Pieris napi chromosome 2, 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\nFR997695.1.\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.
DNA N6-methyl methyltransferase, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
DNA N6-methyl methyltransferase isoform X1
DNA N6-methyl methyltransferase, 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 32 samples with support for all annotated introns
DNA N6-methyl methyltransferase isoform X2
UDP-glucose 4-epimerase-like, transcript variant X2
UDP-glucose 4-epimerase-like, transcript variant X1
trimeric intracellular cation channel type 1B.1, transcript variant X2
trimeric intracellular cation channel type 1B.1, transcript variant X1
trimeric intracellular cation channel type 1B.1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon CGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125055673, transcript variant X2
uncharacterized LOC125055673, transcript variant X1
uncharacterized protein LOC125055673 isoform X1
uncharacterized protein LOC125055673 isoform X2
uncharacterized LOC125059819, transcript variant X1
uncharacterized LOC125059819, transcript variant X2
uncharacterized protein LOC125059819 isoform X1
uncharacterized protein LOC125059819 isoform X2
calcium and integrin-binding protein 1-like, transcript variant X2
calcium and integrin-binding protein 1-like, transcript variant X1
calcium and integrin-binding protein 1-like isoform X1
calcium and integrin-binding protein 1-like 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 7 samples with support for all annotated introns
uncharacterized LOC125061559, transcript variant X2
uncharacterized LOC125061559, transcript variant X1
uncharacterized LOC125060303, transcript variant X1
uncharacterized LOC125060303, transcript variant X2
glycine-rich cell wall structural protein-like
glycine, alanine and asparagine-rich protein-like
GATA zinc finger domain-containing protein 14-like, transcript variant X4
GATA zinc finger domain-containing protein 14-like, transcript variant X3
GATA zinc finger domain-containing protein 14-like, transcript variant X2
GATA zinc finger domain-containing protein 14-like, transcript variant X1
GATA zinc finger domain-containing protein 14-like, transcript variant X5
GATA zinc finger domain-containing protein 14-like, transcript variant X7
GATA zinc finger domain-containing protein 14-like, transcript variant X6
GATA zinc finger domain-containing protein 14-like, transcript variant X8
GATA zinc finger domain-containing protein 14-like, transcript variant X9
GATA zinc finger domain-containing protein 14-like, transcript variant X11
GATA zinc finger domain-containing protein 14-like, transcript variant X10
uncharacterized protein LOC125062439 isoform X11
GATA zinc finger domain-containing protein 14-like isoform X5
GATA zinc finger domain-containing protein 14-like isoform X7
uncharacterized protein LOC125062439 isoform X10
uncharacterized protein LOC125062439 isoform X9
uncharacterized protein LOC125062439 isoform X8
GATA zinc finger domain-containing protein 14-like isoform X6
uncharacterized protein LOC125062439 isoform X4
GATA zinc finger domain-containing protein 14-like isoform X2
GATA zinc finger domain-containing protein 14-like isoform X3
uncharacterized protein LOC125062439 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
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
putative uncharacterized protein DDB_G0282133
receptor-type tyrosine-protein phosphatase kappa, transcript variant X1
receptor-type tyrosine-protein phosphatase kappa, transcript variant X2
receptor-type tyrosine-protein phosphatase kappa isoform X1
receptor-type tyrosine-protein phosphatase kappa 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X5
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X2
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X1
aldehyde dehydrogenase, dimeric NADP-preferring isoform X2
aldehyde dehydrogenase, dimeric NADP-preferring isoform X1
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X3
aldehyde dehydrogenase, dimeric NADP-preferring isoform X3
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X4
aldehyde dehydrogenase, dimeric NADP-preferring isoform X4
ras-like GTP-binding protein Rho1, transcript variant X2
ras-like GTP-binding protein Rho1, transcript variant X1
ras-like GTP-binding protein Rho1 isoform X1
ras-like GTP-binding protein Rho1 isoform X2
ATP synthase subunit alpha, mitochondrial
PX domain-containing protein kinase-like protein, transcript variant X1
PX domain-containing protein kinase-like protein, transcript variant X2
PX domain-containing protein kinase-like protein, transcript variant X3
PX domain-containing protein kinase-like protein isoform X1
PX domain-containing protein kinase-like protein isoform X2
PX domain-containing protein kinase-like protein isoform X3
guanine nucleotide exchange factor subunit Rich
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 63 samples with support for all annotated introns
protein bicaudal D, transcript variant X1
protein bicaudal D, transcript variant X2
BAG family molecular chaperone regulator 2
ras-related protein Rab-23, transcript variant X1
ras-related protein Rab-23, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
ubiquitin carboxyl-terminal hydrolase 14
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
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
DNA replication licensing factor MCM4, transcript variant X1
DNA replication licensing factor MCM4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
DNA replication licensing factor MCM4 isoform X1
DNA replication licensing factor MCM4 isoform X2
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X3
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X1
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X4
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X2
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X3
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X1
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X4
(Lyso)-N-acylphosphatidylethanolamine lipase 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 6 samples with support for all annotated introns
adipokinetic hormone/corazonin-related peptide receptor variant I, transcript variant X1
adipokinetic hormone/corazonin-related peptide receptor variant I, transcript variant X2
adipokinetic hormone/corazonin-related peptide receptor variant I
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 43 samples with support for all annotated introns
zinc finger protein 239-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 143 samples with support for all annotated introns
zinc finger protein 239-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 164 samples with support for all annotated introns
cyclin-dependent kinases regulatory subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
SNAPIN protein homolog, transcript variant X1
methyltransferase N6AMT1-like isoform X1
SNAPIN protein homolog, transcript variant X2
leucine-rich repeat-containing protein 49
glutamate receptor ionotropic, kainate glr-3-like, transcript variant X5
glutamate receptor ionotropic, kainate glr-3-like, transcript variant X1
glutamate receptor ionotropic, kainate glr-3-like, transcript variant X3
glutamate receptor ionotropic, kainate glr-3-like, transcript variant X2
glutamate receptor ionotropic, kainate glr-3-like isoform X1
uncharacterized protein LOC125061586 isoform X2
uncharacterized protein LOC125061586 isoform X3
glutamate receptor ionotropic, kainate glr-3-like, transcript variant X4
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
uncharacterized protein LOC125061586 isoform X4
uncharacterized protein LOC125061586 isoform X5
cartilage oligomeric matrix protein, transcript variant X1
cartilage oligomeric matrix protein, transcript variant X3
cartilage oligomeric matrix protein, transcript variant X2
cartilage oligomeric matrix protein isoform X1
cartilage oligomeric matrix protein isoform X2
transient receptor potential cation channel trpm, transcript variant X9
transient receptor potential cation channel trpm, transcript variant X2
transient receptor potential cation channel trpm, transcript variant X4
transient receptor potential cation channel trpm, transcript variant X10
transient receptor potential cation channel trpm, transcript variant X12
transient receptor potential cation channel trpm, transcript variant X5
transient receptor potential cation channel trpm, transcript variant X1
transient receptor potential cation channel trpm, transcript variant X3
transient receptor potential cation channel trpm, transcript variant X7
transient receptor potential cation channel trpm, transcript variant X8
transient receptor potential cation channel trpm, transcript variant X6
transient receptor potential cation channel trpm, transcript variant X11
transient receptor potential cation channel trpm isoform X8
transient receptor potential cation channel trpm isoform X2
transient receptor potential cation channel trpm isoform X4
transient receptor potential cation channel trpm isoform X9
transient receptor potential cation channel trpm isoform X11
transient receptor potential cation channel trpm isoform X5
transient receptor potential cation channel trpm isoform X1
transient receptor potential cation channel trpm isoform X3
transient receptor potential cation channel trpm isoform X7
transient receptor potential cation channel trpm isoform X6
transient receptor potential cation channel trpm isoform X10
transient receptor potential cation channel trpm, transcript variant X13
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 2 samples with support for all annotated introns
transient receptor potential cation channel trpm isoform X12
uncharacterized LOC125056065, 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 30 samples with support for all annotated introns
uncharacterized LOC125056065, transcript variant X1
uncharacterized protein LOC125056065 isoform X1
uncharacterized protein LOC125056065 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 26 samples with support for all annotated introns
ejaculatory bulb-specific protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
5-formyltetrahydrofolate cyclo-ligase, transcript variant X1
5-formyltetrahydrofolate cyclo-ligase isoform X1
5-formyltetrahydrofolate cyclo-ligase, transcript variant X2
5-formyltetrahydrofolate cyclo-ligase isoform X2
uncharacterized LOC125062771, transcript variant X2
uncharacterized LOC125062771, transcript variant X1
uncharacterized LOC125062771, transcript variant X3
uncharacterized protein LOC125062771 isoform X2
uncharacterized protein LOC125062771 isoform X1
protein fem-1 homolog B, transcript variant X2
protein fem-1 homolog B, transcript variant X1
protein fem-1 homolog B, transcript variant X4
protein fem-1 homolog B, transcript variant X3
protein fem-1 homolog B, transcript variant X5
solute carrier family 35 member F5, transcript variant X1
solute carrier family 35 member F5, transcript variant X2
solute carrier family 35 member F5 isoform X1
uncharacterized transporter C405.03c isoform X2
eukaryotic translation elongation factor 1 epsilon-1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 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 149 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 64 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 111 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 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
EF-hand domain-containing family member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
allergen Tha p 1-like, transcript variant X1
allergen Tha p 1-like, transcript variant X2
ejaculatory bulb-specific protein 3-like, transcript variant X2
ejaculatory bulb-specific protein 3-like, transcript variant X1
ejaculatory bulb-specific protein 3-like isoform X1
ejaculatory bulb-specific protein 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial, transcript variant X2
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial, transcript variant X4
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial, transcript variant X3
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial, transcript variant X1
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial isoform X2
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial isoform X3
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial isoform X1
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial isoform X4
uncharacterized LOC125063010, transcript variant X2
uncharacterized LOC125063010, transcript variant X1
uncharacterized protein LOC125063010 isoform X1
uncharacterized protein LOC125063010 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 109 samples with support for all annotated introns
CREB-regulated transcription coactivator 1-like, transcript variant X1
CREB-regulated transcription coactivator 1-like, transcript variant X2
CREB-regulated transcription coactivator 1-like, transcript variant X3
CREB-regulated transcription coactivator 1-like, transcript variant X5
CREB-regulated transcription coactivator 1-like, transcript variant X7
CREB-regulated transcription coactivator 1-like, transcript variant X4
CREB-regulated transcription coactivator 1-like, transcript variant X6
CREB-regulated transcription coactivator 1-like, transcript variant X8
CREB-regulated transcription coactivator 2-like isoform X1
CREB-regulated transcription coactivator 3-like isoform X2
CREB-regulated transcription coactivator 1-like isoform X4
CREB-regulated transcription coactivator 3-like isoform X3
CREB-regulated transcription coactivator 1-like isoform X5
CREB-regulated transcription coactivator 1-like isoform X7
CREB-regulated transcription coactivator 2-like isoform X6
CREB-regulated transcription coactivator 3-like isoform 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 5 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 52 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 62 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 84 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 72 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 165 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 40 samples with support for all annotated introns
uncharacterized protein LOC125055947 isoform X5
uncharacterized protein LOC125055947 isoform X3
uncharacterized protein LOC125055947 isoform X2
uncharacterized protein LOC125055947 isoform X4
uncharacterized protein LOC125055947 isoform X1
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.
coiled-coil domain-containing protein 112-like, transcript variant X1
coiled-coil domain-containing protein 112-like isoform X1
coiled-coil domain-containing protein 112-like, transcript variant X2
uncharacterized protein LOC125055832 isoform X2
zinc finger protein 729-like, transcript variant X1
zinc finger protein 729-like, transcript variant X2
zinc finger protein 729-like, transcript variant X3
zinc finger protein 729-like, transcript variant X4
E3 SUMO-protein ligase ZBED1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
E3 SUMO-protein ligase ZBED1-like, transcript variant X3
E3 SUMO-protein ligase ZBED1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
zinc finger BED domain-containing protein 6-like isoform X1
E3 SUMO-protein ligase ZBED1-like isoform X2
tetratricopeptide repeat protein 19 homolog, mitochondrial
transmembrane protein adipocyte-associated 1 homolog
serine/threonine-protein kinase PRP4 homolog, transcript variant X7
serine/threonine-protein kinase PRP4 homolog, transcript variant X6
serine/threonine-protein kinase PRP4 homolog, transcript variant X4
serine/threonine-protein kinase PRP4 homolog, transcript variant X5
serine/threonine-protein kinase PRP4 homolog, transcript variant X3
serine/threonine-protein kinase PRP4 homolog, transcript variant X1
serine/threonine-protein kinase PRP4 homolog, transcript variant X2
serine/threonine-protein kinase PRP4 homolog, transcript variant X8
serine/threonine-protein kinase PRP4 homolog
pentatricopeptide repeat-containing protein 2, mitochondrial-like
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 92 samples with support for all annotated introns
diuretic hormone receptor, 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 18 samples with support for all annotated introns
diuretic hormone receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
diuretic hormone receptor, 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 52 samples with support for all annotated introns
diuretic hormone receptor, transcript variant X4
proton-coupled folate transporter-like, transcript variant X1
proton-coupled folate transporter-like isoform X1
proton-coupled folate transporter-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 149 samples with support for all annotated introns
proton-coupled folate transporter-like isoform X2
proton-coupled folate transporter-like, transcript variant X3
proton-coupled folate transporter-like isoform X3
thrombospondin type-1 domain-containing protein 4-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 9 samples with support for all annotated introns
peptidyl-alpha-hydroxyglycine alpha-amidating lyase 2-like
uncharacterized LOC125056798, transcript variant X2
uncharacterized LOC125056798, transcript variant X1
uncharacterized protein LOC125056798 isoform X2
uncharacterized protein LOC125056798 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
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 168 samples with support for all annotated introns
carbohydrate sulfotransferase 11-like, transcript variant X4
carbohydrate sulfotransferase 11-like, transcript variant X2
carbohydrate sulfotransferase 11-like, transcript variant X3
carbohydrate sulfotransferase 11-like, transcript variant X1
carbohydrate sulfotransferase 11-like, transcript variant X5
carbohydrate sulfotransferase 11-like isoform X2
carbohydrate sulfotransferase 11-like isoform X1
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125061894, 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 16 samples with support for all annotated introns
uncharacterized LOC125061894, 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 12 samples with support for all annotated introns
DNA-directed RNA polymerases I, II, and III subunit RPABC1
leptin receptor overlapping transcript-like 1, transcript variant X2
leptin receptor overlapping transcript-like 1, transcript variant X1
leptin receptor overlapping transcript-like 1 isoform X2
leptin receptor overlapping transcript-like 1 isoform X1
Down syndrome cell adhesion molecule-like protein Dscam2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125057152, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125057152, 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 16 samples with support for all annotated introns
uncharacterized protein LOC125057152 isoform X2
uncharacterized protein LOC125057152 isoform X1
uncharacterized LOC125060732, transcript variant X1
uncharacterized protein LOC125060732 isoform X1
uncharacterized LOC125060732, 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 24 samples with support for all annotated introns
uncharacterized protein LOC125060732 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
peroxisomal multifunctional enzyme type 2-like, transcript variant X1
peroxisomal multifunctional enzyme type 2-like isoform X1
peroxisomal multifunctional enzyme type 2-like, transcript variant X2
peroxisomal multifunctional enzyme type 2-like, transcript variant X3
peroxisomal multifunctional enzyme type 2-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 140 samples with support for all annotated introns
uncharacterized LOC125057335, transcript variant X1
uncharacterized LOC125057335, transcript variant X2
uncharacterized LOC125057335, transcript variant X3
uncharacterized protein LOC125057335 isoform X1
uncharacterized protein LOC125057335 isoform X2
uncharacterized protein LOC125057335 isoform 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 1 sample with support for all annotated introns
gamma-tubulin complex component 4, transcript variant X1
gamma-tubulin complex component 4, transcript variant X2
gamma-tubulin complex component 4 isoform X1
gamma-tubulin complex component 4 isoform X2
probable protein arginine N-methyltransferase 6.1
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 75 samples with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD1-like, 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 50 samples with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD1-like isoform X3
mitotic spindle assembly checkpoint protein MAD1-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 43 samples with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD1-like, 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 167 samples with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD1-like isoform X2
mitotic spindle assembly checkpoint protein MAD1-like isoform X1
mitotic spindle assembly checkpoint protein MAD1-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 133 samples with support for all annotated introns
angiogenic factor with G patch and FHA domains 1, transcript variant X3
angiogenic factor with G patch and FHA domains 1, transcript variant X4
angiogenic factor with G patch and FHA domains 1, transcript variant X1
angiogenic factor with G patch and FHA domains 1, transcript variant X2
angiogenic factor with G patch and FHA domains 1 isoform X2
angiogenic factor with G patch and FHA domains 1 isoform X4
angiogenic factor with G patch and FHA domains 1 isoform X1
angiogenic factor with G patch and FHA domains 1 isoform X3
tRNA selenocysteine 1-associated protein 1
transcription factor TFIIIB component B''
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 154 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X5
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X6
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X12
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X11
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X9
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X10
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X7
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X8
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X5
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X6
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X7
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X8
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X9
uncharacterized LOC125061003, 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 3 samples with support for all annotated introns
uncharacterized LOC125061003, transcript variant X1
uncharacterized protein LOC125061003 isoform X2
uncharacterized protein LOC125061003 isoform X1
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
GPI ethanolamine phosphate transferase 3, transcript variant X2
GPI ethanolamine phosphate transferase 3, transcript variant X1
GPI ethanolamine phosphate transferase 3 isoform X2
GPI ethanolamine phosphate transferase 3 isoform X1
EF-hand calcium-binding domain-containing protein 14, transcript variant X3
uncharacterized protein LOC125057389 isoform X2
EF-hand calcium-binding domain-containing protein 14, transcript variant X1
EF-hand calcium-binding domain-containing protein 14, transcript variant X2
EF-hand calcium-binding domain-containing protein 14 isoform X1
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial
alpha-amylase 2-like, transcript variant X1
alpha-amylase 2-like, transcript variant X2
twisted gastrulation protein homolog 1-A
transcription factor HNF-4 homolog, transcript variant X3
transcription factor HNF-4 homolog isoform X3
transcription factor HNF-4 homolog, transcript variant X4
transcription factor HNF-4 homolog isoform X4
transcription factor HNF-4 homolog, transcript variant X1
transcription factor HNF-4 homolog, transcript variant X2
hepatocyte nuclear factor 4-gamma isoform X1
hepatocyte nuclear factor 4-gamma isoform X2
fanconi-associated nuclease 1-like, transcript variant X3
fanconi-associated nuclease 1-like, transcript variant X1
fanconi-associated nuclease 1-like, transcript variant X2
fanconi-associated nuclease 1-like isoform X2
fanconi-associated nuclease 1-like isoform X1
synaptic vesicle membrane protein VAT-1 homolog-like, transcript variant X2
synaptic vesicle membrane protein VAT-1 homolog-like, transcript variant X1
synaptic vesicle membrane protein VAT-1 homolog-like isoform X2
synaptic vesicle membrane protein VAT-1 homolog-like isoform X1
uncharacterized LOC125059121, transcript variant X1
uncharacterized LOC125059121, transcript variant X2
uncharacterized LOC125059121, transcript variant X3
uncharacterized protein LOC125059121 isoform X1
uncharacterized protein LOC125059121 isoform X2
uncharacterized protein LOC125059121 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 89 samples with support for all annotated introns
polyadenylate-binding protein 2, transcript variant X1
polyadenylate-binding protein 2 isoform X1
polyadenylate-binding protein 2, transcript variant X2
polyadenylate-binding protein 2 isoform X2
probable splicing factor, arginine/serine-rich 7, transcript variant X1
probable splicing factor, arginine/serine-rich 7, transcript variant X2
probable splicing factor, arginine/serine-rich 7 isoform X1
splicing regulatory glutamine/lysine-rich protein 1 isoform X2
probable splicing factor, arginine/serine-rich 7, 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 158 samples with support for all annotated introns
probable splicing factor, arginine/serine-rich 7, transcript variant X3
probable splicing factor, arginine/serine-rich 7 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 3 samples with support for all annotated introns
store-operated calcium entry regulator STIMATE-like
heterogeneous nuclear ribonucleoprotein K, transcript variant X2
heterogeneous nuclear ribonucleoprotein K, transcript variant X1
heterogeneous nuclear ribonucleoprotein K isoform X1
heterogeneous nuclear ribonucleoprotein K, transcript variant X3
heterogeneous nuclear ribonucleoprotein K isoform X2
lysM and putative peptidoglycan-binding domain-containing protein 3, transcript variant X3
lysM and putative peptidoglycan-binding domain-containing protein 3, transcript variant X1
lysM and putative peptidoglycan-binding domain-containing protein 3, transcript variant X2
lysM and putative peptidoglycan-binding domain-containing protein 3 isoform X2
lysM and putative peptidoglycan-binding domain-containing protein 3 isoform X1
lysM and putative peptidoglycan-binding domain-containing protein 3 isoform X3
myb-like protein X, transcript variant X2
myb-like protein X, transcript variant X3
myb-like protein X, transcript variant X1
uncharacterized protein LOC125056610 isoform X1
uncharacterized LOC125055904, transcript variant X2
uncharacterized LOC125055904, transcript variant X1
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase
microtubule-associated protein RP/EB family member 1, transcript variant X2
microtubule-associated protein RP/EB family member 1, transcript variant X1
microtubule-associated protein RP/EB family member 1 isoform X1
microtubule-associated protein RP/EB family member 1 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 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 15 samples with support for all annotated introns
ATP-dependent RNA helicase vasa, transcript variant X4
ATP-dependent RNA helicase vasa, transcript variant X2
ATP-dependent RNA helicase vasa, transcript variant X3
ATP-dependent RNA helicase vasa, transcript variant X1
ATP-dependent RNA helicase vasa isoform X4
ATP-dependent RNA helicase vasa isoform X2
ATP-dependent RNA helicase vasa isoform X3
ATP-dependent RNA helicase vasa isoform X1
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 isoform X2
G-protein coupled receptor dmsr-1-like isoform X1
uncharacterized LOC125056406, transcript variant X3
uncharacterized LOC125056406, transcript variant X2
uncharacterized LOC125056406, transcript variant X4
uncharacterized LOC125056406, transcript variant X1
uncharacterized protein LOC125056406 isoform X3
uncharacterized protein LOC125056406 isoform X2
uncharacterized protein LOC125056406 isoform X4
uncharacterized protein LOC125056406 isoform X1
uncharacterized LOC125056423, transcript variant X2
uncharacterized LOC125056423, transcript variant X1
uncharacterized LOC125059803, transcript variant X1
uncharacterized LOC125059803, 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 67 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 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 95 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 87 samples with support for all annotated introns
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
mitochondrial fission process protein 1, transcript variant X1
mitochondrial fission process protein 1, transcript variant X2
mitochondrial fission process protein 1 isoform X2
mitochondrial fission process protein 1 isoform X1
mitochondrial fission process protein 1, transcript variant X3
mitochondrial fission process protein 1 isoform X3
cholesterol transporter ABCA5-like, 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 50 samples with support for all annotated introns
cholesterol transporter ABCA5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 91 samples with support for all annotated introns
cholesterol transporter ABCA5-like isoform X2
cholesterol transporter ABCA5-like isoform X1
leucine-rich repeat-containing protein 47-like
DNA repair and recombination protein RAD54-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 6 samples with support for all annotated introns
dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase
two pore channel protein 1-like, transcript variant X1
two pore channel protein 1-like, transcript variant X3
two pore channel protein 1-like, transcript variant X4
two pore channel protein 1-like, transcript variant X2
two pore calcium channel protein 1-like isoform X1
two pore channel protein 1-like isoform X3
two pore channel protein 1-like isoform X2
two pore channel protein 1-like isoform X4
60S ribosomal protein L6, transcript variant X1
60S ribosomal protein L6, transcript variant X2
SANT and BTB domain regulator of class switch recombination
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125057305, transcript variant X1
uncharacterized LOC125057305, transcript variant X3
uncharacterized LOC125057305, transcript variant X2
uncharacterized protein LOC125057305 isoform X1
uncharacterized protein LOC125057305 isoform X2
U1 small nuclear ribonucleoprotein 70 kDa, transcript variant X1
U1 small nuclear ribonucleoprotein 70 kDa, transcript variant X2
arginine/serine-rich coiled-coil protein 2 isoform X1
U1 small nuclear ribonucleoprotein 70 kDa isoform X2
protein strawberry notch-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 119 samples with support for all annotated introns
protein strawberry notch-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 68 samples with support for all annotated introns
protein strawberry notch-like isoform X1
protein strawberry notch-like 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 12 samples with support for all annotated introns
LIM domain kinase 1, transcript variant X1
LIM domain kinase 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 79 samples with support for all annotated introns
LIM domain kinase 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 93 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase kinase 2-like
eEF1A lysine and N-terminal methyltransferase homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX55 homolog
translation machinery-associated protein 16 homolog
cell division control protein 45 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 97 samples with support for all annotated introns
required for meiotic nuclear division protein 1 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 52 samples with support for all annotated introns
required for meiotic nuclear division protein 1 homolog, transcript variant X2
required for meiotic nuclear division protein 1 homolog isoform X1
required for meiotic nuclear division protein 1 homolog isoform X2
required for meiotic nuclear division protein 1 homolog, 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 52 samples with support for all annotated introns
required for meiotic nuclear division protein 1 homolog isoform X3
GAS2-like protein pickled eggs, transcript variant X2
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
GAS2-like protein pickled eggs, 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 44 samples with support for all annotated introns
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 101 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase kinase 2
uncharacterized LOC125063037, 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 18 samples with support for all annotated introns
uncharacterized LOC125063037, transcript variant X2
uncharacterized LOC125063037, 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 4 samples with support for all annotated introns
uncharacterized LOC125063037, 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 2 samples with support for all annotated introns
uncharacterized protein LOC125063037 isoform X1
uncharacterized protein LOC125063037 isoform X2
uncharacterized protein LOC125063037 isoform X3
uncharacterized protein LOC125063037 isoform X4
AT-rich interactive domain-containing protein 2-like, transcript variant X2
AT-rich interactive domain-containing protein 2-like, transcript variant X1
AT-rich interactive domain-containing protein 2-like isoform X2
serine/threonine-protein kinase pakG-like 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 20 samples with support for all annotated introns
phenoloxidase subunit 1, transcript variant X2
phenoloxidase subunit 1, transcript variant X1
2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like
uncharacterized LOC125057895, transcript variant X2
uncharacterized LOC125057895, transcript variant X1
uncharacterized LOC125057895, transcript variant X3
uncharacterized protein LOC125057895 isoform X1
uncharacterized protein LOC125057895 isoform X2
nose resistant to fluoxetine protein 6-like, transcript variant X2
nose resistant to fluoxetine protein 6-like, transcript variant X1
nose resistant to fluoxetine protein 6-like isoform X2
nose resistant to fluoxetine protein 6-like isoform X1
regulator of hypoxia-inducible factor 1-like, transcript variant X1
regulator of hypoxia-inducible factor 1-like, 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 41 samples with support for all annotated introns
regulator of hypoxia-inducible factor 1-like isoform X1
regulator of hypoxia-inducible factor 1-like isoform X2
O-acyltransferase like protein-like, transcript variant X2
O-acyltransferase like protein-like, transcript variant X1
myosin tail region-interacting protein MTI1-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 104 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 1 sample with support for all annotated introns
O-acyltransferase like protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
O-acyltransferase like protein-like isoform X3
uncharacterized protein LOC125062971 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
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
vacuolar protein sorting-associated protein 45
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 164 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 88 samples with support for all annotated introns
GPI transamidase component PIG-S, transcript variant X1
GPI transamidase component PIG-S, transcript variant X2
GPI transamidase component PIG-S isoform X1
GPI transamidase component PIG-S isoform X2
alpha-tocopherol transfer protein-like, 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 36 samples with support for all annotated introns
alpha-tocopherol transfer protein-like, transcript variant X2
alpha-tocopherol transfer protein-like isoform X1
alpha-tocopherol transfer protein-like isoform X2
uncharacterized LOC125062709, transcript variant X1
uncharacterized LOC125062709, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125061951, transcript variant X3
uncharacterized LOC125061951, transcript variant X1
uncharacterized LOC125061951, transcript variant X2
uncharacterized protein LOC125061951 isoform X3
uncharacterized protein LOC125061951 isoform X1
uncharacterized protein LOC125061951 isoform 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
Meckel syndrome type 1 protein 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 121 samples with support for all annotated introns
Meckel syndrome type 1 protein homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 103 samples with support for all annotated introns
uncharacterized protein LOC125057259 isoform X1
Meckel syndrome type 1 protein homolog isoform X2
rhomboid-related protein 2, transcript variant X1
rhomboid-related protein 2, transcript variant X2
rhomboid-related protein 2, transcript variant X3
rhomboid-related protein 2, transcript variant X4
rhomboid-related protein 2, transcript variant X5
carboxypeptidase D-like, transcript variant X1
carboxypeptidase D-like, transcript variant X2
uncharacterized protein KIAA2013 homolog
mitochondrial inner membrane protease subunit 2
yrdC domain-containing protein, mitochondrial
DNA-directed RNA polymerase III subunit RPC10
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 169 samples with support for all annotated introns
ceramide synthase 5, transcript variant X1
ceramide synthase 5, transcript variant X2
ceramide synthase 5, transcript variant X4
ceramide synthase 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 108 samples with support for all annotated introns
sex-lethal homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 118 samples with support for all annotated introns
sex-lethal homolog, transcript variant X3
sex-lethal homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 163 samples with support for all annotated introns
sex-lethal homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
sex-lethal homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
serine proteinase stubble-like isoform X3
somatomedin-B and thrombospondin type-1 domain-containing protein-like, transcript variant X2
somatomedin-B and thrombospondin type-1 domain-containing protein-like, transcript variant X1
somatomedin-B and thrombospondin type-1 domain-containing protein-like
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
caveolae-associated protein 4-like, transcript variant X7
caveolae-associated protein 4-like, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
caveolae-associated protein 4-like, 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 7 samples with support for all annotated introns
caveolae-associated protein 4-like, transcript variant X5
caveolae-associated protein 4-like, transcript variant X11
caveolae-associated protein 4-like, transcript variant X10
caveolae-associated protein 4-like, transcript variant X2
caveolae-associated protein 4-like, transcript variant X3
caveolae-associated protein 4-like, transcript variant X12
caveolae-associated protein 4-like, transcript variant X13
caveolae-associated protein 4-like, transcript variant X6
caveolae-associated protein 4-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 9 samples with support for all annotated introns
caveolae-associated protein 4-like, transcript variant X1
caveolae-associated protein 4-like, transcript variant X9
caveolae-associated protein 4-like, transcript variant X17
caveolae-associated protein 4-like, transcript variant X14
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
caveolae-associated protein 4-like, transcript variant X8
uncharacterized protein LOC125063019 isoform X2
probable serine/threonine-protein kinase DDB_G0278845 isoform X5
uncharacterized protein LOC125063019 isoform X15
uncharacterized protein LOC125063019 isoform X1
uncharacterized protein LOC125063019 isoform X3
caveolae-associated protein 4-like isoform X8
uncharacterized protein LOC125063019 isoform X13
uncharacterized protein LOC125063019 isoform X4
caveolae-associated protein 4-like isoform X14
uncharacterized protein LOC125063019 isoform X10
uncharacterized protein LOC125063019 isoform X16
uncharacterized protein LOC125063019 isoform X7
uncharacterized protein LOC125063019 isoform X6
uncharacterized protein LOC125063019 isoform X11
uncharacterized protein LOC125063019 isoform X9
uncharacterized protein LOC125063019 isoform X12
uncharacterized protein LOC125063019 isoform X17
uncharacterized LOC125062061, transcript variant X1
uncharacterized LOC125062061, transcript variant X2
eukaryotic translation initiation factor 4E transporter-like, transcript variant X3
eukaryotic translation initiation factor 4E transporter-like, transcript variant X1
eukaryotic translation initiation factor 4E transporter-like, transcript variant X2
eukaryotic translation initiation factor 4E transporter-like isoform X3
eukaryotic translation initiation factor 4E transporter-like isoform X2
eukaryotic translation initiation factor 4E transporter-like isoform X1
protein suppressor of white apricot, transcript variant X1
protein suppressor of white apricot isoform X1
protein suppressor of white apricot, transcript variant X2
protein suppressor of white apricot isoform 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 47 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized protein LOC125057548 isoform X3
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
39S ribosomal protein L18, mitochondrial
eukaryotic translation initiation factor 3 subunit A
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 108 samples with support for all annotated introns
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fructose-bisphosphate aldolase, transcript variant X2
fructose-bisphosphate aldolase, transcript variant X3
fructose-bisphosphate aldolase isoform X2
fructose-bisphosphate aldolase isoform X3
fructose-bisphosphate aldolase, transcript variant X1
fructose-bisphosphate aldolase isoform X1
sodium/calcium exchanger regulatory protein 1-like
DNA cross-link repair 1A protein-like, transcript variant X2
DNA cross-link repair 1A protein-like, transcript variant X3
DNA cross-link repair 1A protein-like isoform X2
DNA cross-link repair 1A protein-like, transcript variant X1
DNA cross-link repair 1A protein-like isoform X1
iron-sulfur cluster co-chaperone protein HscB
transcription initiation protein SPT3 homolog
TWiK family of potassium channels protein 9-like, transcript variant X1
TWiK family of potassium channels protein 9-like, transcript variant X2
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
TWiK family of potassium channels protein 9-like
uncharacterized LOC125063050, transcript variant X2
uncharacterized LOC125063050, transcript variant X1
uncharacterized LOC125063050, transcript variant X3
uncharacterized LOC125057115, 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 1 sample with support for all annotated introns
uncharacterized LOC125057115, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC125057115 isoform X2
uncharacterized protein LOC125057115 isoform X3
uncharacterized LOC125057115, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized protein LOC125057115 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 104 samples with support for all annotated introns
potassium channel subfamily K member 18-like
probable ATP-dependent RNA helicase kurz
uncharacterized LOC125063005, transcript variant X2
uncharacterized LOC125063005, 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 147 samples with support for all annotated introns
uncharacterized protein LOC125063005 isoform X2
uncharacterized protein LOC125063005 isoform X1
uncharacterized LOC125056958, transcript variant X2
uncharacterized LOC125056958, transcript variant X1
glutamate receptor ionotropic, kainate 2-like
glutamate receptor ionotropic, kainate 2, transcript variant X2
glutamate receptor ionotropic, kainate 2, transcript variant X1
glutamate receptor ionotropic, kainate 2, transcript variant X3
glutamate receptor ionotropic, kainate 2, transcript variant X5
glutamate receptor ionotropic, kainate 2, transcript variant X4
glutamate receptor ionotropic, kainate 2, transcript variant X6
glutamate receptor ionotropic, kainate 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2 isoform X2
glutamate receptor ionotropic, kainate 2 isoform X1
glutamate receptor ionotropic, kainate 2 isoform X3
glutamate receptor ionotropic, kainate 2 isoform X5
glutamate receptor ionotropic, kainate 2 isoform X4
glutamate receptor ionotropic, kainate 2 isoform X6
glutamate receptor ionotropic, kainate 2 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 130 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2-like isoform X2
glutamate receptor ionotropic, kainate 2-like isoform 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
uncharacterized LOC125061380, transcript variant X1
uncharacterized LOC125061380, transcript variant X2
uncharacterized LOC125061380, transcript variant X3
uncharacterized protein LOC125061380 isoform X1
uncharacterized protein LOC125061380 isoform X2
uncharacterized protein LOC125061380 isoform X3
palmitoleoyl-protein carboxylesterase NOTUM
protein unc-13 homolog 4B, transcript variant X3
protein unc-13 homolog 4B, transcript variant X2
protein unc-13 homolog 4B, transcript variant X1
protein unc-13 homolog 4B, transcript variant X4
protein unc-13 homolog 4B, transcript variant X6
protein unc-13 homolog 4B, transcript variant X5
protein unc-13 homolog 4B, transcript variant X7
uncharacterized LOC125061215, transcript variant X1
ribonuclease H2 subunit A, transcript variant X1
ribonuclease H2 subunit A, transcript variant X2
uncharacterized LOC125061215, transcript variant X2
protein FRA10AC1 homolog, transcript variant X2
protein FRA10AC1 homolog, transcript variant X1
cytosolic purine 5'-nucleotidase, transcript variant X2
cytosolic purine 5'-nucleotidase, transcript variant X1
cytosolic purine 5'-nucleotidase, transcript variant X5
cytosolic purine 5'-nucleotidase, transcript variant X4
cytosolic purine 5'-nucleotidase, transcript variant X3
cytosolic purine 5'-nucleotidase isoform X2
cytosolic purine 5'-nucleotidase isoform X1
cytosolic purine 5'-nucleotidase isoform X3
Hermansky-Pudlak syndrome 1 protein homolog, transcript variant X2
Hermansky-Pudlak syndrome 1 protein homolog, transcript variant X1
Hermansky-Pudlak syndrome 1 protein homolog isoform X2
Hermansky-Pudlak syndrome 1 protein homolog isoform X1
dihydroorotate dehydrogenase (quinone), mitochondrial, transcript variant X2
dihydroorotate dehydrogenase (quinone), mitochondrial, transcript variant X1
dihydroorotate dehydrogenase (quinone), mitochondrial isoform X1
dihydroorotate dehydrogenase (quinone), mitochondrial isoform X2
hexokinase type 2, transcript variant X3
hexokinase type 2, transcript variant X4
hexokinase type 2, transcript variant X2
hexokinase type 2, transcript variant X1
proto-oncogene tyrosine-protein kinase ROS, transcript variant X1
proto-oncogene tyrosine-protein kinase ROS, transcript variant X2
proto-oncogene tyrosine-protein kinase ROS, transcript variant X3
proto-oncogene tyrosine-protein kinase ROS, transcript variant X4
proto-oncogene tyrosine-protein kinase ROS, transcript variant X5
proto-oncogene tyrosine-protein kinase ROS isoform X1
proto-oncogene tyrosine-protein kinase ROS isoform X5
proto-oncogene tyrosine-protein kinase ROS isoform X2
proto-oncogene tyrosine-protein kinase ROS isoform X3
proto-oncogene tyrosine-protein kinase ROS isoform X4
smad nuclear-interacting protein 1, transcript variant X4
smad nuclear-interacting protein 1, transcript variant X2
smad nuclear-interacting protein 1, transcript variant X1
smad nuclear-interacting protein 1, transcript variant X3
smad nuclear-interacting protein 1 isoform X4
smad nuclear-interacting protein 1 isoform X2
smad nuclear-interacting protein 1 isoform X3
smad nuclear-interacting protein 1 isoform X1
armadillo-like helical domain-containing protein 3, 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 69 samples with support for all annotated introns
armadillo-like helical domain-containing protein 3, 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 164 samples with support for all annotated introns
armadillo-like helical domain-containing protein 3 isoform X1
armadillo-like helical domain-containing protein 3 isoform X2
coiled-coil domain-containing protein 149
HIG1 domain family member 2A, mitochondrial, transcript variant X3
HIG1 domain family member 2A, mitochondrial, transcript variant X2
HIG1 domain family member 2A, mitochondrial, transcript variant X1
HIG1 domain family member 2A, mitochondrial
uncharacterized LOC125056079, transcript variant X1
uncharacterized protein LOC125056079 isoform X1
uncharacterized LOC125056079, transcript variant X2
uncharacterized protein LOC125056079 isoform X2
LOW QUALITY PROTEIN: protein couch potato
PRADC1-like protein, transcript variant X2
PRADC1-like protein, transcript variant X1
endoribonuclease Dicer, transcript variant X3
endoribonuclease Dicer, transcript variant X1
endoribonuclease Dicer, transcript variant X5
endoribonuclease Dicer, transcript variant X6
endoribonuclease Dicer, transcript variant X7
endoribonuclease Dicer, transcript variant X2
endoribonuclease Dicer, transcript variant X4
juvenile hormone epoxide hydrolase-like, transcript variant X2
juvenile hormone epoxide hydrolase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
ubiquinone biosynthesis O-methyltransferase, mitochondrial-like
structure-specific endonuclease subunit SLX1 homolog
zinc finger HIT domain-containing protein 2
phosphatidylinositol 4-kinase alpha, transcript variant X2
phosphatidylinositol 4-kinase alpha, transcript variant X1
phosphatidylinositol 4-kinase alpha, transcript variant X3
phosphatidylinositol 4-kinase alpha isoform X2
phosphatidylinositol 4-kinase alpha isoform X3
phosphatidylinositol 4-kinase alpha isoform X1
uncharacterized LOC125058752, transcript variant X1
uncharacterized LOC125058752, transcript variant X2
uncharacterized LOC125058752, transcript variant X3
trafficking protein particle complex subunit 3, transcript variant X1
trafficking protein particle complex subunit 3, transcript variant X2
trafficking protein particle complex subunit 3 isoform X1
trafficking protein particle complex subunit 3 isoform X2
optomotor-blind protein-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 114 samples with support for all annotated introns
optomotor-blind protein-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 77 samples with support for all annotated introns
optomotor-blind protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 149 samples with support for all annotated introns
optomotor-blind protein-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 143 samples with support for all annotated introns
optomotor-blind protein-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 116 samples with support for all annotated introns
optomotor-blind protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 103 samples with support for all annotated introns
optomotor-blind protein-like, transcript variant X7
T-box transcription factor TBX3-like isoform X7
Fanconi anemia group J protein homolog, transcript variant X1
Fanconi anemia group J protein homolog, transcript variant X2
Fanconi anemia group J protein homolog, transcript variant X3
Fanconi anemia group J protein homolog isoform X1
Fanconi anemia group J protein homolog isoform X2
Fanconi anemia group J protein homolog isoform X3
fatty acid-binding protein, adipocyte-like
transport and Golgi organization protein 2, transcript variant X2
transport and Golgi organization protein 2, transcript variant X1
transport and Golgi organization protein 2 isoform X1
transport and Golgi organization protein 2 isoform X2
serine--tRNA synthetase-like protein Slimp
clathrin heavy chain, transcript variant X1
clathrin heavy chain, transcript variant X2
ubiquitin recognition factor in ER-associated degradation protein 1, transcript variant X1
ubiquitin recognition factor in ER-associated degradation protein 1, transcript variant X2
ubiquitin fusion degradation protein 1 homolog isoform X1
ubiquitin recognition factor in ER-associated degradation protein 1 isoform X2
actin-related protein 2/3 complex subunit 4
leucine-zipper-like transcriptional regulator 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 25 samples with support for all annotated introns
leucine-zipper-like transcriptional regulator 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 127 samples with support for all annotated introns
leucine-zipper-like transcriptional regulator 1 isoform X2
leucine-zipper-like transcriptional regulator 1 homolog isoform X1
ran-specific GTPase-activating protein-like, transcript variant X2
ran-specific GTPase-activating protein-like, transcript variant X1
ran-specific GTPase-activating protein-like isoform X2
ran-specific GTPase-activating protein-like isoform X1
RIMS-binding protein 2, transcript variant X1
RIMS-binding protein 2, transcript variant X4
RIMS-binding protein 2, transcript variant X5
RIMS-binding protein 2, transcript variant X6
RIMS-binding protein 2, transcript variant X7
RIMS-binding protein 2, transcript variant X3
RIMS-binding protein 2, transcript variant X2
RIMS-binding protein 2, transcript variant X9
RIMS-binding protein 2, transcript variant X8
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 31 samples with support for all annotated introns
serine protease gd-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 159 samples with support for all annotated introns
serine protease gd-like, transcript variant X3
serine protease gd-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 158 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 166 samples with support for all annotated introns
AP-1 complex subunit beta-1, transcript variant X2
AP-1 complex subunit beta-1, transcript variant X1
uncharacterized LOC125063058, 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 3 samples with support for all annotated introns
uncharacterized LOC125063058, transcript variant X1
uncharacterized LOC125063058, transcript variant X4
uncharacterized LOC125063058, transcript variant X5
uncharacterized protein LOC125063058 isoform X2
uncharacterized protein LOC125063058 isoform X1
uncharacterized protein LOC125063058 isoform X4
uncharacterized protein LOC125063058 isoform X5
uncharacterized LOC125063058, transcript variant X3
uncharacterized protein LOC125063058 isoform X3
uncharacterized LOC125059020, transcript variant X2
uncharacterized LOC125059020, transcript variant X1
myosin regulatory light chain sqh, transcript variant X1
myosin regulatory light chain sqh, transcript variant X3
myosin regulatory light chain sqh, 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 16 samples with support for all annotated introns
dnaJ homolog subfamily C member 30, mitochondrial
vacuolar protein sorting-associated protein 37B
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase, transcript variant X1
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase, transcript variant X2
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase isoform X1
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase isoform X2
phosphatidylinositol transfer protein alpha isoform
uncharacterized LOC125057989, transcript variant X13
uncharacterized LOC125057989, transcript variant X7
uncharacterized LOC125057989, transcript variant X4
uncharacterized LOC125057989, transcript variant X3
uncharacterized LOC125057989, transcript variant X11
uncharacterized LOC125057989, transcript variant X1
uncharacterized LOC125057989, transcript variant X12
uncharacterized LOC125057989, transcript variant X8
uncharacterized LOC125057989, transcript variant X5
uncharacterized LOC125057989, transcript variant X14
uncharacterized LOC125057989, transcript variant X2
uncharacterized LOC125057989, transcript variant X10
uncharacterized LOC125057989, transcript variant X9
uncharacterized LOC125057989, transcript variant X6
uncharacterized protein LOC125057989 isoform X3
uncharacterized protein LOC125057989 isoform X2
uncharacterized protein LOC125057989 isoform X1
macrophage migration inhibitory factor-like, transcript variant X1
macrophage migration inhibitory factor-like, transcript variant X2
macrophage migration inhibitory factor-like
uncharacterized LOC125059138, transcript variant X1
uncharacterized LOC125059138, 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 169 samples with support for all annotated introns
uncharacterized protein LOC125059138 isoform X1
uncharacterized protein LOC125059138 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1 isoform X1
RILP-like protein homolog, transcript variant X9
RILP-like protein homolog, transcript variant X6
RILP-like protein 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 88 samples with support for all annotated introns
RILP-like protein homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 113 samples with support for all annotated introns
RILP-like protein 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 128 samples with support for all annotated introns
RILP-like protein homolog, 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 115 samples with support for all annotated introns
RILP-like protein homolog, 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 130 samples with support for all annotated introns
RILP-like protein homolog, transcript variant X7
RILP-like protein homolog, transcript variant X8
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 144 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 45 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 60 samples with support for all annotated introns
28S ribosomal protein S15, mitochondrial
neo-calmodulin-like, transcript variant X3
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 22 samples with support for all annotated introns
neo-calmodulin-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
neo-calmodulin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
serine/threonine-protein phosphatase Pgam5, mitochondrial, transcript variant X3
serine/threonine-protein phosphatase Pgam5, mitochondrial, transcript variant X2
serine/threonine-protein phosphatase Pgam5, mitochondrial, transcript variant X1
serine/threonine-protein phosphatase Pgam5, mitochondrial isoform X3
serine/threonine-protein phosphatase Pgam5, mitochondrial isoform X2
serine/threonine-protein phosphatase Pgam5, mitochondrial isoform X1
cytochrome P450 4C1-like, transcript variant X1
cytochrome P450 4C1-like, transcript variant X2
luciferin 4-monooxygenase-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 23 samples with support for all annotated introns
luciferin 4-monooxygenase-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 88 samples with support for all annotated introns
luciferin 4-monooxygenase-like isoform X1
luciferin 4-monooxygenase-like isoform X2
luciferin 4-monooxygenase-like, transcript variant X4
luciferin 4-monooxygenase-like, transcript variant X3
luciferin 4-monooxygenase-like, transcript variant X5
luciferin 4-monooxygenase-like isoform X3
luciferin 4-monooxygenase-like isoform X4
protein FRG1 homolog, transcript variant X1
protein FRG1 homolog, transcript variant X2
uncharacterized LOC125060930, transcript variant X2
uncharacterized LOC125060930, transcript variant X1
uncharacterized protein LOC125060930 isoform X1
uncharacterized protein LOC125060930 isoform X2
death-associated inhibitor of apoptosis 2-like, transcript variant X3
death-associated inhibitor of apoptosis 2-like, transcript variant X1
death-associated inhibitor of apoptosis 2-like, transcript variant X2
death-associated inhibitor of apoptosis 2-like isoform X1
baculoviral IAP repeat-containing protein 7-like isoform X2
death-associated inhibitor of apoptosis 1-like, transcript variant X3
death-associated inhibitor of apoptosis 1-like, transcript variant X4
death-associated inhibitor of apoptosis 1-like, transcript variant X1
death-associated inhibitor of apoptosis 1-like, transcript variant X2
death-associated inhibitor of apoptosis 1-like isoform X1
death-associated inhibitor of apoptosis 1-like, transcript variant X5
death-associated inhibitor of apoptosis 1-like isoform X2
death-associated inhibitor of apoptosis 1-like, transcript variant X6
death-associated inhibitor of apoptosis 1-like isoform X3
putative uncharacterized protein DDB_G0289263, transcript variant X1
putative uncharacterized protein DDB_G0289263, transcript variant X2
putative uncharacterized protein DDB_G0289263 isoform X1
uncharacterized LOC125063082, transcript variant X1
uncharacterized LOC125063082, 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 138 samples with support for all annotated introns
uncharacterized protein LOC125063082 isoform X2
uncharacterized protein LOC125063082 isoform X1
monocarboxylate transporter 10-like, transcript variant X1
monocarboxylate transporter 10-like, transcript variant X5
monocarboxylate transporter 10-like, transcript variant X2
monocarboxylate transporter 10-like, transcript variant X4
monocarboxylate transporter 10-like, transcript variant X3
monocarboxylate transporter 10-like isoform X1
monocarboxylate transporter 10-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 3-like
SR-related and CTD-associated factor 4, transcript variant X3
SR-related and CTD-associated factor 4, transcript variant X4
SR-related and CTD-associated factor 4, transcript variant X2
SR-related and CTD-associated factor 4, transcript variant X1
SR-related and CTD-associated factor 4 isoform X3
SR-related and CTD-associated factor 4 isoform X4
SR-related and CTD-associated factor 4 isoform X2
SR-related and CTD-associated factor 4 isoform X1
tubulin-folding cofactor B, transcript variant X2
tubulin-folding cofactor B, 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 66 samples with support for all annotated introns
potassium channel subfamily K member 1-like, transcript variant X2
potassium channel subfamily K member 1-like isoform X2
potassium channel subfamily K member 1-like, transcript variant X1
potassium channel subfamily K member 1-like isoform X1
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X6
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X5
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X2
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X1
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X3
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X7
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X8
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X4
nucleolar and coiled-body phosphoprotein 1-like isoform X3
bifunctional lysine-specific demethylase and histidyl-hydroxylase NO66
serum response factor homolog, transcript variant X3
serum response factor homolog, transcript variant X2
serum response factor homolog, transcript variant X1
serum response factor homolog isoform X2
serum response factor homolog isoform X1
guanine nucleotide-binding protein subunit beta-like protein 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 74 samples with support for all annotated introns
membrane-bound transcription factor site-2 protease
probable cysteine--tRNA ligase, mitochondrial
uncharacterized LOC125059325, transcript variant X6
uncharacterized LOC125059325, transcript variant X3
uncharacterized LOC125059325, transcript variant X5
uncharacterized LOC125059325, transcript variant X4
uncharacterized LOC125059325, transcript variant X1
uncharacterized LOC125059325, transcript variant X2
uncharacterized protein LOC125059325 isoform X4
uncharacterized protein LOC125059325 isoform X3
uncharacterized protein LOC125059325 isoform X2
uncharacterized protein LOC125059325 isoform X1
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
UDP-N-acetylglucosamine transferase subunit ALG13 homolog
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
transmembrane emp24 domain-containing protein eca
KAT8 regulatory NSL complex subunit 1, transcript variant X3
KAT8 regulatory NSL complex subunit 1, transcript variant X4
KAT8 regulatory NSL complex subunit 1, transcript variant X1
KAT8 regulatory NSL complex subunit 1, transcript variant X2
uncharacterized LOC125057734, transcript variant X1
uncharacterized LOC125057734, transcript variant X2
uncharacterized protein LOC125057734 isoform X1
uncharacterized protein LOC125057734 isoform 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 13 samples with support for all annotated introns
uncharacterized LOC125062995, transcript variant X1
uncharacterized LOC125062995, 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 156 samples with support for all annotated introns
uncharacterized LOC125056556, 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 28 samples with support for all annotated introns
uncharacterized LOC125056556, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125056556, 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 20 samples with support for all annotated introns
uncharacterized protein LOC125056556 isoform X1
uncharacterized protein LOC125056556 isoform X2
uncharacterized protein LOC125056556 isoform X3
probable methylthioribulose-1-phosphate dehydratase, transcript variant X2
probable methylthioribulose-1-phosphate dehydratase, transcript variant X1
probable methylthioribulose-1-phosphate dehydratase isoform X2
probable methylthioribulose-1-phosphate dehydratase isoform X1
uncharacterized LOC125056536, transcript variant X1
uncharacterized LOC125056536, transcript variant X2
uncharacterized LOC125056536, transcript variant X4
uncharacterized protein LOC125056536 isoform X1
uncharacterized protein LOC125056536 isoform X2
uncharacterized protein LOC125056536 isoform X4
uncharacterized LOC125056536, transcript variant X3
uncharacterized protein LOC125056536 isoform X3
proline-rich receptor-like protein kinase PERK9
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: 97% coverage of the annotated genomic feature by RNAseq alignments, including 140 samples with support for all annotated introns
MMS19 nucleotide excision repair protein homolog
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
U6 snRNA-associated Sm-like protein LSm1
rho GTPase-activating protein 19, transcript variant X1
rho GTPase-activating protein 19, transcript variant X2
rho GTPase-activating protein 19 isoform X1
rho GTPase-activating protein 19 isoform X2
delta-1-pyrroline-5-carboxylate synthase, 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 163 samples with support for all annotated introns
delta-1-pyrroline-5-carboxylate synthase isoform X1
delta-1-pyrroline-5-carboxylate synthase, 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 156 samples with support for all annotated introns
delta-1-pyrroline-5-carboxylate synthase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 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 35% coverage of the annotated genomic feature by RNAseq alignments
microsomal glutathione S-transferase 1-like
crossover junction endonuclease MUS81, transcript variant X1
crossover junction endonuclease MUS81 isoform X1
crossover junction endonuclease MUS81, 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 69 samples with support for all annotated introns
crossover junction endonuclease MUS81 isoform X2
RNA polymerase-associated protein CTR9 homolog, transcript variant X2
RNA polymerase-associated protein CTR9 homolog, transcript variant X1
RNA polymerase-associated protein CTR9 homolog
5'-3' exonuclease PLD3-like, 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 36 samples with support for all annotated introns
5'-3' exonuclease PLD3-like, transcript variant X2
5'-3' exonuclease PLD3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 163 samples with support for all annotated introns
structural maintenance of chromosomes protein 3
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 161 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
histone-lysine N-trimethyltransferase SMYD5
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 157 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
circadian clock-controlled protein daywake-like
circadian clock-controlled protein daywake-like, transcript variant X2
circadian clock-controlled protein daywake-like isoform X2
circadian clock-controlled protein daywake-like, transcript variant X1
circadian clock-controlled protein daywake-like isoform X1
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 136 samples with support for all annotated introns
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X1
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X2
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, 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 136 samples with support for all annotated introns
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, 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 150 samples with support for all annotated introns
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X4
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform 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 53 samples with support for all annotated introns
uncharacterized LOC125061029, transcript variant X2
uncharacterized LOC125061029, transcript variant X1
acetyl-CoA acetyltransferase, mitochondrial, transcript variant X1
acetyl-CoA acetyltransferase, mitochondrial, transcript variant X2
acetyl-CoA acetyltransferase, mitochondrial isoform X1
acetyl-CoA acetyltransferase, mitochondrial isoform X2
sodium-dependent transporter bedraggled, transcript variant X2
sodium-dependent transporter bedraggled, transcript variant X1
sodium-dependent transporter bedraggled, transcript variant X3
sodium-dependent transporter bedraggled isoform X1
sodium-dependent transporter bedraggled isoform X2
uncharacterized LOC125059006, transcript variant X1
uncharacterized LOC125059006, transcript variant X2
protein ALP1-like, transcript variant X1
protein ALP1-like, transcript variant X2
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like isoform X2
apoptotic protease-activating factor 1, 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 120 samples with support for all annotated introns
apoptotic protease-activating factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
apoptotic protease-activating factor 1 isoform X1
apoptotic protease-activating factor 1 isoform X2
toll-like receptor 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
toll-like receptor 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
collagen alpha-2(V) chain-like, transcript variant X2
collagen alpha-2(V) chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
collagen alpha-2(V) chain-like isoform X1
collagen alpha-1(XI) chain-like isoform X2
uncharacterized LOC125055910, transcript variant X1
uncharacterized protein LOC125055910 isoform X1
uncharacterized LOC125055910, transcript variant X2
uncharacterized protein LOC125055910 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 115 samples with support for all annotated introns
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
organic cation transporter protein-like, transcript variant X2
organic cation transporter protein-like, transcript variant X1
solute carrier family 22 member 3-like isoform X2
organic cation transporter protein-like isoform X1
organic cation transporter protein-like, transcript variant X3
organic cation transporter protein-like isoform X3
ribosomal protein S6 kinase 2 beta, transcript variant X1
ribosomal protein S6 kinase 2 beta isoform X1
ribosomal protein S6 kinase 2 beta, transcript variant X2
ribosomal protein S6 kinase 2 beta isoform X2
aminoacyl tRNA synthase complex-interacting multifunctional protein 1
polycomb protein Scm, transcript variant X2
polycomb protein Scm, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 119 samples with support for all annotated introns
lysocardiolipin acyltransferase 1-like, 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 5 samples with support for all annotated introns
lysocardiolipin acyltransferase 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
lysocardiolipin acyltransferase 1-like, transcript variant X2
organic cation transporter protein-like 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 113 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 108 samples with support for all annotated introns
histone deacetylase complex subunit SAP18, transcript variant X2
histone deacetylase complex subunit SAP18, transcript variant X1
histone deacetylase complex subunit SAP18
organic cation transporter protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
organic cation transporter protein isoform X1
organic cation transporter protein, transcript variant X2
organic cation transporter protein, transcript variant X4
organic cation transporter protein isoform X2
organic cation transporter protein isoform X4
organic cation transporter protein, transcript variant X3
organic cation transporter protein isoform X3
E3 UFM1-protein ligase 1 homolog, transcript variant X1
E3 UFM1-protein ligase 1 homolog, transcript variant X2
E3 UFM1-protein ligase 1 homolog, transcript variant X3
guanine nucleotide-binding protein subunit gamma-1
DNA fragmentation factor subunit alpha-like, transcript variant X2
DNA fragmentation factor subunit alpha-like, transcript variant X1
DNA fragmentation factor subunit alpha-like
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X2
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial isoform X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial isoform X2
uncharacterized LOC125062789, 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 31 samples with support for all annotated introns
uncharacterized LOC125062789, 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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
eukaryotic translation initiation factor 2 subunit 3-like, transcript variant X1
eukaryotic translation initiation factor 2 subunit 3-like, transcript variant X2
eukaryotic translation initiation factor 2 subunit 3-like isoform X2
histone-lysine N-methyltransferase SUV39H2-like isoform X1
peroxisomal N(1)-acetyl-spermine/spermidine oxidase, transcript variant X1
peroxisomal N(1)-acetyl-spermine/spermidine oxidase, transcript variant X2
peroxisomal N(1)-acetyl-spermine/spermidine oxidase isoform X1
peroxisomal N(1)-acetyl-spermine/spermidine oxidase isoform X2
early growth response protein 3, transcript variant X1
early growth response protein 3, transcript variant X2
early growth response protein 3 isoform X1
early growth response protein 3 isoform X2
uncharacterized LOC125062552, transcript variant X3
uncharacterized LOC125062552, transcript variant X2
uncharacterized LOC125062552, transcript variant X1
uncharacterized LOC125062539, transcript variant X3
uncharacterized LOC125062539, transcript variant X1
uncharacterized LOC125062539, transcript variant X2
phosphatidylethanolamine-binding protein 1-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 17 samples with support for all annotated introns
asparagine synthetase [glutamine-hydrolyzing]
protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
uncharacterized LOC125056828, transcript variant X1
uncharacterized LOC125056828, transcript variant X4
uncharacterized LOC125056828, transcript variant X3
uncharacterized LOC125056828, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
juvenile hormone esterase-like, transcript variant X2
juvenile hormone esterase-like, transcript variant X1
uncharacterized protein LOC125056828 isoform X1
uncharacterized protein LOC125056828 isoform X2
cilia- and flagella-associated protein 157
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 84% 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 13 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 167 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 3 samples with support for all annotated introns
solute carrier family 22 member 1-like, transcript variant X2
solute carrier family 22 member 1-like, transcript variant X3
solute carrier family 22 member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
solute carrier family 22 member 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 22 member 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
solute carrier family 22 member 4-like isoform X1
solute carrier family 22 member 4-like isoform X2
solute carrier family 22 member 2-like, transcript variant X2
solute carrier family 22 member 2-like, 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 11 samples with support for all annotated introns
solute carrier family 22 member 2-like isoform X2
solute carrier family 22 member 2-like isoform 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 1 sample with support for all annotated introns
organic cation transporter protein-like, transcript variant X4
tetratricopeptide repeat protein 7B, transcript variant X1
tetratricopeptide repeat protein 7B, transcript variant X2
tetratricopeptide repeat protein 7B isoform X1
tetratricopeptide repeat protein 7B isoform X2
alpha-ketoglutarate-dependent dioxygenase alkB homolog 6
cytochrome c oxidase assembly protein COX15 homolog, transcript variant X2
cytochrome c oxidase assembly protein COX15 homolog, transcript variant X1
cytochrome c oxidase assembly protein COX15 homolog
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 48 samples with support for all annotated introns
protein takeout-like, transcript variant X2
protein takeout-like, transcript variant X1
ribonuclease P protein subunit p40-like, transcript variant X1
ribonuclease P protein subunit p40-like, transcript variant X2
uncharacterized LOC125062143, transcript variant X1
uncharacterized LOC125062143, transcript variant X4
uncharacterized LOC125062143, transcript variant X2
uncharacterized LOC125062143, transcript variant X3
uncharacterized LOC125062143, transcript variant X5
uncharacterized protein LOC125062143 isoform X1
uncharacterized protein LOC125062143 isoform X2
GTP 3',8-cyclase, mitochondrial, transcript variant X2
GTP 3',8-cyclase, mitochondrial, transcript variant X1
molybdenum cofactor biosynthesis protein 1 isoform X1
GTP 3',8-cyclase, mitochondrial, 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 32 samples with support for all annotated introns
GTP 3',8-cyclase, mitochondrial isoform X2
major facilitator superfamily domain-containing protein 8
collagen alpha-2(I) chain-like, transcript variant X2
collagen alpha-2(I) chain-like, transcript variant X1
collagen alpha-2(I) chain-like isoform X2
collagen alpha-2(I) chain-like isoform X1
solute carrier family 22 member 13-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
solute carrier family 22 member 13-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
solute carrier family 22 member 13-like isoform X2
uncharacterized LOC125063078, transcript variant X3
uncharacterized LOC125063078, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125063078, 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