Stegostoma fasciatum isolate 6-17 chromosome 32, 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\nCM039258.1.\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.
glutamate receptor, ionotropic, kainate 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glutamate receptor, ionotropic, kainate 4, transcript variant X3
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
glutamate receptor, ionotropic, kainate 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glutamate receptor, ionotropic, kainate 4, transcript variant X4
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 1 sample with support for all annotated introns
glutamate receptor ionotropic, kainate 4 isoform X1
glutamate receptor ionotropic, kainate 4 isoform X3
glutamate receptor ionotropic, kainate 4 isoform X2
glutamate receptor ionotropic, kainate 4 isoform X4
tubulin folding cofactor E-like b, 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 17 samples with support for all annotated introns
tubulin folding cofactor E-like b, 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 9 samples with support for all annotated introns
tubulin folding cofactor E-like b, 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 6 samples with support for all annotated introns
tubulin-specific chaperone cofactor E-like protein isoform X1
tubulin-specific chaperone cofactor E-like protein isoform X2
COORDINATES: polyA evidence [ECO:0006239]
rho guanine nucleotide exchange factor 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 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 98% coverage of the annotated genomic feature by RNAseq alignments
POU class 2 homeobox 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POU class 2 homeobox 3, transcript variant X1
POU domain, class 2, transcription factor 3 isoform X2
POU domain, class 2, transcription factor 3 isoform 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 21 samples with support for all annotated introns
myelin protein zero-like protein 3, transcript variant X1
myelin protein zero-like protein 3 isoform X1
myelin protein zero-like protein 3, 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 10 samples with support for all annotated introns
myelin protein zero-like protein 3, transcript variant X4
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 4 samples with support for all annotated introns
myelin protein zero-like protein 3, transcript variant X5
myelin protein zero-like protein 3, transcript variant X3
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 11 samples with support for all annotated introns
myelin protein zero-like protein 3 isoform X2
myelin protein zero-like protein 3 isoform 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 17 samples with support for all annotated introns
T-cell surface glycoprotein CD3 epsilon chain-like
T-cell surface glycoprotein CD3 delta chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
T-cell surface glycoprotein CD3 gamma chain-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 1 sample with support for all annotated introns
T-cell surface glycoprotein CD3 gamma chain-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 5 samples with support for all annotated introns
T-cell surface glycoprotein CD3 gamma chain-like, 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 4 samples with support for all annotated introns
T-cell surface glycoprotein CD3 gamma chain-like isoform X1
T-cell surface glycoprotein CD3 gamma chain-like isoform X2
uncharacterized LOC125466990, 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 2 samples with support for all annotated introns
uncharacterized LOC125466990, transcript variant X1
uncharacterized LOC125466990, 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 3 samples with support for all annotated introns
uncharacterized LOC125466990, 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 1 sample with support for all annotated introns
uncharacterized protein LOC125466990 isoform X1
uncharacterized protein LOC125466990 isoform X2
uncharacterized protein LOC125466990 isoform X4
uncharacterized protein LOC125466990 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125467025, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC125467025, 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 22 samples with support for all annotated introns
uncharacterized LOC125467025, 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 24 samples with support for all annotated introns
uncharacterized LOC125467025, transcript variant X7
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
uncharacterized LOC125467025, transcript variant X5
uncharacterized protein LOC125467025 isoform X5
uncharacterized protein LOC125467025 isoform X4
uncharacterized protein LOC125467025 isoform X1
uncharacterized protein LOC125467025 isoform X7
uncharacterized protein LOC125467025 isoform X6
uncharacterized LOC125467025, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein LOC125467025 isoform X2
uncharacterized LOC125467025, transcript variant X3
uncharacterized protein LOC125467025 isoform 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
HOATZ cilia and flagella associated protein, transcript variant X1
HOATZ cilia and flagella associated protein, transcript variant X2
HOATZ cilia and flagella associated protein, transcript variant X4
HOATZ cilia and flagella associated protein, 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 6 samples with support for all annotated introns
cilia- and flagella-associated protein HOATZ isoform X2
cilia- and flagella-associated protein HOATZ isoform X4
cilia- and flagella-associated protein HOATZ isoform X1
cilia- and flagella-associated protein HOATZ isoform 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 6 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 2-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 5 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 2-like, transcript variant X6
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 1 sample with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 2-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 2-like, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 2-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 2-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 3 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 2-like isoform X1
ubiquitin carboxyl-terminal hydrolase 2-like isoform X2
ubiquitin carboxyl-terminal hydrolase 2-like, transcript variant X7
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 16 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 2-like isoform X3
membrane frizzled-related protein, 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 2 samples with support for all annotated introns
membrane frizzled-related protein, transcript variant X1
membrane frizzled-related protein, transcript variant X4
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 2 samples with support for all annotated introns
membrane frizzled-related protein, 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 1 sample with support for all annotated introns
membrane frizzled-related protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
membrane frizzled-related protein isoform X1
membrane frizzled-related protein isoform X3
membrane frizzled-related protein isoform X2
membrane frizzled-related protein isoform X4
complement C1q tumor necrosis factor-related protein 5
melanoma cell adhesion molecule b, transcript variant X2
melanoma cell adhesion molecule b, transcript variant X1
melanoma cell adhesion molecule b, transcript variant X3
melanoma cell adhesion molecule b isoform X1
melanoma cell adhesion molecule b isoform X3
melanoma cell adhesion molecule b isoform X2
Cbl proto-oncogene, E3 ubiquitin protein ligase, 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 3 samples with support for all annotated introns
Cbl proto-oncogene, E3 ubiquitin protein ligase, 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 12 samples with support for all annotated introns
Cbl proto-oncogene, E3 ubiquitin protein ligase, transcript variant X3
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
E3 ubiquitin-protein ligase CBL isoform X2
E3 ubiquitin-protein ligase CBL isoform X1
E3 ubiquitin-protein ligase CBL isoform X3
coiled-coil domain-containing protein 153
intraflagellar transport 46 homolog (Chlamydomonas), transcript variant X2
intraflagellar transport 46 homolog (Chlamydomonas), transcript variant X1
intraflagellar transport protein 46 homolog isoform X2
intraflagellar transport protein 46 homolog isoform X1
VPS11 core subunit of CORVET and HOPS complexes
vacuolar protein sorting-associated protein 11 homolog
hypoxia up-regulated 1, transcript variant X1
hypoxia up-regulated 1, transcript variant X2
hypoxia up-regulated 1, transcript variant X4
hypoxia up-regulated 1, transcript variant X3
hypoxia up-regulated 1, transcript variant X5
trehalase (brush-border membrane glycoprotein)
uncharacterized LOC125467043, 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
uncharacterized LOC125467043, 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 24 samples with support for all annotated introns
probable ATP-dependent RNA helicase ddx6
C-X-C chemokine receptor type 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
C-X-C chemokine receptor type 5, 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
C-X-C chemokine receptor type 5 isoform X1
C-X-C chemokine receptor type 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 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: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
TEN1 subunit of CST complex, transcript variant X2
TEN1 subunit of CST complex, transcript variant X1
TEN1 subunit of CST complex, transcript variant X3
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 7 samples with support for all annotated introns
sortilin-related receptor, L(DLR class) A repeats containing, transcript variant X1
sortilin-related receptor, L(DLR class) A repeats containing, transcript variant X2
ubiquitin-associated and SH3 domain-containing protein 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 2 samples with support for all annotated introns
ubiquitin-associated and SH3 domain-containing protein B-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 11 samples with support for all annotated introns
ubiquitin-associated and SH3 domain-containing protein B-like isoform X2
ubiquitin-associated and SH3 domain-containing protein B-like isoform X1
succinate dehydrogenase complex, subunit D, integral membrane protein b
succinate dehydrogenase [ubiquinone] cytochrome b small subunit B, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology-like domain, family B, member 1b
pleckstrin homology-like domain family B member 1
NLR family member X1, 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 1 sample with support for all annotated introns
NLR family member X1, transcript variant X1
Na(+)/H(+) exchange regulatory cofactor NHE-RF3-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 5 samples with support for all annotated introns
Na(+)/H(+) exchange regulatory cofactor NHE-RF3-like, transcript variant X2
Na(+)/H(+) exchange regulatory cofactor NHE-RF3-like, transcript variant X4
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
Na(+)/H(+) exchange regulatory cofactor NHE-RF3-like, transcript variant X5
Na(+)/H(+) exchange regulatory cofactor NHE-RF3-like isoform X1
Na(+)/H(+) exchange regulatory cofactor NHE-RF3-like isoform X2
Na(+)/H(+) exchange regulatory cofactor NHE-RF3-like isoform X4
Na(+)/H(+) exchange regulatory cofactor NHE-RF3-like, transcript variant X3
Na(+)/H(+) exchange regulatory cofactor NHE-RF3-like isoform X3
ubiquitination factor E4A (UFD2 homolog, yeast)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ATP synthase, H+ transporting, mitochondrial F0 complex, subunit g
lysine (K)-specific methyltransferase 2A, transcript variant X4
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
lysine (K)-specific methyltransferase 2A, 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 3 samples with support for all annotated introns
lysine (K)-specific methyltransferase 2A, 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 6 samples with support for all annotated introns
lysine (K)-specific methyltransferase 2A, 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 7 samples with support for all annotated introns
histone-lysine N-methyltransferase 2A isoform X1
histone-lysine N-methyltransferase 2A isoform X2
histone-lysine N-methyltransferase 2A isoform X3
histone-lysine N-methyltransferase 2A isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
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 4 samples with support for all annotated introns
transmembrane protein 25, transcript variant X1
transmembrane protein 25, 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 9 samples with support for all annotated introns
transmembrane protein 25, transcript variant X3
FXYD domain containing ion transport regulator 6
FXYD domain-containing ion transport regulator 6
transmembrane serine protease 13a, transcript variant X2
transmembrane serine protease 13a, transcript variant X1
transmembrane protease serine 13a isoform X2
transmembrane protease serine 13a isoform X1
marginal zone B- and B1-cell-specific protein-like, transcript variant X1
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 19 samples with support for all annotated introns
marginal zone B- and B1-cell-specific protein-like, transcript variant X2
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 20 samples with support for all annotated introns
marginal zone B- and B1-cell-specific protein-like, transcript variant X3
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 17 samples with support for all annotated introns
marginal zone B- and B1-cell-specific protein-like, 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 13 samples with support for all annotated introns
marginal zone B- and B1-cell-specific protein-like, transcript variant X6
marginal zone B- and B1-cell-specific protein-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 5 samples with support for all annotated introns
marginal zone B- and B1-cell-specific protein-like, transcript variant X8
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 8 samples with support for all annotated introns
marginal zone B- and B1-cell-specific protein-like, transcript variant X7
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 7 samples with support for all annotated introns
marginal zone B- and B1-cell-specific protein-like, transcript variant X9
marginal zone B- and B1-cell-specific protein-like
interleukin-20 receptor subunit alpha-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
interleukin-20 receptor subunit alpha-like isoform X1
interleukin-20 receptor subunit alpha-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 7 samples with support for all annotated introns
uncharacterized protein LOC125467076 isoform X2
transmembrane serine protease 4a, 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 4 samples with support for all annotated introns
transmembrane protease serine 4a isoform X2
transmembrane serine protease 4a, transcript variant X1
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 3 samples with support for all annotated introns
transmembrane serine protease 4a, transcript variant X4
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
transmembrane protease serine 4a isoform X1
transmembrane serine protease 4a, transcript variant X3
transmembrane protease serine 4a isoform X3
transmembrane protease serine 4a isoform X4
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 6 samples with support for all annotated introns
sodium channel, voltage-gated, type II, beta, 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 2 samples with support for all annotated introns
sodium channel, voltage-gated, type II, beta, 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 9 samples with support for all annotated introns
sodium channel subunit beta-2 isoform X1
sodium channel, voltage-gated, type II, beta, 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 9 samples with support for all annotated introns
sodium channel subunit beta-2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 64% coverage of the annotated genomic feature by RNAseq alignments
sterol-C5-desaturase, transcript variant X1
sterol-C5-desaturase, transcript variant X2
glucuronokinase with putative uridyl pyrophosphorylase
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
carotenoid-cleaving dioxygenase, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
carotenoid-cleaving dioxygenase, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
carotenoid-cleaving dioxygenase, mitochondrial-like, transcript variant X3
carotenoid-cleaving dioxygenase, mitochondrial-like isoform X1
carotenoid-cleaving dioxygenase, mitochondrial-like isoform X3
carotenoid-cleaving dioxygenase, mitochondrial-like isoform X2
carotenoid-cleaving dioxygenase, mitochondrial-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
carotenoid-cleaving dioxygenase, mitochondrial-like isoform X5
carotenoid-cleaving dioxygenase, mitochondrial-like, transcript variant X4
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 5 samples with support for all annotated introns
carotenoid-cleaving dioxygenase, mitochondrial-like isoform X4
uncharacterized LOC125467014, 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 5 samples with support for all annotated introns
uncharacterized LOC125467014, transcript variant X2
uncharacterized protein LOC125467014 isoform X1
uncharacterized protein LOC125467014 isoform X2
zinc finger and BTB domain containing 16a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain-containing protein 16-A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
5-hydroxytryptamine (serotonin) receptor 3B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ubiquitin specific peptidase 28, transcript variant X7
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
ubiquitin specific peptidase 28, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
ubiquitin specific peptidase 28, transcript variant X1
ubiquitin specific peptidase 28, transcript variant X3
ubiquitin specific peptidase 28, transcript variant X4
ubiquitin specific peptidase 28, transcript variant X5
ubiquitin specific peptidase 28, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 28 isoform X1
ubiquitin carboxyl-terminal hydrolase 28 isoform X3
ubiquitin carboxyl-terminal hydrolase 28 isoform X4
ubiquitin carboxyl-terminal hydrolase 28 isoform X5
ubiquitin carboxyl-terminal hydrolase 28 isoform X2
ubiquitin carboxyl-terminal hydrolase 28 isoform X7
ubiquitin specific peptidase 28, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 28 isoform X6
ankyrin repeat and kinase domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and protein kinase domain-containing protein 1
transmembrane serine protease 5, transcript variant X1
transmembrane serine protease 5, transcript variant X2
transmembrane protease serine 5 isoform X1
transmembrane protease serine 5 isoform X2
transmembrane serine protease 5, transcript variant X3
transmembrane protease serine 5 isoform X3
D(2) dopamine receptor B-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 1 sample with support for all annotated introns
D(2) dopamine receptor B-like, transcript variant X1
D(2) dopamine receptor B-like isoform X1
D(2) dopamine receptor B-like isoform X2
centromere/kinetochore protein zw10 homolog
G protein-activated inward rectifier potassium channel 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G protein-activated inward rectifier potassium channel 4-like, transcript variant X1
G protein-activated inward rectifier potassium channel 4-like, transcript variant X3
G protein-activated inward rectifier potassium channel 3-like isoform X1
G protein-activated inward rectifier potassium channel 4-like isoform X2
grass carp reovirus (GCRV)-induced gene 2o
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: grass carp reovirus (GCRV)-induced gene 2o
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATP-binding cassette sub-family G member 4 isoform X1
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X2
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X3
ATP-binding cassette sub-family G member 4 isoform X2
ATP-binding cassette sub-family G member 4 isoform X3
RING finger protein 214-like, transcript variant X1
RING finger protein 214-like, transcript variant X2
RING finger protein 214-like, transcript variant X3
RING finger protein 214-like, transcript variant X4
RING finger protein 214-like, transcript variant X5
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 13 samples with support for all annotated introns
centrosomal protein of 164 kDa-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
centrosomal protein of 164 kDa-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 3 samples with support for all annotated introns
centrosomal protein of 164 kDa-like isoform X1
centrosomal protein of 164 kDa-like isoform X2
Down syndrome cell adhesion molecule-like protein 1 homolog, transcript variant X1
Down syndrome cell adhesion molecule-like protein 1 homolog isoform X1
Down syndrome cell adhesion molecule-like protein 1 homolog, transcript variant X2
Down syndrome cell adhesion molecule-like protein 1 homolog isoform X2
phospholipid transfer protein C2CD2L isoform X2
phospholipid transfer protein C2CD2L isoform X1
histone H4 transcription factor, 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 21 samples with support for all annotated introns
histone H4 transcription factor, 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 8 samples with support for all annotated introns
histone H4 transcription factor, 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 24 samples with support for all annotated introns
histone H4 transcription factor isoform X1
histone H4 transcription factor isoform 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
dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
uncharacterized protein LOC553749 homolog, transcript variant X3
uncharacterized protein LOC553749 homolog, transcript variant X2
uncharacterized protein LOC553749 homolog, transcript variant X1
uncharacterized protein zgc:113279 isoform X3
receptor-interacting serine/threonine-protein kinase 4 isoform X2
uncharacterized protein zgc:113279 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
colorectal cancer associated 2 isoform X1
colorectal cancer associated 2 isoform X3
colorectal cancer associated 2 isoform X2
uncharacterized protein C11orf53 homolog, transcript variant X1
uncharacterized protein C11orf53 homolog, transcript variant X2
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
uncharacterized protein C11orf53 homolog isoform X1
uncharacterized protein C11orf53 homolog isoform 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 10 samples with support for all annotated introns
apolipoprotein A-I-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 3 samples with support for all annotated introns
apolipoprotein A-I-like, 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 1 sample with support for all annotated introns
SIK family kinase 3, transcript variant X3
SIK family kinase 3, transcript variant X4
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 13 samples with support for all annotated introns
SIK family kinase 3, 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 8 samples with support for all annotated introns
SIK family kinase 3, 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 12 samples with support for all annotated introns
serine/threonine-protein kinase SIK3 homolog isoform X2
serine/threonine-protein kinase SIK3 homolog isoform X3
serine/threonine-protein kinase SIK3 homolog isoform X1
platelet-activating factor acetylhydrolase IB subunit alpha2-like, transcript variant X2
platelet-activating factor acetylhydrolase IB subunit alpha2-like, transcript variant X1
platelet-activating factor acetylhydrolase IB subunit alpha2-like
SID1 transmembrane family, member 2, transcript variant 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 3 samples with support for all annotated introns
SID1 transmembrane family, member 2, 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, including 7 samples with support for all annotated introns
SID1 transmembrane family member 2 isoform X1
SID1 transmembrane family member 2 isoform X2
palmitoyl-protein thioesterase ABHD10, mitochondrial-like
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 16 samples with support for all annotated introns
proprotein convertase subtilisin/kexin type 7, transcript variant X1
proprotein convertase subtilisin/kexin type 7, transcript variant X2
proprotein convertase subtilisin/kexin type 7
glucose-6-phosphate exchanger SLC37A4-like, transcript variant X2
glucose-6-phosphate exchanger SLC37A4-like, transcript variant X4
glucose-6-phosphate exchanger SLC37A4-like, transcript variant X1
glucose-6-phosphate exchanger SLC37A4-like, transcript variant X3
glucose-6-phosphate exchanger SLC37A4-like isoform X2
glucose-6-phosphate exchanger SLC37A4-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
centrosomal AT-AC splicing factor, transcript variant X1
centrosomal AT-AC splicing factor, transcript variant X2
coiled-coil domain-containing protein 84 isoform X1
coiled-coil domain-containing protein 84 isoform X2
trafficking protein particle complex subunit 4, transcript variant X1
trafficking protein particle complex subunit 4 isoform X1
trafficking protein particle complex subunit 4, transcript variant X2
trafficking protein particle complex subunit 4 isoform X2
serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform
ALG9 alpha-1,2-mannosyltransferase, 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 11 samples with support for all annotated introns
ALG9 alpha-1,2-mannosyltransferase, transcript variant X2
ALG9 alpha-1,2-mannosyltransferase, transcript variant X5
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 10 samples with support for all annotated introns
alpha-1,2-mannosyltransferase ALG9 isoform X2
alpha-1,2-mannosyltransferase ALG9 isoform X1
alpha-1,2-mannosyltransferase ALG9 isoform X5
ALG9 alpha-1,2-mannosyltransferase, transcript variant X3
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
alpha-1,2-mannosyltransferase ALG9 isoform X3
ALG9 alpha-1,2-mannosyltransferase, 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 6 samples with support for all annotated introns
alpha-1,2-mannosyltransferase ALG9 isoform X4
ferredoxin-fold anticodon binding domain containing 1, 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 10 samples with support for all annotated introns
ferredoxin-fold anticodon binding domain containing 1, transcript variant X1
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 14 samples with support for all annotated introns
ferredoxin-fold anticodon binding domain containing 1, transcript variant X3
ferredoxin-fold anticodon binding domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ferredoxin-fold anticodon-binding domain-containing protein 1 isoform X1
ferredoxin-fold anticodon-binding domain-containing protein 1 isoform X2
crystallin, alpha B, b, transcript variant X1
crystallin, alpha B, b, transcript variant X2
heat shock protein, alpha-crystallin-related, b2
uncharacterized protein C11orf52 homolog
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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 9 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 11 samples with support for all annotated introns
dihydrolipoamide S-acetyltransferase (E2 component of pyruvate dehydrogenase complex)
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial
PIH1 domain containing 2, transcript variant 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 13 samples with support for all annotated introns
PIH1 domain containing 2, transcript variant X8
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 6 samples with support for all annotated introns
PIH1 domain containing 2, transcript variant X4
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 4 samples with support for all annotated introns
PIH1 domain containing 2, transcript variant X6
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 2 samples with support for all annotated introns
PIH1 domain containing 2, transcript variant X2
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
PIH1 domain containing 2, transcript variant X5
PIH1 domain containing 2, transcript variant X10
PIH1 domain containing 2, transcript variant X9
PIH1 domain containing 2, transcript variant X7
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 5 samples with support for all annotated introns
PIH1 domain containing 2, transcript variant X11
PIH1 domain containing 2, transcript variant X3
PIH1 domain containing 2, transcript variant X12
NKAP domain containing 1, transcript variant X3
NKAP domain containing 1, transcript variant X1
NKAP domain containing 1, transcript variant X4
NKAP domain containing 1, transcript variant X2
NKAP domain containing 1, transcript variant X5
cell adhesion molecule 1a, transcript variant X2
cell adhesion molecule 1a, transcript variant X4
cell adhesion molecule 1a, transcript variant X5
cell adhesion molecule 1a, transcript variant X3
cell adhesion molecule 1a, transcript variant X1
uncharacterized LOC125466851, transcript variant X1
uncharacterized LOC125466851, transcript variant X2
cytotoxic and regulatory T-cell molecule, transcript variant X1
cytotoxic and regulatory T-cell molecule, transcript variant X2
cytotoxic and regulatory T-cell molecule isoform X1
cytotoxic and regulatory T-cell molecule isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 15-like
A disintegrin and metalloproteinase with thrombospondin motifs 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 8-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 14 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 8-like isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 8-like isoform X2
zinc finger and BTB domain containing 44, transcript variant X4
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
zinc finger and BTB domain containing 44, transcript variant X3
zinc finger and BTB domain containing 44, transcript variant X2
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 14 samples with support for all annotated introns
zinc finger and BTB domain containing 44, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 44 isoform X2
zinc finger and BTB domain-containing protein 44 isoform X1
neural cell adhesion molecule 1a, transcript variant X2
neural cell adhesion molecule 1a, transcript variant X3
neural cell adhesion molecule 1a, transcript variant X10
neural cell adhesion molecule 1a, transcript variant X9
neural cell adhesion molecule 1a, transcript variant X8
neural cell adhesion molecule 1a, transcript variant X6
neural cell adhesion molecule 1a, transcript variant X5
neural cell adhesion molecule 1a, transcript variant X4
neural cell adhesion molecule 1a, transcript variant X1
neural cell adhesion molecule 1a, transcript variant X18
neural cell adhesion molecule 1a, transcript variant X11
neural cell adhesion molecule 1a, transcript variant X7
neural cell adhesion molecule 1a, transcript variant X13
neural cell adhesion molecule 1a, transcript variant X12
neural cell adhesion molecule 1a, transcript variant X14
neural cell adhesion molecule 1a, transcript variant X19
neural cell adhesion molecule 1a isoform X3
neural cell adhesion molecule 1a isoform X19
neural cell adhesion molecule 1a isoform X18
neural cell adhesion molecule 1a isoform X11
neural cell adhesion molecule 1a isoform X7
neural cell adhesion molecule 1a isoform X14
neural cell adhesion molecule 1a isoform X10
neural cell adhesion molecule 1a isoform X9
neural cell adhesion molecule 1a isoform X8
neural cell adhesion molecule 1a isoform X6
neural cell adhesion molecule 1a isoform X5
neural cell adhesion molecule 1a isoform X4
neural cell adhesion molecule 1a isoform X13
neural cell adhesion molecule 1a isoform X2
neural cell adhesion molecule 1a isoform X12
neural cell adhesion molecule 1a isoform X1
neural cell adhesion molecule 1a, transcript variant X15
neural cell adhesion molecule 1a, transcript variant X16
neural cell adhesion molecule 1a, transcript variant X17
neural cell adhesion molecule 1a isoform X17
neural cell adhesion molecule 1a isoform X16
neural cell adhesion molecule 1a isoform X15
uncharacterized protein YBL113C-like, transcript variant X1
uncharacterized protein YBL113C-like, transcript variant X2
uncharacterized protein YBL113C-like isoform X1
uncharacterized protein YBL113C-like isoform X2
placenta-expressed transcript 1 protein-like
nicotinamide N-methyltransferase-like, 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
nicotinamide N-methyltransferase-like isoform X2
nicotinamide N-methyltransferase-like, transcript variant X1
nicotinamide N-methyltransferase-like isoform 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 12 samples with support for all annotated introns
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 24 samples with support for all annotated introns
vacuolar protein sorting-associated protein 26B-like
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 23 samples with support for all annotated introns
non-SMC condensin II complex, subunit D3, transcript variant X1
non-SMC condensin II complex, subunit D3, transcript variant X2
non-SMC condensin II complex, subunit D3, transcript variant X3
condensin-2 complex subunit D3 isoform X1
condensin-2 complex subunit D3 isoform X2
condensin-2 complex subunit D3 isoform X3
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 21 samples with support for all annotated introns
immunoglobulin superfamily, member 9Bb, transcript variant X1
immunoglobulin superfamily, member 9Bb, transcript variant X2
immunoglobulin superfamily, member 9Bb, transcript variant X3
immunoglobulin superfamily, member 9Bb, transcript variant X4
immunoglobulin superfamily, member 9Bb, transcript variant X5
RNA-binding protein 7-like, transcript variant X5
RNA-binding protein 7-like, transcript variant X6
RNA-binding protein 7-like, transcript variant X7
RNA-binding protein 7-like, transcript variant X1
RNA-binding protein 7-like, transcript variant X4
RNA-binding protein 7-like, transcript variant X2
RNA-binding protein 7-like, transcript variant X3
RNA-binding protein 7-like, transcript variant X8
mth938 domain-containing protein-like, 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 18 samples with support for all annotated introns
mth938 domain-containing protein-like, 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 5 samples with support for all annotated introns
mth938 domain-containing protein-like, 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 13 samples with support for all annotated introns
mth938 domain-containing protein-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 20 samples with support for all annotated introns
CXADR-like membrane protein, transcript variant X1
CXADR-like membrane protein, transcript variant X2
GRAM domain containing 1Ba, 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
GRAM domain containing 1Ba, transcript variant X2
GRAM domain containing 1Ba, transcript variant X4
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 1 sample with support for all annotated introns
GRAM domain containing 1Ba, transcript variant X3
GRAM domain containing 1Ba, transcript variant X5
GRAM domain containing 1Ba, transcript variant X6
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 1 sample with support for all annotated introns
GRAM domain containing 1Ba, transcript variant X7
sodium channel, voltage-gated, type III, beta, transcript variant X5
sodium channel, voltage-gated, type III, beta, transcript variant X4
sodium channel, voltage-gated, type III, beta, transcript variant X3
sodium channel, voltage-gated, type III, beta, transcript variant X2
sodium channel, voltage-gated, type III, beta, transcript variant X1
sodium channel subunit beta-3 isoform X2
sodium channel subunit beta-3 isoform X1
potassium-transporting ATPase alpha chain 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 232 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium-transporting ATPase alpha chain 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 232 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium-transporting ATPase alpha chain 2-like, transcript variant X3
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 1 sample with support for all annotated introns
potassium-transporting ATPase alpha chain 2-like isoform X1
potassium-transporting ATPase alpha chain 2-like isoform X3
potassium-transporting ATPase alpha chain 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 174 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium-transporting ATPase alpha chain 2-like, transcript variant X5
potassium-transporting ATPase alpha chain 2-like isoform X2
uncharacterized protein CXorf65 homolog, transcript variant X2
uncharacterized protein CXorf65 homolog, transcript variant X3
uncharacterized protein CXorf65 homolog, transcript variant X1
uncharacterized protein LOC125466993 isoform X2
uncharacterized protein LOC125466993 isoform X3
uncharacterized protein CXorf65 homolog isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like, transcript variant X2
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like, transcript variant X3
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like, transcript variant X1
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like, transcript variant X6
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like, transcript variant X5
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like, transcript variant X4
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like, transcript variant X7
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like
beta-galactosidase-1-like protein 2, transcript variant X1
beta-galactosidase-1-like protein 2, transcript variant X2
beta-galactosidase-1-like protein 2 isoform X1
beta-galactosidase-1-like protein 2 isoform X2
junctional cadherin complex regulator, transcript variant X2
junctional cadherin complex regulator, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
myb/SANT-like DNA-binding domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 30% 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
uncharacterized LOC125467047, 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 16 samples with support for all annotated introns
uncharacterized LOC125467047, 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 11 samples with support for all annotated introns
uncharacterized LOC125467047, 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 18 samples with support for all annotated introns
opioid-binding protein/cell adhesion molecule homolog, transcript variant X8
opioid-binding protein/cell adhesion molecule homolog, transcript variant X7
opioid-binding protein/cell adhesion molecule homolog, transcript variant X5
opioid-binding protein/cell adhesion molecule homolog, transcript variant X6
opioid-binding protein/cell adhesion molecule homolog, transcript variant X2
opioid-binding protein/cell adhesion molecule homolog, transcript variant X4
opioid-binding protein/cell adhesion molecule homolog, transcript variant X1
opioid-binding protein/cell adhesion molecule homolog, transcript variant X9
opioid-binding protein/cell adhesion molecule homolog, transcript variant X10
opioid-binding protein/cell adhesion molecule homolog, transcript variant X3
opioid-binding protein/cell adhesion molecule homolog isoform X8
opioid-binding protein/cell adhesion molecule homolog isoform X7
opioid-binding protein/cell adhesion molecule homolog isoform X5
opioid-binding protein/cell adhesion molecule homolog isoform X6
opioid-binding protein/cell adhesion molecule homolog isoform X2
opioid-binding protein/cell adhesion molecule homolog isoform X4
opioid-binding protein/cell adhesion molecule homolog isoform X1
opioid-binding protein/cell adhesion molecule homolog isoform X9
opioid-binding protein/cell adhesion molecule homolog isoform X10
opioid-binding protein/cell adhesion molecule homolog isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
neurogranin (protein kinase C substrate, RC3) a, transcript variant X1
neurogranin (protein kinase C substrate, RC3) a, transcript variant X2
neurogranin (protein kinase C substrate, RC3) a isoform X1
neurogranin (protein kinase C substrate, RC3) a isoform X2
sperm autoantigenic protein 17, transcript variant X2
sperm autoantigenic protein 17, 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 11 samples with support for all annotated introns
V-set and immunoglobulin domain-containing protein 2-like, transcript variant X2
V-set and immunoglobulin domain-containing protein 2-like, transcript variant X1
V-set and immunoglobulin domain-containing protein 2-like isoform X2
V-set and immunoglobulin domain-containing protein 2-like isoform X1
endothelial cell-selective adhesion molecule-like, transcript variant X2
endothelial cell-selective adhesion molecule-like, transcript variant X1
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
endothelial cell-selective adhesion molecule-like isoform X1
endothelial cell-selective adhesion molecule-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 22 samples with support for all annotated introns
roundabout, axon guidance receptor, homolog 3 (Drosophila), transcript variant X1
roundabout, axon guidance receptor, homolog 3 (Drosophila), 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 3 samples with support for all annotated introns
roundabout, axon guidance receptor, homolog 3 (Drosophila), transcript variant X3
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 7 samples with support for all annotated introns
roundabout, axon guidance receptor, homolog 3 (Drosophila), transcript variant X4
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 5 samples with support for all annotated introns
roundabout, axon guidance receptor, homolog 3 (Drosophila), transcript variant X5
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
roundabout, axon guidance receptor, homolog 4 (Drosophila), transcript variant X1
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 5 samples with support for all annotated introns
roundabout, axon guidance receptor, homolog 4 (Drosophila), transcript variant X2
pbx/knotted 1 homeobox 2, transcript variant X18
pbx/knotted 1 homeobox 2, transcript variant X15
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 9 samples with support for all annotated introns
pbx/knotted 1 homeobox 2, transcript variant X14
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
pbx/knotted 1 homeobox 2, transcript variant X13
pbx/knotted 1 homeobox 2, transcript variant X17
pbx/knotted 1 homeobox 2, transcript variant X16
pbx/knotted 1 homeobox 2, transcript variant X12
pbx/knotted 1 homeobox 2, transcript variant X4
pbx/knotted 1 homeobox 2, transcript variant X6
pbx/knotted 1 homeobox 2, transcript variant X9
pbx/knotted 1 homeobox 2, transcript variant X1
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 10 samples with support for all annotated introns
pbx/knotted 1 homeobox 2, transcript variant X2
pbx/knotted 1 homeobox 2, transcript variant X7
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 3 samples with support for all annotated introns
pbx/knotted 1 homeobox 2, transcript variant X5
pbx/knotted 1 homeobox 2, transcript variant X11
pbx/knotted 1 homeobox 2, transcript variant X3
pbx/knotted 1 homeobox 2, transcript variant X10
pbx/knotted 1 homeobox 2, transcript variant X8
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
transmembrane protein 218, 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
transmembrane protein 218, 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 1 sample with support for all annotated introns
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A
glucose-6-phosphate exchanger SLC37A2-like
coiled-coil domain containing 15, transcript variant X2
coiled-coil domain containing 15, transcript variant X1
coiled-coil domain-containing protein 15 isoform X2
coiled-coil domain-containing protein 15 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
hepatic and glial cell adhesion molecule b, transcript variant X1
hepatic and glial cell adhesion molecule b, transcript variant X2
hepatic and glial cell adhesion molecule b isoform X1
hepatic and glial cell adhesion molecule b isoform X2
arginyl-tRNA--protein transferase 1-like
fasciculation and elongation protein zeta 1 (zygin I)
fasciculation and elongation protein zeta-1
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X5
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 10 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, 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, including 20 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X2
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 4 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X3
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X4
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
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, 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 1 sample with support for all annotated introns
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4 isoform X2
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4 isoform X4
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4 isoform X1
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4 isoform X3
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
toll-interleukin 1 receptor (TIR) domain containing adaptor protein, 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, including 20 samples with support for all annotated introns
toll-interleukin 1 receptor (TIR) domain containing adaptor protein, transcript variant 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 4 samples with support for all annotated introns
toll-interleukin 1 receptor (TIR) domain containing adaptor protein, transcript variant X4
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 10 samples with support for all annotated introns
toll-interleukin 1 receptor (TIR) domain containing adaptor protein, transcript variant X3
toll-interleukin 1 receptor (TIR) domain containing adaptor protein, transcript variant X5
toll-interleukin 1 receptor (TIR) domain containing adaptor protein, transcript variant X6
toll/interleukin-1 receptor domain-containing adapter protein
FAD-dependent oxidoreductase domain containing 1, transcript variant X3
FAD-dependent oxidoreductase domain containing 1, transcript variant X2
FAD-dependent oxidoreductase domain containing 1, transcript variant X1
FAD-dependent oxidoreductase domain-containing protein 1 isoform X3
FAD-dependent oxidoreductase domain-containing protein 1 isoform X2
FAD-dependent oxidoreductase domain-containing protein 1 isoform X1
SRP receptor subunit alpha, transcript variant X2
SRP receptor subunit alpha, transcript variant X1
signal recognition particle receptor subunit alpha isoform X1
signal recognition particle receptor subunit alpha isoform X2
family with sequence similarity 118 member B, transcript variant X3
family with sequence similarity 118 member B, transcript variant X4
family with sequence similarity 118 member B, transcript variant X6
family with sequence similarity 118 member B, transcript variant X7
family with sequence similarity 118 member B, transcript variant X1
family with sequence similarity 118 member B, transcript variant X2
family with sequence similarity 118 member B, transcript variant X5
ilvB (bacterial acetolactate synthase)-like
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 22 samples with support for all annotated introns
V-set and immunoglobulin domain-containing protein 10-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
cell adhesion associated, oncogene regulated
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
cell adhesion molecule-related/down-regulated by oncogenes
uncharacterized LOC125467000, transcript variant X4
uncharacterized protein LOC125467000 isoform X3
uncharacterized LOC125467000, transcript variant X2
uncharacterized LOC125467000, transcript variant X3
uncharacterized LOC125467000, transcript variant X1
uncharacterized protein LOC125467000 isoform X2
uncharacterized protein LOC125467000 isoform X1
checkpoint kinase 1, transcript variant X4
checkpoint kinase 1, transcript variant X1
checkpoint kinase 1, transcript variant X3
checkpoint kinase 1, transcript variant X2
STT3 oligosaccharyltransferase complex catalytic subunit A, transcript variant X1
STT3 oligosaccharyltransferase complex catalytic subunit A, transcript variant X2
STT3 oligosaccharyltransferase complex catalytic subunit A, transcript variant X3
STT3 oligosaccharyltransferase complex catalytic subunit A, transcript variant X4
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A isoform X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A isoform X2
EI24 autophagy associated transmembrane protein, transcript variant X1
EI24 autophagy associated transmembrane protein, transcript variant X2
EI24 autophagy associated transmembrane protein, transcript variant X3
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4-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 1 sample with support for all annotated introns
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4-like isoform X1
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4-like isoform X2
kirre like nephrin family adhesion molecule 3a, 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, including 5 samples with support for all annotated introns
kirre like nephrin family adhesion molecule 3a, 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 6 samples with support for all annotated introns
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X5
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X3
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X2
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X4
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X7
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X1
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X9
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X6
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X8
Friend leukemia integration 1 transcription factor isoform X3
Friend leukemia integration 1 transcription factor isoform X1
Friend leukemia integration 1 transcription factor isoform X2
Friend leukemia integration 1 transcription factor isoform X4
v-ets avian erythroblastosis virus E26 oncogene homolog 1, transcript variant X1
v-ets avian erythroblastosis virus E26 oncogene homolog 1, transcript variant X2
v-ets avian erythroblastosis virus E26 oncogene homolog 1, transcript variant X3
potassium inwardly rectifying channel subfamily J member 1b, transcript variant X4
ATP-sensitive inward rectifier potassium channel 1b isoform X2
potassium inwardly rectifying channel subfamily J member 1b, transcript variant X5
ATP-sensitive inward rectifier potassium channel 1b isoform X3
potassium inwardly rectifying channel subfamily J member 1b, transcript variant X1
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, including 3 samples with support for all annotated introns
potassium inwardly rectifying channel subfamily J member 1b, transcript variant X2
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, including 2 samples with support for all annotated introns
potassium inwardly rectifying channel subfamily J member 1b, transcript variant X3
ATP-sensitive inward rectifier potassium channel 1b isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 4-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 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: 142 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 4-like
rho GTPase-activating protein 32-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
rho GTPase-activating protein 32-like, transcript variant X2
rho GTPase-activating protein 32-like, transcript variant X3
rho GTPase-activating protein 32-like, transcript variant X5
rho GTPase-activating protein 32-like, transcript variant X4
rho GTPase-activating protein 32-like, transcript variant X6
rho GTPase-activating protein 32-like, transcript variant X7
rho GTPase-activating protein 32-like, transcript variant X8
rho GTPase-activating protein 32-like, transcript variant X9
rho GTPase-activating protein 32-like isoform X1
rho GTPase-activating protein 32-like isoform X2
rho GTPase-activating protein 32-like isoform X3
rho GTPase-activating protein 32-like isoform X4
rho GTPase-activating protein 32-like isoform X5
rho GTPase-activating protein 32-like isoform X6
rho GTPase-activating protein 32-like isoform X7
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
homeobox protein BarH-like 2, 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 5 samples with support for all annotated introns
homeobox protein BarH-like 2, transcript variant X2
transmembrane protein 45B, transcript variant X1
transmembrane protein 45B, transcript variant X2
nuclear factor related to kappaB binding protein, transcript variant X2
nuclear factor related to kappaB binding protein, transcript variant X3
nuclear factor related to kappaB binding protein, transcript variant X4
nuclear factor related to kappaB binding protein, transcript variant X1
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 11 samples with support for all annotated introns
nuclear factor related to kappa-B-binding protein isoform X2
nuclear factor related to kappa-B-binding protein isoform X3
nuclear factor related to kappa-B-binding protein isoform X4
nuclear factor related to kappa-B-binding protein isoform X1
PR domain containing 10, transcript variant X4
PR domain containing 10, transcript variant X6
PR domain containing 10, transcript variant X9
PR domain containing 10, transcript variant X7
PR domain containing 10, transcript variant X8
PR domain containing 10, transcript variant X1
PR domain containing 10, transcript variant X2
PR domain containing 10, transcript variant X3
PR domain containing 10, transcript variant X5
PR domain zinc finger protein 10 isoform X2
PR domain zinc finger protein 10 isoform X5
PR domain zinc finger protein 10 isoform X3
PR domain zinc finger protein 10 isoform X4
PR domain zinc finger protein 10 isoform X1
amyloid beta (A4) precursor-like protein 2, transcript variant X1
amyloid beta (A4) precursor-like protein 2, transcript variant X2
amyloid beta (A4) precursor-like protein 2, transcript variant X3
suppressor of tumorigenicity 14 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: isobutyryl-CoA dehydrogenase, mitochondrial
sialic acid acetylesterase, transcript variant X1
sialic acid acetylesterase, transcript variant X3
sialic acid acetylesterase, transcript variant X2
thymocyte expressed, positive selection associated 1, transcript variant X2
thymocyte expressed, positive selection associated 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
thymocyte expressed, positive selection associated 1, transcript variant X3
thymocyte expressed, positive selection associated 1, transcript variant X6
thymocyte expressed, positive selection associated 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
thymocyte expressed, positive selection associated 1, transcript variant X5
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 107 like, transcript variant X2
transmembrane protein 107 like, transcript variant X1
transmembrane protein 107 like, transcript variant X3
transmembrane protein 107 like, transcript variant X4
transmembrane protein 107 like, transcript variant X5
transmembrane protein 107 like isoform X1
transmembrane protein 107 like isoform X2
uncharacterized LOC125466941, transcript variant X4
uncharacterized LOC125466941, transcript variant X3
uncharacterized LOC125466941, transcript variant X2
uncharacterized LOC125466941, transcript variant X1
uncharacterized protein LOC125466941 isoform X4
uncharacterized protein LOC125466941 isoform X3
uncharacterized protein LOC125466941 isoform X2
uncharacterized protein LOC125466941 isoform X1