Chrysemys picta bellii isolate RCT428 chromosome 11, Chrysemys_picta_BioNano-3.0.4, whole genome shotgun sequence.
Chrysemys picta bellii (western painted turtle)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Testudinata; Testudines; Cryptodira; Durocryptodira; Testudinoidea; Emydidae; Chrysemys.
Physical Mapping and Refinement of the Painted Turtle Genome (Chrysemys picta) Inform Amniote Genome Evolution and Challenge Turtle-Bird Chromosomal Conservation
REFSEQ INFORMATION: The reference sequence is identical to\nCM002664.2.\nOn Aug 10, 2021 this sequence version replaced NC_024227.1.\nAssembly name: Chrysemys_picta_BioNano-3.0.4\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Painted turtle genome\nsequencing consortium on 2020/08/21. The original whole-genome\nshotgun project has the accession AHGY00000000.3.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Painted turtle genome sequencing\n consortium\nAssembly Method :: Newbler v. 2.6\nAssembly Name :: Chrysemys_picta_BioNano-3.0.4\nGenome Coverage :: 19.2x\nSequencing Technology :: 454 Life Sciences\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Chrysemys picta Annotation Release\n 103\nAnnotation Version :: 103\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
small lake 1.3 miles south of Potholes Reservoir
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 39 member 10, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
solute carrier family 39 member 10, transcript variant X2
solute carrier family 39 member 10, transcript variant X3
dynein axonemal heavy chain 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
dynein axonemal heavy chain 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein axonemal heavy chain 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
dynein axonemal heavy chain 7 isoform X2
dynein axonemal heavy chain 7 isoform X3
dynein axonemal heavy chain 7 isoform X1
baculoviral IAP repeat-containing protein 5.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine kinase 17b, transcript variant X1
serine/threonine kinase 17b, transcript variant X2
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X4
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X1
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X3
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X2
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X5
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X8
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X7
E3 ubiquitin-protein ligase HECW2 isoform X2
E3 ubiquitin-protein ligase HECW2 isoform X1
E3 ubiquitin-protein ligase HECW2 isoform X3
E3 ubiquitin-protein ligase HECW2 isoform X5
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X6
E3 ubiquitin-protein ligase HECW2 isoform X4
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase HECW2 isoform X6
coiled-coil domain containing 150, transcript variant X1
coiled-coil domain containing 150, transcript variant X4
coiled-coil domain containing 150, transcript variant X2
coiled-coil domain containing 150, transcript variant X3
coiled-coil domain-containing protein 150 isoform X1
coiled-coil domain-containing protein 150 isoform X4
coiled-coil domain-containing protein 150 isoform X2
coiled-coil domain-containing protein 150 isoform X3
coiled-coil domain containing 150, transcript variant X5
coiled-coil domain-containing protein 150 isoform X5
uncharacterized LOC122173857, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC122173857, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
coiled-coil domain containing 150, transcript variant X6
coiled-coil domain-containing protein 150 isoform X6
coiled-coil domain containing 150, transcript variant X7
coiled-coil domain containing 150, transcript variant X8
coiled-coil domain-containing protein 150 isoform X7
general transcription factor IIIC subunit 3, transcript variant X1
general transcription factor 3C polypeptide 3
general transcription factor IIIC subunit 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
general transcription factor IIIC subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
post-GPI attachment to proteins inositol deacylase 1, transcript variant X2
post-GPI attachment to proteins inositol deacylase 1, transcript variant X1
post-GPI attachment to proteins inositol deacylase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
ankyrin repeat domain 44, transcript variant X7
ankyrin repeat domain 44, transcript variant X3
ankyrin repeat domain 44, transcript variant X2
ankyrin repeat domain 44, transcript variant X1
ankyrin repeat domain 44, transcript variant X8
ankyrin repeat domain 44, transcript variant X6
ankyrin repeat domain 44, transcript variant X12
ankyrin repeat domain 44, transcript variant X5
ankyrin repeat domain 44, transcript variant X4
ankyrin repeat domain 44, transcript variant X9
ankyrin repeat domain 44, transcript variant X10
ankyrin repeat domain 44, transcript variant X14
ankyrin repeat domain 44, transcript variant X11
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X13
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X11
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X8
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X9
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X7
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X6
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X5
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X4
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X2
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X3
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X10
ankyrin repeat domain 44, transcript variant X13
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X12
splicing factor 3b subunit 1, transcript variant X2
splicing factor 3b subunit 1, transcript variant X1
splicing factor 3b subunit 1, transcript variant X3
splicing factor 3b subunit 1, transcript variant X4
splicing factor 3b subunit 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
splicing factor 3b subunit 1, transcript variant X5
uncharacterized LOC101948872, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC101948872, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
uncharacterized LOC101948872, transcript variant X1
uncharacterized LOC101948872, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
coenzyme Q-binding protein COQ10 homolog B, mitochondrial isoform X1
coenzyme Q-binding protein COQ10 homolog B, mitochondrial isoform X2
coenzyme Q-binding protein COQ10 homolog B, mitochondrial isoform X3
heat shock protein family D (Hsp60) member 1
60 kDa heat shock protein, mitochondrial
MOB-like protein phocein, transcript variant X4
MOB-like protein phocein, transcript variant X3
10 kDa heat shock protein, mitochondrial isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
MOB-like protein phocein, transcript variant X1
MOB-like protein phocein, transcript variant X2
raftlin family member 2, transcript variant X1
raftlin family member 2, transcript variant X2
raftlin family member 2, transcript variant X3
raftlin family member 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
formiminotransferase cyclodeaminase N-terminal like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
formiminotransferase N-terminal subdomain-containing protein isoform X4
formiminotransferase cyclodeaminase N-terminal like, transcript variant X6
formiminotransferase cyclodeaminase N-terminal like, transcript variant X1
formiminotransferase cyclodeaminase N-terminal like, transcript variant X5
formiminotransferase cyclodeaminase N-terminal like, transcript variant X3
formiminotransferase cyclodeaminase N-terminal like, transcript variant X2
formiminotransferase cyclodeaminase N-terminal like, transcript variant X4
formiminotransferase N-terminal subdomain-containing protein isoform X3
formiminotransferase N-terminal subdomain-containing protein isoform X1
formiminotransferase N-terminal subdomain-containing protein isoform X2
tRNA-yW synthesizing protein 5, transcript variant X4
tRNA-yW synthesizing protein 5, transcript variant X6
tRNA-yW synthesizing protein 5, transcript variant X5
tRNA-yW synthesizing protein 5, transcript variant X3
tRNA-yW synthesizing protein 5, transcript variant X1
tRNA-yW synthesizing protein 5, transcript variant X8
tRNA-yW synthesizing protein 5, transcript variant X9
tRNA-yW synthesizing protein 5, transcript variant X2
tRNA-yW synthesizing protein 5, transcript variant X7
tRNA wybutosine-synthesizing protein 5 isoform X2
tRNA wybutosine-synthesizing protein 5 isoform X1
tRNA wybutosine-synthesizing protein 5 isoform X3
tRNA wybutosine-synthesizing protein 5 isoform X4
matrix AAA peptidase interacting protein 1, transcript variant X2
matrix AAA peptidase interacting protein 1, transcript variant X3
m-AAA protease-interacting protein 1, mitochondrial isoform X2
m-AAA protease-interacting protein 1, mitochondrial isoform X3
matrix AAA peptidase interacting protein 1, transcript variant X1
m-AAA protease-interacting protein 1, mitochondrial isoform X1
spermatogenesis associated serine rich 2 like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
spermatogenesis associated serine rich 2 like, transcript variant X2
spermatogenesis associated serine rich 2 like, transcript variant X1
spermatogenesis associated serine rich 2 like, transcript variant X5
spermatogenesis associated serine rich 2 like, transcript variant X4
spermatogenesis associated serine rich 2 like, transcript variant X3
spermatogenesis associated serine rich 2 like, transcript variant X7
potassium channel tetramerization domain containing 18, transcript variant X3
potassium channel tetramerization domain containing 18, transcript variant X1
potassium channel tetramerization domain containing 18, transcript variant X2
BTB/POZ domain-containing protein KCTD18 isoform X2
BTB/POZ domain-containing protein KCTD18 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
aldehyde oxidase 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
aldehyde oxidase 1, transcript variant X1
aldehyde oxidase 1, transcript variant X3
aldehyde oxidase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: BestRefSeq.
aldehyde oxidase 1, transcript variant X4
aldehyde oxidase-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
basic leucine zipper and W2 domains 1, transcript variant X3
basic leucine zipper and W2 domains 1, transcript variant X1
basic leucine zipper and W2 domains 1, transcript variant X2
basic leucine zipper and W2 domain-containing protein 1 isoform X1
basic leucine zipper and W2 domains 1, transcript variant X4
basic leucine zipper and W2 domain-containing protein 1 isoform X2
CDC like kinase 1, transcript variant X3
CDC like kinase 1, transcript variant X1
CDC like kinase 1, transcript variant X2
dual specificity protein kinase CLK1 isoform X2
dual specificity protein kinase CLK1 isoform X1
NGG1 interacting factor 3 like 1, transcript variant X3
peptidylprolyl isomerase like 3, transcript variant X1
peptidylprolyl isomerase like 3, transcript variant X2
peptidyl-prolyl cis-trans isomerase-like 3
NGG1 interacting factor 3 like 1, transcript variant X1
NGG1 interacting factor 3 like 1, transcript variant X2
origin recognition complex subunit 2, transcript variant X2
origin recognition complex subunit 2, transcript variant X4
origin recognition complex subunit 2, transcript variant X1
origin recognition complex subunit 2, transcript variant X3
origin recognition complex subunit 2, transcript variant X5
origin recognition complex subunit 2, transcript variant X6
origin recognition complex subunit 2 isoform X2
origin recognition complex subunit 2 isoform X1
origin recognition complex subunit 2 isoform X3
origin recognition complex subunit 2 isoform X4
family with sequence similarity 126 member B, transcript variant X4
family with sequence similarity 126 member B, transcript variant X1
family with sequence similarity 126 member B, transcript variant X5
family with sequence similarity 126 member B, transcript variant X2
family with sequence similarity 126 member B, transcript variant X9
family with sequence similarity 126 member B, transcript variant X8
family with sequence similarity 126 member B, transcript variant X7
family with sequence similarity 126 member B, transcript variant X10
family with sequence similarity 126 member B, transcript variant X3
family with sequence similarity 126 member B, transcript variant X6
NADH:ubiquinone oxidoreductase subunit B3, transcript variant X2
NADH:ubiquinone oxidoreductase subunit B3, transcript variant X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
flagellum associated containing coiled-coil domains 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
flagellum associated containing coiled-coil domains 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
flagellum-associated coiled-coil domain-containing protein 1 isoform X2
flagellum-associated coiled-coil domain-containing protein 1 isoform X1
trafficking kinesin protein 2, transcript variant X1
trafficking kinesin protein 2, transcript variant X2
trafficking kinesin protein 2, transcript variant X3
trafficking kinesin-binding protein 2 isoform X3
trafficking kinesin-binding protein 2 isoform X2
trafficking kinesin-binding protein 2 isoform X1
STE20 related adaptor beta, transcript variant X2
STE20 related adaptor beta, transcript variant X1
STE20 related adaptor beta, transcript variant X4
STE20 related adaptor beta, transcript variant X3
STE20-related kinase adapter protein beta isoform X1
STE20-related kinase adapter protein beta isoform X2
C2 calcium dependent domain containing 6, transcript variant X3
C2 calcium dependent domain containing 6, transcript variant X2
C2 calcium dependent domain containing 6, transcript variant X1
C2 calcium dependent domain containing 6, transcript variant X6
C2 calcium dependent domain containing 6, transcript variant X7
C2 calcium-dependent domain-containing protein 6 isoform X3
C2 calcium-dependent domain-containing protein 6 isoform X2
C2 calcium-dependent domain-containing protein 6 isoform X1
C2 calcium-dependent domain-containing protein 6 isoform X6
C2 calcium-dependent domain-containing protein 6 isoform X7
C2 calcium dependent domain containing 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
C2 calcium dependent domain containing 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
C2 calcium-dependent domain-containing protein 6 isoform X4
C2 calcium-dependent domain-containing protein 6 isoform X5
transmembrane protein 237, transcript variant X3
transmembrane protein 237, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
transmembrane protein 237, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
transmembrane protein 237, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
transmembrane protein 237, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X5
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X6
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X7
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X1
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X3
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X2
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X4
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
cyclin dependent kinase 15, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclin dependent kinase 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cyclin dependent kinase 15, transcript variant X2
KIAA2012 ortholog, transcript variant X5
KIAA2012 ortholog, transcript variant X3
KIAA2012 ortholog, transcript variant X1
KIAA2012 ortholog, transcript variant X4
KIAA2012 ortholog, transcript variant X2
uncharacterized protein KIAA2012 homolog isoform X1
uncharacterized protein KIAA2012 homolog isoform X3
uncharacterized protein KIAA2012 homolog isoform X4
uncharacterized protein KIAA2012 homolog isoform X2
NOP58 ribonucleoprotein, transcript variant X2
NOP58 ribonucleoprotein, transcript variant X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00575
COORDINATES: nucleotide motif:Rfam:12.0:RF01192
COORDINATES: nucleotide motif:Rfam:12.0:RF01182
bone morphogenetic protein receptor type 2, transcript variant X1
bone morphogenetic protein receptor type-2 isoform X1
bone morphogenetic protein receptor type 2, transcript variant X2
bone morphogenetic protein receptor type-2 isoform X2
family with sequence similarity 117 member B
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
islet cell autoantigen 1 like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
islet cell autoantigen 1 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
islet cell autoantigen 1 like, transcript variant X1
islet cell autoantigen 1-like protein isoform X1
islet cell autoantigen 1-like protein isoform X2
calcium responsive transcription factor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium responsive transcription factor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
calcium responsive transcription factor, transcript variant X2
calcium responsive transcription factor, transcript variant X1
calcium-responsive transcription factor isoform X1
calcium-responsive transcription factor isoform X2
calcium-responsive transcription factor isoform X4
calcium-responsive transcription factor isoform X3
calcium responsive transcription factor, transcript variant X5
calcium-responsive transcription factor isoform X5
cyclic nucleotide binding domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide-binding domain-containing protein 2
neurobeachin like 1, transcript variant X1
neurobeachin like 1, transcript variant X2
neurobeachin like 1, transcript variant X3
neurobeachin like 1, transcript variant X4
alpha-aspartyl dipeptidase-like, transcript variant X3
alpha-aspartyl dipeptidase-like, transcript variant X2
alpha-aspartyl dipeptidase-like, transcript variant X1
alpha-aspartyl dipeptidase-like isoform X3
alpha-aspartyl dipeptidase-like isoform X2
alpha-aspartyl dipeptidase-like isoform X1
cytochrome P450 20A1, transcript variant X2
cytochrome P450 20A1, transcript variant X1
cytochrome P450 20A1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
cytochrome P450 20A1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
abl interactor 2, transcript variant X13
abl interactor 2, transcript variant X14
abl interactor 2, transcript variant X15
abl interactor 2, transcript variant X16
abl interactor 2, transcript variant X11
abl interactor 2, transcript variant X10
abl interactor 2, transcript variant X12
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1, transcript variant X4
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1, transcript variant X3
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1, transcript variant X2
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1, transcript variant X5
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1, transcript variant X1
ras-associated and pleckstrin homology domains-containing protein 1 isoform X4
ras-associated and pleckstrin homology domains-containing protein 1 isoform X3
ras-associated and pleckstrin homology domains-containing protein 1 isoform X2
ras-associated and pleckstrin homology domains-containing protein 1 isoform X1
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1, transcript variant X6
ras-associated and pleckstrin homology domains-containing protein 1 isoform X5
ras-associated and pleckstrin homology domains-containing protein 1 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
T-cell-specific surface glycoprotein CD28
cytotoxic T-lymphocyte associated protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns