Pieris rapae chromosome 3, ilPieRapa1.1, 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\nLR990585.1.\nAssembly name: ilPieRapa1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Wellcome Sanger Institute on\n2021/01/28. The original whole-genome shotgun project has the\naccession CAJHWY000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris rapae Annotation Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
UDP-glucose 4-epimerase-like, transcript variant X1
UDP-glucose 4-epimerase-like, transcript variant X2
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 LOC111002635, transcript variant X4
uncharacterized LOC111002635, transcript variant X1
uncharacterized LOC111002635, transcript variant X3
uncharacterized LOC111002635, transcript variant X2
uncharacterized protein LOC111002635 isoform X3
uncharacterized protein LOC111002635 isoform X1
uncharacterized protein LOC111002635 isoform X2
uncharacterized LOC111002610, transcript variant X2
uncharacterized LOC111002610, transcript variant X1
uncharacterized protein LOC111002610 isoform X1
uncharacterized protein LOC111002610 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 11 samples with support for all annotated introns
uncharacterized LOC111002630, transcript variant X2
uncharacterized LOC111002630, transcript variant X3
uncharacterized LOC111002630, transcript variant X1
glycine, alanine and asparagine-rich protein-like
uncharacterized LOC111002652, transcript variant X7
uncharacterized LOC111002652, transcript variant X2
uncharacterized LOC111002652, transcript variant X8
uncharacterized LOC111002652, transcript variant X11
uncharacterized LOC111002652, transcript variant X10
uncharacterized LOC111002652, transcript variant X4
uncharacterized LOC111002652, transcript variant X5
uncharacterized LOC111002652, transcript variant X9
uncharacterized LOC111002652, transcript variant X6
uncharacterized LOC111002652, transcript variant X3
uncharacterized LOC111002652, transcript variant X1
uncharacterized LOC111002652, transcript variant X12
uncharacterized protein LOC111002652 isoform X8
uncharacterized protein LOC111002652 isoform X11
uncharacterized protein LOC111002652 isoform X12
uncharacterized protein LOC111002652 isoform X10
uncharacterized protein LOC111002652 isoform X4
uncharacterized protein LOC111002652 isoform X5
uncharacterized protein LOC111002652 isoform X9
uncharacterized protein LOC111002652 isoform X6
uncharacterized protein LOC111002652 isoform X7
uncharacterized protein LOC111002652 isoform X3
uncharacterized protein LOC111002652 isoform X2
uncharacterized protein LOC111002652 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
putative uncharacterized protein DDB_G0282499, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
putative uncharacterized protein DDB_G0282499, 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 11 samples with support for all annotated introns
putative uncharacterized protein DDB_G0282499 isoform X2
uncharacterized protein LOC111002696 isoform X1
receptor-type tyrosine-protein phosphatase kappa, 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 13 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase kappa, 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 15 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase kappa isoform X1
receptor-type tyrosine-protein phosphatase kappa isoform X2
juvenile hormone esterase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
juvenile hormone esterase-like isoform X2
juvenile hormone esterase-like, transcript variant X1
juvenile hormone esterase-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 105 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 109 samples with support for all annotated introns
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X3
aldehyde dehydrogenase, dimeric NADP-preferring isoform X3
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X2
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X1
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
aldehyde dehydrogenase, dimeric NADP-preferring isoform X2
aldehyde dehydrogenase, dimeric NADP-preferring isoform X1
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 X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
PX domain-containing protein kinase-like protein, transcript variant X4
PX domain-containing protein kinase-like protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
PX domain-containing protein kinase-like protein, transcript variant X2
PX domain-containing protein kinase-like protein, transcript variant X1
PX domain-containing protein kinase-like protein, transcript variant X7
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 16 samples with support for all annotated introns
PX domain-containing protein kinase-like protein, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
PX domain-containing protein kinase-like protein, transcript variant X8
PX domain-containing protein kinase-like protein isoform X1
PX domain-containing protein kinase-like protein isoform X4
PX domain-containing protein kinase-like protein isoform X3
PX domain-containing protein kinase-like protein isoform X5
PX domain-containing protein kinase-like protein isoform X6
PX domain-containing protein kinase-like protein isoform X7
PX domain-containing protein kinase-like protein isoform X2
PX domain-containing protein kinase-like protein isoform X8
guanine nucleotide exchange factor subunit Rich, transcript variant X2
guanine nucleotide exchange factor subunit Rich, transcript variant X1
guanine nucleotide exchange factor subunit Rich, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
guanine nucleotide exchange factor subunit Rich isoform X1
guanine nucleotide exchange factor subunit Rich isoform X2
guanine nucleotide exchange factor subunit Rich, transcript variant X3
guanine nucleotide exchange factor subunit Rich isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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
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 20 samples with support for all annotated introns
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: 6 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: 3 Proteins, and 96% 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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X2
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X1
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X3
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X2
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X1
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X3
Bardet-Biedl syndrome 2 protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Bardet-Biedl syndrome 2 protein, transcript variant X2
Bardet-Biedl syndrome 2 protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Bardet-Biedl syndrome 2 protein isoform X1
Bardet-Biedl syndrome 2 protein homolog 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 15 samples with support for all annotated introns
adipokinetic hormone/corazonin-related peptide receptor variant I
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
excitatory amino acid transporter 3, transcript variant X1
excitatory amino acid transporter 3, transcript variant X2
zinc finger protein 891, 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
zinc finger protein 891, transcript variant X2
gastrula zinc finger protein XlCGF7.1 isoform X2
cyclin-dependent kinases regulatory subunit
glutathione S-transferase 1, transcript variant X1
glutathione S-transferase 1, transcript variant X2
SNAPIN protein homolog, transcript variant X1
SNAPIN protein homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
leucine-rich repeat-containing protein 49
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
glutamate receptor ionotropic, delta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cartilage oligomeric matrix protein, transcript variant X1
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 X8
transient receptor potential cation channel trpm, transcript variant X13
transient receptor potential cation channel trpm, transcript variant X12
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 X14
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 X6
transient receptor potential cation channel trpm, transcript variant X11
transient receptor potential cation channel trpm isoform X9
transient receptor potential cation channel trpm isoform X8
transient receptor potential cation channel trpm isoform X13
transient receptor potential cation channel trpm isoform X12
transient receptor potential cation channel trpm isoform X2
transient receptor potential cation channel trpm isoform X4
transient receptor potential cation channel trpm isoform X10
transient receptor potential cation channel trpm isoform X14
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 X11
transient receptor potential cation channel trpm isoform X7
transient receptor potential cation channel trpm isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
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 8 samples with support for all annotated introns
5-formyltetrahydrofolate cyclo-ligase, transcript variant X1
5-formyltetrahydrofolate cyclo-ligase, transcript variant X2
5-formyltetrahydrofolate cyclo-ligase isoform X1
5-formyltetrahydrofolate cyclo-ligase isoform X2
uncharacterized LOC111002660, 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 4 samples with support for all annotated introns
uncharacterized LOC111002660, 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 8 samples with support for all annotated introns
uncharacterized protein LOC111002660 isoform X2
uncharacterized protein LOC111002660 isoform X1
protein fem-1 homolog B, transcript variant X2
protein fem-1 homolog B, transcript variant X3
protein fem-1 homolog B, transcript variant X1
protein fem-1 homolog B, transcript variant X5
protein fem-1 homolog B, 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
putative deoxyribonuclease TATDN1, transcript variant X1
putative deoxyribonuclease TATDN1, transcript variant X2
putative deoxyribonuclease TATDN1 isoform X1
putative deoxyribonuclease TATDN1 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 16 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 2
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC111002644, 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 9 samples with support for all annotated introns
uncharacterized LOC111002644, transcript variant X1
uncharacterized LOC111002644, transcript variant X4
uncharacterized LOC111002644, transcript variant X2
uncharacterized LOC111002644, transcript variant X5
uncharacterized LOC111002644, transcript variant X6
uncharacterized LOC111002644, transcript variant X7
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 LOC111002644, 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 18 samples with support for all annotated introns
uncharacterized LOC111002644, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized protein LOC111002644 isoform X2
uncharacterized protein LOC111002644 isoform X1
uncharacterized protein LOC111002644 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 59 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 3 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: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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: 1 mRNA, 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
EF-hand domain-containing family member B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 220 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 159 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial, transcript variant X1
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial, transcript variant X2
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial isoform X2
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial isoform X1
uncharacterized LOC110991528, transcript variant X2
uncharacterized LOC110991528, transcript variant X1
uncharacterized protein LOC110991528 isoform X1
uncharacterized protein LOC110991528 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CREB-regulated transcription coactivator 3, transcript variant X1
CREB-regulated transcription coactivator 3, transcript variant X2
CREB-regulated transcription coactivator 3, transcript variant X3
CREB-regulated transcription coactivator 3, transcript variant X4
CREB-regulated transcription coactivator 3 isoform X1
CREB-regulated transcription coactivator 3 isoform X2
CREB-regulated transcription coactivator 3 isoform X3
CREB-regulated transcription coactivator 3 isoform X4
GATA zinc finger domain-containing protein 14-like
uncharacterized LOC110991520, transcript variant X9
uncharacterized LOC110991520, transcript variant X2
uncharacterized LOC110991520, transcript variant X4
uncharacterized LOC110991520, transcript variant X8
uncharacterized LOC110991520, transcript variant X3
uncharacterized LOC110991520, transcript variant X7
uncharacterized LOC110991520, transcript variant X6
uncharacterized LOC110991520, transcript variant X5
uncharacterized LOC110991520, transcript variant X1
uncharacterized protein LOC110991520 isoform X2
uncharacterized protein LOC110991520 isoform X4
uncharacterized protein LOC110991520 isoform X8
uncharacterized protein LOC110991520 isoform X3
uncharacterized protein LOC110991520 isoform X9
uncharacterized protein LOC110991520 isoform X7
uncharacterized protein LOC110991520 isoform X6
uncharacterized protein LOC110991520 isoform X5
uncharacterized protein LOC110991520 isoform X1
coiled-coil domain-containing protein 112-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tetratricopeptide repeat protein 19 homolog, mitochondrial
transmembrane protein adipocyte-associated 1 homolog
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 X2
serine/threonine-protein kinase PRP4 homolog, transcript variant X1
serine/threonine-protein kinase PRP4 homolog, transcript variant X3
serine/threonine-protein kinase PRP4 homolog
pentatricopeptide repeat-containing protein 2, mitochondrial
diuretic hormone receptor, 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 10 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
diuretic hormone receptor, 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 9 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
diuretic hormone receptor, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
proton-coupled folate transporter, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
proton-coupled folate transporter isoform X1
proton-coupled folate transporter, 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 24 samples with support for all annotated introns
proton-coupled folate transporter 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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
thrombospondin type-1 domain-containing protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-alpha-hydroxyglycine alpha-amidating lyase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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 97 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 21 samples with support for all annotated introns
carbohydrate sulfotransferase 11, transcript variant X3
carbohydrate sulfotransferase 11, transcript variant X1
carbohydrate sulfotransferase 11, transcript variant X2
carbohydrate sulfotransferase 11, transcript variant X4
carbohydrate sulfotransferase 11, transcript variant X5
carbohydrate sulfotransferase 11 isoform X2
carbohydrate sulfotransferase 11 isoform X1
carbohydrate sulfotransferase 11 isoform 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 8 samples with support for all annotated introns
transfer RNA leucine (anticodon AAG); 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 X3
leptin receptor overlapping transcript-like 1, transcript variant X1
leptin receptor overlapping transcript-like 1, transcript variant X2
leptin receptor overlapping transcript-like 1 isoform X2
leptin receptor overlapping transcript-like 1 isoform X1
leptin receptor overlapping transcript-like 1, transcript variant X4
leptin receptor gene-related protein isoform X3
Down syndrome cell adhesion molecule-like protein Dscam2
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 LOC110992002, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC110992002, 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 6 samples with support for all annotated introns
uncharacterized LOC110992002, 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 7 samples with support for all annotated introns
uncharacterized protein LOC110992002 isoform X2
uncharacterized protein LOC110992002 isoform X3
uncharacterized protein LOC110992002 isoform X1
uncharacterized LOC110991838, transcript variant X2
uncharacterized LOC110991838, transcript variant X1
uncharacterized protein LOC110991838 isoform X2
uncharacterized protein LOC110991838 isoform X1
peroxisomal multifunctional enzyme type 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 36 samples with support for all annotated introns
uncharacterized LOC123690681, transcript variant X1
uncharacterized LOC123690681, transcript variant X3
uncharacterized LOC123690681, 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 27 samples with support for all annotated introns
zinc carboxypeptidase A 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc carboxypeptidase A 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc carboxypeptidase A 1-like isoform X1
zinc carboxypeptidase A 1-like isoform X2
inactive metallocarboxypeptidase ECM14-like
probable protein arginine N-methyltransferase 6.1
mitotic spindle assembly checkpoint protein MAD1
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 X1
angiogenic factor with G patch and FHA domains 1 isoform X2
tRNA selenocysteine 1-associated protein 1
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 56 samples with support for all annotated introns
transcription factor TFIIIB component B''
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 X5
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X9
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X11
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X10
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X12
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X7
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X6
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X8
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X6
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X5
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
GPI ethanolamine phosphate transferase 3
EF-hand calcium-binding domain-containing protein 14, transcript variant X2
uncharacterized protein LOC110991610 isoform X2
EF-hand calcium-binding domain-containing protein 14, transcript variant X1
EF-hand calcium-binding domain-containing protein 14 isoform X1
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial
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
transcription factor HNF-4 homolog, transcript variant X5
hepatocyte nuclear factor 4-gamma isoform X1
hepatocyte nuclear factor 4-gamma isoform X2
transcription factor HNF-4 homolog isoform X5
fanconi-associated nuclease 1, transcript variant X3
fanconi-associated nuclease 1, transcript variant X1
fanconi-associated nuclease 1, transcript variant X2
fanconi-associated nuclease 1 isoform X2
fanconi-associated nuclease 1 isoform X1
synaptic vesicle membrane protein VAT-1 homolog-like, transcript variant X1
synaptic vesicle membrane protein VAT-1 homolog-like, transcript variant X2
synaptic vesicle membrane protein VAT-1 homolog-like isoform X2
synaptic vesicle membrane protein VAT-1 homolog-like isoform X1
putative ribosome-binding factor A, mitochondrial
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
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 isoform X1
probable splicing factor, arginine/serine-rich 7, transcript variant X2
probable splicing factor, arginine/serine-rich 7 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 10 samples with support for all annotated introns
store-operated calcium entry regulator STIMATE
heterogeneous nuclear ribonucleoprotein K, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein K, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein K, 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 10 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein K isoform X1
heterogeneous nuclear ribonucleoprotein K, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
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
putative uncharacterized protein DDB_G0282133, transcript variant X2
putative uncharacterized protein DDB_G0282133, transcript variant X1
putative uncharacterized protein DDB_G0282133 isoform X1
uncharacterized protein MAL13P1.304 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 4 samples with support for all annotated introns
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase
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 33 samples with support for all annotated introns
putative uncharacterized protein DDB_G0282133
microtubule-associated protein RP/EB family member 1, transcript variant X1
microtubule-associated protein RP/EB family member 1, transcript variant X2
microtubule-associated protein RP/EB family member 1 isoform X1
microtubule-associated protein RP/EB family member 1 isoform X2
uncharacterized protein LOC110991953 isoform X2
ATP-dependent RNA helicase vasa, transcript variant X2
ATP-dependent RNA helicase vasa, transcript variant X1
ATP-dependent RNA helicase vasa isoform X2
ATP-dependent RNA helicase vasa isoform X1
G-protein coupled receptor dmsr-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
G-protein coupled receptor dmsr-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
G-protein coupled receptor dmsr-1 isoform X2
G-protein coupled receptor dmsr-1 isoform X1
ejaculatory bulb-specific protein 3, transcript variant X1
ejaculatory bulb-specific protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC110991378, transcript variant X4
uncharacterized LOC110991378, transcript variant X2
uncharacterized LOC110991378, transcript variant X3
uncharacterized LOC110991378, transcript variant X1
uncharacterized protein LOC110991378 isoform X4
uncharacterized protein LOC110991378 isoform X2
uncharacterized protein LOC110991378 isoform X3
uncharacterized protein LOC110991378 isoform X1
uncharacterized LOC110996594, transcript variant X2
uncharacterized LOC110996594, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cholesterol transporter ABCA5, transcript variant X2
cholesterol transporter ABCA5, transcript variant X1
cholesterol transporter ABCA5 isoform X2
cholesterol transporter ABCA5 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
protein adenylyltransferase SelO, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
two pore channel protein 1, transcript variant X1
two pore channel protein 1, transcript variant X4
two pore channel protein 1, transcript variant X3
two pore channel protein 1, transcript variant X2
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.
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 53 samples with support for all annotated introns
TRAF-type zinc finger domain-containing protein 1, transcript variant X1
TRAF-type zinc finger domain-containing protein 1, transcript variant X2
TRAF-type zinc finger domain-containing protein 1 isoform X1
TRAF-type zinc finger domain-containing protein 1 isoform X2
U1 small nuclear ribonucleoprotein 70 kDa, transcript variant X1
U1 small nuclear ribonucleoprotein 70 kDa, transcript variant X2
U1 small nuclear ribonucleoprotein 70 kDa isoform X1
U1 small nuclear ribonucleoprotein 70 kDa isoform X2
protein strawberry notch, transcript variant X1
protein strawberry notch, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LIM domain kinase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
LIM domain kinase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
LIM domain kinase 1, transcript variant X1
probable ATP-dependent RNA helicase DDX55 homolog
translation machinery-associated protein 16 homolog
cell division control protein 45 homolog
venom serine carboxypeptidase, transcript variant X2
venom serine carboxypeptidase, transcript variant X3
venom serine carboxypeptidase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
required for meiotic nuclear division protein 1 homolog, 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 8 samples with support for all annotated introns
required for meiotic nuclear division protein 1 homolog
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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 23 samples with support for all annotated introns
uncharacterized LOC111002939, transcript variant X2
uncharacterized LOC111002939, transcript variant X1
uncharacterized protein LOC111002939 isoform X2
uncharacterized protein LOC111002939 isoform X1
calcium/calmodulin-dependent protein kinase kinase 2, transcript variant X1
calcium/calmodulin-dependent protein kinase kinase 2 isoform X1
calcium/calmodulin-dependent protein kinase kinase 2, transcript variant X2
calcium/calmodulin-dependent protein kinase kinase 2 isoform X2
myosin-G heavy chain-like, transcript variant X2
myosin-G heavy 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 6 samples with support for all annotated introns
uncharacterized protein C622.15c-like isoform X2
phenoloxidase subunit 1, transcript variant X2
phenoloxidase subunit 1, transcript variant X1
2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial
uncharacterized LOC110997043, transcript variant X1
uncharacterized LOC110997043, transcript variant X2
uncharacterized LOC110997043, transcript variant X3
uncharacterized protein LOC110997043 isoform X1
uncharacterized protein LOC110997043 isoform X2
uncharacterized protein LOC110997043 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nose resistant to fluoxetine protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 786, transcript variant X3
zinc finger protein 786, transcript variant X1
zinc finger protein 786, transcript variant X2
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial, 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 16 samples with support for all annotated introns
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial isoform X1
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial isoform X2
uncharacterized LOC110997052, transcript variant X1
uncharacterized LOC110997052, transcript variant X2
uncharacterized LOC110997052, transcript variant X3
probable malate dehydrogenase, mitochondrial
vacuolar protein sorting-associated protein 45
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 11 samples with support for all annotated introns
GPI transamidase component PIG-S, transcript variant X2
GPI transamidase component PIG-S, transcript variant X1
GPI transamidase component PIG-S isoform X1
GPI transamidase component PIG-S isoform X2
general transcriptional corepressor trfA
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
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
uncharacterized LOC110997082, transcript variant X3
uncharacterized LOC110997082, transcript variant X1
uncharacterized LOC110997082, transcript variant X2
uncharacterized protein LOC110997082 isoform X3
uncharacterized protein LOC110997082 isoform X1
uncharacterized protein LOC110997082 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
Meckel syndrome type 1 protein homolog, transcript variant X2
Meckel syndrome type 1 protein homolog, 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
Meckel syndrome type 1 protein homolog isoform X2
Meckel syndrome type 1 protein homolog isoform X1
rhomboid-related protein 2, 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 30 samples with support for all annotated introns
rhomboid-related protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
rhomboid-related protein 2, 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 89 samples with support for all annotated introns
carboxypeptidase D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
carboxypeptidase D, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized protein KIAA2013 homolog
mitochondrial inner membrane protease subunit 2, transcript variant X2
mitochondrial inner membrane protease subunit 2, transcript variant X1
mitochondrial inner membrane protease subunit 2
yrdC domain-containing protein, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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 103 samples with support for all annotated introns
ceramide synthase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
ceramide synthase 5, transcript variant X2
ceramide synthase 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
sex-lethal homolog, transcript variant X1
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 27 samples with support for all annotated introns
sex-lethal homolog, transcript variant X3
sex-lethal homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
serine protease gd, transcript variant X3
serine protease gd, transcript variant X2
serine protease gd, transcript variant X1
uncharacterized LOC123690713, 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 13 samples with support for all annotated introns
uncharacterized LOC123690713, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
somatomedin-B and thrombospondin type-1 domain-containing protein
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC110997085, transcript variant X3
uncharacterized LOC110997085, transcript variant X2
uncharacterized LOC110997085, transcript variant X1
uncharacterized LOC110997085, transcript variant X4
uncharacterized protein LOC110997085 isoform X1
uncharacterized protein LOC110997085 isoform X4
uncharacterized protein LOC110997085 isoform X2
uncharacterized protein LOC110997085 isoform X3
uncharacterized LOC110997101, transcript variant X1
uncharacterized LOC110997101, transcript variant X3
uncharacterized LOC110997101, transcript variant X2
eukaryotic translation initiation factor 4E transporter, transcript variant X3
eukaryotic translation initiation factor 4E transporter, transcript variant X1
eukaryotic translation initiation factor 4E transporter, transcript variant X2
eukaryotic translation initiation factor 4E transporter isoform X3
eukaryotic translation initiation factor 4E transporter isoform X2
eukaryotic translation initiation factor 4E transporter isoform X1
protein suppressor of white apricot, 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 21 samples with support for all annotated introns
protein suppressor of white apricot isoform X1
protein suppressor of white apricot, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
protein suppressor of white apricot, transcript variant X3
protein suppressor of white apricot isoform X2
uncharacterized protein LOC110997058 isoform X3
uncharacterized protein LOC110997058 isoform X2
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
TBC1 domain family member whacked, transcript variant X2
39S ribosomal protein L18, mitochondrial
TBC1 domain family member whacked, transcript variant X1
TBC1 domain family member whacked isoform X1
TBC1 domain family member whacked 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 33 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit A
bleomycin hydrolase, transcript variant X1
bleomycin hydrolase, 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 14 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fructose-bisphosphate aldolase, transcript variant X1
fructose-bisphosphate aldolase, transcript variant X3
fructose-bisphosphate aldolase isoform X1
fructose-bisphosphate aldolase isoform X3
fructose-bisphosphate aldolase, transcript variant X2
fructose-bisphosphate aldolase isoform X2
sodium/calcium exchanger regulatory protein 1
DNA cross-link repair 1A protein, transcript variant X2
DNA cross-link repair 1A protein, transcript variant X3
DNA cross-link repair 1A protein, transcript variant X1
iron-sulfur cluster co-chaperone protein HscB
transcription initiation protein SPT3 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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 34 samples with support for all annotated introns
TWiK family of potassium channels protein 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC110993333, transcript variant X1
uncharacterized LOC110993333, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
alpha-tocopherol transfer protein, transcript variant X1
alpha-tocopherol transfer protein, transcript variant X2
alpha-tocopherol transfer protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
alpha-tocopherol transfer protein-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 6 samples with support for all annotated introns
uncharacterized LOC110993265, transcript variant X1
uncharacterized LOC110993265, transcript variant X2
uncharacterized LOC110993265, transcript variant X3
uncharacterized protein LOC110993265 isoform X1
uncharacterized protein LOC110993265 isoform X2
potassium channel subfamily K member 18-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 7 samples with support for all annotated introns
probable ATP-dependent RNA helicase kurz
glutamate receptor ionotropic, kainate 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
palmitoleoyl-protein carboxylesterase NOTUM, transcript variant X2
palmitoleoyl-protein carboxylesterase NOTUM, transcript variant X1
palmitoleoyl-protein carboxylesterase NOTUM isoform X2
palmitoleoyl-protein carboxylesterase NOTUM isoform X1
protein unc-13 homolog 4B, transcript variant X2
protein unc-13 homolog 4B, transcript variant X1
protein unc-13 homolog 4B, transcript variant X3
protein unc-13 homolog 4B, transcript variant X5
protein unc-13 homolog 4B, transcript variant X4
protein unc-13 homolog 4B, transcript variant X6
protein unc-13 homolog 4B, transcript variant X7
ribonuclease H2 subunit A, transcript variant X1
ribonuclease H2 subunit A, transcript variant X2
protein FRA10AC1 homolog, transcript variant X2
protein FRA10AC1 homolog, transcript variant X3
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 X3
cytosolic purine 5'-nucleotidase, transcript variant X4
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 X4
hexokinase type 2, transcript variant X2
hexokinase type 2, transcript variant X1
hexokinase type 2, transcript variant X5
hexokinase type 2, transcript variant X3
proto-oncogene tyrosine-protein kinase ROS, 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 10 samples with support for all annotated introns
proto-oncogene tyrosine-protein kinase ROS, 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 11 samples with support for all annotated introns
proto-oncogene tyrosine-protein kinase ROS isoform X1
proto-oncogene tyrosine-protein kinase ROS isoform X2
smad nuclear-interacting protein 1, transcript variant X4
smad nuclear-interacting protein 1, transcript variant X2
smad nuclear-interacting protein 1, transcript variant X3
smad nuclear-interacting protein 1, transcript variant X1
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
coiled-coil domain-containing protein 149
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
threonine aspartase 1, transcript variant X2
threonine aspartase 1, transcript variant X1
HIG1 domain family member 2A, mitochondrial, transcript variant X2
HIG1 domain family member 2A, mitochondrial, transcript variant X1
HIG1 domain family member 2A, mitochondrial isoform X1
HIG1 domain family member 2A, mitochondrial isoform X2
uncharacterized LOC110993199, transcript variant X1
uncharacterized protein LOC110993199 isoform X1
uncharacterized LOC110993199, transcript variant X2
uncharacterized protein LOC110993199 isoform X2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein couch potato
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 32 samples with support for all annotated introns
endoribonuclease Dicer, transcript variant X2
endoribonuclease Dicer, 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 98 samples with support for all annotated introns
uncharacterized LOC110993242, transcript variant X2
uncharacterized LOC110993242, 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 4 samples with support for all annotated introns
uncharacterized protein LOC110993242 isoform X2
uncharacterized protein LOC110993242 isoform X1
ubiquinone biosynthesis O-methyltransferase, mitochondrial-like
structure-specific endonuclease subunit SLX1 homolog
zinc finger HIT domain-containing protein 2
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 41 samples with support for all annotated introns
phosphatidylinositol 4-kinase alpha, transcript variant X6
phosphatidylinositol 4-kinase alpha, transcript variant X5
phosphatidylinositol 4-kinase alpha, transcript variant X4
phosphatidylinositol 4-kinase alpha, transcript variant X2
phosphatidylinositol 4-kinase alpha, transcript variant X3
phosphatidylinositol 4-kinase alpha, transcript variant X1
phosphatidylinositol 4-kinase alpha isoform X6
phosphatidylinositol 4-kinase alpha isoform X5
phosphatidylinositol 4-kinase alpha isoform X4
phosphatidylinositol 4-kinase alpha isoform X2
phosphatidylinositol 4-kinase alpha isoform X3
phosphatidylinositol 4-kinase alpha isoform X1
uncharacterized LOC110993221, transcript variant X1
uncharacterized LOC110993221, transcript variant X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
optomotor-blind protein, transcript variant X2
optomotor-blind protein, transcript variant X4
optomotor-blind protein, transcript variant X3
optomotor-blind protein, transcript variant X5
optomotor-blind protein, transcript variant X6
optomotor-blind protein, transcript variant X1
optomotor-blind protein, transcript variant X7
T-box transcription factor TBX3 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
transport and Golgi organization protein 2
serine--tRNA synthetase-like protein Slimp
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 homolog
ran-specific GTPase-activating protein, transcript variant X2
ran-specific GTPase-activating protein, transcript variant X1
ran-specific GTPase-activating protein isoform X2
ran-specific GTPase-activating protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
RIMS-binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RIMS-binding protein 2, transcript variant X5
RIMS-binding protein 2, transcript variant X4
RIMS-binding protein 2, transcript variant X6
RIMS-binding protein 2, transcript variant X2
RIMS-binding protein 2, transcript variant X3
RIMS-binding protein 2, transcript variant X8
RIMS-binding protein 2, transcript variant X7
peripheral-type benzodiazepine receptor-associated protein 1 isoform X1
peripheral-type benzodiazepine receptor-associated protein 1 isoform X2
peripheral-type benzodiazepine receptor-associated protein 1 isoform X3
peripheral-type benzodiazepine receptor-associated protein 1 isoform X8
peripheral-type benzodiazepine receptor-associated protein 1 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: phospholipase A2-like
N-glycosylase/DNA lyase, transcript variant X1
N-glycosylase/DNA lyase, 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 14 samples with support for all annotated introns
PAX-interacting protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
PAX-interacting protein 1, transcript variant X1
AP-1 complex subunit beta-1, transcript variant X1
AP-1 complex subunit beta-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
putative nuclease HARBI1, transcript variant X1
putative nuclease HARBI1, transcript variant X2
uncharacterized protein LOC123690717 isoform X2
transcription factor stalky-like, transcript variant X2
transcription factor stalky-like isoform X2
transcription factor stalky-like, transcript variant X1
transcription factor stalky-like isoform X1
transcription factor stalky-like, transcript variant X3
uncharacterized protein LOC110993188 isoform X3
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, including 2 samples with support for all annotated introns
myosin regulatory light chain sqh, transcript variant X2
myosin regulatory light chain sqh, transcript variant X1
myosin regulatory light chain sqh, transcript variant X3
dnaJ homolog subfamily C member 30, mitochondrial
vacuolar protein sorting-associated protein 37B
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase, 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 33 samples with support for all annotated introns
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase, 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 42 samples with support for all annotated introns
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase isoform X1
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase isoform X2
phosphatidylinositol transfer protein alpha isoform
uncharacterized LOC110993275, transcript variant X2
uncharacterized LOC110993275, transcript variant X1
uncharacterized LOC110993318, 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 29 samples with support for all annotated introns
uncharacterized LOC110993318, transcript variant X1
uncharacterized protein LOC110993318 isoform X1
uncharacterized protein LOC110993318 isoform X2
serine/arginine repetitive matrix protein 1 isoform X1
RILP-like protein homolog, transcript variant X7
RILP-like protein homolog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 49 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 58 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 62 samples with support for all annotated introns
RILP-like protein 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 78 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: 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
28S ribosomal protein S15, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 115 samples with support for all annotated introns
baculoviral IAP repeat-containing protein 7, transcript variant X2
baculoviral IAP repeat-containing protein 7, transcript variant X1
baculoviral IAP repeat-containing protein 7 isoform X1
baculoviral IAP repeat-containing protein 7 isoform X2
uncharacterized LOC110993168, transcript variant X1
uncharacterized LOC110993168, 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 8 samples with support for all annotated introns
uncharacterized LOC110993167, transcript variant X2
uncharacterized LOC110993167, 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 3 samples with support for all annotated introns
death-associated inhibitor of apoptosis 1, transcript variant X3
death-associated inhibitor of apoptosis 1, transcript variant X2
death-associated inhibitor of apoptosis 1, transcript variant X1
death-associated inhibitor of apoptosis 1, transcript variant X6
death-associated inhibitor of apoptosis 1 isoform X1
death-associated inhibitor of apoptosis 1, transcript variant X4
death-associated inhibitor of apoptosis 1 isoform X2
death-associated inhibitor of apoptosis 1, transcript variant X5
death-associated inhibitor of apoptosis 1 isoform X3
homeobox protein 2, transcript variant X1
homeobox protein 2, transcript variant X2
uncharacterized protein LOC110993149 isoform X2
uncharacterized LOC110993165, transcript variant X2
uncharacterized LOC110993165, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
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
glutamate receptor ionotropic, kainate 3
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
potassium channel subfamily K member 1, transcript variant X2
potassium channel subfamily K member 1 isoform X2
potassium channel subfamily K member 1, 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 70 samples with support for all annotated introns
potassium channel subfamily K member 1 isoform X1
potassium channel subfamily K member 1, transcript variant X3
potassium channel subfamily K member 1 isoform X3
nascent polypeptide-associated complex subunit alpha, muscle-specific form isoform X2
bifunctional lysine-specific demethylase and histidyl-hydroxylase NO66, transcript variant X1
bifunctional lysine-specific demethylase and histidyl-hydroxylase NO66, transcript variant X2
bifunctional lysine-specific demethylase and histidyl-hydroxylase NO66
muscarinic acetylcholine receptor DM1, transcript variant X1
muscarinic acetylcholine receptor DM1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
serum response factor homolog, transcript variant X2
serum response factor homolog, transcript variant X1
serum response factor homolog isoform X1
serum response factor homolog isoform X2
guanine nucleotide-binding protein subunit beta-like protein 1, transcript variant X2
guanine nucleotide-binding protein subunit beta-like protein 1, transcript variant X1
guanine nucleotide-binding protein subunit beta-like protein 1 isoform X1
guanine nucleotide-binding protein subunit beta-like protein 1 isoform X2
membrane-bound transcription factor site-2 protease, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
membrane-bound transcription factor site-2 protease, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
membrane-bound transcription factor site-2 protease isoform X1
membrane-bound transcription factor site-2 protease isoform X2
probable cysteine--tRNA ligase, mitochondrial
uncharacterized LOC110993360, transcript variant X6
uncharacterized LOC110993360, transcript variant X3
uncharacterized LOC110993360, transcript variant X5
uncharacterized LOC110993360, transcript variant X4
uncharacterized LOC110993360, transcript variant X1
uncharacterized LOC110993360, transcript variant X2
uncharacterized protein LOC110993360 isoform X4
uncharacterized protein LOC110993360 isoform X3
uncharacterized protein LOC110993360 isoform X2
uncharacterized protein LOC110993360 isoform X1
transfer RNA leucine (anticodon CAG); 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: 52 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: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
UDP-N-acetylglucosamine transferase subunit ALG13 homolog
transmembrane emp24 domain-containing protein eca
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
DDRGK domain-containing protein 1, transcript variant X1
DDRGK domain-containing protein 1, transcript variant X2
DDRGK domain-containing protein 1 isoform X1
DDRGK domain-containing protein 1 isoform X2
KAT8 regulatory NSL complex subunit 1, transcript variant X2
KAT8 regulatory NSL complex subunit 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
myosin heavy chain, cardiac muscle isoform, transcript variant X2
myosin heavy chain, cardiac muscle isoform, transcript variant X1
myosin heavy chain, cardiac muscle isoform, transcript variant X3
myosin heavy chain, cardiac muscle isoform isoform X1
axoneme-associated protein mst101(2) isoform X2
myosin heavy chain, cardiac muscle isoform, transcript variant X4
myosin heavy chain, cardiac muscle isoform 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 9 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 80% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable methylthioribulose-1-phosphate dehydratase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
MMS19 nucleotide excision repair protein homolog
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 80 samples with support for all annotated introns
U6 snRNA-associated Sm-like protein LSm1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
delta-1-pyrroline-5-carboxylate synthase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
delta-1-pyrroline-5-carboxylate synthase isoform X2
microsomal glutathione S-transferase 1-like
RNA polymerase-associated protein CTR9 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
5'-3' exonuclease PLD3, transcript variant X1
5'-3' exonuclease PLD3, transcript variant X2
structural maintenance of chromosomes protein 3
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 29 samples with support for all annotated introns
organic cation transporter protein, transcript variant X2
organic cation transporter protein, transcript variant X1
organic cation transporter protein isoform X1
organic cation transporter protein isoform X2
histone-lysine N-trimethyltransferase SMYD5
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
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
circadian clock-controlled protein daywake-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
circadian clock-controlled protein daywake, 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 5 samples with support for all annotated introns
circadian clock-controlled protein daywake, transcript variant X2
circadian clock-controlled protein daywake isoform X2
circadian clock-controlled protein daywake isoform X3
circadian clock-controlled protein daywake, transcript variant X1
circadian clock-controlled protein daywake isoform 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
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, transcript variant X1
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, transcript variant X2
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X1
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X2
uncharacterized LOC110999318, transcript variant X1
uncharacterized LOC110999318, transcript variant X2
uncharacterized protein LOC110999318 isoform X1
uncharacterized protein LOC110999318 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
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
apoptotic protease-activating factor 1, transcript variant X1
apoptotic protease-activating factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123690715, 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 29 samples with support for all annotated introns
uncharacterized LOC123690715, 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 52 samples with support for all annotated introns
uncharacterized LOC123690715, transcript variant X3
uncharacterized protein LOC123690715 isoform X1
uncharacterized protein LOC123690715 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
transfer RNA lysine (anticodon CUU); 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: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 108 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 89% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
organic cation transporter protein, transcript variant X3
organic cation transporter protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
histone deacetylase complex subunit SAP18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
E3 UFM1-protein ligase 1 homolog, transcript variant X1
E3 UFM1-protein ligase 1 homolog, transcript variant X2
guanine nucleotide-binding protein subunit gamma-1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
eukaryotic translation initiation factor 2 subunit 3, transcript variant X1
eukaryotic translation initiation factor 2 subunit 3, transcript variant X2
eukaryotic translation initiation factor 2 subunit 3 isoform X2
histone-lysine N-methyltransferase SUV39H2 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 30 samples with support for all annotated introns
peroxisomal N(1)-acetyl-spermine/spermidine oxidase
early growth response protein 3, 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 12 samples with support for all annotated introns
early growth response protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
early growth response protein 3 isoform X1
early growth response protein 3 isoform X2
phosphatidylethanolamine-binding protein 1-like
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 13 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
asparagine synthetase [glutamine-hydrolyzing]
protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
juvenile hormone esterase, transcript variant X2
juvenile hormone esterase, transcript variant X3
juvenile hormone esterase, transcript variant X4
juvenile hormone esterase, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 157
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
uncharacterized LOC110997683, transcript variant X1
uncharacterized LOC110997683, 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 114 samples with support for all annotated introns
uncharacterized protein LOC110997683 isoform X1
uncharacterized protein LOC110997683 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 7 samples with support for all annotated introns
solute carrier family 22 member 4-like, transcript variant X2
solute carrier family 22 member 4-like, transcript variant X1
organic cation transporter protein-like isoform X1
solute carrier family 22 member 4-like isoform X2
organic cation transporter protein-like, transcript variant X2
organic cation transporter protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
organic cation transporter protein-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 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 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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
tubulin alpha chain-like, transcript variant X2
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 2 samples with support for all annotated introns
tubulin alpha chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 388 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
circadian clock-controlled protein daywake
uncharacterized LOC110997685, transcript variant X2
uncharacterized LOC110997685, transcript variant X1
uncharacterized LOC110997685, transcript variant X3
uncharacterized protein LOC110997685 isoform X1
uncharacterized protein LOC110997685 isoform X3
uncharacterized protein LOC110997685 isoform X2
uncharacterized LOC110997684, transcript variant X1
uncharacterized LOC110997684, transcript variant X2
uncharacterized protein LOC110997684 isoform X1
uncharacterized protein LOC110997684 isoform X2
exocyst complex component 1, transcript variant X2
exocyst complex component 1, transcript variant X1
GTP 3',8-cyclase, mitochondrial, transcript variant X3
GTP 3',8-cyclase, mitochondrial, 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 16 samples with support for all annotated introns
GTP 3',8-cyclase, mitochondrial, 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 48 samples with support for all annotated introns
molybdenum cofactor biosynthesis protein 1 isoform X1
molybdenum cofactor biosynthesis protein 1 isoform X2
GTP 3',8-cyclase, mitochondrial, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
GTP 3',8-cyclase, mitochondrial isoform X3
major facilitator superfamily domain-containing protein 8, transcript variant X3
major facilitator superfamily domain-containing protein 8 isoform X2
major facilitator superfamily domain-containing protein 8, transcript variant X2
major facilitator superfamily domain-containing protein 8, transcript variant X1
major facilitator superfamily domain-containing protein 8 isoform X1