Rhincodon typus isolate 14 chromosome 22, sRhiTyp1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Rhincodontidae; Rhincodon.
REFSEQ INFORMATION: The reference sequence is identical to\nCM038819.1.\nAssembly name: sRhiTyp1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/03. The\noriginal whole-genome shotgun project has the accession\nJAHMAH000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Supernova v. 2.1.1; P_RNA_scaffolder v.\n commit 7941e0f; Tigmint v. 1.1.2; ARKS v.\n 1.1.0; 3D-DNA v. 180922\nAssembly Name :: sRhiTyp1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 46.7x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Rhincodon typus Annotation Release\n 101\nAnnotation Version :: 101\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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Cbl proto-oncogene-like 1, E3 ubiquitin protein ligase, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
E3 ubiquitin-protein ligase Hakai isoform X1
Cbl proto-oncogene-like 1, E3 ubiquitin protein ligase, transcript variant X2
E3 ubiquitin-protein ligase Hakai isoform X2
dihydrolipoyl dehydrogenase, mitochondrial
uncharacterized protein C12orf45 homolog
aldehyde dehydrogenase 1 family, member L2
mitochondrial 10-formyltetrahydrofolate dehydrogenase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 8 Proteins, and 98% 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2, transcript variant X1
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 8 samples with support for all annotated introns
DCC-interacting protein 13-beta isoform X2
DCC-interacting protein 13-beta isoform X1
uncharacterized LOC109920070, transcript variant X1
uncharacterized LOC109920070, transcript variant X2
NUAK family, SNF1-like kinase, 1b, 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 1 sample with support for all annotated introns
NUAK family, SNF1-like kinase, 1b, transcript variant X2
NUAK family, SNF1-like kinase, 1b, 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 2 samples with support for all annotated introns
NUAK family, SNF1-like kinase, 1b, 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 1 sample with support for all annotated introns
NUAK family SNF1-like kinase 1 isoform X4
NUAK family SNF1-like kinase 1 isoform X2
NUAK family SNF1-like kinase 1 isoform X1
NUAK family SNF1-like kinase 1 isoform X3
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
phosphate carrier protein, mitochondrial, transcript variant X1
phosphate carrier protein, mitochondrial, transcript variant X2
phosphate carrier protein, mitochondrial isoform X2
phosphate carrier protein, mitochondrial isoform X1
lamina-associated polypeptide 2, isoforms beta/delta/epsilon/gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
dynein axonemal heavy chain 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein axonemal heavy chain 3-like, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
uncharacterized LOC125485773, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125485773, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
NEDD1 gamma-tubulin ring complex targeting factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
NEDD1 gamma-tubulin ring complex targeting factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
NEDD1 gamma-tubulin ring complex targeting factor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NEDD1 gamma-tubulin ring complex targeting factor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
NEDD1 gamma-tubulin ring complex targeting factor, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cilia- and flagella-associated protein 54
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 54-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
histidine ammonia-lyase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
histidine ammonia-lyase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cilia- and flagella-associated protein 100-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 44
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
small nuclear ribonucleoprotein polypeptide F
ubiquitin carboxyl-terminal hydrolase 44-like
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 protein C3orf20-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein C3orf20-like, transcript variant X2
vezatin, adherens junctions transmembrane protein, transcript variant X2
vezatin, adherens junctions transmembrane protein, transcript variant X4
vezatin, adherens junctions transmembrane protein, transcript variant X5
vezatin, adherens junctions transmembrane protein, transcript variant X3
vezatin, adherens junctions transmembrane protein, transcript variant X1
FYVE, RhoGEF and PH domain containing 6, 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 3 samples with support for all annotated introns
FYVE, RhoGEF and PH domain containing 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FYVE, RhoGEF and PH domain-containing protein 6
FYVE, RhoGEF and PH domain containing 5b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
FYVE, RhoGEF and PH domain-containing protein 5b
nuclear receptor subfamily 2, group C, member 1, transcript variant X5
nuclear receptor subfamily 2, group C, member 1, transcript variant X9
nuclear receptor subfamily 2, group C, member 1, transcript variant X13
nuclear receptor subfamily 2, group C, member 1, transcript variant X6
nuclear receptor subfamily 2, group C, member 1, transcript variant X7
nuclear receptor subfamily 2, group C, member 1, transcript variant X10
nuclear receptor subfamily 2, group C, member 1, transcript variant X1
nuclear receptor subfamily 2, group C, member 1, transcript variant X3
nuclear receptor subfamily 2, group C, member 1, transcript variant X2
nuclear receptor subfamily 2, group C, member 1, transcript variant X4
nuclear receptor subfamily 2, group C, member 1, transcript variant X8
nuclear receptor subfamily 2, group C, member 1, transcript variant X11
nuclear receptor subfamily 2, group C, member 1, transcript variant X12
nuclear receptor subfamily 2 group C member 1-A isoform X1
nuclear receptor subfamily 2 group C member 1-A isoform X3
nuclear receptor subfamily 2 group C member 1-A isoform X2
nuclear receptor subfamily 2 group C member 1-A isoform X4
nuclear receptor subfamily 2 group C member 1-A isoform X8
nuclear receptor subfamily 2 group C member 1-A isoform X6
nuclear receptor subfamily 2 group C member 1-A isoform X7
nuclear receptor subfamily 2 group C member 1-A isoform X10
nuclear receptor subfamily 2 group C member 1-A isoform X11
nuclear receptor subfamily 2 group C member 1-A isoform X12
nuclear receptor subfamily 2 group C member 1-A isoform X5
nuclear receptor subfamily 2 group C member 1-A isoform X9
nuclear receptor subfamily 2 group C member 1-A isoform X13
NADH:ubiquinone oxidoreductase subunit A12
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12
transmembrane and coiled-coil domain family 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transmembrane and coiled-coil domain protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 5 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: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitochondrial ribosomal protein L42, transcript variant X2
mitochondrial ribosomal protein L42, transcript variant X1
39S ribosomal protein L42, mitochondrial isoform X1
39S ribosomal protein L42, mitochondrial isoform X2
ubiquitin-conjugating enzyme E2 N, transcript variant X4
ubiquitin-conjugating enzyme E2 N, transcript variant X2
ubiquitin-conjugating enzyme E2 N, transcript variant X1
ubiquitin-conjugating enzyme E2 N, transcript variant X3
ubiquitin-conjugating enzyme E2 E1 isoform X1
ubiquitin-conjugating enzyme E2 N isoform X2
ubiquitin-conjugating enzyme E2 N isoform X3
ubiquitin-conjugating enzyme E2 N isoform X4
diphosphoinositol polyphosphate phosphohydrolase 2-like, transcript variant X3
diphosphoinositol polyphosphate phosphohydrolase 2-like, transcript variant X5
diphosphoinositol polyphosphate phosphohydrolase 2-like, transcript variant X2
diphosphoinositol polyphosphate phosphohydrolase 2-like, transcript variant X4
diphosphoinositol polyphosphate phosphohydrolase 2-like, transcript variant X1
diphosphoinositol polyphosphate phosphohydrolase 2-like isoform X3
diphosphoinositol polyphosphate phosphohydrolase 2-like isoform X2
diphosphoinositol polyphosphate phosphohydrolase 2-like isoform X1
diphosphoinositol polyphosphate phosphohydrolase 2-like isoform X4
early endosome antigen 1, transcript variant X4
early endosome antigen 1, transcript variant X5
early endosome antigen 1, transcript variant X2
early endosome antigen 1, transcript variant X3
early endosome antigen 1, transcript variant X1
early endosome antigen 1, transcript variant X6
pleckstrin homology domain containing, family G (with RhoGef domain) member 7, 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 2 samples with support for all annotated introns
pleckstrin homology domain containing, family G (with RhoGef domain) member 7, transcript variant X6
pleckstrin homology domain containing, family G (with RhoGef domain) member 7, 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 1 sample with support for all annotated introns
pleckstrin homology domain containing, family G (with RhoGef domain) member 7, transcript variant X3
pleckstrin homology domain containing, family G (with RhoGef domain) member 7, 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
pleckstrin homology domain containing, family G (with RhoGef domain) member 7, 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
pleckstrin homology domain-containing family G member 7 isoform X2
pleckstrin homology domain-containing family G member 7 isoform X6
pleckstrin homology domain-containing family G member 7 isoform X4
pleckstrin homology domain-containing family G member 7 isoform X3
pleckstrin homology domain-containing family G member 7 isoform X1
pleckstrin homology domain-containing family G member 7 isoform X5
integrator complex subunit 13, transcript variant X1
integrator complex subunit 13, transcript variant X2
integrator complex subunit 13, transcript variant X3
integrator complex subunit 13 isoform X1
integrator complex subunit 13 isoform X2
integrator complex subunit 13 isoform X3
inositol 1,4,5-trisphosphate receptor, type 2
inositol 1,4,5-trisphosphate receptor type 2
sarcospan (Kras oncogene-associated gene)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
basic helix-loop-helix family, member e41, transcript variant X3
basic helix-loop-helix family, member e41, transcript variant X1
class E basic helix-loop-helix protein 41 isoform X1
basic helix-loop-helix family, member e41, transcript variant X4
basic helix-loop-helix family, member e41, transcript variant X2
basic helix-loop-helix family, member e41, transcript variant X5
class E basic helix-loop-helix protein 41 isoform X2
class E basic helix-loop-helix protein 41 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
ras association domain-containing protein 8b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
lamin tail domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lamin tail domain-containing protein 1-like, transcript variant X1
lamin tail domain-containing protein 1-like isoform X2
lamin tail domain-containing protein 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 133 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC109931500, transcript variant X5
uncharacterized LOC109931500, transcript variant X3
uncharacterized LOC109931500, transcript variant X2
uncharacterized LOC109931500, transcript variant X4
uncharacterized LOC109931500, transcript variant X1
uncharacterized protein LOC109931500 isoform X2
uncharacterized protein LOC109931500 isoform X1
uncharacterized protein LOC109931500 isoform X3
electron transfer flavoprotein regulatory factor 1
dynein axonemal intermediate chain 7, transcript variant X1
dynein axonemal intermediate chain 7 isoform X1
dynein axonemal intermediate chain 7, transcript variant X2
dynein axonemal intermediate chain 7 isoform X2
lymphoid-restricted membrane protein, transcript variant X4
lymphoid-restricted membrane protein, transcript variant X3
lymphoid-restricted membrane protein, transcript variant X1
lymphoid-restricted membrane protein, transcript variant X2
inositol 1,4,5-triphosphate receptor associated 2 isoform X3
inositol 1,4,5-triphosphate receptor associated 2 isoform X2
inositol 1,4,5-triphosphate receptor associated 2 isoform X1
branched chain amino-acid transaminase 1, cytosolic
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
branched-chain-amino-acid aminotransferase, cytosolic
SRY-box transcription factor 5, transcript variant X3
SRY-box transcription factor 5, transcript variant X2
SRY-box transcription factor 5, transcript variant X1
ethanolamine kinase 1, transcript variant X1
ethanolamine kinase 1, transcript variant X2
ethanolamine kinase 1, transcript variant X8
ethanolamine kinase 1, transcript variant X6
ethanolamine kinase 1, transcript variant X5
ethanolamine kinase 1, transcript variant X4
ethanolamine kinase 1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ethanolamine kinase 1, transcript variant X7
ethanolamine kinase 1, transcript variant X3
C2 calcium dependent domain containing 5, transcript variant X10
C2 calcium dependent domain containing 5, transcript variant X1
C2 calcium dependent domain containing 5, transcript variant X5
C2 calcium dependent domain containing 5, transcript variant X2
C2 calcium dependent domain containing 5, transcript variant X4
C2 calcium dependent domain containing 5, transcript variant X8
C2 calcium dependent domain containing 5, transcript variant X3
C2 calcium dependent domain containing 5, transcript variant X6
C2 calcium dependent domain containing 5, 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 5 samples with support for all annotated introns
C2 domain-containing protein 5 isoform X10
C2 domain-containing protein 5 isoform X1
C2 domain-containing protein 5 isoform X5
C2 domain-containing protein 5 isoform X2
C2 domain-containing protein 5 isoform X4
C2 domain-containing protein 5 isoform X8
C2 domain-containing protein 5 isoform X3
C2 domain-containing protein 5 isoform X6
C2 domain-containing protein 5 isoform X7
C2 calcium dependent domain containing 5, transcript variant X9
C2 domain-containing protein 5 isoform X9
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
alpha-N-acetylneuraminide alpha-2,8-sialyltransferase
cytidine monophosphate N-acetylneuraminic acid synthetase a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 long SRA reads, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
N-acylneuraminate cytidylyltransferase A
ATP-binding cassette, sub-family C (CFTR/MRP), member 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATP-binding cassette, sub-family C (CFTR/MRP), member 9, transcript variant 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 4 samples with support for all annotated introns
ATP-binding cassette, sub-family C (CFTR/MRP), member 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATP-binding cassette, sub-family C (CFTR/MRP), member 9, 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 4 samples with support for all annotated introns
ATP-binding cassette sub-family C member 9 isoform X1
ATP-binding cassette sub-family C member 9 isoform X3
ATP-binding cassette sub-family C member 9 isoform X2
ATP-binding cassette sub-family C member 9 isoform X4
ATP-binding cassette, sub-family C (CFTR/MRP), member 9, transcript variant X5
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
ATP-binding cassette, sub-family C (CFTR/MRP), member 9, 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 1 sample with support for all annotated introns
ATP-binding cassette sub-family C member 9 isoform X5
ATP-sensitive inward rectifier potassium channel 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
L-lactate dehydrogenase B chain, transcript variant X1
L-lactate dehydrogenase B chain isoform X1
L-lactate dehydrogenase B chain, transcript variant X2
L-lactate dehydrogenase B chain isoform X2
glycogen synthase 2, transcript variant X2
glycogen synthase 2, transcript variant X1
glycogen [starch] synthase, liver isoform X1
glycogen [starch] synthase, liver isoform X2
RecQ helicase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RecQ helicase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
RecQ helicase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pyridine nucleotide-disulphide oxidoreductase domain 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pyridine nucleotide-disulphide oxidoreductase domain 1, transcript variant X1
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1
calcitonin gene-related peptide, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcitonin gene-related peptide, transcript variant X1
calcitonin gene-related peptide, transcript variant X3
solute carrier organic anion transporter family member 1C1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
cGMP-inhibited 3',5'-cyclic phosphodiesterase A
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 LOC125485784, transcript variant X2
uncharacterized LOC125485784, 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
pleckstrin homology domain-containing family A member 5-like
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
pleckstrin homology domain containing, family A member 5
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
pleckstrin homology domain-containing family A member 5
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase zeta-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 54% coverage of the annotated genomic feature by RNAseq alignments
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
ras-related and estrogen-regulated growth inhibitor-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor (GEF) 39
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho guanine nucleotide exchange factor 39
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
LIM domain only 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LIM domain only 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LIM domain only 3, transcript variant X8
LIM domain only 3, transcript variant X5
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
LIM domain only 3, transcript variant X4
LIM domain only 3, transcript variant X6
LIM domain only 3, transcript variant X11
LIM domain only 3, transcript variant X9
LIM domain only 3, 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
LIM domain only 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LIM domain only 3, transcript variant X7
microsomal glutathione S-transferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
deoxyribose-phosphate aldolase (putative)
serine/threonine kinase receptor associated protein, transcript variant X1
serine/threonine kinase receptor associated protein, transcript variant X2
serine-threonine kinase receptor-associated protein isoform X1
serine-threonine kinase receptor-associated protein isoform X2
epidermal growth factor receptor pathway substrate 8a, transcript variant X4
epidermal growth factor receptor pathway substrate 8a, transcript variant X3
epidermal growth factor receptor pathway substrate 8a, transcript variant X1
epidermal growth factor receptor pathway substrate 8a, transcript variant X2
epidermal growth factor receptor kinase substrate 8a isoform X3
epidermal growth factor receptor kinase substrate 8a isoform X1
epidermal growth factor receptor kinase substrate 8a isoform X2
epidermal growth factor receptor pathway substrate 8a, transcript variant X5
epidermal growth factor receptor kinase substrate 8a isoform X4
protein tyrosine phosphatase receptor type O
receptor-type tyrosine-protein phosphatase O
RAS-like, estrogen-regulated, growth inhibitor
ras-related and estrogen-regulated growth inhibitor
troponin T, fast skeletal muscle-like, transcript variant X1
troponin T, fast skeletal muscle-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 48 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
CWF19 like cell cycle control factor 1, transcript variant X2
CWF19 like cell cycle control factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 15 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel subfamily A member 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 171 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily A member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily A member 1 isoform X2
potassium voltage-gated channel subfamily A member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 171 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily A member 1 isoform X1
potassium voltage-gated channel subfamily A member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 long SRA reads, 163 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
potassium voltage-gated channel subfamily A member 1-like, transcript variant X2
potassium voltage-gated channel subfamily A member 1-like
Tp53rk binding protein, transcript variant X2
Tp53rk binding protein, transcript variant X5
Tp53rk binding protein, transcript variant X1
Tp53rk binding protein, transcript variant X3
Tp53rk binding protein, transcript variant X6
Tp53rk binding protein, transcript variant X7
Tp53rk binding protein, transcript variant X4
EKC/KEOPS complex subunit TPRKB isoform X3
EKC/KEOPS complex subunit TPRKB isoform X4
EKC/KEOPS complex subunit TPRKB isoform X1
EKC/KEOPS complex subunit TPRKB isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kinesin-like protein KIF21A, transcript variant X3
kinesin-like protein KIF21A, transcript variant X4
kinesin-like protein KIF21A, transcript variant X1
kinesin-like protein KIF21A, transcript variant X2
kinesin-like protein KIF21A, transcript variant X5
ATP-binding cassette sub-family D member 2-like, transcript variant X1
ATP-binding cassette sub-family D member 2-like
ATP-binding cassette sub-family D member 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat serine/threonine-protein kinase 2-like, transcript variant X1
leucine-rich repeat serine/threonine-protein kinase 2-like, transcript variant X2
leucine-rich repeat serine/threonine-protein kinase 2-like isoform X1
leucine-rich repeat serine/threonine-protein kinase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 long SRA reads, 19 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
leucine-rich repeat serine/threonine-protein kinase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
actin-related protein 6-like, transcript variant X1
actin-related protein 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
T-complex protein 11-like protein 2, transcript variant X4
T-complex protein 11-like protein 2, transcript variant X7
T-complex protein 11-like protein 2, transcript variant X8
T-complex protein 11-like protein 2, transcript variant X6
T-complex protein 11-like protein 2, transcript variant X5
T-complex protein 11-like protein 2, transcript variant X3
T-complex protein 11-like protein 2, transcript variant X1
T-complex protein 11-like protein 2, transcript variant X2
T-complex protein 11-like protein 2 isoform X1
T-complex protein 11-like protein 2 isoform X2
T-complex protein 11-like protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 87
apoptotic peptidase activating factor 1, transcript variant X1
apoptotic peptidase activating factor 1, transcript variant X2
apoptotic protease-activating factor 1 isoform X1
apoptotic protease-activating factor 1 isoform X2
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X6
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X5
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X7
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X3
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X1
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X8
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X10
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X9
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X14
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X15
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X13
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X12
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X11
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X5
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X4
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X3
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X1
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X7
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X9
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X8
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X11
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X10
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X12
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X4
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X6
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X2
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X2
UHRF1 binding protein 1-like, transcript variant X2
UHRF1 binding protein 1-like, transcript variant X1
UHRF1 binding protein 1-like, transcript variant X3
cytoskeleton-associated protein 4, 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 10 samples with support for all annotated introns
cytoskeleton-associated protein 4 isoform X1
cytoskeleton-associated protein 4, 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 2 samples with support for all annotated introns
cytoskeleton-associated protein 4 isoform X2
inhibitor of nuclear factor kappa-B kinase-interacting protein, transcript variant X3
inhibitor of nuclear factor kappa-B kinase-interacting protein, transcript variant X1
inhibitor of nuclear factor kappa-B kinase-interacting protein, transcript variant X4
inhibitor of nuclear factor kappa-B kinase-interacting protein, transcript variant X7
inhibitor of nuclear factor kappa-B kinase-interacting protein, transcript variant X8
inhibitor of nuclear factor kappa-B kinase-interacting protein, transcript variant X5
inhibitor of nuclear factor kappa-B kinase-interacting protein, transcript variant X6
inhibitor of nuclear factor kappa-B kinase-interacting protein isoform X3
inhibitor of nuclear factor kappa-B kinase-interacting protein isoform X1
inhibitor of nuclear factor kappa-B kinase-interacting protein isoform X4
inhibitor of nuclear factor kappa-B kinase-interacting protein isoform X5
inhibitor of nuclear factor kappa-B kinase-interacting protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
inhibitor of nuclear factor kappa-B kinase-interacting protein isoform X2
cAMP-dependent protein kinase type II-beta regulatory subunit-like, transcript variant X3
coiled-coil domain-containing protein 71L
cAMP-dependent protein kinase type II-beta regulatory subunit-like, transcript variant X4
cAMP-dependent protein kinase type II-beta regulatory subunit-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cAMP-dependent protein kinase type II-beta regulatory subunit-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cAMP-dependent protein kinase type II-beta regulatory subunit-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 73% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cAMP-dependent protein kinase type II-beta regulatory subunit-like isoform X1
cAMP-dependent protein kinase type II-beta regulatory subunit-like isoform X2
G1/S-specific cyclin-D2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G1/S-specific cyclin-D2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
conserved oligomeric Golgi complex subunit 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
dihydrouridine synthase 4-like (S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
tRNA-dihydrouridine(20a/20b) synthase [NAD(P)+]-like
B cell receptor associated protein 29, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
B cell receptor associated protein 29, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
B-cell receptor-associated protein 31-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125485743, transcript variant X1
uncharacterized LOC125485743, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TP53 induced glycolysis regulatory phosphatase a
probable fructose-2,6-bisphosphatase TIGAR A
chromosome 22 C12orf4 homolog, transcript variant X1
chromosome 22 C12orf4 homolog, transcript variant X2
chromosome 22 C12orf4 homolog, transcript variant X3
chromosome 22 C12orf4 homolog, transcript variant X4
RAD51 associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
RAD51 associated protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
RAD51 associated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
RAD51 associated protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
dual specificity tyrosine-phosphorylation-regulated kinase 4
NADH:ubiquinone oxidoreductase subunit A9a
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochondrial
G-2 and S-phase expressed 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
G-2 and S-phase expressed 1, transcript variant X2
G-2 and S-phase expressed 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G2 and S phase-expressed protein 1 isoform X1
G2 and S phase-expressed protein 1 isoform X2
G2 and S phase-expressed protein 1 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 98% 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable serine racemase
tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
mitochondrial tRNA-specific 2-thiouridylase 1
cadherin EGF LAG seven-pass G-type receptor 1a, transcript variant X3
cadherin EGF LAG seven-pass G-type receptor 1a, transcript variant X2
cadherin EGF LAG seven-pass G-type receptor 1a, transcript variant X1
cadherin EGF LAG seven-pass G-type receptor 1 isoform X2
cadherin EGF LAG seven-pass G-type receptor 1 isoform X3
cadherin EGF LAG seven-pass G-type receptor 1 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
bromodomain containing 1a, transcript variant X1
bromodomain containing 1a, transcript variant X4
bromodomain containing 1a, transcript variant X2
bromodomain containing 1a, transcript variant X3
bromodomain containing 1a, transcript variant X5
bromodomain-containing protein 1 isoform X2
bromodomain-containing protein 1 isoform X1
bromodomain-containing protein 1 isoform X3
ALG12 alpha-1,6-mannosyltransferase, transcript variant X2
ALG12 alpha-1,6-mannosyltransferase, transcript variant X1
dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase isoform X2
dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase isoform X1
cysteine-rich with EGF-like domains 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cysteine-rich with EGF-like domains 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cysteine-rich with EGF-like domains 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cysteine-rich with EGF-like domains 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cysteine-rich with EGF-like domains 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cysteine-rich with EGF-like domains 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cysteine-rich with EGF-like domain protein 2 isoform X1
cysteine-rich with EGF-like domain protein 2 isoform X2
cysteine-rich with EGF-like domain protein 2 isoform X3
cysteine-rich with EGF-like domain protein 2 isoform X4
uncharacterized LOC125485785, transcript variant X1
uncharacterized LOC125485785, transcript variant X2
serine/threonine-protein kinase pim-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% 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: 7 Proteins, and 42% 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 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
transcriptional regulator QRICH1-like, transcript variant X4
transcriptional regulator QRICH1-like, transcript variant X1
transcriptional regulator QRICH1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcriptional regulator QRICH1-like, transcript variant X2
transcriptional regulator QRICH1-like, transcript variant X5
transcriptional regulator QRICH1-like, transcript variant X6
transcriptional regulator QRICH1-like isoform X1
transcriptional regulator QRICH1-like isoform X2
transcriptional regulator QRICH1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transcriptional regulator QRICH1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA opal suppressor (anticodon UCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
traB domain-containing protein-like, transcript variant X4
traB domain-containing protein-like, transcript variant X2
traB domain-containing protein-like, transcript variant X5
traB domain-containing protein-like, transcript variant X1
traB domain-containing protein-like, transcript variant X3
traB domain-containing protein-like isoform X1
traB domain-containing protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
TraB domain containing, transcript variant X1
TraB domain containing, transcript variant X4
TraB domain containing, transcript variant X7
TraB domain containing, transcript variant X10
TraB domain containing, transcript variant X8
TraB domain containing, transcript variant X11
TraB domain containing, transcript variant X2
TraB domain containing, transcript variant X9
TraB domain containing, transcript variant X12
TraB domain containing, transcript variant X5
TraB domain containing, transcript variant X6
TraB domain containing, transcript variant X3
traB domain-containing protein isoform X3
traB domain-containing protein isoform X4
traB domain-containing protein isoform X1
traB domain-containing protein isoform X2
traB domain-containing protein isoform X5
traB domain-containing protein isoform X6
protein adenylyltransferase SelO, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
secreted frizzled-related protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitogen-activated protein kinase 12, transcript variant X2
mitogen-activated protein kinase 12, transcript variant X1
mitogen-activated protein kinase 12 isoform X1
mitogen-activated protein kinase 12 isoform X2
mitogen-activated protein kinase 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 long SRA reads, 166 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
mitogen-activated protein kinase 11 isoform X1
mitogen-activated protein kinase 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 92 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
mitogen-activated protein kinase 11 isoform X2
voltage-dependent calcium channel subunit alpha-2/delta-1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins
hepatocyte growth factor, transcript variant X2
hepatocyte growth factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% coverage of the annotated genomic feature by RNAseq alignments
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 79% 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
guanine nucleotide-binding protein G(i) subunit alpha-1, transcript variant X3
guanine nucleotide-binding protein G(i) subunit alpha-1, transcript variant X1
guanine nucleotide-binding protein G(i) subunit alpha-1, transcript variant X2
guanine nucleotide-binding protein G(i) subunit alpha-1
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X12
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X13
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
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X2
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X7
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
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X3
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X14
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X1
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X5
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X4
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X6
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X1
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X2
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X7
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X9
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X3
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X5
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X4
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X6
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X13
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X10
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X11
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X12
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X8
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 associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X9
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X8
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
tyrosine-protein phosphatase non-receptor type 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 146
family with sequence similarity 185 member A, transcript variant X3
family with sequence similarity 185 member A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
family with sequence similarity 185 member A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
family with sequence similarity 185 member A, transcript variant X1
F-box and leucine-rich repeat protein 13
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 1 sample with support for all annotated introns
leucine-rich repeat-containing protein 17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X6
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X9
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X1
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D isoform X1
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X4
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X5
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X7
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X8
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X2
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D isoform X2
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D isoform X3
armadillo repeat containing 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
armadillo repeat containing 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
armadillo repeat-containing protein 10 isoform X1
armadillo repeat-containing protein 10 isoform X2
peptidase, mitochondrial processing subunit beta
mitochondrial-processing peptidase subunit beta
DnaJ (Hsp40) homolog, subfamily C, member 2
solute carrier family 26 member 5, transcript variant X1
solute carrier family 26 member 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
origin recognition complex, subunit 5, transcript variant X2
origin recognition complex, subunit 5, transcript variant X4
origin recognition complex, subunit 5, transcript variant X1
origin recognition complex, subunit 5, transcript variant X3
origin recognition complex subunit 5 isoform X2
origin recognition complex subunit 5 isoform X1
origin recognition complex, subunit 5, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
origin recognition complex subunit 5 isoform X3
LHFPL tetraspan subfamily member 3 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
lysine (K)-specific methyltransferase 2E, transcript variant X1
lysine (K)-specific methyltransferase 2E, transcript variant X4
lysine (K)-specific methyltransferase 2E, transcript variant X3
lysine (K)-specific methyltransferase 2E, transcript variant X2
lysine (K)-specific methyltransferase 2E, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
inactive histone-lysine N-methyltransferase 2E isoform X1
inactive histone-lysine N-methyltransferase 2E isoform X4
inactive histone-lysine N-methyltransferase 2E isoform X3
inactive histone-lysine N-methyltransferase 2E isoform X2
inactive histone-lysine N-methyltransferase 2E isoform X5
SRSF protein kinase 2-like, transcript variant X5
SRSF protein kinase 2-like, transcript variant X1
SRSF protein kinase 2-like, transcript variant X3
SRSF protein kinase 2-like, transcript variant X2
SRSF protein kinase 2-like, transcript variant X4
uncharacterized LOC125485759, 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 11 samples with support for all annotated introns
uncharacterized LOC125485759, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
GRIP and coiled-coil domain containing 1, transcript variant X2
GRIP and coiled-coil domain containing 1, transcript variant X1
GRIP and coiled-coil domain containing 1, transcript variant X3
GRIP and coiled-coil domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: lipase maturation factor 2a
non-SMC condensin II complex, subunit H2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 8 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
non-SMC condensin II complex, subunit H2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
condensin-2 complex subunit H2 isoform X1
condensin-2 complex subunit H2 isoform X2
sarcolemmal membrane-associated protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 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: 28 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
uridylate-specific endoribonuclease B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
snaclec macrovipecetin subunit beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
interferon regulatory factor 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
interferon regulatory factor 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 97% 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: 95% coverage of the annotated genomic feature by RNAseq alignments
inosine-5'-monophosphate dehydrogenase 1, transcript variant X2
inosine-5'-monophosphate dehydrogenase 1, transcript variant X1
inosine-5'-monophosphate dehydrogenase 1, transcript variant X5
inosine-5'-monophosphate dehydrogenase 1, transcript variant X4
inosine-5'-monophosphate dehydrogenase 1, transcript variant X3
inosine-5'-monophosphate dehydrogenase 1, transcript variant X6
inosine-5'-monophosphate dehydrogenase 1 isoform X3
inosine-5'-monophosphate dehydrogenase 1 isoform X4
inosine-5'-monophosphate dehydrogenase 1 isoform X6
inosine-5'-monophosphate dehydrogenase 1b isoform X1
inosine-5'-monophosphate dehydrogenase 1b isoform X2
inosine-5'-monophosphate dehydrogenase 1b isoform X5
inosine-5'-monophosphate dehydrogenase 1, transcript variant X7
inosine-5'-monophosphate dehydrogenase 1a isoform X7
uncharacterized protein LOC393862 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
SH3 and multiple ankyrin repeat domains 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
SH3 and multiple ankyrin repeat domains protein 3
RAB, member of RAS oncogene family-like 2, transcript variant X2
RAB, member of RAS oncogene family-like 2, transcript variant X1
RAB, member of RAS oncogene family-like 2, transcript variant X3
RAB, member of RAS oncogene family-like 2 isoform X1
RAB, member of RAS oncogene family-like 2 isoform X2
hematopoietic cell-specific Lyn substrate 1
thymidine phosphorylase, transcript variant X6
thymidine phosphorylase, transcript variant X1
thymidine phosphorylase, transcript variant X2
thymidine phosphorylase, transcript variant X7
thymidine phosphorylase, transcript variant X3
thymidine phosphorylase, transcript variant X5
thymidine phosphorylase, transcript variant X4
mitogen-activated protein kinase 8 interacting protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
staphylococcal nuclease domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
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 20 samples with support for all annotated introns
staphylococcal nuclease domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
uncharacterized protein LOC565091 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein si:dkey-5i3.5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
uncharacterized LOC109912298, transcript variant X3
uncharacterized LOC109912298, transcript variant X2
uncharacterized LOC109912298, transcript variant X1
peroxisomal succinyl-coenzyme A thioesterase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
V-set domain-containing T-cell activation inhibitor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
general transcription factor IIIC, polypeptide 6, alpha, transcript variant X2
general transcription factor IIIC, polypeptide 6, alpha, transcript variant X1
general transcription factor 3C polypeptide 6 isoform X2
general transcription factor 3C polypeptide 6 isoform 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 6 samples with support for all annotated introns
uncharacterized LOC125485753, transcript variant X1
uncharacterized LOC125485753, transcript variant X2
adenosylhomocysteinase like 2b, transcript variant X1
adenosylhomocysteinase like 2b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
adenosylhomocysteinase like 2b, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 45 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
adenosylhomocysteinase like 2b, transcript variant X4
adenosylhomocysteinase like 2b, transcript variant X5
adenosylhomocysteinase like 2b, transcript variant X2
adenosylhomocysteinase like 2b, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 42 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
adenosylhomocysteinase like 2b isoform X1
adenosylhomocysteinase like 2b isoform X4
adenosylhomocysteinase like 2b isoform X5
adenosylhomocysteinase like 2b isoform X2
adenosylhomocysteinase like 2b isoform X3
adenosylhomocysteinase like 2b isoform X6
adenosylhomocysteinase like 2b isoform X7
carboxypeptidase A1-like, transcript variant X1
carboxypeptidase A1-like, transcript variant X2
transmembrane protein 209, transcript variant X3
transmembrane protein 209, transcript variant X1
transmembrane protein 209, transcript variant X4
transmembrane protein 209, transcript variant X5
transmembrane protein 209, transcript variant X2
transmembrane protein 209, transcript variant X6
kelch domain containing 10, transcript variant X1
kelch domain containing 10, transcript variant X2
kelch domain containing 10, transcript variant X4
kelch domain containing 10, transcript variant X3
kelch domain containing 10, transcript variant X5
kelch domain-containing protein 10 isoform X1
kelch domain-containing protein 10 isoform X5
kelch domain-containing protein 10 isoform X4
kelch domain-containing protein 10 isoform X3
kelch domain-containing protein 10 isoform X2
zinc finger, C3HC-type containing 1, transcript variant X2
zinc finger, C3HC-type containing 1, transcript variant X3
nuclear-interacting partner of ALK isoform X2
zinc finger, C3HC-type containing 1, transcript variant X4
zinc finger, C3HC-type containing 1, transcript variant X1
nuclear-interacting partner of ALK isoform X1
nuclear-interacting partner of ALK isoform X3
zinc finger, C3HC-type containing 1, transcript variant X5
nuclear-interacting partner of ALK isoform X4
ubiquitin-conjugating enzyme E2H (UBC8 homolog, yeast)
nuclear respiratory factor 1, transcript variant X1
nuclear respiratory factor 1, transcript variant X2
nuclear respiratory factor 1, transcript variant X3
nuclear respiratory factor 1, transcript variant X5
nuclear respiratory factor 1, transcript variant X4
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 60 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COPI coat complex subunit gamma 2, transcript variant X2
COPI coat complex subunit gamma 2, transcript variant X1
mesoderm specific transcript, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mesoderm-specific transcript homolog protein isoform X8
mesoderm specific transcript, transcript variant X5
mesoderm-specific transcript homolog protein isoform X5
mesoderm specific transcript, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mesoderm specific transcript, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mesoderm specific transcript, transcript variant X1
mesoderm-specific transcript homolog protein isoform X3
mesoderm-specific transcript homolog protein isoform X1
mesoderm-specific transcript homolog protein isoform X6
mesoderm specific transcript, transcript variant X7
mesoderm specific transcript, transcript variant X4
mesoderm specific transcript, transcript variant X2
mesoderm-specific transcript homolog protein isoform X4
mesoderm-specific transcript homolog protein isoform X2
mesoderm-specific transcript homolog protein isoform X7
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 1 sample with support for all annotated introns
carboxypeptidase A1-like, transcript variant X5
carboxypeptidase A1-like, transcript variant X7
carboxypeptidase A1-like, transcript variant X6
carboxypeptidase A1-like, transcript variant X4
carboxypeptidase A1-like, transcript variant X3
carboxypeptidase A1-like, transcript variant X8
galactoside alpha-(1,2)-fucosyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 89% 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 41% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 35 member B4, transcript variant X2
solute carrier family 35 member B4, transcript variant X1
UDP-xylose and UDP-N-acetylglucosamine transporter isoform X1
UDP-xylose and UDP-N-acetylglucosamine transporter isoform X2
leucine-rich repeats and guanylate kinase domain containing
leucine-rich repeat and guanylate kinase domain-containing protein
exocyst complex component 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
exocyst complex component 4, transcript variant X3
exocyst complex component 4, 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
coiled-coil-helix-coiled-coil-helix domain containing 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 5 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125485796, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125485796, transcript variant X1
muskelin 1, intracellular mediator containing kelch motifs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125485762, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125485762, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 2 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
ankyrin repeat domain-containing protein 16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
USP6 N-terminal like, transcript variant X1
USP6 N-terminal like, transcript variant X3
USP6 N-terminal like, transcript variant X2
USP6 N-terminal like, transcript variant X4
CUGBP Elav-like family member 2, transcript variant X9
CUGBP Elav-like family member 2, transcript variant X11
CUGBP Elav-like family member 2, transcript variant X13
CUGBP Elav-like family member 2, transcript variant X12
CUGBP Elav-like family member 2, transcript variant X6
CUGBP Elav-like family member 2, transcript variant X10
CUGBP Elav-like family member 2, transcript variant X8
CUGBP Elav-like family member 2, transcript variant X4
CUGBP Elav-like family member 2, transcript variant X2
CUGBP Elav-like family member 2, transcript variant X7
CUGBP Elav-like family member 2, transcript variant X3
CUGBP Elav-like family member 2, transcript variant X5
CUGBP Elav-like family member 2, transcript variant X1
CUGBP Elav-like family member 2 isoform X11
CUGBP Elav-like family member 2 isoform X13
CUGBP Elav-like family member 2 isoform X12
CUGBP Elav-like family member 2 isoform X6
CUGBP Elav-like family member 2 isoform X9
CUGBP Elav-like family member 2 isoform X10
CUGBP Elav-like family member 2 isoform X8
CUGBP Elav-like family member 2 isoform X4
CUGBP Elav-like family member 2 isoform X2
CUGBP Elav-like family member 2 isoform X7
CUGBP Elav-like family member 2 isoform X3
CUGBP Elav-like family member 2 isoform X5
CUGBP Elav-like family member 2 isoform X1
GATA binding protein 3, transcript variant X2
GATA binding protein 3, transcript variant X4
GATA binding protein 3, transcript variant X5
GATA binding protein 3, transcript variant X3
GATA binding protein 3, transcript variant X1
TAF3 RNA polymerase II, TATA box binding protein (TBP)-associated facto
transcription initiation factor TFIID subunit 3
ATP synthase F1 subunit gamma, transcript variant X1
ATP synthase subunit gamma, mitochondrial isoform X1
ATP synthase F1 subunit gamma, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
ATP synthase subunit gamma, mitochondrial isoform X2
inter-alpha-trypsin inhibitor heavy chain 2
inter-alpha-trypsin inhibitor heavy chain H2
inter-alpha-trypsin inhibitor heavy chain 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
inter-alpha-trypsin inhibitor heavy chain H5
scm-like with four MBT domains protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
scm-like with four MBT domains protein 2
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X6
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X3
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X1
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X4
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X5
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3 isoform X3
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3 isoform X5
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3 isoform X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3 isoform X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3 isoform X4
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3 isoform X6
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
enoyl CoA hydratase domain containing 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
enoyl CoA hydratase domain containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
enoyl-CoA hydratase domain-containing protein 3, mitochondrial isoform X2
enoyl-CoA hydratase domain-containing protein 3, mitochondrial isoform 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 8 samples with support for all annotated introns
regulator of nonsense transcripts 2-like
2-oxoadipate dehydrogenase complex component E1-like
UPF2 regulator of nonsense mediated mRNA decay
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
dehydrogenase E1 and transketolase domain containing 1
2-oxoadipate dehydrogenase complex component E1
SEC61 translocon subunit alpha 2, transcript variant X2
SEC61 translocon subunit alpha 2, transcript variant X1
protein transport protein Sec61 subunit alpha isoform X1
protein transport protein Sec61 subunit alpha isoform X2
nudix (nucleoside diphosphate linked moiety X)-type motif 5
cell division cycle 123 homolog (S. cerevisiae)
calcium/calmodulin-dependent protein kinase 1Da
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
calcium/calmodulin-dependent protein kinase type 1D
coiled-coil domain-containing protein 3a
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 14 samples with support for all annotated introns
PRP18 pre-mRNA processing factor 18 homolog (yeast), transcript variant X1
PRP18 pre-mRNA processing factor 18 homolog (yeast), transcript variant X2
phytanoyl-CoA 2-hydroxylase, transcript variant X2
phytanoyl-CoA 2-hydroxylase, transcript variant X1
phytanoyl-CoA dioxygenase, peroxisomal isoform X1
phytanoyl-CoA dioxygenase, peroxisomal isoform X2
upper zone of growth plate and cartilage matrix associated a, transcript variant X1
upper zone of growth plate and cartilage matrix associated a isoform X1
upper zone of growth plate and cartilage matrix associated a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
upper zone of growth plate and cartilage matrix associated a isoform X2
minichromosome maintenance 10 replication initiation factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
minichromosome maintenance 10 replication initiation factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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: 10 Proteins
family with sequence similarity 107 member B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 22 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
family with sequence similarity 107 member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 27 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
cyclin D binding myb-like transcription factor 1
cyclin-D-binding Myb-like transcription factor 1
transmembrane protein 243, mitochondrial b, transcript variant X1
transmembrane protein 243, mitochondrial b, transcript variant X2
meiosis expressed gene 1 protein homolog
DNA cross-link repair 1C, PSO2 homolog (S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
histone-lysine N-methyltransferase SUV39H2
endosome-lysosome associated apoptosis and autophagy regulator family member 2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3Ab
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments