Diprion similis isolate iyDipSimi1 chromosome 7, iyDipSimi1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Tenthredinoidea; Diprionidae; Diprioninae; Diprion.
REFSEQ INFORMATION: The reference sequence is identical to\nCM037725.1.\nAssembly name: iyDipSimi1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the United States Department of\nAgriculture on 2021/12/10. The original whole-genome shotgun\nproject has the accession JAJNQI000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: United States Department of Agriculture\nAssembly Date :: 17-NOV-2021\nAssembly Method :: HiFiASM v. 0.16.1-r375; Juicebox Assembly\n Toolkit v. 1.11\nAssembly Name :: iyDipSimi1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 100.0x\nSequencing Technology :: PacBio Sequel; Illumina NovaSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Diprion similis Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Catherine Linnen, University of Kentucky
Derived by automated computational analysis using gene prediction method: Gnomon.
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X7
COORDINATES: polyA evidence [ECO:0006239]
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X4
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X2
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X3
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X6
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X5
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X1
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X3
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X2
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X1
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 32 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 761-like, transcript variant X1
zinc finger protein 761-like, transcript variant X2
protein-cysteine N-palmitoyltransferase HHAT, transcript variant X2
protein-cysteine N-palmitoyltransferase HHAT, transcript variant X1
protein-cysteine N-palmitoyltransferase HHAT isoform X2
protein-cysteine N-palmitoyltransferase HHAT isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 71 samples with support for all annotated introns
rho GDP-dissociation inhibitor 2, transcript variant X1
rho GDP-dissociation inhibitor 2, transcript variant X2
rho GDP-dissociation inhibitor 1 isoform X1
rho GDP-dissociation inhibitor 2 isoform X2
ribonuclease Z, mitochondrial, transcript variant X3
ribonuclease Z, mitochondrial, transcript variant X4
ribonuclease Z, mitochondrial, transcript variant X2
ribonuclease Z, mitochondrial, transcript variant X1
putative ATP synthase subunit f, mitochondrial, 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 77 samples with support for all annotated introns
putative ATP synthase subunit f, mitochondrial, transcript variant X1
putative ATP synthase subunit f, mitochondrial isoform X2
putative ATP synthase subunit f, mitochondrial isoform X1
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like, transcript variant X2
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like, transcript variant X3
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like, transcript variant X4
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like, transcript variant X1
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like isoform X1
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 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 2 samples with support for all annotated introns
U4/U6 small nuclear ribonucleoprotein Prp31
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; 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 9 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 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC124408102
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
lysophospholipid acyltransferase 6, 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 18 samples with support for all annotated introns
lysophospholipid acyltransferase 6, transcript variant X2
lysophospholipid acyltransferase 6, transcript variant X1
lysophospholipid acyltransferase 6, transcript variant X3
lysophospholipid acyltransferase 6 isoform X4
lysophospholipid acyltransferase 6 isoform X1
lysophospholipid acyltransferase 6 isoform X3
lysophospholipid acyltransferase 6 isoform X2
lysophospholipid acyltransferase 6, transcript variant X5
lysophospholipid acyltransferase 6 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger and SCAN domain-containing protein 21-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
high affinity copper uptake protein 1-like, transcript variant X1
high affinity copper uptake protein 1-like, transcript variant X2
high affinity copper uptake protein 1-like, transcript variant X3
high affinity copper uptake protein 1-like isoform X1
high affinity copper uptake protein 1-like isoform X2
high affinity copper uptake protein 1-like isoform X3
probable cytochrome P450 304a1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
probable cytochrome P450 304a1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable cytochrome P450 304a1 isoform X1
probable cytochrome P450 304a1 isoform X2
TELO2-interacting protein 2-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 17 samples with support for all annotated introns
TELO2-interacting protein 2-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 59 samples with support for all annotated introns
TELO2-interacting protein 2-like isoform X2
TELO2-interacting protein 2-like isoform 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 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 19 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 37 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
uncharacterized LOC124407883, 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 23 samples with support for all annotated introns
uncharacterized LOC124407883, 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 5 samples with support for all annotated introns
uncharacterized protein LOC124407883 isoform X1
uncharacterized protein LOC124407883 isoform X2
39S ribosomal protein L37, mitochondrial
vesicle transport through interaction with t-SNAREs homolog 1B-like, transcript variant X2
vesicle transport through interaction with t-SNAREs homolog 1B-like isoform X2
vesicle transport through interaction with t-SNAREs homolog 1B-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
vesicle transport through interaction with t-SNAREs homolog 1B-like, transcript variant X3
F-box only protein 11, transcript variant X2
F-box only protein 11, transcript variant X1
CAAX prenyl protease 2, 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 56 samples with support for all annotated introns
CAAX prenyl protease 2, 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 9 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD3, 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 5 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD3, 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 7 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD3, 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 14 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD3 isoform X4
BTB/POZ domain-containing protein KCTD3 isoform X3
BTB/POZ domain-containing protein KCTD3 isoform X1
BTB/POZ domain-containing protein KCTD3 isoform X2
zinc finger protein 225-like, transcript variant X1
zinc finger protein 225-like, transcript variant X2
NADPH--cytochrome P450 reductase, transcript variant X2
NADPH--cytochrome P450 reductase, transcript variant X1
NADPH--cytochrome P450 reductase, transcript variant X3
NADPH--cytochrome P450 reductase isoform X1
NADPH--cytochrome P450 reductase isoform X2
NADPH--cytochrome P450 reductase isoform X3
cysteine-rich DPF motif domain-containing protein 1
putative transferase CAF17 homolog, mitochondrial
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 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
unc-112-related protein-like, transcript variant X1
unc-112-related protein-like, transcript variant X2
retinol dehydrogenase 13-like, transcript variant X2
retinol dehydrogenase 13-like, transcript variant X1
retinol dehydrogenase 13-like, transcript variant X3
retinol dehydrogenase 13-like isoform X2
retinol dehydrogenase 13-like isoform X1
retinol dehydrogenase 13-like isoform X3
uncharacterized LOC124408381, transcript variant X1
uncharacterized LOC124408381, transcript variant X2
uncharacterized LOC124408381, transcript variant X5
uncharacterized LOC124408381, transcript variant X6
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
uncharacterized LOC124408381, transcript variant X7
uncharacterized protein LOC124408381 isoform X1
uncharacterized protein LOC124408381 isoform X2
uncharacterized protein LOC124408381 isoform X6
uncharacterized protein LOC124408381 isoform X4
uncharacterized protein LOC124408381 isoform X5
uncharacterized LOC124408381, transcript variant X4
uncharacterized LOC124408381, transcript variant X3
uncharacterized protein LOC124408381 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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 14% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA Delta-9 desaturase-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
acyl-CoA Delta-9 desaturase-like, transcript variant X3
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
acyl-CoA Delta-9 desaturase-like isoform X3
acyl-CoA Delta-9 desaturase-like isoform X6
acyl-CoA Delta-9 desaturase-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
acyl-CoA Delta-9 desaturase-like isoform X2
uncharacterized LOC124408200, transcript variant X3
uncharacterized LOC124408200, transcript variant X2
uncharacterized LOC124408200, transcript variant X1
uncharacterized protein LOC124408200 isoform X3
uncharacterized protein LOC124408200 isoform X2
uncharacterized protein LOC124408200 isoform X1
FK506-binding protein 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
FK506-binding protein 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
FK506-binding protein 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein LOC124408204 isoform X2
insulin-like growth factor-binding protein complex acid labile subunit
lipid storage droplets surface-binding protein 2-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 16 samples with support for all annotated introns
lipid storage droplets surface-binding protein 2-like, transcript variant X1
lipid storage droplets surface-binding protein 2-like isoform X1
lipid storage droplets surface-binding protein 2-like isoform X2
lipid storage droplets surface-binding protein 2-like
uncharacterized LOC124408211, transcript variant X2
uncharacterized LOC124408211, transcript variant X1
uncharacterized protein LOC124408211 isoform X1
uncharacterized protein LOC124408211 isoform X2
zinc finger CCCH domain-containing protein 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-CoA Delta-9 desaturase-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-CoA Delta-9 desaturase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acyl-CoA Delta-9 desaturase-like, transcript variant X4
acyl-CoA Delta-9 desaturase-like isoform X5
acyl-CoA Delta-9 desaturase-like isoform X1
acyl-CoA Delta-9 desaturase-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
rho GTPase-activating protein 21-A, transcript variant X3
rho GTPase-activating protein 21-A, transcript variant X2
rho GTPase-activating protein 21-A, transcript variant X1
rho GTPase-activating protein 21-A, transcript variant X5
rho GTPase-activating protein 21-A, transcript variant X6
rho GTPase-activating protein 21-A, transcript variant X8
rho GTPase-activating protein 21-A, transcript variant X7
rho GTPase-activating protein 21-A, transcript variant X4
uncharacterized protein LOC124408260 isoform X2
rho GTPase-activating protein 21 isoform X5
uncharacterized protein LOC124408260 isoform X8
uncharacterized protein LOC124408260 isoform X7
uncharacterized protein LOC124408260 isoform X4
uncharacterized protein LOC124408260 isoform X6
uncharacterized protein LOC124408260 isoform X3
uncharacterized protein LOC124408260 isoform X1
rho GTPase-activating protein 21-A, transcript variant X9
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
rho GTPase-activating protein 21-A isoform X9
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: 80% coverage of the annotated genomic feature by RNAseq alignments
ribosome biogenesis protein NOP53, 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 45 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ribosome biogenesis protein NOP53, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 71 samples with support for all annotated introns
integrin alpha-PS2-like, transcript variant X1
integrin alpha-PS2-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 4 samples with support for all annotated introns
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, transcript variant X3
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, transcript variant X2
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, transcript variant X1
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X3
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X2
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X1
uncharacterized LOC124408213, 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 8 samples with support for all annotated introns
uncharacterized LOC124408213, 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 5 samples with support for all annotated introns
uncharacterized LOC124408213, transcript variant X1
uncharacterized protein LOC124408213 isoform X2
uncharacterized protein LOC124408213 isoform X1
uncharacterized LOC124407848, 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
uncharacterized LOC124407848, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC124407848 isoform X1
uncharacterized protein LOC124407848 isoform X2
testis-specific serine/threonine-protein kinase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00274
zinc transporter 7, transcript variant X2
zinc transporter 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
CDAN1-interacting nuclease 1, transcript variant X1
CDAN1-interacting nuclease 1, transcript variant X2
protein FAM50 homolog, transcript variant X1
protein FAM50 homolog, transcript variant X2
mitochondrial inner membrane protease ATP23 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 62% coverage of the annotated genomic feature by RNAseq alignments
pre-rRNA 2'-O-ribose RNA methyltransferase FTSJ3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nuclear hormone receptor E75-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ecdysone-inducible protein E75-like isoform X1
nuclear hormone receptor E75-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear hormone receptor E75-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nuclear hormone receptor E75-like isoform X2
nuclear hormone receptor E75-like isoform X3
KH domain-containing protein akap-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
KH domain-containing protein akap-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
RNA-binding protein cabeza-like, transcript variant X2
RNA-binding protein cabeza-like, transcript variant X1
RNA-binding protein cabeza-like isoform X2
RNA-binding protein cabeza-like isoform X1
mediator of RNA polymerase II transcription subunit 19
RNA-binding protein with serine-rich domain 1-B-like
uncharacterized LOC124407853, transcript variant X5
uncharacterized LOC124407853, transcript variant X3
uncharacterized LOC124407853, transcript variant X2
uncharacterized LOC124407853, transcript variant X4
uncharacterized LOC124407853, transcript variant X1
uncharacterized protein LOC124407853 isoform X1
uncharacterized protein LOC124407853 isoform X2
vitamin K epoxide reductase complex subunit 1-like protein 1
spermatogenesis-associated protein 20, transcript variant X1
spermatogenesis-associated protein 20, transcript variant X2
SUMO-conjugating enzyme UBC9-B, transcript variant X2
SUMO-conjugating enzyme UBC9-B, transcript variant X1
spermatogenesis-associated protein 20, transcript variant X5
spermatogenesis-associated protein 20, transcript variant X3
spermatogenesis-associated protein 20, transcript variant X4
spermatogenesis-associated protein 20, transcript variant X6
spermatogenesis-associated protein 20 isoform X1
spermatogenesis-associated protein 20 isoform X2
voltage-dependent T-type calcium channel subunit alpha-1G-like, transcript variant X3
voltage-dependent T-type calcium channel subunit alpha-1G-like, transcript variant X1
voltage-dependent T-type calcium channel subunit alpha-1G-like, transcript variant X2
voltage-dependent T-type calcium channel subunit alpha-1G-like isoform X3
voltage-dependent T-type calcium channel subunit alpha-1G-like isoform X1
voltage-dependent T-type calcium channel subunit alpha-1G-like isoform X2
probable glucosamine 6-phosphate N-acetyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
FAD synthase-like, 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
FAD synthase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FAD synthase-like, 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 16 samples with support for all annotated introns
FAD synthase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TOX high mobility group box family member 4-like, transcript variant X1
TOX high mobility group box family member 4-like, transcript variant X2
TOX high mobility group box family member 4-like, transcript variant X3
TOX high mobility group box family member 4-like, transcript variant X6
TOX high mobility group box family member 3-like isoform X1
TOX high mobility group box family member 3-like isoform X2
TOX high mobility group box family member 4-like isoform X3
TOX high mobility group box family member 3-like isoform X6
TOX high mobility group box family member 4-like, transcript variant X4
TOX high mobility group box family member 3-like isoform X4
TOX high mobility group box family member 4-like, transcript variant X5
TOX high mobility group box family member 3-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
lethal(3)malignant brain tumor-like protein 3, transcript variant X2
lethal(3)malignant brain tumor-like protein 3, transcript variant X1
lethal(3)malignant brain tumor-like protein 3, transcript variant X5
lethal(3)malignant brain tumor-like protein 3, transcript variant X4
lethal(3)malignant brain tumor-like protein 3, transcript variant X3
lethal(3)malignant brain tumor-like protein 3 isoform X2
lethal(3)malignant brain tumor-like protein 3 isoform X1
lethal(3)malignant brain tumor-like protein 3 isoform X3
protein-L-isoaspartate O-methyltransferase domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
protein-L-isoaspartate O-methyltransferase domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
protein-L-isoaspartate O-methyltransferase domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
electron transfer flavoprotein beta subunit lysine methyltransferase-like
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
nuclear receptor-binding protein homolog, transcript variant X2
nuclear receptor-binding protein homolog, transcript variant X1
nuclear receptor-binding protein homolog isoform X2
nuclear receptor-binding protein homolog isoform X1
kinase D-interacting substrate of 220 kDa, transcript variant X6
kinase D-interacting substrate of 220 kDa, transcript variant X7
kinase D-interacting substrate of 220 kDa, transcript variant X3
kinase D-interacting substrate of 220 kDa, transcript variant X1
kinase D-interacting substrate of 220 kDa, transcript variant X2
kinase D-interacting substrate of 220 kDa B isoform X3
kinase D-interacting substrate of 220 kDa B isoform X2
kinase D-interacting substrate of 220 kDa B isoform X1
kinase D-interacting substrate of 220 kDa B isoform X6
kinase D-interacting substrate of 220 kDa, transcript variant X8
kinase D-interacting substrate of 220 kDa, transcript variant X4
kinase D-interacting substrate of 220 kDa, transcript variant X5
kinase D-interacting substrate of 220 kDa B isoform X5
kinase D-interacting substrate of 220 kDa B isoform X4
kinase D-interacting substrate of 220 kDa isoform X7
tRNA (guanine-N(7)-)-methyltransferase, transcript variant X2
tRNA (guanine-N(7)-)-methyltransferase, transcript variant X1
tRNA (guanine-N(7)-)-methyltransferase isoform X1
tRNA (guanine-N(7)-)-methyltransferase isoform X2
cilia- and flagella-associated protein 65-like
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cilia- and flagella-associated protein 65-like
acylamino-acid-releasing enzyme-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
acylamino-acid-releasing enzyme-like, transcript variant X1
protein-lysine N-methyltransferase EEF2KMT
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
MICAL-like protein 1, transcript variant X1
MICAL-like protein 1, 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
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 5 samples with support for all annotated introns
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT6-like
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 5 samples with support for all annotated introns
meiosis regulator and mRNA stability factor 1, transcript variant X3
meiosis regulator and mRNA stability factor 1, transcript variant X1
meiosis regulator and mRNA stability factor 1, transcript variant X2
meiosis regulator and mRNA stability factor 1, transcript variant X4
meiosis regulator and mRNA stability factor 1 isoform X2
meiosis regulator and mRNA stability factor 1 isoform X1
meiosis regulator and mRNA stability factor 1 isoform X3
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q, transcript variant X1
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q, transcript variant X2
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q, transcript variant X3
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q isoform X1
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q isoform X2
N-acetylglucosaminyl-phosphatidylinositol biosynthetic protein gpi1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein chibby homolog 1, transcript variant X2
protein chibby homolog 1, transcript variant X1
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
meiosis-specific with OB domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124408316, transcript variant X3
uncharacterized LOC124408316, transcript variant X1
uncharacterized LOC124408316, transcript variant X2
uncharacterized LOC124408316, transcript variant X4
uncharacterized protein LOC124408316 isoform X1
uncharacterized protein LOC124408316 isoform X2
uncharacterized protein LOC124408316 isoform X3
hrp65 protein-like, transcript variant X2
hrp65 protein-like, transcript variant X1
U11/U12 small nuclear ribonucleoprotein 48 kDa protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% 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 96% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF01174
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10
serine/threonine-protein kinase fused, transcript variant X1
serine/threonine-protein kinase fused, transcript variant X2
serine/threonine-protein kinase fused isoform X1
serine/threonine-protein kinase fused isoform X2
cytochrome P450 306a1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cytochrome P450 306a1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glycolipid transfer protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glycolipid transfer protein, transcript variant X2
glycolipid transfer protein, transcript variant X1
tRNA (uracil-5-)-methyltransferase homolog A
INO80 complex subunit E, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
INO80 complex subunit E, 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 76 samples with support for all annotated introns
INO80 complex subunit E, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
sin3 histone deacetylase corepressor complex component SDS3, transcript variant X2
sin3 histone deacetylase corepressor complex component SDS3, transcript variant X1
sin3 histone deacetylase corepressor complex component SDS3 isoform X2
sin3 histone deacetylase corepressor complex component SDS3 isoform X1
aldo-keto reductase family 1 member A1-A
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 74 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
uncharacterized LOC124408088, transcript variant X4
uncharacterized LOC124408088, transcript variant X3
uncharacterized LOC124408088, transcript variant X1
uncharacterized LOC124408088, transcript variant X2
uncharacterized protein LOC124408088 isoform X1
uncharacterized protein LOC124408088 isoform X2
uncharacterized protein LOC124408088 isoform X3
uncharacterized protein LOC124408088 isoform X4
carboxypeptidase M, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
carboxypeptidase M, transcript variant X1
carboxypeptidase M, transcript variant X3
cytoplasmic phosphatidylinositol transfer protein 1
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 13 samples with support for all annotated introns
probable tRNA (uracil-O(2)-)-methyltransferase
lysophospholipase-like protein 1, transcript variant X2
lysophospholipase-like protein 1, transcript variant X1
lysophospholipase-like protein 1, transcript variant X3
lysophospholipase-like protein 1 isoform X1
lysophospholipase-like protein 1 isoform X2
transcription factor IIIB 90 kDa subunit, 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 1 sample with support for all annotated introns
protein kinase C, brain isozyme, transcript variant X1
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 2 samples with support for all annotated introns
protein kinase C, brain isozyme, 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 31 samples with support for all annotated introns
protein kinase C, brain isozyme, 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 33 samples with support for all annotated introns
protein kinase C, brain isozyme, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein kinase C, brain isozyme isoform X3
protein kinase C, brain isozyme isoform X2
protein kinase C, brain isozyme isoform X1
protein kinase C, brain isozyme isoform X4
developmentally-regulated GTP-binding protein 2, 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 19 samples with support for all annotated introns
developmentally-regulated GTP-binding protein 2, transcript variant X1
developmentally-regulated GTP-binding protein 2
transcription factor IIIB 90 kDa subunit, 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 11 samples with support for all annotated introns
transcription factor IIIB 90 kDa subunit isoform X1
BTB/POZ domain-containing protein 3, transcript variant X1
BTB/POZ domain-containing protein 3, transcript variant X2
BTB/POZ domain-containing protein 3, transcript variant X5
BTB/POZ domain-containing protein 3, transcript variant X4
BTB/POZ domain-containing protein 3, transcript variant X3
BTB/POZ domain-containing protein 6-B isoform X1
BTB/POZ domain-containing protein 6-B isoform X2
BTB/POZ domain-containing protein 6 isoform X4
BTB/POZ domain-containing protein 6-B isoform X3
BTB/POZ domain-containing protein 3 isoform X5
transcription factor IIIB 90 kDa subunit, transcript variant X4
transcription factor IIIB 90 kDa subunit, transcript variant X3
transcription factor IIIB 90 kDa subunit isoform X2
transcription factor IIIB 90 kDa subunit isoform X3
dual specificity protein phosphatase 23-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dual specificity protein phosphatase 23-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 6 samples with support for all annotated introns
dual specificity protein phosphatase 23-like, transcript variant X2
dual specificity protein phosphatase 23-like isoform X3
dual specificity protein phosphatase 23-like isoform X2
dual specificity protein phosphatase 23-like isoform X1
lutropin-choriogonadotropic hormone receptor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 18 samples with support for all annotated introns
sterol O-acyltransferase 1, transcript variant X3
sterol O-acyltransferase 1, transcript variant X1
sterol O-acyltransferase 1, transcript variant X2
mediator of RNA polymerase II transcription subunit 1, transcript variant X2
mediator of RNA polymerase II transcription subunit 1, transcript variant X1
mediator of RNA polymerase II transcription subunit 1 isoform X2
mediator of RNA polymerase II transcription subunit 1 isoform X1
uncharacterized LOC124408126, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 15-like isoform X1
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X2
double-stranded RNA-specific editase 1-like isoform X2
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X3
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X4
mediator of RNA polymerase II transcription subunit 15-like isoform X3
intraflagellar transport protein 22 homolog
uncharacterized LOC124408126, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124408126, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
proteasome activator complex subunit 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
tubulin--tyrosine ligase-like protein 12
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
7SK snRNA methylphosphate capping enzyme bin3-like
echinoderm microtubule-associated protein-like CG42247
28S rRNA (cytosine-C(5))-methyltransferase
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 14 samples with support for all annotated introns
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
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 4 samples with support for all annotated introns
ER degradation-enhancing alpha-mannosidase-like protein 2
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 75 samples with support for all annotated introns
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1, transcript variant X2
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1, transcript variant X1
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 isoform X2
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124408315, 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 5 samples with support for all annotated introns
uncharacterized LOC124408315, 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 52 samples with support for all annotated introns
lipid storage droplets surface-binding protein 1-like, transcript variant X1
lipid storage droplets surface-binding protein 1-like, transcript variant X2
lipid storage droplets surface-binding protein 1-like, transcript variant X3
lipid storage droplets surface-binding protein 1-like isoform X2
lipid storage droplets surface-binding protein 1-like isoform X3
lipid storage droplets surface-binding protein 1-like isoform X1
lipid storage droplets surface-binding protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
lipid storage droplets surface-binding protein 1-like isoform X4
calcium-activated potassium channel slowpoke, transcript variant X43
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
calcium-activated potassium channel slowpoke, transcript variant X23
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 2 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, transcript variant X45
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
calcium-activated potassium channel slowpoke, transcript variant X29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, transcript variant X22
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
calcium-activated potassium channel slowpoke, transcript variant X48
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 4 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, transcript variant X19
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 4 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, transcript variant X5
calcium-activated potassium channel slowpoke, transcript variant X42
calcium-activated potassium channel slowpoke, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, transcript variant X20
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
calcium-activated potassium channel slowpoke, transcript variant X41
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
calcium-activated potassium channel slowpoke, transcript variant X13
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
calcium-activated potassium channel slowpoke, transcript variant X44
calcium-activated potassium channel slowpoke, transcript variant X28
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, transcript variant X50
calcium-activated potassium channel slowpoke, transcript variant X18
calcium-activated potassium channel slowpoke, transcript variant X47
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
calcium-activated potassium channel slowpoke, transcript variant X17
calcium-activated potassium channel slowpoke, transcript variant X31
calcium-activated potassium channel slowpoke, transcript variant X40
calcium-activated potassium channel slowpoke, transcript variant X35
calcium-activated potassium channel slowpoke, transcript variant X46
calcium-activated potassium channel slowpoke, transcript variant X15
calcium-activated potassium channel slowpoke, transcript variant X39
calcium-activated potassium channel slowpoke, transcript variant X21
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
calcium-activated potassium channel slowpoke, transcript variant X9
calcium-activated potassium channel slowpoke, transcript variant X37
calcium-activated potassium channel slowpoke, transcript variant X36
calcium-activated potassium channel slowpoke, transcript variant X12
calcium-activated potassium channel slowpoke, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, transcript variant X34
calcium-activated potassium channel slowpoke, transcript variant X10
calcium-activated potassium channel slowpoke, transcript variant X30
calcium-activated potassium channel slowpoke, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, 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 6 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, transcript variant X32
calcium-activated potassium channel slowpoke, transcript variant X7
calcium-activated potassium channel slowpoke, transcript variant X24
calcium-activated potassium channel slowpoke, transcript variant X26
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
calcium-activated potassium channel slowpoke, transcript variant X2
calcium-activated potassium channel slowpoke, transcript variant X27
calcium-activated potassium channel slowpoke, transcript variant X3
calcium-activated potassium channel slowpoke, transcript variant X49
calcium-activated potassium channel slowpoke, transcript variant X14
calcium-activated potassium channel slowpoke, transcript variant X6
calcium-activated potassium channel slowpoke, transcript variant X25
calcium-activated potassium channel slowpoke, transcript variant X33
calcium-activated potassium channel slowpoke, transcript variant X38
calcium-activated potassium channel slowpoke isoform X16
calcium-activated potassium channel slowpoke isoform X20
calcium-activated potassium channel slowpoke isoform X41
calcium-activated potassium channel slowpoke isoform X49
calcium-activated potassium channel slowpoke isoform X14
calcium-activated potassium channel slowpoke isoform X13
calcium-activated potassium channel slowpoke isoform X44
calcium-activated potassium channel slowpoke isoform X28
calcium-activated potassium channel slowpoke isoform X50
calcium-activated potassium channel slowpoke isoform X18
calcium-activated potassium channel slowpoke isoform X43
calcium-activated potassium channel slowpoke isoform X23
calcium-activated potassium channel slowpoke isoform X45
calcium-activated potassium channel slowpoke isoform X29
calcium-activated potassium channel slowpoke isoform X47
calcium-activated potassium channel slowpoke isoform X17
calcium-activated potassium channel slowpoke isoform X22
calcium-activated potassium channel slowpoke isoform X31
calcium-activated potassium channel slowpoke isoform X40
calcium-activated potassium channel slowpoke isoform X35
calcium-activated potassium channel slowpoke isoform X46
calcium-activated potassium channel slowpoke isoform X15
calcium-activated potassium channel slowpoke isoform X39
calcium-activated potassium channel slowpoke isoform X21
calcium-activated potassium channel slowpoke isoform X9
calcium-activated potassium channel slowpoke isoform X48
calcium-activated potassium channel slowpoke isoform X19
calcium-activated potassium channel slowpoke isoform X6
calcium-activated potassium channel slowpoke isoform X37
calcium-activated potassium channel slowpoke isoform X36
calcium-activated potassium channel slowpoke isoform X12
calcium-activated potassium channel slowpoke isoform X25
calcium-activated potassium channel slowpoke isoform X11
calcium-activated potassium channel slowpoke isoform X33
calcium-activated potassium channel slowpoke isoform X34
calcium-activated potassium channel slowpoke isoform X10
calcium-activated potassium channel slowpoke isoform X30
calcium-activated potassium channel slowpoke isoform X8
calcium-activated potassium channel slowpoke isoform X1
calcium-activated potassium channel slowpoke isoform X32
calcium-activated potassium channel slowpoke isoform X7
calcium-activated potassium channel slowpoke isoform X24
calcium-activated potassium channel slowpoke isoform X26
calcium-activated potassium channel slowpoke isoform X2
calcium-activated potassium channel slowpoke isoform X4
calcium-activated potassium channel slowpoke isoform X5
calcium-activated potassium channel slowpoke isoform X42
calcium-activated potassium channel slowpoke isoform X27
calcium-activated potassium channel slowpoke isoform X3
calcium-activated potassium channel slowpoke isoform X38
set1/Ash2 histone methyltransferase complex subunit ASH2
DNA-binding transcriptional regulator BolA, transcript variant X3
DNA-binding transcriptional regulator BolA, transcript variant X2
DNA-binding transcriptional regulator BolA, transcript variant X1
DNA-binding transcriptional regulator BolA isoform X2
DNA-binding transcriptional regulator BolA isoform X1
DNA-binding transcriptional regulator BolA isoform X3
homeobox protein SIX3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
homeobox protein SIX3-like, 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 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
disintegrin and metalloproteinase domain-containing protein 10, transcript variant X1
disintegrin and metalloproteinase domain-containing protein 10, transcript variant X2
disintegrin and metalloproteinase domain-containing protein 10 isoform X2
disintegrin and metalloproteinase domain-containing protein 10 isoform X1
transmembrane protein 161B, transcript variant X2
transmembrane protein 161B, transcript variant X1
uncharacterized LOC124408064, transcript variant X3
uncharacterized LOC124408064, transcript variant X2
uncharacterized LOC124408064, transcript variant X1
uncharacterized protein LOC124408064 isoform X3
uncharacterized protein LOC124408064 isoform X2
uncharacterized protein LOC124408064 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC124407929
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 76% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor D and EGF domain-containing protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC124408068
tyrosine-protein kinase receptor Tie-2-like, transcript variant X2
tyrosine-protein kinase receptor Tie-2-like, transcript variant X1
uncharacterized protein LOC124408059 isoform X2
tyrosine-protein kinase receptor Tie-2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
proline-rich protein 4-like, transcript variant X1
skin secretory protein xP2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized transmembrane protein DDB_G0289901-like, transcript variant X1
uncharacterized transmembrane protein DDB_G0289901-like, transcript variant X2
uncharacterized transmembrane protein DDB_G0289901-like, transcript variant X3
uncharacterized protein LOC124408057 isoform X1
uncharacterized transmembrane protein DDB_G0289901-like isoform X2
uncharacterized transmembrane protein DDB_G0289901-like isoform X3
proline-rich protein 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase kinase kinase 15, 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 16 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 15, 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 25 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 15, 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 8 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 15, transcript variant X3
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 33 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 15, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 15 isoform X2
mitogen-activated protein kinase kinase kinase 15 isoform X1
mitogen-activated protein kinase kinase kinase 15 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial
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: 46 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: 45 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: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rab GTPase-binding effector protein 1, transcript variant X4
rab GTPase-binding effector protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
rab GTPase-binding effector protein 1, transcript variant X1
rab GTPase-binding effector protein 1, transcript variant X3
rab GTPase-binding effector protein 1 isoform X1
rab GTPase-binding effector protein 1 isoform X3
rab GTPase-binding effector protein 1 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 1 sample with support for all annotated introns
uncharacterized LOC124407912, transcript variant X1
uncharacterized LOC124407912, transcript variant X2
uncharacterized protein LOC124407912 isoform X1
uncharacterized protein LOC124407912 isoform 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
group 3 secretory phospholipase A2, transcript variant X3
group 3 secretory phospholipase A2, transcript variant X2
group 3 secretory phospholipase A2, transcript variant X1
group 3 secretory phospholipase A2 isoform X1
group 3 secretory phospholipase A2 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 13 samples with support for all annotated introns
ribosomal L1 domain-containing protein 1
pterin-4-alpha-carbinolamine dehydratase
serine/threonine-protein kinase D3, 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 13 samples with support for all annotated introns
serine/threonine-protein kinase D3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
serine/threonine-protein kinase D3, 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 7 samples with support for all annotated introns
serine/threonine-protein kinase D3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
serine/threonine-protein kinase D3 isoform X3
serine/threonine-protein kinase D3 isoform X1
serine/threonine-protein kinase D3 isoform 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 10 samples with support for all annotated introns
protoheme IX farnesyltransferase, mitochondrial, transcript variant X1
protoheme IX farnesyltransferase, mitochondrial, transcript variant X2
protoheme IX farnesyltransferase, mitochondrial, transcript variant X5
protoheme IX farnesyltransferase, mitochondrial, transcript variant X4
protoheme IX farnesyltransferase, mitochondrial, transcript variant X3
protoheme IX farnesyltransferase, mitochondrial isoform X1
protoheme IX farnesyltransferase, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX31
V-type proton ATPase 116 kDa subunit a1-like, transcript variant X2
V-type proton ATPase 116 kDa subunit a1-like, transcript variant X4
V-type proton ATPase 116 kDa subunit a1-like, transcript variant X3
V-type proton ATPase 116 kDa subunit a1-like, transcript variant X1
V-type proton ATPase 116 kDa subunit a1-like isoform X2
V-type proton ATPase 116 kDa subunit a1-like isoform X4
V-type proton ATPase 116 kDa subunit a1-like isoform X3
V-type proton ATPase 116 kDa subunit a1-like isoform X1
lys-63-specific deubiquitinase BRCC36-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
lys-63-specific deubiquitinase BRCC36-like, transcript variant X1
lys-63-specific deubiquitinase BRCC36-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 39 samples with support for all annotated introns
L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 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: 102 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
trypsin delta-like, transcript variant X2
trypsin delta-like, transcript variant X1
disintegrin and metalloproteinase domain-containing protein 10
origin recognition complex subunit 2, transcript variant X1
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, including 1 sample 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 2 samples with support for all annotated introns
origin recognition complex subunit 2, transcript variant X2
signal peptidase complex catalytic subunit SEC11A
LOW QUALITY PROTEIN: signal peptidase complex catalytic subunit SEC11A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATPase H(+)-transporting accessory protein 2, transcript variant X3
ATPase H(+)-transporting accessory protein 2, transcript variant X1
ATPase H(+)-transporting accessory protein 2 isoform X3
ATPase H(+)-transporting accessory protein 2 isoform X1
ATPase H(+)-transporting accessory protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATPase H(+)-transporting accessory protein 2 isoform X2
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X1
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X2
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X4
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X3
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X1
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X2
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X3
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X4
myc box-dependent-interacting protein 1, transcript variant X4
myc box-dependent-interacting protein 1, transcript variant X1
myc box-dependent-interacting protein 1, transcript variant X2
myc box-dependent-interacting protein 1, transcript variant X3
myc box-dependent-interacting protein 1 isoform X2
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X5
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X4
guanine nucleotide-binding protein G(q) subunit alpha, 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 21 samples with support for all annotated introns
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
guanine nucleotide-binding protein G(q) subunit alpha isoform X5
guanine nucleotide-binding protein G(q) subunit alpha isoform X4
guanine nucleotide-binding protein G(q) subunit alpha isoform X2
guanine nucleotide-binding protein G(q) subunit alpha isoform X6
uncharacterized LOC124407879, transcript variant X3
uncharacterized LOC124407879, transcript variant X2
uncharacterized LOC124407879, transcript variant X1
facilitated trehalose transporter Tret1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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 55% 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 80 samples with support for all annotated introns
uncharacterized LOC124407975, transcript variant X1
uncharacterized protein LOC124407975 isoform X1
uncharacterized LOC124407975, transcript variant X2
uncharacterized LOC124407975, transcript variant X4
uncharacterized LOC124407975, transcript variant X3
uncharacterized protein LOC124407975 isoform X2
transcriptional adapter 2B, transcript variant X3
transcriptional adapter 2B, transcript variant X1
transcriptional adapter 2B, 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 20 samples with support for all annotated introns
TRAF3-interacting protein 1, transcript variant X4
TRAF3-interacting protein 1, transcript variant X3
TRAF3-interacting protein 1, transcript variant X2
TRAF3-interacting protein 1, transcript variant X1
TRAF3-interacting protein 1, transcript variant X5
lysM and putative peptidoglycan-binding domain-containing protein 2, transcript variant X3
lysM and putative peptidoglycan-binding domain-containing protein 2, transcript variant X4
lysM and putative peptidoglycan-binding domain-containing protein 2, transcript variant X5
lysM and putative peptidoglycan-binding domain-containing protein 2, transcript variant X1
lysM and putative peptidoglycan-binding domain-containing protein 2, transcript variant X2
lysM and putative peptidoglycan-binding domain-containing protein 2 isoform X2
lysM and putative peptidoglycan-binding domain-containing protein 2 isoform X1
lysM and putative peptidoglycan-binding domain-containing protein 2 isoform X3
lysM and putative peptidoglycan-binding domain-containing protein 2 isoform X5
lysM and putative peptidoglycan-binding domain-containing protein 2 isoform X4
transcription initiation factor IIA subunit 2
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1
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
sedoheptulokinase-like, transcript variant X5
sedoheptulokinase-like, transcript variant X1
sedoheptulokinase-like, transcript variant X2
sedoheptulokinase-like, transcript variant X3
sedoheptulokinase-like, transcript variant X6
sedoheptulokinase-like, transcript variant X4
uncharacterized LOC124407990, transcript variant X1
uncharacterized LOC124407990, transcript variant X2
uncharacterized LOC124407976, transcript variant X1
uncharacterized protein LOC124407976 isoform X1
uncharacterized LOC124407976, transcript variant X4
uncharacterized LOC124407976, transcript variant X2
uncharacterized LOC124407976, transcript variant X3
uncharacterized protein LOC124407976 isoform X2
uncharacterized LOC124408220, 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 6 samples with support for all annotated introns
uncharacterized LOC124408220, 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 33 samples with support for all annotated introns
uncharacterized LOC124408220, transcript variant X3
uncharacterized protein LOC124408220 isoform X1
uncharacterized protein LOC124408220 isoform X2
uncharacterized protein LOC124408220 isoform X3
bifunctional glutamate/proline--tRNA ligase
DNA-directed RNA polymerases I and III subunit RPAC1
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 52 samples with support for all annotated introns
DNA polymerase epsilon catalytic subunit 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DNA polymerase epsilon catalytic subunit 1 isoform X1
DNA polymerase epsilon catalytic subunit 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DNA polymerase epsilon catalytic subunit 1 isoform X2
ATP synthase-coupling factor 6, mitochondrial
transforming protein p54/c-ets-1, transcript variant X1
transforming protein p54/c-ets-1, transcript variant X2
transforming protein p54/c-ets-1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
14 kDa phosphohistidine phosphatase-like
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial
eEF1A lysine and N-terminal methyltransferase homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
aminopeptidase N-like, transcript variant X1
aminopeptidase N-like, transcript variant X2
ras association domain-containing protein 4, transcript variant X1
ras association domain-containing protein 4 isoform X1
ras association domain-containing protein 4, transcript variant X2
ras association domain-containing protein 4 isoform X2
zinc finger and BTB domain-containing protein 7C-like, 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 8 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 7C-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger and BTB domain-containing protein 7C-like isoform X1
zinc finger and BTB domain-containing protein 7C-like isoform X2
zinc finger and BTB domain-containing protein 7C-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB7
vascular endothelial growth factor receptor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial mRNA pseudouridine synthase Trub2
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 78 samples with support for all annotated introns
39S ribosomal protein L16, mitochondrial
transmembrane protein 132E, transcript variant X2
transmembrane protein 132E, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
rRNA methyltransferase 3A, mitochondrial
GATOR complex protein Iml1, transcript variant X1
GATOR complex protein Iml1, transcript variant X2
GATOR complex protein Iml1, transcript variant X3
GATOR complex protein Iml1, transcript variant X4
arrestin domain-containing protein 17-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 31% 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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
putative polypeptide N-acetylgalactosaminyltransferase 9 isoform X1
putative polypeptide N-acetylgalactosaminyltransferase 9 isoform X2
serine-enriched 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
serine-enriched protein, transcript variant X2
serine-enriched protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 340 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 448 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: 447 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: 318 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like, transcript variant X4
acetylcholine receptor subunit alpha-like, transcript variant X2
acetylcholine receptor subunit alpha-like, transcript variant X3
acetylcholine receptor subunit alpha-like, transcript variant X1
acetylcholine receptor subunit alpha-like, transcript variant X6
acetylcholine receptor subunit alpha-like, transcript variant X5
acetylcholine receptor subunit alpha-like isoform X4
acetylcholine receptor subunit alpha-like isoform X2
acetylcholine receptor subunit alpha-like isoform X3
acetylcholine receptor subunit alpha-like isoform X1
acetylcholine receptor subunit alpha-like isoform X5
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
NK1 transcription factor-related protein 1-like
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 20 samples with support for all annotated introns
synaptic vesicle glycoprotein 2C-like, transcript variant X2
synaptic vesicle glycoprotein 2C-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 19 samples with support for all annotated introns
synaptic vesicle glycoprotein 2C-like isoform X2
synaptic vesicle glycoprotein 2C-like isoform X1
proton-associated sugar transporter A, transcript variant X1
proton-associated sugar transporter A, transcript variant X2
proton-associated sugar transporter A isoform X1
proton-associated sugar transporter A isoform X2
tetratricopeptide repeat protein 21B-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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transfer RNA tryptophan (anticodon CCA); 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 9-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
major facilitator superfamily domain-containing protein 9-like isoform X1
major facilitator superfamily domain-containing protein 9-like, transcript variant X2
major facilitator superfamily domain-containing protein 9-like isoform X2
LOW QUALITY PROTEIN: uncharacterized protein LOC124407993
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
signal recognition particle 19 kDa protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 samples with support for all annotated introns
carbonic anhydrase 7-like, transcript variant X1
carbonic anhydrase 7-like, transcript variant X2
transcription elongation factor B polypeptide 3
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
ATP-binding cassette sub-family C member 11-like, transcript variant X1
ATP-binding cassette sub-family C member 11-like, transcript variant X3
ATP-binding cassette sub-family C member 11-like isoform X1
ATP-binding cassette sub-family C member 12-like isoform X3
ATP-binding cassette sub-family C member 11-like, transcript variant X2
ATP-binding cassette sub-family C member 5-like isoform X2
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X3
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X2
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X1
LIM and senescent cell antigen-like-containing domain protein 1 isoform X2
LIM and senescent cell antigen-like-containing domain protein 1 isoform X1
LIM and senescent cell antigen-like-containing domain protein 1 isoform X3
protein artichoke-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein artichoke-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 67% 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 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
neurogenic locus notch homolog protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PH and SEC7 domain-containing protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
PH and SEC7 domain-containing protein isoform X4
PH and SEC7 domain-containing protein, transcript variant X6
PH and SEC7 domain-containing protein, transcript variant X7
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 4 samples with support for all annotated introns
PH and SEC7 domain-containing protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
PH and SEC7 domain-containing protein isoform X5
PH and SEC7 domain-containing protein isoform X6
PH and SEC7 domain-containing protein isoform X2
PH and SEC7 domain-containing protein, 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 10 samples with support for all annotated introns
PH and SEC7 domain-containing protein isoform X3
PH and SEC7 domain-containing protein, 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 6 samples with support for all annotated introns
PH and SEC7 domain-containing protein, transcript variant X1
PH and SEC7 domain-containing protein isoform X1
CDGSH iron-sulfur domain-containing protein 2 homolog
isovaleryl-CoA dehydrogenase, mitochondrial, transcript variant X2
isovaleryl-CoA dehydrogenase, mitochondrial, 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 25 samples with support for all annotated introns
isovaleryl-CoA dehydrogenase, mitochondrial isoform X1
isovaleryl-CoA dehydrogenase, mitochondrial isoform X2
DNA-dependent protein kinase catalytic subunit-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
uncharacterized LOC124407864, 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 9 samples with support for all annotated introns
uncharacterized LOC124407864, transcript variant X1
uncharacterized protein LOC124407864 isoform X1
uncharacterized protein LOC124407864 isoform X2
uncharacterized LOC124408166, transcript variant X1
uncharacterized protein LOC124408166 isoform X1
uncharacterized LOC124408166, transcript variant X2
uncharacterized protein LOC124408166 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
inorganic pyrophosphatase, transcript variant X1
inorganic pyrophosphatase, transcript variant X2
transcription factor MafK-like, transcript variant X1
transcription factor MafK-like, transcript variant X2
transcription factor MafK-like isoform X1
transcription factor MafK-like isoform X2
uncharacterized LOC124408171, 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 8 samples with support for all annotated introns
uncharacterized LOC124408171, 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 1 sample with support for all annotated introns
ankyrin repeat and KH domain-containing protein 1-like
phenylalanine--tRNA ligase beta subunit, transcript variant X1
phenylalanine--tRNA ligase beta subunit, transcript variant X2
phenylalanine--tRNA ligase beta subunit isoform X1
phenylalanine--tRNA ligase beta subunit isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 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 27 samples with support for all annotated introns
neutral and basic amino acid transport protein rBAT, transcript variant X1
neutral and basic amino acid transport protein rBAT, 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 61 samples with support for all annotated introns
neutral and basic amino acid transport protein rBAT isoform X1
neutral and basic amino acid transport protein rBAT isoform X2
JNK1/MAPK8-associated membrane protein, transcript variant X1
JNK1/MAPK8-associated membrane protein, transcript variant X2
JNK1/MAPK8-associated membrane protein isoform X1
JNK1/MAPK8-associated membrane protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC124407952
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit epsilon isoform, transcript variant X2
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit epsilon isoform, transcript variant X1
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit epsilon isoform
mitochondrial arginine transporter BAC2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 25 member 45-like, transcript variant X2
solute carrier family 25 member 45-like isoform X2
solute carrier family 25 member 45-like, transcript variant X3
solute carrier family 25 member 45-like, transcript variant X1
solute carrier family 25 member 45-like, transcript variant X4
solute carrier family 25 member 47-A-like isoform X3
solute carrier family 25 member 45-like isoform X1
RNA-binding protein Pasilla, transcript variant X1
RNA-binding protein Pasilla, transcript variant X2
RNA-binding protein Pasilla, 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 32 samples with support for all annotated introns
RNA-binding protein Pasilla, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
molybdopterin synthase sulfur carrier subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
molybdopterin synthase catalytic subunit
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 48 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 39% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124407873, transcript variant X1
uncharacterized LOC124407873, transcript variant X2
uncharacterized LOC124408001, transcript variant X2
uncharacterized LOC124408001, 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 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 88% coverage of the annotated genomic feature by RNAseq alignments
N-alpha-acetyltransferase 80-like, transcript variant X1
N-alpha-acetyltransferase 80-like, transcript variant X3
N-alpha-acetyltransferase 80-like, transcript variant X2
N-alpha-acetyltransferase 80-like, transcript variant X4
N-alpha-acetyltransferase 80-like isoform X1
N-alpha-acetyltransferase 80-like isoform X2
protein O-mannosyl-transferase 2, transcript variant X1
protein O-mannosyl-transferase 2, transcript variant X2
protein O-mannosyl-transferase 2, transcript variant X3
protein O-mannosyl-transferase 2, transcript variant X4
protein O-mannosyl-transferase 2, transcript variant X6
protein O-mannosyl-transferase 2, transcript variant X8
protein O-mannosyl-transferase 2, transcript variant X5
protein O-mannosyl-transferase 2, transcript variant X7
protein O-mannosyl-transferase 2 isoform X1
protein O-mannosyl-transferase 2 isoform X2
protein O-mannosyl-transferase 2 isoform X3
protein O-mannosyl-transferase 2 isoform X4
protein O-mannosyl-transferase 2 isoform X6
protein O-mannosyl-transferase 2 isoform X8
protein O-mannosyl-transferase 2 isoform X5
protein O-mannosyl-transferase 2 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51% coverage of the annotated genomic feature by RNAseq alignments
post-GPI attachment to proteins factor 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 34% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 11% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF01960
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
COORDINATES: nucleotide motif:Rfam:12.0:RF02543