Hypomesus transpacificus isolate Combined female chromosome 7, fHypTra1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Stomiati; Osmeriformes; Osmeridae; Hypomesus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM038978.1.\nAssembly name: fHypTra1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Genomic Variation Lab at\nUniversity of California Davis on 2022/02/04. The original\nwhole-genome shotgun project has the accession JAJTOO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Genomic Variation Lab at University of\n California Davis\nAssembly Date :: 21-APR-2021\nAssembly Method :: IPA v. 1.3.1; scaff10x v. 4.2; SALSA2 v.\n NA; Chromonomer v. 1.13\nAssembly Name :: fHypTra1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 120.0x\nSequencing Technology :: 10X; PacBio Sequel; Hi-C\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Hypomesus transpacificus Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
USA: Fish Conservation and Culture Laboratory, Discovery Bay, California
Derived by automated computational analysis using gene prediction method: Gnomon.
CUGBP Elav-like family member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CUGBP Elav-like family member 2, transcript variant X3
CUGBP Elav-like family member 2, transcript variant X4
CUGBP Elav-like family member 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
CUGBP Elav-like family member 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 2 samples with support for all annotated introns
CUGBP Elav-like family member 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CUGBP Elav-like family member 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
CUGBP Elav-like family member 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
CUGBP Elav-like family member 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
CUGBP Elav-like family member 2 isoform X1
CUGBP Elav-like family member 2 isoform X3
CUGBP Elav-like family member 2 isoform X4
CUGBP Elav-like family member 2 isoform X5
CUGBP Elav-like family member 2 isoform X2
CUGBP Elav-like family member 2 isoform X9
CUGBP Elav-like family member 2 isoform X6
CUGBP Elav-like family member 2 isoform X8
CUGBP Elav-like family member 2 isoform X7
USP6 N-terminal like, transcript variant X4
COORDINATES: polyA evidence [ECO:0006239]
USP6 N-terminal like, transcript variant X2
USP6 N-terminal like, transcript variant X1
USP6 N-terminal like, transcript variant X3
enoyl-CoA hydratase domain-containing protein 3, mitochondrial
proline and serine-rich protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
proline and serine-rich protein 2, 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 16 samples with support for all annotated introns
UPF2 regulator of nonsense mediated mRNA decay
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: regulator of nonsense transcripts 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 351 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 606 Proteins, and 95% 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: 686 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interferon regulatory factor 5, transcript variant X2
interferon regulatory factor 5, transcript variant X1
cadherin-related family member 5, related sequence, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cadherin-related family member 5 isoform X2
cadherin-related family member 5, related sequence, 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
cadherin-related family member 5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
late endosomal/lysosomal adaptor, MAPK and MTOR activator 4
GRIP and coiled-coil domain containing 1, transcript variant X3
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 protein 1
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 42 samples with support for all annotated introns
microtubule associated monooxygenase, calponin and LIM domain containing 3b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
microtubule associated monooxygenase, calponin and LIM domain containing 3b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
microtubule associated monooxygenase, calponin and LIM domain containing 3b, transcript variant X3
protein-methionine sulfoxide oxidase mical3b isoform X3
protein-methionine sulfoxide oxidase mical3b isoform X2
protein-methionine sulfoxide oxidase mical3b isoform 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 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
poly (ADP-ribose) polymerase family, member 12b
protein mono-ADP-ribosyltransferase PARP12b
SLIT-ROBO Rho GTPase activating protein 1b
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
SLIT-ROBO Rho GTPase-activating protein 1b
acyl-CoA thioesterase 18, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
acyl-CoA thioesterase 18, 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 40 samples with support for all annotated introns
transmembrane and coiled-coil domain protein 3-like, transcript variant X2
transmembrane and coiled-coil domain protein 3-like, transcript variant X3
transmembrane and coiled-coil domain protein 3-like, transcript variant X1
transmembrane and coiled-coil domain protein 3-like isoform X2
transmembrane and coiled-coil domain protein 3-like isoform X3
transmembrane and coiled-coil domain protein 3-like isoform X1
NADH:ubiquinone oxidoreductase subunit A12
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12
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 34 samples with support for all annotated introns
FYVE, RhoGEF and PH domain-containing protein 6
vezatin, adherens junctions transmembrane protein, 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 37 samples with support for all annotated introns
vezatin, adherens junctions transmembrane protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
methionyl aminopeptidase 2a, transcript variant X1
methionyl aminopeptidase 2a, transcript variant X2
ubiquitin specific peptidase 44, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
ubiquitin specific peptidase 44, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
nuclear receptor interacting protein 2, transcript variant X1
nuclear receptor interacting protein 2, transcript variant X2
nuclear receptor-interacting protein 2 isoform X1
nuclear receptor-interacting protein 2 isoform X2
integrin alpha FG-GAP repeat containing 2, transcript variant X1
KICSTOR complex protein ITFG2 isoform X1
integrin alpha FG-GAP repeat containing 2, transcript variant X2
KICSTOR complex protein ITFG2 isoform X2
achaete-scute family bHLH transcription factor 1a
phenylalanine hydroxylase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
phenylalanine hydroxylase, 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 21 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 12 samples with support for all annotated introns
PARP1 binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
PARP1 binding protein, transcript variant X2
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 24 samples with support for all annotated introns
PARP1 binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
insulin-like growth factor 1, transcript variant X1
insulin-like growth factor 1, transcript variant X3
insulin-like growth factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
DNA-damage regulated autophagy modulator 1, 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 29 samples with support for all annotated introns
DNA-damage regulated autophagy modulator 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
DNA damage-regulated autophagy modulator protein 1 isoform X2
DNA damage-regulated autophagy modulator protein 1 isoform X1
N-acetylglucosamine-1-phosphate transferase subunits alpha and beta, transcript variant X1
N-acetylglucosamine-1-phosphate transferase subunits alpha and beta, transcript variant X2
N-acetylglucosamine-1-phosphotransferase subunits alpha/beta isoform X1
N-acetylglucosamine-1-phosphotransferase subunits alpha/beta isoform X2
myosin binding protein C1, transcript variant X19
myosin binding protein C1, transcript variant X18
myosin binding protein C1, transcript variant X16
myosin binding protein C1, transcript variant X14
myosin binding protein C1, transcript variant X17
myosin binding protein C1, transcript variant X15
myosin binding protein C1, transcript variant X13
myosin binding protein C1, transcript variant X12
myosin binding protein C1, transcript variant X11
myosin binding protein C1, transcript variant X10
myosin binding protein C1, transcript variant X8
myosin binding protein C1, transcript variant X5
myosin binding protein C1, transcript variant X9
myosin binding protein C1, transcript variant X6
myosin binding protein C1, transcript variant X4
myosin binding protein C1, transcript variant X2
myosin binding protein C1, transcript variant X3
myosin binding protein C1, transcript variant X1
myosin binding protein C1, transcript variant X7
myosin-binding protein C, slow-type isoform X19
myosin-binding protein C, slow-type isoform X18
myosin-binding protein C, slow-type isoform X16
myosin-binding protein C, slow-type isoform X14
myosin-binding protein C, slow-type isoform X17
myosin-binding protein C, slow-type isoform X15
myosin-binding protein C, slow-type isoform X13
myosin-binding protein C, slow-type isoform X12
myosin-binding protein C, slow-type isoform X11
myosin-binding protein C, slow-type isoform X10
myosin-binding protein C, slow-type isoform X8
myosin-binding protein C, slow-type isoform X5
myosin-binding protein C, slow-type isoform X9
myosin-binding protein C, slow-type isoform X6
myosin-binding protein C, slow-type isoform X4
myosin-binding protein C, slow-type isoform X2
myosin-binding protein C, slow-type isoform X3
myosin-binding protein C, slow-type isoform X1
myosin-binding protein C, slow-type isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Spi-C transcription factor (Spi-1/PU.1 related)
uncharacterized protein LOC559160 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC559160 homolog, 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 45 samples with support for all annotated introns
ATPase H+ transporting V1 subunit E1b, transcript variant X1
ATPase H+ transporting V1 subunit E1b, transcript variant X2
adenosine deaminase 2b, transcript variant X1
adenosine deaminase 2b, transcript variant X2
probable polypeptide N-acetylgalactosaminyltransferase 8
dual specificity tyrosine-phosphorylation-regulated kinase 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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 40 samples with support for all annotated introns
fibroblast growth factor 23, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fibroblast growth factor 23, transcript variant X2
TP53 induced glycolysis regulatory phosphatase b
peroxisomal biogenesis factor 26, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
peroxisomal biogenesis factor 26, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
peroxisome assembly protein 26 isoform X1
peroxisome assembly protein 26 isoform X2
LLP homolog, long-term synaptic facilitation factor, transcript variant X2
LLP homolog, long-term synaptic facilitation factor, transcript variant X1
hematopoietic cell-specific Lyn substrate 1
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: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LHFPL tetraspan subfamily member 3 protein
lysine (K)-specific methyltransferase 2E
inactive histone-lysine N-methyltransferase 2E
NADH:ubiquinone oxidoreductase subunit B2, transcript variant X2
NADH:ubiquinone oxidoreductase subunit B2, transcript variant X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 2, mitochondrial
lysine (K)-specific demethylase 7Aa, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
lysine (K)-specific demethylase 7Aa, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
endoplasmic reticulum-Golgi intermediate compartment protein 2-like, transcript variant X2
endoplasmic reticulum-Golgi intermediate compartment protein 2-like, transcript variant X1
endoplasmic reticulum-Golgi intermediate compartment protein 2-like, transcript variant X3
endoplasmic reticulum-Golgi intermediate compartment protein 2-like
fatty acyl-CoA reductase 1, transcript variant X3
fatty acyl-CoA reductase 1, transcript variant X2
fatty acyl-CoA reductase 1, transcript variant X1
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 1
guanine nucleotide-binding protein G(i) subunit alpha-1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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: 33 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
tripartite motif containing 35-14, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
tripartite motif containing 35-14, transcript variant X2
tripartite motif containing 35-14, transcript variant X1
protein mono-ADP-ribosyltransferase TIPARP-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
TUB like protein 3, transcript variant X2
TUB like protein 3, transcript variant X3
TUB like protein 3, transcript variant X5
TUB like protein 3, transcript variant X1
TUB like protein 3, transcript variant X4
RAD9-HUS1-RAD1 interacting nuclear orphan 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
RAD9-HUS1-RAD1 interacting nuclear orphan 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
RAD9, HUS1, RAD1-interacting nuclear orphan protein 1
acyl-CoA synthetase short chain family member 3, transcript variant X1
acyl-CoA synthetase short chain family member 3, transcript variant X2
acyl-CoA synthetase short-chain family member 3, mitochondrial isoform X1
acyl-CoA synthetase short-chain family member 3, mitochondrial isoform X2
acyl-CoA synthetase short chain family member 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
acyl-CoA synthetase short-chain family member 3, mitochondrial isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
protein phosphatase 1, regulatory subunit 12A, 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 31 samples with support for all annotated introns
protein phosphatase 1, regulatory subunit 12A, transcript variant X2
protein phosphatase 1 regulatory subunit 12A isoform X1
protein phosphatase 1 regulatory subunit 12A isoform X2
PRKC, apoptosis, WT1, regulator, transcript variant X2
PRKC, apoptosis, WT1, regulator, transcript variant X1
liprin-beta-1-like, transcript variant X2
liprin-beta-1-like, transcript variant X3
liprin-beta-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 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: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transcription termination factor 2, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
transcription termination factor 2, mitochondrial-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transcription termination factor 2, mitochondrial-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transcription termination factor 2, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
transcription termination factor 2, mitochondrial-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
transcription termination factor 2, mitochondrial-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
transcription termination factor 2, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
transcription termination factor 2, mitochondrial-like, transcript variant X6
transcription termination factor 2, mitochondrial-like, transcript variant X8
transcription termination factor 2, mitochondrial-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 42 samples with support for all annotated introns
ankyrin repeat and BTB/POZ domain-containing protein BTBD11-A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
APEX nuclease (multifunctional DNA repair enzyme) 1
DNA-(apurinic or apyrimidinic site) endonuclease
LOW QUALITY PROTEIN: probable tRNA N6-adenosine threonylcarbamoyltransferase
uncharacterized protein LOC558894 homolog
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 43 samples with support for all annotated introns
uncharacterized protein si:ch211-214j24.10
zinc finger protein 260-like, transcript variant X8
zinc finger protein 260-like, transcript variant X5
zinc finger protein 260-like, transcript variant X4
zinc finger protein 260-like, transcript variant X3
zinc finger protein 260-like, transcript variant X7
zinc finger protein 260-like, transcript variant X2
zinc finger protein 260-like, transcript variant X6
zinc finger protein 260-like, transcript variant X1
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: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: neuron navigator 3-like
zinc finger DHHC-type palmitoyltransferase 17
oxysterol binding protein-like 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
oxysterol binding protein-like 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
oxysterol binding protein-like 8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
oxysterol-binding protein-related protein 8 isoform X1
oxysterol-binding protein-related protein 8 isoform X2
oxysterol-binding protein-related protein 8 isoform X3
oxysterol binding protein-like 8, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
oxysterol-binding protein-related protein 8 isoform X4
nucleosome assembly protein 1-like 1, transcript variant X3
nucleosome assembly protein 1-like 1, transcript variant X1
nucleosome assembly protein 1-like 1, transcript variant X2
nucleosome assembly protein 1-like 1 isoform X1
nucleosome assembly protein 1-like 1 isoform X2
nucleosome assembly protein 1-like 1 isoform X3
pleckstrin homology-like domain, family A, member 1
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
pleckstrin homology-like domain family A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
cytidine monophospho-N-acetylneuraminic acid hydroxylase, transcript variant X1
cytidine monophospho-N-acetylneuraminic acid hydroxylase, transcript variant X2
cytidine monophospho-N-acetylneuraminic acid hydroxylase, transcript variant X4
cytidine monophospho-N-acetylneuraminic acid hydroxylase, transcript variant X5
cytidine monophospho-N-acetylneuraminic acid hydroxylase, transcript variant X3
cytidine monophosphate-N-acetylneuraminic acid hydroxylase isoform X1
cytidine monophosphate-N-acetylneuraminic acid hydroxylase isoform X3
cytidine monophosphate-N-acetylneuraminic acid hydroxylase isoform X2
coiled-coil domain-containing protein 107
potassium voltage-gated channel, Shaw-related subfamily, member 2, transcript variant X1
potassium voltage-gated channel subfamily C member 2 isoform X1
potassium voltage-gated channel, Shaw-related subfamily, member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily C member 2 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 X2
solute carrier family 26 member 5, transcript variant X1
RAS-like, estrogen-regulated, growth inhibitor
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 42 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor
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
protein mono-ADP-ribosyltransferase PARP12-like
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 43 samples with support for all annotated introns
ETS variant transcription factor 6, transcript variant X1
ETS variant transcription factor 6, transcript variant X2
chemokine-like protein TAFA-2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chemokine-like protein TAFA-2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
chemokine-like protein TAFA-2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
chemokine-like protein TAFA-2 isoform X1
chemokine-like protein TAFA-2 isoform X2
monocarboxylate transporter 2-like, transcript variant X1
monocarboxylate transporter 2-like, transcript variant X2
leucine-rich repeats and immunoglobulin-like domains 3
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: leucine-rich repeats and immunoglobulin-like domains protein 3
ATP23 metallopeptidase and ATP synthase assembly factor homolog
mitochondrial inner membrane protease ATP23 homolog
RNA polymerase II associated protein 3, transcript variant X1
RNA polymerase II associated protein 3, transcript variant X2
RNA polymerase II-associated protein 3 isoform X1
RNA polymerase II-associated protein 3 isoform X2
hemicentin-1-like, transcript variant X1
hemicentin-1-like, transcript variant X2
carcinoembryonic antigen-related cell adhesion molecule 5-like
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
mitogen-activated protein kinase 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chaperonin containing TCP1, subunit 2 (beta)
cleavage and polyadenylation specific factor 6, transcript variant X1
cleavage and polyadenylation specific factor 6, transcript variant X2
cleavage and polyadenylation specific factor 6, transcript variant X3
cleavage and polyadenylation specific factor 6, transcript variant X4
cleavage and polyadenylation specificity factor subunit 6 isoform X1
cleavage and polyadenylation specificity factor subunit 6 isoform X2
cleavage and polyadenylation specificity factor subunit 6 isoform X3
cleavage and polyadenylation specificity factor subunit 6 isoform X4
fibroblast growth factor receptor substrate 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
fibroblast growth factor receptor substrate 2a, transcript variant X2
fibroblast growth factor receptor substrate 2a
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X3
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X1
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D isoform X1
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X2
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D isoform X2
calcium channel, voltage-dependent, L type, alpha 1C subunit
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: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: voltage-dependent L-type calcium channel subunit alpha-1C
voltage-dependent calcium channel subunit alpha-2/delta-4-like
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
MDM2 proto-oncogene, transcript variant X2
MDM2 proto-oncogene, transcript variant X4
MDM2 proto-oncogene, transcript variant X3
MDM2 proto-oncogene, 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 6 samples with support for all annotated introns
striatin interacting protein 2, transcript variant X2
striatin interacting protein 2, transcript variant X1
striatin-interacting protein 1 homolog isoform X2
striatin-interacting protein 1 homolog isoform X1
MORN repeat containing 2, 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 12 samples with support for all annotated introns
MORN repeat containing 2, 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 14 samples with support for all annotated introns
MORN repeat-containing protein 2 isoform X2
MORN repeat-containing protein 2 isoform X1
DEAH (Asp-Glu-Ala-Asp/His) box polypeptide 57
putative ATP-dependent RNA helicase DHX57
small lysine-rich protein 1, transcript variant X2
small lysine-rich protein 1, transcript variant X1
FYVE, RhoGEF and PH domain-containing protein 4-like, transcript variant X1
FYVE, RhoGEF and PH domain-containing protein 4-like isoform X1
FYVE, RhoGEF and PH domain-containing protein 4-like, transcript variant X2
FYVE, RhoGEF and PH domain-containing protein 4-like isoform X2
DENN domain-containing protein 11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DENN domain-containing protein 11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
UTP20 small subunit processome component
small subunit processome component 20 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium-coupled monocarboxylate transporter 1
inositol 1,4,5-triphosphate receptor associated 2
branched-chain-amino-acid aminotransferase, cytosolic-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 9 bases in 7 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 9 bases in 7 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: branched-chain-amino-acid aminotransferase, cytosolic-like
RAB3A interacting protein (rabin3), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
RAB3A interacting protein (rabin3), transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
RAB3A interacting protein (rabin3), transcript variant X1
RAB3A interacting protein (rabin3), 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 15 samples with support for all annotated introns
RAB3A interacting protein (rabin3), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
RAB3A interacting protein (rabin3), transcript variant X6
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 28 samples with support for all annotated introns
RAB3A interacting protein (rabin3), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
RAB3A interacting protein (rabin3), transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
Cbl proto-oncogene-like 1, E3 ubiquitin protein ligase
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 41 samples with support for all annotated introns
protein phosphatase 6, regulatory subunit 2a, transcript variant X2
protein phosphatase 6, regulatory subunit 2a, transcript variant X1
protein phosphatase 6, regulatory subunit 2a, transcript variant X3
serine/threonine-protein phosphatase 6 regulatory subunit 2a isoform X1
serine/threonine-protein phosphatase 6 regulatory subunit 2a isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF01229
SET binding factor 1, transcript variant X6
SET binding factor 1, transcript variant X5
SET binding factor 1, transcript variant X4
SET binding factor 1, transcript variant X2
SET binding factor 1, transcript variant X3
SET binding factor 1, transcript variant X1
myotubularin-related protein 5 isoform X6
myotubularin-related protein 5 isoform X5
myotubularin-related protein 5 isoform X4
myotubularin-related protein 5 isoform X2
myotubularin-related protein 5 isoform X3
myotubularin-related protein 5 isoform X1
adrenomedullin 2a, transcript variant X1
adrenomedullin 2a, 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
heat shock protein 90, beta (grp94), member 1
glycosyltransferase 8 domain containing 2, transcript variant X3
glycosyltransferase 8 domain containing 2, transcript variant X5
glycosyltransferase 8 domain containing 2, transcript variant X4
glycosyltransferase 8 domain containing 2, transcript variant X6
glycosyltransferase 8 domain containing 2, transcript variant X2
glycosyltransferase 8 domain containing 2, transcript variant X1
glycosyltransferase 8 domain-containing protein 2 isoform X4
glycosyltransferase 8 domain-containing protein 2 isoform X3
glycosyltransferase 8 domain-containing protein 2 isoform X2
glycosyltransferase 8 domain-containing protein 2 isoform X1
glycosyltransferase 8 domain-containing protein 2 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
ankyrin repeat domain-containing protein 16
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
rab GDP dissociation inhibitor beta-like
ankyrin repeat and SOCS box containing 13a, tandem duplicate 1
ankyrin repeat and SOCS box protein 13a.1
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 25 samples with support for all annotated introns
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 42 samples with support for all annotated introns
interleukin-1 receptor-associated kinase 3, transcript variant X1
interleukin-1 receptor-associated kinase 3, transcript variant X2
interleukin-1 receptor-associated kinase 3 isoform X1
interleukin-1 receptor-associated kinase 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 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: beta-2-microglobulin-like
transmembrane BAX inhibitor motif containing 4
methionine sulfoxide reductase B3, transcript variant X2
methionine sulfoxide reductase B3, transcript variant X3
methionine sulfoxide reductase B3, transcript variant X1
methionine-R-sulfoxide reductase B3 isoform X2
methionine-R-sulfoxide reductase B3 isoform X1
methionine-R-sulfoxide reductase B3 isoform X3
high mobility group AT-hook 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
high mobility group AT-hook 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 41 samples with support for all annotated introns
high mobility group protein HMGI-C isoform X2
high mobility group protein HMGI-C isoform X1
deoxyribose-phosphate aldolase (putative)
microsomal glutathione S-transferase 1-like, transcript variant X1
microsomal glutathione S-transferase 1-like, transcript variant X2
microsomal glutathione S-transferase 1-like
microsomal glutathione S-transferase 1.1, transcript variant X2
microsomal glutathione S-transferase 1.1, transcript variant X1
microsomal glutathione S-transferase 1.1
LIM domain only 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
LIM domain only 3, transcript variant X2
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 7 samples with support for all annotated introns
LIM domain only 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 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: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 39, transcript variant X1
Rho guanine nucleotide exchange factor (GEF) 39, transcript variant X2
Rho guanine nucleotide exchange factor (GEF) 39, transcript variant X3
rho guanine nucleotide exchange factor 39 isoform X1
rho guanine nucleotide exchange factor 39 isoform X3
rho guanine nucleotide exchange factor 39 isoform X2
ras-related and estrogen-regulated growth inhibitor-like protein
interleukin 17 receptor A1a, transcript variant X1
interleukin 17 receptor A1a, 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
probable E3 ubiquitin-protein ligase makorin-1
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 20 samples with support for all annotated introns
CCR4-NOT transcription complex, subunit 4b, transcript variant X1
CCR4-NOT transcription complex, subunit 4b, transcript variant X2
CCR4-NOT transcription complex subunit 4 isoform X1
CCR4-NOT transcription complex subunit 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mitochondrial ribosomal protein S33, transcript variant X1
mitochondrial ribosomal protein S33, transcript variant X2
28S ribosomal protein S33, mitochondrial
B-Raf proto-oncogene, serine/threonine kinase, transcript variant X1
B-Raf proto-oncogene, serine/threonine kinase, transcript variant X2
serine/threonine-protein kinase B-raf isoform X1
serine/threonine-protein kinase B-raf isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LARGE xylosyl- and glucuronyltransferase 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: LARGE xylosyl- and glucuronyltransferase 1
stimulated by retinoic acid gene 8 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
rho GTPase-activating protein 8-like, transcript variant X1
rho GTPase-activating protein 8-like, transcript variant X2
nuclear pore complex protein Nup50 isoform X1
nuclear pore complex protein Nup50 isoform X2
uncharacterized protein KIAA0930 homolog
microfibril-associated glycoprotein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
RNA 2',3'-cyclic phosphate and 5'-OH ligase
exportin, tRNA (nuclear export receptor for tRNAs), transcript variant X2
exportin, tRNA (nuclear export receptor for tRNAs), transcript variant X5
exportin, tRNA (nuclear export receptor for tRNAs), transcript variant X3
exportin, tRNA (nuclear export receptor for tRNAs), transcript variant X4
exportin, tRNA (nuclear export receptor for tRNAs), transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00263
parathyroid hormone-like hormone a, transcript variant X4
parathyroid hormone-like hormone a, transcript variant X3
parathyroid hormone-like hormone a, transcript variant X1
parathyroid hormone-like hormone a, transcript variant X2
uncharacterized protein C11orf98 homolog
MANSC domain containing 1, transcript variant X4
MANSC domain containing 1, transcript variant X3
MANSC domain containing 1, transcript variant X2
MANSC domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
MANSC domain-containing protein 1 isoform X1
MANSC domain-containing protein 1 isoform X2
low density lipoprotein receptor-related protein 6, transcript variant X1
low density lipoprotein receptor-related protein 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
low-density lipoprotein receptor-related protein 6 isoform X1
low-density lipoprotein receptor-related protein 6 isoform X2
TANK-binding kinase 1, transcript variant X2
TANK-binding kinase 1, transcript variant X3
TANK-binding kinase 1, 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 9 samples with support for all annotated introns
cAMP responsive element binding protein-like 2
cAMP-responsive element-binding protein-like 2
epidermal growth factor receptor pathway substrate 8a, 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 4 samples with support for all annotated introns
epidermal growth factor receptor pathway substrate 8a, 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 32 samples with support for all annotated introns
epidermal growth factor receptor pathway substrate 8a, transcript variant X5
epidermal growth factor receptor pathway substrate 8a, transcript variant X6
epidermal growth factor receptor pathway substrate 8a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
epidermal growth factor receptor pathway substrate 8a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8a isoform X2
epidermal growth factor receptor kinase substrate 8a isoform X1
epidermal growth factor receptor kinase substrate 8a isoform X3
protein tyrosine phosphatase receptor type O, transcript variant X3
protein tyrosine phosphatase receptor type O, 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 3 samples with support for all annotated introns
protein tyrosine phosphatase receptor type O, transcript variant X1
receptor-type tyrosine-protein phosphatase O isoform X3
receptor-type tyrosine-protein phosphatase O isoform X2
receptor-type tyrosine-protein phosphatase O isoform X1
CASP2 and RIPK1 domain containing adaptor with death domain
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 46 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
non-SMC condensin II complex, subunit H2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; 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, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC124469611
tripartite motif-containing protein 29-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
tripartite motif-containing protein 29-like, transcript variant X3
tripartite motif-containing protein 29-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tripartite motif-containing protein 29-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00393
COORDINATES: nucleotide motif:Rfam:12.0:RF00425
COORDINATES: nucleotide motif:Rfam:12.0:RF00342
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
kyphoscoliosis peptidase-like, transcript variant X2
kyphoscoliosis peptidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
serine/threonine kinase 38 like, transcript variant X1
serine/threonine kinase 38 like, transcript variant X3
serine/threonine kinase 38 like, transcript variant X2
serine/threonine kinase 38 like, transcript variant X5
serine/threonine kinase 38 like, transcript variant X4
serine/threonine-protein kinase 38-like isoform X1
serine/threonine-protein kinase 38-like isoform X3
serine/threonine-protein kinase 38-like isoform X4
serine/threonine-protein kinase 38-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 21
patatin-like phospholipase domain containing 3
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: 9 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: patatin-like phospholipase domain containing 3
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
metallophosphoesterase domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
metallophosphoesterase domain-containing protein 1
signal peptide, CUB domain, EGF-like 1, 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 30 samples with support for all annotated introns
signal peptide, CUB domain, EGF-like 1, 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
signal peptide, CUB domain, EGF-like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
signal peptide, CUB and EGF-like domain-containing protein 1 isoform X3
signal peptide, CUB and EGF-like domain-containing protein 1 isoform X2
signal peptide, CUB and EGF-like domain-containing protein 1 isoform X1
sorting and assembly machinery component 50 homolog, like
sorting and assembly machinery component 50 homolog B
aldehyde dehydrogenase 1 family, member L2
mitochondrial 10-formyltetrahydrofolate dehydrogenase
uncharacterized protein C12orf45 homolog
solute carrier family 41 member 2b, transcript variant X2
solute carrier family 41 member 2b, transcript variant X1
solute carrier family 41 member 2b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 50% coverage of the annotated genomic feature by RNAseq alignments
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
carbohydrate (chondroitin 4) sulfotransferase 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
carbohydrate (chondroitin 4) sulfotransferase 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
carbohydrate (chondroitin 4) sulfotransferase 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
carbohydrate sulfotransferase 11 isoform X2
carbohydrate sulfotransferase 11 isoform X1
carbohydrate sulfotransferase 11 isoform X3
nuclear transcription factor Y, beta a, transcript variant X2
nuclear transcription factor Y, beta a, transcript variant X6
nuclear transcription factor Y, beta a, transcript variant X1
nuclear transcription factor Y, beta a, transcript variant X4
nuclear transcription factor Y, beta a, transcript variant X3
nuclear transcription factor Y, beta a, transcript variant X5
nuclear transcription factor Y, beta a isoform X1
nuclear transcription factor Y, beta a isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 60% 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
muskelin 1, intracellular mediator containing kelch motifs, transcript variant X2
muskelin 1, intracellular mediator containing kelch motifs, transcript variant X1
muskelin 1, intracellular mediator containing kelch motifs, transcript variant X3
uncharacterized LOC124469328, transcript variant X2
uncharacterized protein LOC124469328 isoform X2
uncharacterized LOC124469328, transcript variant X1
uncharacterized LOC124469328, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC124469328 isoform X1
uncharacterized protein LOC124469328 isoform X3
neuroepithelial cell-transforming gene 1 protein
t-complex 11, testis-specific-like 2, transcript variant X1
t-complex 11, testis-specific-like 2, transcript variant X3
t-complex 11, testis-specific-like 2, transcript variant X4
t-complex 11, testis-specific-like 2, transcript variant X2
T-complex protein 11-like protein 2 isoform X1
T-complex protein 11-like protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124469486, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
uncharacterized LOC124469486, 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 43 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 24 samples with support for all annotated introns
uncharacterized LOC124469563, transcript variant X2
uncharacterized LOC124469563, 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 38 samples with support for all annotated introns
uncharacterized LOC124469564, transcript variant X1
uncharacterized LOC124469564, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC124469564, transcript variant X3
DEP domain containing 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
DEP domain containing 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
DEP domain-containing protein 4 isoform X1
DEP domain-containing protein 4 isoform X2
dihydrouridine synthase 4-like (S. cerevisiae), 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 44 samples with support for all annotated introns
dihydrouridine synthase 4-like (S. cerevisiae), 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 44 samples with support for all annotated introns
tRNA-dihydrouridine(20a/20b) synthase [NAD(P)+]-like isoform X2
tRNA-dihydrouridine(20a/20b) synthase [NAD(P)+]-like isoform X1
conserved oligomeric Golgi complex subunit 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit A5
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5
ankyrin repeat and SOCS box protein 15-like
LOW QUALITY PROTEIN: ubiquitin-conjugating enzyme E2 N-like
39S ribosomal protein L42, mitochondrial
zinc finger protein 502, transcript variant X4
zinc finger protein 502, transcript variant X5
zinc finger protein 502, transcript variant X6
zinc finger protein 502, transcript variant X2
zinc finger protein 502, transcript variant X1
zinc finger protein 502, transcript variant X3
uncharacterized protein si:dkey-14d8.1 isoform X3
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: 29 Proteins
LOW QUALITY PROTEIN: C-X-C chemokine receptor type 4-like
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: 2 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase TRIM39-like
E3 ubiquitin-protein ligase Mdm2-like, transcript variant X1
E3 ubiquitin-protein ligase Mdm2-like, transcript variant X2
E3 ubiquitin-protein ligase Mdm2-like isoform X2
uncharacterized LOC124469599, transcript variant X2
uncharacterized LOC124469599, transcript variant X1
PDZ domain-containing RING finger protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
zinc finger CCHC-type and RNA binding motif 1
zinc finger CCHC-type and RNA-binding motif-containing protein 1
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 39 samples with support for all annotated introns
prickle-like protein 1, transcript variant X2
prickle-like protein 1, transcript variant X1
pseudouridine synthase 7 like, transcript variant X3
pseudouridine synthase 7 like, transcript variant X2
pseudouridine synthase 7 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
pseudouridylate synthase 7 homolog-like protein
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
LOW QUALITY PROTEIN: NUAK family SNF1-like kinase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
kinesin-like protein KIF21A, transcript variant X4
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 7 samples with support for all annotated introns
kinesin-like protein KIF21A, transcript variant X3
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 11 samples with support for all annotated introns
kinesin-like protein KIF21A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
kinesin-like protein KIF21A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ATP-binding cassette sub-family D member 2-like
uncharacterized LOC124469310, transcript variant X1
uncharacterized LOC124469310, transcript variant X2
uncharacterized LOC124469310, transcript variant X3
uncharacterized LOC124469310, transcript variant X4
uncharacterized LOC124469310, transcript variant X7
uncharacterized protein LOC124469310 isoform X1
uncharacterized protein LOC124469310 isoform X2
uncharacterized protein LOC124469310 isoform X3
uncharacterized protein LOC124469310 isoform X4
uncharacterized protein LOC124469310 isoform X7
uncharacterized LOC124469310, transcript variant X5
uncharacterized LOC124469310, transcript variant X6
uncharacterized protein LOC124469310 isoform X5
uncharacterized protein LOC124469310 isoform X6
uncharacterized LOC124469310, transcript variant X8
uncharacterized protein LOC124469310 isoform X8
solute carrier organic anion transporter family member 1C1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 41% 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 25% coverage of the annotated genomic feature by RNAseq alignments
pyridine nucleotide-disulphide oxidoreductase domain 1
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1
RecQ helicase-like, transcript variant X1
ATP-dependent DNA helicase Q1 isoform X1
RecQ helicase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
RecQ helicase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
RecQ helicase-like, transcript variant X2
ATP-dependent DNA helicase Q1 isoform X2
glycogen synthase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
glycogen synthase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
glycogen [starch] synthase, liver isoform X2
glycogen [starch] synthase, liver isoform X1
lactate dehydrogenase Ba, transcript variant X1
lactate dehydrogenase Ba, transcript variant X2
solute carrier family 25 member 3a, transcript variant X1
solute carrier family 25 member 3a, transcript variant X2
solute carrier family 25 member 3a isoform X1
solute carrier family 25 member 3a isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
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
serine/threonine kinase receptor associated protein, transcript variant X4
serine/threonine kinase receptor associated protein, transcript variant X2
serine/threonine kinase receptor associated protein, transcript variant X3
serine/threonine kinase receptor associated protein, transcript variant X1
serine/threonine kinase receptor associated protein, transcript variant X6
serine/threonine kinase receptor associated protein, transcript variant X5
serine-threonine kinase receptor-associated protein isoform X4
serine-threonine kinase receptor-associated protein isoform X3
serine-threonine kinase receptor-associated protein isoform X2
serine-threonine kinase receptor-associated protein isoform X1
ATPase plasma membrane Ca2+ transporting 1a
LOW QUALITY PROTEIN: plasma membrane calcium-transporting ATPase 1a
mesoderm specific transcript, transcript variant X1
mesoderm specific transcript, transcript variant X2
mesoderm-specific transcript homolog protein isoform X1
mesoderm-specific transcript homolog protein isoform X2
uncharacterized protein LOC559444 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
MAPK-interacting and spindle-stabilizing protein-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 31 samples with support for all annotated introns
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1, transcript variant X1
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1, transcript variant X2
alpha-N-acetylneuraminide alpha-2,8-sialyltransferase isoform X1
alpha-N-acetylneuraminide alpha-2,8-sialyltransferase isoform X2
troponin I, slow skeletal muscle-like, transcript variant X2
troponin I, slow skeletal muscle-like, transcript variant X1
troponin I, slow skeletal muscle-like isoform X1
troponin I, slow skeletal muscle-like isoform X2
IQ motif and SEC7 domain-containing protein 3-like
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
sodium- and chloride-dependent GABA transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 114 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
sodium- and chloride-dependent betaine transporter-like, transcript variant X2
sodium- and chloride-dependent betaine transporter-like, transcript variant X1
sodium- and chloride-dependent betaine transporter-like
protein mono-ADP-ribosyltransferase PARP11-like
protein mono-ADP-ribosyltransferase PARP11-like, transcript variant X1
protein mono-ADP-ribosyltransferase PARP11-like, transcript variant X2
protein mono-ADP-ribosyltransferase PARP11-like isoform X2
protein mono-ADP-ribosyltransferase PARP11-like isoform X1
protein mono-ADP-ribosyltransferase PARP11-like, transcript variant X3
protein mono-ADP-ribosyltransferase PARP11-like isoform X3
transmembrane O-mannosyltransferase targeting cadherins 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
transmembrane O-mannosyltransferase targeting cadherins 2a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein O-mannosyl-transferase TMTC2 isoform X1
protein O-mannosyl-transferase TMTC2 isoform X3
transmembrane O-mannosyltransferase targeting cadherins 2a, 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 8 samples with support for all annotated introns
protein O-mannosyl-transferase TMTC2 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
methyltransferase like 25, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
methyltransferase like 25, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
methyltransferase like 25, transcript variant X2
methyltransferase-like protein 25 isoform X2
methyltransferase-like protein 25 isoform X3
methyltransferase-like protein 25 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
thyroid transcription factor 1-associated protein 26 homolog
calcium release activated channel regulator 2Ab
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
EF-hand calcium-binding domain-containing protein 4B
protein arginine N-methyltransferase 8-B
LOW QUALITY PROTEIN: nuclear factor 7, brain-like
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3Aa
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
piccolo presynaptic cytomatrix protein a
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: 2 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
calcium channel, voltage-dependent, alpha 2/delta subunit 1a, transcript variant X1
calcium channel, voltage-dependent, alpha 2/delta subunit 1a, transcript variant X2
calcium channel, voltage-dependent, alpha 2/delta subunit 1a, transcript variant X3
calcium channel, voltage-dependent, alpha 2/delta subunit 1a, transcript variant X4
voltage-dependent calcium channel subunit alpha-2/delta-1a isoform X1
voltage-dependent calcium channel subunit alpha-2/delta-1a isoform X2
voltage-dependent calcium channel subunit alpha-2/delta-1a isoform X3
voltage-dependent calcium channel subunit alpha-2/delta-1a isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 29% coverage of the annotated genomic feature by RNAseq alignments
staphylococcal nuclease and tudor domain containing 1
staphylococcal nuclease domain-containing protein 1
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
LOW QUALITY PROTEIN: myoD family inhibitor domain-containing protein
protein phosphatase 1, regulatory subunit 3Aa
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1 regulatory subunit 3A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
uncharacterized LOC124469286, transcript variant X2
uncharacterized LOC124469286, transcript variant X1
uncharacterized protein LOC124469286 isoform X2
uncharacterized protein LOC124469286 isoform X1
interferon-related developmental regulator 1, transcript variant X1
interferon-related developmental regulator 1, transcript variant X2
interferon-related developmental regulator 1 isoform X2
interferon-related developmental regulator 1 isoform X1
uncharacterized LOC124469289, transcript variant X1
uncharacterized LOC124469289, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
protein PHTF2-like, transcript variant X5
protein PHTF2-like, transcript variant X7
protein PHTF2-like, transcript variant X1
protein PHTF2-like, transcript variant X3
protein PHTF2-like, transcript variant X4
protein PHTF2-like, transcript variant X6
protein PHTF2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase non-receptor type 12, transcript variant X4
protein tyrosine phosphatase non-receptor type 12, transcript variant X1
protein tyrosine phosphatase non-receptor type 12, transcript variant X2
protein tyrosine phosphatase non-receptor type 12, transcript variant X3
protein tyrosine phosphatase non-receptor type 12, transcript variant X5
tyrosine-protein phosphatase non-receptor type 12 isoform X3
tyrosine-protein phosphatase non-receptor type 12 isoform X2
tyrosine-protein phosphatase non-receptor type 12 isoform X5
tyrosine-protein phosphatase non-receptor type 12 isoform X1
tyrosine-protein phosphatase non-receptor type 12 isoform X4
gamma-secretase activating protein, transcript variant X3
gamma-secretase activating protein, transcript variant X2
gamma-secretase activating protein, transcript variant X1
gamma-secretase-activating protein isoform X2
gamma-secretase-activating protein 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
coiled-coil domain-containing protein 146
leucine-rich repeat-containing protein 17
short transmembrane mitochondrial protein 1, transcript variant X3
short transmembrane mitochondrial protein 1, transcript variant X2
short transmembrane mitochondrial protein 1, transcript variant X1
short transmembrane mitochondrial protein 1
aldo-keto reductase family 1 member B1-like, transcript variant X2
aldo-keto reductase family 1 member B1-like, transcript variant X1
aldo-keto reductase family 1 member B1-like
aldo-keto reductase family 1 member B1-like isoform X1
aldo-keto reductase family 1 member B1-like isoform X2
A-kinase anchor protein 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
A-kinase anchor protein 5-like, transcript variant X2
A-kinase anchor protein 5-like isoform X1
A-kinase anchor protein 5-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
LOW QUALITY PROTEIN: proline-rich protein 5-like
interleukin-15 receptor subunit alpha-like, transcript variant X1
interleukin-15 receptor subunit alpha-like, transcript variant X2
interleukin-15 receptor subunit alpha-like isoform X1
interleukin-15 receptor subunit alpha-like isoform X2
F-box DNA helicase 1, transcript variant X2
F-box DNA helicase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
nudix (nucleoside diphosphate linked moiety X)-type motif 5, transcript variant X1
nudix (nucleoside diphosphate linked moiety X)-type motif 5, transcript variant X2
cell division cycle 123 homolog (S. cerevisiae), transcript variant X1
cell division cycle 123 homolog (S. cerevisiae), transcript variant X2
coiled-coil domain-containing protein 3a
minichromosome maintenance 10 replication initiation factor
upper zone of growth plate and cartilage matrix associated a
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 43 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: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cyclin-dependent kinase 17
LOW QUALITY PROTEIN: ETS domain-containing protein Elk-3
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 41 samples with support for all annotated introns
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon AAC); 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 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 77% coverage of the annotated genomic feature by RNAseq alignments
zinc finger, C3HC-type containing 1, transcript variant X1
zinc finger, C3HC-type containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
nuclear-interacting partner of ALK isoform X1
nuclear-interacting partner of ALK isoform X2
ubiquitin-conjugating enzyme E2H (UBC8 homolog, yeast), transcript variant X1
ubiquitin-conjugating enzyme E2H (UBC8 homolog, yeast), transcript variant X2
nuclear respiratory factor 1, transcript variant X2
nuclear respiratory factor 1, transcript variant X1
N-acetylated alpha-linked acidic dipeptidase like 1
endoplasmic reticulum aminopeptidase 1b, transcript variant X1
endoplasmic reticulum aminopeptidase 1b, transcript variant X2
endoplasmic reticulum aminopeptidase 1b isoform X1
endoplasmic reticulum aminopeptidase 1b isoform X2
general transcription factor IIH, polypeptide 2, transcript variant X1
general transcription factor IIH, polypeptide 2, transcript variant X3
general transcription factor IIH, polypeptide 2, transcript variant X2
general transcription factor IIH subunit 2
protein prenyltransferase alpha subunit repeat containing 1, transcript variant X2
protein prenyltransferase alpha subunit repeat containing 1, transcript variant X1
protein prenyltransferase alpha subunit repeat-containing protein 1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
dihydrofolate reductase, transcript variant X1
dihydrofolate reductase, transcript variant X2
ankyrin repeat domain 34Bb, 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 10 samples with support for all annotated introns
ankyrin repeat domain 34Bb, 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 36 samples with support for all annotated introns
family with sequence similarity 151 member B
coiled-coil domain containing 125, transcript variant X2
coiled-coil domain containing 125, transcript variant X1
coiled-coil domain-containing protein 125 isoform X2
coiled-coil domain-containing protein 125 isoform X1
RAD17 checkpoint clamp loader component, 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 19 samples with support for all annotated introns
RAD17 checkpoint clamp loader component, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
MARVEL domain containing 2b, transcript variant X4
MARVEL domain containing 2b, transcript variant X1
MARVEL domain containing 2b, transcript variant X3
MARVEL domain containing 2b, transcript variant X2
amyloid-beta A4 precursor protein-binding family A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
family with sequence similarity 189 member A2
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
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: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
LOW QUALITY PROTEIN: tight junction protein ZO-2-like
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 14 samples with support for all annotated introns
3-hydroxy-3-methylglutaryl-CoA reductase a
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
ankyrin repeat domain-containing protein 31-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4
family with sequence similarity 169 member Ab, transcript variant X1
family with sequence similarity 169 member Ab, transcript variant X3
family with sequence similarity 169 member Ab, transcript variant X2
ectoderm-neural cortex protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
ectoderm-neural cortex protein 1-like, transcript variant X2
cell division cycle 14B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
cell division cycle 14B, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
cell division cycle 14B, 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 14 samples with support for all annotated introns
cell division cycle 14B, transcript variant X2
cell division cycle 14B, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
cell division cycle 14B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
cell division cycle 14B, transcript variant X9
dual specificity protein phosphatase CDC14B isoform X6
dual specificity protein phosphatase CDC14B isoform X7
dual specificity protein phosphatase CDC14B isoform X1
dual specificity protein phosphatase CDC14B isoform X3
dual specificity protein phosphatase CDC14B isoform X4
dual specificity protein phosphatase CDC14B isoform X2
cell division cycle 14B, transcript variant X5
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 39 samples with support for all annotated introns
cell division cycle 14B, transcript variant X7
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 16 samples with support for all annotated introns
dual specificity protein phosphatase CDC14B isoform X5
leucine zipper, putative tumor suppressor family member 3b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
leucine zipper putative tumor suppressor 3
U-box domain containing 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
U-box domain containing 5, 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 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
solute carrier family 35 member D2, transcript variant X3
solute carrier family 35 member D2, transcript variant X1
solute carrier family 35 member D2, transcript variant X2
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter isoform X1
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter isoform X2
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
glutamate receptor-interacting protein 1-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 34 samples with support for all annotated introns
uncharacterized LOC124469535, transcript variant X1
uncharacterized protein LOC124469535 isoform X1
uncharacterized LOC124469535, 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 38 samples with support for all annotated introns
uncharacterized protein LOC124469535 isoform X2
SH3 and multiple ankyrin repeat domains 3b
LOW QUALITY PROTEIN: SH3 and multiple ankyrin repeat domains protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LSM8 homolog, U6 small nuclear RNA associated
uncharacterized LOC124469507, transcript variant X2
uncharacterized LOC124469507, transcript variant X1
ATP-binding cassette sub-family C member 9-like
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: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: ATP-binding cassette sub-family C member 9-like
potassium inwardly rectifying channel subfamily J member 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ATP-sensitive inward rectifier potassium channel 8
cytidine monophosphate N-acetylneuraminic acid synthetase a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
N-acylneuraminate cytidylyltransferase A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 31% 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 79% 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: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
FAM3 metabolism regulating signaling molecule C
B-cell translocation gene 1, anti-proliferative
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC568385 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized protein LOC568385 homolog, 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 36 samples with support for all annotated introns
uncharacterized protein si:dkeyp-38g8.5 isoform X1
uncharacterized LOC124469629, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
uncharacterized LOC124469629, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
uncharacterized protein LOC124469629 isoform X1
uncharacterized protein LOC124469629 isoform X4
uncharacterized LOC124469629, transcript variant X3
uncharacterized LOC124469629, transcript variant X2
uncharacterized protein LOC124469629 isoform X2
uncharacterized protein LOC124469629 isoform X3
B cell receptor associated protein 29, transcript variant X1
B cell receptor associated protein 29, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
AE binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
AE binding protein 2, 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 40 samples with support for all annotated introns
pleckstrin homology domain containing, family A member 5, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology domain-containing family A member 5 isoform X5
pleckstrin homology domain containing, family A member 5, transcript variant X7
pleckstrin homology domain containing, family A member 5, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
pleckstrin homology domain containing, family A member 5, transcript variant X4
pleckstrin homology domain containing, family A member 5, transcript variant X3
pleckstrin homology domain containing, family A member 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
pleckstrin homology domain containing, family A member 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
pleckstrin homology domain containing, family A member 5, transcript variant X5
pleckstrin homology domain containing, family A member 5, transcript variant X6
pleckstrin homology domain-containing family A member 5 isoform X4
pleckstrin homology domain-containing family A member 5 isoform X3
pleckstrin homology domain-containing family A member 5 isoform X2
pleckstrin homology domain-containing family A member 5 isoform X1
protein bicaudal D homolog 1-like, transcript variant X2
protein bicaudal D homolog 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
protein bicaudal D homolog 1-like isoform X2
protein bicaudal D homolog 1-like isoform X1
suppressor APC domain containing 1, transcript variant X3
suppressor APC domain containing 1, transcript variant X1
suppressor APC domain containing 1, transcript variant X5
suppressor APC domain containing 1, transcript variant X2
suppressor APC domain containing 1, transcript variant X6
suppressor APC domain containing 1, transcript variant X4
suppressor APC domain-containing protein 1 isoform X2
suppressor APC domain-containing protein 1 isoform X1
suppressor APC domain-containing protein 1 isoform X4
suppressor APC domain-containing protein 1 isoform X3
cyclin-dependent kinase inhibitor 1D, transcript variant X1
cyclin-dependent kinase inhibitor 1D, transcript variant X2
solute carrier family 37 member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
solute carrier family 37 member 3, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 15-like, 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 23 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 15-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 15-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 15-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 15-like isoform X2
ubiquitin carboxyl-terminal hydrolase 15-like isoform X1
ubiquitin carboxyl-terminal hydrolase 15-like isoform X3
ubiquitin carboxyl-terminal hydrolase 15-like isoform X4
sodium- and chloride-dependent GABA transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
lysine (K)-specific demethylase 5A, transcript variant X3
lysine (K)-specific demethylase 5A, transcript variant X2
lysine (K)-specific demethylase 5A, transcript variant X1
lysine-specific demethylase 5A isoform X2
lysine-specific demethylase 5A isoform X3
lysine-specific demethylase 5A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
transcription intermediary factor 1-alpha
cysteine rich DPF motif domain containing 1
cysteine-rich DPF motif domain-containing protein 1