Vespa crabro chromosome 23, iyVesCrab1.2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Apocrita; Aculeata; Vespoidea; Vespidae; Vespinae; Vespa.
REFSEQ INFORMATION: The reference sequence is identical to\nOU342422.1.\nAssembly name: iyVesCrab1.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/02/09. The original whole-genome shotgun project has the\naccession CAJUUB000000000.2.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Vespa crabro Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
uncharacterized LOC124432002, transcript variant X3
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC124432002, transcript variant X2
uncharacterized LOC124432002, transcript variant X1
histone-lysine N-methyltransferase SETMAR-like
calcium homeostasis endoplasmic reticulum protein, transcript variant X1
calcium homeostasis endoplasmic reticulum protein, transcript variant X2
calcium homeostasis endoplasmic reticulum protein isoform X1
calcium homeostasis endoplasmic reticulum protein isoform X2
eukaryotic translation initiation factor 3 subunit G
neprilysin-2-like, transcript variant X1
neprilysin-2-like, transcript variant X3
neprilysin-2-like, transcript variant X2
neprilysin-2-like, transcript variant X4
neprilysin-2-like, transcript variant X5
DNA-directed RNA polymerase II subunit Rpb4-like, 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 16 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit Rpb4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit Rpb4-like, transcript variant X3
DNA-directed RNA polymerase II subunit Rpb4-like isoform X2
transcriptional adapter 2-alpha-like isoform X1
uncharacterized LOC124432043, transcript variant X5
uncharacterized LOC124432043, transcript variant X1
uncharacterized LOC124432043, transcript variant X4
uncharacterized LOC124432043, transcript variant X3
uncharacterized LOC124432043, transcript variant X2
uncharacterized protein LOC124432043 isoform X1
uncharacterized protein LOC124432043 isoform X2
putative uncharacterized protein DDB_G0291608, 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 11 samples with support for all annotated introns
putative uncharacterized protein DDB_G0291608, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
putative uncharacterized protein DDB_G0291608
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
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X5
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X6
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X4
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X1
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X2
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X3
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X7
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X8
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X4
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X2
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X1
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X3
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X5
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X6
uncharacterized LOC124432118, transcript variant X1
uncharacterized LOC124432118, transcript variant X2
uncharacterized protein LOC124432118 isoform X1
uncharacterized protein LOC124432118 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 15 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 16 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 16 samples with support for all annotated introns
transmembrane protein 47, transcript variant X2
transmembrane protein 47, transcript variant X3
transmembrane protein 47, transcript variant X1
cysteine-rich with EGF-like domain protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
THUMP domain-containing protein 3-like, transcript variant X1
THUMP domain-containing protein 3-like, transcript variant X2
THUMP domain-containing protein 3-like isoform X1
THUMP domain-containing protein 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
lipase maturation factor 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 9 samples with support for all annotated introns
lipase maturation factor 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
lipase maturation factor 2-like isoform X1
lipase maturation factor 2-like isoform X2
snRNA-activating protein complex subunit 4
AP2-associated protein kinase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
AP2-associated protein kinase 1, transcript variant X1
AP2-associated protein kinase 1, transcript variant X2
AP2-associated protein kinase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
AP2-associated protein kinase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
AP2-associated protein kinase 1 isoform X1
AP2-associated protein kinase 1 isoform X2
AP2-associated protein kinase 1 isoform X3
AP2-associated protein kinase 1 isoform X4
AP2-associated protein kinase 1 isoform X5
uncharacterized LOC124432008, transcript variant X1
uncharacterized LOC124432008, transcript variant X2
uncharacterized LOC124432008, transcript variant X7
uncharacterized LOC124432008, transcript variant X4
uncharacterized LOC124432008, transcript variant X5
uncharacterized LOC124432008, transcript variant X3
uncharacterized LOC124432008, transcript variant X6
mitochondrial import inner membrane translocase subunit Tim23, transcript variant X3
mitochondrial import inner membrane translocase subunit Tim23, transcript variant X2
mitochondrial import inner membrane translocase subunit Tim23 isoform X2
mitochondrial import inner membrane translocase subunit Tim23, transcript variant X1
mitochondrial import inner membrane translocase subunit Tim23 isoform X1
protein phosphatase 1B, transcript variant X2
protein phosphatase 1B, transcript variant X1
protein phosphatase 1B, 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 18 samples with support for all annotated introns
beclin 1-associated autophagy-related key regulator, transcript variant X3
beclin 1-associated autophagy-related key regulator, transcript variant X2
beclin 1-associated autophagy-related key regulator, transcript variant X1
beclin 1-associated autophagy-related key regulator isoform X3
beclin 1-associated autophagy-related key regulator isoform X2
beclin 1-associated autophagy-related key regulator isoform X1
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X4
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X2
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X3
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X5
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X1
probable cleavage and polyadenylation specificity factor subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC124432124, transcript variant X2
uncharacterized LOC124432124, transcript variant X1
uncharacterized protein LOC124432124 isoform X1
uncharacterized protein LOC124432124 isoform X2
glutamic acid-rich protein-like, transcript variant X1
glutamic acid-rich protein-like, transcript variant X2
glutamic acid-rich protein-like isoform X1
glutamic acid-rich protein-like isoform X2
neprilysin-4-like, transcript variant X1
neprilysin-4-like, transcript variant X2
p21-activated protein kinase-interacting protein 1-like
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial, transcript variant X1
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial, transcript variant X2
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial, transcript variant X3
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X1
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X2
CCR4-NOT transcription complex subunit 1, transcript variant X2
CCR4-NOT transcription complex subunit 1, transcript variant X1
CCR4-NOT transcription complex subunit 1 isoform X2
CCR4-NOT transcription complex subunit 1 isoform X1
endothelial differentiation-related factor 1 homolog
39S ribosomal protein L46, mitochondrial, transcript variant X1
39S ribosomal protein L46, mitochondrial, transcript variant X2
39S ribosomal protein L46, mitochondrial
lariat debranching enzyme, 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 14 samples with support for all annotated introns
lariat debranching enzyme, 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 18 samples with support for all annotated introns
survival of motor neuron-related-splicing factor 30, transcript variant X4
survival of motor neuron-related-splicing factor 30, transcript variant X2
survival of motor neuron-related-splicing factor 30, transcript variant X3
survival of motor neuron-related-splicing factor 30, transcript variant X1
survival of motor neuron-related-splicing factor 30
uncharacterized LOC124432105, transcript variant X2
uncharacterized LOC124432105, transcript variant X4
uncharacterized LOC124432105, transcript variant X1
uncharacterized LOC124432105, transcript variant X3
uncharacterized protein LOC124432105 isoform X1
uncharacterized protein LOC124432105 isoform X2
E3 ubiquitin-protein ligase TRIM33-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 5 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM33-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 12 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM33-like isoform X2
E3 ubiquitin-protein ligase TRIM33-like isoform X1
dyslexia-associated protein KIAA0319, transcript variant X2
dyslexia-associated protein KIAA0319, transcript variant X1
dyslexia-associated protein KIAA0319, 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 15 samples with support for all annotated introns
androgen-induced gene 1 protein-like, transcript variant X6
androgen-induced gene 1 protein-like, transcript variant X1
androgen-induced gene 1 protein-like, transcript variant X5
androgen-induced gene 1 protein-like, transcript variant X7
androgen-induced gene 1 protein-like, transcript variant X4
androgen-induced gene 1 protein-like, transcript variant X3
androgen-induced gene 1 protein-like, transcript variant X2
androgen-induced gene 1 protein-like isoform X1
androgen-induced gene 1 protein-like isoform X3
androgen-induced gene 1 protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
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 6 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
fatty-acid amide hydrolase 2, transcript variant X9
fatty-acid amide hydrolase 2, transcript variant X8
fatty-acid amide hydrolase 2, transcript variant X5
fatty-acid amide hydrolase 2, transcript variant X4
fatty-acid amide hydrolase 2, transcript variant X3
fatty-acid amide hydrolase 2, transcript variant X2
fatty-acid amide hydrolase 2, transcript variant X10
fatty-acid amide hydrolase 2, transcript variant X1
fatty-acid amide hydrolase 2, transcript variant X6
fatty-acid amide hydrolase 2, transcript variant X7
fatty-acid amide hydrolase 2, transcript variant X11
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 14 samples with support for all annotated introns
fatty-acid amide hydrolase 2, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
cytochrome b5 reductase 4, transcript variant X3
cytochrome b5 reductase 4, transcript variant X1
cytochrome b5 reductase 4, transcript variant X2
cytochrome b5 reductase 4, transcript variant X4
monocarboxylate transporter 10-like, transcript variant X1
monocarboxylate transporter 10-like, transcript variant X2
monocarboxylate transporter 10-like, transcript variant X3
monocarboxylate transporter 10-like isoform X1
monocarboxylate transporter 10-like isoform X2
monocarboxylate transporter 10-like isoform X3
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X3
polypeptide N-acetylgalactosaminyltransferase 5 isoform X1
polypeptide N-acetylgalactosaminyltransferase 5 isoform X2
SH3 domain-binding glutamic acid-rich protein homolog
uracil phosphoribosyltransferase homolog
ATP-dependent DNA/RNA helicase DHX36, transcript variant X1
ATP-dependent DNA/RNA helicase DHX36, transcript variant X3
ATP-dependent DNA/RNA helicase DHX36, transcript variant X2
ATP-dependent DNA/RNA helicase DHX36, transcript variant X4
ATP-dependent DNA/RNA helicase DHX36 isoform X1
ATP-dependent DNA/RNA helicase DHX36 isoform X3
ATP-dependent DNA/RNA helicase DHX36 isoform X2
ATP-dependent DNA/RNA helicase DHX36 isoform X4
probable G-protein coupled receptor Mth-like 1
protein MTO1 homolog, mitochondrial, transcript variant X2
protein MTO1 homolog, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
serine/threonine-protein kinase Genghis Khan, transcript variant X3
serine/threonine-protein kinase Genghis Khan, transcript variant X2
serine/threonine-protein kinase Genghis Khan, transcript variant X1
serine/threonine-protein kinase Genghis Khan isoform X2
serine/threonine-protein kinase Genghis Khan isoform X1
dihydropyrimidinase, transcript variant X3
dihydropyrimidinase, transcript variant X2
dihydropyrimidinase, transcript variant X1
epidermal growth factor receptor kinase substrate 8-like, transcript variant X4
epidermal growth factor receptor kinase substrate 8-like, transcript variant X2
epidermal growth factor receptor kinase substrate 8-like, transcript variant X5
epidermal growth factor receptor kinase substrate 8-like, transcript variant X3
epidermal growth factor receptor kinase substrate 8-like, transcript variant X1
epidermal growth factor receptor kinase substrate 8-like, transcript variant X6
epidermal growth factor receptor kinase substrate 8-like
lysine-specific demethylase lid, transcript variant X2
lysine-specific demethylase lid, transcript variant X5
lysine-specific demethylase lid, transcript variant X3
lysine-specific demethylase lid, transcript variant X7
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 14 samples with support for all annotated introns
lysine-specific demethylase lid, transcript variant X1
lysine-specific demethylase lid, transcript variant X4
lysine-specific demethylase lid, transcript variant X6
lysine-specific demethylase lid isoform X2
lysine-specific demethylase lid isoform X1
lysine-specific demethylase lid isoform X5
lysine-specific demethylase lid isoform X3
lysine-specific demethylase lid isoform X4
lysine-specific demethylase lid isoform X6
lysine-specific demethylase lid isoform X7
lysine-specific demethylase lid, transcript variant X8
lysine-specific demethylase lid isoform X8
lysine-specific demethylase lid, transcript variant X9
lysine-specific demethylase lid isoform X9
uncharacterized LOC124431991, transcript variant X1
uncharacterized LOC124431991, transcript variant X2
uncharacterized protein LOC124431991 isoform X1
uncharacterized protein LOC124431991 isoform X2
uncharacterized LOC124432026, transcript variant X1
uncharacterized LOC124432026, transcript variant X2
uncharacterized LOC124432026, transcript variant X3
uncharacterized LOC124432064, transcript variant X2
uncharacterized LOC124432064, transcript variant X1
uncharacterized LOC124432064, transcript variant X3
uncharacterized protein LOC124432064 isoform X2
uncharacterized protein LOC124432064 isoform X1
uncharacterized protein LOC124432064 isoform X3
serine/threonine-protein kinase HRK1-like
ataxin-7-like protein 1, 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
ataxin-7-like protein 1, transcript variant X1
ataxin-7-like protein 1, transcript variant X3
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X1
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X4
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X3
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X2
KN motif and ankyrin repeat domain-containing protein 1 isoform X1
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X5
KN motif and ankyrin repeat domain-containing protein 1 isoform X2
plasma membrane calcium-transporting ATPase 3, transcript variant X9
plasma membrane calcium-transporting ATPase 3, transcript variant X7
plasma membrane calcium-transporting ATPase 3, transcript variant X8
plasma membrane calcium-transporting ATPase 3, transcript variant X6
plasma membrane calcium-transporting ATPase 2 isoform X6
plasma membrane calcium-transporting ATPase 2 isoform X4
plasma membrane calcium-transporting ATPase 2 isoform X5
plasma membrane calcium-transporting ATPase 2 isoform X3
plasma membrane calcium-transporting ATPase 3, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X13
plasma membrane calcium-transporting ATPase 3, transcript variant X10
plasma membrane calcium-transporting ATPase 3, transcript variant X16
plasma membrane calcium-transporting ATPase 3 isoform X7
plasma membrane calcium-transporting ATPase 3, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X3
plasma membrane calcium-transporting ATPase 3, transcript variant X5
plasma membrane calcium-transporting ATPase 3, transcript variant X1
plasma membrane calcium-transporting ATPase 3, transcript variant X2
plasma membrane calcium-transporting ATPase 3, transcript variant X4
plasma membrane calcium-transporting ATPase 2 isoform X2
plasma membrane calcium-transporting ATPase 2 isoform X1
plasma membrane calcium-transporting ATPase 3, transcript variant X15
plasma membrane calcium-transporting ATPase 3, transcript variant X11
plasma membrane calcium-transporting ATPase 3 isoform X8
uncharacterized LOC124431982, transcript variant X2
uncharacterized LOC124431982, transcript variant X1
uncharacterized protein LOC124431982 isoform X2
uncharacterized protein LOC124431982 isoform X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9
GTP-binding protein Rit2-like, transcript variant X1
GTP-binding protein Rit2-like, transcript variant X2
GTP-binding protein Rit2-like isoform X1
GTP-binding protein Rit2-like isoform X2
uncharacterized LOC124432022, transcript variant X4
uncharacterized LOC124432022, transcript variant X3
uncharacterized LOC124432022, transcript variant X2
uncharacterized LOC124432022, transcript variant X1
uncharacterized LOC124432022, transcript variant X5
uncharacterized protein LOC124432022 isoform X2
uncharacterized protein LOC124432022 isoform X1
putative ATP synthase subunit f, mitochondrial
mediator of RNA polymerase II transcription subunit 6
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 9 samples with support for all annotated introns
F-box only protein 11, transcript variant X3
F-box only protein 11, transcript variant X4
F-box only protein 11, transcript variant X2
F-box only protein 11, transcript variant X5
F-box only protein 11, transcript variant X6
F-box only protein 11, transcript variant X7
F-box only protein 11, 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 15 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD3, transcript variant X3
BTB/POZ domain-containing protein KCTD3, transcript variant X2
BTB/POZ domain-containing protein KCTD3, transcript variant X1
BTB/POZ domain-containing protein KCTD3, transcript variant X4
BTB/POZ domain-containing protein KCTD3 isoform X3
BTB/POZ domain-containing protein KCTD3 isoform X2
BTB/POZ domain-containing protein KCTD3 isoform X1
BTB/POZ domain-containing protein KCTD3 isoform X4
dynein axonemal assembly factor 11, transcript variant X1
dynein axonemal assembly factor 11, transcript variant X6
dynein axonemal assembly factor 11, transcript variant X4
dynein axonemal assembly factor 11, transcript variant X5
dynein axonemal assembly factor 11, transcript variant X3
dynein axonemal assembly factor 11, transcript variant X2
dynein axonemal assembly factor 11 isoform X4
uncharacterized protein LOC124432078 isoform X2
dynein axonemal assembly factor 11 isoform X3
dynein axonemal assembly factor 11 isoform X1
spliceosome-associated protein CWC27 homolog
mitochondrial dicarboxylate carrier, transcript variant X1
mitochondrial dicarboxylate carrier, transcript variant X2
immunoglobulin superfamily member 10-like, transcript variant X2
immunoglobulin superfamily member 10-like, transcript variant X1
immunoglobulin superfamily member 10-like
igLON family member 5-like, transcript variant X1
igLON family member 5-like, transcript variant X2
dopamine D2-like receptor, transcript variant X1
dopamine D2-like receptor, transcript variant X4
dopamine D2-like receptor, transcript variant X2
dopamine D2-like receptor, transcript variant X8
dopamine D2-like receptor, transcript variant X3
dopamine D2-like receptor, transcript variant X6
dopamine D2-like receptor, transcript variant X5
dopamine D2-like receptor, transcript variant X7
dopamine D2-like receptor, transcript variant X10
dopamine D2-like receptor, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear pore complex protein DDB_G0274915-like
putative uncharacterized protein DDB_G0282129
mediator of RNA polymerase II transcription subunit 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 69% 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC124432065, 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 3 samples with support for all annotated introns
uncharacterized protein LOC124432065 isoform X1
uncharacterized LOC124432065, 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 LOC124432065 isoform X2
tRNA N(3)-methylcytidine methyltransferase METTL6
Derived by automated computational analysis using gene prediction method: cmsearch.
small nucleolar RNA snR60/Z15/Z230/Z193/J17
COORDINATES: nucleotide motif:Rfam:12.0:RF00309
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X2
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial
adult-specific cuticular protein ACP-22-like
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 63% 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: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
cuticle protein 7-like, 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 1 sample with support for all annotated introns
cuticle protein 7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC124432136 isoform X1
odorant receptor 67c-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
odorant receptor 67c-like, 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 2 samples with support for all annotated introns
odorant receptor 67c-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
odorant receptor 67c-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 4 samples with support for all annotated introns
uncharacterized protein LOC124432135 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 26% 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 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 46% 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: odorant receptor 30a-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
probable ribonuclease ZC3H12C, 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
probable ribonuclease ZC3H12C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable ribonuclease ZC3H12C, transcript variant X3
probable ribonuclease ZC3H12C isoform X3
ubiquitin carboxyl-terminal hydrolase 45
uncharacterized LOC124432075, transcript variant X2
uncharacterized LOC124432075, transcript variant X3
uncharacterized LOC124432075, transcript variant X1
uncharacterized LOC124432075, transcript variant X4
uncharacterized LOC124432075, transcript variant X5
uncharacterized protein LOC124432075 isoform X3
uncharacterized protein LOC124432075 isoform X1
uncharacterized protein LOC124432075 isoform X2
uncharacterized protein LOC124432075 isoform X4
28S ribosomal protein S15, mitochondrial
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 1 sample with support for all annotated introns
chromatin modification-related protein MEAF6
uncharacterized LOC124432032, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC124432032, 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 14 samples with support for all annotated introns
uncharacterized protein LOC124432032 isoform X1
uncharacterized protein LOC124432032 isoform X2
recQ-mediated genome instability protein 1-like
probable V-type proton ATPase subunit D 2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
calcium uptake protein 1 homolog, mitochondrial, transcript variant X1
calcium uptake protein 1 homolog, mitochondrial, transcript variant X2
calcium uptake protein 1 homolog, mitochondrial isoform X1
calcium uptake protein 1 homolog, mitochondrial isoform X2
coiled-coil domain-containing protein 6, transcript variant X2
coiled-coil domain-containing protein 6, transcript variant X1
coiled-coil domain-containing protein 6, transcript variant X3
coiled-coil domain-containing protein 6 isoform X1
coiled-coil domain-containing protein 6 isoform X2
puratrophin-1-like, transcript variant X1
puratrophin-1-like, transcript variant X2
uncharacterized protein LOC124432083 isoform X1
puratrophin-1-like, transcript variant X3
uncharacterized protein LOC124432083 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
puratrophin-1-like, transcript variant X4
ras guanine nucleotide exchange factor P-like, transcript variant X1
ras guanine nucleotide exchange factor P-like, transcript variant X2
ras guanine nucleotide exchange factor P-like isoform X1
ras guanine nucleotide exchange factor P-like isoform X2
farnesol dehydrogenase-like, 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 3 samples with support for all annotated introns
farnesol dehydrogenase-like, transcript variant X3
farnesol dehydrogenase-like, transcript variant X2
uncharacterized LOC124431974, transcript variant X4
uncharacterized LOC124431974, transcript variant X1
uncharacterized LOC124431974, transcript variant X3
uncharacterized LOC124431974, transcript variant X2
segmentation polarity homeobox protein engrailed-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124431976, 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 LOC124431976, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC124431976, transcript variant X3
Krueppel-like factor 6, transcript variant X2
Krueppel-like factor 6, transcript variant X4
Krueppel-like factor 6, transcript variant X1
Krueppel-like factor 6, transcript variant X6
Krueppel-like factor 6, transcript variant X5
Krueppel-like factor 6, transcript variant X3
uncharacterized LOC124431975, transcript variant X3
uncharacterized LOC124431975, transcript variant X2
uncharacterized LOC124431975, transcript variant X1
uncharacterized LOC124432119, transcript variant X2
uncharacterized LOC124432119, transcript variant X3
uncharacterized LOC124432119, transcript variant X1
uncharacterized protein LOC124432119 isoform X2
uncharacterized protein LOC124432119 isoform X1
uncharacterized LOC124432119, 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 2 samples with support for all annotated introns
uncharacterized protein LOC124432119 isoform X3
bestrophin homolog 15, transcript variant X2
bestrophin homolog 15, transcript variant X1
bestrophin homolog 15, transcript variant X3
uncharacterized protein LOC124431997 isoform 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 16 samples with support for all annotated introns