Chiloscyllium plagiosum isolate BGI_BamShark_2017 chromosome 30, ASM401019v2, whole genome shotgun sequence.
Chiloscyllium plagiosum (whitespotted bambooshark)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Hemiscylliidae; Chiloscyllium.
REFSEQ INFORMATION: The reference sequence is identical to\nCM012985.1.\nAssembly name: ASM401019v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the BGI on 2019/01/10. The\noriginal whole-genome shotgun project has the accession\nQPFF00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: BGI\nAssembly Method :: platanus v. 1.2.4; 3ddna v. 170123\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 280.0x\nSequencing Technology :: BGIseq-500\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Chiloscyllium plagiosum Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
zinc finger protein 239-like, transcript variant X11
COORDINATES: polyA evidence [ECO:0006239]
zinc finger protein 239-like, transcript variant X6
zinc finger protein 239-like, transcript variant X9
zinc finger protein 239-like, transcript variant X1
zinc finger protein 239-like, transcript variant X4
zinc finger protein 239-like, transcript variant X10
zinc finger protein 239-like, transcript variant X12
zinc finger protein 239-like, transcript variant X7
zinc finger protein 239-like, transcript variant X2
zinc finger protein 239-like, transcript variant X8
zinc finger protein 239-like, transcript variant X3
zinc finger protein 239-like, transcript variant X5
gastrula zinc finger protein XlCGF7.1-like
uncharacterized LOC122564680, 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
uncharacterized LOC122564680, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gastrula zinc finger protein XlCGF7.1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gastrula zinc finger protein XlCGF7.1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gastrula zinc finger protein XlCGF7.1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon UAU); 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: 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 12 samples with support for all annotated introns
uncharacterized LOC122564687, transcript variant X1
uncharacterized LOC122564687, 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 9 samples with support for all annotated introns
ectonucleoside triphosphate diphosphohydrolase 8-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ectonucleoside triphosphate diphosphohydrolase 8-like, transcript variant X3
ectonucleoside triphosphate diphosphohydrolase 8-like, transcript variant X1
ectonucleoside triphosphate diphosphohydrolase 8-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ectonucleoside triphosphate diphosphohydrolase 8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ectonucleoside triphosphate diphosphohydrolase 8-like isoform X1
ectonucleoside triphosphate diphosphohydrolase 8-like isoform X2
ectonucleoside triphosphate diphosphohydrolase 8-like isoform X4
ectonucleoside triphosphate diphosphohydrolase 8-like isoform X3
NOTCH regulated ankyrin repeat protein a
notch-regulated ankyrin repeat-containing protein A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
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 25 samples with support for all annotated introns
complement component 8, gamma polypeptide
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
F-box and WD repeat domain containing 5, transcript variant X2
F-box and WD repeat domain containing 5, transcript variant X1
F-box/WD repeat-containing protein 5 isoform X2
F-box/WD repeat-containing protein 5 isoform X1
rab-like protein 6, 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 12 samples with support for all annotated introns
rab-like protein 6, 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 26 samples with support for all annotated introns
rab-like protein 6, 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ectonucleoside triphosphate diphosphohydrolase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 58% coverage of the annotated genomic feature by RNAseq alignments
peptidylprolyl isomerase (cyclophilin)-like 3
peptidyl-prolyl cis-trans isomerase-like 3
ectonucleoside triphosphate diphosphohydrolase 2-like
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 15 samples with support for all annotated introns
uncharacterized protein LOC449555 homolog
3-oxoacyl-[acyl-carrier-protein] reductase FabG
coenzyme Q4 homolog (S. cerevisiae), transcript variant X2
coenzyme Q4 homolog (S. cerevisiae), transcript variant X1
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial isoform X1
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial isoform X2
TruB pseudouridine (psi) synthase family member 2, transcript variant X3
TruB pseudouridine (psi) synthase family member 2, transcript variant X2
TruB pseudouridine (psi) synthase family member 2, transcript variant X1
mitochondrial mRNA pseudouridine synthase TRUB2 isoform X2
mitochondrial mRNA pseudouridine synthase TRUB2 isoform X1
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
suppressor APC domain-containing protein 2
endothelial differentiation-related factor 1, transcript variant X1
endothelial differentiation-related factor 1, transcript variant X2
endothelial differentiation-related factor 1 homolog isoform X1
endothelial differentiation-related factor 1 homolog isoform X2
UDP-N-acetylglucosamine pyrophosphorylase 1, like 1
UDP-N-acetylhexosamine pyrophosphorylase-like protein 1
sodium-dependent phosphate transport protein 2B-like
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 3 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 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: 458 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tubulin beta chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 456 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tubulin beta chain-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tubulin beta chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
aminolevulinate dehydratase, transcript variant X2
aminolevulinate dehydratase, transcript variant X1
aminolevulinate dehydratase, transcript variant X3
NADPH dependent diflavin oxidoreductase 1, transcript variant X1
NADPH-dependent diflavin oxidoreductase 1 isoform X1
NADPH dependent diflavin oxidoreductase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
NADPH-dependent diflavin oxidoreductase 1 isoform X2
transmembrane protein 203, transcript variant X2
transmembrane protein 203, transcript variant X1
Sjogren syndrome nuclear autoantigen 1, transcript variant X1
Sjogren syndrome nuclear autoantigen 1, transcript variant X2
Sjoegren syndrome nuclear autoantigen 1 isoform X1
Sjoegren syndrome nuclear autoantigen 1 isoform X2
anaphase promoting complex subunit 2, transcript variant X1
anaphase promoting complex subunit 2, transcript variant X2
anaphase-promoting complex subunit 2 isoform X1
anaphase-promoting complex subunit 2 isoform X2
uncharacterized LOC122564714, transcript variant X2
uncharacterized LOC122564714, 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
lectin BRA-3-like, transcript variant X2
lectin BRA-3-like, transcript variant X1
lectin BRA-3-like, transcript variant X3
C-type mannose receptor 2-like isoform X2
uncharacterized protein LOC122564717 isoform X1
glutamate receptor, ionotropic, N-methyl D-aspartate 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
nuclear speckle splicing regulatory protein 1-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tetratricopeptide repeat protein 28-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 10 samples with support for all annotated introns
discoidin domain-containing receptor 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 504 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 435 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
haloacid dehalogenase-like hydrolase domain containing 3, transcript variant X3
haloacid dehalogenase-like hydrolase domain containing 3, transcript variant X1
haloacid dehalogenase-like hydrolase domain containing 3, transcript variant X2
haloacid dehalogenase-like hydrolase domain-containing protein 3
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 17 samples with support for all annotated introns
B box and SPRY domain-containing protein
WD repeat domain 31, transcript variant X4
WD repeat domain 31, transcript variant X1
WD repeat domain 31, transcript variant X2
WD repeat domain 31, transcript variant X5
WD repeat-containing protein 31 isoform X1
WD repeat-containing protein 31 isoform X3
WD repeat domain 31, transcript variant X3
WD repeat-containing protein 31 isoform X2
WD repeat-containing protein 31 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
PRP4 pre-mRNA processing factor 4 homolog (yeast), transcript variant X2
PRP4 pre-mRNA processing factor 4 homolog (yeast), transcript variant X1
U4/U6 small nuclear ribonucleoprotein Prp4 isoform X1
U4/U6 small nuclear ribonucleoprotein Prp4 isoform X2
anaphase-promoting complex subunit CDC26
solute carrier family 31 member 1, transcript variant X3
solute carrier family 31 member 1, transcript variant X4
solute carrier family 31 member 1, transcript variant X1
solute carrier family 31 member 1, transcript variant X2
high affinity copper uptake protein 1 isoform X1
high affinity copper uptake protein 1 isoform X2
high affinity copper uptake protein 1 isoform 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
FK506-binding protein 15-like, transcript variant X2
FK506-binding protein 15-like, transcript variant X1
FK506-binding protein 15-like isoform X2
FK506-binding protein 15-like isoform X1
leucine rich repeat and sterile alpha motif containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
leucine rich repeat and sterile alpha motif containing 1, transcript variant X4
leucine rich repeat and sterile alpha motif containing 1, transcript variant X2
leucine rich repeat and sterile alpha motif containing 1, transcript variant X1
leucine rich repeat and sterile alpha motif containing 1, transcript variant X5
E3 ubiquitin-protein ligase LRSAM1 isoform X2
E3 ubiquitin-protein ligase LRSAM1 isoform X1
E3 ubiquitin-protein ligase LRSAM1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
polymerase (DNA directed), epsilon 3 (p17 subunit), transcript variant X1
polymerase (DNA directed), epsilon 3 (p17 subunit), transcript variant X3
polymerase (DNA directed), epsilon 3 (p17 subunit), transcript variant X8
polymerase (DNA directed), epsilon 3 (p17 subunit), transcript variant X4
polymerase (DNA directed), epsilon 3 (p17 subunit), transcript variant X7
polymerase (DNA directed), epsilon 3 (p17 subunit), transcript variant X6
polymerase (DNA directed), epsilon 3 (p17 subunit), transcript variant X2
polymerase (DNA directed), epsilon 3 (p17 subunit), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
cellular communication network factor 1, like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
NMDA receptor synaptonuclear signaling and neuronal migration factor b, transcript variant X2
NMDA receptor synaptonuclear signaling and neuronal migration factor b, transcript variant X1
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X2
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X1
zinc finger MYND domain-containing protein 19
diphthamide biosynthesis 7, 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 26 samples with support for all annotated introns
diphthamide biosynthesis 7, 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 22 samples with support for all annotated introns
diphthamide biosynthesis 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitochondrial ribosomal protein L41, transcript variant X1
mitochondrial ribosomal protein L41, transcript variant X3
mitochondrial ribosomal protein L41, transcript variant X2
39S ribosomal protein L41, mitochondrial
patatin-like phospholipase domain containing 7b, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
patatin-like phospholipase domain containing 7b, transcript variant X1
patatin-like phospholipase domain containing 7b, transcript variant X3
patatin-like phospholipase domain-containing protein 7 isoform X1
patatin-like phospholipase domain-containing protein 7 isoform X3
patatin-like phospholipase domain-containing protein 7 isoform X5
patatin-like phospholipase domain containing 7b, transcript variant X4
patatin-like phospholipase domain containing 7b, transcript variant X5
patatin-like phospholipase domain containing 7b, transcript variant X2
patatin-like phospholipase domain-containing protein 7 isoform X2
patatin-like phospholipase domain-containing protein 7 isoform X4
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
neural proliferation differentiation and control protein 1-like
POU domain, class 5, transcription factor 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ATP-binding cassette, sub-family A (ABC1), member 2, transcript variant X1
ATP-binding cassette, sub-family A (ABC1), member 2, transcript variant X4
ATP-binding cassette, sub-family A (ABC1), member 2, transcript variant X5
ATP-binding cassette, sub-family A (ABC1), member 2, transcript variant X2
ATP-binding cassette sub-family A member 2 isoform X1
ATP-binding cassette sub-family A member 2 isoform X4
ATP-binding cassette sub-family A member 2 isoform X5
ATP-binding cassette sub-family A member 2 isoform X2
ATP-binding cassette, sub-family A (ABC1), member 2, transcript variant X3
ATP-binding cassette sub-family A member 2 isoform X3
chloride intracellular channel protein 4-like, transcript variant X1
chloride intracellular channel protein 4-like, transcript variant X2
chloride intracellular channel protein 4-like, transcript variant X3
chloride intracellular channel protein 5-like isoform X2
chloride intracellular channel protein 4-like isoform X1
PAXX non-homologous end joining factor, transcript variant X3
PAXX non-homologous end joining factor, transcript variant X2
PAXX non-homologous end joining factor, transcript variant X1
uncharacterized LOC122564755, 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 5 samples with support for all annotated introns
uncharacterized LOC122564755, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC122564755 isoform X1
uncharacterized protein LOC122564755 isoform X2
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC122564649, transcript variant X2
uncharacterized LOC122564649, transcript variant X1
bone morphogenetic protein/retinoic acid inducible neural-specific 1, transcript variant X1
bone morphogenetic protein/retinoic acid inducible neural-specific 1, transcript variant X4
bone morphogenetic protein/retinoic acid inducible neural-specific 1, transcript variant X3
bone morphogenetic protein/retinoic acid inducible neural-specific 1, transcript variant X2
BMP/retinoic acid-inducible neural-specific protein 1
zinc finger and SCAN domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
astrotactin-2-like, transcript variant X2
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
ferritin heavy chain, oocyte isoform-like
astrotactin-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
tripartite motif containing 32, transcript variant X2
tripartite motif containing 32, transcript variant X3
tripartite motif containing 32, transcript variant X1
tripartite motif containing 32, transcript variant X4
pappalysin-1-like, transcript variant X3
pappalysin-1-like, transcript variant X2
pappalysin-1-like, transcript variant X1
dual specificity testis-specific protein kinase 2-like, transcript variant X2
dual specificity testis-specific protein kinase 2-like, transcript variant X1
dual specificity testis-specific protein kinase 2-like, transcript variant X3
dual specificity testis-specific protein kinase 2-like isoform X1
dual specificity testis-specific protein kinase 2-like isoform X2
flocculation protein FLO11-like, transcript variant X1
flocculation protein FLO11-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 21 samples with support for all annotated introns
flocculation protein FLO11-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
flocculation protein FLO11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
flocculation protein FLO11-like, transcript variant X5
flocculation protein FLO11-like, transcript variant X6
flocculation protein FLO11-like isoform X1
uncharacterized protein LOC122564766 isoform X2
flocculation protein FLO11-like isoform X4
flocculation protein FLO11-like isoform X3
flocculation protein FLO11-like isoform X5
flocculation protein FLO11-like isoform X6
mannosidase, alpha, class 1B, member 1b, transcript variant X3
mannosidase, alpha, class 1B, member 1b, transcript variant X1
mannosidase, alpha, class 1B, member 1b, transcript variant X2
mannosidase, alpha, class 1B, member 1b isoform X2
mannosidase, alpha, class 1B, member 1b isoform X1
probable voltage-dependent N-type calcium channel subunit alpha-1B, transcript variant X9
probable voltage-dependent N-type calcium channel subunit alpha-1B, transcript variant X5
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
probable voltage-dependent N-type calcium channel subunit alpha-1B, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable voltage-dependent N-type calcium channel subunit alpha-1B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable voltage-dependent N-type calcium channel subunit alpha-1B, transcript variant X2
probable voltage-dependent N-type calcium channel subunit alpha-1B, transcript variant X3
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
probable voltage-dependent N-type calcium channel subunit alpha-1B, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable voltage-dependent N-type calcium channel subunit alpha-1B, transcript variant X8
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
probable voltage-dependent N-type calcium channel subunit alpha-1B, transcript variant X1
probable voltage-dependent N-type calcium channel subunit alpha-1B isoform X9
probable voltage-dependent N-type calcium channel subunit alpha-1B isoform X5
probable voltage-dependent N-type calcium channel subunit alpha-1B isoform X6
probable voltage-dependent N-type calcium channel subunit alpha-1B isoform X4
probable voltage-dependent N-type calcium channel subunit alpha-1B isoform X2
probable voltage-dependent N-type calcium channel subunit alpha-1B isoform X3
probable voltage-dependent N-type calcium channel subunit alpha-1B isoform X7
probable voltage-dependent N-type calcium channel subunit alpha-1B isoform X8
probable voltage-dependent N-type calcium channel subunit alpha-1B isoform X1
probable voltage-dependent N-type calcium channel subunit alpha-1B, transcript variant X10
probable voltage-dependent N-type calcium channel subunit alpha-1B isoform X10
histone-lysine N-methyltransferase EHMT1-like, transcript variant X5
histone-lysine N-methyltransferase EHMT1-like, transcript variant X3
histone-lysine N-methyltransferase EHMT1-like, transcript variant X1
histone-lysine N-methyltransferase EHMT1-like, transcript variant X2
histone-lysine N-methyltransferase EHMT1-like, transcript variant X4
histone-lysine N-methyltransferase EHMT1-like isoform X5
histone-lysine N-methyltransferase EHMT1-like isoform X3
histone-lysine N-methyltransferase EHMT1-like isoform X1
histone-lysine N-methyltransferase EHMT1-like isoform X2
histone-lysine N-methyltransferase EHMT1-like isoform X4
histone-lysine N-methyltransferase EHMT1-like, transcript variant X6
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 17 samples with support for all annotated introns
histone-lysine N-methyltransferase EHMT1-like isoform X6
arrestin domain-containing protein 1-like, transcript variant X1
arrestin domain-containing protein 1-like, transcript variant X2
arrestin domain-containing protein 1-like, transcript variant X3
arrestin domain-containing protein 1-like isoform X1
arrestin domain-containing protein 1-like isoform X2
P2Y purinoceptor 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
P2Y purinoceptor 4-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 9 samples with support for all annotated introns
P2Y purinoceptor 4-like, transcript variant X3
P2Y purinoceptor 4-like, 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 4 samples with support for all annotated introns
P2Y purinoceptor 4-like, transcript variant X6
P2Y purinoceptor 4-like, transcript variant X5
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
negative elongation factor complex member B
ER degradation-enhancing alpha-mannosidase-like protein 3, transcript variant X1
ER degradation-enhancing alpha-mannosidase-like protein 3, transcript variant X2
ER degradation-enhancing alpha-mannosidase-like protein 3 isoform X2
ER degradation-enhancing alpha-mannosidase-like protein 3 isoform X1
solute carrier family 31 member 2, 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 11 samples with support for all annotated introns
solute carrier family 31 member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
solute carrier family 31 member 2, 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 25 samples with support for all annotated introns
probable low affinity copper uptake protein 2 isoform X3
probable low affinity copper uptake protein 2 isoform X1
probable low affinity copper uptake protein 2 isoform X2
syntaxin-binding protein 1, transcript variant X1
syntaxin-binding protein 1, transcript variant X2
AT-hook transcription factor, transcript variant X5
AT-hook transcription factor, transcript variant X4
AT-hook transcription factor, transcript variant X6
AT-hook transcription factor, transcript variant X1
AT-hook transcription factor, transcript variant X3
AT-hook transcription factor, transcript variant X2
microtubule organization protein AKNA isoform X2
microtubule organization protein AKNA isoform X1
AT-hook transcription factor, transcript variant X8
microtubule organization protein AKNA isoform X4
AT-hook transcription factor, transcript variant X7
microtubule organization protein AKNA isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane protein 268-like, transcript variant X2
transmembrane protein 268-like, transcript variant X3
transmembrane protein 268-like, transcript variant X1
transmembrane protein 268-like, transcript variant X4
transmembrane protein 268-like isoform X1
transmembrane protein 268-like isoform X2
transmembrane protein 268-like isoform X3
tumor necrosis factor ligand superfamily member 15-like
tumor necrosis factor ligand superfamily member 15-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 15-like isoform X2
tumor necrosis factor ligand superfamily member 15-like, transcript variant X1
tumor necrosis factor ligand superfamily member 15-like isoform X1
multiple epidermal growth factor-like domains protein 9
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
regulator of G protein signaling 3a, transcript variant X2
regulator of G protein signaling 3a, transcript variant X8
regulator of G protein signaling 3a, transcript variant X7
regulator of G protein signaling 3a, transcript variant X9
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
regulator of G protein signaling 3a, transcript variant X10
regulator of G protein signaling 3a, transcript variant X5
regulator of G protein signaling 3a, transcript variant X3
regulator of G protein signaling 3a, transcript variant X1
regulator of G protein signaling 3a, transcript variant X6
regulator of G-protein signaling 3a isoform X1
regulator of G-protein signaling 3a isoform X4
regulator of G-protein signaling 3a isoform X2
regulator of G-protein signaling 3a isoform X8
regulator of G-protein signaling 3a isoform X9
regulator of G-protein signaling 3a isoform X6
regulator of G-protein signaling 3a isoform X7
regulator of G protein signaling 3a, transcript variant X4
regulator of G-protein signaling 3a isoform X3
regulator of G-protein signaling 3a isoform X5
regulator of G protein signaling 3a, transcript variant X11
regulator of G-protein signaling 3a isoform X10
regulator of G protein signaling 3a, transcript variant X12
regulator of G-protein signaling 3a isoform X11
regulator of G protein signaling 3a, transcript variant X14
regulator of G protein signaling 3a, transcript variant X15
regulator of G protein signaling 3a, transcript variant X13
regulator of G-protein signaling 3a isoform X12
regulator of G-protein signaling 3a isoform X13
regulator of G protein signaling 3a, transcript variant X16
regulator of G-protein signaling 3a isoform X14
regulator of G protein signaling 3a, transcript variant X18
regulator of G-protein signaling 3a isoform X16
regulator of G protein signaling 3a, transcript variant X17
regulator of G-protein signaling 3a isoform X15
uncharacterized LOC122564801, transcript variant X1
uncharacterized LOC122564801, 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
uncharacterized LOC122564658, transcript variant X2
uncharacterized LOC122564658, transcript variant X1
zinc finger protein 618, transcript variant X2
zinc finger protein 618, transcript variant X3
zinc finger protein 618, transcript variant X4
zinc finger protein 618, transcript variant X1
zinc finger protein 618, transcript variant X5
zinc finger protein 618, transcript variant X7
zinc finger protein 618, transcript variant X6
zinc finger protein 618, transcript variant X8
zinc finger protein 618, transcript variant X9
zinc finger protein 618, transcript variant X10
zinc finger protein 486-like, transcript variant X1
zinc finger protein 486-like, transcript variant X12
zinc finger protein 486-like, transcript variant X4
zinc finger protein 486-like, transcript variant X10
zinc finger protein 486-like, transcript variant X5
zinc finger protein 486-like, transcript variant X9
zinc finger protein 486-like, transcript variant X2
zinc finger protein 486-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger protein 486-like, transcript variant X8
zinc finger protein 486-like, transcript variant X7
zinc finger protein 486-like, transcript variant X3
zinc finger protein 486-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
PR domain zinc finger protein 5-like isoform X5
zinc finger protein 486-like, transcript variant X13
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
probable G-protein coupled receptor 82, transcript variant X3
probable G-protein coupled receptor 82, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
probable G-protein coupled receptor 82, transcript variant X4
probable G-protein coupled receptor 82, transcript variant X2
uncharacterized LOC122564810, transcript variant X4
uncharacterized LOC122564810, transcript variant X3
uncharacterized LOC122564810, transcript variant X2
uncharacterized LOC122564810, transcript variant X1
uncharacterized LOC122564810, transcript variant X5
uncharacterized LOC122564810, transcript variant X6
uncharacterized protein LOC122564810 isoform X1
uncharacterized protein LOC122564810 isoform X2
uncharacterized LOC122564812, transcript variant X1
uncharacterized LOC122564812, transcript variant X2
uncharacterized protein LOC122564812 isoform X1
uncharacterized protein LOC122564812 isoform X2
prostaglandin G/H synthase 1-like, transcript variant X2
prostaglandin G/H synthase 1-like, transcript variant X1
prostaglandin G/H synthase 1-like, transcript variant X3
prostaglandin G/H synthase 1-like, transcript variant X4
prostaglandin G/H synthase 1-like isoform X3
prostaglandin G/H synthase 1-like isoform X2
prostaglandin G/H synthase 1-like isoform X1
prostaglandin G/H synthase 1-like isoform X4
mitochondrial ribosome recycling factor, transcript variant X1
mitochondrial ribosome recycling factor, transcript variant X2
ribosome-recycling factor, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
MORN repeat containing 5, 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 5 samples with support for all annotated introns
MORN repeat containing 5, 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 19 samples with support for all annotated introns
NADH:ubiquinone oxidoreductase subunit A8
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8
uncharacterized protein LOC559906 homolog, transcript variant X1
uncharacterized protein LOC559906 homolog, transcript variant X2
keratin, type I cytoskeletal 18 isoform X1
keratin, type I cytoskeletal 18 isoform X2
zinc finger and BTB domain containing 26, 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 1 sample with support for all annotated introns
zinc finger and BTB domain-containing protein 26 isoform X2
zinc finger and BTB domain containing 26, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
zinc finger and BTB domain containing 26, transcript variant X4
zinc finger and BTB domain containing 26, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 26 isoform X1
zinc finger and BTB domain-containing protein 26 isoform X3
ring finger and CCCH-type domains 2, transcript variant X1
ring finger and CCCH-type domains 2, transcript variant X5
ring finger and CCCH-type domains 2, transcript variant X4
ring finger and CCCH-type domains 2, transcript variant X2
ring finger and CCCH-type domains 2, transcript variant X3
rab GTPase-activating protein 1, transcript variant X1
rab GTPase-activating protein 1 isoform X1
rab GTPase-activating protein 1, transcript variant X2
rab GTPase-activating protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
rab GTPase-activating protein 1, transcript variant X3
rab GTPase-activating protein 1 isoform X3
spermatid perinuclear RNA binding protein, transcript variant X5
spermatid perinuclear RNA binding protein, transcript variant X1
spermatid perinuclear RNA binding protein, transcript variant X4
spermatid perinuclear RNA binding protein, transcript variant X2
spermatid perinuclear RNA binding protein, transcript variant X3
spermatid perinuclear RNA-binding protein isoform X3
spermatid perinuclear RNA-binding protein isoform X2
spermatid perinuclear RNA-binding protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein crumbs homolog 1-like, transcript variant X1
protein crumbs homolog 1-like, transcript variant X2
protein crumbs homolog 1-like isoform X1
protein crumbs homolog 1-like isoform X2
DENN/MADD domain containing 1A, transcript variant X2
DENN/MADD domain containing 1A, transcript variant X1
DENN/MADD domain containing 1A, transcript variant X4
DENN/MADD domain containing 1A, transcript variant X3
DENN/MADD domain containing 1A, transcript variant X5
DENN domain-containing protein 1A isoform X4
DENN domain-containing protein 1A isoform X2
DENN domain-containing protein 1A isoform X3
DENN domain-containing protein 1A isoform X1
DENN domain-containing protein 1A isoform X5
DENN/MADD domain containing 1A, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DENN domain-containing protein 1A isoform X6
uncharacterized LOC122564835, transcript variant X2
uncharacterized LOC122564835, transcript variant X1
uncharacterized LOC122564835, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
The sequence of the model RefSeq 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: LIM/homeobox protein Lhx2-like
serine/threonine-protein kinase Nek6, transcript variant X3
serine/threonine-protein kinase Nek6, transcript variant X6
serine/threonine-protein kinase Nek6, transcript variant X5
serine/threonine-protein kinase Nek6, transcript variant X2
serine/threonine-protein kinase Nek6, transcript variant X7
serine/threonine-protein kinase Nek6, transcript variant X4
serine/threonine-protein kinase Nek6, transcript variant X1
serine/threonine-protein kinase Nek6, transcript variant X8
serine/threonine-protein kinase Nek6 isoform X1
serine/threonine-protein kinase Nek6, transcript variant X9
serine/threonine-protein kinase Nek6 isoform X2
serine/threonine-protein kinase Nek6, transcript variant X10
serine/threonine-protein kinase Nek6 isoform X3
adhesion G protein-coupled receptor D2, transcript variant X2
adhesion G protein-coupled receptor D2, transcript variant X4
adhesion G protein-coupled receptor D2, transcript variant X6
adhesion G protein-coupled receptor D2, transcript variant X1
adhesion G protein-coupled receptor D2, transcript variant X3
adhesion G protein-coupled receptor D2, transcript variant X5
adhesion G-protein coupled receptor D2 isoform X1
adhesion G-protein coupled receptor D2 isoform X2
nuclear receptor subfamily 5 group A member 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear receptor subfamily 5 group A member 2-like, transcript variant X2
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, including 1 sample with support for all annotated introns
nuclear receptor subfamily 5 group A member 2-like isoform X1
nuclear receptor subfamily 5 group A member 2-like isoform X2
nuclear receptor subfamily 6 group A member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear receptor subfamily 6 group A member 1, 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 3 samples with support for all annotated introns
nuclear receptor subfamily 6 group A member 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear receptor subfamily 6 group A member 1, transcript variant X5
nuclear receptor subfamily 6 group A member 1, transcript variant X6
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 9 samples with support for all annotated introns
nuclear receptor subfamily 6 group A member 1 isoform X2
nuclear receptor subfamily 6 group A member 1 isoform X1
nuclear receptor subfamily 6 group A member 1 isoform X7
nuclear receptor subfamily 6 group A member 1 isoform X5
nuclear receptor subfamily 6 group A member 1 isoform X6
nuclear receptor subfamily 6 group A member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear receptor subfamily 6 group A member 1, transcript variant X4
nuclear receptor subfamily 6 group A member 1 isoform X3
nuclear receptor subfamily 6 group A member 1 isoform X4
nuclear receptor subfamily 6 group A member 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear receptor subfamily 6 group A member 1 isoform X8
olfactomedin-like protein 2A, transcript variant X2
olfactomedin-like protein 2A, 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 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
actin related protein 2/3 complex, subunit 5-like, b
Rab9 effector protein with kelch motifs, transcript variant X3
Rab9 effector protein with kelch motifs, transcript variant X1
rab9 effector protein with kelch motifs isoform X1
rab9 effector protein with kelch motifs isoform X3
Rab9 effector protein with kelch motifs, transcript variant X2
rab9 effector protein with kelch motifs isoform X2
protein phosphatase 6, catalytic subunit
serine/threonine-protein phosphatase 6 catalytic subunit
Rab9 effector protein with kelch motifs, transcript variant X5
Rab9 effector protein with kelch motifs, transcript variant X4
Rab9 effector protein with kelch motifs, transcript variant X6
rab9 effector protein with kelch motifs isoform X4
heat shock protein 5, transcript variant X1
heat shock protein 5, transcript variant X2
GTPase activating protein and VPS9 domains 1, transcript variant X3
GTPase activating protein and VPS9 domains 1, transcript variant X1
GTPase activating protein and VPS9 domains 1, transcript variant X7
GTPase activating protein and VPS9 domains 1, transcript variant X2
GTPase activating protein and VPS9 domains 1, transcript variant X5
GTPase activating protein and VPS9 domains 1, transcript variant X6
GTPase activating protein and VPS9 domains 1, transcript variant X9
GTPase activating protein and VPS9 domains 1, transcript variant X8
GTPase activating protein and VPS9 domains 1, transcript variant X10
GTPase activating protein and VPS9 domains 1, transcript variant X11
GTPase activating protein and VPS9 domains 1, transcript variant X4
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X1
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X2
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X5
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X4
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X6
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X7
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X3
MAPK associated protein 1, transcript variant X4
MAPK associated protein 1, transcript variant X1
MAPK associated protein 1, transcript variant X3
MAPK associated protein 1, transcript variant X6
MAPK associated protein 1, transcript variant X7
MAPK associated protein 1, transcript variant X8
target of rapamycin complex 2 subunit MAPKAP1 isoform X1
target of rapamycin complex 2 subunit MAPKAP1 isoform X3
target of rapamycin complex 2 subunit MAPKAP1 isoform X4
target of rapamycin complex 2 subunit MAPKAP1 isoform X6
target of rapamycin complex 2 subunit MAPKAP1 isoform X7
MAPK associated protein 1, transcript variant X2
target of rapamycin complex 2 subunit MAPKAP1 isoform X2
MAPK associated protein 1, 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 13 samples with support for all annotated introns
target of rapamycin complex 2 subunit MAPKAP1 isoform X5
pre-B-cell leukemia transcription factor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
pre-B-cell leukemia transcription factor 3, transcript variant X1
pre-B-cell leukemia transcription factor 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
pre-B-cell leukemia transcription factor 3 isoform X1
pre-B-cell leukemia transcription factor 3 isoform X2
pre-B-cell leukemia transcription factor 3 isoform X5
pre-B-cell leukemia transcription factor 3, transcript variant X3
pre-B-cell leukemia transcription factor 3 isoform X3
pre-B-cell leukemia transcription factor 3, transcript variant X4
pre-B-cell leukemia transcription factor 3 isoform X4
tigger transposable element-derived protein 1-like
multivesicular body subunit 12Ba, 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 9 samples with support for all annotated introns
multivesicular body subunit 12Ba, 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 8 samples with support for all annotated introns
multivesicular body subunit 12Ba, 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 11 samples with support for all annotated introns
multivesicular body subunit 12Ba, transcript variant X3
multivesicular body subunit 12Ba isoform X3
multivesicular body subunit 12Ba isoform X4
multivesicular body subunit 12Ba isoform X1
multivesicular body subunit 12Ba isoform X2
LIM/homeobox protein LMX-1.2, 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 1 sample with support for all annotated introns
LIM/homeobox protein LMX-1.2, transcript variant X3
LIM/homeobox protein LMX-1.2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LIM/homeobox protein LMX-1.2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger and BTB domain containing 43, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger and BTB domain containing 43, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 43 isoform X1
zinc finger and BTB domain-containing protein 43 isoform X2
zinc finger and BTB domain containing 43, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger and BTB domain containing 43, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger and BTB domain containing 43, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger and BTB domain containing 43, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 43 isoform X3
zinc finger and BTB domain-containing protein 43 isoform X4
family with sequence similarity 183 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
zinc finger and BTB domain containing 34, transcript variant X4
zinc finger and BTB domain containing 34, transcript variant X2
zinc finger and BTB domain containing 34, transcript variant X5
zinc finger and BTB domain containing 34, transcript variant X1
zinc finger and BTB domain containing 34, transcript variant X3
zinc finger and BTB domain-containing protein 34 isoform X1
zinc finger and BTB domain-containing protein 34 isoform X2
ras-specific guanine nucleotide-releasing factor RalGPS1-like, transcript variant X1
ras-specific guanine nucleotide-releasing factor RalGPS1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ras-specific guanine nucleotide-releasing factor RalGPS1-like, transcript variant X2
ras-specific guanine nucleotide-releasing factor RalGPS1-like, transcript variant X3
ras-specific guanine nucleotide-releasing factor RalGPS1-like isoform X1
ras-specific guanine nucleotide-releasing factor RalGPS1-like isoform X2
angiopoietin-like 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
angiopoietin-like 2b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
F-box and WD repeat domain containing 2, transcript variant X1
F-box and WD repeat domain containing 2, transcript variant X2
F-box and WD repeat domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 8
GTPase activating Rap/RanGAP domain like 3, transcript variant X3
GTPase activating Rap/RanGAP domain like 3, transcript variant X2
GTPase activating Rap/RanGAP domain like 3, transcript variant X5
GTPase activating Rap/RanGAP domain like 3, transcript variant X4
GTPase activating Rap/RanGAP domain like 3, transcript variant X1
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X3
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X5
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X2
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X4
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein, transcript variant X2
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein, 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 5 samples with support for all annotated introns
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein isoform X1
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein isoform X2
transfer RNA lysine (anticodon UUU); 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: 10 Proteins
tubulin tyrosine ligase-like family, member 11, 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 18 samples with support for all annotated introns
tubulin tyrosine ligase-like family, member 11, 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 9 samples with support for all annotated introns
tubulin tyrosine ligase-like family, member 11, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
tubulin tyrosine ligase-like family, member 11, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
tubulin tyrosine ligase-like family, member 11, transcript variant X6
tubulin tyrosine ligase-like family, member 11, transcript variant X2
tubulin tyrosine ligase-like family, member 11, 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 10 samples with support for all annotated introns
tubulin polyglutamylase TTLL11 isoform X3
tubulin polyglutamylase TTLL11 isoform X6
tubulin polyglutamylase TTLL11 isoform X5
tubulin polyglutamylase TTLL11 isoform X1
tubulin polyglutamylase TTLL11 isoform X4
tubulin polyglutamylase TTLL11 isoform X2
tubulin polyglutamylase TTLL11 isoform X8
tubulin tyrosine ligase-like family, member 11, transcript variant X7
tubulin tyrosine ligase-like family, member 11, transcript variant X8
tubulin polyglutamylase TTLL11 isoform X7
tubulin tyrosine ligase-like family, member 11, transcript variant X10
tubulin polyglutamylase TTLL11 isoform X9
disabled homolog 2-interacting protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
disabled homolog 2-interacting protein-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
disabled homolog 2-interacting protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
disabled homolog 2-interacting protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
disabled homolog 2-interacting protein-like, transcript variant X3
disabled homolog 2-interacting protein-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
disabled homolog 2-interacting protein-like, transcript variant X8
disabled homolog 2-interacting protein-like, transcript variant X11
disabled homolog 2-interacting protein-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
disabled homolog 2-interacting protein-like, transcript variant X6
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 6 samples with support for all annotated introns
disabled homolog 2-interacting protein-like, transcript variant X9
disabled homolog 2-interacting protein-like isoform X1
disabled homolog 2-interacting protein-like isoform X2
disabled homolog 2-interacting protein-like isoform X5
disabled homolog 2-interacting protein-like isoform X3
disabled homolog 2-interacting protein-like isoform X7
disabled homolog 2-interacting protein-like isoform X6
disabled homolog 2-interacting protein-like isoform X8
disabled homolog 2-interacting protein-like isoform X4
PHD finger protein 19, transcript variant X2
PHD finger protein 19, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
TNF receptor-associated factor 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
TNF receptor-associated factor 1-like, transcript variant X3
TNF receptor-associated factor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
TNF receptor-associated factor 1-like, transcript variant X5
TNF receptor-associated factor 1-like, transcript variant X2
TNF receptor-associated factor 1-like, transcript variant X6
TNF receptor-associated factor 1-like isoform X2
TNF receptor-associated factor 1-like isoform X1
TNF receptor-associated factor 1-like isoform X3
TNF receptor-associated factor 1-like, transcript variant X7
TNF receptor-associated factor 1-like isoform X4
uncharacterized LOC122564884, transcript variant X2
uncharacterized LOC122564884, transcript variant X1
complement component 5, transcript variant X1
complement component 5, transcript variant X2
complement component 5, 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 5 samples with support for all annotated introns
uncharacterized LOC122564889, transcript variant X2
uncharacterized LOC122564889, transcript variant X1
ras-related protein Rab-14, transcript variant X3
ras-related protein Rab-14, transcript variant X4
ras-related protein Rab-14, transcript variant X1
ras-related protein Rab-14, transcript variant X2
erythrocyte band 7 integral membrane protein
tetratricopeptide repeat protein 16-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
sperm acrosome associated 9, transcript variant X9
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
sperm acrosome associated 9, transcript variant X8
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
sperm acrosome associated 9, transcript variant X7
sperm acrosome-associated protein 9 isoform X3
sperm acrosome-associated protein 9 isoform X2
sperm acrosome associated 9, transcript variant X12
sperm acrosome-associated protein 9 isoform X6
sperm acrosome associated 9, transcript variant X2
sperm acrosome associated 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sperm acrosome associated 9, transcript variant X4
sperm acrosome associated 9, transcript variant X5
sperm acrosome associated 9, transcript variant X6
sperm acrosome associated 9, transcript variant X3
sperm acrosome associated 9, transcript variant X10
sperm acrosome-associated protein 9 isoform X1
sperm acrosome-associated protein 9 isoform X4
sperm acrosome associated 9, transcript variant X11
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
sperm acrosome-associated protein 9 isoform X5
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
adenylate kinase 8, 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 5 samples with support for all annotated introns
adenylate kinase 8, transcript variant X2
adenylate kinase 8, 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 3 samples with support for all annotated introns
adenylate kinase 8, transcript variant X4
general transcription factor IIIC, polypeptide 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
general transcription factor IIIC, polypeptide 4, 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 14 samples with support for all annotated introns
general transcription factor 3C polypeptide 4 isoform X1
general transcription factor 3C polypeptide 4 isoform X2
general transcription factor IIIC, polypeptide 4, transcript variant X3
general transcription factor 3C polypeptide 4 isoform X3
DEAD (Asp-Glu-Ala-Asp) box polypeptide 31, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 31, transcript variant X1
probable ATP-dependent RNA helicase DDX31 isoform X1
probable ATP-dependent RNA helicase DDX31 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cilia and flagella associated protein 77
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cilia- and flagella-associated protein 77
transcription termination factor 1-like, transcript variant X2
transcription termination factor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
transcription termination factor 1-like, transcript variant X4
transcription termination factor 1-like, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00614
mediator complex subunit 27, transcript variant X1
mediator complex subunit 27, transcript variant X2
mediator of RNA polymerase II transcription subunit 27 isoform X1
mediator of RNA polymerase II transcription subunit 27 isoform X2
rap guanine nucleotide exchange factor 1-like, transcript variant X2
rap guanine nucleotide exchange factor 1-like, transcript variant X4
rap guanine nucleotide exchange factor 1-like, transcript variant X1
rap guanine nucleotide exchange factor 1-like, transcript variant X3
rap guanine nucleotide exchange factor 1-like, transcript variant X5
rap guanine nucleotide exchange factor 1-like, transcript variant X6
rap guanine nucleotide exchange factor 1-like, transcript variant X7
rap guanine nucleotide exchange factor 1-like, transcript variant X8
rap guanine nucleotide exchange factor 1-like, transcript variant X9
rap guanine nucleotide exchange factor 1-like isoform X1
rap guanine nucleotide exchange factor 1-like isoform X5
rap guanine nucleotide exchange factor 1-like isoform X3
rap guanine nucleotide exchange factor 1-like isoform X6
rap guanine nucleotide exchange factor 1-like isoform X7
rap guanine nucleotide exchange factor 1-like isoform X8
rap guanine nucleotide exchange factor 1-like isoform X9
rap guanine nucleotide exchange factor 1-like isoform X2
rap guanine nucleotide exchange factor 1-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
phytanoyl-CoA dioxygenase domain containing 1, transcript variant X2
phytanoyl-CoA dioxygenase domain containing 1, transcript variant X3
phytanoyl-CoA dioxygenase domain containing 1, transcript variant X1
phytanoyl-CoA dioxygenase domain-containing protein 1 isoform X2
phytanoyl-CoA dioxygenase domain-containing protein 1 isoform X3
phytanoyl-CoA dioxygenase domain-containing protein 1 isoform X1
volume-regulated anion channel subunit LRRC8D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeat containing 8 VRAC subunit Aa, transcript variant X1
leucine rich repeat containing 8 VRAC subunit Aa, transcript variant X2
leucine rich repeat containing 8 VRAC subunit Aa isoform X1
leucine rich repeat containing 8 VRAC subunit Aa isoform X2
kynurenine--oxoglutarate transaminase 1-like, 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 20 samples with support for all annotated introns
kynurenine--oxoglutarate transaminase 1-like, transcript variant X2
kynurenine--oxoglutarate transaminase 1-like, transcript variant X1
kynurenine--oxoglutarate transaminase 1-like, transcript variant X5
kynurenine--oxoglutarate transaminase 1-like, transcript variant X6
kynurenine--oxoglutarate transaminase 1-like, transcript variant X4
kynurenine--oxoglutarate transaminase 1-like isoform X2
kynurenine--oxoglutarate transaminase 1-like isoform X1
kynurenine--oxoglutarate transaminase 1-like isoform X3
kynurenine--oxoglutarate transaminase 3-like isoform X4
uncharacterized protein LOC122564914 isoform X4
folylpolyglutamate synthase, transcript variant X2
folylpolyglutamate synthase, transcript variant X1
folylpolyglutamate synthase, mitochondrial isoform X2
folylpolyglutamate synthase, mitochondrial isoform X1
cyclin-dependent kinase 9 (CDC2-related kinase), transcript variant X1
cyclin-dependent kinase 9 (CDC2-related kinase), transcript variant X2
uncharacterized LOC122564923, transcript variant X2
uncharacterized LOC122564923, transcript variant X1
formin-binding protein 1, transcript variant X4
formin-binding protein 1, transcript variant X12
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
formin-binding protein 1, transcript variant X10
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
formin-binding protein 1, transcript variant X5
formin-binding protein 1, transcript variant X11
formin-binding protein 1, transcript variant X1
formin-binding protein 1, transcript variant X13
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 6 samples with support for all annotated introns
formin-binding protein 1, transcript variant X8
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 6 samples with support for all annotated introns
formin-binding protein 1, transcript variant X6
formin-binding protein 1, transcript variant X2
formin-binding protein 1, transcript variant X9
formin-binding protein 1, transcript variant X7
formin-binding protein 1, transcript variant X3
protein GPR107-like, transcript variant X2
protein GPR107-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein GPR107-like, transcript variant X3
protein GPR107-like, transcript variant X4
protein GPR107-like, transcript variant X6
protein GPR107-like, transcript variant X5
neuronal calcium sensor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
neuronal calcium sensor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neuronal calcium sensor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
far upstream element-binding protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
far upstream element-binding protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
far upstream element-binding protein 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
far upstream element-binding protein 3-like isoform X2
far upstream element-binding protein 3-like isoform X1
far upstream element-binding protein 3-like isoform X4
far upstream element-binding protein 3-like, transcript variant X3
far upstream element-binding protein 3-like isoform X3
argininosuccinate synthase 1, transcript variant X1
argininosuccinate synthase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
adenylate kinase isoenzyme 1-like, transcript variant X1
adenylate kinase isoenzyme 1-like, transcript variant X3
adenylate kinase isoenzyme 1-like, transcript variant X2
adenylate kinase isoenzyme 5-like isoform X1
adenylate kinase isoenzyme 1-like isoform X3
adenylate kinase isoenzyme 1-like isoform X2
spermatogenesis- and oogenesis-specific basic helix-loop-helix-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
proteasome 26S subunit, non-ATPase 5, transcript variant X1
proteasome 26S subunit, non-ATPase 5, transcript variant X2
26S proteasome non-ATPase regulatory subunit 5 isoform X2
26S proteasome non-ATPase regulatory subunit 5 isoform X1
coiled-coil domain-containing protein 180-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 180-like, transcript variant X1
coiled-coil domain-containing protein 180-like, transcript variant X2
coiled-coil domain-containing protein 180-like isoform X1
coiled-coil domain-containing protein 180-like isoform X2
ral guanine nucleotide dissociation stimulator-like, transcript variant X3
ral guanine nucleotide dissociation stimulator-like isoform X3
ral guanine nucleotide dissociation stimulator-like, transcript variant X2
ral guanine nucleotide dissociation stimulator-like isoform X2
ral guanine nucleotide dissociation stimulator-like, transcript variant X4
ral guanine nucleotide dissociation stimulator-like, transcript variant X1
ral guanine nucleotide dissociation stimulator-like isoform X1
ral guanine nucleotide dissociation stimulator-like isoform X4
cilia and flagella associated protein 157
cilia- and flagella-associated protein 157
cerebral endothelial cell adhesion molecule, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
procollagen galactosyltransferase 2 isoform X1
cerebral endothelial cell adhesion molecule, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
procollagen galactosyltransferase 1 isoform X2
long-chain fatty acid transport protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6, transcript variant X5
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 2 samples with support for all annotated introns
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6, transcript variant X3
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 11 samples with support for all annotated introns
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6, transcript variant X2
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6, transcript variant X4
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6, transcript variant X6
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 13 samples with support for all annotated introns
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6
potassium sodium-activated channel subfamily T member 1b, transcript variant X1
potassium sodium-activated channel subfamily T member 1b, transcript variant X2
potassium sodium-activated channel subfamily T member 1b, transcript variant X3
potassium sodium-activated channel subfamily T member 1b, transcript variant X4
potassium channel subfamily T member 1 isoform X1
potassium channel subfamily T member 1 isoform X2
potassium sodium-activated channel subfamily T member 1b, transcript variant X5
potassium channel subfamily T member 1 isoform X3
uncharacterized LOC122564944, transcript variant X5
uncharacterized LOC122564944, transcript variant X4
uncharacterized LOC122564944, transcript variant X3
uncharacterized LOC122564944, transcript variant X2
uncharacterized LOC122564944, transcript variant X1
uncharacterized protein LOC122564944 isoform X2
uncharacterized protein LOC122564944 isoform X1
uncharacterized protein LOC122564944 isoform X3
calmodulin regulated spectrin-associated protein 1b, transcript variant X1
calmodulin regulated spectrin-associated protein 1b, transcript variant X5
calmodulin regulated spectrin-associated protein 1b, transcript variant X3
calmodulin regulated spectrin-associated protein 1b, transcript variant X2
calmodulin regulated spectrin-associated protein 1b, transcript variant X6
calmodulin regulated spectrin-associated protein 1b, transcript variant X4
calmodulin-regulated spectrin-associated protein 1-B isoform X6
calmodulin-regulated spectrin-associated protein 1-B isoform X5
calmodulin-regulated spectrin-associated protein 1-B isoform X4
calmodulin-regulated spectrin-associated protein 1-B isoform X3
calmodulin-regulated spectrin-associated protein 1-B isoform X2
calmodulin-regulated spectrin-associated protein 1-B isoform X1
ubiquitin-associated domain-containing protein 1
xenotropic and polytropic retrovirus receptor 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
nucleus accumbens-associated protein 2-like, transcript variant X9
nucleus accumbens-associated protein 2-like, transcript variant X2
nucleus accumbens-associated protein 2-like, transcript variant X4
nucleus accumbens-associated protein 2-like, transcript variant X5
nucleus accumbens-associated protein 2-like, transcript variant X1
nucleus accumbens-associated protein 2-like, transcript variant X3
nucleus accumbens-associated protein 2-like, transcript variant X6
nucleus accumbens-associated protein 2-like, transcript variant X8
nucleus accumbens-associated protein 2-like, transcript variant X7
nucleus accumbens-associated protein 2-like, transcript variant X10
nucleus accumbens-associated protein 2-like, transcript variant X11
nucleus accumbens-associated protein 2-like
transmembrane protein 250, transcript variant X2
transmembrane protein 250, 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
centrosome-associated protein 350-like, transcript variant X4
centrosome-associated protein 350-like, transcript variant X5
centrosome-associated protein 350-like, transcript variant X3
centrosome-associated protein 350-like, transcript variant X1
centrosome-associated protein 350-like, transcript variant X8
centrosome-associated protein 350-like, transcript variant X6
centrosome-associated protein 350-like, transcript variant X7
centrosome-associated protein 350-like, transcript variant X2
centrosome-associated protein 350-like isoform X4
centrosome-associated protein 350-like isoform X5
centrosome-associated protein 350-like isoform X3
centrosome-associated protein 350-like isoform X1
centrosome-associated protein 350-like isoform X2
centrosome-associated protein 350-like isoform X6
G protein signaling modulator 1b, transcript variant X6
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
G protein signaling modulator 1b, transcript variant X4
G protein signaling modulator 1b, transcript variant X7
G-protein-signaling modulator 1b isoform X4
G protein signaling modulator 1b, transcript variant X1
G-protein-signaling modulator 1b isoform X1
G-protein-signaling modulator 1b isoform X6
G protein signaling modulator 1b, transcript variant X8
G-protein-signaling modulator 1b isoform X7
G protein signaling modulator 1b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
G-protein-signaling modulator 1b isoform X5
G protein signaling modulator 1b, 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 2 samples with support for all annotated introns
G-protein-signaling modulator 1b isoform X2
G protein signaling modulator 1b, transcript variant X3
G-protein-signaling modulator 1b isoform X3
G-protein-signaling modulator 1-like, transcript variant X1
G-protein-signaling modulator 1-like, transcript variant X2
G-protein-signaling modulator 1-like isoform X1
G-protein-signaling modulator 1-like 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 13 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 25 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 20
telomere length and silencing protein 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
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 8 samples with support for all annotated introns
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 21 samples with support for all annotated introns
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 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
calcium-binding mitochondrial carrier protein SCaMC-2-B-like
protein FAM102A-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 23 samples with support for all annotated introns
protein FAM102A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized LOC122564967, transcript variant X2
uncharacterized LOC122564967, transcript variant X1
dolichyl-phosphate mannosyltransferase subunit 2, regulatory, transcript variant X7
dolichyl-phosphate mannosyltransferase subunit 2, regulatory, transcript variant X9
dolichyl-phosphate mannosyltransferase subunit 2, regulatory, transcript variant X6
dolichyl-phosphate mannosyltransferase subunit 2, regulatory, transcript variant X1
dolichyl-phosphate mannosyltransferase subunit 2, regulatory, transcript variant X4
dolichyl-phosphate mannosyltransferase subunit 2, regulatory, transcript variant X3
dolichyl-phosphate mannosyltransferase subunit 2, regulatory, transcript variant X5
dolichyl-phosphate mannosyltransferase subunit 2, regulatory, transcript variant X2
dolichyl-phosphate mannosyltransferase subunit 2, regulatory, transcript variant X8
dolichol phosphate-mannose biosynthesis regulatory protein isoform X1
dolichol phosphate-mannose biosynthesis regulatory protein isoform X2
phosphatidylinositol-4-phosphate 5-kinase-like 1, transcript variant X1
phosphatidylinositol-4-phosphate 5-kinase-like 1, transcript variant X2
phosphatidylinositol 4-phosphate 5-kinase-like protein 1
protein-O-mannosyltransferase 1, transcript variant X2
protein-O-mannosyltransferase 1, transcript variant X1
protein-O-mannosyltransferase 1, transcript variant X3
protein O-mannosyl-transferase 1 isoform X2
protein O-mannosyl-transferase 1 isoform X1
protein O-mannosyl-transferase 1 isoform X3
proline-rich coiled-coil 2B, transcript variant X4
proline-rich coiled-coil 2B, transcript variant X2
proline-rich coiled-coil 2B, transcript variant X3
proline-rich coiled-coil 2B, transcript variant X5
proline-rich coiled-coil 2B, transcript variant X1
proline-rich coiled-coil 2B, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00153
inactive phospholipid phosphatase 7-like
family with sequence similarity 78 member Ab
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
fibrinogen C domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
c-abl oncogene 1, non-receptor tyrosine kinase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
exosome component 2, transcript variant X3
exosome component 2, transcript variant X1
exosome component 2, transcript variant X2
exosome complex component RRP4 isoform X2
exosome complex component RRP4 isoform X1
cip1-interacting zinc finger protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
cip1-interacting zinc finger protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
cip1-interacting zinc finger protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
cip1-interacting zinc finger protein-like isoform X1
cip1-interacting zinc finger protein-like isoform X2
cip1-interacting zinc finger protein-like isoform X4
cip1-interacting zinc finger protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized protein LOC122564982 isoform X3
bublin coiled coil protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
UPF0184 protein C9orf16 homolog isoform X2
bublin coiled coil protein, transcript variant X1
UPF0184 protein C9orf16 homolog isoform X1
bublin coiled coil protein, transcript variant X3
UPF0184 protein C9orf16 homolog isoform X3
bublin coiled coil protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
UPF0184 protein C9orf16 homolog isoform X4
prostaglandin E synthase 2-like, 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
prostaglandin E synthase 2-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 28 samples with support for all annotated introns
outer dense fiber protein 2-like, transcript variant X2
outer dense fiber protein 2-like isoform X2
outer dense fiber protein 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
outer dense fiber protein 2-like, transcript variant X5
outer dense fiber protein 2-like, transcript variant X1
outer dense fiber protein 2-like isoform X1
outer dense fiber protein 2-like isoform X4
outer dense fiber protein 2-like, transcript variant X3
outer dense fiber protein 2-like isoform X3
GLE1 RNA export mediator, transcript variant X1
GLE1 RNA export mediator, transcript variant X2
GLE1 RNA export mediator, transcript variant X3
GLE1 RNA export mediator, transcript variant X4
spectrin alpha, non-erythrocytic 1, transcript variant X3
spectrin alpha, non-erythrocytic 1, transcript variant X1
spectrin alpha, non-erythrocytic 1, transcript variant X6
spectrin alpha, non-erythrocytic 1, transcript variant X8
spectrin alpha, non-erythrocytic 1, transcript variant X2
spectrin alpha, non-erythrocytic 1, transcript variant X7
spectrin alpha, non-erythrocytic 1, transcript variant X4
spectrin alpha, non-erythrocytic 1, transcript variant X5
spectrin alpha, non-erythrocytic 1, transcript variant X9
spectrin alpha, non-erythrocytic 1, transcript variant X10
spectrin alpha chain, non-erythrocytic 1 isoform X1
spectrin alpha chain, non-erythrocytic 1 isoform X6
spectrin alpha chain, non-erythrocytic 1 isoform X8
spectrin alpha chain, non-erythrocytic 1 isoform X2
spectrin alpha chain, non-erythrocytic 1 isoform X7
spectrin alpha chain, non-erythrocytic 1 isoform X4
spectrin alpha chain, non-erythrocytic 1 isoform X5
spectrin alpha chain, non-erythrocytic 1 isoform X9
spectrin alpha chain, non-erythrocytic 1 isoform X10
spectrin alpha chain, non-erythrocytic 1 isoform X3
uncharacterized protein LOC558400 homolog
zinc finger DHHC-type palmitoyltransferase 12a
zyg-11 related, cell cycle regulator, transcript variant X1
zyg-11 related, cell cycle regulator, transcript variant X2
SPOUT domain containing methyltransferase 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 14 samples with support for all annotated introns
SPOUT domain containing methyltransferase 1, transcript variant X1
putative methyltransferase C9orf114 homolog isoform X2
putative methyltransferase C9orf114 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
general transcription factor IIIC, polypeptide 5
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 29 samples with support for all annotated introns
general transcription factor 3C polypeptide 5
TSC complex subunit 1b, transcript variant X4
TSC complex subunit 1b, transcript variant X3
TSC complex subunit 1b, transcript variant X2
TSC complex subunit 1b, transcript variant X1
TSC complex subunit 1b, transcript variant X5
TSC complex subunit 1b, transcript variant X6
zinc finger protein Gfi-1b-like, transcript variant X2
zinc finger protein Gfi-1b-like, transcript variant X1
zinc finger protein Gfi-1b-like isoform X1
zinc finger protein Gfi-1b-like isoform X2
carnitine O-acetyltransferase a, transcript variant X1
carnitine O-acetyltransferase a, transcript variant X2
carnitine O-acetyltransferase isoform X1
carnitine O-acetyltransferase isoform X2
protein phosphatase 2 phosphatase activator
serine/threonine-protein phosphatase 2A activator
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
immediate early response gene 5-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
ankyrin repeat and SOCS box containing 6
endosome associated trafficking regulator 1
endosome-associated-trafficking regulator 1
small nuclear RNA activating complex, polypeptide 4, transcript variant X1
small nuclear RNA activating complex, polypeptide 4, transcript variant X2
snRNA-activating protein complex subunit 4 isoform X1
snRNA-activating protein complex subunit 4 isoform X2
small nuclear RNA activating complex, polypeptide 4, transcript variant X3
snRNA-activating protein complex subunit 4 isoform X3
neurogenic locus notch homolog protein 1-like
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X4
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X3
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X1
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X8
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X7
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X6
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X5
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X2
protein transport protein Sec16A isoform X1
protein transport protein Sec16A isoform X4
protein transport protein Sec16A isoform X3
protein transport protein Sec16A isoform X2
inositol polyphosphate-5-phosphatase E, transcript variant X1
inositol polyphosphate-5-phosphatase E, transcript variant X4
inositol polyphosphate-5-phosphatase E, transcript variant X3
inositol polyphosphate-5-phosphatase E, transcript variant X2
phosphatidylinositol polyphosphate 5-phosphatase type IV isoform X1
phosphatidylinositol polyphosphate 5-phosphatase type IV isoform X2
peptidase, mitochondrial processing subunit alpha
mitochondrial-processing peptidase subunit alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine kinase-like domain-containing protein STKLD1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
REX4 homolog, 3'-5' exonuclease, transcript variant X2
REX4 homolog, 3'-5' exonuclease, transcript variant X5
REX4 homolog, 3'-5' exonuclease, transcript variant X1
REX4 homolog, 3'-5' exonuclease, transcript variant X4
REX4 homolog, 3'-5' exonuclease, transcript variant X3
ADAM metallopeptidase with thrombospondin type 1 motif, 13
A disintegrin and metalloproteinase with thrombospondin motifs 13
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 5 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 6
calcium channel flower domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
mediator complex subunit 22, transcript variant X2
mediator of RNA polymerase II transcription subunit 22 isoform X2
mediator complex subunit 22, transcript variant X3
mediator complex subunit 22, transcript variant X1
mediator complex subunit 22, transcript variant X5
mediator complex subunit 22, transcript variant X4
mediator of RNA polymerase II transcription subunit 22 isoform X5
mediator of RNA polymerase II transcription subunit 22 isoform X4
mediator of RNA polymerase II transcription subunit 22 isoform X3
mediator of RNA polymerase II transcription subunit 22 isoform X1
mediator complex subunit 22, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 22 isoform X6
DNL-type zinc finger, transcript variant X1
DNL-type zinc finger, 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 29 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00069
COORDINATES: nucleotide motif:Rfam:12.0:RF00049
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC122565022, transcript variant X3
uncharacterized LOC122565022, transcript variant X4
uncharacterized LOC122565022, transcript variant X5
uncharacterized LOC122565022, transcript variant X2
uncharacterized LOC122565022, transcript variant X1
1-acylglycerol-3-phosphate O-acyltransferase 2 (lysophosphatidic acid acyltransferase, beta)
1-acyl-sn-glycerol-3-phosphate acyltransferase beta
uncharacterized LOC122565023, transcript variant X1
uncharacterized LOC122565023, transcript variant X2
divergent protein kinase domain 1B, transcript variant X4
divergent protein kinase domain 1B isoform X4
divergent protein kinase domain 1B, transcript variant X1
divergent protein kinase domain 1B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
divergent protein kinase domain 1B isoform X1
divergent protein kinase domain 1B isoform X2
divergent protein kinase domain 1B, transcript variant X3
divergent protein kinase domain 1B isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns