Plutella xylostella chromosome 17, ilPluXylo3.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Yponomeutoidea; Plutellidae; Plutella.
REFSEQ INFORMATION: The reference sequence is identical to\nOW026572.1.\nAssembly name: ilPluXylo3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/03/10. The original whole-genome shotgun project has the\naccession CAKNZZ000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Plutella xylostella Annotation\n Release 103\nAnnotation Version :: 103\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.
serine hydroxymethyltransferase, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
serine hydroxymethyltransferase isoform X1
serine hydroxymethyltransferase, transcript variant X2
serine hydroxymethyltransferase isoform X2
DNA topoisomerase 3-alpha, transcript variant X2
DNA topoisomerase 3-alpha, transcript variant X1
protein chibby homolog 1, transcript variant X3
protein chibby homolog 1, transcript variant X2
protein chibby homolog 1, transcript variant X1
major facilitator superfamily domain-containing protein 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
transcription initiation factor TFIID subunit 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription initiation factor TFIID subunit 4, 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
transcription initiation factor TFIID subunit 4 isoform X2
nascent polypeptide-associated complex subunit alpha, muscle-specific form isoform X1
glucose-induced degradation protein 4 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119691537, 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 30 samples with support for all annotated introns
uncharacterized LOC119691537, 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 19 samples with support for all annotated introns
uncharacterized protein LOC119691537 isoform X1
uncharacterized protein LOC119691537 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
extracellular serine/threonine protein CG31145, transcript variant X5
extracellular serine/threonine protein CG31145, transcript variant X4
extracellular serine/threonine protein CG31145, transcript variant X2
extracellular serine/threonine protein CG31145, transcript variant X3
extracellular serine/threonine protein CG31145, transcript variant X1
extracellular serine/threonine protein CG31145 isoform X4
extracellular serine/threonine protein CG31145 isoform X2
extracellular serine/threonine protein CG31145 isoform X3
extracellular serine/threonine protein CG31145 isoform X1
extracellular serine/threonine protein CG31145 isoform X5
extracellular serine/threonine protein CG31145, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
zinc finger protein 271, transcript variant X1
zinc finger protein 271, transcript variant X2
zinc finger protein 271, transcript variant X7
zinc finger protein 271, transcript variant X9
zinc finger protein 271, transcript variant X5
zinc finger protein 271, transcript variant X6
zinc finger protein 271, transcript variant X8
zinc finger protein 271, transcript variant X3
zinc finger protein 271, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent T-type calcium channel subunit alpha-1G
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
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 38 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 56 samples with support for all annotated introns
dentin sialophosphoprotein, transcript variant X1
dentin sialophosphoprotein, transcript variant X2
mitochondrial glycine transporter B, transcript variant X1
mitochondrial glycine transporter B isoform X1
mitochondrial glycine transporter B, transcript variant X2
mitochondrial glycine transporter B isoform 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 17 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 89% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105398536, transcript variant X3
uncharacterized LOC105398536, transcript variant X1
uncharacterized LOC105398536, transcript variant X2
uncharacterized protein LOC105398536 isoform X2
uncharacterized protein LOC105398536 isoform X1
uncharacterized protein K02A2.6, transcript variant X2
uncharacterized protein K02A2.6, transcript variant X1
uncharacterized protein K02A2.6 isoform X1
uncharacterized protein LOC119691631 isoform X2
retrovirus-related Pol polyprotein from transposon TNT 1-94
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase CHIP, 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 34 samples with support for all annotated introns
E3 ubiquitin-protein ligase CHIP, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L12, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
cytosolic Fe-S cluster assembly factor NUBP2 homolog
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
sulfotransferase 1C4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
sulfotransferase 1C4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 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 19 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 41 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% 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
uncharacterized LOC105389661, transcript variant X2
uncharacterized LOC105389661, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC105389653, 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
uncharacterized LOC105389653, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
40S ribosomal protein S24; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309110.1
annotated by transcript or proteomic data
The RefSeq transcript has 8 substitutions, 2 frameshifts, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001296039.1
The RefSeq protein has 1 substitution, 2 frameshifts compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
pyridoxal-dependent decarboxylase domain-containing protein 1, transcript variant X2
pyridoxal-dependent decarboxylase domain-containing protein 1, transcript variant X1
pyridoxal-dependent decarboxylase domain-containing protein 1
uncharacterized LOC125489824, transcript variant X1
uncharacterized LOC125489824, transcript variant X2
uncharacterized protein LOC125489824 isoform X1
uncharacterized protein LOC125489824 isoform X2
NADH-ubiquinone oxidoreductase subunit 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
cytochrome P450 9e2-like, transcript variant X3
cytochrome P450 9e2-like, transcript variant X1
cytochrome P450 9e2-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 41 samples with support for all annotated introns
pyridoxal-dependent decarboxylase domain-containing protein 1-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 73 samples with support for all annotated introns
pyridoxal-dependent decarboxylase domain-containing protein 1-like isoform X1
pyridoxal-dependent decarboxylase domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
pyridoxal-dependent decarboxylase domain-containing protein 1-like isoform X2
pyridoxal-dependent decarboxylase domain-containing protein 1-like, transcript variant X3
putative pyridoxal-dependent decarboxylase domain-containing protein 2 isoform X3
cytochrome P450 9e2, transcript variant X2
cytochrome P450 9e2, transcript variant X4
cytochrome P450 9e2, transcript variant X1
cytochrome P450 9e2, 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 78 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 75 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
uncharacterized LOC125489826, transcript variant X1
uncharacterized LOC125489826, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
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: tRNAscan-SE.
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125489830, 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 62 samples with support for all annotated introns
uncharacterized LOC125489830, 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 60 samples with support for all annotated introns
uncharacterized LOC125489830, 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 19 samples with support for all annotated introns
uncharacterized LOC125489830, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein LOC125489830 isoform X1
uncharacterized protein LOC125489830 isoform X2
uncharacterized LOC125488556, transcript variant X1
uncharacterized LOC125488556, transcript variant X2
uncharacterized protein LOC125488556 isoform X1
uncharacterized protein LOC125488556 isoform X2
probable cytochrome P450 9f2, transcript variant X1
probable cytochrome P450 9f2, transcript variant X2
ubiquitin carboxyl-terminal hydrolase nonstop
rhomboid-related protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
rhomboid-related protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial
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 24 samples with support for all annotated introns
zinc finger CCCH domain-containing protein 10-like
zinc finger protein 26-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 54 samples with support for all annotated introns
zinc finger protein 26-like, transcript variant X1
zinc finger protein 62 homolog isoform X2
zinc finger protein 37, 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 35 samples with support for all annotated introns
zinc finger protein 37, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
zinc finger protein 37, transcript variant X4
zinc finger protein 37, transcript variant X1
uncharacterized LOC125489748, transcript variant X5
uncharacterized protein LOC125489748 isoform X5
uncharacterized LOC125489748, transcript variant X2
uncharacterized LOC125489748, transcript variant X1
uncharacterized LOC125489748, transcript variant X4
uncharacterized LOC125489748, transcript variant X3
uncharacterized protein LOC125489748 isoform X4
uncharacterized protein LOC125489748 isoform X3
uncharacterized protein LOC125489748 isoform X2
uncharacterized protein LOC125489748 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 98% 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: 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 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, 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 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 66% 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 97% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
sodium-independent sulfate anion transporter
uncharacterized LOC105390281, transcript variant X4
uncharacterized LOC105390281, transcript variant X1
uncharacterized LOC105390281, transcript variant X3
uncharacterized LOC105390281, transcript variant X2
uncharacterized protein LOC105390281 isoform X2
uncharacterized protein LOC105390281 isoform X1
15-hydroxyprostaglandin dehydrogenase [NAD(+)]
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 51 samples with support for all annotated introns
3-oxoacyl-[acyl-carrier-protein] reductase FabG, transcript variant X2
3-oxoacyl-[acyl-carrier-protein] reductase FabG, transcript variant X1
3-oxoacyl-[acyl-carrier-protein] reductase FabG isoform X1
3-oxoacyl-[acyl-carrier-protein] reductase FabG isoform X2
monocarboxylate transporter 9, 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 68 samples with support for all annotated introns
monocarboxylate transporter 9, 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 59 samples with support for all annotated introns
monocarboxylate transporter 9, 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 15 samples with support for all annotated introns
baculoviral IAP repeat-containing protein 5
cilia- and flagella-associated protein 52
sodium-independent sulfate anion transporter, transcript variant X1
sodium-independent sulfate anion transporter, transcript variant X2
sodium-independent sulfate anion transporter, transcript variant X4
sodium-independent sulfate anion transporter, transcript variant X3
sodium-independent sulfate anion transporter isoform X1
sodium-independent sulfate anion transporter isoform X2
sodium-independent sulfate anion transporter isoform X3
coiled-coil domain-containing protein 137
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X1
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X2
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X3
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
WD repeat domain phosphoinositide-interacting protein 2 isoform X1
WD repeat domain phosphoinositide-interacting protein 2 isoform X3
WD repeat domain phosphoinositide-interacting protein 2 isoform X2
WD repeat domain phosphoinositide-interacting protein 2 isoform X4
nuclear protein localization protein 4 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-prolyl cis-trans isomerase F, mitochondrial
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
uncharacterized LOC105392153, transcript variant X2
uncharacterized LOC105392153, 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 17 samples with support for all annotated introns
protein winged eye, transcript variant X1
protein winged eye, transcript variant X3
protein winged eye, transcript variant X2
senecionine N-oxygenase, transcript variant X1
senecionine N-oxygenase, transcript variant X2
uncharacterized LOC105384324, transcript variant X1
uncharacterized LOC105384324, transcript variant X2
uncharacterized protein LOC105384324 isoform X1
uncharacterized protein LOC105384324 isoform X2
uncharacterized LOC105384320, transcript variant X1
uncharacterized LOC105384320, transcript variant X2
uncharacterized LOC105385457, transcript variant X2
uncharacterized LOC105385457, transcript variant X1
uncharacterized LOC105385457, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
uncharacterized protein LOC105385457 isoform X2
uncharacterized protein LOC105385457 isoform X3
uncharacterized protein LOC105385457 isoform X1
uncharacterized LOC105384319, transcript variant X2
uncharacterized LOC105384319, transcript variant X1
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 18 samples with support for all annotated introns
28 kDa heat- and acid-stable phosphoprotein
WAS/WASL-interacting protein family member 3, transcript variant X1
WAS/WASL-interacting protein family member 3, transcript variant X2
WAS/WASL-interacting protein family member 3 isoform X1
WAS/WASL-interacting protein family member 3 isoform X2
uncharacterized LOC125489756, transcript variant X2
uncharacterized LOC125489756, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 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 18 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 1 sample with support for all annotated introns
putative RNA-binding protein Luc7-like 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
putative RNA-binding protein Luc7-like 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
putative RNA-binding protein Luc7-like 2, 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 57 samples with support for all annotated introns
putative RNA-binding protein Luc7-like 2 isoform X1
putative RNA-binding protein Luc7-like 1 isoform X2
putative RNA-binding protein Luc7-like 1 isoform X3
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q
nuclear distribution protein nudE homolog 1
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 69 samples with support for all annotated introns
thioredoxin domain-containing protein 11
sodium-dependent nutrient amino acid transporter 1
eukaryotic peptide chain release factor GTP-binding subunit ERF3A, transcript variant X1
eukaryotic peptide chain release factor GTP-binding subunit ERF3A, transcript variant X2
eukaryotic peptide chain release factor GTP-binding subunit ERF3A isoform X1
eukaryotic peptide chain release factor GTP-binding subunit ERF3A isoform X2
eukaryotic peptide chain release factor GTP-binding subunit ERF3A, transcript variant X3
eukaryotic peptide chain release factor GTP-binding subunit ERF3A isoform X3
lysophospholipid acyltransferase 6, transcript variant X2
lysophospholipid acyltransferase 6, transcript variant X1
lysophospholipid acyltransferase 6 isoform X1
lysophospholipid acyltransferase 6 isoform X2
26S proteasome non-ATPase regulatory subunit 10-like
mitochondrial dicarboxylate carrier, transcript variant X1
mitochondrial dicarboxylate carrier, transcript variant X2
dual specificity mitogen-activated protein kinase kinase 4, transcript variant X1
dual specificity mitogen-activated protein kinase kinase 4, transcript variant X3
dual specificity mitogen-activated protein kinase kinase 4, transcript variant X2
dual specificity mitogen-activated protein kinase kinase 4 isoform X1
dual specificity mitogen-activated protein kinase kinase 4 isoform X3
dual specificity mitogen-activated protein kinase kinase 4 isoform X2
DNA-directed RNA polymerase I subunit RPA43
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 20 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
major royal jelly protein 1, transcript variant X2
major royal jelly protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC105396433, transcript variant X2
uncharacterized LOC105396433, transcript variant X1
uncharacterized protein LOC105396433 isoform X2
uncharacterized protein LOC105396433 isoform X1
lysosomal-associated transmembrane protein 4B, transcript variant X1
lysosomal-associated transmembrane protein 4B, transcript variant X2
uncharacterized protein LOC105395753 isoform X1
lysosomal-associated transmembrane protein 4B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 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 32 samples with support for all annotated introns
uncharacterized LOC119694689, transcript variant X2
uncharacterized LOC119694689, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
ribosomal L1 domain-containing protein CG13096
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 36 samples with support for all annotated introns
intraflagellar transport protein 140 homolog
translation factor GUF1 homolog, mitochondrial
WD repeat domain phosphoinositide-interacting protein 3
BAG domain-containing protein Samui, transcript variant X3
BAG domain-containing protein Samui isoform X3
BAG domain-containing protein Samui, transcript variant X1
BAG domain-containing protein Samui isoform X1
BAG domain-containing protein Samui, transcript variant X2
BAG domain-containing protein Samui isoform X2
vacuolar protein sorting-associated protein 18 homolog, transcript variant X2
vacuolar protein sorting-associated protein 18 homolog, transcript variant X1
vacuolar protein sorting-associated protein 18 homolog isoform X2
vacuolar protein sorting-associated protein 18 homolog isoform X1
short-chain specific acyl-CoA dehydrogenase, mitochondrial
sulfide:quinone oxidoreductase, mitochondrial, transcript variant X3
sulfide:quinone oxidoreductase, mitochondrial, transcript variant X2
sulfide:quinone oxidoreductase, mitochondrial, transcript variant X1
sulfide:quinone oxidoreductase, mitochondrial isoform X2
sulfide:quinone oxidoreductase, mitochondrial isoform X3
sulfide:quinone oxidoreductase, mitochondrial isoform 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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
TATA-binding protein-associated factor 172, transcript variant X3
TATA-binding protein-associated factor 172, transcript variant X2
TATA-binding protein-associated factor 172, transcript variant X1
TATA-binding protein-associated factor 172, transcript variant X4
TATA-binding protein-associated factor 172 isoform X3
TATA-binding protein-associated factor 172 isoform X2
TATA-binding protein-associated factor 172 isoform X1
TATA-binding protein-associated factor 172 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
sodium-independent sulfate anion transporter isoform X4
ATP-sensitive inward rectifier potassium channel 12, transcript variant X3
ATP-sensitive inward rectifier potassium channel 12, transcript variant X1
ATP-sensitive inward rectifier potassium channel 12, transcript variant X2
ATP-sensitive inward rectifier potassium channel 12, transcript variant X4
ATP-sensitive inward rectifier potassium channel 12, transcript variant X6
ATP-sensitive inward rectifier potassium channel 12, transcript variant X5
inward rectifier potassium channel 2 isoform X1
inward rectifier potassium channel 2 isoform X2
G protein-activated inward rectifier potassium channel 3 isoform X5
G protein-activated inward rectifier potassium channel 3 isoform X4
ATP-sensitive inward rectifier potassium channel 11 isoform X6
inward rectifier potassium channel 2 isoform X3
ATP-sensitive inward rectifier potassium channel 12, transcript variant X10
ATP-sensitive inward rectifier potassium channel 12, transcript variant X7
ATP-sensitive inward rectifier potassium channel 12, transcript variant X9
ATP-sensitive inward rectifier potassium channel 12, transcript variant X8
ATP-sensitive inward rectifier potassium channel 12 isoform X7
G protein-activated inward rectifier potassium channel 3 isoform X8
ATP-sensitive inward rectifier potassium channel 11 isoform X9
ATP-sensitive inward rectifier potassium channel 11 isoform X10
G protein-activated inward rectifier potassium channel 3, transcript variant X1
G protein-activated inward rectifier potassium channel 3, transcript variant X6
G protein-activated inward rectifier potassium channel 3, transcript variant X3
G protein-activated inward rectifier potassium channel 3, transcript variant X4
G protein-activated inward rectifier potassium channel 3 isoform X1
G protein-activated inward rectifier potassium channel 3 isoform X6
G protein-activated inward rectifier potassium channel 3 isoform X3
G protein-activated inward rectifier potassium channel 3, transcript variant X2
G protein-activated inward rectifier potassium channel 3, transcript variant X5
G protein-activated inward rectifier potassium channel 3 isoform X2
G protein-activated inward rectifier potassium channel 4
hepatocyte growth factor-regulated tyrosine kinase substrate, transcript variant X1
hepatocyte growth factor-regulated tyrosine kinase substrate, transcript variant X2
hepatocyte growth factor-regulated tyrosine kinase substrate isoform X1
hepatocyte growth factor-regulated tyrosine kinase substrate isoform X2
hepatocyte growth factor-regulated tyrosine kinase substrate, transcript variant X3
hepatocyte growth factor-regulated tyrosine kinase substrate, transcript variant X4
hepatocyte growth factor-regulated tyrosine kinase substrate isoform X3
hepatocyte growth factor-regulated tyrosine kinase substrate isoform X4
U6 snRNA-associated Sm-like protein LSm5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 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: 2 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: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
elongation of very long chain fatty acids protein-like
suppressor of cytokine signaling 2, transcript variant X2
suppressor of cytokine signaling 2 isoform X2
suppressor of cytokine signaling 2, transcript variant X1
suppressor of cytokine signaling 2 isoform X1
homeobox protein unc-4, transcript variant X2
homeobox protein unc-4, transcript variant X1
probable methyltransferase-like protein 15 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105394234, transcript variant X1
uncharacterized LOC105394234, transcript variant X2
uncharacterized protein LOC105394234 isoform X1
uncharacterized protein LOC105394234 isoform X2
zinc-type alcohol dehydrogenase-like protein SERP1785
TBC1 domain family member 16, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
TBC1 domain family member 16, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
TBC1 domain family member 16, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
TBC1 domain family member 16, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
TBC1 domain family member 16, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
(E3-independent) E2 ubiquitin-conjugating enzyme
probable low-specificity L-threonine aldolase 2
signal recognition particle subunit SRP68
eukaryotic translation initiation factor 3 subunit D
facilitated trehalose transporter Tret1-2 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 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 3 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 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: 94% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
putative nuclease HARBI1, transcript variant X1
putative nuclease HARBI1, transcript variant X2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: translation initiation factor IF-2-like
abnormal spindle-like microcephaly-associated protein homolog
uncharacterized LOC105394995, transcript variant X1
uncharacterized LOC105394995, transcript variant X2
uncharacterized protein LOC105394995 isoform X1
uncharacterized protein LOC105394995 isoform X2
insulin-like growth factor-binding protein complex acid labile subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
ecdysone oxidase-like, transcript variant X1
ecdysone oxidase-like, transcript variant X2
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 26 samples with support for all annotated introns
phosphoribosyl pyrophosphate synthase-associated protein 2
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 83 samples with support for all annotated introns
rho GTPase-activating protein 44, transcript variant X1
rho GTPase-activating protein 44, transcript variant X2
rho GTPase-activating protein 44 isoform X1
rho GTPase-activating protein 44 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
transmembrane protein 70 homolog, mitochondrial
28S ribosomal protein S23, mitochondrial
meteorin-like protein, transcript variant X1
meteorin-like protein, transcript variant X2
testis-expressed protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
testis-expressed protein 2, 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 48 samples with support for all annotated introns
testis-expressed protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
testis-expressed protein 2, transcript variant X4
uncharacterized LOC119693625, transcript variant X2
uncharacterized LOC119693625, transcript variant X1
serine/threonine-protein kinase/endoribonuclease IRE1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
ankyrin repeat domain-containing protein 27
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
Down syndrome cell adhesion molecule-like protein Dscam2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 7 isoform X2
ubiquitin carboxyl-terminal hydrolase 7 isoform X3
ubiquitin carboxyl-terminal hydrolase 7 isoform X4
ubiquitin carboxyl-terminal hydrolase 7 isoform X1
ubiquitin carboxyl-terminal hydrolase 7 isoform X6
ubiquitin carboxyl-terminal hydrolase 7 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitochondrial uncoupling protein 4, transcript variant X5
mitochondrial uncoupling protein 4, transcript variant X1
mitochondrial uncoupling protein 4, transcript variant X2
mitochondrial uncoupling protein 4, transcript variant X4
mitochondrial uncoupling protein 4, transcript variant X3
growth factor receptor-bound protein 2, transcript variant X2
growth factor receptor-bound protein 2, transcript variant X1
growth factor receptor-bound protein 2 isoform X2
growth factor receptor-bound protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
inactive rhomboid protein 1, transcript variant X1
inactive rhomboid protein 1, transcript variant X2
inactive rhomboid protein 1, transcript variant X3
uncharacterized LOC125489776, transcript variant X1
uncharacterized LOC125489776, 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 55 samples with support for all annotated introns
uncharacterized LOC125489776, 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 58 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
putative inorganic phosphate cotransporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
coiled-coil domain-containing protein 96
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
voltage-dependent calcium channel gamma-4 subunit, transcript variant X3
voltage-dependent calcium channel gamma-4 subunit, transcript variant X1
voltage-dependent calcium channel gamma-4 subunit, transcript variant X2
uncharacterized protein LOC105389272 isoform X3
voltage-dependent calcium channel gamma-4 subunit isoform X1
voltage-dependent calcium channel gamma-4 subunit isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
translation initiation factor IF-2, transcript variant X1
translation initiation factor IF-2, transcript variant X2
translation initiation factor IF-2 isoform X1
translation initiation factor IF-2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
putative inorganic phosphate cotransporter, transcript variant X1
putative inorganic phosphate cotransporter, transcript variant X2
putative inorganic phosphate cotransporter isoform X1
putative inorganic phosphate cotransporter isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 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: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
inositol polyphosphate 5-phosphatase E, 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 25 samples with support for all annotated introns
inositol polyphosphate 5-phosphatase E, transcript variant X2
inositol polyphosphate 5-phosphatase E isoform X2
inositol polyphosphate 5-phosphatase E isoform X1
26S proteasome non-ATPase regulatory subunit 12
meiosis regulator and mRNA stability factor 1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10
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 4 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 12 samples with support for all annotated introns
glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial
DNA polymerase subunit gamma-2, mitochondrial
ragulator complex protein LAMTOR2 homolog
developmentally-regulated GTP-binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC105380457, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC105380457, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat extensin-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
alkyldihydroxyacetonephosphate synthase, transcript variant X2
alkyldihydroxyacetonephosphate synthase, transcript variant X1
alkyldihydroxyacetonephosphate synthase isoform X1
alkyldihydroxyacetonephosphate synthase isoform X2
probable aconitate hydratase, mitochondrial
uncharacterized protein K02A2.6-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 11 samples with support for all annotated introns
uncharacterized protein LOC125489808 isoform X2
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein K02A2.6-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC105391893
hydroxysteroid dehydrogenase-like protein 2, transcript variant X2
hydroxysteroid dehydrogenase-like protein 2, transcript variant X1
hydroxysteroid dehydrogenase-like protein 2 isoform X2
hydroxysteroid dehydrogenase-like protein 2 isoform X1
uncharacterized LOC105391894, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC105391894, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
uncharacterized LOC105391894, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
uncharacterized protein LOC105391894 isoform X2
uncharacterized protein LOC105391894 isoform X1
eukaryotic translation initiation factor 3 subunit B
multiple inositol polyphosphate phosphatase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 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 15 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1 isoform X1
multiple inositol polyphosphate phosphatase 1 isoform X2
DNA-directed RNA polymerase III subunit RPC5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dihydropyrimidine dehydrogenase [NADP(+)], transcript variant X6
dihydropyrimidine dehydrogenase [NADP(+)], transcript variant X1
dihydropyrimidine dehydrogenase [NADP(+)], transcript variant X4
dihydropyrimidine dehydrogenase [NADP(+)], transcript variant X5
dihydropyrimidine dehydrogenase [NADP(+)], transcript variant X3
dihydropyrimidine dehydrogenase [NADP(+)], transcript variant X2
dihydropyrimidine dehydrogenase [NADP(+)], transcript variant X8
dihydropyrimidine dehydrogenase [NADP(+)], transcript variant X7
dihydropyrimidine dehydrogenase [NADP(+)] isoform X4
dihydropyrimidine dehydrogenase [NADP(+)] isoform X3
dihydropyrimidine dehydrogenase [NADP(+)] isoform X2
dihydropyrimidine dehydrogenase [NADP(+)] isoform X1
dihydropyrimidine dehydrogenase [NADP(+)] isoform X5
ras-related protein Rac1, transcript variant X2
ras-related protein Rac1, 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
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 55 samples with support for all annotated introns
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
heparan sulfate glucosamine 3-O-sulfotransferase 3B1
hydroxyacylglutathione hydrolase, mitochondrial, transcript variant X1
hydroxyacylglutathione hydrolase, mitochondrial, transcript variant X2
hydroxyacylglutathione hydrolase, mitochondrial isoform X1
hydroxyacylglutathione hydrolase, mitochondrial isoform X2
small subunit processome component 20 homolog
uncharacterized LOC105385026, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC105385026, 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 7 samples with support for all annotated introns
uncharacterized LOC105385026, 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 18 samples with support for all annotated introns
uncharacterized protein LOC105385026 isoform X1
uncharacterized protein LOC105385026 isoform X2
uncharacterized protein LOC105385026 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
transcription initiation factor TFIID subunit 1
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC125488553, transcript variant X2
uncharacterized LOC125488553, transcript variant X1
uncharacterized protein LOC125488553 isoform X2
uncharacterized protein LOC125488553 isoform X1
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial
D-beta-hydroxybutyrate dehydrogenase, mitochondrial
UDP-N-acetylglucosamine transferase subunit ALG14 homolog
GPI inositol-deacylase, transcript variant X1
GPI inositol-deacylase, transcript variant X2
serine-threonine kinase receptor-associated protein
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 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
PDZ and LIM domain protein 3, transcript variant X1
PDZ and LIM domain protein 3, transcript variant X2
uncharacterized protein LOC105390645 isoform 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 16 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 49 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 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, including 33 samples with support for all annotated introns
uncharacterized LOC105380129, transcript variant X1
uncharacterized protein LOC105380129 isoform X1
uncharacterized LOC105380129, transcript variant X2
uncharacterized protein LOC105380129 isoform X2
transcription factor Sp3, 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 6 samples with support for all annotated introns
transcription factor Sp3, transcript variant X1
uridine 5'-monophosphate synthase, transcript variant X2
uridine 5'-monophosphate synthase, transcript variant X1
uridine 5'-monophosphate synthase isoform X1
uridine 5'-monophosphate synthase isoform X2
sodium/potassium-transporting ATPase subunit alpha-2
coiled-coil domain-containing protein 40
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 71 samples with support for all annotated introns
lethal(2) giant larvae protein, transcript variant X2
lethal(2) giant larvae protein, transcript variant X3
lethal(2) giant larvae protein, transcript variant X4
lethal(2) giant larvae protein, transcript variant X6
lethal(2) giant larvae protein, transcript variant X1
lethal(2) giant larvae protein, transcript variant X5
lethal(2) giant larvae protein isoform X3
lethal(2) giant larvae protein isoform X1
lethal(2) giant larvae protein isoform X2
lethal(2) giant larvae protein isoform X4
lethal(2) giant larvae protein isoform X6
lethal(2) giant larvae protein isoform X5
thrombospondin type-1 domain-containing protein 7A, transcript variant X1
thrombospondin type-1 domain-containing protein 7A, 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 1 sample with support for all annotated introns
thrombospondin type-1 domain-containing protein 7A isoform X1
thrombospondin type-1 domain-containing protein 7A isoform X2
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial-like
uncharacterized LOC105385949, transcript variant X1
uncharacterized LOC105385949, 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 30 samples with support for all annotated introns
U3 small nucleolar RNA-interacting protein 2
protein shuttle craft, 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 8 samples with support for all annotated introns
protein shuttle craft, 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 5 samples with support for all annotated introns
uncharacterized protein LOC105380219 isoform X1
serine/arginine-rich splicing factor 2, transcript variant X1
serine/arginine-rich splicing factor 2, transcript variant X2
ribosome biogenesis regulatory protein homolog
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 81 samples with support for all annotated introns
dual specificity mitogen-activated protein kinase kinase 6
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ribonuclease Z, mitochondrial, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
ribonuclease Z, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
ribonuclease Z, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
ribonuclease Z, mitochondrial isoform X1
ribonuclease Z, mitochondrial isoform X2
ribonuclease Z, mitochondrial isoform X3
26S proteasome non-ATPase regulatory subunit 4
putative ATP synthase subunit f, mitochondrial
mesencephalic astrocyte-derived neurotrophic factor homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 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 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105398424, 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 10 samples with support for all annotated introns
uncharacterized LOC105398424, 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 23 samples with support for all annotated introns
uncharacterized protein LOC105398424 isoform X1
uncharacterized protein LOC105398424 isoform X2
malignant fibrous histiocytoma-amplified sequence 1 homolog
forkhead box protein K1, transcript variant X3
forkhead box protein K1, transcript variant X2
forkhead box protein K1, transcript variant X1
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 24 samples with support for all annotated introns
GSK3-beta interaction protein, transcript variant X1
GSK3-beta interaction protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
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
transmembrane channel-like protein 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transmembrane channel-like protein 3, transcript variant X4
transmembrane channel-like protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
transmembrane channel-like protein 3, transcript variant X3
transmembrane channel-like protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
beta-1,3-galactosyltransferase brn-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309088.1
The RefSeq transcript has 5 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001296017.1
The RefSeq protein has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
myosin heavy chain, non-muscle, transcript variant X3
myosin heavy chain, non-muscle, transcript variant X1
myosin heavy chain, non-muscle, transcript variant X2
myosin heavy chain, non-muscle isoform X1
myosin heavy chain, non-muscle isoform X3
myosin heavy chain, non-muscle isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 99% 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 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 98% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein subunit gamma-e
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, including 34 samples with support for all annotated introns
uncharacterized LOC105393518, transcript variant X1
uncharacterized LOC105393518, transcript variant X3
uncharacterized LOC105393518, transcript variant X2
uncharacterized protein LOC105393518 isoform X1
uncharacterized LOC105393518, transcript variant X4
uncharacterized protein LOC105393518 isoform X2
probable enoyl-CoA hydratase, mitochondrial
nascent polypeptide-associated complex subunit alpha, muscle-specific form, transcript variant X2
nascent polypeptide-associated complex subunit alpha, muscle-specific form, transcript variant X1
nascent polypeptide-associated complex subunit alpha, muscle-specific form, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105380630, transcript variant X2
uncharacterized LOC105380630, transcript variant X1
uncharacterized protein LOC105380630 isoform X2
uncharacterized protein LOC105380630 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 83 samples with support for all annotated introns
transcription factor Adf-1, transcript variant X1
transcription factor Adf-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 48 samples with support for all annotated introns
geranylgeranyl transferase type-2 subunit beta
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 84 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 53% coverage of the annotated genomic feature by RNAseq alignments
oxidoreductase-like domain-containing protein 1
rho GDP-dissociation inhibitor 1, transcript variant X1
rho GDP-dissociation inhibitor 1, transcript variant X3
rho GDP-dissociation inhibitor 1, transcript variant X2
rho GDP-dissociation inhibitor 1 isoform X1
rho GDP-dissociation inhibitor 1 isoform X2
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 71 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 52 samples with support for all annotated introns
uncharacterized LOC125489781, 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 28 samples with support for all annotated introns
uncharacterized LOC125489781, transcript variant X2
oxidized purine nucleoside triphosphate hydrolase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
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 25 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
peptidyl-tRNA hydrolase ICT1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC105383220, transcript variant X1
uncharacterized LOC105383220, transcript variant X2
uncharacterized protein LOC105383220 isoform X2
uncharacterized protein LOC105383220 isoform X1
cytosolic endo-beta-N-acetylglucosaminidase
beta-1,4-N-acetylgalactosaminyltransferase bre-4-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 83 samples with support for all annotated introns
beta-1,4-N-acetylgalactosaminyltransferase bre-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
beta-1,4-N-acetylgalactosaminyltransferase bre-4-like
vacuolar protein sorting-associated protein 41 homolog
enoyl-CoA hydratase domain-containing protein 2, mitochondrial
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 77 samples with support for all annotated introns
28S ribosomal protein S33, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
rhodanese domain-containing protein CG4456
protein artichoke, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein artichoke, 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 44 samples with support for all annotated introns
NAD-dependent protein deacetylase sirtuin-7
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 36 samples with support for all annotated introns