Vespula pensylvanica isolate Volc-1 chromosome 21, ASM1446617v1, whole genome shotgun sequence.
Vespula pensylvanica (western yellowjacket)
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Apocrita; Aculeata; Vespoidea; Vespidae; Vespinae; Vespula.
High-Quality Assemblies for Three Invasive Social Wasps from the Vespula Genus
Publication Status: Available-Online prior to print
REFSEQ INFORMATION: The reference sequence is identical to\nCM025356.1.\nAssembly name: ASM1446617v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the University of Otago on\n2020/09/09. The original whole-genome shotgun project has the\naccession JACSDY000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: University of Otago\nAssembly Date :: 03-JUL-2020\nAssembly Method :: meraculous v. 2.2.6\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 644x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Vespula pensylvanica Annotation\n 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.
calcium homeostasis endoplasmic reticulum protein, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
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 X3
neprilysin-2-like, transcript variant X2
neprilysin-2-like, transcript variant X1
neprilysin-2-like, transcript variant X4
neprilysin-2-like, transcript variant X6
neprilysin-2-like, transcript variant X5
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 10 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit Rpb4-like, transcript variant X1
DNA-directed RNA polymerase II subunit Rpb4-like, 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 15 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit Rpb4-like, 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 34 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit Rpb4-like, transcript variant X5
transcriptional adapter 2-alpha-like isoform X1
DNA-directed RNA polymerase II subunit Rpb4-like isoform X3
transcriptional adapter 2-alpha-like isoform X2
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A, transcript variant X1
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform X1
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A, transcript variant X2
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 56% 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 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: 93% coverage of the annotated genomic feature by RNAseq alignments
amyloid beta A4 precursor protein-binding family B member 1-interacting protein, transcript variant X4
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 30 samples with support for all annotated introns
amyloid beta A4 precursor protein-binding family B member 1-interacting protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
amyloid beta A4 precursor protein-binding family B member 1-interacting protein, 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 19 samples with support for all annotated introns
amyloid beta A4 precursor protein-binding family B member 1-interacting protein, 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 21 samples with support for all annotated introns
amyloid beta A4 precursor protein-binding family B member 1-interacting protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
amyloid beta A4 precursor protein-binding family B member 1-interacting protein, transcript variant X6
amyloid beta A4 precursor protein-binding family B member 1-interacting protein isoform X4
amyloid beta A4 precursor protein-binding family B member 1-interacting protein isoform X3
amyloid beta A4 precursor protein-binding family B member 1-interacting protein isoform X2
amyloid beta A4 precursor protein-binding family B member 1-interacting protein isoform X1
amyloid beta A4 precursor protein-binding family B member 1-interacting protein isoform X5
amyloid beta A4 precursor protein-binding family B member 1-interacting protein isoform X6
uncharacterized LOC122636266, transcript variant X1
uncharacterized LOC122636266, transcript variant X2
uncharacterized protein LOC122636266 isoform X1
uncharacterized protein LOC122636266 isoform X2
zinc finger protein 678-like, transcript variant X2
zinc finger protein 678-like, transcript variant X1
zinc finger protein 678-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
transmembrane protein 47, transcript variant X2
transmembrane protein 47, transcript variant X4
transmembrane protein 47, transcript variant X3
transmembrane protein 47, transcript variant X1
cysteine-rich with EGF-like domain protein 2
uncharacterized LOC122636336, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC122636336, transcript variant X2
THUMP domain-containing protein 3-like, transcript variant X1
THUMP domain-containing protein 3-like isoform X1
THUMP domain-containing protein 3-like, transcript variant X2
THUMP domain-containing protein 3-like isoform X2
snRNA-activating protein complex subunit 4 homolog
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
BMP-2-inducible protein kinase, transcript variant X1
BMP-2-inducible protein kinase, transcript variant X2
BMP-2-inducible protein kinase, transcript variant X3
BMP-2-inducible protein kinase, transcript variant X5
BMP-2-inducible protein kinase, transcript variant X6
BMP-2-inducible protein kinase, transcript variant X4
BMP-2-inducible protein kinase, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
BMP-2-inducible protein kinase isoform X1
BMP-2-inducible protein kinase isoform X2
BMP-2-inducible protein kinase isoform X3
BMP-2-inducible protein kinase isoform X4
BMP-2-inducible protein kinase isoform X5
BMP-2-inducible protein kinase isoform X6
AP2-associated protein kinase 1 isoform X7
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 44 samples with support for all annotated introns
uncharacterized LOC122636335, transcript variant X1
uncharacterized LOC122636335, transcript variant X2
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 X1
protein phosphatase 1B, transcript variant X3
protein phosphatase 1B, 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 44 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 X2
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X3
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X4
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X1
probable cleavage and polyadenylation specificity factor subunit 2 isoform X1
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X5
probable cleavage and polyadenylation specificity factor subunit 2 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 43 samples 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122636302, transcript variant X3
uncharacterized LOC122636302, transcript variant X1
uncharacterized LOC122636302, transcript variant X2
uncharacterized protein LOC122636302 isoform X1
uncharacterized protein LOC122636302 isoform X2
dipeptidase 1-like, transcript variant X2
dipeptidase 1-like, transcript variant X1
neprilysin-4-like, transcript variant X4
neprilysin-4-like, transcript variant X1
neprilysin-4-like, transcript variant X2
neprilysin-4-like, transcript variant X3
p21-activated protein kinase-interacting protein 1-like
DNA topoisomerase 3-beta-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 25 samples with support for all annotated introns
DNA topoisomerase 3-beta-1, transcript variant X3
DNA topoisomerase 3-beta-1, transcript variant X2
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial, transcript variant X1
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial, transcript variant X2
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X1
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X2
CCR4-NOT transcription complex subunit 1, transcript variant X3
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 X3
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 X2
39S ribosomal protein L46, mitochondrial, transcript variant X1
39S ribosomal protein L46, mitochondrial
lariat debranching enzyme, transcript variant X2
lariat debranching enzyme, transcript variant X1
lariat debranching enzyme, transcript variant X3
survival of motor neuron-related-splicing factor 30, transcript variant X4
survival of motor neuron-related-splicing factor 30, transcript variant X3
survival of motor neuron-related-splicing factor 30, transcript variant X2
survival of motor neuron-related-splicing factor 30, transcript variant X1
survival of motor neuron-related-splicing factor 30
tripartite motif-containing protein 45-like
androgen-induced gene 1 protein-like, transcript variant X3
androgen-induced gene 1 protein-like, transcript variant X7
androgen-induced gene 1 protein-like, transcript variant X2
androgen-induced gene 1 protein-like, transcript variant X8
androgen-induced gene 1 protein-like, transcript variant X9
androgen-induced gene 1 protein-like, transcript variant X4
androgen-induced gene 1 protein-like, transcript variant X5
androgen-induced gene 1 protein-like, transcript variant X6
androgen-induced gene 1 protein-like, transcript variant X1
androgen-induced gene 1 protein-like isoform X2
androgen-induced gene 1 protein-like isoform X1
fatty-acid amide hydrolase 2, transcript variant X3
fatty-acid amide hydrolase 2, transcript variant X12
fatty-acid amide hydrolase 2, transcript variant X2
fatty-acid amide hydrolase 2, transcript variant X11
fatty-acid amide hydrolase 2, transcript variant X9
fatty-acid amide hydrolase 2, transcript variant X6
fatty-acid amide hydrolase 2, transcript variant X4
fatty-acid amide hydrolase 2, transcript variant X1
fatty-acid amide hydrolase 2, transcript variant X5
fatty-acid amide hydrolase 2, transcript variant X7
fatty-acid amide hydrolase 2, transcript variant X8
fatty-acid amide hydrolase 2, transcript variant X10
fatty-acid amide hydrolase 2, transcript variant X13
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
fatty-acid amide hydrolase 2, transcript variant X14
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 X1
cytochrome b5 reductase 4, transcript variant X2
monocarboxylate transporter 10-like, transcript variant X1
monocarboxylate transporter 10-like, transcript variant X2
monocarboxylate transporter 10-like isoform X1
monocarboxylate transporter 10-like isoform X2
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X3
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 5 isoform X1
polypeptide N-acetylgalactosaminyltransferase 5 isoform X2
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X2
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X3
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X1
SH3 domain-binding glutamic acid-rich protein homolog
uracil phosphoribosyltransferase homolog
ATP-dependent DNA/RNA helicase DHX36, transcript variant X2
ATP-dependent DNA/RNA helicase DHX36, transcript variant X3
ATP-dependent DNA/RNA helicase DHX36, transcript variant X1
ATP-dependent DNA/RNA helicase DHX36, transcript variant X4
ATP-dependent DNA/RNA helicase DHX36 isoform X1
ATP-dependent DNA/RNA helicase DHX36 isoform X2
probable G-protein coupled receptor Mth-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
deubiquitinase DESI2, transcript variant X1
deubiquitinase DESI2, transcript variant X2
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 X4
serine/threonine-protein kinase Genghis Khan, transcript variant X5
serine/threonine-protein kinase Genghis Khan, transcript variant X1
serine/threonine-protein kinase Genghis Khan, transcript variant X6
serine/threonine-protein kinase Genghis Khan isoform X3
serine/threonine-protein kinase Genghis Khan isoform X1
serine/threonine-protein kinase Genghis Khan 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 39 samples with support for all annotated introns
dihydropyrimidinase, transcript variant X1
dihydropyrimidinase, transcript variant X2
epidermal growth factor receptor kinase substrate 8-like, transcript variant X2
epidermal growth factor receptor kinase substrate 8-like, transcript variant X1
epidermal growth factor receptor kinase substrate 8-like, transcript variant X3
epidermal growth factor receptor kinase substrate 8-like
cytochrome b-c1 complex subunit 8, transcript variant X2
cytochrome b-c1 complex subunit 8, transcript variant X1
lysine-specific demethylase lid, 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 18 samples with support for all annotated introns
lysine-specific demethylase lid, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
lysine-specific demethylase lid, 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 16 samples with support for all annotated introns
lysine-specific demethylase lid, transcript variant X3
lysine-specific demethylase lid, transcript variant X2
lysine-specific demethylase lid isoform X2
lysine-specific demethylase lid isoform X1
uncharacterized protein DDB_G0284311-like
vitellogenin-like, transcript variant X2
vitellogenin-like, transcript variant X1
uncharacterized LOC122636347, transcript variant X2
uncharacterized LOC122636347, transcript variant X1
uncharacterized protein LOC122636347 isoform X2
uncharacterized protein LOC122636347 isoform X1
uncharacterized LOC122636353, transcript variant X2
uncharacterized LOC122636353, transcript variant X1
ataxin-7-like protein 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 4 samples with support for all annotated introns
ataxin-7-like protein 1, 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 33 samples with support for all annotated introns
ataxin-7-like protein 1, 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 30 samples with support for all annotated introns
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X5
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X2
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X1
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X3
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X4
KN motif and ankyrin repeat domain-containing protein 1 isoform X1
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X6
KN motif and ankyrin repeat domain-containing protein 1 isoform X2
uncharacterized LOC122636354, transcript variant X1
uncharacterized LOC122636354, transcript variant X2
plasma membrane calcium-transporting ATPase 3, 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 32 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, 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 27 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 2 isoform X5
plasma membrane calcium-transporting ATPase 2 isoform X3
plasma membrane calcium-transporting ATPase 2 isoform X4
plasma membrane calcium-transporting ATPase 3, transcript variant X15
plasma membrane calcium-transporting ATPase 3, 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 14 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X10
plasma membrane calcium-transporting ATPase 3 isoform X9
plasma membrane calcium-transporting ATPase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, 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 38 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X3
plasma membrane calcium-transporting ATPase 2 isoform X2
plasma membrane calcium-transporting ATPase 2 isoform X1
plasma membrane calcium-transporting ATPase 3, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X11
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 28 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X12
plasma membrane calcium-transporting ATPase 3, transcript variant X9
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
plasma membrane calcium-transporting ATPase 3 isoform X8
plasma membrane calcium-transporting ATPase 3 isoform X7
plasma membrane calcium-transporting ATPase 3, transcript variant X8
plasma membrane calcium-transporting ATPase 2 isoform X6
uncharacterized LOC122636342, transcript variant X2
uncharacterized LOC122636342, transcript variant X3
uncharacterized LOC122636342, transcript variant X4
uncharacterized LOC122636342, transcript variant X1
uncharacterized LOC122636342, transcript variant X6
uncharacterized LOC122636342, transcript variant X5
uncharacterized protein LOC122636342 isoform X3
uncharacterized protein LOC122636342 isoform X2
uncharacterized protein LOC122636342 isoform X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9
uncharacterized LOC122636351, transcript variant X3
uncharacterized protein LOC122636351 isoform X3
uncharacterized LOC122636351, transcript variant X2
uncharacterized protein LOC122636351 isoform X2
uncharacterized LOC122636351, 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 41 samples with support for all annotated introns
uncharacterized protein LOC122636351 isoform X1
putative ATP synthase subunit f, mitochondrial
mediator of RNA polymerase II transcription subunit 6
F-box only protein 11, transcript variant X1
F-box only protein 11, transcript variant X2
BTB/POZ domain-containing protein KCTD3, transcript variant X4
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 isoform X4
BTB/POZ domain-containing protein KCTD3 isoform X2
BTB/POZ domain-containing protein KCTD3 isoform X3
BTB/POZ domain-containing protein KCTD3 isoform X1
dynein axonemal assembly factor 11, transcript variant X3
dynein axonemal assembly factor 11, transcript variant X2
dynein axonemal assembly factor 11, transcript variant X1
dynein axonemal assembly factor 11, transcript variant X5
dynein axonemal assembly factor 11, transcript variant X4
dynein axonemal assembly factor 11 isoform X4
dynein axonemal assembly factor 11 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
mitochondrial dicarboxylate carrier, transcript variant X3
uncharacterized LOC122636210, transcript variant X1
uncharacterized LOC122636210, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC122636250, transcript variant X3
uncharacterized LOC122636250, transcript variant X2
uncharacterized LOC122636250, 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 LOC122636245, transcript variant X2
uncharacterized LOC122636245, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
igLON family member 5-like, transcript variant X1
igLON family member 5-like, transcript variant X3
igLON family member 5-like, transcript variant X2
dopamine D2-like receptor, transcript variant X5
dopamine D2-like receptor, transcript variant X6
dopamine D2-like receptor, transcript variant X8
dopamine D2-like receptor, transcript variant X2
dopamine D2-like receptor, transcript variant X4
dopamine D2-like receptor, transcript variant X1
dopamine D2-like receptor, transcript variant X7
dopamine D2-like receptor, transcript variant X3
dopamine D2-like receptor, transcript variant X9
dopamine D2-like receptor, transcript variant X10
uncharacterized LOC122636296, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC122636296, 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 2 samples with support for all annotated introns
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, transcript variant X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X4
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X3
uncharacterized LOC122636294, transcript variant X2
uncharacterized LOC122636294, transcript variant X1
uncharacterized protein LOC122636294 isoform X2
uncharacterized protein LOC122636294 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 80% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein DDB_G0282133
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
myb-like protein AA, transcript variant X3
myb-like protein AA, transcript variant X1
myb-like protein AA, transcript variant X2
uncharacterized protein DDB_G0283357-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable ATP-dependent RNA helicase ddx17, 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 11 samples with support for all annotated introns
probable ATP-dependent RNA helicase ddx17, 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
probable ATP-dependent RNA helicase ddx17, 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 12 samples with support for all annotated introns
probable ATP-dependent RNA helicase ddx17 isoform X3
probable ATP-dependent RNA helicase ddx17 isoform X2
probable ATP-dependent RNA helicase ddx17 isoform X1
uncharacterized LOC122636275, 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 4 samples with support for all annotated introns
uncharacterized protein LOC122636275 isoform X3
uncharacterized LOC122636275, 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 6 samples with support for all annotated introns
uncharacterized LOC122636275, 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
uncharacterized protein LOC122636275 isoform X2
uncharacterized protein LOC122636275 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 47 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
tRNA N(3)-methylcytidine methyltransferase METTL6, 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 7 samples with support for all annotated introns
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
tRNA N(3)-methylcytidine methyltransferase METTL6
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X2
D-beta-hydroxybutyrate dehydrogenase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 86% 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 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: 14 Proteins, and 69% 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cuticle protein 7-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 7 samples with support for all annotated introns
cuticle protein 7-like, transcript variant X3
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
cuticle protein 7-like, transcript variant X4
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 4 samples 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
cuticle protein 7-like, transcript variant X5
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 2 samples with support for all annotated introns
cuticle protein 7-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 29 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: 100% coverage of the annotated genomic feature by RNAseq alignments
charged multivesicular body protein 1b, transcript variant X3
charged multivesicular body protein 1b, transcript variant X1
charged multivesicular body protein 1b, transcript variant X2
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 34 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized protein LOC122636310 isoform X1
uncharacterized protein LOC122636310 isoform X2
probable ribonuclease ZC3H12C, 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 10 samples with support for all annotated introns
probable ribonuclease ZC3H12C isoform X3
probable ribonuclease ZC3H12C, 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 35 samples with support for all annotated introns
probable ribonuclease ZC3H12C isoform X4
ubiquitin carboxyl-terminal hydrolase 45, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 45, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 45, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 45, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 16 isoform X2
ubiquitin carboxyl-terminal hydrolase 45 isoform X1
uncharacterized LOC122636311, 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 9 samples with support for all annotated introns
uncharacterized LOC122636311, 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 1 sample with support for all annotated introns
uncharacterized LOC122636311, transcript variant X4
uncharacterized LOC122636311, transcript variant X5
uncharacterized LOC122636311, 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 10 samples with support for all annotated introns
uncharacterized protein LOC122636311 isoform X3
uncharacterized protein LOC122636311 isoform X1
uncharacterized protein LOC122636311 isoform X2
uncharacterized protein LOC122636311 isoform X4
28S ribosomal protein S15, mitochondrial, transcript variant X1
28S ribosomal protein S15, mitochondrial, transcript variant X2
28S ribosomal protein S15, mitochondrial isoform X1
28S ribosomal protein S15, mitochondrial isoform X2
cuticle protein 19-like, transcript variant X3
larval cuticle protein A3A-like isoform X2
cuticle protein 19-like, transcript variant X1
cuticle protein 19-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC122636239 isoform X1
cuticle protein 19-like, transcript variant X4
chromatin modification-related protein MEAF6
uncharacterized LOC122636236, transcript variant X1
uncharacterized LOC122636236, transcript variant X2
uncharacterized protein LOC122636236 isoform X1
uncharacterized protein LOC122636236 isoform X2
recQ-mediated genome instability protein 1-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 16 samples with support for all annotated introns
recQ-mediated genome instability 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 28 samples with support for all annotated introns
recQ-mediated genome instability protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
recQ-mediated genome instability protein 1-like isoform X2
recQ-mediated genome instability protein 1-like isoform X1
recQ-mediated genome instability protein 1-like isoform X3
V-type proton ATPase subunit D-like, transcript variant X1
V-type proton ATPase subunit D-like, transcript variant X2
probable V-type proton ATPase subunit D 2 isoform X1
V-type proton ATPase subunit D-like isoform X2
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.
uncharacterized LOC122636254, 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 5 samples with support for all annotated introns
uncharacterized protein LOC122636254 isoform X1
uncharacterized LOC122636254, transcript variant X2
uncharacterized protein LOC122636254 isoform X2
uncharacterized LOC122636255, transcript variant X2
uncharacterized LOC122636255, transcript variant X1
uncharacterized protein LOC122636255 isoform X2
uncharacterized protein LOC122636255 isoform X1
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 X2
calcium uptake protein 1 homolog, mitochondrial isoform X1
coiled-coil domain-containing protein 6, transcript variant X1
coiled-coil domain-containing protein 6, transcript variant X2
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 LOC122636288 isoform X1
uncharacterized protein LOC122636288 isoform X2
puratrophin-1-like, transcript variant X3
uncharacterized protein LOC122636288 isoform X3
puratrophin-1-like, transcript variant X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
probable WRKY transcription factor protein 1
farnesol dehydrogenase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
farnesol dehydrogenase-like, transcript variant X6
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 3 samples with support for all annotated introns
farnesol dehydrogenase-like, transcript variant X7
farnesol dehydrogenase-like, transcript variant X2
farnesol dehydrogenase-like, transcript variant X5
farnesol dehydrogenase-like, transcript variant X8
farnesol dehydrogenase-like, transcript variant X1
farnesol dehydrogenase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized LOC122636246, transcript variant X2
uncharacterized LOC122636246, transcript variant X1
uncharacterized protein LOC122636246 isoform X2
uncharacterized protein LOC122636246 isoform X1
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
Krueppel-like factor 6, transcript variant X1
Krueppel-like factor 6, transcript variant X2
serine/arginine repetitive matrix protein 2-like, transcript variant X2
serine/arginine repetitive matrix protein 2-like, transcript variant X1
serine/arginine repetitive matrix protein 2-like, transcript variant X4
serine/arginine repetitive matrix protein 2-like isoform X2
serine/arginine repetitive matrix protein 2-like isoform X1
serine/arginine repetitive matrix protein 2-like isoform X4
serine/arginine repetitive matrix protein 2-like, 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 1 sample with support for all annotated introns
serine/arginine repetitive matrix protein 2-like 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 5 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 26 samples with support for all annotated introns
pyridoxine/pyridoxamine 5'-phosphate oxidase-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 3 samples with support for all annotated introns
pyridoxine/pyridoxamine 5'-phosphate oxidase-like, transcript variant X1
pyridoxine/pyridoxamine 5'-phosphate oxidase-like
uncharacterized LOC122636364, transcript variant X3
uncharacterized LOC122636364, transcript variant X2
uncharacterized LOC122636364, transcript variant X1