Pieris napi chromosome 12, ilPieNapi1.2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Pieridae; Pierinae; Pieris.
REFSEQ INFORMATION: The reference sequence is identical to\nFR997706.1.\nAssembly name: ilPieNapi1.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/01/30. The original whole-genome shotgun project has the\naccession CAJQFT000000000.2.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris napi Annotation 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.
COORDINATES: polyA evidence [ECO:0006239]
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 71 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 96% coverage of the annotated genomic feature by RNAseq alignments
pyrethroid hydrolase Ces2e-like isoform X1
pyrethroid hydrolase Ces2e-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
pyrethroid hydrolase Ces2e-like isoform 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 8 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 8 samples with support for all annotated introns
zinc finger protein 62 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized protein LOC125054822 isoform X4
zinc finger protein 62 homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized protein LOC125054822 isoform X5
zinc finger protein 62 homolog, transcript variant X2
zinc finger protein 62 homolog isoform X2
zinc finger protein 62 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 136 samples with support for all annotated introns
zinc finger protein 62 homolog, 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 24 samples with support for all annotated introns
uncharacterized protein LOC125054822 isoform X3
RNA-binding protein Pasilla, transcript variant X1
RNA-binding protein Pasilla, transcript variant X2
RNA-binding protein Pasilla, transcript variant X4
RNA-binding protein Pasilla, transcript variant X3
RNA-binding protein Pasilla, transcript variant X6
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 58 samples with support for all annotated introns
RNA-binding protein Pasilla, transcript variant X5
putative inactive tyrosine-protein kinase Wsck
putative uncharacterized protein DDB_G0282133
hippocampus abundant transcript 1 protein
putative phospholipase B-like 2, transcript variant X2
putative phospholipase B-like 2, transcript variant X1
integrator complex subunit 1, transcript variant X1
integrator complex subunit 1, transcript variant X2
peptidyl-prolyl cis-trans isomerase FKBP4
uncharacterized LOC125054646, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
uncharacterized LOC125054646, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 161 samples with support for all annotated introns
ATP synthase-coupling factor 6, mitochondrial
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
AMP deaminase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 505 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
AMP deaminase 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 458 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
AMP deaminase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 505 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
AMP deaminase 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
AMP deaminase 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 502 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ribosome-releasing factor 2, mitochondrial
retinol dehydrogenase 12-like, transcript variant X1
retinol dehydrogenase 12-like, transcript variant X2
retinol dehydrogenase 12-like isoform X2
retinol dehydrogenase 12-like isoform X1
DNA-directed RNA polymerase III subunit RPC1
bromodomain adjacent to zinc finger domain protein 1A, transcript variant X1
bromodomain adjacent to zinc finger domain protein 1A, transcript variant X6
bromodomain adjacent to zinc finger domain protein 1A, transcript variant X8
bromodomain adjacent to zinc finger domain protein 1A, transcript variant X3
bromodomain adjacent to zinc finger domain protein 1A, transcript variant X7
bromodomain adjacent to zinc finger domain protein 1A, transcript variant X2
bromodomain adjacent to zinc finger domain protein 1A, transcript variant X9
bromodomain adjacent to zinc finger domain protein 1A, transcript variant X4
bromodomain adjacent to zinc finger domain protein 1A, transcript variant X5
bromodomain adjacent to zinc finger domain protein 1A isoform X1
bromodomain adjacent to zinc finger domain protein 1A isoform X6
bromodomain adjacent to zinc finger domain protein 1A isoform X8
bromodomain adjacent to zinc finger domain protein 1A isoform X3
bromodomain adjacent to zinc finger domain protein 1A isoform X7
bromodomain adjacent to zinc finger domain protein 1A isoform X2
bromodomain adjacent to zinc finger domain protein 1A isoform X9
bromodomain adjacent to zinc finger domain protein 1A isoform X4
bromodomain adjacent to zinc finger domain protein 1A isoform X5
uncharacterized LOC125054452, transcript variant X1
uncharacterized LOC125054452, transcript variant X2
kinesin-like protein Klp98A, transcript variant X3
kinesin-like protein Klp98A, transcript variant X1
kinesin-like protein Klp98A, 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 169 samples with support for all annotated introns
mitochondrial GTPase 1, 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 168 samples with support for all annotated introns
mitochondrial GTPase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ribosome quality control complex subunit NEMF homolog
all trans-polyprenyl-diphosphate synthase PDSS2-like
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
homeobox protein homothorax, transcript variant X5
homeobox protein homothorax, transcript variant X4
homeobox protein homothorax, transcript variant X2
homeobox protein homothorax, transcript variant X3
homeobox protein homothorax, transcript variant X1
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial, transcript variant X2
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial isoform X2
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial isoform X1
tubulin polyglutamylase TTLL5, 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 10 samples with support for all annotated introns
tubulin polyglutamylase TTLL5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
tubulin polyglutamylase TTLL5, transcript variant X4
tubulin polyglutamylase TTLL5, 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 11 samples with support for all annotated introns
tubulin polyglutamylase TTLL5, 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 9 samples with support for all annotated introns
tubulin polyglutamylase TTLL5, 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 20 samples with support for all annotated introns
tubulin polyglutamylase TTLL5 isoform X1
uncharacterized protein LOC125054554 isoform X3
uncharacterized protein LOC125054554 isoform X2
uncharacterized protein LOC125054554 isoform X4
tubulin polyglutamylase TTLL5 isoform X5
RNA-binding protein 4.1, transcript variant X1
RNA-binding protein 4.1, transcript variant X3
RNA-binding protein 4.1, transcript variant X2
transcription termination factor 2, transcript variant X3
transcription termination factor 2, transcript variant X2
transcription termination factor 2, transcript variant X1
transcription termination factor 2 isoform X2
transcription termination factor 2 isoform X3
transcription termination factor 2 isoform 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 166 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 100 samples with support for all annotated introns
protein sel-1 homolog 1, 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 166 samples with support for all annotated introns
protein sel-1 homolog 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 168 samples with support for all annotated introns
molybdopterin synthase catalytic subunit
molybdopterin synthase sulfur carrier subunit, 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 126 samples with support for all annotated introns
molybdopterin synthase sulfur carrier subunit, 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 136 samples with support for all annotated introns
molybdopterin synthase sulfur carrier subunit, 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 34 samples with support for all annotated introns
molybdopterin synthase sulfur carrier subunit, 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 91 samples with support for all annotated introns
molybdopterin synthase sulfur carrier subunit
intraflagellar transport protein 46 homolog
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 42 samples with support for all annotated introns
cell growth regulator with RING finger domain protein 1-like
cyclin-dependent kinase-like 4, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclin-dependent kinase-like 4, transcript variant X1
cyclin-dependent kinase-like 4, transcript variant X3
cyclin-dependent kinase-like 4, transcript variant X4
cyclin-dependent kinase-like 4, transcript variant X6
cyclin-dependent kinase-like 4 isoform X1
cyclin-dependent kinase-like 4 isoform X3
cyclin-dependent kinase-like 4 isoform X6
cyclin-dependent kinase-like 1 isoform X4
cyclin-dependent kinase-like 1 isoform X9
cyclin-dependent kinase-like 4, transcript variant X7
cyclin-dependent kinase-like 4, transcript variant X2
cyclin-dependent kinase-like 4, transcript variant X5
cyclin-dependent kinase-like 4, transcript variant X8
cyclin-dependent kinase-like 4 isoform X2
cyclin-dependent kinase-like 4 isoform X5
cyclin-dependent kinase-like 4 isoform X8
cyclin-dependent kinase-like 4 isoform X7
polyribonucleotide nucleotidyltransferase 1, mitochondrial
sodium/calcium exchanger 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
sodium/calcium exchanger 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 105 samples with support for all annotated introns
uncharacterized LOC125054482, transcript variant X1
uncharacterized LOC125054482, 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125054274, 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 24 samples with support for all annotated introns
uncharacterized LOC125054274, 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 18 samples with support for all annotated introns
uncharacterized protein K02A2.6-like, transcript variant X3
uncharacterized protein K02A2.6-like, transcript variant X2
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein K02A2.6-like isoform X1
uncharacterized protein K02A2.6-like isoform X2
uncharacterized protein LOC125054273 isoform X3
uncharacterized LOC125054274, 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 101 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 13% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125054737, transcript variant X2
uncharacterized LOC125054737, transcript variant X1
bilin-binding protein, transcript variant X1
bilin-binding protein, transcript variant X2
uncharacterized LOC125054729, transcript variant X1
uncharacterized LOC125054729, transcript variant X2
uncharacterized LOC125054729, transcript variant X3
uncharacterized protein LOC125054729 isoform X1
uncharacterized protein LOC125054729 isoform X2
uncharacterized protein LOC125054729 isoform X3
uncharacterized LOC125054377, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125054377, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125054377, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125054377, transcript variant X1
uncharacterized protein LOC125054377 isoform X4
uncharacterized protein LOC125054377 isoform X1
uncharacterized protein LOC125054377 isoform X2
uncharacterized protein LOC125054377 isoform X3
uncharacterized LOC125054499, transcript variant X2
uncharacterized protein LOC125054499 isoform X2
uncharacterized LOC125054499, transcript variant X1
uncharacterized protein LOC125054499 isoform X1
N-acetylneuraminate lyase-like, transcript variant X1
N-acetylneuraminate lyase-like isoform X1
N-acetylneuraminate lyase-like, transcript variant X2
N-acetylneuraminate lyase-like isoform X2
adenylosuccinate synthetase, transcript variant X2
adenylosuccinate synthetase, transcript variant X1
post-GPI attachment to proteins factor 6
putative FERM domain-containing protein FRMD8P1
dynein regulatory complex subunit 7, transcript variant X1
dynein regulatory complex subunit 7, transcript variant X2
dynein regulatory complex subunit 7, transcript variant X3
dynein regulatory complex subunit 7 isoform X1
dynein regulatory complex subunit 7 isoform X2
protein transport protein Sec23A, transcript variant X2
protein transport protein Sec23A, transcript variant X1
protein transport protein Sec23A isoform X2
protein transport protein Sec23A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
metastasis-associated protein MTA3, transcript variant X1
metastasis-associated protein MTA3, transcript variant X2
metastasis-associated protein MTA3 isoform X1
metastasis-associated protein MTA3 isoform X2
eukaryotic initiation factor 4A-III, transcript variant X2
eukaryotic initiation factor 4A-III, transcript variant X1
eukaryotic initiation factor 4A-III, transcript variant X3
eukaryotic initiation factor 4A-III, transcript variant X4
tubulin--tyrosine ligase-like protein 12
28S ribosomal protein S5, mitochondrial, transcript variant X1
28S ribosomal protein S5, mitochondrial, transcript variant X2
autophagy-related protein 2 homolog A, 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 50 samples with support for all annotated introns
autophagy-related protein 2 homolog A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 130 samples with support for all annotated introns
autophagy-related protein 2 homolog A isoform X2
autophagy-related protein 2 homolog A isoform X1
5-hydroxytryptamine receptor 1A-alpha-like
39S ribosomal protein L40, mitochondrial
uncharacterized LOC125054697, transcript variant X1
uncharacterized LOC125054697, 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 13 samples with support for all annotated introns
uncharacterized protein LOC125054697 isoform X1
uncharacterized protein LOC125054697 isoform X2
uncharacterized LOC125054463, transcript variant X1
uncharacterized LOC125054463, 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 64 samples with support for all annotated introns
uncharacterized LOC125054463, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
uncharacterized LOC125054463, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
uncharacterized protein LOC125054463 isoform X1
uncharacterized protein LOC125054463 isoform X2
lysM and putative peptidoglycan-binding domain-containing protein 2
myosin-I heavy chain, 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 38 samples with support for all annotated introns
myosin-I heavy chain, 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 38 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB7
ras-related protein Rab-8A-like, transcript variant X1
ras-related protein Rab-8A-like, transcript variant X2
ras-related protein Rab-8A-like isoform X1
ras-related protein Rab-8A-like isoform X2
DNA polymerase epsilon catalytic subunit 1
DDB1- and CUL4-associated factor 10 homolog, 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 126 samples with support for all annotated introns
DDB1- and CUL4-associated factor 10 homolog, 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 130 samples with support for all annotated introns
DDB1- and CUL4-associated factor 10 homolog, 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 17 samples with support for all annotated introns
DDB1- and CUL4-associated factor 10 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 107 samples with support for all annotated introns
DDB1- and CUL4-associated factor 10 homolog, transcript variant X5
DDB1- and CUL4-associated factor 10 isoform X1
DDB1- and CUL4-associated factor 10 isoform X2
DDB1- and CUL4-associated factor 10 isoform X3
DDB1- and CUL4-associated factor 10 homolog isoform X4
DDB1- and CUL4-associated factor 10 homolog isoform X5
electron transfer flavoprotein subunit beta
signal recognition particle 54 kDa protein
CCA tRNA nucleotidyltransferase 1, mitochondrial, transcript variant X2
CCA tRNA nucleotidyltransferase 1, mitochondrial, transcript variant X1
CCA tRNA nucleotidyltransferase 1, mitochondrial isoform X1
CCA tRNA nucleotidyltransferase 1, mitochondrial isoform X2
abscission/NoCut checkpoint regulator, transcript variant X2
abscission/NoCut checkpoint regulator, transcript variant X1
abscission/NoCut checkpoint regulator isoform X2
abscission/NoCut checkpoint regulator isoform X1
L-threonine ammonia-lyase-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 2 samples with support for all annotated introns
L-threonine ammonia-lyase-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 4 samples with support for all annotated introns
L-threonine dehydratase catabolic TdcB-like isoform X2
L-threonine ammonia-lyase-like isoform X1
L-threonine dehydratase catabolic TdcB-like
DNA-directed RNA polymerase II subunit RPB3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
photoreceptor outer segment membrane glycoprotein 2-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 2 samples with support for all annotated introns
isopentenyl-diphosphate Delta-isomerase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 127 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC125054703, transcript variant X1
uncharacterized LOC125054703, transcript variant X2
uncharacterized protein LOC125054703 isoform X1
uncharacterized protein LOC125054703 isoform X2
transmembrane protein 245, transcript variant X2
transmembrane protein 245, transcript variant X1
transmembrane protein 245, transcript variant X3
transmembrane protein 245, transcript variant X4
uncharacterized LOC125054812, transcript variant X2
uncharacterized LOC125054812, transcript variant X3
uncharacterized LOC125054812, transcript variant X1
uncharacterized LOC125054812, transcript variant X4
uncharacterized LOC125054812, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC125054812 isoform X4
uncharacterized protein LOC125054812 isoform X1
uncharacterized protein LOC125054812 isoform X2
uncharacterized protein LOC125054812 isoform X3
uncharacterized protein LOC125054812 isoform X5
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B, transcript variant X3
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B, transcript variant X4
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B, transcript variant X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B isoform X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B isoform X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 147 samples with support for all annotated introns
uncharacterized LOC125054832, transcript variant X2
uncharacterized LOC125054832, transcript variant X1
uncharacterized LOC125054781, transcript variant X22
uncharacterized LOC125054781, transcript variant X10
uncharacterized LOC125054781, transcript variant X21
uncharacterized LOC125054781, transcript variant X26
uncharacterized LOC125054781, transcript variant X18
uncharacterized LOC125054781, transcript variant X11
uncharacterized LOC125054781, transcript variant X24
uncharacterized LOC125054781, transcript variant X19
uncharacterized LOC125054781, transcript variant X6
uncharacterized LOC125054781, transcript variant X4
uncharacterized LOC125054781, transcript variant X7
uncharacterized LOC125054781, transcript variant X14
uncharacterized LOC125054781, transcript variant X20
uncharacterized LOC125054781, transcript variant X25
uncharacterized LOC125054781, transcript variant X12
uncharacterized LOC125054781, transcript variant X17
uncharacterized LOC125054781, transcript variant X23
uncharacterized LOC125054781, transcript variant X8
uncharacterized LOC125054781, transcript variant X13
uncharacterized LOC125054781, transcript variant X5
uncharacterized LOC125054781, transcript variant X3
uncharacterized LOC125054781, transcript variant X2
uncharacterized LOC125054781, transcript variant X1
uncharacterized LOC125054781, transcript variant X9
uncharacterized protein LOC125054781 isoform X3
uncharacterized protein LOC125054781 isoform X20
uncharacterized protein LOC125054781 isoform X19
uncharacterized protein LOC125054781 isoform X18
uncharacterized protein LOC125054781 isoform X16
uncharacterized protein LOC125054781 isoform X9
uncharacterized protein LOC125054781 isoform X23
uncharacterized protein LOC125054781 isoform X17
uncharacterized protein LOC125054781 isoform X10
uncharacterized protein LOC125054781 isoform X4
uncharacterized protein LOC125054781 isoform X15
uncharacterized protein LOC125054781 isoform X21
uncharacterized protein LOC125054781 isoform X6
uncharacterized protein LOC125054781 isoform X2
uncharacterized protein LOC125054781 isoform X5
uncharacterized protein LOC125054781 isoform X12
uncharacterized protein LOC125054781 isoform X11
uncharacterized protein LOC125054781 isoform X1
uncharacterized protein LOC125054781 isoform X7
uncharacterized protein LOC125054781 isoform X8
uncharacterized protein LOC125054781 isoform X24
uncharacterized protein LOC125054781 isoform X22
uncharacterized LOC125054781, 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 10 samples with support for all annotated introns
uncharacterized LOC125054781, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC125054781 isoform X14
uncharacterized protein LOC125054781 isoform X13
uncharacterized LOC125054783, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC125054783, 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 151 samples with support for all annotated introns
uncharacterized LOC125054783, transcript variant X3
uncharacterized LOC125054783, transcript variant X2
transient receptor potential channel pyrexia-like, transcript variant X3
transient receptor potential channel pyrexia-like isoform X3
ubiquinone biosynthesis monooxygenase COQ6, mitochondrial
transient receptor potential channel pyrexia-like, transcript variant X2
transient receptor potential channel pyrexia-like isoform X2
transient receptor potential channel pyrexia-like, transcript variant X1
transient receptor potential channel pyrexia-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein LOC125054800 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
CLIP domain-containing serine protease HP8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
synaptosomal-associated protein 25, transcript variant X5
synaptosomal-associated protein 25, transcript variant X1
synaptosomal-associated protein 25, transcript variant X2
synaptosomal-associated protein 25, transcript variant X3
synaptosomal-associated protein 25, transcript variant X4
synaptosomal-associated protein 25 isoform X1
synaptosomal-associated protein 25 isoform X2
synaptosomal-associated protein 25 isoform X3
synaptosomal-associated protein 25 isoform X4
synaptosomal-associated protein 25 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins
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 129 samples with support for all annotated introns
beta-1,3-galactosyltransferase 5-like, transcript variant X4
beta-1,3-galactosyltransferase 5-like, transcript variant X5
beta-1,3-galactosyltransferase 5-like, transcript variant X1
beta-1,3-galactosyltransferase 5-like, transcript variant X3
beta-1,3-galactosyltransferase 5-like, transcript variant X2
beta-1,3-galactosyltransferase 5-like isoform X1
beta-1,3-galactosyltransferase 5-like isoform X2
uncharacterized LOC125054395, transcript variant X1
uncharacterized LOC125054395, transcript variant X2
uncharacterized protein LOC125054395 isoform X2
uncharacterized protein LOC125054395 isoform X1
uncharacterized LOC125054878, transcript variant X1
uncharacterized LOC125054878, transcript variant X2
zinc finger protein 239-like, transcript variant X5
zinc finger protein 239-like, transcript variant X2
zinc finger protein 239-like, transcript variant X4
zinc finger protein 239-like, transcript variant X1
zinc finger protein 239-like, transcript variant X6
zinc finger protein 239-like, transcript variant X3
RNA helicase aquarius-like, transcript variant X1
RNA helicase aquarius-like, transcript variant X2
probable G-protein coupled receptor Mth-like 5, transcript variant X4
probable G-protein coupled receptor Mth-like 5, transcript variant X3
probable G-protein coupled receptor Mth-like 5 isoform X4
probable G-protein coupled receptor Mth-like 5 isoform X3
probable G-protein coupled receptor Mth-like 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 149 samples with support for all annotated introns
probable G-protein coupled receptor Mth-like 5 isoform X2
uncharacterized LOC125054881, transcript variant X1
uncharacterized LOC125054881, 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 5 samples with support for all annotated introns
probable G-protein coupled receptor Mth-like 5, transcript variant X1
probable G-protein coupled receptor Mth-like 5 isoform X1
probable G-protein coupled receptor Mth-like 4
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 160 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cytochrome P450 4V2-like, transcript variant X3
cytochrome P450 4V2-like, transcript variant X1
cytochrome P450 4V2-like, transcript variant X2
cytochrome P450 4V2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ubiquitin-like domain-containing CTD phosphatase 1
uncharacterized LOC125054541, transcript variant X2
uncharacterized LOC125054541, transcript variant X1
uncharacterized protein LOC125054541 isoform X2
uncharacterized protein LOC125054541 isoform X1
rho-related BTB domain-containing protein 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 20 samples with support for all annotated introns
rho-related BTB domain-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
rho-related BTB domain-containing protein 1, 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 27 samples with support for all annotated introns
rho-related BTB domain-containing protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
rho-related BTB domain-containing protein 1 isoform X2
rho-related BTB domain-containing protein 1 isoform X1
rho-related BTB domain-containing protein 1 isoform X3
H/ACA ribonucleoprotein complex subunit 2-like protein
uncharacterized LOC125054895, 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 42 samples with support for all annotated introns
uncharacterized LOC125054895, 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 1 sample with support for all annotated introns
myb/SANT-like DNA-binding domain-containing protein 3, transcript variant X2
myb/SANT-like DNA-binding domain-containing protein 3, transcript variant X1
myb/SANT-like DNA-binding domain-containing protein 3
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
uncharacterized LOC125054868, transcript variant X1
uncharacterized LOC125054868, transcript variant X3
uncharacterized LOC125054868, transcript variant X4
uncharacterized LOC125054868, transcript variant X2
uncharacterized LOC125054868, transcript variant X5
uncharacterized protein LOC125054868 isoform X1
uncharacterized protein LOC125054868 isoform X2
uncharacterized protein LOC125054868 isoform X5
uncharacterized protein LOC125054868 isoform X4
uncharacterized protein LOC125054868 isoform X3
uncharacterized LOC125054773, transcript variant X2
uncharacterized LOC125054773, transcript variant X1
uncharacterized protein LOC125054773 isoform X2
uncharacterized protein LOC125054773 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 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 12 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 23 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 10 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 91% 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, including 20 samples with support for all annotated introns
cGMP-specific 3',5'-cyclic phosphodiesterase-like, transcript variant X2
cGMP-specific 3',5'-cyclic phosphodiesterase-like, transcript variant X1
cGMP-specific 3',5'-cyclic phosphodiesterase-like isoform X1
cGMP-specific 3',5'-cyclic phosphodiesterase-like isoform X2
acyl-CoA Delta-9 desaturase-like, transcript variant X2
acyl-CoA Delta-9 desaturase-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 1 sample with support for all annotated introns
leucine-rich repeat-containing protein 27-like
protein glass-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
protein glass-like, transcript variant X3
protein glass-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 26 samples with support for all annotated introns
F-box/LRR-repeat protein 2, transcript variant X2
F-box/LRR-repeat protein 2, transcript variant X3
F-box/LRR-repeat protein 2, transcript variant X1
C-terminal-binding protein, transcript variant X1
C-terminal-binding protein, transcript variant X2
cilia- and flagella-associated protein 58-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
alpha-sarcoglycan, transcript variant X2
alpha-sarcoglycan, 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 70 samples with support for all annotated introns
uncharacterized protein LOC125054517 isoform X1
inositol polyphosphate-5-phosphatase A, transcript variant X2
inositol polyphosphate-5-phosphatase A, transcript variant X3
inositol polyphosphate-5-phosphatase A, transcript variant X1
inositol polyphosphate-5-phosphatase A isoform X2
inositol polyphosphate-5-phosphatase A isoform X3
inositol polyphosphate-5-phosphatase A isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
octopamine receptor beta-2R, transcript variant X2
octopamine receptor beta-2R, transcript variant X1
sodium-coupled monocarboxylate transporter 2, transcript variant X1
sodium-coupled monocarboxylate transporter 2, transcript variant X2
sodium-coupled monocarboxylate transporter 2
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 40 samples with support for all annotated introns
dedicator of cytokinesis protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 108 samples with support for all annotated introns
dedicator of cytokinesis protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
dedicator of cytokinesis protein 1, 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 98 samples with support for all annotated introns
dedicator of cytokinesis protein 1, 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 54 samples with support for all annotated introns
dedicator of cytokinesis protein 1 isoform X5
dedicator of cytokinesis protein 1 isoform X2
dedicator of cytokinesis protein 1 isoform X3
dedicator of cytokinesis protein 1 isoform X1
dedicator of cytokinesis protein 1, transcript variant X4
dedicator of cytokinesis protein 1 isoform X4
uncharacterized LOC125054906, transcript variant X4
uncharacterized LOC125054906, transcript variant X3
uncharacterized LOC125054906, transcript variant X2
uncharacterized LOC125054906, transcript variant X1
uncharacterized protein LOC125054906 isoform X1
uncharacterized protein LOC125054906 isoform X3
uncharacterized protein LOC125054906 isoform X2
uncharacterized protein LOC125054906 isoform X4
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine protease HTRA2, mitochondrial, transcript variant X1
serine protease HTRA2, mitochondrial isoform X1
serine protease HTRA2, mitochondrial, transcript variant X2
serine protease HTRA2, mitochondrial isoform X2
probable phospholipid hydroperoxide glutathione peroxidase
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
facilitated trehalose transporter Tret1-like
uncharacterized LOC125054698, transcript variant X3
uncharacterized LOC125054698, transcript variant X2
uncharacterized LOC125054698, transcript variant X1
uncharacterized protein LOC125054698 isoform X2
uncharacterized protein LOC125054698 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 109 samples with support for all annotated introns
glutamine-dependent NAD(+) synthetase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC125054929, transcript variant X2
uncharacterized LOC125054929, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
nucleoplasmin-like protein, transcript variant X2
nucleoplasmin-like protein, transcript variant X1
actin-binding LIM protein 2, transcript variant X5
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 20 samples with support for all annotated introns
actin-binding LIM protein 2, transcript variant X4
actin-binding LIM protein 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 90 samples with support for all annotated introns
actin-binding LIM protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
actin-binding LIM protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 150 samples with support for all annotated introns
actin-binding LIM protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 159 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 159 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 136 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 116 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
pyridoxal phosphate homeostasis protein, transcript variant X2
pyridoxal phosphate homeostasis protein, transcript variant X1
uncharacterized LOC125054569, transcript variant X1
uncharacterized LOC125054569, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125054412, transcript variant X1
uncharacterized LOC125054412, transcript variant X2
serine/threonine-protein phosphatase PP2A 65 kDa regulatory subunit
4-hydroxybutyrate coenzyme A transferase
casein kinase I-like, transcript variant X2
casein kinase I-like, transcript variant X1
casein kinase I-like, transcript variant X3
casein kinase I-like, transcript variant X4
probable sodium/potassium/calcium exchanger CG1090
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
fumarylacetoacetate hydrolase domain-containing protein 2
39S ribosomal protein L35, mitochondrial, transcript variant X1
39S ribosomal protein L35, mitochondrial, transcript variant X2
39S ribosomal protein L35, mitochondrial isoform X1
39S ribosomal protein L35, mitochondrial isoform X2
MICOS complex subunit Mic60, transcript variant X1
MICOS complex subunit Mic60, transcript variant X2
serine/threonine-protein kinase pelle-like
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 169 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
myrosinase 1-like, transcript variant X4
myrosinase 1-like, transcript variant X2
myrosinase 1-like, transcript variant X3
myrosinase 1-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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 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 97% coverage of the annotated genomic feature by RNAseq alignments
lateral signaling target protein 2 homolog, transcript variant X1
lateral signaling target protein 2 homolog, transcript variant X2
lateral signaling target protein 2 homolog isoform X1
lateral signaling target protein 2 homolog isoform 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 72 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 95% coverage of the annotated genomic feature by RNAseq alignments
methenyltetrahydrofolate synthase domain-containing protein
cell growth-regulating nucleolar protein
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
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
DNA mismatch repair protein Mlh1, transcript variant X2
DNA mismatch repair protein Mlh1, transcript variant X1
DNA mismatch repair protein Mlh1 isoform X2
DNA mismatch repair protein Mlh1 isoform X1
DNA mismatch repair protein Mlh1, transcript variant X3
snRNA-activating protein complex subunit 4
uncharacterized LOC125054720, transcript variant X5
uncharacterized LOC125054720, transcript variant X4
uncharacterized LOC125054720, transcript variant X1
uncharacterized LOC125054720, transcript variant X3
uncharacterized LOC125054720, transcript variant X2
uncharacterized LOC125054720, transcript variant X6
uncharacterized protein LOC125054720 isoform X3
uncharacterized protein LOC125054720 isoform X2
uncharacterized protein LOC125054720 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 40 samples with support for all annotated introns
somatostatin receptor type 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
somatostatin receptor type 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
somatostatin receptor type 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
nuclear receptor-binding protein homolog
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 83 samples with support for all annotated introns
uncharacterized protein DDB_G0283697-like
lymphokine-activated killer T-cell-originated protein kinase
ankyrin repeat domain-containing protein 29
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein tiptop-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
protein tiptop-like, 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 107 samples with support for all annotated introns
probable peroxisomal membrane protein PEX13
probable DNA replication complex GINS protein PSF2
TNF receptor-associated factor 4, transcript variant X3
TNF receptor-associated factor 4, transcript variant X1
TNF receptor-associated factor 4, transcript variant X2
TNF receptor-associated factor 4, transcript variant X4
TNF receptor-associated factor 4 isoform X3
TNF receptor-associated factor 4 isoform X1
TNF receptor-associated factor 4 isoform X2
TNF receptor-associated factor 4 isoform X4
cytochrome b5 domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
serine/threonine-protein kinase Aurora-2
glutamate receptor ionotropic, kainate glr-3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 3-like, transcript variant X1
peroxisomal acyl-coenzyme A oxidase 3-like, transcript variant X2
peroxisomal acyl-coenzyme A oxidase 3-like
beta-1,3-glucosyltransferase, transcript variant X2
beta-1,3-glucosyltransferase, transcript variant X1
integrin alpha-PS2, transcript variant X2
integrin alpha-PS2, transcript variant X1
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
39S ribosomal protein L50, mitochondrial
mediator of RNA polymerase II transcription subunit 13, transcript variant X2
mediator of RNA polymerase II transcription subunit 13, transcript variant X1
mediator of RNA polymerase II transcription subunit 13 isoform X1
mediator of RNA polymerase II transcription subunit 13 isoform 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 169 samples with support for all annotated introns
protein outspread-like, transcript variant X1
protein outspread-like, transcript variant X2
protein outspread-like, transcript variant X3
leucine-rich repeat-containing protein 74B-like
NLR family CARD domain-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 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 63 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 3-like isoform X1
peroxisomal acyl-coenzyme A oxidase 3-like, transcript variant X3
peroxisomal acyl-coenzyme A oxidase 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 139 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 3-like isoform X2
peroxisomal acyl-coenzyme A oxidase 3-like isoform X3
SH3 domain-binding protein 5 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 164 samples with support for all annotated introns
SH3 domain-binding protein 5 homolog, 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 164 samples with support for all annotated introns
SH3 domain-binding protein 5 homolog isoform X2
SH3 domain-binding protein 5 homolog isoform X1
sin3 histone deacetylase corepressor complex component SDS3
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 168 samples with support for all annotated introns
tumor protein p63-regulated gene 1-like 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 22 samples with support for all annotated introns
tumor protein p63-regulated gene 1-like protein, 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 139 samples with support for all annotated introns
tumor protein p63-regulated gene 1-like protein, 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 156 samples with support for all annotated introns
tumor protein p63-regulated gene 1-like protein isoform X1
tumor protein p63-regulated gene 1-like protein isoform X2
tumor protein p63-regulated gene 1-like protein isoform X3
transfer RNA alanine (anticodon AGC); 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
uncharacterized LOC125054803, 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 33 samples with support for all annotated introns
uncharacterized LOC125054803, 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 45 samples with support for all annotated introns
uncharacterized protein LOC125054803 isoform X1
uncharacterized protein LOC125054803 isoform X2
uncharacterized LOC125054803, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC125054803 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 25 member 35-like, transcript variant X6
solute carrier family 25 member 35-like, transcript variant X2
solute carrier family 25 member 35-like, transcript variant X1
solute carrier family 25 member 35-like, transcript variant X7
solute carrier family 25 member 35-like, transcript variant X3
solute carrier family 25 member 35-like, transcript variant X4
solute carrier family 25 member 35-like isoform X6
solute carrier family 25 member 35-like isoform X2
solute carrier family 25 member 35-like isoform X1
solute carrier family 25 member 35-like isoform X3
solute carrier family 25 member 35-like isoform X4
solute carrier family 25 member 35-like isoform X7
solute carrier family 25 member 35-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
solute carrier family 25 member 35-like isoform X5
solute carrier family 25 member 35-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 168 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 168 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 121 samples with support for all annotated introns
solute carrier family 25 member 34-like isoform X2
solute carrier family 2, facilitated glucose transporter member 3-like, transcript variant X1
solute carrier family 2, facilitated glucose transporter member 3-like, transcript variant X3
solute carrier family 2, facilitated glucose transporter member 3-like, transcript variant X2
solute carrier family 2, facilitated glucose transporter member 3-like, transcript variant X4
solute carrier family 2, facilitated glucose transporter member 5-like isoform X1
solute carrier family 2, facilitated glucose transporter member 5-like isoform X2
solute carrier family 2, facilitated glucose transporter member 3-like isoform X3
protein HIRA homolog, transcript variant X1
protein HIRA homolog, transcript variant X2
death-associated protein kinase related, transcript variant X1
death-associated protein kinase related, transcript variant X2
death-associated protein kinase related isoform X2
death-associated protein kinase related isoform X1
DNA-directed RNA polymerase III subunit RPC9-like, transcript variant X4
DNA-directed RNA polymerase III subunit RPC9-like, transcript variant X5
DNA-directed RNA polymerase III subunit RPC9-like, transcript variant X2
DNA-directed RNA polymerase III subunit RPC9-like, transcript variant X6
DNA-directed RNA polymerase III subunit RPC9-like, transcript variant X3
DNA-directed RNA polymerase III subunit RPC9-like, transcript variant X1
DNA-directed RNA polymerase III subunit RPC9-like
glutamine synthetase 1, mitochondrial-like
plasminogen activator inhibitor 1 RNA-binding protein-like
E3 ubiquitin-protein ligase HECW2, transcript variant X2
E3 ubiquitin-protein ligase HECW2, transcript variant X1
E3 ubiquitin-protein ligase HECW2, transcript variant X3
E3 ubiquitin-protein ligase HECW2, transcript variant X4
uncharacterized protein LOC125054366 isoform X2
uncharacterized protein LOC125054366 isoform X1
E3 ubiquitin-protein ligase HECW2 isoform X3
E3 ubiquitin-protein ligase HECW2 isoform X4
uncharacterized LOC125054368, transcript variant X1
uncharacterized LOC125054368, transcript variant X2
uncharacterized LOC125054368, transcript variant X3
uncharacterized protein LOC125054368 isoform X1
uncharacterized protein LOC125054368 isoform X2
uncharacterized protein LOC125054368 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 166 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 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
uncharacterized LOC125054622, transcript variant X1
uncharacterized protein LOC125054622 isoform X1
uncharacterized LOC125054622, transcript variant X2
uncharacterized protein LOC125054622 isoform X2
serine/arginine repetitive matrix protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
serine/arginine repetitive matrix protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
serine/arginine repetitive matrix protein 2, 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 37 samples with support for all annotated introns
serine/arginine repetitive matrix protein 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
serine/arginine repetitive matrix protein 2, transcript variant X7
serine/arginine repetitive matrix protein 2, transcript variant X6
serine/arginine repetitive matrix protein 2, transcript variant X9
serine/arginine repetitive matrix protein 2, transcript variant X8
serine/arginine repetitive matrix protein 2, transcript variant X10
serine/arginine repetitive matrix protein 2, transcript variant X12
serine/arginine repetitive matrix protein 2, transcript variant X11
serine/arginine repetitive matrix protein 2 isoform X1
serine/arginine repetitive matrix protein 2 isoform X3
serine/arginine repetitive matrix protein 2 isoform X4
serine/arginine repetitive matrix protein 2 isoform X5
serine/arginine repetitive matrix protein 2 isoform X6
serine/arginine repetitive matrix protein 2 isoform X8
serine/arginine repetitive matrix protein 2 isoform X10
serine/arginine repetitive matrix protein 2 isoform X7
serine/arginine repetitive matrix protein 2 isoform X9
serine/arginine repetitive matrix protein 2 isoform X11
serine/arginine repetitive matrix protein 2 isoform X12
serine/arginine repetitive matrix protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
serine/arginine repetitive matrix protein 2, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase G isoform X2
peptidyl-prolyl cis-trans isomerase G isoform X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 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 117 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125054778
thioredoxin domain-containing protein 17-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 163 samples with support for all annotated introns
armadillo repeat-containing protein gudu
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 167 samples with support for all annotated introns
RNA polymerase I-specific transcription initiation factor RRN3
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 166 samples with support for all annotated introns
guanine nucleotide-binding protein subunit alpha homolog
integrin alpha-D-like, transcript variant X2
integrin alpha-D-like, transcript variant X1
uncharacterized LOC125054523, transcript variant X1
uncharacterized LOC125054523, 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 18 samples with support for all annotated introns
serine/threonine-protein kinase NLK, transcript variant X1
serine/threonine-protein kinase NLK, transcript variant X2
serine/threonine-protein kinase NLK, transcript variant X3
serine/threonine-protein kinase NLK isoform X2
serine/threonine-protein kinase NLK isoform X1
serine/threonine-protein kinase NLK isoform X3
ankyrin repeat and MYND domain-containing protein 2
zinc finger CCHC domain-containing protein 8 homolog
28S ribosomal protein S22, mitochondrial
calcium release-activated calcium channel protein 1, transcript variant X1
calcium release-activated calcium channel protein 1, transcript variant X5
calcium release-activated calcium channel protein 1, transcript variant X4
calcium release-activated calcium channel protein 1, transcript variant X3
calcium release-activated calcium channel protein 1, transcript variant X2
calcium release-activated calcium channel protein 1 isoform X1
calcium release-activated calcium channel protein 1 isoform X2
FGGY carbohydrate kinase domain-containing protein
uncharacterized LOC125054776, transcript variant X2
uncharacterized LOC125054776, transcript variant X3
uncharacterized LOC125054776, transcript variant X4
uncharacterized LOC125054776, transcript variant X1
uncharacterized protein LOC125054776 isoform X2
uncharacterized protein LOC125054776 isoform X3
uncharacterized protein LOC125054776 isoform X1
uncharacterized LOC125054776, transcript variant X6
uncharacterized LOC125054776, transcript variant X9
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
uncharacterized LOC125054776, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC125054776 isoform X5
uncharacterized LOC125054776, transcript variant X5
uncharacterized LOC125054776, transcript variant X7
uncharacterized protein LOC125054776 isoform X4
uncharacterized LOC125054776, transcript variant X11
uncharacterized LOC125054776, transcript variant X10
uncharacterized protein LOC125054776 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 132 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
sulfotransferase 1C4-like, transcript variant X2
sulfotransferase 1C4-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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 4 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium/calcium exchanger regulatory protein 1-like, transcript variant X1
sodium/calcium exchanger regulatory protein 1-like, transcript variant X2
sodium/calcium exchanger regulatory protein 1-like
ADP-ribosylation factor-like protein 6-interacting protein 1
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X5
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X2
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X4
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X1
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X7
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X6
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X3
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X8
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase isoform X7
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase isoform X4
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase isoform X6
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase isoform X5
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase isoform X2
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase isoform X3
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase isoform X1
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X10
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 70 samples with support for all annotated introns
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X9
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase isoform X8
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase, transcript variant X11
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase isoform X9
probable tRNA (uracil-O(2)-)-methyltransferase
putative aldehyde dehydrogenase family 7 member A1 homolog
rRNA N6-adenosine-methyltransferase Mettl5, transcript variant X1
rRNA N6-adenosine-methyltransferase Mettl5 isoform X1
rRNA N6-adenosine-methyltransferase Mettl5, 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 42 samples with support for all annotated introns
rRNA N6-adenosine-methyltransferase METTL5 isoform X2
protein tramtrack, alpha isoform-like, transcript variant X2
protein tramtrack, alpha isoform-like, transcript variant X1
protein tramtrack, alpha isoform-like isoform X2
protein tramtrack, alpha isoform-like isoform X1
3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial
neuferricin homolog, transcript variant X2
neuferricin homolog, transcript variant X1
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type, transcript variant X4
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type, transcript variant X5
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type isoform X2
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type isoform X3
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type, transcript variant X2
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type, transcript variant X1
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type, transcript variant X3
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type isoform X1
pre-piRNA 3'-exonuclease trimmer-like, transcript variant X1
pre-piRNA 3'-exonuclease trimmer-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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 154 samples with support for all annotated introns
slit homolog 1 protein, 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 36 samples with support for all annotated introns
slit homolog 1 protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
slit homolog 1 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 39 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 72% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA histidin (anticodon GUG); 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: 47 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 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: 8 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: 45 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
kelch domain-containing protein 10 homolog
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 168 samples with support for all annotated introns
zinc finger CW-type PWWP domain protein 1-like, transcript variant X1
zinc finger CW-type PWWP domain protein 1-like, transcript variant X2
zinc finger CW-type PWWP domain protein 1-like isoform X1
zinc finger CW-type PWWP domain protein 1-like, transcript variant X3
zinc finger CW-type PWWP domain protein 1-like isoform X2
GTP-binding nuclear protein Ran, transcript variant X1
GTP-binding nuclear protein Ran, 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 159 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 167 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB11
putative autophagy-related protein 11, transcript variant X1
putative autophagy-related protein 11, transcript variant X2
putative autophagy-related protein 11 isoform X1
putative autophagy-related protein 11 isoform X2
uncharacterized LOC125054628, 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 3 samples with support for all annotated introns
uncharacterized LOC125054628, 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 17 samples with support for all annotated introns
uncharacterized LOC125054628, transcript variant X2
uncharacterized protein LOC125054628 isoform X1
uncharacterized protein LOC125054628 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase N2, transcript variant X4
receptor-type tyrosine-protein phosphatase N2, transcript variant X3
receptor-type tyrosine-protein phosphatase N2, transcript variant X1
receptor-type tyrosine-protein phosphatase N2, transcript variant X6
receptor-type tyrosine-protein phosphatase N2, transcript variant X5
receptor-type tyrosine-protein phosphatase N2, transcript variant X2
receptor-type tyrosine-protein phosphatase N2 isoform X5
receptor-type tyrosine-protein phosphatase N2 isoform X4
uncharacterized protein LOC125054292 isoform X3
receptor-type tyrosine-protein phosphatase N2 isoform X2
receptor-type tyrosine-protein phosphatase N2 isoform X1
activated Cdc42 kinase Ack, transcript variant X2
activated Cdc42 kinase Ack, transcript variant X1
cilia- and flagella-associated protein 65-like
S1 RNA-binding domain-containing protein 1
protein-lysine N-methyltransferase EEF2KMT
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 164 samples with support for all annotated introns
mitochondrial inner membrane protease ATP23 homolog
glycine receptor subunit alpha-3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
glycine receptor subunit alpha-3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
glycine receptor subunit alpha-3-like, transcript variant X1
glycine receptor subunit alpha-3-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
glycine receptor subunit alpha-3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 80 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit delta-like isoform X2
glycine receptor subunit alpha-3-like isoform X5
glycine receptor subunit alpha-4-like isoform X3
glycine receptor subunit alpha-4-like isoform X1
glycine receptor subunit alpha-4-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1
7SK snRNA methylphosphate capping enzyme bin3-like
inositol-trisphosphate 3-kinase homolog, transcript variant X1
inositol-trisphosphate 3-kinase homolog, transcript variant X4
inositol-trisphosphate 3-kinase homolog, transcript variant X2
inositol-trisphosphate 3-kinase homolog, transcript variant X3
inositol-trisphosphate 3-kinase homolog isoform X1
inositol-trisphosphate 3-kinase homolog isoform X4
inositol-trisphosphate 3-kinase homolog isoform X2
inositol-trisphosphate 3-kinase homolog 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 55 samples with support for all annotated introns
vacuolar protein sorting-associated protein 53 homolog, transcript variant X1
vacuolar protein sorting-associated protein 53 homolog isoform X1
vacuolar protein sorting-associated protein 53 homolog, transcript variant X2
vacuolar protein sorting-associated protein 53 homolog isoform X2
kinase D-interacting substrate of 220 kDa B, transcript variant X8
kinase D-interacting substrate of 220 kDa B, transcript variant X1
kinase D-interacting substrate of 220 kDa B, transcript variant X3
kinase D-interacting substrate of 220 kDa B, transcript variant X2
kinase D-interacting substrate of 220 kDa B, transcript variant X4
kinase D-interacting substrate of 220 kDa B isoform X1
kinase D-interacting substrate of 220 kDa B isoform X3
kinase D-interacting substrate of 220 kDa B isoform X2
kinase D-interacting substrate of 220 kDa B isoform X4
kinase D-interacting substrate of 220 kDa B, transcript variant X10
kinase D-interacting substrate of 220 kDa B, transcript variant X5
kinase D-interacting substrate of 220 kDa B isoform X5
kinase D-interacting substrate of 220 kDa B, transcript variant X6
kinase D-interacting substrate of 220 kDa B isoform X6
kinase D-interacting substrate of 220 kDa B, transcript variant X9
kinase D-interacting substrate of 220 kDa B, transcript variant X7
kinase D-interacting substrate of 220 kDa B isoform X7
kinase D-interacting substrate of 220 kDa B isoform X8
late secretory pathway protein AVL9 homolog
serine/threonine-protein kinase tousled-like 2, transcript variant X2
serine/threonine-protein kinase tousled-like 2, transcript variant X4
serine/threonine-protein kinase tousled-like 2, transcript variant X6
serine/threonine-protein kinase tousled-like 2 isoform X2
serine/threonine-protein kinase tousled-like 2 isoform X4
serine/threonine-protein kinase tousled-like 2, transcript variant X1
serine/threonine-protein kinase tousled-like 2, transcript variant X3
serine/threonine-protein kinase tousled-like 2, transcript variant X7
serine/threonine-protein kinase tousled-like 2 isoform X1
serine/threonine-protein kinase tousled-like 2 isoform X3
serine/threonine-protein kinase tousled-like 2, transcript variant X5
serine/threonine-protein kinase tousled-like 2, transcript variant X8
serine/threonine-protein kinase tousled-like 2 isoform X5
serine/threonine-protein kinase tousled-like 2, transcript variant X9
serine/threonine-protein kinase tousled-like 2 isoform X6
Ca(2+)/calmodulin-responsive adenylate cyclase, transcript variant X2
Ca(2+)/calmodulin-responsive adenylate cyclase, transcript variant X1
Ca(2+)/calmodulin-responsive adenylate cyclase, transcript variant X3
histone-lysine N-methyltransferase SETMAR-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
Ca(2+)/calmodulin-responsive adenylate cyclase isoform X1
Ca(2+)/calmodulin-responsive adenylate cyclase isoform X2
Ca(2+)/calmodulin-responsive adenylate cyclase isoform X3
partitioning defective 3 homolog, transcript variant X1
partitioning defective 3 homolog, transcript variant X5
partitioning defective 3 homolog, transcript variant X9
partitioning defective 3 homolog, transcript variant X10
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
partitioning defective 3 homolog isoform X1
partitioning defective 3 homolog isoform X3
partitioning defective 3 homolog isoform X5
partitioning defective 3 homolog, transcript variant X2
partitioning defective 3 homolog, transcript variant X4
partitioning defective 3 homolog, transcript variant X3
partitioning defective 3 homolog isoform X2
partitioning defective 3 homolog, transcript variant X6
partitioning defective 3 homolog, transcript variant X7
partitioning defective 3 homolog, transcript variant X8
partitioning defective 3 homolog isoform X4
diacylglycerol lipase-beta, transcript variant X2
diacylglycerol lipase-beta, transcript variant X1
diacylglycerol lipase-beta, transcript variant X4
diacylglycerol lipase-beta, transcript variant X3
diacylglycerol lipase-beta, 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 69 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
intraflagellar transport protein 20 homolog A-like
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3
heparan sulfate glucosamine 3-O-sulfotransferase 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 5
NCK-interacting protein with SH3 domain, transcript variant X1
NCK-interacting protein with SH3 domain, transcript variant X2
NCK-interacting protein with SH3 domain, transcript variant X3
NCK-interacting protein with SH3 domain, transcript variant X4
NCK-interacting protein with SH3 domain isoform X1
NCK-interacting protein with SH3 domain isoform X3
NCK-interacting protein with SH3 domain isoform X2
NCK-interacting protein with SH3 domain isoform X4
plasma membrane ascorbate-dependent reductase CYBRD1-like, transcript variant X4
plasma membrane ascorbate-dependent reductase CYBRD1-like, transcript variant X1
plasma membrane ascorbate-dependent reductase CYBRD1-like, transcript variant X3
plasma membrane ascorbate-dependent reductase CYBRD1-like, transcript variant X6
plasma membrane ascorbate-dependent reductase CYBRD1-like, transcript variant X5
plasma membrane ascorbate-dependent reductase CYBRD1-like isoform X4
plasma membrane ascorbate-dependent reductase CYBRD1-like isoform X1
plasma membrane ascorbate-dependent reductase CYBRD1-like isoform X3
plasma membrane ascorbate-dependent reductase CYBRD1-like isoform X6
plasma membrane ascorbate-dependent reductase CYBRD1-like isoform X5
plasma membrane ascorbate-dependent reductase CYBRD1-like, transcript variant X2
plasma membrane ascorbate-dependent reductase CYBRD1-like isoform X2
25S rRNA (cytosine-C(5))-methyltransferase nop2
coenzyme Q-binding protein COQ10 homolog A, mitochondrial
NAD(+) hydrolase sarm1, transcript variant X1
NAD(+) hydrolase sarm1, transcript variant X2
NAD(+) hydrolase sarm1, transcript variant X3
NAD(+) hydrolase sarm1, transcript variant X4
NAD(+) hydrolase sarm1, transcript variant X6
NAD(+) hydrolase sarm1, transcript variant X5
NAD(+) hydrolase sarm1, transcript variant X7
NAD(+) hydrolase sarm1-like, transcript variant X1
NAD(+) hydrolase sarm1-like, transcript variant X3
NAD(+) hydrolase sarm1-like, transcript variant X2
NAD(+) hydrolase sarm1-like, transcript variant X4
NAD(+) hydrolase sarm1-like, transcript variant X5
NAD(+) hydrolase sarm1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
putative fatty acyl-CoA reductase CG5065, transcript variant X2
putative fatty acyl-CoA reductase CG5065, transcript variant X1
putative fatty acyl-CoA reductase CG5065
macrophage mannose receptor 1-like, transcript variant X2
macrophage mannose receptor 1-like, transcript variant X3
macrophage mannose receptor 1-like isoform X2
macrophage mannose receptor 1-like, transcript variant X1
macrophage mannose receptor 1-like isoform X1
ecdysone receptor, transcript variant X4
ecdysone receptor, transcript variant X3
ecdysone receptor, transcript variant X5
ecdysone receptor, transcript variant X1
ecdysone receptor, transcript variant X2
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
patched domain-containing protein 3, transcript variant X1
patched domain-containing protein 3, transcript variant X2
patched domain-containing protein 3 isoform X1
patched domain-containing protein 3 isoform X2
uncharacterized LOC125054284, transcript variant X4
uncharacterized LOC125054284, transcript variant X3
uncharacterized LOC125054284, transcript variant X2
uncharacterized LOC125054284, transcript variant X1
uncharacterized protein LOC125054284 isoform X3
uncharacterized protein LOC125054284 isoform X2
uncharacterized protein LOC125054284 isoform X1
uncharacterized LOC125054891, transcript variant X2
uncharacterized LOC125054891, transcript variant X1
uncharacterized protein LOC125054891 isoform X1
uncharacterized protein LOC125054891 isoform X2
G-protein coupled receptor dmsr-1-like, transcript variant X4
G-protein coupled receptor dmsr-1-like, transcript variant X3
G-protein coupled receptor dmsr-1-like, transcript variant X1
G-protein coupled receptor dmsr-1-like, transcript variant X2
G-protein coupled receptor dmsr-1-like, transcript variant X5