC100505592
type: SO_0000704
gene: LOC100505592
note: Derived by automated computational analysis using gene prediction method: Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3466248..3478976
location: region:3466248-3478976:1
SIO_010080: LOC100505592

100505592
SIO_000068: ncbigene

position:3466248:1
position: 3466248
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3478976:1
position: 3478976
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC100505592
type: SO_0000673
gene: LOC100505592
product: uncharacterized LOC100505592, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 92% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XR_243821.1
so part of: LOC100505592
location: join(3466248..3466355,3467125..3467268,3478754..3478974)
location: region:3466248-3478974:1

GI:530425019
SIO_000068: ncbigi

position:3478974:1
position: 3478974
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3466248-3466355:1/exon

position:3466355:1
position: 3466355
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3467125-3467268:1/exon

position:3467125:1
position: 3467125
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3467268:1
position: 3467268
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3478754-3478974:1/exon

position:3478754:1
position: 3478754
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LOC100505592
type: SO_0000673
gene: LOC100505592
product: uncharacterized LOC100505592, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 95% coverage by RNAseq alignments
transcript id: XR_109463.2
so part of: LOC100505592
location: join(3466277..3466355,3467125..3467294,3478754..3478976)
location: region:3466277-3478976:1

GI:530425020
SIO_000068: ncbigi

position:3466277:1
position: 3466277
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3466277-3466355:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3467125-3467294:1/exon

position:3467294:1
position: 3467294
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3478754-3478976:1/exon

DLGAP1
type: SO_0000704
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: discs, large (Drosophila) homolog-associated protein 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(3496030..4455310)
location: region:3496030-4455310:-1
SIO_010080: DLGAP1

9229
SIO_000068: ncbigene

2905
SIO_000068: hgnc

09260
SIO_000068: hprd

605445
SIO_000068: omim

position:3496030:-1
position: 3496030
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:4455310:-1
position: 4455310
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 48 ESTs, 6 Proteins, and 99% coverage by RNAseq alignments
transcript id: XM_005258171.1
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3879112..3880140,4005116..4005201,4151180..4151287,4455006..4455310))
location: region:3496030-4455310:-1

GI:530424994
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:4455006-4455310:-1/exon

position:4455006:-1
position: 4455006
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:4151180-4151287:-1/exon

position:4151180:-1
position: 4151180
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:4151287:-1
position: 4151287
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:4005116-4005201:-1/exon

position:4005116:-1
position: 4005116
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:4005201:-1
position: 4005201
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:3879112-3880140:-1/exon

position:3879112:-1
position: 3879112
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3880140:-1
position: 3880140
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:3814059-3814273:-1/exon

position:3814059:-1
position: 3814059
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3814273:-1
position: 3814273
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:3742335-3742512:-1/exon

position:3742335:-1
position: 3742335
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3742512:-1
position: 3742512
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:3729135-3729375:-1/exon

position:3729135:-1
position: 3729135
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3729375:-1
position: 3729375
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:3656084-3656113:-1/exon

position:3656084:-1
position: 3656084
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3656113:-1
position: 3656113
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:3581873-3582246:-1/exon

position:3581873:-1
position: 3581873
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3582246:-1
position: 3582246
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:3567488-3567579:-1/exon

position:3567488:-1
position: 3567488
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3567579:-1
position: 3567579
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:3534192-3534613:-1/exon

position:3534192:-1
position: 3534192
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3534613:-1
position: 3534613
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:3508568-3508659:-1/exon

position:3508568:-1
position: 3508568
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3508659:-1
position: 3508659
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:3502491-3502643:-1/exon

position:3502491:-1
position: 3502491
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3502643:-1
position: 3502643
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:3496030-3499392:-1/exon

position:3499392:-1
position: 3499392
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 44 ESTs, 6 Proteins, and 99% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XM_005258172.1
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3879112..3880140,4005116..4005201,4151180..4151282,4455006..4455307))
location: region:3496030-4455307:-1

GI:530424996
SIO_000068: ncbigi

position:4455307:-1
position: 4455307
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:4455006-4455307:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:4151180-4151282:-1/exon

position:4151282:-1
position: 4151282
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:4005116-4005201:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3879112-3880140:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_004746.3
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3729135..3729375,3742335..3742512,3814059..3814273,3879112..3880140,4005116..4005201,4151180..4151287,4455006..4455266))
location: region:3496030-4455266:-1

GI:338221668
SIO_000068: ncbigi

position:4455266:-1
position: 4455266
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:4455006-4455266:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:4151180-4151287:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:4005116-4005201:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3879112-3880140:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant 4
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001242762.1
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582162,3729135..3729375,3742335..3742512,3814059..3814273,3874614..3874767))
location: region:3496030-3874767:-1

GI:338221673
SIO_000068: ncbigi

position:3874767:-1
position: 3874767
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3874614-3874767:-1/exon

position:3874614:-1
position: 3874614
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3581873-3582162:-1/exon

position:3582162:-1
position: 3582162
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant 5
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001242763.1
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3874614..3874767))
location: region:3496030-3874767:-1

GI:338221675
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3874614-3874767:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 35 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XM_005258173.1
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3821892..3822005,3874614..3874750))
location: region:3496030-3874750:-1

GI:530424998
SIO_000068: ncbigi

position:3874750:-1
position: 3874750
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3874614-3874750:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3821892-3822005:-1/exon

position:3821892:-1
position: 3821892
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3822005:-1
position: 3822005
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant X4
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 36 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258174.1
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3874148..3874451))
location: region:3496030-3874451:-1

GI:530425000
SIO_000068: ncbigi

position:3874451:-1
position: 3874451
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3874148-3874451:-1/exon

position:3874148:-1
position: 3874148
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant X5
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 41 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258175.1
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3874154..3874305))
location: region:3496030-3874305:-1

GI:530425002
SIO_000068: ncbigi

position:3874305:-1
position: 3874305
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3874154-3874305:-1/exon

position:3874154:-1
position: 3874154
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant 6
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001242764.1
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3729135..3729375,3742335..3742512,3814059..3814273,3874154..3874253))
location: region:3496030-3874253:-1

GI:338221677
SIO_000068: ncbigi

position:3874253:-1
position: 3874253
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3874154-3874253:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant X6
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 35 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XM_005258176.1
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3845564..3845592))
location: region:3496030-3845592:-1

GI:530425004
SIO_000068: ncbigi

position:3845592:-1
position: 3845592
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3845564-3845592:-1/exon

position:3845564:-1
position: 3845564
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001003809.2
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3729135..3729375,3742335..3742512,3814059..3814273,3845232..3845358))
location: region:3496030-3845358:-1

GI:338221672
SIO_000068: ncbigi

position:3845358:-1
position: 3845358
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3845232-3845358:-1/exon

position:3845232:-1
position: 3845232
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant 8
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001242766.1
so part of: DLGAP1
location: complement(join(3496030..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3845232..3845358))
location: region:3496030-3845358:-1

GI:338221679
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3845232-3845358:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3496030-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: isoform 1 is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: disks large-associated protein 1 isoform 1
translation: MKGLSGSRSHHHGVTCDSACDSLSHHSDRKPYLLSPVEHHPADHPYYTQRNSFQAECVGPFSDPLASSTFPRRHYTSQQELKDECALVPRTLATKANRIPANLLDQFERQLPLSRDGYHTLQYKRTAVEHRSDSPGRIRHLVHSVQKLFTKSHSLEGPSKGSVNGGKASPDEAQAARYGKRSKSKERRAEPKARPSTSPGWWSSDDNLDGDMCIYHAPSGVMTMGRCPDRSASQYFLEAYNTISEQAVKASRSNNDVKCSTCANLPVSLDTPLLKKSAWSSTLTVSRAREVYQKASVNMDQAMVKSESCQQERSCQYLQVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3729135..3729375,3742335..3742512,3814059..3814273,3879112..3880068))
location: region:3499183-3880068:-1

NP_004737.2
SIO_000068: ncbiprotein

GI:19923274
SIO_000068: ncbigi

CCDS11836.1
SIO_000068: ccds

position:3499183:-1
position: 3499183
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3880068:-1
position: 3880068
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3879112-3880068:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: disks large-associated protein 1 isoform X1
translation: MKGLSGSRSHHHGVTCDSACDSLSHHSDRKPYLLSPVEHHPADHPYYTQRNSFQAECVGPFSDPLASSTFPRRHYTSQQELKDECALVPRTLATKANRIPANLLDQFERQLPLSRDGYHTLQYKRTAVEHRSDSPGRIRHLVHSVQKLFTKSHSLEGPSKGSVNGGKASPDEAQAARYGKRSKSKERRAEPKARPSTSPGWWSSDDNLDGDMCIYHAPSGVMTMGRCPDRSASQYFLEAYNTISEQAVKASRSNNDVKCSTCANLPVSLDTPLLKKSAWSSTLTVSRAREVYQKASVNMDQAMVKSESCQQERSCQYLQVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTGVIKLSSAVEVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3879112..3880068))
location: region:3499183-3880068:-1

XP_005258228.1
SIO_000068: ncbiprotein

GI:530424995
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3879112-3880068:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: disks large-associated protein 1 isoform X2
translation: MKGLSGSRSHHHGVTCDSACDSLSHHSDRKPYLLSPVEHHPADHPYYTQRNSFQAECVGPFSDPLASSTFPRRHYTSQQELKDECALVPRTLATKANRIPANLLDQFERQLPLSRDGYHTLQYKRTAVEHRSDSPGRIRHLVHSVQKLFTKSHSLEGPSKGSVNGGKASPDEAQAARYGKRSKSKERRAEPKARPSTSPGWWSSDDNLDGDMCIYHAPSGVMTMGRCPDRSASQYFLEAYNTISEQAVKASRSNNDVKCSTCANLPVSLDTPLLKKSAWSSTLTVSRAREVYQKASVNMDQAMVKSESCQQERSCQYLQVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTGVIKLSSAVEVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3879112..3880068))
location: region:3499183-3880068:-1

XP_005258229.1
SIO_000068: ncbiprotein

GI:530424997
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3879112-3880068:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: isoform 4 is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: disks large-associated protein 1 isoform 4
translation: MDLKTLKLFNSQLRCGWLLYIWNKAFMAHLRVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582162,3729135..3729375,3742335..3742512,3814059..3814273,3874614..3874706))
location: region:3499183-3874706:-1

NP_001229691.1
SIO_000068: ncbiprotein

GI:338221674
SIO_000068: ncbigi

CCDS56052.1
SIO_000068: ccds

position:3874706:-1
position: 3874706
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3874614-3874706:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3581873-3582162:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: isoform 5 is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: disks large-associated protein 1 isoform 5
translation: MDLKTLKLFNSQLRCGWLLYIWNKAFMAHLRVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTGVIKLSSAVEVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3874614..3874706))
location: region:3499183-3874706:-1

NP_001229692.1
SIO_000068: ncbiprotein

GI:338221676
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3874614-3874706:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: disks large-associated protein 1 isoform X3
translation: MDLKTLKLFNSQLRCGWLLYIWNKAFMAHLRSKLKRLKGHLSQVAFVKVKAVWSRKAVLPAAKKMQRNRVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTGVIKLSSAVEVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3821892..3822005,3874614..3874706))
location: region:3499183-3874706:-1

XP_005258230.1
SIO_000068: ncbiprotein

GI:530424999
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3874614-3874706:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3821892-3822005:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: isoform 6 is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: disks large-associated protein 1 isoform 6
translation: MIDLFKAEWVSSVCVQVSRNGRTDQVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3729135..3729375,3742335..3742512,3814059..3814273,3874154..3874228))
location: region:3499183-3874228:-1

NP_001229693.1
SIO_000068: ncbiprotein

GI:338221678
SIO_000068: ncbigi

CCDS56051.1
SIO_000068: ccds

position:3874228:-1
position: 3874228
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3874154-3874228:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: disks large-associated protein 1 isoform X5
translation: MIDLFKAEWVSSVCVQVSRNGRTDQVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTGVIKLSSAVEVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3874154..3874228))
location: region:3499183-3874228:-1

XP_005258232.1
SIO_000068: ncbiprotein

GI:530425003
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3874154-3874228:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: disks large-associated protein 1 isoform X4
translation: MIDLFKAEWVSSVCVQVSRNGRTDQVWVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTGVIKLSSAVEVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3874148..3874228))
location: region:3499183-3874228:-1

XP_005258231.1
SIO_000068: ncbiprotein

GI:530425001
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3874148-3874228:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: disks large-associated protein 1 isoform X6
translation: MPDSVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTGVIKLSSAVEVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3845564..3845575))
location: region:3499183-3845575:-1

XP_005258233.1
SIO_000068: ncbiprotein

GI:530425005
SIO_000068: ncbigi

position:3845575:-1
position: 3845575
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3845564-3845575:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: isoform 2 is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: disks large-associated protein 1 isoform 2
translation: MNLIFHKDILFGIPANKVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3729135..3729375,3742335..3742512,3814059..3814273,3845232..3845282))
location: region:3499183-3845282:-1

NP_001003809.1
SIO_000068: ncbiprotein

GI:51339031
SIO_000068: ncbigi

CCDS42406.1
SIO_000068: ccds

position:3845282:-1
position: 3845282
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3845232-3845282:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: isoform 8 is encoded by transcript variant 8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: disks large-associated protein 1 isoform 8
translation: MNLIFHKDILFGIPANKVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTGVIKLSSAVEVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKERRAPPPVPKKPAKGPAPLIRERSLESSQRQEARKRLMAAKRAASVRQNSATESAESIEIYIPEAQTRL
so part of: DLGAP1
location: complement(join(3499183..3499392,3502491..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3656084..3656113,3729135..3729375,3742335..3742512,3814059..3814273,3845232..3845282))
location: region:3499183-3845282:-1

NP_001229695.1
SIO_000068: ncbiprotein

GI:338221680
SIO_000068: ncbigi

CCDS56050.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:3845232-3845282:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3656084-3656113:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3502491-3502643:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3499183-3499392:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001242761.1
so part of: DLGAP1
location: complement(join(3502143..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3729135..3729375,3742335..3742512,3814059..3814273,3879112..3880140,4005116..4005201,4151180..4151287,4455006..4455266))
location: region:3502143-4455266:-1

GI:338221670
SIO_000068: ncbigi

position:3502143:-1
position: 3502143
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:4455006-4455266:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:4151180-4151287:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:4005116-4005201:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3879112-3880140:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:3502143-3502643:-1/exon

DLGAP1
type: SO_0000234
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
product: discs, large (Drosophila) homolog-associated protein 1, transcript variant 7
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001242765.1
so part of: DLGAP1
location: complement(join(3502143..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3729135..3729375,3742335..3742512,3814059..3814273,3845232..3845358))
location: region:3502143-3845358:-1

GI:338221688
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3845232-3845358:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3502143-3502643:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: isoform 3 is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: disks large-associated protein 1 isoform 3
translation: MKGLSGSRSHHHGVTCDSACDSLSHHSDRKPYLLSPVEHHPADHPYYTQRNSFQAECVGPFSDPLASSTFPRRHYTSQQELKDECALVPRTLATKANRIPANLLDQFERQLPLSRDGYHTLQYKRTAVEHRSDSPGRIRHLVHSVQKLFTKSHSLEGPSKGSVNGGKASPDEAQAARYGKRSKSKERRAEPKARPSTSPGWWSSDDNLDGDMCIYHAPSGVMTMGRCPDRSASQYFLEAYNTISEQAVKASRSNNDVKCSTCANLPVSLDTPLLKKSAWSSTLTVSRAREVYQKASVNMDQAMVKSESCQQERSCQYLQVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKVEQCRFCMVHLKTCTNTGQSK
so part of: DLGAP1
location: complement(join(3502425..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3729135..3729375,3742335..3742512,3814059..3814273,3879112..3880068))
location: region:3502425-3880068:-1

NP_001229690.1
SIO_000068: ncbiprotein

GI:338221671
SIO_000068: ncbigi

CCDS56053.1
SIO_000068: ccds

position:3502425:-1
position: 3502425
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3879112-3880068:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3502425-3502643:-1/exon

DLGAP1
type: SO_0000316
alternative label: DAP-1
alternative label: DAP-1-ALPHA
alternative label: DAP-1-BETA
alternative label: GKAP
alternative label: hGKAP
alternative label: SAPAP1
gene: DLGAP1
gene synonym: DAP-1; DAP-1-ALPHA; DAP-1-BETA; GKAP; hGKAP; SAPAP1
note: isoform 7 is encoded by transcript variant 7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: disks large-associated protein 1 isoform 7
translation: MNLIFHKDILFGIPANKVPQDEWTGYTPRGKDDEIPCRRMRSGSYIKAMGDEDSGDSDTSPKPSPKVAARRESYLKATQPSLTELTTLKISNEHSPKLQIRSHSYLRAVSEVSINRSLDSLDPAGLLTSPKFRSRNESYMRAMSTISQVSEMEVNGQFESVCESVFSELESQAVEALDLPMPGCFRMRSHSYVRAIEKGCSQDDECVSLRSSSPPRTTTTVRTIQSSTVSSCITTYKKTPPPVPPRTTTKPFISITAQSSTESAQDAYMDGQGQRGDIISQSGLSNSTESLDSMKALTAAIEAANAQIHGPASQHMGNNTATVTTTTTIATVTTEDRKKDHFKKNRCLSIGIQVDDAEEPDKTGENKAPSKFQSVGVQVEEEKCFRRFTRSNSVTTAVQADLDFHDNLENSLESIEDNSCPGPMARQFSRDASTSTVSIQGSGNHYHACAADDDFDTDFDPSILPPPDPWIDSITEDPLEAVQRSVCHRDGHWFLKLLQAERDRMEGWCQQMEREERENNLPEDILGKIRTAVGSAQLLMAQKFYQFRELCEENLNPNAHPRPTSQDLAGFWDMLQLSIENISMKFDELHQLKANNWKQMDPLDKKVEQCRFCMVHLKTCTNTGQSK
so part of: DLGAP1
location: complement(join(3502425..3502643,3508568..3508659,3534192..3534613,3567488..3567579,3581873..3582246,3729135..3729375,3742335..3742512,3814059..3814273,3845232..3845282))
location: region:3502425-3845282:-1

NP_001229694.1
SIO_000068: ncbiprotein

GI:338221689
SIO_000068: ncbigi

CCDS56049.1
SIO_000068: ccds

urn:…
SIO_000300: 1
SIO_000628: feature:3845232-3845282:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3814059-3814273:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3742335-3742512:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:3729135-3729375:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:3581873-3582246:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:3567488-3567579:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:3534192-3534613:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:3508568-3508659:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:3502425-3502643:-1/exon

LOC100419892
type: SO_0000704
gene: LOC100419892
note: zinc finger protein 592 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3580158..3580754
location: region:3580158-3580754:1

100419892
SIO_000068: ncbigene

position:3580158:1
position: 3580158
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3580754:1
position: 3580754
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

DLGAP1-AS1
type: SO_0000704
alternative label: HsT914
gene: DLGAP1-AS1
gene synonym: HsT914
note: DLGAP1 antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3594112..>3597377
location: region:3594112-3597377:1
SIO_010080: DLGAP1-AS1

649446
SIO_000068: ncbigene

31676
SIO_000068: hgnc

position:3594112:1
position: 3594112
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3597377:1
position: 3597377
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: FuzzyPosition

DLGAP1-AS1
type: SO_0000673
alternative label: HsT914
gene: DLGAP1-AS1
gene synonym: HsT914
product: DLGAP1 antisense RNA 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_024101.1
so part of: DLGAP1-AS1
location: join(3594112..3594238,3594418..3594482,3596577..>3597377)
location: region:3594112-3597377:1

GI:197209866
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3594112-3594238:1/exon

position:3594238:1
position: 3594238
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3594418-3594482:1/exon

position:3594418:1
position: 3594418
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3594482:1
position: 3594482
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3596577-3597377:1/exon

position:3596577:1
position: 3596577
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

DLGAP1-AS3
type: SO_0000704
gene: DLGAP1-AS3
note: DLGAP1 antisense RNA 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3878180..3897069
location: region:3878180-3897069:1
SIO_010080: DLGAP1-AS3

201477
SIO_000068: ncbigene

27317
SIO_000068: hgnc

position:3878180:1
position: 3878180
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3897069:1
position: 3897069
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

DLGAP1-AS3
type: SO_0000673
gene: DLGAP1-AS3
product: DLGAP1 antisense RNA 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_038895.1
so part of: DLGAP1-AS3
location: join(3878180..3878291,3895771..3896003,3896157..3897069)
location: region:3878180-3897069:1

GI:336455111
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:3878180-3878291:1/exon

position:3878291:1
position: 3878291
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3895771-3896003:1/exon

position:3895771:1
position: 3895771
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3896003:1
position: 3896003
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3896157-3897069:1/exon

position:3896157:1
position: 3896157
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

DLGAP1-AS4
type: SO_0000704
gene: DLGAP1-AS4
note: DLGAP1 antisense RNA 4; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 3962353..4014094
location: region:3962353-4014094:1
SIO_010080: DLGAP1-AS4

101410534
SIO_000068: ncbigene

44333
SIO_000068: hgnc

position:3962353:1
position: 3962353
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:4014094:1
position: 4014094
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

DLGAP1-AS4
type: SO_0000673
gene: DLGAP1-AS4
product: DLGAP1 antisense RNA 4
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_102696.1
so part of: DLGAP1-AS4
location: join(3962353..3962430,3993091..3993202,3995217..3995349,3995608..3995716,4013619..4013943)
location: region:3962353-4013943:1

GI:482661662
SIO_000068: ncbigi

position:4013943:1
position: 4013943
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3962353-3962430:1/exon

position:3962430:1
position: 3962430
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:3993091-3993202:1/exon

position:3993091:1
position: 3993091
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3993202:1
position: 3993202
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:3995217-3995349:1/exon

position:3995217:1
position: 3995217
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3995349:1
position: 3995349
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:3995608-3995716:1/exon

position:3995608:1
position: 3995608
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:3995716:1
position: 3995716
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:4013619-4013943:1/exon

position:4013619:1
position: 4013619
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

GAPDHP66
type: SO_0000704
alternative label: GAPDHL11
alternative label: GAPDL11
gene: GAPDHP66
gene synonym: GAPDHL11; GAPDL11
note: glyceraldehyde-3-phosphate dehydrogenase pseudogene 66; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(3977457..3978686)
location: region:3977457-3978686:-1
SIO_010080: GAPDHP66

645256
SIO_000068: ncbigene

4144
SIO_000068: hgnc

position:3977457:-1
position: 3977457
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:3978686:-1
position: 3978686
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

GAPDHP66
type: SO_0000147
alternative label: GAPDHL11
alternative label: GAPDL11
gene: GAPDHP66
gene synonym: GAPDHL11; GAPDL11
note: Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: GAPDHP66
location: complement(3977457..3978686)
location: region:3977457-3978686:-1

DLGAP1-AS4
type: SO_0000673
gene: DLGAP1-AS4
product: DLGAP1 antisense RNA 4, transcript variant X1
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 3 samples with support for all introns
transcript id: XR_243797.1
so part of: DLGAP1-AS4
location: join(3993083..3993202,3995217..3995349,3995608..3995716,4013619..4014094)
location: region:3993083-4014094:1

GI:530424785
SIO_000068: ncbigi

position:3993083:1
position: 3993083
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:3993083-3993202:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:3995217-3995349:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:3995608-3995716:1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:4013619-4014094:1/exon

DLGAP1-AS5
type: SO_0000704
gene: DLGAP1-AS5
note: DLGAP1 antisense RNA 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 4264602..4296000
location: region:4264602-4296000:1
SIO_010080: DLGAP1-AS5

284215
SIO_000068: ncbigene

27586
SIO_000068: hgnc

position:4264602:1
position: 4264602
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:4296000:1
position: 4296000
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

DLGAP1-AS5
type: SO_0000673
gene: DLGAP1-AS5
product: DLGAP1 antisense RNA 5
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_036489.1
so part of: DLGAP1-AS5
location: join(4264602..4264901,4275301..4275379,4293160..4296000)
location: region:4264602-4296000:1

GI:302318970
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:4264602-4264901:1/exon

position:4264901:1
position: 4264901
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:4275301-4275379:1/exon

position:4275301:1
position: 4275301
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:4275379:1
position: 4275379
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:4293160-4296000:1/exon

position:4293160:1
position: 4293160
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

PPIAP14
type: SO_0000704
alternative label: PPIP4
gene: PPIAP14
gene synonym: PPIP4
note: peptidylprolyl isomerase A (cyclophilin A) pseudogene 14; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(5002511..5003328)
location: region:5002511-5003328:-1

5486
SIO_000068: ncbigene

9267
SIO_000068: hgnc

position:5002511:-1
position: 5002511
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5003328:-1
position: 5003328
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LOC100129355
type: SO_0000704
gene: LOC100129355
note: biorientation of chromosomes in cell division 1 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(5131199..5133350)
location: region:5131199-5133350:-1

100129355
SIO_000068: ncbigene

position:5131199:-1
position: 5131199
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5133350:-1
position: 5133350
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C18orf42
type: SO_0000704
gene: C18orf42
note: chromosome 18 open reading frame 42; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(5143672..5197507)
location: region:5143672-5197507:-1
SIO_010080: C18orf42

642597
SIO_000068: ncbigene

28285
SIO_000068: hgnc

position:5143672:-1
position: 5143672
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5197507:-1
position: 5197507
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C18orf42
type: SO_0000234
gene: C18orf42
product: chromosome 18 open reading frame 42
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001145194.1
so part of: C18orf42
location: complement(join(5143672..5145754,5197037..5197255))
location: region:5143672-5197255:-1

GI:223633926
SIO_000068: ncbigi

position:5197255:-1
position: 5197255
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5197037-5197255:-1/exon

position:5197037:-1
position: 5197037
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5143672-5145754:-1/exon

position:5145754:-1
position: 5145754
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

C18orf42
type: SO_0000234
gene: C18orf42
product: chromosome 18 open reading frame 42, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 2 Proteins, and 96% coverage by RNAseq alignments
transcript id: XM_005258129.1
so part of: C18orf42
location: complement(join(5143674..5145754,5197451..5197507))
location: region:5143674-5197507:-1

GI:530424909
SIO_000068: ncbigi

position:5143674:-1
position: 5143674
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5197451-5197507:-1/exon

position:5197451:-1
position: 5197451
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5143674-5145754:-1/exon

C18orf42
type: SO_0000316
gene: C18orf42
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: putative uncharacterized protein C18orf42 isoform X1
translation: MSVQYPRRRATAGEKPGNEPEEVKLQNASKQIVQNAILQAVQQVSQESQRREERISDNRDHIQLGVGELTKKHEKK
so part of: C18orf42
location: complement(join(5145561..5145754,5197451..5197487))
location: region:5145561-5197487:-1

XP_005258186.1
SIO_000068: ncbiprotein

GI:530424910
SIO_000068: ncbigi

position:5145561:-1
position: 5145561
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5197487:-1
position: 5197487
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5197451-5197487:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5145561-5145754:-1/exon

C18orf42
type: SO_0000316
gene: C18orf42
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: putative uncharacterized protein C18orf42
translation: MVFAPGEKPGNEPEEVKLQNASKQIVQNAILQAVQQVSQESQRREERISDNRDHIQLGVGELTKKHEKK
so part of: C18orf42
location: complement(join(5145561..5145754,5197037..5197052))
location: region:5145561-5197052:-1

NP_001138666.1
SIO_000068: ncbiprotein

GI:223633927
SIO_000068: ncbigi

CCDS54179.1
SIO_000068: ccds

position:5197052:-1
position: 5197052
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5197037-5197052:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5145561-5145754:-1/exon

LINC00526
type: SO_0000704
alternative label: C18orf18
alternative label: HsT959
gene: LINC00526
gene synonym: C18orf18; HsT959
note: long intergenic non-protein coding RNA 526; Derived by automated computational analysis using gene prediction method: BestRefSeq.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(<5236723..5238028)
location: region:5236723-5238028:-1
SIO_010080: LINC00526

147525
SIO_000068: ncbigene

28278
SIO_000068: hgnc

position:5236723:-1
position: 5236723
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: FuzzyPosition

position:5238028:-1
position: 5238028
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

LINC00526
type: SO_0000673
alternative label: C18orf18
alternative label: HsT959
gene: LINC00526
gene synonym: C18orf18; HsT959
product: long intergenic non-protein coding RNA 526
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_026849.1
so part of: LINC00526
location: complement(<5236723..5238028)
location: region:5236723-5238028:-1

GI:223633928
SIO_000068: ncbigi

LINC00667
type: SO_0000704
gene: LINC00667
note: long intergenic non-protein coding RNA 667; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: 5238041..5246507
location: region:5238041-5246507:1
SIO_010080: LINC00667

339290
SIO_000068: ncbigene

27906
SIO_000068: hgnc

position:5238041:1
position: 5238041
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:5246507:1
position: 5246507
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LINC00667
type: SO_0000673
gene: LINC00667
product: long intergenic non-protein coding RNA 667, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 39 ESTs, and 84% coverage by RNAseq alignments, including 5 samples with support for all introns
transcript id: XR_243801.1
so part of: LINC00667
location: join(5238041..5241254,5241698..5241888,5243593..5246507)
location: region:5238041-5246507:1

GI:530424851
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5238041-5241254:1/exon

position:5241254:1
position: 5241254
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5241698-5241888:1/exon

position:5241698:1
position: 5241698
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

position:5241888:1
position: 5241888
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:5243593-5246507:1/exon

position:5243593:1
position: 5243593
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

LINC00667
type: SO_0000673
gene: LINC00667
product: long intergenic non-protein coding RNA 667, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 38 ESTs, and 89% coverage by RNAseq alignments, including 5 samples with support for all introns
transcript id: XR_243799.1
so part of: LINC00667
location: join(5238041..5241811,5243593..5245191)
location: region:5238041-5245191:1

GI:530424849
SIO_000068: ncbigi

position:5245191:1
position: 5245191
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5238041-5241811:1/exon

position:5241811:1
position: 5241811
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5243593-5245191:1/exon

LINC00667
type: SO_0000673
gene: LINC00667
product: long intergenic non-protein coding RNA 667, transcript variant X4
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 34 ESTs, and 88% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XR_243802.1
so part of: LINC00667
location: join(5238041..5241254,5243593..5245191)
location: region:5238041-5245191:1

GI:530424852
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5238041-5241254:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5243593-5245191:1/exon

LINC00667
type: SO_0000673
gene: LINC00667
product: long intergenic non-protein coding RNA 667, transcript variant X5
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 33 ESTs, and 86% coverage by RNAseq alignments, including 1 sample with support for all introns
transcript id: XR_243803.1
so part of: LINC00667
location: join(5238041..5240614,5241698..5241811,5243593..5245191)
location: region:5238041-5245191:1

GI:530424853
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5238041-5240614:1/exon

position:5240614:1
position: 5240614
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5241698-5241811:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:5243593-5245191:1/exon

LINC00667
type: SO_0000673
gene: LINC00667
product: long intergenic non-protein coding RNA 667, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 38 ESTs, and 88% coverage by RNAseq alignments, including 2 samples with support for all introns
transcript id: XR_243800.1
so part of: LINC00667
location: join(5238041..5240276,5240647..5241811,5243593..5245191)
location: region:5238041-5245191:1

GI:530424850
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5238041-5240276:1/exon

position:5240276:1
position: 5240276
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5240647-5241811:1/exon

position:5240647:1
position: 5240647
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:5243593-5245191:1/exon

LINC00667
type: SO_0000673
gene: LINC00667
product: long intergenic non-protein coding RNA 667, transcript variant X6
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 27 ESTs, and 85% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XR_243804.1
so part of: LINC00667
location: join(5238041..5239048,5240647..5241811,5243593..5245191)
location: region:5238041-5245191:1

GI:530424854
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5238041-5239048:1/exon

position:5239048:1
position: 5239048
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5240647-5241811:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:5243593-5245191:1/exon

LINC00667
type: SO_0000673
gene: LINC00667
product: long intergenic non-protein coding RNA 667
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NR_015389.1
so part of: LINC00667
location: join(5238099..5239048,5241698..5241811,5243593..5246507)
location: region:5238099-5246507:1

GI:213972557
SIO_000068: ncbigi

position:5238099:1
position: 5238099
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ForwardStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5238099-5239048:1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5241698-5241811:1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:5243593-5246507:1/exon

LOC100422274
type: SO_0000704
gene: LOC100422274
note: transforming, acidic coiled-coil containing protein 3 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
pseudo: true
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(5240262..5241145)
location: region:5240262-5241145:-1

100422274
SIO_000068: ncbigene

position:5240262:-1
position: 5240262
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5241145:-1
position: 5241145
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ZBTB14
type: SO_0000704
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
note: zinc finger and BTB domain containing 14; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(5289018..5297052)
location: region:5289018-5297052:-1
SIO_010080: ZBTB14

7541
SIO_000068: ncbigene

12860
SIO_000068: hgnc

602126
SIO_000068: omim

position:5289018:-1
position: 5289018
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5297052:-1
position: 5297052
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ZBTB14
type: SO_0000234
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
product: zinc finger and BTB domain containing 14, transcript variant 4
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001243704.1
so part of: ZBTB14
location: complement(join(5289018..5292203,5293243..5293326,5293971..5294000,5297011..5297052))
location: region:5289018-5297052:-1

GI:343962590
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5297011-5297052:-1/exon

position:5297011:-1
position: 5297011
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5293971-5294000:-1/exon

position:5293971:-1
position: 5293971
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5294000:-1
position: 5294000
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:5293243-5293326:-1/exon

position:5293243:-1
position: 5293243
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5293326:-1
position: 5293326
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:5289018-5292203:-1/exon

position:5292203:-1
position: 5292203
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

ZBTB14
type: SO_0000234
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
product: zinc finger and BTB domain containing 14, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_003409.4
so part of: ZBTB14
location: complement(join(5289018..5292203,5293243..5293326,5295812..5296194))
location: region:5289018-5296194:-1

GI:343962592
SIO_000068: ncbigi

position:5296194:-1
position: 5296194
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5295812-5296194:-1/exon

position:5295812:-1
position: 5295812
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5293243-5293326:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:5289018-5292203:-1/exon

ZBTB14
type: SO_0000234
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
product: zinc finger and BTB domain containing 14, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001143823.2
so part of: ZBTB14
location: complement(join(5289018..5292203,5293243..5293326,5293971..5294000,5295812..5296194))
location: region:5289018-5296194:-1

GI:343962593
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5295812-5296194:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5293971-5294000:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:5293243-5293326:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:5289018-5292203:-1/exon

ZBTB14
type: SO_0000234
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
product: zinc finger and BTB domain containing 14, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001243702.1
so part of: ZBTB14
location: complement(join(5289018..5292203,5293243..5293326,5293971..5294000,5295651..5295701))
location: region:5289018-5295701:-1

GI:343962586
SIO_000068: ncbigi

position:5295701:-1
position: 5295701
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5295651-5295701:-1/exon

position:5295651:-1
position: 5295651
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5293971-5294000:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:5293243-5293326:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:5289018-5292203:-1/exon

ZBTB14
type: SO_0000234
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
product: zinc finger and BTB domain containing 14, transcript variant X2
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 27 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 7 samples with support for all introns
transcript id: XM_005258142.1
so part of: ZBTB14
location: complement(join(5289018..5292203,5293243..5293326,5293971..5294000,5294800..5295107))
location: region:5289018-5295107:-1

GI:530424936
SIO_000068: ncbigi

position:5295107:-1
position: 5295107
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5294800-5295107:-1/exon

position:5294800:-1
position: 5294800
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5293971-5294000:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:5293243-5293326:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:5289018-5292203:-1/exon

ZBTB14
type: SO_0000234
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
product: zinc finger and BTB domain containing 14, transcript variant X1
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 27 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 16 samples with support for all introns
transcript id: XM_005258141.1
so part of: ZBTB14
location: complement(join(5289018..5292203,5293243..5293326,5293971..5294785))
location: region:5289018-5294785:-1

GI:530424934
SIO_000068: ncbigi

position:5294785:-1
position: 5294785
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5293971-5294785:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5293243-5293326:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:5289018-5292203:-1/exon

ZBTB14
type: SO_0000234
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
product: zinc finger and BTB domain containing 14, transcript variant X3
note: Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 27 ESTs, 3 Proteins, and 100% coverage by RNAseq alignments, including 3 samples with support for all introns
transcript id: XM_005258143.1
so part of: ZBTB14
location: complement(join(5289376..5292203,5293243..5293326,5294800..5295107))
location: region:5289376-5295107:-1

GI:530424938
SIO_000068: ncbigi

position:5289376:-1
position: 5289376
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5294800-5295107:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5293243-5293326:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:5289376-5292203:-1/exon

ZBTB14
type: SO_0000316
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: zinc finger and BTB domain-containing protein 14
translation: MEFFISMSETIKYNDDDHKTLFLKTLNEQRLEGEFCDIAIVVEDVKFRAHRCVLAACSTYFKKLFKKLEVDSSSVIEIDFLRSDIFEEVLNYMYTAKISVKKEDVNLMMSSGQILGIRFLDKLCSQKRDVSSPDENNGQSKSKYCLKINRPIGDAADTQDDDVEEIGDQDDSPSDDTVEGTPPSQEDGKSPTTTLRVQEAILKELGSEEVRKVNCYGQEVESMETPESKDLGSQTPQALTFNDGMSEVKDEQTPGWTTAASDMKFEYLLYGHHREQIACQACGKTFSDEGRLRKHEKLHTADRPFVCEMCTKGFTTQAHLKEHLKIHTGYKPYSCEVCGKSFIRAPDLKKHERVHSNERPFACHMCDKAFKHKSHLKDHERRHRGEKPFVCGSCTKAFAKASDLKRHENNMHSERKQVTPSAIQSETEQLQAAAMAAEAEQQLETIACS
so part of: ZBTB14
location: complement(join(5290857..5292203,5293243..5293245))
location: region:5290857-5293245:-1

NP_001230631.1
SIO_000068: ncbiprotein

GI:343962587
SIO_000068: ncbigi

CCDS11837.1
SIO_000068: ccds

position:5290857:-1
position: 5290857
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5293245:-1
position: 5293245
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5293243-5293245:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5290857-5292203:-1/exon

ZBTB14
type: SO_0000316
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: zinc finger and BTB domain-containing protein 14
translation: MEFFISMSETIKYNDDDHKTLFLKTLNEQRLEGEFCDIAIVVEDVKFRAHRCVLAACSTYFKKLFKKLEVDSSSVIEIDFLRSDIFEEVLNYMYTAKISVKKEDVNLMMSSGQILGIRFLDKLCSQKRDVSSPDENNGQSKSKYCLKINRPIGDAADTQDDDVEEIGDQDDSPSDDTVEGTPPSQEDGKSPTTTLRVQEAILKELGSEEVRKVNCYGQEVESMETPESKDLGSQTPQALTFNDGMSEVKDEQTPGWTTAASDMKFEYLLYGHHREQIACQACGKTFSDEGRLRKHEKLHTADRPFVCEMCTKGFTTQAHLKEHLKIHTGYKPYSCEVCGKSFIRAPDLKKHERVHSNERPFACHMCDKAFKHKSHLKDHERRHRGEKPFVCGSCTKAFAKASDLKRHENNMHSERKQVTPSAIQSETEQLQAAAMAAEAEQQLETIACS
so part of: ZBTB14
location: complement(join(5290857..5292203,5293243..5293245))
location: region:5290857-5293245:-1

NP_001230633.1
SIO_000068: ncbiprotein

GI:343962591
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5293243-5293245:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5290857-5292203:-1/exon

ZBTB14
type: SO_0000316
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: zinc finger and BTB domain-containing protein 14
translation: MEFFISMSETIKYNDDDHKTLFLKTLNEQRLEGEFCDIAIVVEDVKFRAHRCVLAACSTYFKKLFKKLEVDSSSVIEIDFLRSDIFEEVLNYMYTAKISVKKEDVNLMMSSGQILGIRFLDKLCSQKRDVSSPDENNGQSKSKYCLKINRPIGDAADTQDDDVEEIGDQDDSPSDDTVEGTPPSQEDGKSPTTTLRVQEAILKELGSEEVRKVNCYGQEVESMETPESKDLGSQTPQALTFNDGMSEVKDEQTPGWTTAASDMKFEYLLYGHHREQIACQACGKTFSDEGRLRKHEKLHTADRPFVCEMCTKGFTTQAHLKEHLKIHTGYKPYSCEVCGKSFIRAPDLKKHERVHSNERPFACHMCDKAFKHKSHLKDHERRHRGEKPFVCGSCTKAFAKASDLKRHENNMHSERKQVTPSAIQSETEQLQAAAMAAEAEQQLETIACS
so part of: ZBTB14
location: complement(join(5290857..5292203,5293243..5293245))
location: region:5290857-5293245:-1

NP_003400.2
SIO_000068: ncbiprotein

GI:19923242
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5293243-5293245:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5290857-5292203:-1/exon

ZBTB14
type: SO_0000316
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
codon start: 1
product: zinc finger and BTB domain-containing protein 14
translation: MEFFISMSETIKYNDDDHKTLFLKTLNEQRLEGEFCDIAIVVEDVKFRAHRCVLAACSTYFKKLFKKLEVDSSSVIEIDFLRSDIFEEVLNYMYTAKISVKKEDVNLMMSSGQILGIRFLDKLCSQKRDVSSPDENNGQSKSKYCLKINRPIGDAADTQDDDVEEIGDQDDSPSDDTVEGTPPSQEDGKSPTTTLRVQEAILKELGSEEVRKVNCYGQEVESMETPESKDLGSQTPQALTFNDGMSEVKDEQTPGWTTAASDMKFEYLLYGHHREQIACQACGKTFSDEGRLRKHEKLHTADRPFVCEMCTKGFTTQAHLKEHLKIHTGYKPYSCEVCGKSFIRAPDLKKHERVHSNERPFACHMCDKAFKHKSHLKDHERRHRGEKPFVCGSCTKAFAKASDLKRHENNMHSERKQVTPSAIQSETEQLQAAAMAAEAEQQLETIACS
so part of: ZBTB14
location: complement(join(5290857..5292203,5293243..5293245))
location: region:5290857-5293245:-1

NP_001137295.1
SIO_000068: ncbiprotein

GI:219689126
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5293243-5293245:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5290857-5292203:-1/exon

ZBTB14
type: SO_0000316
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: zinc finger and BTB domain-containing protein 14 isoform X1
translation: MEFFISMSETIKYNDDDHKTLFLKTLNEQRLEGEFCDIAIVVEDVKFRAHRCVLAACSTYFKKLFKKLEVDSSSVIEIDFLRSDIFEEVLNYMYTAKISVKKEDVNLMMSSGQILGIRFLDKLCSQKRDVSSPDENNGQSKSKYCLKINRPIGDAADTQDDDVEEIGDQDDSPSDDTVEGTPPSQEDGKSPTTTLRVQEAILKELGSEEVRKVNCYGQEVESMETPESKDLGSQTPQALTFNDGMSEVKDEQTPGWTTAASDMKFEYLLYGHHREQIACQACGKTFSDEGRLRKHEKLHTADRPFVCEMCTKGFTTQAHLKEHLKIHTGYKPYSCEVCGKSFIRAPDLKKHERVHSNERPFACHMCDKAFKHKSHLKDHERRHRGEKPFVCGSCTKAFAKASDLKRHENNMHSERKQVTPSAIQSETEQLQAAAMAAEAEQQLETIACS
so part of: ZBTB14
location: complement(join(5290857..5292203,5293243..5293245))
location: region:5290857-5293245:-1

XP_005258198.1
SIO_000068: ncbiprotein

GI:530424935
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5293243-5293245:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5290857-5292203:-1/exon

ZBTB14
type: SO_0000316
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: zinc finger and BTB domain-containing protein 14 isoform X2
translation: MEFFISMSETIKYNDDDHKTLFLKTLNEQRLEGEFCDIAIVVEDVKFRAHRCVLAACSTYFKKLFKKLEVDSSSVIEIDFLRSDIFEEVLNYMYTAKISVKKEDVNLMMSSGQILGIRFLDKLCSQKRDVSSPDENNGQSKSKYCLKINRPIGDAADTQDDDVEEIGDQDDSPSDDTVEGTPPSQEDGKSPTTTLRVQEAILKELGSEEVRKVNCYGQEVESMETPESKDLGSQTPQALTFNDGMSEVKDEQTPGWTTAASDMKFEYLLYGHHREQIACQACGKTFSDEGRLRKHEKLHTADRPFVCEMCTKGFTTQAHLKEHLKIHTGYKPYSCEVCGKSFIRAPDLKKHERVHSNERPFACHMCDKAFKHKSHLKDHERRHRGEKPFVCGSCTKAFAKASDLKRHENNMHSERKQVTPSAIQSETEQLQAAAMAAEAEQQLETIACS
so part of: ZBTB14
location: complement(join(5290857..5292203,5293243..5293245))
location: region:5290857-5293245:-1

XP_005258199.1
SIO_000068: ncbiprotein

GI:530424937
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5293243-5293245:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5290857-5292203:-1/exon

ZBTB14
type: SO_0000316
alternative label: ZF5
alternative label: ZFP-161
alternative label: ZFP-5
alternative label: ZFP161
alternative label: ZNF478
gene: ZBTB14
gene synonym: ZF5; ZFP-161; ZFP-5; ZFP161; ZNF478
note: Derived by automated computational analysis using gene prediction method: Gnomon.
codon start: 1
product: zinc finger and BTB domain-containing protein 14 isoform X3
translation: MEFFISMSETIKYNDDDHKTLFLKTLNEQRLEGEFCDIAIVVEDVKFRAHRCVLAACSTYFKKLFKKLEVDSSSVIEIDFLRSDIFEEVLNYMYTAKISVKKEDVNLMMSSGQILGIRFLDKLCSQKRDVSSPDENNGQSKSKYCLKINRPIGDAADTQDDDVEEIGDQDDSPSDDTVEGTPPSQEDGKSPTTTLRVQEAILKELGSEEVRKVNCYGQEVESMETPESKDLGSQTPQALTFNDGMSEVKDEQTPGWTTAASDMKFEYLLYGHHREQIACQACGKTFSDEGRLRKHEKLHTADRPFVCEMCTKGFTTQAHLKEHLKIHTGYKPYSCEVCGKSFIRAPDLKKHERVHSNERPFACHMCDKAFKHKSHLKDHERRHRGEKPFVCGSCTKAFAKASDLKRHENNMHSERKQVTPSAIQSETEQLQAAAMAAEAEQQLETIACS
so part of: ZBTB14
location: complement(join(5290857..5292203,5293243..5293245))
location: region:5290857-5293245:-1

XP_005258200.1
SIO_000068: ncbiprotein

GI:530424939
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5293243-5293245:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5290857-5292203:-1/exon

EPB41L3
type: SO_0000704
alternative label: 4.1B
alternative label: DAL-1
alternative label: DAL1
gene: EPB41L3
gene synonym: 4.1B; DAL-1; DAL1
note: erythrocyte membrane protein band 4.1-like 3; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
so part of: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
location: complement(5392380..5630662)
location: region:5392380-5630662:-1
SIO_010080: EPB41L3
SIO_010080: feature:5392385-5630662:-1/mRNA:98
SIO_010080: feature:5392385-5610269:-1/mRNA:99
SIO_010080: feature:5392385-5610269:-1/mRNA:100
SIO_010080: feature:5392385-5610269:-1/mRNA:101
SIO_010080: feature:5392385-5610269:-1/mRNA:102
SIO_010080: feature:5392385-5610269:-1/mRNA:103
SIO_010080: feature:5392385-5610269:-1/mRNA:104
SIO_010080: feature:5392385-5610269:-1/mRNA:105
SIO_010080: feature:5393472-5489182:-1/CDS:94
SIO_010080: feature:5394682-5610269:-1/CDS:95
SIO_010080: feature:5394682-5610269:-1/CDS:96
SIO_010080: feature:5394682-5610269:-1/CDS:97
SIO_010080: feature:5394682-5610269:-1/CDS:98
SIO_010080: feature:5394682-5610269:-1/CDS:99
SIO_010080: feature:5394682-5610269:-1/CDS:100
SIO_010080: feature:5394682-5610269:-1/CDS:101
SIO_010080: feature:5394682-5489182:-1/CDS:102
SIO_010080: feature:5394682-5489182:-1/CDS:103
SIO_010080: feature:5394682-5489182:-1/CDS:104
SIO_010080: feature:5394682-5478293:-1/CDS:105

23136
SIO_000068: ncbigene

3380
SIO_000068: hgnc

05622
SIO_000068: hprd

605331
SIO_000068: omim

position:5392380:-1
position: 5392380
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5630662:-1
position: 5630662
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

EPB41L3
type: SO_0000234
alternative label: 4.1B
alternative label: DAL-1
alternative label: DAL1
gene: EPB41L3
gene synonym: 4.1B; DAL-1; DAL1
product: erythrocyte membrane protein band 4.1-like 3, transcript variant 4
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001281535.1
so part of: EPB41L3
location: complement(join(5392380..5393477,5394676..5394792,5395066..5395146,5395608..5395706,5396200..5396331,5397057..5397425,5406776..5406967,5410565..5410618,5419710..5419930,5423377..5423552,5424261..5424358,5428312..5428464,5433468..5433555,5433902..5434120,5438034..5438109,5443837..5443879,5445139..5445243,5478240..5478437,5489000..5489160,5612339..5612427,5614350..5614422,5628921..5628990))
location: region:5392380-5628990:-1

GI:528281422
SIO_000068: ncbigi

position:5628990:-1
position: 5628990
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5628921-5628990:-1/exon

position:5628921:-1
position: 5628921
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5614350-5614422:-1/exon

position:5614350:-1
position: 5614350
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5614422:-1
position: 5614422
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:5612339-5612427:-1/exon

position:5612339:-1
position: 5612339
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5612427:-1
position: 5612427
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 4
SIO_000628: feature:5489000-5489160:-1/exon

position:5489000:-1
position: 5489000
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5489160:-1
position: 5489160
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 5
SIO_000628: feature:5478240-5478437:-1/exon

position:5478240:-1
position: 5478240
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5478437:-1
position: 5478437
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 6
SIO_000628: feature:5445139-5445243:-1/exon

position:5445139:-1
position: 5445139
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5445243:-1
position: 5445243
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 7
SIO_000628: feature:5443837-5443879:-1/exon

position:5443837:-1
position: 5443837
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5443879:-1
position: 5443879
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 8
SIO_000628: feature:5438034-5438109:-1/exon

position:5438034:-1
position: 5438034
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5438109:-1
position: 5438109
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 9
SIO_000628: feature:5433902-5434120:-1/exon

position:5433902:-1
position: 5433902
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5434120:-1
position: 5434120
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 10
SIO_000628: feature:5433468-5433555:-1/exon

position:5433468:-1
position: 5433468
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5433555:-1
position: 5433555
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 11
SIO_000628: feature:5428312-5428464:-1/exon

position:5428312:-1
position: 5428312
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5428464:-1
position: 5428464
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 12
SIO_000628: feature:5424261-5424358:-1/exon

position:5424261:-1
position: 5424261
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5424358:-1
position: 5424358
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:5423377-5423552:-1/exon

position:5423377:-1
position: 5423377
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5423552:-1
position: 5423552
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:5419710-5419930:-1/exon

position:5419710:-1
position: 5419710
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5419930:-1
position: 5419930
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 15
SIO_000628: feature:5410565-5410618:-1/exon

position:5410565:-1
position: 5410565
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5410618:-1
position: 5410618
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:5406776-5406967:-1/exon

position:5406776:-1
position: 5406776
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5406967:-1
position: 5406967
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 17
SIO_000628: feature:5397057-5397425:-1/exon

position:5397057:-1
position: 5397057
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5397425:-1
position: 5397425
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 18
SIO_000628: feature:5396200-5396331:-1/exon

position:5396200:-1
position: 5396200
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5396331:-1
position: 5396331
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 19
SIO_000628: feature:5395608-5395706:-1/exon

position:5395608:-1
position: 5395608
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5395706:-1
position: 5395706
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 20
SIO_000628: feature:5395066-5395146:-1/exon

position:5395066:-1
position: 5395066
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5395146:-1
position: 5395146
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 21
SIO_000628: feature:5394676-5394792:-1/exon

position:5394676:-1
position: 5394676
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5394792:-1
position: 5394792
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 22
SIO_000628: feature:5392380-5393477:-1/exon

position:5393477:-1
position: 5393477
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

EPB41L3
type: SO_0000234
alternative label: 4.1B
alternative label: DAL-1
alternative label: DAL1
gene: EPB41L3
gene synonym: 4.1B; DAL-1; DAL1
product: erythrocyte membrane protein band 4.1-like 3, transcript variant 1
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_012307.3
so part of: EPB41L3
location: complement(join(5392380..5393477,5394676..5394792,5395066..5395146,5395608..5395706,5396200..5396331,5397057..5397425,5398020..5398142,5406776..5406967,5407700..5407735,5410565..5410618,5415817..5416377,5419710..5419876,5423377..5423552,5424261..5424358,5428312..5428464,5433468..5433555,5433902..5434120,5438034..5438109,5443837..5443879,5445139..5445243,5478240..5478437,5489000..5489193,5543912..5544309))
location: region:5392380-5544309:-1

GI:528281417
SIO_000068: ncbigi

position:5544309:-1
position: 5544309
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5543912-5544309:-1/exon

position:5543912:-1
position: 5543912
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 2
SIO_000628: feature:5489000-5489193:-1/exon

position:5489193:-1
position: 5489193
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 3
SIO_000628: feature:5478240-5478437:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:5445139-5445243:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:5443837-5443879:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:5438034-5438109:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:5433902-5434120:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:5433468-5433555:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:5428312-5428464:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:5424261-5424358:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:5423377-5423552:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:5419710-5419876:-1/exon

position:5419876:-1
position: 5419876
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 13
SIO_000628: feature:5415817-5416377:-1/exon

position:5415817:-1
position: 5415817
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5416377:-1
position: 5416377
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 14
SIO_000628: feature:5410565-5410618:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:5407700-5407735:-1/exon

position:5407700:-1
position: 5407700
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5407735:-1
position: 5407735
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 16
SIO_000628: feature:5406776-5406967:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:5398020-5398142:-1/exon

position:5398020:-1
position: 5398020
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

position:5398142:-1
position: 5398142
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 18
SIO_000628: feature:5397057-5397425:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:5396200-5396331:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:5395608-5395706:-1/exon

urn:…
SIO_000300: 21
SIO_000628: feature:5395066-5395146:-1/exon

urn:…
SIO_000300: 22
SIO_000628: feature:5394676-5394792:-1/exon

urn:…
SIO_000300: 23
SIO_000628: feature:5392380-5393477:-1/exon

EPB41L3
type: SO_0000234
alternative label: 4.1B
alternative label: DAL-1
alternative label: DAL1
gene: EPB41L3
gene synonym: 4.1B; DAL-1; DAL1
product: erythrocyte membrane protein band 4.1-like 3, transcript variant 3
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001281534.1
so part of: EPB41L3
location: complement(join(5392380..5393477,5394676..5394792,5395066..5395146,5395608..5395706,5396200..5396331,5397057..5397425,5406776..5406967,5410565..5410618,5419710..5419930,5423377..5423552,5424261..5424358,5428312..5428464,5433468..5433555,5433902..5434120,5438034..5438109,5443837..5443879,5445139..5445243,5478240..5478437,5489000..5489193,5543912..5544309))
location: region:5392380-5544309:-1

GI:528281420
SIO_000068: ncbigi

urn:…
SIO_000300: 1
SIO_000628: feature:5543912-5544309:-1/exon

urn:…
SIO_000300: 2
SIO_000628: feature:5489000-5489193:-1/exon

urn:…
SIO_000300: 3
SIO_000628: feature:5478240-5478437:-1/exon

urn:…
SIO_000300: 4
SIO_000628: feature:5445139-5445243:-1/exon

urn:…
SIO_000300: 5
SIO_000628: feature:5443837-5443879:-1/exon

urn:…
SIO_000300: 6
SIO_000628: feature:5438034-5438109:-1/exon

urn:…
SIO_000300: 7
SIO_000628: feature:5433902-5434120:-1/exon

urn:…
SIO_000300: 8
SIO_000628: feature:5433468-5433555:-1/exon

urn:…
SIO_000300: 9
SIO_000628: feature:5428312-5428464:-1/exon

urn:…
SIO_000300: 10
SIO_000628: feature:5424261-5424358:-1/exon

urn:…
SIO_000300: 11
SIO_000628: feature:5423377-5423552:-1/exon

urn:…
SIO_000300: 12
SIO_000628: feature:5419710-5419930:-1/exon

urn:…
SIO_000300: 13
SIO_000628: feature:5410565-5410618:-1/exon

urn:…
SIO_000300: 14
SIO_000628: feature:5406776-5406967:-1/exon

urn:…
SIO_000300: 15
SIO_000628: feature:5397057-5397425:-1/exon

urn:…
SIO_000300: 16
SIO_000628: feature:5396200-5396331:-1/exon

urn:…
SIO_000300: 17
SIO_000628: feature:5395608-5395706:-1/exon

urn:…
SIO_000300: 18
SIO_000628: feature:5395066-5395146:-1/exon

urn:…
SIO_000300: 19
SIO_000628: feature:5394676-5394792:-1/exon

urn:…
SIO_000300: 20
SIO_000628: feature:5392380-5393477:-1/exon

EPB41L3
type: SO_0000234
alternative label: 4.1B
alternative label: DAL-1
alternative label: DAL1
gene: EPB41L3
gene synonym: 4.1B; DAL-1; DAL1
product: erythrocyte membrane protein band 4.1-like 3, transcript variant 2
note: Derived by automated computational analysis using gene prediction method: BestRefSeq.
transcript id: NM_001281533.1
so part of: EPB41L3
location: complement(join(5392380..5393477,5395066..5395146,5395608..5395706,5396200..5396331,5397057..5397425,5398020..5398142,5406776..5406967,5407700..5407735,5410565..5410618,5419710..5419930,5423377..5423552,5424261..5424358,5428312..5428464,5433468..5433555,5433902..5434120,5438034..5438109,5443837..5443879,5445139..5445243,5478240..5478437,5489000..5489193,5540339..5540555))
location: region:5392380-5540555:-1

GI:528281418
SIO_000068: ncbigi

position:5540555:-1
position: 5540555
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition

urn:…
SIO_000300: 1
SIO_000628: feature:5540339-5540555:-1/exon

position:5540339:-1
position: 5540339
reference: Homo sapiens chromosome 18, GRCh37.p13 Primary Assembly.
type: ReverseStrandPosition
type: ExactPosition