Chiloscyllium plagiosum isolate BGI_BamShark_2017 chromosome 39, 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\nCM012994.1.\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.
transcriptional enhancer factor TEF-1-like, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
transcriptional enhancer factor TEF-1-like, transcript variant X5
transcriptional enhancer factor TEF-1-like, transcript variant X4
transcriptional enhancer factor TEF-1-like, transcript variant X3
transcriptional enhancer factor TEF-1-like, transcript variant X2
transcriptional enhancer factor TEF-1-like, transcript variant X6
transcriptional enhancer factor TEF-1-like isoform X1
transcriptional enhancer factor TEF-1-like isoform X3
transcriptional enhancer factor TEF-1-like isoform X2
transcriptional enhancer factor TEF-1-like isoform X4
sodium-dependent neutral amino acid transporter B(0)AT2-like, transcript variant X3
sodium-dependent neutral amino acid transporter B(0)AT2-like, transcript variant X1
sodium-dependent neutral amino acid transporter B(0)AT2-like, transcript variant X2
sodium-dependent neutral amino acid transporter B(0)AT2-like, transcript variant X4
sodium-dependent neutral amino acid transporter B(0)AT2-like isoform X3
sodium-dependent neutral amino acid transporter B(0)AT2-like isoform X1
sodium-dependent neutral amino acid transporter B(0)AT2-like isoform X2
uncharacterized LOC122542067, transcript variant X12
uncharacterized LOC122542067, transcript variant X5
uncharacterized LOC122542067, transcript variant X4
uncharacterized LOC122542067, transcript variant X1
uncharacterized LOC122542067, transcript variant X14
uncharacterized LOC122542067, transcript variant X8
uncharacterized LOC122542067, transcript variant X7
uncharacterized LOC122542067, transcript variant X9
uncharacterized LOC122542067, transcript variant X10
uncharacterized LOC122542067, transcript variant X11
uncharacterized LOC122542067, transcript variant X3
uncharacterized LOC122542067, transcript variant X6
uncharacterized LOC122542067, transcript variant X13
cytidine deaminase-like, transcript variant X2
cytidine deaminase-like, transcript variant X1
uncharacterized LOC122542067, transcript variant X2
uncharacterized protein LOC122542067 isoform X1
uncharacterized protein LOC122542067 isoform X2
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, including 7 samples with support for all annotated introns
uncharacterized LOC122542069, 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 2 samples with support for all annotated introns
uncharacterized LOC122542069, 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 3 samples with support for all annotated introns
uncharacterized LOC122542069, 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
uncharacterized protein LOC122542069 isoform X1
uncharacterized protein LOC122542069 isoform X2
uncharacterized protein LOC122542069 isoform X3
protein phosphatase 1 regulatory subunit 15B-like
branched chain amino-acid transaminase 2, mitochondrial
branched-chain-amino-acid aminotransferase, mitochondrial
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 20-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 66% 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: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
RNA binding protein fox-1 homolog 2-like, transcript variant X2
RNA binding protein fox-1 homolog 2-like, transcript variant X1
RNA binding protein fox-1 homolog 2-like, transcript variant X11
RNA binding protein fox-1 homolog 2-like, transcript variant X7
RNA binding protein fox-1 homolog 2-like, transcript variant X10
RNA binding protein fox-1 homolog 2-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RNA binding protein fox-1 homolog 2-like isoform X2
RNA binding protein fox-1 homolog 1-like isoform X1
RNA binding protein fox-1 homolog 1-like isoform X11
RNA binding protein fox-1 homolog 1-like isoform X7
RNA binding protein fox-1 homolog 1-like isoform X10
RNA binding protein fox-1 homolog 1-like isoform X9
RNA binding protein fox-1 homolog 2-like, transcript variant X8
RNA binding protein fox-1 homolog 2-like, transcript variant X3
RNA binding protein fox-1 homolog 1-like isoform X3
RNA binding protein fox-1 homolog 2-like isoform X8
RNA binding protein fox-1 homolog 2-like, transcript variant X6
RNA binding protein fox-1 homolog 1-like isoform X6
RNA binding protein fox-1 homolog 2-like, transcript variant X4
RNA binding protein fox-1 homolog 2-like isoform X4
RNA binding protein fox-1 homolog 2-like, transcript variant X5
RNA binding protein fox-1 homolog 2-like isoform X5
formation of mitochondrial complex V assembly factor 1 homolog
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
coiled-coil domain containing 96, 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 4 samples with support for all annotated introns
coiled-coil domain containing 96, 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 10 samples with support for all annotated introns
coiled-coil domain containing 96, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
coiled-coil domain-containing protein 96 isoform X2
coiled-coil domain containing 96, 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 2 samples with support for all annotated introns
coiled-coil domain-containing protein 96 isoform X1
coiled-coil domain containing 96, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
coiled-coil domain-containing protein 96 isoform X3
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-like
CCR4-NOT transcription complex subunit 3-like, transcript variant X5
CCR4-NOT transcription complex subunit 3-like, transcript variant X1
CCR4-NOT transcription complex subunit 3-like, transcript variant X4
CCR4-NOT transcription complex subunit 3-like, transcript variant X3
CCR4-NOT transcription complex subunit 3-like, transcript variant X2
CCR4-NOT transcription complex subunit 3-like, transcript variant X6
CCR4-NOT transcription complex subunit 3-like isoform X1
CCR4-NOT transcription complex subunit 3-like isoform X3
CCR4-NOT transcription complex subunit 3-like isoform X4
CCR4-NOT transcription complex subunit 3-like isoform X2
CCR4-NOT transcription complex subunit 3-like isoform X5
G-protein coupled receptor family C group 5 member B-like
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 14 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 11 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 47
probable ATP-dependent RNA helicase DDX47
osteocalcin 2-like, transcript variant X5
osteocalcin 2-like, transcript variant X10
osteocalcin 2-like, transcript variant X8
osteocalcin 2-like, transcript variant X4
osteocalcin 2-like, transcript variant X3
osteocalcin 2-like, transcript variant X6
osteocalcin 2-like, transcript variant X12
osteocalcin 2-like, transcript variant X1
osteocalcin 2-like, transcript variant X7
osteocalcin 2-like, transcript variant X15
osteocalcin 2-like, transcript variant X13
otolith matrix protein OMM-64-like isoform X4
otolith matrix protein OMM-64-like isoform X5
otolith matrix protein OMM-64-like isoform X1
osteocalcin 2-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 5 samples with support for all annotated introns
osteocalcin 2-like, transcript variant X16
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
osteocalcin 2-like, transcript variant X14
osteocalcin 2-like, transcript variant X9
osteocalcin 2-like, transcript variant X2
otolith matrix protein OMM-64-like isoform X11
otolith matrix protein OMM-64-like isoform X9
cilia- and flagella-associated protein 251-like isoform X2
endoplasmic reticulum resident protein 27-like
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
dynein axonemal light chain 4-like, transcript variant X1
dynein axonemal light chain 4-like, transcript variant X2
chromobox protein homolog 6-like, transcript variant X5
chromobox protein homolog 6-like, transcript variant X1
chromobox protein homolog 6-like, transcript variant X4
chromobox protein homolog 6-like, transcript variant X2
chromobox protein homolog 6-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
chromobox protein homolog 6-like isoform 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 26 samples with support for all annotated introns
GTP-binding protein 1-like, transcript variant X1
GTP-binding protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
eukaryotic translation initiation factor 3, subunit D, transcript variant X2
eukaryotic translation initiation factor 3, subunit D, transcript variant X1
eukaryotic translation initiation factor 3 subunit D
synaptogyrin-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
synaptogyrin-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00593
intraflagellar transport 27 homolog (Chlamydomonas), transcript variant X4
intraflagellar transport protein 27 homolog isoform X4
intraflagellar transport 27 homolog (Chlamydomonas), transcript variant X5
intraflagellar transport 27 homolog (Chlamydomonas), transcript variant X3
intraflagellar transport protein 27 homolog isoform X5
intraflagellar transport protein 27 homolog isoform X3
intraflagellar transport 27 homolog (Chlamydomonas), transcript variant X2
intraflagellar transport protein 27 homolog isoform X2
intraflagellar transport 27 homolog (Chlamydomonas), transcript variant X1
intraflagellar transport protein 27 homolog isoform X1
calcium channel, voltage-dependent, gamma subunit 2a
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 5 samples with support for all annotated introns
uncharacterized LOC122541961, transcript variant X2
uncharacterized LOC122541961, transcript variant X1
trinucleotide repeat containing adaptor 6Ba, transcript variant X3
trinucleotide repeat containing adaptor 6Ba, transcript variant X1
trinucleotide repeat containing adaptor 6Ba, transcript variant X8
trinucleotide repeat containing adaptor 6Ba, transcript variant X2
trinucleotide repeat-containing gene 6B protein isoform X1
trinucleotide repeat-containing gene 6B protein isoform X5
trinucleotide repeat containing adaptor 6Ba, transcript variant X6
trinucleotide repeat containing adaptor 6Ba, transcript variant X9
trinucleotide repeat containing adaptor 6Ba, transcript variant X5
trinucleotide repeat-containing gene 6B protein isoform X3
trinucleotide repeat containing adaptor 6Ba, transcript variant X4
trinucleotide repeat containing adaptor 6Ba, transcript variant X7
trinucleotide repeat-containing gene 6B protein isoform X2
trinucleotide repeat-containing gene 6B protein isoform X4
RNA polymerase II, I and III subunit F, transcript variant X1
DNA-directed RNA polymerases I, II, and III subunit RPABC2 isoform X1
RNA polymerase II, I and III subunit F, 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
DNA-directed RNA polymerases I, II, and III subunit RPABC2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 186 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
calcium voltage-gated channel subunit alpha1 Ia, transcript variant X3
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
calcium voltage-gated channel subunit alpha1 Ia, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcium voltage-gated channel subunit alpha1 Ia, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium voltage-gated channel subunit alpha1 Ia, transcript variant X1
voltage-dependent T-type calcium channel subunit alpha-1I isoform X2
voltage-dependent T-type calcium channel subunit alpha-1I isoform X3
voltage-dependent T-type calcium channel subunit alpha-1I isoform X1
voltage-dependent T-type calcium channel subunit alpha-1I isoform X4
arf-GAP with dual PH domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
lectin, galactoside-binding, soluble, 2b
ATP synthase subunit f, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
probable G-protein coupled receptor 146, 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 3 samples with support for all annotated introns
probable G-protein coupled receptor 146, transcript variant X1
lysoplasmalogenase-like protein TMEM86A, 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 6 samples with support for all annotated introns
lysoplasmalogenase-like protein TMEM86A isoform X3
lysoplasmalogenase-like protein TMEM86A, 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
lysoplasmalogenase-like protein TMEM86A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
lysoplasmalogenase-like protein TMEM86A isoform X1
lysoplasmalogenase-like protein TMEM86A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
lysoplasmalogenase-like protein TMEM86A isoform X2
lysoplasmalogenase-like protein TMEM86A isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ATP-sensitive inward rectifier potassium channel 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SR-related CTD-associated factor 1, transcript variant X1
SR-related CTD-associated factor 1, transcript variant X3
SR-related CTD-associated factor 1, transcript variant X2
serine/arginine repetitive matrix protein 2 isoform X1
serine/arginine repetitive matrix protein 2 isoform X2
interferon regulatory factor 3-like, transcript variant X2
interferon regulatory factor 3-like, transcript variant X5
interferon regulatory factor 3-like, transcript variant X3
interferon regulatory factor 3-like, transcript variant X4
interferon regulatory factor 3-like, transcript variant X1
interferon regulatory factor 3-like isoform X4
interferon regulatory factor 3-like isoform X2
interferon regulatory factor 3-like isoform X3
interferon regulatory factor 3-like isoform 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
apoptosis facilitator Bcl-2-like protein 14
DNA-directed RNA polymerases I, II, and III subunit RPABC5
adaptor related protein complex 2 subunit alpha 1, transcript variant X1
adaptor related protein complex 2 subunit alpha 1, transcript variant X2
adaptor related protein complex 2 subunit alpha 1, transcript variant X3
fuzzy planar cell polarity 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 21 samples with support for all annotated introns
fuzzy planar cell polarity protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
fuzzy planar cell polarity protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
fuzzy planar cell polarity protein, 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 15 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 38% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily C member 1-like, transcript variant X1
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 6 samples with support for all annotated introns
potassium voltage-gated channel subfamily C member 1-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 6 samples with support for all annotated introns
potassium voltage-gated channel subfamily C member 1-like isoform X2
potassium voltage-gated channel subfamily C member 1-like isoform X1
TBC1 domain family, member 17, transcript variant X2
TBC1 domain family, member 17, transcript variant X3
TBC1 domain family, member 17, transcript variant X1
TBC1 domain family, member 17, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
ferritin, heavy subunit-like, transcript variant X2
ferritin, heavy subunit-like, transcript variant X1
ferritin heavy chain, oocyte isoform-like
ferritin heavy chain A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 92% 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ferritin heavy chain A-like, transcript variant X3
ferritin heavy chain A-like, transcript variant X1
ferritin heavy chain A-like, transcript variant X4
ferritin heavy chain A-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 180 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: 97 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: 17 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
charged multivesicular body protein 2A, transcript variant X1
charged multivesicular body protein 2A, transcript variant X2
charged multivesicular body protein 2A, transcript variant X3
ferritin heavy chain, oocyte isoform-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 141 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
ferritin heavy chain, oocyte isoform-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 141 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase H-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
transcription intermediary factor 1-beta-like, transcript variant X3
transcription intermediary factor 1-beta-like, transcript variant X2
transcription intermediary factor 1-beta-like, transcript variant X1
transcription intermediary factor 1-beta-like isoform X3
transcription intermediary factor 1-beta-like isoform X2
transcription intermediary factor 1-beta-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
PTPRF interacting protein alpha 3, transcript variant X1
PTPRF interacting protein alpha 3, transcript variant X6
PTPRF interacting protein alpha 3, transcript variant X5
PTPRF interacting protein alpha 3, transcript variant X9
PTPRF interacting protein alpha 3, transcript variant X7
PTPRF interacting protein alpha 3, transcript variant X2
PTPRF interacting protein alpha 3, transcript variant X4
PTPRF interacting protein alpha 3, transcript variant X3
PTPRF interacting protein alpha 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neurotrophin-4-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neurotrophin-4-like, transcript variant X3
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 2 samples with support for all annotated introns
neurotrophin-4-like, transcript variant X4
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 1 sample with support for all annotated introns
neurotrophin-4-like, transcript variant X1
neurotrophin-4-like, transcript variant X8
neurotrophin-4-like, transcript variant X7
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 11 samples with support for all annotated introns
neurotrophin-4-like, transcript variant X6
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 4 samples with support for all annotated introns
neurotrophin-4-like, transcript variant X2
neurotrophin-4-like, transcript variant X9
neurotrophin-4-like, transcript variant X10
kinesin-like protein KIF18A, transcript variant X1
kinesin-like protein KIF18A, transcript variant X2
potassium voltage-gated channel subfamily A member 2-like
synaptotagmin-1-like, transcript variant X1
synaptotagmin-1-like, transcript variant X2
dynein axonemal assembly factor 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
dynein axonemal assembly factor 3-like, transcript variant X2
dynein axonemal assembly factor 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
troponin T type 1 (skeletal, slow), transcript variant X2
troponin T type 1 (skeletal, slow), transcript variant X1
troponin T, slow skeletal muscle isoform X1
troponin T, slow skeletal muscle isoform X2
protein phosphatase 1 regulatory subunit 12C-like
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
U1 small nuclear ribonucleoprotein 70 kDa
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 153 Proteins, and 46% 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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
PIH1 domain containing 1, transcript variant X1
PIH1 domain containing 1, transcript variant X2
aldehyde dehydrogenase 16 family, member A1, 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 21 samples with support for all annotated introns
aldehyde dehydrogenase 16 family, member A1, transcript variant X1
aldehyde dehydrogenase family 16 member A1 isoform X2
aldehyde dehydrogenase family 16 member A1 isoform X1
uncharacterized LOC122542184, transcript variant X3
uncharacterized LOC122542184, 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 9 samples with support for all annotated introns
uncharacterized LOC122542184, transcript variant X5
uncharacterized LOC122542184, transcript variant X4
uncharacterized LOC122542184, transcript variant X2
uncharacterized protein LOC122542184 isoform X2
uncharacterized protein LOC122542184 isoform X1
excitatory amino acid transporter 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
excitatory amino acid transporter 2-like, transcript variant X2
excitatory amino acid transporter 2-like
epidermal growth factor receptor kinase substrate 8-like protein 1, transcript variant X1
epidermal growth factor receptor kinase substrate 8-like protein 1, transcript variant X3
epidermal growth factor receptor kinase substrate 8-like protein 1, transcript variant X2
epidermal growth factor receptor kinase substrate 8-like protein 1 isoform X1
epidermal growth factor receptor kinase substrate 8-like protein 1 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
SH3 and multiple ankyrin repeat domains protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% 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: 74% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein C19orf81
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
SH3 and multiple ankyrin repeat domains protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/arginine-rich splicing factor 3-like
DNA ligase 1-like, transcript variant X2
DNA ligase 1-like, transcript variant X1
leucine rich repeat containing 4Ba, transcript variant X6
leucine rich repeat containing 4Ba, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
leucine rich repeat containing 4Ba, transcript variant X5
leucine rich repeat containing 4Ba, transcript variant X7
leucine rich repeat containing 4Ba, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine rich repeat containing 4Ba, transcript variant X2
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 5 samples with support for all annotated introns
leucine rich repeat containing 4Ba, transcript variant X4
leucine-rich repeat-containing protein 4B
E3 SUMO-protein ligase ZBED1-like, transcript variant X3
E3 SUMO-protein ligase ZBED1-like, transcript variant X1
E3 SUMO-protein ligase ZBED1-like, transcript variant X2
E3 SUMO-protein ligase ZBED1-like isoform X1
E3 SUMO-protein ligase ZBED1-like isoform X2
ETS homologous factor-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 5 samples with support for all annotated introns
ETS homologous factor-like, transcript variant X4
transcription factor ETV6-like isoform X1
ETS homologous factor-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 2 samples with support for all annotated introns
ETS homologous factor-like, transcript variant X3
myosin binding protein Ca, transcript variant X2
myosin binding protein Ca, transcript variant X1
transcription factor Spi-B-like, transcript variant X2
transcription factor Spi-B-like, transcript variant X3
transcription factor Spi-B-like, transcript variant X1
transcription factor Spi-B-like isoform X2
transcription factor PU.1-like isoform X3
transcription factor Spi-B-like isoform X1
polymerase (DNA directed), delta 1, catalytic subunit, 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 10 samples with support for all annotated introns
polymerase (DNA directed), delta 1, catalytic subunit, transcript variant X2
oxysterols receptor LXR-beta-like, transcript variant X1
oxysterols receptor LXR-beta-like, transcript variant X2
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X3
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X1
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X2
protein kinase C and casein kinase substrate in neurons protein 3 isoform X1
protein kinase C and casein kinase substrate in neurons protein 1 isoform X2
mediator complex subunit 25, transcript variant X4
mediator complex subunit 25, transcript variant X3
mediator complex subunit 25, transcript variant X1
mediator complex subunit 25, transcript variant X2
mediator of RNA polymerase II transcription subunit 25 isoform X2
mediator of RNA polymerase II transcription subunit 25 isoform X3
mediator of RNA polymerase II transcription subunit 25 isoform X1
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X3
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X4
proline rich Gla (G-carboxyglutamic acid) 2, 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 23 samples with support for all annotated introns
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X5
transmembrane gamma-carboxyglutamic acid protein 2
nitric oxide synthase interacting protein, transcript variant X3
nitric oxide synthase interacting protein, transcript variant X2
nitric oxide synthase interacting protein, transcript variant X1
nitric oxide synthase-interacting protein
reticulocalbin 3, EF-hand calcium binding domain, 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 10 samples with support for all annotated introns
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X2
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
F-box only protein 47-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 1 sample with support for all annotated introns
F-box only protein 47-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
F-box only protein 47-like, transcript variant X2
paired box protein Pax-6-like, transcript variant X5
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
paired box protein Pax-6-like, transcript variant X1
paired box protein Pax-6-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
paired box protein Pax-6-like, transcript variant X6
paired box protein Pax-6-like, transcript variant X7
paired box protein Pax-6-like, transcript variant X3
paired box protein Pax-6-like, transcript variant X2
paired box protein Pax-6-like isoform X1
paired box protein Pax-6-like isoform X2
paired box protein Pax-6-like isoform X3
paired box protein Pax-6-like isoform X4
paired box protein Pax-6-like isoform X5
tumor protein p53-inducible protein 11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tumor protein p53-inducible protein 11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
tumor protein p53-inducible protein 11-like
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
carnitine O-palmitoyltransferase 1, liver isoform-like, transcript variant X1
carnitine O-palmitoyltransferase 1, liver isoform-like, transcript variant X3
carnitine O-palmitoyltransferase 1, liver isoform-like, transcript variant X2
carnitine O-palmitoyltransferase 1, liver isoform-like isoform X1
carnitine O-palmitoyltransferase 1, liver isoform-like isoform X2
transportin-3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
transportin-3-like, transcript variant X3
transportin-3-like, transcript variant X1
transportin-3-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 2 samples with support for all annotated introns
transportin-3-like, transcript variant X5
ras-related and estrogen-regulated growth inhibitor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel, subfamily M, member 4a
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
transient receptor potential cation channel subfamily M member 4a
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cyclin-dependent kinase inhibitor 1B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
dual specificity protein phosphatase 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine/threonine-protein kinase BRSK2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 6 regulatory subunit 3-like
HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1, transcript variant X1
HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1, transcript variant X3
HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1, transcript variant X4
HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1, transcript variant X5
HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1, transcript variant X6
HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1, transcript variant X2
histone-lysine N-methyltransferase KMT5C-like, 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 11 samples with support for all annotated introns
histone-lysine N-methyltransferase KMT5C-like, 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 1 sample with support for all annotated introns
histone-lysine N-methyltransferase KMT5C-like, transcript variant X5
histone-lysine N-methyltransferase KMT5C-like, 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 3 samples with support for all annotated introns
histone-lysine N-methyltransferase KMT5C-like, transcript variant X1
histone-lysine N-methyltransferase KMT5C-like
modulator of macroautophagy TMEM150B-like, transcript variant X5
modulator of macroautophagy TMEM150B-like, transcript variant X4
modulator of macroautophagy TMEM150B-like, transcript variant X3
modulator of macroautophagy TMEM150B-like, transcript variant X8
modulator of macroautophagy TMEM150B-like, transcript variant X6
modulator of macroautophagy TMEM150B-like, transcript variant X11
modulator of macroautophagy TMEM150B-like, transcript variant X1
modulator of macroautophagy TMEM150B-like, transcript variant X10
modulator of macroautophagy TMEM150B-like, transcript variant X9
modulator of macroautophagy TMEM150B-like, transcript variant X7
modulator of macroautophagy TMEM150B-like, transcript variant X2
modulator of macroautophagy TMEM150B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ferritin, middle subunit-like, transcript variant X2
ferritin, middle subunit-like, transcript variant X1
ferritin, middle subunit-like isoform X2
ferritin, middle subunit-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 166 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ferritin, middle subunit-like, transcript variant X4
ferritin, middle subunit-like isoform X4
ferritin, middle subunit-like, transcript variant X3
ferritin, middle subunit-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 144 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 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: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 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: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
golgi-associated, gamma adaptin ear containing, ARF binding protein 1, transcript variant X2
golgi-associated, gamma adaptin ear containing, ARF binding protein 1, transcript variant X1
golgi-associated, gamma adaptin ear containing, ARF binding protein 1, transcript variant X3
golgi-associated, gamma adaptin ear containing, ARF binding protein 1, transcript variant X4
ADP-ribosylation factor-binding protein GGA1 isoform X1
ADP-ribosylation factor-binding protein GGA1 isoform X2
ADP-ribosylation factor-binding protein GGA1 isoform X3
ADP-ribosylation factor-binding protein GGA1 isoform X4
ras-related C3 botulinum toxin substrate 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 216 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ras-related C3 botulinum toxin substrate 1-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 3 samples with support for all annotated introns
ras-related C3 botulinum toxin substrate 1-like, transcript variant X3
ras-related C3 botulinum toxin substrate 1-like isoform X1
ras-related C3 botulinum toxin substrate 1-like isoform X2
ras-related C3 botulinum toxin substrate 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
ras-related C3 botulinum toxin substrate 1-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
somatostatin receptor type 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00096
somatostatin receptor type 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
complement C1q tumor necrosis factor-related protein 1-like
brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2, transcript variant X1
brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2, transcript variant X2
brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2 isoform X1
brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2 isoform X2
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X7
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X1
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X3
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X5
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X6
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X4
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X2
85/88 kDa calcium-independent phospholipase A2 isoform X2
85/88 kDa calcium-independent phospholipase A2 isoform X1
transcription factor MafK-like, transcript variant X1
transcription factor MafK-like, transcript variant X3
transcription factor MafK-like, transcript variant X2
transcription factor MafK-like isoform X1
transcription factor MafK-like isoform X2
transmembrane protein 184B-like, transcript variant X3
transmembrane protein 184B-like, transcript variant X1
transmembrane protein 184B-like, transcript variant X2
discs, large (Drosophila) homolog-associated protein 5
protein phosphatase 1 regulatory subunit 29-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 29-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 4 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 29-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
protein phosphatase 1 regulatory subunit 29-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 29-like, transcript variant X4
protein phosphatase 1 regulatory subunit 29-like isoform X2
protein phosphatase 1 regulatory subunit 29-like isoform X1
cytochrome P450 2D17-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cytochrome P450 2D17-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
beta-1,3-N-acetylglucosaminyltransferase lunatic fringe-like
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 20 samples with support for all annotated introns
guanine nucleotide-binding protein subunit alpha-12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 106 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
caspase recruitment domain-containing protein 11-like
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 17 samples with support for all annotated introns
cytokine receptor common subunit beta-like, transcript variant X1
cytokine receptor common subunit beta-like, transcript variant X2
cytokine receptor common subunit beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
interleukin-2 receptor subunit beta-like, transcript variant X2
interleukin-2 receptor subunit beta-like, transcript variant X1
interleukin-2 receptor subunit beta-like, transcript variant X3
interleukin-2 receptor subunit beta-like, transcript variant X4
interleukin-2 receptor subunit beta-like
transmembrane protease serine 6, transcript variant X1
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 4 samples with support for all annotated introns
transmembrane protease serine 6 isoform X1
transmembrane protease serine 6, transcript variant X2
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 1 sample with support for all annotated introns
transmembrane protease serine 6 isoform X2
BTB/POZ domain-containing protein KCTD5-like, transcript variant X1
BTB/POZ domain-containing protein KCTD5-like, transcript variant X2
BTB/POZ domain-containing protein KCTD5-like isoform X2
BTB/POZ domain-containing protein KCTD5-like isoform X1
testis-expressed protein 33, 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
testis-expressed protein 33, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC122542257 isoform X1
testis-expressed protein 33, 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 18 samples with support for all annotated introns
SUMO-conjugating enzyme UBC9, transcript variant X2
SUMO-conjugating enzyme UBC9, transcript variant X1
uncharacterized LOC122542263, transcript variant X1
uncharacterized LOC122542263, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
3-mercaptopyruvate sulfurtransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
3-mercaptopyruvate sulfurtransferase-like, transcript variant X2
3-mercaptopyruvate sulfurtransferase-like, transcript variant X3
3-mercaptopyruvate sulfurtransferase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclic AMP-dependent transcription factor ATF-4
MIEF1 upstream open reading frame protein-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 29 samples with support for all annotated introns
MIEF1 upstream open reading frame protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
MIEF1 upstream open reading frame protein-like
eukaryotic translation initiation factor 3, subunit 6 interacting protein, transcript variant X1
eukaryotic translation initiation factor 3, subunit 6 interacting protein, transcript variant X2
eukaryotic translation initiation factor 3 subunit L isoform X1
eukaryotic translation initiation factor 3 subunit L isoform X2
ankyrin repeat domain-containing protein 54
activating transcription factor 7-interacting protein 1-like, transcript variant X17
activating transcription factor 7-interacting protein 1-like, transcript variant X16
activating transcription factor 7-interacting protein 1-like, transcript variant X18
activating transcription factor 7-interacting protein 1-like isoform X7
activating transcription factor 7-interacting protein 1-like isoform X6
activating transcription factor 7-interacting protein 1-like isoform X5
activating transcription factor 7-interacting protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1-like, transcript variant X7
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 28 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1-like, transcript variant X5
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 23 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1-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 16 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1-like, transcript variant X12
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
activating transcription factor 7-interacting protein 1-like, transcript variant X8
activating transcription factor 7-interacting protein 1-like, transcript variant X13
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 19 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1-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
activating transcription factor 7-interacting protein 1-like, transcript variant X14
activating transcription factor 7-interacting protein 1-like, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1-like, 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 20 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1-like, transcript variant X11
activating transcription factor 7-interacting protein 1-like, transcript variant X2
activating transcription factor 7-interacting protein 1-like, transcript variant X4
activating transcription factor 7-interacting protein 1-like, transcript variant X9
activating transcription factor 7-interacting protein 1-like isoform X3
activating transcription factor 7-interacting protein 1-like isoform X1
activating transcription factor 7-interacting protein 1-like isoform X4
activating transcription factor 7-interacting protein 1-like isoform X2
glutamate receptor ionotropic, NMDA 2B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glutamate receptor ionotropic, NMDA 2B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor ionotropic, NMDA 2B-like isoform X1
glutamate receptor ionotropic, NMDA 2B-like, transcript variant X3
glutamate receptor ionotropic, NMDA 2B-like isoform X2
uncharacterized LOC122542274, transcript variant X2
uncharacterized LOC122542274, 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 30 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 13B-like
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
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
WW domain-binding protein 2-like, transcript variant X2
WW domain-binding protein 2-like, transcript variant X1
WW domain-binding protein 2-like, transcript variant X3
WW domain-binding protein 2-like isoform X2
WW domain-binding protein 2-like isoform X1
WW domain-binding protein 2-like 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 10 samples with support for all annotated introns
uncharacterized LOC122542279, 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 12 samples with support for all annotated introns
uncharacterized LOC122542279, transcript variant X2
uncharacterized protein LOC122542279 isoform X1
uncharacterized protein LOC122542279 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
X-ray repair complementing defective repair in Chinese hamster cells 6, transcript variant X2
X-ray repair complementing defective repair in Chinese hamster cells 6, transcript variant X1
X-ray repair cross-complementing protein 6 isoform X1
X-ray repair cross-complementing protein 6 isoform X2
cytochrome b-c1 complex subunit 2, mitochondrial-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 14 samples with support for all annotated introns
cytochrome b-c1 complex subunit 2, mitochondrial-like isoform X2
cytochrome b-c1 complex subunit 2, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome b-c1 complex subunit 2, mitochondrial-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 6 samples with support for all annotated introns
cytochrome b-c1 complex subunit 2, mitochondrial-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome b-c1 complex subunit 2, mitochondrial-like, transcript variant X6
cytochrome b-c1 complex subunit 2, mitochondrial-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytochrome b-c1 complex subunit 2, mitochondrial-like isoform X3
cytochrome b-c1 complex subunit 2, mitochondrial-like isoform X1
cytochrome b-c1 complex subunit 2, mitochondrial-like isoform X7
cytochrome b-c1 complex subunit 2, mitochondrial-like isoform X5
cytochrome b-c1 complex subunit 2, mitochondrial-like isoform X6
cytochrome b-c1 complex subunit 2, mitochondrial-like, transcript variant X4
cytochrome b-c1 complex subunit 2, mitochondrial-like, transcript variant X5
cytochrome b-c1 complex subunit 2, mitochondrial-like, transcript variant X9
cytochrome b-c1 complex subunit 2, mitochondrial-like isoform X4
cytochrome b-c1 complex subunit 2, mitochondrial-like isoform X8
myocardin-related transcription factor A-like, transcript variant X3
myocardin-related transcription factor A-like, transcript variant X1
myocardin-related transcription factor A-like, transcript variant X5
myocardin-related transcription factor A-like, transcript variant X2
myocardin-related transcription factor A-like, transcript variant X4
myocardin-related transcription factor A-like isoform X3
myocardin-related transcription factor A-like isoform X1
myocardin-related transcription factor A-like isoform X2
myocardin-related transcription factor A-like isoform X5
myocardin-related transcription factor A-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X1
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X3
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X4
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X2
DNA-directed RNA polymerase III subunit RPC8
PHD finger-like domain-containing protein 5A
protein Tob2-like, transcript variant X1
protein Tob2-like, transcript variant X3
protein Tob2-like, transcript variant X4
protein Tob2-like, transcript variant X2
thyrotroph embryonic factor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
thyrotroph embryonic factor-like isoform X1
thyrotroph embryonic factor-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
thyrotroph embryonic factor-like isoform X3
thyrotroph embryonic factor-like, transcript variant X2
thyrotroph embryonic factor-like isoform X2
zinc finger CCCH-type containing 7Bb, transcript variant X1
zinc finger CCCH-type containing 7Bb, transcript variant X2
zinc finger CCCH domain-containing protein 7B
Ran GTPase activating protein 1b, transcript variant X1
Ran GTPase activating protein 1b, transcript variant X5
Ran GTPase activating protein 1b, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Ran GTPase activating protein 1b, transcript variant X3
Ran GTPase activating protein 1b, transcript variant X4
Ran GTPase activating protein 1b, transcript variant X2
ran GTPase-activating protein 1b isoform X1
ran GTPase-activating protein 1b isoform X2
ran GTPase-activating protein 1b isoform X3
chondroadherin-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
chondroadherin-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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
L3MBTL histone methyl-lysine binding protein 2, transcript variant X5
L3MBTL histone methyl-lysine binding protein 2, transcript variant X4
L3MBTL histone methyl-lysine binding protein 2, transcript variant X2
L3MBTL histone methyl-lysine binding protein 2, transcript variant X1
L3MBTL histone methyl-lysine binding protein 2, transcript variant X3
lethal(3)malignant brain tumor-like protein 2 isoform X1
lethal(3)malignant brain tumor-like protein 2 isoform X2
lethal(3)malignant brain tumor-like protein 2 isoform X3
lethal(3)malignant brain tumor-like protein 2 isoform X4
uncharacterized LOC122541984, transcript variant X2
uncharacterized LOC122541984, transcript variant X1
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
X-prolyl aminopeptidase 3, mitochondrial, transcript variant X1
X-prolyl aminopeptidase 3, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ankyrin repeat and fibronectin type-III domain-containing protein 1-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glycine C-acetyltransferase, transcript variant X1
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial isoform X1
glycine C-acetyltransferase, transcript variant X2
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial isoform X2
TRIO and F-actin-binding protein-like, transcript variant X2
TRIO and F-actin-binding protein-like, transcript variant X5
TRIO and F-actin-binding protein-like, transcript variant X6
TRIO and F-actin-binding protein-like, transcript variant X4
TRIO and F-actin-binding protein-like, transcript variant X1
TRIO and F-actin-binding protein-like, transcript variant X3
TRIO and F-actin-binding protein-like, transcript variant X8
TRIO and F-actin-binding protein-like isoform X2
TRIO and F-actin-binding protein-like isoform X5
TRIO and F-actin-binding protein-like isoform X6
TRIO and F-actin-binding protein-like isoform X8
TRIO and F-actin-binding protein-like isoform X4
TRIO and F-actin-binding protein-like isoform X1
TRIO and F-actin-binding protein-like isoform X3
TRIO and F-actin-binding protein-like, transcript variant X9
uncharacterized protein LOC122542310 isoform X9
TRIO and F-actin-binding protein-like, transcript variant X7
uncharacterized protein LOC122542310 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
nucleolar protein 12, transcript variant X1
nucleolar protein 12, transcript variant X2
nucleolar protein 12, transcript variant X3
sterol regulatory element binding transcription factor 2
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 28 samples with support for all annotated introns
sterol regulatory element-binding protein 2
coiled-coil domain-containing protein 134-like, transcript variant X2
coiled-coil domain-containing protein 134-like, transcript variant X1
coiled-coil domain-containing protein 134-like
target of myb1 membrane trafficking protein, transcript variant X4
target of myb1 membrane trafficking protein, transcript variant X2
target of myb1 membrane trafficking protein, transcript variant X1
target of myb1 membrane trafficking protein, transcript variant X3
target of myb1 membrane trafficking protein, 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 22 samples with support for all annotated introns
target of myb1 membrane trafficking protein, 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 7 samples with support for all annotated introns
HMG box domain containing 4a, 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 23 samples with support for all annotated introns
HMG box domain containing 4a, 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 22 samples with support for all annotated introns
HMG box domain containing 4a, transcript variant X3
HMG box domain containing 4a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
HMG box domain containing 4a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
HMG domain-containing protein 4a isoform X1
HMG domain-containing protein 4a isoform X2
HMG domain-containing protein 4a isoform X3
heat-stable enterotoxin receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
heat-stable enterotoxin receptor-like, transcript variant X1
heat-stable enterotoxin receptor-like isoform X1
heat-stable enterotoxin receptor-like isoform X2
tetratricopeptide repeat domain 26, 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 6 samples with support for all annotated introns
tetratricopeptide repeat domain 26, transcript variant X1
tetratricopeptide repeat domain 26, transcript variant X3
intraflagellar transport protein 56 isoform X1
intraflagellar transport protein 56 isoform X3
intraflagellar transport protein 56 isoform X4
tetratricopeptide repeat domain 26, transcript variant X2
intraflagellar transport protein 56 isoform X2
ubinuclein-2-like, transcript variant X6
ubinuclein-2-like, transcript variant X4
ubinuclein-2-like, transcript variant X3
ubinuclein-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ubinuclein-2-like, transcript variant X5
ubinuclein-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 11 samples with support for all annotated introns
small nucleolar RNA SNORA62/SNORA6 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
FAD-dependent oxidoreductase domain containing 2, transcript variant X6
FAD-dependent oxidoreductase domain containing 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
FAD-dependent oxidoreductase domain containing 2, transcript variant X4
FAD-dependent oxidoreductase domain containing 2, transcript variant X2
FAD-dependent oxidoreductase domain containing 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
FAD-dependent oxidoreductase domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
FAD-dependent oxidoreductase domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 2 isoform X2
FAD-dependent oxidoreductase domain-containing protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
minichromosome maintenance complex component 5
NADH:ubiquinone oxidoreductase subunit A6
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6
single-pass membrane protein with aspartate-rich tail 1b
serine hydrolase like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
serine hydrolase like, transcript variant X4
N-acetylgalactosaminidase, alpha, transcript variant X2
N-acetylgalactosaminidase, alpha, transcript variant X1
alpha-N-acetylgalactosaminidase isoform X2
alpha-N-acetylgalactosaminidase isoform X1
serine hydrolase like, transcript variant X3
serine hydrolase like, transcript variant X1
serine hydrolase-like protein isoform X1
serine hydrolase like, transcript variant X5
serine hydrolase-like protein isoform X2
putative RNA-binding protein Luc7-like 2, transcript variant X1
putative RNA-binding protein Luc7-like 2, transcript variant X3
putative RNA-binding protein Luc7-like 2, transcript variant X2
putative RNA-binding protein Luc7-like 2, transcript variant X4
putative RNA-binding protein Luc7-like 2, transcript variant X8
putative RNA-binding protein Luc7-like 2, transcript variant X7
putative RNA-binding protein Luc7-like 2, transcript variant X5
putative RNA-binding protein Luc7-like 2, transcript variant X6
putative RNA-binding protein Luc7-like 2 isoform X3
putative RNA-binding protein Luc7-like 2 isoform X2
putative RNA-binding protein Luc7-like 2 isoform X1
putative RNA-binding protein Luc7-like 2 isoform X5
putative RNA-binding protein Luc7-like 2 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59
probable ATP-dependent RNA helicase DDX59
family with sequence similarity 234 member B
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
platelet-derived growth factor subunit B-like
extracellular serine/threonine protein kinase FAM20C
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 13 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 94% coverage of the annotated genomic feature by RNAseq alignments
protein interacting with prkca 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
protein interacting with prkca 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
translocase of outer mitochondrial membrane 22 homolog (yeast)
mitochondrial import receptor subunit TOM22 homolog
COORDINATES: nucleotide motif:Rfam:12.0:RF00007
ribosomal RNA-processing protein 7 homolog A
MICAL-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
MICAL-like protein 1, 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 6 samples with support for all annotated introns
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X4
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X2
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X5
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X1
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X3
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X6
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like isoform X1
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like isoform X3
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
TGF-beta activated kinase 1/MAP3K7 binding protein 1
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1
extracellular serine/threonine protein kinase FAM20C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
Sad1 and UNC84 domain containing 2, transcript variant X3
Sad1 and UNC84 domain containing 2, transcript variant X1
Sad1 and UNC84 domain containing 2, transcript variant X4
Sad1 and UNC84 domain containing 2, transcript variant X2
SUN domain-containing protein 2 isoform X1
SUN domain-containing protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
meiotic recombination protein DMC1/LIM15 homolog
probable ATP-dependent RNA helicase DDX17, transcript variant X2
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 26 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX17, transcript variant X1
probable ATP-dependent RNA helicase DDX17
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X1
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X2
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X3
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X4
ATP-sensitive inward rectifier potassium channel 12-like
small G protein signaling modulator 3, transcript variant X1
small G protein signaling modulator 3, transcript variant X2
small G protein signaling modulator 3 isoform X1
small G protein signaling modulator 3 isoform X2
gastrula zinc finger protein XlCGF71.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
NACHT, LRR and PYD domains-containing protein 3-like, 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 4 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X4
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X1
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X10
NACHT, LRR and PYD domains-containing protein 3-like isoform X2
NACHT, LRR and PYD domains-containing protein 3-like isoform X1
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X7
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X6
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X8
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X9
NACHT, LRR and PYD domains-containing protein 3-like isoform 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 7 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 5 samples with support for all annotated introns
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon ACU); 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: 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
centromere protein K, transcript variant X1
centromere protein K, transcript variant X2
UDP-glucuronosyltransferase 2C1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
UDP-glucuronosyltransferase 2C1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
UDP-glucuronosyltransferase 2C1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
UDP-glucuronosyltransferase 2C1-like isoform X1
UDP-glucuronosyltransferase 2C1-like isoform X2
UDP-glucuronosyltransferase 2C1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
troponin C, slow skeletal and cardiac muscles-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 92% 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: 16 Proteins, and 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: 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122542357, transcript variant X5
uncharacterized LOC122542357, transcript variant X4
uncharacterized LOC122542357, transcript variant X3
uncharacterized LOC122542357, transcript variant X2
uncharacterized LOC122542357, transcript variant X1
uncharacterized LOC122542357, 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 21 samples with support for all annotated introns
structural maintenance of chromosomes protein 1A
hydroxysteroid (17-beta) dehydrogenase 10, transcript variant X1
hydroxysteroid (17-beta) dehydrogenase 10, transcript variant X2
3-hydroxyacyl-CoA dehydrogenase type-2 isoform X1
3-hydroxyacyl-CoA dehydrogenase type-2 isoform X2
hydroxysteroid (17-beta) dehydrogenase 10, transcript variant X3
3-hydroxyacyl-CoA dehydrogenase type-2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
interleukin-1 receptor-associated kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
interleukin-1 receptor-associated kinase 1, transcript variant X1
interleukin-1 receptor-associated kinase 1 isoform X1
interleukin-1 receptor-associated kinase 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 64% 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 100% coverage of the annotated genomic feature by RNAseq alignments
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X1
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X8
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X5
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X7
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X9
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X4
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X12
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X11
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X6
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X13
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X3
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X10
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1, transcript variant X2
E3 ubiquitin-protein ligase HUWE1 isoform X1
E3 ubiquitin-protein ligase HUWE1 isoform X7
E3 ubiquitin-protein ligase HUWE1 isoform X4
E3 ubiquitin-protein ligase HUWE1 isoform X6
E3 ubiquitin-protein ligase HUWE1 isoform X8
E3 ubiquitin-protein ligase HUWE1 isoform X3
E3 ubiquitin-protein ligase HUWE1 isoform X11
E3 ubiquitin-protein ligase HUWE1 isoform X10
E3 ubiquitin-protein ligase HUWE1 isoform X5
E3 ubiquitin-protein ligase HUWE1 isoform X12
E3 ubiquitin-protein ligase HUWE1 isoform X2
E3 ubiquitin-protein ligase HUWE1 isoform X9
transmembrane and coiled-coil domain protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NPR3-like, GATOR1 complex subunit, transcript variant X2
NPR3-like, GATOR1 complex subunit, transcript variant X3
NPR3-like, GATOR1 complex subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
FUS RNA binding protein, transcript variant X1
FUS RNA binding protein, transcript variant X2
3-methyl-2-oxobutanoate dehydrogenase [lipoamide] kinase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
vitamin K epoxide reductase complex subunit 1-like protein 1
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 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
Snf2-related CREBBP activator protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Snf2-related CREBBP activator protein, transcript variant X1
Snf2-related CREBBP activator protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Snf2-related CREBBP activator protein, 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 15 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 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial ribosomal protein L24, transcript variant X3
mitochondrial ribosomal protein L24, transcript variant X2
mitochondrial ribosomal protein L24, transcript variant X4
mitochondrial ribosomal protein L24, transcript variant X1
probable 39S ribosomal protein L24, mitochondrial isoform X1
probable 39S ribosomal protein L24, mitochondrial isoform X2
diamine acetyltransferase 1-like, transcript variant X2
diamine acetyltransferase 1-like, transcript variant X1
diamine acetyltransferase 1-like isoform X2
diamine acetyltransferase 1-like isoform X1
hyaluronan and proteoglycan link protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 92% 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 85% coverage of the annotated genomic feature by RNAseq alignments
hemagglutinin/amebocyte aggregation factor-like, transcript variant X2
hemagglutinin/amebocyte aggregation factor-like isoform X2
hemagglutinin/amebocyte aggregation factor-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 13 samples with support for all annotated introns
hemagglutinin/amebocyte aggregation factor-like, transcript variant X1
hemagglutinin/amebocyte aggregation factor-like isoform X3
hemagglutinin/amebocyte aggregation factor-like isoform X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
immunoglobulin lambda variable 5-39-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
immunoglobulin lambda variable 5-37-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC122541995, transcript variant X1
uncharacterized LOC122541995, transcript variant X2
uncharacterized LOC122541995, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin lambda-1 light chain-like
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