Stegostoma fasciatum isolate 6-17 chromosome 27, sSteFas1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Stegostomatidae; Stegostoma.
REFSEQ INFORMATION: The reference sequence is identical to\nCM039253.1.\nAssembly name: sSteFas1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/17. The\noriginal whole-genome shotgun project has the accession\nJAFIRC000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Platanus v. 1.2.4; P_RNA_scaffolder v.\n commit 7941e0f on May 30, at github;\n 3D-DNA v. 180922\nAssembly Name :: sSteFas1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 95.8x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Stegostoma fasciatum Annotation\n Release 100\nAnnotation Version :: 100\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##
Derived by automated computational analysis using gene prediction method: Gnomon.
granulocyte colony-stimulating factor receptor-like, 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 1 sample with support for all annotated introns
granulocyte colony-stimulating factor receptor-like, 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 4 samples with support for all annotated introns
granulocyte colony-stimulating factor receptor-like isoform X2
granulocyte colony-stimulating factor receptor-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
NIPA like domain containing 3, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
NIPA like domain containing 3, transcript variant X2
potassium voltage-gated channel subfamily S member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 24% 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
uncharacterized LOC125464850, 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 5 samples with support for all annotated introns
uncharacterized LOC125464850, transcript variant X1
uncharacterized LOC125464850, transcript variant X2
uncharacterized LOC125464850, 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 2 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 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 14 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 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 22 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 1-like, transcript variant X1
KH domain-containing, RNA-binding, signal transduction-associated protein 1-like
mitochondrial ribosomal protein S15, transcript variant X2
mitochondrial ribosomal protein S15, transcript variant X1
28S ribosomal protein S15, mitochondrial isoform X2
28S ribosomal protein S15, mitochondrial isoform X1
tubulointerstitial nephritis antigen-like 1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tubulointerstitial nephritis antigen-like
potassium voltage-gated channel subfamily KQT member 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125465120, 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 7 samples with support for all annotated introns
uncharacterized LOC125465120, transcript variant X2
uncharacterized LOC125465120, transcript variant X3
nuclear transcription factor Y, gamma, transcript variant X6
nuclear transcription factor Y, gamma, transcript variant X2
nuclear transcription factor Y, gamma, transcript variant X5
nuclear transcription factor Y, gamma, transcript variant X1
nuclear transcription factor Y, gamma, transcript variant X4
nuclear transcription factor Y, gamma, transcript variant X3
nuclear transcription factor Y subunit gamma isoform X1
nuclear transcription factor Y subunit gamma isoform X2
regulating synaptic membrane exocytosis 3, transcript variant X7
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 4 samples with support for all annotated introns
regulating synaptic membrane exocytosis 3, transcript variant 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 1 sample with support for all annotated introns
regulating synaptic membrane exocytosis 3, transcript variant X2
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 6 samples with support for all annotated introns
regulating synaptic membrane exocytosis 3, transcript variant X4
regulating synaptic membrane exocytosis 3, transcript variant X3
regulating synaptic membrane exocytosis 3, transcript variant X1
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 7 samples with support for all annotated introns
regulating synaptic membrane exocytosis 3, transcript variant X8
regulating synaptic membrane exocytosis 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
regulating synaptic membrane exocytosis 3, transcript variant X5
regulating synaptic membrane exocytosis protein 3 isoform X1
regulating synaptic membrane exocytosis protein 3 isoform X2
regulating synaptic membrane exocytosis protein 3 isoform X3
stromal membrane-associated protein 2-like, transcript variant X2
stromal membrane-associated protein 2-like, transcript variant X1
stromal membrane-associated protein 2-like isoform X2
stromal membrane-associated protein 2-like isoform X1
procollagen, type IX, alpha 2, transcript variant X1
procollagen, type IX, alpha 2, 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 3 samples with support for all annotated introns
tRNA isopentenyltransferase 1, transcript variant X1
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 22 samples with support for all annotated introns
tRNA isopentenyltransferase 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 6 samples with support for all annotated introns
tRNA isopentenyltransferase 1, transcript variant X2
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 19 samples with support for all annotated introns
tRNA dimethylallyltransferase isoform X1
tRNA dimethylallyltransferase isoform X2
mucosal pentraxin-like, transcript variant X2
mucosal pentraxin-like, transcript variant X1
collagen, type XVI, alpha 1, transcript variant X2
collagen, type XVI, alpha 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
adhesion G protein-coupled receptor B2, 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 2 samples with support for all annotated introns
adhesion G protein-coupled receptor B2, transcript variant X5
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 4 samples with support for all annotated introns
adhesion G protein-coupled receptor B2, 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 3 samples with support for all annotated introns
adhesion G protein-coupled receptor B2, transcript variant X1
adhesion G protein-coupled receptor B2, transcript variant X2
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
adhesion G protein-coupled receptor B2, transcript variant X3
adhesion G protein-coupled receptor B2, transcript variant X9
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 1 sample with support for all annotated introns
adhesion G protein-coupled receptor B2, transcript variant X10
adhesion G protein-coupled receptor B2 isoform X5
adhesion G protein-coupled receptor B2 isoform X3
adhesion G protein-coupled receptor B2 isoform X2
adhesion G protein-coupled receptor B2 isoform X1
adhesion G protein-coupled receptor B2 isoform X6
adhesion G protein-coupled receptor B2 isoform X7
adhesion G protein-coupled receptor B2, transcript variant X8
adhesion G protein-coupled receptor B2, transcript variant X6
adhesion G protein-coupled receptor B2 isoform X4
adhesion G protein-coupled receptor B2, transcript variant X11
adhesion G protein-coupled receptor B2 isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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
PHD finger protein 3-like, transcript variant X1
PHD finger protein 3-like, transcript variant X2
protein tyrosine phosphatase type IVA 2-like, transcript variant X3
protein tyrosine phosphatase type IVA 2-like, transcript variant X1
protein tyrosine phosphatase type IVA 2-like, transcript variant X2
protein tyrosine phosphatase type IVA 2-like
U7 snRNA-associated Sm-like protein LSm10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
cornifelin homolog, transcript variant X1
cornifelin homolog, transcript variant X2
mitogen-activated protein kinase kinase kinase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitogen-activated protein kinase kinase kinase 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitogen-activated protein kinase kinase kinase 5 isoform X2
mitogen-activated protein kinase kinase kinase 5 isoform X1
mitogen-activated protein kinase kinase kinase 5 isoform X3
MAP7 domain containing 1a, transcript variant X2
MAP7 domain containing 1a, transcript variant X1
MAP7 domain containing 1a, transcript variant X3
MAP7 domain containing 1a, transcript variant X5
MAP7 domain-containing protein 1a isoform X1
MAP7 domain-containing protein 1a isoform X2
MAP7 domain-containing protein 1a isoform X3
MAP7 domain-containing protein 1a isoform X5
MAP7 domain containing 1a, transcript variant X4
MAP7 domain-containing protein 1a isoform X4
thyroid hormone receptor-associated protein 3-like, transcript variant X1
thyroid hormone receptor-associated protein 3-like, transcript variant X6
thyroid hormone receptor-associated protein 3-like, transcript variant X5
thyroid hormone receptor-associated protein 3-like, transcript variant X3
thyroid hormone receptor-associated protein 3-like, transcript variant X7
thyroid hormone receptor-associated protein 3-like, transcript variant X2
thyroid hormone receptor-associated protein 3-like isoform X1
thyroid hormone receptor-associated protein 3-like isoform X5
thyroid hormone receptor-associated protein 3-like isoform X4
thyroid hormone receptor-associated protein 3-like isoform X2
thyroid hormone receptor-associated protein 3-like isoform X6
thyroid hormone receptor-associated protein 3-like, transcript variant X4
thyroid hormone receptor-associated protein 3-like isoform X3
protein eva-1 homolog B-like, transcript variant X3
protein eva-1 homolog B-like, transcript variant X2
protein eva-1 homolog B-like, transcript variant X1
protein eva-1 homolog B-like, transcript variant X4
serine/threonine kinase 40, transcript variant X1
serine/threonine kinase 40, transcript variant X2
serine/threonine-protein kinase 40 isoform X1
serine/threonine-protein kinase 40 isoform X2
inositol polyphosphate-5-phosphatase B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X1
inositol polyphosphate-5-phosphatase B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X2
inositol polyphosphate-5-phosphatase B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X3
inositol polyphosphate-5-phosphatase B, transcript variant X4
inositol polyphosphate-5-phosphatase B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X4
yrdC N(6)-threonylcarbamoyltransferase domain containing
yrdC domain-containing protein, mitochondrial
glycoprotein endo-alpha-1,2-mannosidase-like protein
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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
c19h1orf109 homolog (H. sapiens), transcript variant X1
c19h1orf109 homolog (H. sapiens), transcript variant X2
uncharacterized protein C1orf109 homolog isoform X1
uncharacterized protein C1orf109 homolog isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
glutamate receptor ionotropic, kainate 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 114 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor ionotropic, kainate 3 isoform X2
glutamate receptor ionotropic, kainate 3 isoform X1
glutamate receptor ionotropic, kainate 3 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
MYST/Esa1-associated factor 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
MYST/Esa1-associated factor 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
chromatin modification-related protein MEAF6 isoform X2
chromatin modification-related protein MEAF6 isoform X1
dynein, axonemal, light intermediate chain 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
axonemal dynein light intermediate polypeptide 1
guanine nucleotide binding protein-like 2 (nucleolar), transcript variant X2
guanine nucleotide binding protein-like 2 (nucleolar), transcript variant X1
nucleolar GTP-binding protein 2 isoform X2
nucleolar GTP-binding protein 2 isoform X1
uncharacterized LOC125464897, transcript variant X2
uncharacterized LOC125464897, transcript variant X1
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 17 samples with support for all annotated introns
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CUB and sushi domain-containing protein 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
CUB and sushi domain-containing protein 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
gap junction alpha-4 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 117 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gap junction alpha-4 protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
gap junction alpha-4 protein-like, transcript variant X4
gap junction alpha-4 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
gap junction alpha-4 protein-like isoform X2
gap junction alpha-4 protein-like isoform X1
zinc finger MYM-type protein 4-like, transcript variant X3
zinc finger MYM-type protein 4-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger MYM-type protein 4-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger MYM-type protein 4-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger MYM-type protein 4-like, transcript variant X1
zinc finger MYM-type protein 4-like, transcript variant X2
zinc finger MYM-type protein 4-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
zinc finger MYM-type protein 4-like isoform X4
zinc finger MYM-type protein 4-like isoform X3
zinc finger MYM-type protein 4-like isoform X2
zinc finger MYM-type protein 4-like isoform X1
zinc finger MYM-type protein 4-like isoform X5
splicing factor, proline- and glutamine-rich-like, transcript variant X1
splicing factor, proline- and glutamine-rich-like, transcript variant X2
splicing factor, proline- and glutamine-rich-like isoform X2
splicing factor, proline- and glutamine-rich-like isoform X1
platelet-activating factor receptor-like
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 7 samples with support for all annotated introns
discs, large (Drosophila) homolog-associated protein 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
discs, large (Drosophila) homolog-associated protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
discs, large (Drosophila) homolog-associated protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
discs, large (Drosophila) homolog-associated protein 3, transcript variant X3
discs, large (Drosophila) homolog-associated protein 3, transcript variant X4
discs, large (Drosophila) homolog-associated protein 3, transcript variant X6
small integral membrane protein 12, transcript variant X3
small integral membrane protein 12, transcript variant X2
small integral membrane protein 12, transcript variant X1
small integral membrane protein 12 isoform X1
small integral membrane protein 12 isoform X2
interferon alpha-inducible protein 6-like, transcript variant X1
interferon alpha-inducible protein 6-like, transcript variant X2
interferon alpha-inducible protein 6-like
interferon alpha-inducible protein 27-like protein 2A, transcript variant X2
interferon alpha-inducible protein 27-like protein 2A, transcript variant X1
interferon alpha-inducible protein 27-like protein 2A
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
transmembrane channel-like protein, transcript variant X1
transmembrane channel-like protein, transcript variant X2
four and a half LIM domains 3a, transcript variant X1
four and a half LIM domains 3a, transcript variant X4
four and a half LIM domains 3a, transcript variant X2
four and a half LIM domains 3a, transcript variant X3
UTP11 small subunit processome component
probable U3 small nucleolar RNA-associated protein 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
POU domain, class 3, transcription factor 1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
gap junction protein alpha 9a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gap junction protein alpha 9a, transcript variant X3
gap junction protein alpha 9a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gap junction protein alpha 9a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, 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: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
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 9 samples with support for all annotated introns
uncharacterized LOC125464919, transcript variant X2
uncharacterized LOC125464919, transcript variant X1
zinc finger and BTB domain-containing protein 8A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 8A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 8A-like
zinc finger and BTB domain-containing protein 8B-like, transcript variant X3
zinc finger and BTB domain-containing protein 8B-like, transcript variant X4
zinc finger and BTB domain-containing protein 8B-like, transcript variant X2
zinc finger and BTB domain-containing protein 8B-like, transcript variant X1
zinc finger and BTB domain-containing protein 8B-like
hairy/enhancer-of-split related with YRPW motif-like protein, transcript variant X2
hairy/enhancer-of-split related with YRPW motif-like protein, 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 6 samples with support for all annotated introns
hairy/enhancer-of-split related with YRPW motif-like protein isoform X2
hairy/enhancer-of-split related with YRPW motif protein 1-like isoform X1
NADH:ubiquinone oxidoreductase subunit S5, transcript variant X2
NADH:ubiquinone oxidoreductase subunit S5, transcript variant X1
NADH dehydrogenase [ubiquinone] iron-sulfur protein 5
microtubule actin crosslinking factor 1a, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
microtubule actin crosslinking factor 1a, transcript variant X19
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 2 samples with support for all annotated introns
microtubule actin crosslinking factor 1a, transcript variant X12
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 2 samples with support for all annotated introns
microtubule actin crosslinking factor 1a, transcript variant X1
microtubule actin crosslinking factor 1a, transcript variant X7
microtubule actin crosslinking factor 1a, transcript variant X3
microtubule actin crosslinking factor 1a, transcript variant X8
microtubule actin crosslinking factor 1a, transcript variant X2
microtubule actin crosslinking factor 1a, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
microtubule actin crosslinking factor 1a, transcript variant X10
microtubule actin crosslinking factor 1a, transcript variant X4
microtubule actin crosslinking factor 1a, transcript variant X6
microtubule actin crosslinking factor 1a, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
microtubule actin crosslinking factor 1a, transcript variant X20
microtubule actin crosslinking factor 1a, transcript variant X15
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 3 samples with support for all annotated introns
microtubule actin crosslinking factor 1a, transcript variant X13
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 1 sample with support for all annotated introns
microtubule actin crosslinking factor 1a, transcript variant X14
microtubule actin crosslinking factor 1a, transcript variant X16
microtubule actin crosslinking factor 1a, transcript variant X17
microtubule-actin cross-linking factor 1 isoform X1
microtubule-actin cross-linking factor 1 isoform X7
microtubule-actin cross-linking factor 1 isoform X3
microtubule-actin cross-linking factor 1 isoform X8
microtubule-actin cross-linking factor 1 isoform X2
microtubule-actin cross-linking factor 1, isoforms 1/2/3/4/5 isoform X9
microtubule-actin cross-linking factor 1, isoforms 1/2/3/4/5 isoform X10
microtubule-actin cross-linking factor 1 isoform X4
microtubule-actin cross-linking factor 1 isoform X13
microtubule-actin cross-linking factor 1 isoform X6
microtubule-actin cross-linking factor 1 isoform X18
microtubule-actin cross-linking factor 1 isoform X20
microtubule-actin cross-linking factor 1, isoforms 1/2/3/4/5 isoform X15
microtubule-actin cross-linking factor 1 isoform X14
microtubule-actin cross-linking factor 1 isoform X16
microtubule-actin cross-linking factor 1 isoform X17
microtubule-actin cross-linking factor 1 isoform X11
microtubule-actin cross-linking factor 1 isoform X12
microtubule-actin cross-linking factor 1, isoforms 1/2/3/4/5 isoform X19
microtubule actin crosslinking factor 1a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
microtubule-actin cross-linking factor 1 isoform X5
bone morphogenetic protein 7-like, transcript variant X2
bone morphogenetic protein 7-like, transcript variant X1
bone morphogenetic protein 7-like isoform X1
bone morphogenetic protein 7-like isoform X2
3-hydroxy-3-methylglutaryl-CoA lyase, transcript variant X2
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 16 samples with support for all annotated introns
hydroxymethylglutaryl-CoA lyase, mitochondrial isoform X2
3-hydroxy-3-methylglutaryl-CoA lyase, transcript variant X1
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 24 samples with support for all annotated introns
hydroxymethylglutaryl-CoA lyase, mitochondrial isoform X1
PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1, transcript variant X3
PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 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 19 samples with support for all annotated introns
PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1, transcript variant X1
PITH domain-containing protein 1 isoform X1
PITH domain-containing protein 1 isoform X3
PITH domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
UDP-galactose-4-epimerase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
UDP-galactose-4-epimerase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
UDP-galactose-4-epimerase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
UDP-galactose-4-epimerase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
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 8 samples with support for all annotated introns
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 22 samples with support for all annotated introns
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 1 sample with support for all annotated introns
kelch-like protein 31, transcript variant X1
kelch-like protein 31, transcript variant X2
palmitoyl-protein thioesterase 1-like, transcript variant X2
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 6 samples with support for all annotated introns
palmitoyl-protein thioesterase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
palmitoyl-protein thioesterase 1-like isoform X1
palmitoyl-protein thioesterase 1-like isoform X2
palmitoyl-protein thioesterase 1 (ceroid-lipofuscinosis, neuronal 1, infantile)
CAP, adenylate cyclase-associated protein 1 (yeast), transcript variant X1
CAP, adenylate cyclase-associated protein 1 (yeast), transcript variant X2
RNA-binding protein 24-B-like, 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 5 samples with support for all annotated introns
RNA-binding protein 24-B-like isoform X2
RNA-binding protein 24-B-like, 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 4 samples with support for all annotated introns
RNA-binding protein 24-B-like, 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 19 samples with support for all annotated introns
tektin 2 (testicular), transcript variant X1
tektin 2 (testicular), transcript variant X2
protein argonaute-3, transcript variant X2
protein argonaute-3, transcript variant X1
protein argonaute-3, transcript variant X3
uncharacterized LOC125464960, transcript variant X6
uncharacterized LOC125464960, transcript variant X4
uncharacterized LOC125464960, transcript variant X2
uncharacterized LOC125464960, transcript variant X5
uncharacterized LOC125464960, transcript variant X3
uncharacterized LOC125464960, 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 7 samples with support for all annotated introns
protein argonaute-4, transcript variant X2
protein argonaute-4, transcript variant X1
transient receptor potential cation channel subfamily A member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
transcription factor AP-2-beta-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
transcription factor AP-2-beta-like isoform X1
transcription factor AP-2-beta-like, transcript variant X2
transcription factor AP-2-beta-like isoform X2
uncharacterized LOC125464824, transcript variant X1
uncharacterized LOC125464824, transcript variant X2
UPF0500 protein C1orf216 homolog, transcript variant X8
UPF0500 protein C1orf216 homolog, transcript variant X5
UPF0500 protein C1orf216 homolog, transcript variant X7
UPF0500 protein C1orf216 homolog, transcript variant X3
UPF0500 protein C1orf216 homolog, transcript variant X9
UPF0500 protein C1orf216 homolog, transcript variant X1
UPF0500 protein C1orf216 homolog, transcript variant X2
UPF0500 protein C1orf216 homolog, transcript variant X6
UPF0500 protein C1orf216 homolog, transcript variant X4
UPF0500 protein C1orf216 homolog, transcript variant X10
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 8 samples with support for all annotated introns
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 10 samples with support for all annotated introns
KIAA0319-like ortholog, transcript variant X2
dyslexia-associated protein KIAA0319-like protein isoform X2
KIAA0319-like ortholog, transcript variant X5
KIAA0319-like ortholog, transcript variant X6
KIAA0319-like ortholog, transcript variant X1
KIAA0319-like ortholog, transcript variant X3
dyslexia-associated protein KIAA0319-like protein isoform X4
dyslexia-associated protein KIAA0319-like protein isoform X5
dyslexia-associated protein KIAA0319-like protein isoform X1
KIAA0319-like ortholog, transcript variant X4
dyslexia-associated protein KIAA0319-like protein isoform X3
KIAA0319-like ortholog, transcript variant X8
KIAA0319-like ortholog, transcript variant X7
dyslexia-associated protein KIAA0319-like protein isoform X6
ADP-ribosylserine hydrolase, transcript variant X4
ADP-ribosylserine hydrolase, transcript variant X5
ADP-ribosylserine hydrolase, transcript variant X2
ADP-ribosylserine hydrolase, transcript variant X3
ADP-ribosylserine hydrolase, transcript variant X1
ADP-ribosylserine hydrolase, transcript variant X6
sperm-tail PG-rich repeat containing 1, transcript variant X2
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 2 samples with support for all annotated introns
sperm-tail PG-rich repeat containing 1, transcript variant X1
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 3 samples with support for all annotated introns
ribonucleotide reductase M2 polypeptide, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ribonucleoside-diphosphate reductase subunit M2 isoform X1
ribonucleotide reductase M2 polypeptide, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ribonucleotide reductase M2 polypeptide, transcript variant X5
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
ribonucleoside-diphosphate reductase subunit M2 isoform X3
ribonucleotide reductase M2 polypeptide, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ribonucleoside-diphosphate reductase subunit M2 isoform X2
ribonucleotide reductase M2 polypeptide, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ribonucleoside-diphosphate reductase subunit M2 isoform X4
ribonucleoside-diphosphate reductase subunit M2 isoform X5
keratinocyte-associated protein 3-like, transcript variant X3
keratinocyte-associated protein 3-like, 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 2 samples with support for all annotated introns
keratinocyte-associated protein 3-like, transcript variant X1
calcipressin-3-like, transcript variant X1
calcipressin-3-like, transcript variant X2
calcipressin-3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
non-compact myelin associated protein, transcript variant X1
noncompact myelin-associated protein isoform X1
non-compact myelin associated protein, transcript variant X2
noncompact myelin-associated protein isoform X2
serine/arginine repetitive matrix 1, transcript variant X1
serine/arginine repetitive matrix 1, transcript variant X3
serine/arginine repetitive matrix 1, transcript variant X2
serine/arginine repetitive matrix protein 1 isoform X1
serine/arginine repetitive matrix protein 1 isoform X3
serine/arginine repetitive matrix protein 1 isoform X2
serine/arginine repetitive matrix 1, transcript variant X4
serine/arginine repetitive matrix protein 1 isoform X4
chloride intracellular channel protein 4
RUNX family transcription factor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RUNX family transcription factor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
runt-related transcription factor 3 isoform X2
runt-related transcription factor 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
arginine/serine-rich protein 1, transcript variant X1
arginine/serine-rich protein 1, transcript variant X4
arginine/serine-rich protein 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 23 samples with support for all annotated introns
arginine/serine-rich protein 1, transcript variant X6
arginine/serine-rich protein 1, transcript variant X5
arginine/serine-rich protein 1, transcript variant X7
arginine/serine-rich protein 1, transcript variant X2
small nuclear ribonucleoprotein polypeptide C
transmembrane protein 50A, transcript variant X2
transmembrane protein 50A, transcript variant X1
low density lipoprotein receptor adaptor protein 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
low density lipoprotein receptor adaptor protein 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
low density lipoprotein receptor adapter protein 1b isoform X1
low density lipoprotein receptor adapter protein 1b isoform X2
low density lipoprotein receptor adaptor protein 1b, transcript variant X3
low density lipoprotein receptor adapter protein 1b isoform X3
fibronectin type III domain containing 5a
fibronectin type III domain-containing protein 5
collagen, type VIII, alpha 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
collagen, type VIII, alpha 2, transcript variant X2
collagen, type VIII, alpha 2, transcript variant X7
collagen, type VIII, alpha 2, transcript variant X5
collagen, type VIII, alpha 2, transcript variant X4
collagen, type VIII, alpha 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
collagen, type VIII, alpha 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
collagen, type VIII, alpha 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
trafficking protein particle complex subunit 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
trafficking protein particle complex subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
trafficking protein particle complex subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
trafficking protein particle complex subunit 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
trafficking protein particle complex subunit 3 isoform X2
trafficking protein particle complex subunit 3 isoform X1
trafficking protein particle complex subunit 3 isoform X3
amine sulfotransferase-like, transcript variant X3
amine sulfotransferase-like, transcript variant X4
amine sulfotransferase-like, transcript variant X1
amine sulfotransferase-like, transcript variant X5
amine sulfotransferase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
fatty acid-binding protein, brain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fatty acid-binding protein, brain-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fatty acid-binding protein, brain-like isoform X1
fatty acid-binding protein, brain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
fatty acid-binding protein, brain-like isoform X2
fatty acid-binding protein, brain-like, transcript variant X4
fatty acid-binding protein, heart-like isoform X3
cAMP-dependent protein kinase inhibitor alpha-like, 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 5 samples with support for all annotated introns
cAMP-dependent protein kinase inhibitor alpha-like, transcript variant X5
cAMP-dependent protein kinase inhibitor alpha-like, 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 13 samples with support for all annotated introns
cAMP-dependent protein kinase inhibitor alpha-like, transcript variant X2
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
cAMP-dependent protein kinase inhibitor alpha-like, transcript variant X4
cAMP-dependent protein kinase inhibitor alpha-like, transcript variant X1
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 21 samples with support for all annotated introns
cAMP-dependent protein kinase inhibitor alpha-like, transcript variant X6
cAMP-dependent protein kinase inhibitor alpha-like isoform X2
cAMP-dependent protein kinase inhibitor alpha-like isoform X1
transcription factor HIVEP3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transcription factor HIVEP3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125464979, transcript variant X2
uncharacterized LOC125464979, transcript variant X3
uncharacterized LOC125464979, transcript variant X4
uncharacterized LOC125464979, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00045
regulator of chromosome condensation 1, transcript variant X1
regulator of chromosome condensation 1, transcript variant X6
regulator of chromosome condensation 1, transcript variant X4
regulator of chromosome condensation isoform X1
regulator of chromosome condensation isoform X3
regulator of chromosome condensation 1, transcript variant X2
regulator of chromosome condensation 1, transcript variant X3
regulator of chromosome condensation 1, transcript variant X5
regulator of chromosome condensation isoform X2
opioid receptor, delta 1b, transcript variant X3
opioid receptor, delta 1b, transcript variant X1
opioid receptor, delta 1b, transcript variant X2
regulator of G-protein signaling 17-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transcription elongation factor A (SII), 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
transcription elongation factor A (SII), 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
transcription elongation factor A protein 3 isoform X2
transcription elongation factor A protein 3 isoform X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2-like, transcript variant X2
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2-like, transcript variant X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2-like isoform X2
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
family with sequence similarity 110 member D, transcript variant X2
family with sequence similarity 110 member D, transcript variant X3
family with sequence similarity 110 member D, transcript variant X5
family with sequence similarity 110 member D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
family with sequence similarity 110 member D, transcript variant X4
family with sequence similarity 110 member D, transcript variant X6
family with sequence similarity 110 member D, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
PDLIM1 interacting kinase 1 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
PDLIM1 interacting kinase 1 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
PDLIM1 interacting kinase 1 like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125464848, transcript variant X2
uncharacterized LOC125464848, transcript variant X1
progestin and adipoQ receptor family member VII, b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
progestin and adipoQ receptor family member VII, b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 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: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
platelet-activating factor acetylhydrolase 2, cytoplasmic-like, transcript variant X2
platelet-activating factor acetylhydrolase 2, cytoplasmic-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
platelet-activating factor acetylhydrolase 2, cytoplasmic-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Mediator of RNA polymerase II transcription subunit 30-like, transcript variant X6
Mediator of RNA polymerase II transcription subunit 30-like, transcript variant X3
Mediator of RNA polymerase II transcription subunit 30-like, transcript variant X2
Mediator of RNA polymerase II transcription subunit 30-like, transcript variant X1
Mediator of RNA polymerase II transcription subunit 30-like, transcript variant X4
Mediator of RNA polymerase II transcription subunit 30-like, transcript variant X5
Mediator of RNA polymerase II transcription subunit 30-like, transcript variant X7
mediator of RNA polymerase II transcription subunit 30-like
zinc transporter 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc transporter 2-like, transcript variant X3
zinc transporter 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM63-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM63-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dnaJ homolog subfamily C member 5-like, transcript variant X2
dnaJ homolog subfamily C member 5-like, transcript variant X1
dnaJ homolog subfamily C member 5-like isoform X1
dnaJ homolog subfamily C member 5-like isoform X2
glucocorticoid modulatory element-binding protein 1-like, transcript variant X1
glucocorticoid modulatory element-binding protein 1-like, transcript variant X2
glucocorticoid modulatory element-binding protein 1-like isoform X1
glucocorticoid modulatory element-binding protein 1-like isoform X2
glucocorticoid modulatory element-binding protein 1-like, transcript variant X3
glucocorticoid modulatory element-binding protein 1-like isoform X3
YTH N(6)-methyladenosine RNA binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
beta/gamma crystallin domain-containing protein 1-like, 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 3 samples with support for all annotated introns
beta/gamma crystallin domain-containing protein 1-like, 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 1 sample with support for all annotated introns
beta/gamma crystallin domain-containing protein 1-like isoform X1
beta/gamma crystallin domain-containing protein 1-like isoform X2
SH3 domain-binding glutamic acid-rich-like protein 3
UBX domain protein 11, transcript variant X3
UBX domain protein 11, transcript variant X2
UBX domain protein 11, transcript variant X1
UBX domain protein 11, transcript variant X4
UBX domain-containing protein 11 isoform X1
UBX domain-containing protein 11 isoform X2
UBX domain protein 11, transcript variant X5
UBX domain-containing protein 11 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
protein lin-28 homolog A-like, transcript variant X1
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
protein lin-28 homolog A-like, transcript variant X2
protein lin-28 homolog A-like isoform X1
protein lin-28 homolog A-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
PR domain zinc finger protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PR domain zinc finger protein 1-like, transcript variant X2
PR domain zinc finger protein 1-like isoform X1
PR domain zinc finger protein 1-like, transcript variant X4
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 2 samples with support for all annotated introns
PR domain zinc finger protein 1-like, transcript variant X3
PR domain zinc finger protein 1-like isoform X2
PR domain zinc finger protein 1-like isoform X3
uncharacterized LOC125465193, transcript variant X2
uncharacterized LOC125465193, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins
cation channel sperm-associated protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
connector enhancer of kinase suppressor of Ras 1
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 506 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ribosomal protein S6 kinase 2 alpha-like, transcript variant X6
ribosomal protein S6 kinase 2 alpha-like, transcript variant X1
ribosomal protein S6 kinase 2 alpha-like, transcript variant X2
ribosomal protein S6 kinase 2 alpha-like isoform X1
ribosomal protein S6 kinase 2 alpha-like isoform X2
ribosomal protein S6 kinase 2 alpha-like, transcript variant X4
ribosomal protein S6 kinase 2 alpha-like isoform X4
ribosomal protein S6 kinase 2 alpha-like, transcript variant X5
ribosomal protein S6 kinase 2 alpha-like, transcript variant X3
ribosomal protein S6 kinase alpha-2-like isoform X3
ribosomal protein S6 kinase 2 alpha-like isoform X5
centrosomal protein 85, transcript variant X1
centrosomal protein of 85 kDa isoform X1
centrosomal protein 85, transcript variant X2
centrosomal protein of 85 kDa isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
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 14 samples with support for all annotated introns
uncharacterized protein C1orf232, transcript variant X1
uncharacterized protein C1orf232 isoform X1
uncharacterized protein C1orf232, transcript variant X3
uncharacterized protein C1orf232, transcript variant X2
uncharacterized protein C1orf232 isoform X2
uncharacterized protein C1orf232 isoform X3
palmitoyltransferase ZDHHC18-like, transcript variant X5
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 4 samples with support for all annotated introns
palmitoyltransferase ZDHHC18-like isoform X4
palmitoyltransferase ZDHHC18-like, transcript variant X1
palmitoyltransferase ZDHHC18-like, transcript variant X2
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 21 samples with support for all annotated introns
palmitoyltransferase ZDHHC18-like isoform X2
palmitoyltransferase ZDHHC18-like isoform X1
palmitoyltransferase ZDHHC18-like, 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 8 samples with support for all annotated introns
palmitoyltransferase ZDHHC18-like, transcript variant X4
palmitoyltransferase ZDHHC18-like isoform X3
phosphatidylinositol glycan anchor biosynthesis, class V, transcript variant X4
phosphatidylinositol glycan anchor biosynthesis, class V, transcript variant X5
phosphatidylinositol glycan anchor biosynthesis, class V, transcript variant X3
phosphatidylinositol glycan anchor biosynthesis, class V, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis, class V, transcript variant X2
palmitoyltransferase ZDHHC18-A isoform X2
palmitoyltransferase ZDHHC18-A isoform X1
palmitoyltransferase ZDHHC18-A isoform X3
AT-rich interactive domain-containing protein 1A-like, transcript variant X2
AT-rich interactive domain-containing protein 1A-like, transcript variant X1
AT-rich interactive domain-containing protein 1A-like isoform X2
AT-rich interactive domain-containing protein 1A-like isoform X1
uncharacterized LOC125464907, transcript variant X3
uncharacterized LOC125464907, transcript variant X5
uncharacterized LOC125464907, transcript variant X6
uncharacterized LOC125464907, transcript variant X1
uncharacterized LOC125464907, transcript variant X4
uncharacterized LOC125464907, transcript variant X2
dehydrodolichyl diphosphate synthase, transcript variant X6
dehydrodolichyl diphosphate synthase, transcript variant X2
dehydrodolichyl diphosphate synthase, transcript variant X7
dehydrodolichyl diphosphate synthase, transcript variant X4
dehydrodolichyl diphosphate synthase, transcript variant X3
dehydrodolichyl diphosphate synthase, transcript variant X1
dehydrodolichyl diphosphate synthase, transcript variant X8
dehydrodolichyl diphosphate synthase, transcript variant X5
dehydrodolichyl diphosphate synthase complex subunit DHDDS
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
nuclear receptor subfamily 0, group B, member 2a
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nuclear receptor subfamily 0 group B member 2a
keratinocyte differentiation factor 1-like, transcript variant X2
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 11 samples with support for all annotated introns
keratinocyte differentiation factor 1-like, transcript variant X4
keratinocyte differentiation factor 1-like, transcript variant X1
keratinocyte differentiation factor 1-like, transcript variant X3
keratinocyte differentiation factor 1-like isoform X2
keratinocyte differentiation factor 1-like isoform X1
V-type proton ATPase subunit d 1-like, transcript variant X2
V-type proton ATPase subunit d 1-like, transcript variant X1
V-type proton ATPase subunit d 2-like isoform X2
V-type proton ATPase subunit d 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
WD and tetratricopeptide repeats protein 1
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 10 samples with support for all annotated introns
mannosyl-oligosaccharide 1,2-alpha-mannosidase IA-like
ring finger protein 19B, transcript variant X2
ring finger protein 19B, transcript variant X1
ring finger protein 19B, transcript variant X4
ring finger protein 19B, transcript variant X3
E3 ubiquitin-protein ligase RNF19B isoform X2
E3 ubiquitin-protein ligase RNF19B isoform X1
E3 ubiquitin-protein ligase RNF19B isoform X3
E3 ubiquitin-protein ligase RNF19B isoform 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 14 samples with support for all annotated introns
adenylate kinase 2, transcript variant X2
adenylate kinase 2, mitochondrial isoform X2
adenylate kinase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
adenylate kinase 2, mitochondrial isoform X1
protein disulfide isomerase family A, member 6
polyadenylate-binding protein 4-like, transcript variant X1
polyadenylate-binding protein 4-like isoform X1
polyadenylate-binding protein 4-like, transcript variant X2
polyadenylate-binding protein 4-like, transcript variant X3
polyadenylate-binding protein 4-like isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00431
peptidylprolyl isomerase E (cyclophilin E)
homeobox-containing protein 1-like, transcript variant X3
homeobox-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
homeobox-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
homeobox-containing protein 1-like isoform X2
homeobox-containing protein 1-like isoform X1
homeobox-containing protein 1-like, transcript variant X4
homeobox-containing protein 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
penta-EF-hand domain containing 1, transcript variant X1
penta-EF-hand domain containing 1, transcript variant X2
CD276 antigen-like, 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 9 samples with support for all annotated introns
CD276 antigen-like, 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 16 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
major facilitator superfamily domain containing 2ab
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
sodium-dependent lysophosphatidylcholine symporter 1-B
U5 small nuclear ribonucleoprotein 40 kDa protein
QKI, KH domain containing, RNA binding a, transcript variant X3
QKI, KH domain containing, RNA binding a, transcript variant X1
QKI, KH domain containing, RNA binding a, transcript variant X4
QKI, KH domain containing, RNA binding a, transcript variant X2
QKI, KH domain containing, RNA binding a, transcript variant X5
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 8 samples with support for all annotated introns
PARK2 co-regulated, transcript variant X2
PARK2 co-regulated, transcript variant X1
parkin coregulated gene protein isoform X1
PARK2 co-regulated, transcript variant X3
parkin coregulated gene protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
DnaJ (Hsp40) homolog, subfamily C, member 8
ATP synthase inhibitory factor subunit 1b
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
small nucleolar RNA Z195/SNORD33/SNORD32 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00133
COORDINATES: nucleotide motif:Rfam:12.0:RF00147
heterogeneous nuclear ribonucleoprotein R, transcript variant X2
heterogeneous nuclear ribonucleoprotein R, transcript variant X3
heterogeneous nuclear ribonucleoprotein R, transcript variant X1
heterogeneous nuclear ribonucleoprotein R, transcript variant X4
heterogeneous nuclear ribonucleoprotein R isoform X1
heterogeneous nuclear ribonucleoprotein R isoform X2
5-hydroxytryptamine (serotonin) receptor 1D, G protein-coupled, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
5-hydroxytryptamine (serotonin) receptor 1D, G protein-coupled, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
5-hydroxytryptamine (serotonin) receptor 1D, G protein-coupled, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine zipper protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
leucine zipper protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
leucine zipper protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
leucine zipper protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane protein 30B, transcript variant X3
transmembrane protein 30B, transcript variant X2
transmembrane protein 30B, transcript variant X1
zinc metallopeptidase, STE24 homolog, transcript variant X2
zinc metallopeptidase, STE24 homolog, transcript variant X1
CAAX prenyl protease 1 homolog isoform X2
CAAX prenyl protease 1 homolog isoform X1
dynein light chain Tctex-type 1-like, transcript variant X2
dynein light chain Tctex-type 1-like, transcript variant X1
dynein light chain Tctex-type 1-like isoform X1
dynein light chain Tctex-type 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
zinc finger protein 593, transcript variant X1
zinc finger protein 593, transcript variant X3
zinc finger protein 593, 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 14 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
nuclear receptor coactivator 7-like, transcript variant X1
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 1 sample with support for all annotated introns
nuclear receptor coactivator 7-like, transcript variant X2
nuclear receptor coactivator 7-like isoform X1
nuclear receptor coactivator 7-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial fission regulator 1-like, transcript variant X2
mitochondrial fission regulator 1-like, transcript variant X1
STKc_SGK domain-containing protein, transcript variant X2
STKc_SGK domain-containing protein isoform X2
STKc_SGK domain-containing protein, transcript variant X1
STKc_SGK domain-containing protein isoform X1
eyes absent homolog 3-like, transcript variant X5
eyes absent homolog 3-like, transcript variant X7
eyes absent homolog 3-like, transcript variant X4
eyes absent homolog 3-like, transcript variant X6
eyes absent homolog 3-like, transcript variant X1
eyes absent homolog 3-like, transcript variant X2
eyes absent homolog 3-like, transcript variant X3
sphingomyelin phosphodiesterase acid like 3B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sphingomyelin phosphodiesterase acid like 3B, transcript variant X2
acid sphingomyelinase-like phosphodiesterase 3b isoform X1
acid sphingomyelinase-like phosphodiesterase 3b isoform X2
sphingomyelin phosphodiesterase acid like 3B, transcript variant X3
acid sphingomyelinase-like phosphodiesterase 3b isoform X3
sphingomyelin phosphodiesterase acid like 3B, transcript variant X6
acid sphingomyelinase-like phosphodiesterase 3b isoform X6
sphingomyelin phosphodiesterase acid like 3B, transcript variant X5
acid sphingomyelinase-like phosphodiesterase 3b isoform X5
sphingomyelin phosphodiesterase acid like 3B, transcript variant X4
acid sphingomyelinase-like phosphodiesterase 3b isoform X4
replication protein A2, transcript variant X4
replication protein A2, transcript variant X3
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 1 sample with support for all annotated introns
replication protein A2, transcript variant X2
replication protein A2, transcript variant X1
replication protein A 32 kDa subunit isoform X1
replication protein A 32 kDa subunit isoform X2
replication protein A2, transcript variant X5
replication protein A 32 kDa subunit isoform X3
thymocyte selection associated family member 2, transcript variant X2
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
thymocyte selection associated family member 2, transcript variant X1
thymocyte selection associated family member 2, transcript variant X4
thymocyte selection associated family member 2, transcript variant X3
receptor-type tyrosine-protein phosphatase U-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial trans-2-enoyl-CoA reductase
enoyl-[acyl-carrier-protein] reductase, mitochondrial
transmembrane protein 244-like, transcript variant X15
transmembrane protein 244-like, transcript variant X12
transmembrane protein 244-like, transcript variant X10
transmembrane protein 244-like, transcript variant X3
transmembrane protein 244-like, transcript variant X8
transmembrane protein 244-like, transcript variant X11
transmembrane protein 244-like, transcript variant X4
transmembrane protein 244-like, transcript variant X6
transmembrane protein 244-like, transcript variant X1
transmembrane protein 244-like, transcript variant X2
transmembrane protein 244-like, transcript variant X13
transmembrane protein 244-like, transcript variant X9
transmembrane protein 244-like, transcript variant X14
transmembrane protein 244-like isoform X3
uncharacterized protein LOC125464905 isoform X4
transmembrane protein 244-like isoform X6
transmembrane protein 244-like isoform X1
transmembrane protein 244-like isoform X2
transmembrane protein 244-like isoform X7
transmembrane protein 244-like, transcript variant X7
transmembrane protein 244-like, transcript variant X5
transmembrane protein 244-like isoform X5
serine/arginine-rich splicing factor 4-like, transcript variant X1
serine/arginine-rich splicing factor 4-like isoform X1
serine/arginine-rich splicing factor 4-like, transcript variant X2
serine/arginine-rich splicing factor 4-like isoform X2
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
erythrocyte membrane protein band 4.1a, transcript variant X2
erythrocyte membrane protein band 4.1a, transcript variant X1
erythrocyte membrane protein band 4.1a, transcript variant X5
erythrocyte membrane protein band 4.1a, transcript variant X4
erythrocyte membrane protein band 4.1a, transcript variant X3
erythrocyte membrane protein band 4.1a, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
tRNA selenocysteine 1-associated protein 1-like, 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 12 samples with support for all annotated introns
tRNA selenocysteine 1-associated protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
tRNA selenocysteine 1-associated protein 1-like, transcript variant X1
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 24 samples with support for all annotated introns
tRNA selenocysteine 1-associated protein 1-like isoform X2
tRNA selenocysteine 1-associated protein 1-like isoform X1
tRNA selenocysteine 1-associated protein 1-like isoform X4
tRNA selenocysteine 1-associated protein 1-like, 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 24 samples with support for all annotated introns
tRNA selenocysteine 1-associated protein 1-like isoform X3
protein phosphatase 1, regulatory subunit 8a
COORDINATES: nucleotide motif:Rfam:12.0:RF00553
lysosomal-associated transmembrane protein 4A-like, transcript variant X2
lysosomal-associated transmembrane protein 4A-like, transcript variant X1
lysosomal-associated transmembrane protein 4A-like isoform X2
lysosomal-associated transmembrane protein 4A-like isoform X1
glutathione hydrolase 1 proenzyme-like, transcript variant X2
glutathione hydrolase 1 proenzyme-like, transcript variant X1
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 3 samples with support for all annotated introns
glutathione hydrolase 1 proenzyme-like isoform X2
glutathione hydrolase 1 proenzyme-like isoform X1
glutathione hydrolase 1 proenzyme-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glutathione hydrolase 1 proenzyme-like, transcript variant X3
glutathione hydrolase 1 proenzyme-like isoform X4
glutathione hydrolase 1 proenzyme-like isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: pumilio homolog 1-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00598
COORDINATES: nucleotide motif:Rfam:12.0:RF00188
rho-related GTP-binding protein RhoB-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 188 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium transporting ATPase interacting 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sodium/potassium transporting ATPase interacting 1, transcript variant X2
sodium/potassium-transporting ATPase subunit beta-1-interacting protein 1 isoform X1
sodium/potassium-transporting ATPase subunit beta-1-interacting protein 1 isoform X2
transcription cofactor vestigial-like protein 2, transcript variant X1
transcription cofactor vestigial-like protein 2, transcript variant X2
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 4 samples with support for all annotated introns
transcription cofactor vestigial-like protein 2 isoform X2
transcription cofactor vestigial-like protein 2 isoform X1
transcription cofactor vestigial-like protein 2, transcript variant X4
transcription cofactor vestigial-like protein 2, transcript variant X3
transcription cofactor vestigial-like protein 2 isoform X3
transcription cofactor vestigial-like protein 2 isoform X4
discoidin, CUB and LCCL domain-containing protein 1, transcript variant X1
discoidin, CUB and LCCL domain-containing protein 1, transcript variant X2
discoidin, CUB and LCCL domain-containing protein 1 isoform X1
discoidin, CUB and LCCL domain-containing protein 1 isoform X2
TAF12 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X1
TAF12 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X3
TAF12 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X2
transcription initiation factor TFIID subunit 12 isoform X1
transcription initiation factor TFIID subunit 12 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
synapse-associated protein 1-like, transcript variant X1
synapse-associated protein 1-like, transcript variant X2
synapse-associated protein 1-like, transcript variant X3
Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 4b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
polycomb protein SCMH1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
polycomb protein SCMH1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
polycomb protein SCMH1-like, transcript variant X8
polycomb protein SCMH1-like, transcript variant X5
polycomb protein SCMH1-like, transcript variant X1
polycomb protein SCMH1-like, transcript variant X6
polycomb protein SCMH1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
polycomb protein SCMH1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
mediator of RNA polymerase II transcription, subunit 18 homolog (yeast)
mediator of RNA polymerase II transcription subunit 18
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 16 samples with support for all annotated introns
G-protein coupled receptor 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G-protein coupled receptor 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
S-adenosylmethionine decarboxylase proenzyme-like
AT hook, DNA binding motif, containing 1, transcript variant X3
AT hook, DNA binding motif, containing 1, transcript variant X1
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 5 samples with support for all annotated introns
AT hook, DNA binding motif, containing 1, transcript variant X2
AT hook, DNA binding motif, containing 1, transcript variant X4
AT hook, DNA binding motif, containing 1, transcript variant X5
AT-hook DNA-binding motif-containing protein 1
proto-oncogene tyrosine-protein kinase Yrk-like, transcript variant X5
proto-oncogene tyrosine-protein kinase Yrk-like, transcript variant X4
proto-oncogene tyrosine-protein kinase Yrk-like, transcript variant X3
proto-oncogene tyrosine-protein kinase Yrk-like, transcript variant X7
proto-oncogene tyrosine-protein kinase Yrk-like, transcript variant X8
proto-oncogene tyrosine-protein kinase Yrk-like, transcript variant X2
proto-oncogene tyrosine-protein kinase Yrk-like, transcript variant X1
proto-oncogene tyrosine-protein kinase Yrk-like, transcript variant X6
tyrosine-protein kinase Fyn-like isoform X2
proto-oncogene tyrosine-protein kinase Yrk-like isoform X1
tyrosine-protein kinase Fyn-like isoform X4
proto-oncogene tyrosine-protein kinase Yrk-like isoform X3
uncharacterized LOC125465128, transcript variant X1
uncharacterized LOC125465128, transcript variant X2
digestive cysteine proteinase 2-like, transcript variant X1
digestive cysteine proteinase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
digestive cysteine proteinase 2-like isoform X1
digestive cysteine proteinase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
digestive cysteine proteinase 2-like, transcript variant X3
digestive cysteine proteinase 2-like isoform X3
interferon lambda receptor 1-like, 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 15 samples with support for all annotated introns
interferon lambda receptor 1-like, transcript variant X3
interferon lambda receptor 1-like isoform X1
interferon lambda receptor 1-like, transcript variant X2
interferon lambda receptor 1-like isoform X2
interferon lambda receptor 1-like isoform X3
interleukin-22 receptor subunit alpha-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
fatty acid binding protein 10a, liver basic
fatty acid-binding protein 10-A, liver basic
gap junction beta-2 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 137 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gap junction beta-2 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 139 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gap junction beta-2 protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 137 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 179 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 179 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gap junction beta-2 protein-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 179 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
gap junction beta-2 protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 179 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125465079, transcript variant X1
uncharacterized LOC125465079, transcript variant X2
uncharacterized protein LOC125465079 isoform X1
uncharacterized protein LOC125465079 isoform X2
serine/arginine-rich splicing factor 10-like
CD276 antigen-like, transcript variant X3
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 16 samples with support for all annotated introns
zinc finger and BTB domain containing 8 opposite strand
IQ motif containing C, 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 18 samples with support for all annotated introns
IQ domain-containing protein C isoform X2
IQ motif containing C, 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 20 samples with support for all annotated introns
IQ motif containing C, 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 10 samples with support for all annotated introns
IQ domain-containing protein C isoform X1
IQ domain-containing protein C isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
doublecortin domain-containing protein 2B
eukaryotic translation initiation factor 3, subunit I
eukaryotic translation initiation factor 3 subunit I
myotubularin-related protein 9-like, transcript variant X2
myotubularin-related protein 9-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
myotubularin-related protein 9-like, transcript variant X1
myotubularin-related protein 9-like, transcript variant X4
myotubularin-related protein 9-like, transcript variant X5
myotubularin-related protein 9-like isoform X2
myotubularin-related protein 9-like isoform X1
myotubularin-related protein 9-like isoform X3
family with sequence similarity 167 member B
LCK proto-oncogene, Src family tyrosine kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LCK proto-oncogene, Src family tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
testis-specific serine/threonine-protein kinase 3-like, transcript variant X3
testis-specific serine/threonine-protein kinase 3-like, transcript variant X1
testis-specific serine/threonine-protein kinase 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
testis-specific serine/threonine-protein kinase 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 6 bases in 3 codons; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 6 bases in 3 codons; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
tumor necrosis factor alpha-induced protein 3-like
uncharacterized protein KIAA1522 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
histone-binding protein RBBP4, transcript variant X3
histone-binding protein RBBP4, transcript variant X2
histone-binding protein RBBP4, transcript variant X1
histone-binding protein RBBP4 isoform X3
histone-binding protein RBBP4 isoform X2
histone-binding protein RBBP4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
coiled-coil domain-containing protein 28B
alpha-taxilin-like, transcript variant X2
alpha-taxilin-like, transcript variant X1
alpha-taxilin-like, transcript variant X3
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 9 samples with support for all annotated introns
transmembrane protein 39B, transcript variant X2
transmembrane protein 39B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
transmembrane protein 39B, transcript variant X3
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 14 samples with support for all annotated introns