Leguminivora glycinivorella isolate SPB_JAAS2020 chromosome 16, LegGlyc_1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Tortricoidea; Tortricidae; Olethreutinae; Grapholitini; Leguminivora.
REFSEQ INFORMATION: The reference sequence is identical to\nCM041136.1.\nAssembly name: LegGlyc_1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the USDA-ARS on 2022/04/22. The\noriginal whole-genome shotgun project has the accession\nJAKXMO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: USDA-ARS\nAssembly Date :: 08-OCT-2021\nAssembly Method :: NextDeNovo v. 2.5.0\nAssembly Name :: LegGlyc_1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 85.48x\nSequencing Technology :: Oxford Nanopore GridION\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Leguminivora glycinivorella\n 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC125235008 isoform X2
uncharacterized LOC125234760, transcript variant X4
uncharacterized LOC125234760, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125234760, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125234760, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125234760, 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 10 samples with support for all annotated introns
uncharacterized protein LOC125234760 isoform X3
uncharacterized protein LOC125234760 isoform X4
uncharacterized LOC125234760, transcript variant X1
uncharacterized LOC125234760, transcript variant X2
uncharacterized protein LOC125234760 isoform X1
uncharacterized protein LOC125234760 isoform X2
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 1 Protein, and 66% 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: 77% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125234968, transcript variant X3
uncharacterized LOC125234968, transcript variant X2
uncharacterized LOC125234968, transcript variant X1
uncharacterized protein LOC125234968 isoform X3
uncharacterized protein LOC125234968 isoform X2
uncharacterized protein LOC125234968 isoform X1
NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
protein VAC14 homolog, 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 7 samples with support for all annotated introns
protein VAC14 homolog, 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 4 samples with support for all annotated introns
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit DAD1
trafficking protein particle complex subunit 11
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: trafficking protein particle complex subunit 11
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: SAP30-binding protein
cysteine and histidine-rich protein 1 homolog, 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 10 samples with support for all annotated introns
cysteine and histidine-rich protein 1 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
cysteine and histidine-rich protein 1 homolog, transcript variant X2
cysteine and histidine-rich protein 1 homolog isoform X1
cysteine and histidine-rich protein 1 homolog isoform X3
cysteine and histidine-rich protein 1 homolog isoform X2
translin-associated factor X-interacting protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ran-binding protein 10, 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 5 samples with support for all annotated introns
ran-binding protein 10, 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 7 samples with support for all annotated introns
ran-binding protein 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cholinesterase 2-like
esterase FE4-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
esterase FE4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
esterase FE4-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
esterase FE4-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
esterase FE4-like, transcript variant X5
esterase FE4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
esterase FE4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 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: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 96% 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: 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
uncharacterized LOC125234998, transcript variant X2
uncharacterized protein LOC125234998 isoform X2
uncharacterized LOC125234998, 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 7 samples with support for all annotated introns
uncharacterized protein LOC125234998 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
serine/threonine-protein kinase SIK3 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
iroquois-class homeodomain protein IRX-5-like, transcript variant X1
iroquois-class homeodomain protein IRX-5-like, transcript variant X2
iroquois-class homeodomain protein IRX-5-like isoform X1
iroquois-class homeodomain protein IRX-2-like isoform X2
DNA repair protein RAD52 homolog, 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
DNA repair protein RAD52 homolog isoform X2
DNA repair protein RAD52 homolog, transcript variant X1
DNA repair and recombination protein rhm52-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
WD repeat-containing protein CG11141, transcript variant X2
WD repeat-containing protein CG11141, 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 9 samples with support for all annotated introns
WD repeat-containing protein CG11141 isoform X2
WD repeat-containing protein CG11141 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 90% coverage of the annotated genomic feature by RNAseq alignments
nose resistant to fluoxetine protein 6-like
CCHC-type zinc finger nucleic acid binding protein
peptidylprolyl isomerase domain and WD repeat-containing protein 1, transcript variant X2
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 1 sample with support for all annotated introns
peptidylprolyl isomerase domain and WD repeat-containing protein 1, transcript variant X1
peptidylprolyl isomerase domain and WD repeat-containing protein 1
eukaryotic translation initiation factor 3 subunit A-like, transcript variant X1
eukaryotic translation initiation factor 3 subunit A-like, transcript variant X2
eukaryotic translation initiation factor 3 subunit A-like isoform X1
uncharacterized protein LOC125234570 isoform X2
insulin-like growth factor-binding protein complex acid labile subunit
phospholipid-transporting ATPase ABCA1-like
phospholipid-transporting ATPase ABCA3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
peroxisomal leader peptide-processing protease-like
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tyrosine (anticodon GUA); 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RING finger and CHY zinc finger domain-containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RING finger and CHY zinc finger domain-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RING finger and CHY zinc finger domain-containing protein 1 isoform X2
RING finger and CHY zinc finger domain-containing protein 1 isoform X1
oxysterol-binding protein-related protein 9
elongation of very long chain fatty acids protein
LOW QUALITY PROTEIN: alpha-protein kinase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 3 subunit J
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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transforming growth factor beta activator LRRC33-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
toll-like receptor 3, 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 2 samples with support for all annotated introns
toll-like receptor 3, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 66% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125234548, transcript variant X1
uncharacterized LOC125234548, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% 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: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tyrosine-protein kinase receptor torso-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] iron-sulfur protein 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
inactive selenide, water dikinase-like protein
probable methylcrotonoyl-CoA carboxylase beta chain, mitochondrial
putative phosphatidate phosphatase, transcript variant X7
putative phosphatidate phosphatase, transcript variant X5
putative phosphatidate phosphatase, transcript variant X3
putative phosphatidate phosphatase, transcript variant X1
putative phosphatidate phosphatase, transcript variant X2
putative phosphatidate phosphatase, transcript variant X4
putative phosphatidate phosphatase, transcript variant X6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: putative phosphatidate phosphatase
mitochondrial potassium channel ATP-binding subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54% coverage of the annotated genomic feature by RNAseq alignments
synaptic vesicle glycoprotein 2C-like, transcript variant X7
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
synaptic vesicle glycoprotein 2C-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
synaptic vesicle glycoprotein 2C-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
synaptic vesicle glycoprotein 2C-like, transcript variant X2
synaptic vesicle glycoprotein 2C-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
synaptic vesicle glycoprotein 2C-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
synaptic vesicle glycoprotein 2C-like isoform X4
synaptic vesicle glycoprotein 2C-like isoform X1
synaptic vesicle glycoprotein 2C-like isoform X2
synaptic vesicle glycoprotein 2C-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 11 samples with support for all annotated introns
synaptic vesicle glycoprotein 2C-like isoform X3
synaptic vesicle glycoprotein 2C-like, transcript variant X8
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
synaptic vesicle glycoprotein 2C-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein artichoke-like, transcript variant X6
protein artichoke-like, transcript variant X5
uncharacterized protein LOC125235026 isoform X3
uncharacterized protein LOC125235026 isoform X2
protein artichoke-like, transcript variant X1
protein artichoke-like, transcript variant X3
protein artichoke-like, transcript variant X4
protein artichoke-like, transcript variant X2
protein artichoke-like, transcript variant X7
uncharacterized protein LOC125235026 isoform X4
uncharacterized LOC125235029, transcript variant X1
uncharacterized LOC125235029, transcript variant X2
transitional endoplasmic reticulum ATPase TER94, transcript variant X1
transitional endoplasmic reticulum ATPase TER94, transcript variant X3
transitional endoplasmic reticulum ATPase TER94, transcript variant X4
transitional endoplasmic reticulum ATPase TER94, transcript variant X2
transitional endoplasmic reticulum ATPase TER94 isoform X1
transitional endoplasmic reticulum ATPase TER94 isoform X2
F-box/LRR-repeat protein 2-like, transcript variant X1
F-box/LRR-repeat protein 2-like, transcript variant X4
F-box/LRR-repeat protein 2-like, transcript variant X5
F-box/LRR-repeat protein 2-like, transcript variant X2
F-box/LRR-repeat protein 2-like isoform X1
uncharacterized protein LOC125234980 isoform X4
uncharacterized protein LOC125234980 isoform X5
F-box/LRR-repeat protein 2-like isoform X2
F-box/LRR-repeat protein 2-like, transcript variant X3
F-box/LRR-repeat protein 2-like isoform X3
uncharacterized LOC125234684, transcript variant X2
uncharacterized LOC125234684, transcript variant X1
uncharacterized protein LOC125234684 isoform X1
uncharacterized protein LOC125234684 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
arp2/3 complex-activating protein rickA-like isoform X2
uncharacterized oxidoreductase YjmC-like, transcript variant X2
uncharacterized oxidoreductase YjmC-like, transcript variant X4
uncharacterized oxidoreductase YjmC-like, transcript variant X5
uncharacterized oxidoreductase YjmC-like, transcript variant X1
uncharacterized oxidoreductase YjmC-like, transcript variant X3
uncharacterized oxidoreductase YjmC-like isoform X2
hydroxycarboxylate dehydrogenase B-like isoform X5
uncharacterized oxidoreductase YjmC-like isoform X1
uncharacterized oxidoreductase YjmC-like isoform X3
uncharacterized oxidoreductase YjmC-like isoform X4
uncharacterized oxidoreductase YjmC-like
probable beta-hexosaminidase fdl, 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 8 samples with support for all annotated introns
probable beta-hexosaminidase fdl, transcript variant X3
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 1 sample with support for all annotated introns
probable beta-hexosaminidase fdl, transcript variant X4
probable beta-hexosaminidase fdl, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nuclear mitotic apparatus protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
thrombospondin type-1 domain-containing protein 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
thrombospondin type-1 domain-containing protein 4-like, transcript variant X1
thrombospondin type-1 domain-containing protein 4-like
ADAMTS-like protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ADAMTS-like protein 4, 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
transmembrane reductase CYB561D2-like, transcript variant X1
transmembrane reductase CYB561D2-like isoform X1
transmembrane reductase CYB561D2-like, transcript variant X2
transmembrane reductase CYB561D2-like isoform X2
ADAMTS-like protein 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
peptidyl-alpha-hydroxyglycine alpha-amidating lyase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125234687, 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 2 samples with support for all annotated introns
uncharacterized LOC125234687, transcript variant X1
uncharacterized LOC125234687, transcript variant X4
uncharacterized LOC125234687, transcript variant X2
uncharacterized protein LOC125234687 isoform X1
uncharacterized protein LOC125234687 isoform X2
tripartite motif-containing protein 2-like
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 12 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LOW QUALITY PROTEIN: carbohydrate sulfotransferase 11
uncharacterized LOC125234763, transcript variant X2
uncharacterized LOC125234763, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC125234985
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125234640, transcript variant X2
uncharacterized LOC125234640, transcript variant X1
uncharacterized LOC125234640, transcript variant X3
uncharacterized protein LOC125234640 isoform X1
uncharacterized protein LOC125234640 isoform X2
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
DNA-directed RNA polymerases I, II, and III subunit RPABC1
transfer RNA alanine (anticodon GGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Down syndrome cell adhesion molecule-like protein Dscam2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% 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: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: Down syndrome cell adhesion molecule-like protein Dscam2
uncharacterized LOC125235021, transcript variant X2
uncharacterized LOC125235021, transcript variant X5
uncharacterized LOC125235021, transcript variant X7
uncharacterized LOC125235021, transcript variant X6
uncharacterized LOC125235021, transcript variant X1
uncharacterized LOC125235021, transcript variant X3
uncharacterized LOC125235021, transcript variant X4
uncharacterized protein LOC125235021 isoform X2
uncharacterized protein LOC125235021 isoform X4
uncharacterized protein LOC125235021 isoform X3
uncharacterized protein LOC125235021 isoform X1
farnesyl pyrophosphate synthase-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 11 samples with support for all annotated introns
farnesyl pyrophosphate synthase-like, transcript variant X2
farnesyl pyrophosphate synthase-like isoform X1
farnesyl pyrophosphate synthase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 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: 60 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: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ras-related protein Rab-2A, transcript variant X2
ras-related protein Rab-2A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125234389, transcript variant X2
uncharacterized LOC125234389, 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 protein LOC125234389 isoform X2
uncharacterized protein LOC125234389 isoform X1
peroxisomal multifunctional enzyme type 2-like
recQ-mediated genome instability protein 2-like
growth arrest-specific protein 1-like, transcript variant X1
growth arrest-specific protein 1-like isoform X1
growth arrest-specific protein 1-like, transcript variant X2
growth arrest-specific protein 1-like isoform X2
zinc carboxypeptidase A 1-like, transcript variant X1
zinc carboxypeptidase A 1-like, transcript variant X2
zinc carboxypeptidase A 1-like isoform X1
zinc carboxypeptidase A 1-like isoform X2
zinc carboxypeptidase-like, transcript variant X1
zinc carboxypeptidase-like, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
angiogenic factor with G patch and FHA domains 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
angiogenic factor with G patch and FHA domains 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
angiogenic factor with G patch and FHA domains 1, transcript variant X3
angiogenic factor with G patch and FHA domains 1 isoform X2
angiogenic factor with G patch and FHA domains 1 isoform X1
angiogenic factor with G patch and FHA domains 1 isoform X3
mitotic spindle assembly checkpoint protein MAD1
probable protein arginine N-methyltransferase 6.1
uncharacterized LOC125234698, transcript variant X2
uncharacterized LOC125234698, transcript variant X1
uncharacterized LOC125235003, transcript variant X1
uncharacterized LOC125235003, transcript variant X2
uncharacterized protein LOC125235003 isoform X1
uncharacterized protein LOC125235003 isoform X2
tRNA selenocysteine 1-associated protein 1, transcript variant X2
tRNA selenocysteine 1-associated protein 1, transcript variant X3
tRNA selenocysteine 1-associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
tRNA selenocysteine 1-associated protein 1 isoform X1
tRNA selenocysteine 1-associated protein 1 isoform X3
tRNA selenocysteine 1-associated protein 1 isoform X2
transcription factor TFIIIB component B'', transcript variant X2
transcription factor TFIIIB component B'', transcript variant X1
transcription factor TFIIIB component B''
uncharacterized LOC125234355, transcript variant X1
uncharacterized LOC125234355, transcript variant X5
uncharacterized LOC125234355, transcript variant X3
uncharacterized LOC125234355, transcript variant X7
uncharacterized LOC125234355, transcript variant X6
uncharacterized LOC125234355, transcript variant X9
uncharacterized LOC125234355, transcript variant X10
uncharacterized LOC125234355, transcript variant X4
uncharacterized LOC125234355, transcript variant X8
uncharacterized LOC125234355, transcript variant X2
uncharacterized protein LOC125234355 isoform X1
uncharacterized protein LOC125234355 isoform X5
uncharacterized protein LOC125234355 isoform X3
uncharacterized protein LOC125234355 isoform X7
uncharacterized protein LOC125234355 isoform X6
uncharacterized protein LOC125234355 isoform X9
uncharacterized protein LOC125234355 isoform X10
uncharacterized protein LOC125234355 isoform X4
uncharacterized protein LOC125234355 isoform X8
uncharacterized protein LOC125234355 isoform X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, 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
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X5
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X10
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X11
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X8
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X9
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X7
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3 isoform X12
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X6
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X5
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X8
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X9
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X10
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X11
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: dynein intermediate chain 2, ciliary
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ribitol 5-phosphate transferase FKRP, 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 12 samples with support for all annotated introns
ribitol 5-phosphate transferase FKRP isoform X2
ribitol 5-phosphate transferase FKRP, transcript variant X1
ribitol 5-phosphate transferase FKRP isoform X1
GPI ethanolamine phosphate transferase 3, transcript variant X1
GPI ethanolamine phosphate transferase 3, transcript variant X2
GPI ethanolamine phosphate transferase 3 isoform X2
GPI ethanolamine phosphate transferase 3 isoform X1
olfactomedin-like protein 2A, transcript variant X2
olfactomedin-like protein 2A, transcript variant X1
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial, transcript variant X2
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial, transcript variant X1
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial, transcript variant X3
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial isoform X1
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial isoform X2
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial isoform X3
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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
synaptic vesicle membrane protein VAT-1 homolog-like
LOW QUALITY PROTEIN: synaptic vesicle membrane protein VAT-1 homolog-like
putative ribosome-binding factor A, mitochondrial, transcript variant X2
putative ribosome-binding factor A, 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 13 samples with support for all annotated introns
putative ribosome-binding factor A, mitochondrial isoform X1
putative ribosome-binding factor A, mitochondrial isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
LOW QUALITY PROTEIN: retinoblastoma-like protein 1
SAGA-associated factor 29, transcript variant X1
SAGA-associated factor 29, 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 3 samples with support for all annotated introns
uncharacterized LOC125234977, transcript variant X2
uncharacterized LOC125234977, transcript variant X1
uncharacterized protein LOC125234977 isoform X2
uncharacterized protein LOC125234977 isoform X1
uncharacterized LOC125234978, transcript variant X1
uncharacterized LOC125234978, transcript variant X2
uncharacterized protein LOC125234978 isoform X1
uncharacterized protein LOC125234978 isoform X2
probable splicing factor, arginine/serine-rich 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
store-operated calcium entry regulator STIMATE-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 12 samples with support for all annotated introns
store-operated calcium entry regulator STIMATE-like, transcript variant X1
store-operated calcium entry regulator STIMATE-like isoform X2
store-operated calcium entry regulator STIMATE-like isoform X1
heterogeneous nuclear ribonucleoprotein K, transcript variant X1
heterogeneous nuclear ribonucleoprotein K, transcript variant X2
heterogeneous nuclear ribonucleoprotein K, transcript variant X4
heterogeneous nuclear ribonucleoprotein K, transcript variant X3
heterogeneous nuclear ribonucleoprotein K isoform X2
heterogeneous nuclear ribonucleoprotein K isoform X1
lysM and putative peptidoglycan-binding domain-containing protein 3, transcript variant X2
lysM and putative peptidoglycan-binding domain-containing protein 3, transcript variant X1
lysM and putative peptidoglycan-binding domain-containing protein 3 isoform X2
lysM and putative peptidoglycan-binding domain-containing protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125234515, transcript variant X2
uncharacterized LOC125234515, transcript variant X1
uncharacterized LOC125234515, transcript variant X3
uncharacterized protein LOC125234515 isoform X1
uncharacterized protein LOC125234515 isoform X3
uncharacterized protein LOC125234515 isoform X2
uncharacterized LOC125234575, transcript variant X2
uncharacterized LOC125234575, transcript variant X3
uncharacterized LOC125234575, transcript variant X1
uncharacterized protein LOC125234575 isoform X1
uncharacterized protein LOC125234575 isoform X2
microtubule-associated protein RP/EB family member 1, transcript variant X1
microtubule-associated protein RP/EB family member 1, transcript variant X2
microtubule-associated protein RP/EB family member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G-protein coupled receptor dmsr-1-like, transcript variant X2
G-protein coupled receptor dmsr-1-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 1 sample with support for all annotated introns
G-protein coupled receptor dmsr-1-like isoform X1
G-protein coupled receptor dmsr-1-like isoform X2
probable alpha-ketoglutarate-dependent hypophosphite dioxygenase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 60% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA aspartic acid (anticodon AUC); 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
tyrosine-protein kinase Src42A, transcript variant X2
tyrosine-protein kinase Src42A isoform X2
tyrosine-protein kinase Src42A, transcript variant X1
tyrosine-protein kinase Src42A, transcript variant X3
tyrosine-protein kinase Src42A isoform X3
uncharacterized protein C1orf112 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
pleckstrin homology domain-containing family F member 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: pleckstrin homology domain-containing family F member 2-like
pleckstrin homology domain-containing family F member 2-like, transcript variant X1
pleckstrin homology domain-containing family F member 2-like, transcript variant X2
pleckstrin homology domain-containing family F member 2-like isoform X1
pleckstrin homology domain-containing family F member 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
testis-specific serine/threonine-protein kinase 3-like, transcript variant X2
testis-specific serine/threonine-protein kinase 3-like, transcript variant X1
testis-specific serine/threonine-protein kinase 3-like isoform X2
testis-specific serine/threonine-protein kinase 3-like isoform 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
uncharacterized LOC125234427, transcript variant X1
uncharacterized LOC125234427, transcript variant X3
uncharacterized LOC125234427, transcript variant X2
uncharacterized LOC125234427, transcript variant X4
uncharacterized protein LOC125234427 isoform X4
uncharacterized protein LOC125234427 isoform X3
uncharacterized protein LOC125234427 isoform X1
uncharacterized protein LOC125234427 isoform X2
cilia- and flagella-associated protein 20-like
cAMP-dependent protein kinase type II regulatory subunit, transcript variant X3
cAMP-dependent protein kinase type II regulatory subunit, transcript variant X4
cAMP-dependent protein kinase type II regulatory subunit, transcript variant X1
cAMP-dependent protein kinase type II regulatory subunit, transcript variant X2
cAMP-dependent protein kinase type II regulatory subunit isoform X1
cAMP-dependent protein kinase type II regulatory subunit isoform X3
cAMP-dependent protein kinase type II regulatory subunit isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein G(o) subunit alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
guanine nucleotide-binding protein G(o) subunit alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
guanine nucleotide-binding protein G(o) subunit alpha isoform X2
guanine nucleotide-binding protein G(o) subunit alpha isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Golgi pH regulator, transcript variant X2
Golgi pH regulator, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments
DNA replication complex GINS protein PSF3
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
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 13 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase FKBP8
GPI ethanolamine phosphate transferase 2, transcript variant X5
GPI ethanolamine phosphate transferase 2, transcript variant X4
GPI ethanolamine phosphate transferase 2, transcript variant X1
GPI ethanolamine phosphate transferase 2, transcript variant X2
GPI ethanolamine phosphate transferase 2, transcript variant X3
GPI ethanolamine phosphate transferase 2 isoform X3
GPI ethanolamine phosphate transferase 2 isoform X2
GPI ethanolamine phosphate transferase 2 isoform X1
GPI ethanolamine phosphate transferase 2 isoform X4
GPI ethanolamine phosphate transferase 2 isoform X5
protein lethal(2)essential for life-like
protein dead ringer, transcript variant X1
protein dead ringer, transcript variant X3
protein dead ringer, transcript variant X2
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X2
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X1
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X2
nitric oxide synthase-interacting protein homolog, transcript variant X3
nitric oxide synthase-interacting protein homolog, transcript variant X2
nitric oxide synthase-interacting protein homolog, transcript variant X1
nitric oxide synthase-interacting protein homolog
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X4
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X4
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X3
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X3
ceramide transfer protein-like, transcript variant X1
ceramide transfer protein-like, transcript variant X3
ceramide transfer protein-like, transcript variant X2
ceramide transfer protein-like isoform X1
ceramide transfer protein-like isoform X2
ceramide transfer protein-like isoform X3
RNA polymerase II subunit A C-terminal domain phosphatase, transcript variant X2
RNA polymerase II subunit A C-terminal domain phosphatase, transcript variant X1
RNA polymerase II subunit A C-terminal domain phosphatase isoform X1
RNA polymerase II subunit A C-terminal domain phosphatase isoform X2
28S ribosomal protein S17, mitochondrial
LOW QUALITY PROTEIN: RNA-binding protein spenito
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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: leukotriene A-4 hydrolase
39S ribosomal protein L13, mitochondrial
protein PRRC1-like, transcript variant X2
protein PRRC1-like, transcript variant X1
protein PRRC1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial
coiled-coil-helix-coiled-coil-helix domain-containing protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
LOW QUALITY PROTEIN: alpha-N-acetylgalactosaminidase
ankyrin repeat and LEM domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA alanine (anticodon CGC); 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: 93% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: E3 SUMO-protein ligase PIAS3
serine/threonine-protein kinase PRP4 homolog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
serine/threonine-protein kinase PRP4 homolog, transcript variant X1
serine/threonine-protein kinase PRP4 homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
serine/threonine-protein kinase PRP4 homolog, transcript variant X4
serine/threonine-protein kinase PRP4 homolog, transcript variant X3
serine/threonine-protein kinase PRP4 homolog, transcript variant X2
serine/threonine-protein kinase PRP4 homolog
transmembrane protein adipocyte-associated 1 homolog, 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
transmembrane protein adipocyte-associated 1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transmembrane protein adipocyte-associated 1 homolog
tetratricopeptide repeat protein 19 homolog, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: ubiquitin-conjugating enzyme E2 R2
putative uncharacterized protein DDB_G0287457, transcript variant X2
putative uncharacterized protein DDB_G0287457, transcript variant X1
putative uncharacterized protein DDB_G0287457 isoform X2
CREB-regulated transcription coactivator 3, transcript variant X2
CREB-regulated transcription coactivator 3, transcript variant X5
CREB-regulated transcription coactivator 3, transcript variant X3
CREB-regulated transcription coactivator 3, transcript variant X1
CREB-regulated transcription coactivator 3, transcript variant X6
CREB-regulated transcription coactivator 3, transcript variant X4
CREB-regulated transcription coactivator 3 isoform X2
CREB-regulated transcription coactivator 3 isoform X5
CREB-regulated transcription coactivator 3 isoform X3
CREB-regulated transcription coactivator 3 isoform X1
CREB-regulated transcription coactivator 3 isoform X4
CREB-regulated transcription coactivator 3 isoform X6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
LOW QUALITY PROTEIN: putative glycerol kinase 5
uncharacterized LOC125234481, transcript variant X2
uncharacterized LOC125234481, transcript variant X1
uncharacterized protein LOC125234481 isoform X1
uncharacterized protein LOC125234481 isoform X2
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial
ejaculatory bulb-specific protein 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 276 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ejaculatory bulb-specific protein 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 276 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ejaculatory bulb-specific protein 3-like, transcript variant X2
ejaculatory bulb-specific protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 276 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ejaculatory bulb-specific protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 126 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 172 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ejaculatory bulb-specific protein 3-like isoform X3
ejaculatory bulb-specific protein 3-like isoform X2
ejaculatory bulb-specific protein 3-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ejaculatory bulb-specific protein 3-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments
salivary glue protein Sgs-3-like, transcript variant X2
salivary glue protein Sgs-3-like, transcript variant X1
TATA-binding protein-associated factor 2N-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
leucine-rich repeat extensin-like protein 3
uncharacterized LOC125234508, transcript variant X1
uncharacterized protein LOC125234508 isoform X1
uncharacterized LOC125234508, transcript variant X2
uncharacterized protein LOC125234508 isoform X2
uncharacterized LOC125234566, transcript variant X2
uncharacterized LOC125234566, transcript variant X1
N(6)-adenine-specific methyltransferase METTL4, transcript variant X2
N(6)-adenine-specific methyltransferase METTL4, 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 11 samples with support for all annotated introns
N(6)-adenine-specific methyltransferase METTL4 isoform X1
N(6)-adenine-specific methyltransferase METTL4 isoform X2
LOW QUALITY PROTEIN: UDP-glucose 4-epimerase-like
trimeric intracellular cation channel type 1B.1
transfer RNA proline (anticodon CGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125234773, transcript variant X2
uncharacterized LOC125234773, transcript variant X3
uncharacterized LOC125234773, transcript variant X1
calcium and integrin-binding protein 1-like
uncharacterized LOC125234628, transcript variant X1
uncharacterized LOC125234628, transcript variant X3
uncharacterized LOC125234628, transcript variant X2
uncharacterized protein LOC125234628 isoform X3
uncharacterized protein LOC125234628 isoform X2
uncharacterized protein LOC125234628 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
glycine-rich cell wall structural protein 1.8-like
uncharacterized LOC125234917, transcript variant X1
uncharacterized LOC125234917, transcript variant X2
uncharacterized LOC125234917, transcript variant X3
uncharacterized protein LOC125234917 isoform X2
uncharacterized protein LOC125234917 isoform X1
uncharacterized protein LOC125234917 isoform X3
mRNA decay activator protein ZFP36L3-like, transcript variant X2
mRNA decay activator protein ZFP36L3-like, transcript variant X1
mRNA decay activator protein ZFP36L3-like isoform X1
mRNA decay activator protein ZFP36L3-like, transcript variant X3
mRNA decay activator protein ZFP36L3-like isoform X3
uncharacterized LOC125234536, transcript variant X3
uncharacterized LOC125234536, transcript variant X1
uncharacterized LOC125234536, transcript variant X2
uncharacterized LOC125234536, transcript variant X4
uncharacterized protein LOC125234536 isoform X4
uncharacterized protein LOC125234536 isoform X3
uncharacterized protein LOC125234536 isoform X2
uncharacterized protein LOC125234536 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: dynein axonemal heavy chain 10
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
putative mediator of RNA polymerase II transcription subunit 29
receptor-type tyrosine-protein phosphatase kappa, transcript variant X1
receptor-type tyrosine-protein phosphatase kappa, transcript variant X3
receptor-type tyrosine-protein phosphatase kappa, transcript variant X2
receptor-type tyrosine-protein phosphatase kappa isoform X1
receptor-type tyrosine-protein phosphatase kappa isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: venom carboxylesterase-6-like
juvenile hormone esterase-like, transcript variant X1
juvenile hormone esterase-like, transcript variant X2
juvenile hormone esterase-like isoform X1
putative inactive carboxylesterase 4 isoform X2
aldehyde dehydrogenase family 3 member A2, transcript variant X3
aldehyde dehydrogenase family 3 member A2, transcript variant X1
aldehyde dehydrogenase family 3 member A2, transcript variant X2
aldehyde dehydrogenase family 3 member A2 isoform X1
aldehyde dehydrogenase family 3 member A2 isoform X2
aldehyde dehydrogenase family 3 member B2 isoform X3
aldehyde dehydrogenase family 3 member A2, transcript variant X5
aldehyde dehydrogenase, dimeric NADP-preferring isoform X5
aldehyde dehydrogenase family 3 member A2, transcript variant X6
aldehyde dehydrogenase family 3 member A2 isoform X6
aldehyde dehydrogenase family 3 member A2, transcript variant X4
aldehyde dehydrogenase, dimeric NADP-preferring isoform X4
ras-like GTP-binding protein Rho1, transcript variant X3
ras-like GTP-binding protein Rho1, transcript variant X2
ras-like GTP-binding protein Rho1, transcript variant X1
ras-like GTP-binding protein Rho1 isoform X1
ras-like GTP-binding protein Rho1 isoform X2
polynucleotide 5'-hydroxyl-kinase NOL9, transcript variant X2
polynucleotide 5'-hydroxyl-kinase NOL9, transcript variant X1
polynucleotide 5'-hydroxyl-kinase NOL9, transcript variant X3
polynucleotide 5'-hydroxyl-kinase NOL9, transcript variant X4
ATP synthase subunit alpha, mitochondrial
PX domain-containing protein kinase-like protein
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
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
uncharacterized LOC125234774, transcript variant X2
uncharacterized LOC125234774, transcript variant X1
uncharacterized protein LOC125234774 isoform X1
uncharacterized protein LOC125234774 isoform X2
guanine nucleotide exchange factor subunit Rich
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ATP-dependent (S)-NAD(P)H-hydrate dehydratase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
BAG family molecular chaperone regulator 2, transcript variant X3
BAG family molecular chaperone regulator 2 isoform X3
BAG family molecular chaperone regulator 2, transcript variant X1
BAG family molecular chaperone regulator 2 isoform X1
BAG family molecular chaperone regulator 2, transcript variant X2
BAG family molecular chaperone regulator 2 isoform X2
ras-related protein Rab-23, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras-related protein Rab-23, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ras-related protein Rab-23, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ras-related protein Rab-23, 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 1 sample with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 14
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DNA replication licensing factor MCM4, 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 2 samples with support for all annotated introns
DNA replication licensing factor MCM4, transcript variant X2
DNA replication licensing factor MCM4 isoform X1
DNA replication licensing factor MCM4 isoform X2
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X1
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X2
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X3
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X1
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X3
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 16 bases in 9 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 16 bases in 9 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: SUMO-activating enzyme subunit 1
adipokinetic hormone/corazonin-related peptide receptor variant I-like
excitatory amino acid transporter 3, transcript variant X1
excitatory amino acid transporter 3, transcript variant X2
excitatory amino acid transporter 3 isoform X1
excitatory amino acid transporter 3 isoform X2
cyclin-dependent kinases regulatory subunit
zinc finger protein 891-like, transcript variant X1
zinc finger protein 891-like, transcript variant X2
gastrula zinc finger protein XlCGF8.2DB-like isoform X1
leucine-rich repeat-containing protein 49, transcript variant X1
leucine-rich repeat-containing protein 49, transcript variant X2
leucine-rich repeat-containing protein 49 isoform X2
leucine-rich repeat-containing protein 49 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: ionotropic receptor 75a-like
cartilage oligomeric matrix protein-like, transcript variant X1
cartilage oligomeric matrix protein-like, transcript variant X2
cartilage oligomeric matrix protein-like isoform X2
cartilage oligomeric matrix protein-like isoform X1
transient receptor potential cation channel trpm
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: transient receptor potential cation channel trpm
transfer RNA serine (anticodon CGA); 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: 113 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
5-formyltetrahydrofolate cyclo-ligase-like, transcript variant X2
5-formyltetrahydrofolate cyclo-ligase-like, transcript variant X1
5-formyltetrahydrofolate cyclo-ligase-like, transcript variant X3
5-formyltetrahydrofolate cyclo-ligase-like
protein fem-1 homolog B, transcript variant X2
protein fem-1 homolog B, transcript variant X1
protein fem-1 homolog B, transcript variant X3
protein fem-1 homolog B, transcript variant X5
protein fem-1 homolog B, transcript variant X4
protein fem-1 homolog B, transcript variant X6
LOW QUALITY PROTEIN: transmembrane protein 214
LOW QUALITY PROTEIN: deoxyribonuclease TATDN1
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase, transcript variant X4
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase, transcript variant X6
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase, transcript variant X5
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase, transcript variant X1
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase, transcript variant X3
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase, transcript variant X2
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase isoform X2
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase isoform X1
sodium/potassium/calcium exchanger Nckx30C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 82% 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 4 samples with support for all annotated introns
uncharacterized LOC125234986, transcript variant X1
uncharacterized LOC125234986, transcript variant X2
uncharacterized protein LOC125234986 isoform X1
uncharacterized protein LOC125234986 isoform X2
zinc finger SWIM domain-containing protein 4-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger SWIM domain-containing protein 4-like
Bardet-Biedl syndrome 4 protein homolog, transcript variant X2
Bardet-Biedl syndrome 4 protein homolog, transcript variant X1
Bardet-Biedl syndrome 4 protein homolog, transcript variant X3
Bardet-Biedl syndrome 4 protein homolog isoform X1
Bardet-Biedl syndrome 4 protein homolog isoform X2
uncharacterized LOC125234633, transcript variant X1
uncharacterized LOC125234633, transcript variant X2
uncharacterized protein LOC125234633 isoform X1
uncharacterized protein LOC125234633 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
hemocyte protein-glutamine gamma-glutamyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: hemocyte protein-glutamine gamma-glutamyltransferase-like
glutamate receptor ionotropic, kainate 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 2-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 2 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2-like isoform X2
glutamate receptor ionotropic, kainate 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125234594, transcript variant X3
uncharacterized LOC125234594, transcript variant X1
uncharacterized LOC125234594, transcript variant X2
uncharacterized protein LOC125234594 isoform X2
uncharacterized protein LOC125234594 isoform X1
uncharacterized protein LOC125234594 isoform X3
threonine--tRNA ligase 1, cytoplasmic, transcript variant X2
threonine--tRNA ligase 1, cytoplasmic isoform X2
threonine--tRNA ligase 1, cytoplasmic, transcript variant X1
threonine--tRNA ligase 1, cytoplasmic isoform X1
BTB/POZ domain-containing protein At4g08455-like
putative mediator of RNA polymerase II transcription subunit 26
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nose resistant to fluoxetine protein 6-like, transcript variant X1
nose resistant to fluoxetine protein 6-like, transcript variant X2
nose resistant to fluoxetine protein 6-like isoform X1
nose resistant to fluoxetine protein 6-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125234705, transcript variant X2
uncharacterized LOC125234705, transcript variant X1
uncharacterized protein LOC125234705 isoform X2
uncharacterized protein LOC125234705 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125235031, transcript variant X2
uncharacterized LOC125235031, transcript variant X1
uncharacterized protein LOC125235031 isoform X2
uncharacterized protein LOC125235031 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
alpha-2-macroglobulin-like, transcript variant X1
alpha-2-macroglobulin-like, transcript variant X2
alpha-2-macroglobulin-like, transcript variant X3
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 11
proline-, glutamic acid- and leucine-rich protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
proline-, glutamic acid- and leucine-rich protein 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 8 samples with support for all annotated introns
proline-, glutamic acid- and leucine-rich protein 1, transcript variant X4
proline-, glutamic acid- and leucine-rich protein 1, transcript variant X2
proline-, glutamic acid- and leucine-rich protein 1, transcript variant X3
proline-, glutamic acid- and leucine-rich protein 1 isoform X3
proline-, glutamic acid- and leucine-rich protein 1 isoform X2
muscle M-line assembly protein unc-89 isoform X5
muscle M-line assembly protein unc-89 isoform 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 5 samples with support for all annotated introns
E3 ubiquitin-protein ligase NEDD4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase NEDD4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase NEDD4, transcript variant X7
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 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase NEDD4, transcript variant X3
E3 ubiquitin-protein ligase NEDD4, transcript variant X5
E3 ubiquitin-protein ligase NEDD4, transcript variant X6
E3 ubiquitin-protein ligase NEDD4, transcript variant X4
E3 ubiquitin-protein ligase Nedd-4 isoform X2
E3 ubiquitin-protein ligase NEDD4 isoform X7
E3 ubiquitin-protein ligase Nedd-4 isoform X1
E3 ubiquitin-protein ligase Nedd-4 isoform X3
E3 ubiquitin-protein ligase Nedd-4 isoform X5
E3 ubiquitin-protein ligase Nedd-4 isoform X6
E3 ubiquitin-protein ligase Nedd-4 isoform X4
nose resistant to fluoxetine protein 6-like, transcript variant X3
CCR4-NOT transcription complex subunit 11, transcript variant X3
CCR4-NOT transcription complex subunit 11, transcript variant X2
CCR4-NOT transcription complex subunit 11, transcript variant X1
CCR4-NOT transcription complex subunit 11 isoform X1
CCR4-NOT transcription complex subunit 11 isoform X2
CCR4-NOT transcription complex subunit 11 isoform X3
acyl-CoA-binding domain-containing protein 6-like
probable methyltransferase-like protein 23
3-ketoacyl-CoA thiolase, mitochondrial-like, transcript variant X1
3-ketoacyl-CoA thiolase, mitochondrial-like, transcript variant X2
3-ketoacyl-CoA thiolase, mitochondrial-like isoform X1
3-ketoacyl-CoA thiolase, mitochondrial-like isoform X2
uncharacterized LOC125234433, transcript variant X2
uncharacterized protein LOC125234433 isoform X2
uncharacterized LOC125234433, transcript variant X1
uncharacterized protein LOC125234433 isoform X1
3-ketoacyl-CoA thiolase, mitochondrial-like
lactosylceramide 4-alpha-galactosyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
RNA polymerase II-associated protein 3-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 6 samples with support for all annotated introns
RNA polymerase II-associated protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
RNA polymerase II-associated protein 3-like isoform X1
RNA polymerase II-associated protein 3-like isoform 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 9 samples with support for all annotated introns
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% 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 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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
endocuticle structural glycoprotein SgAbd-3-like
A disintegrin and metalloproteinase with thrombospondin motifs 19-like
A disintegrin and metalloproteinase with thrombospondin motifs 16-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
phospholipid phosphatase 1-like, transcript variant X1
phospholipid phosphatase 1-like, transcript variant X3
phospholipid phosphatase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
phospholipid phosphatase 1-like, transcript variant X4
phospholipid phosphatase 1-like isoform X1
phospholipid phosphatase 1-like isoform X3
phospholipid phosphatase 1-like isoform X2
phospholipid phosphatase 1-like isoform X4
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
phospholipid phosphatase 2-like, transcript variant X1
phospholipid phosphatase 2-like isoform X1
phospholipid phosphatase 2-like, transcript variant X2
phospholipid phosphatase 2-like isoform X2
epidermal growth factor receptor substrate 15-like 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: epidermal growth factor receptor substrate 15-like 1
glutathione S-transferase E14-like, transcript variant X2
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
glutathione S-transferase E14-like, transcript variant X1
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 13 samples with support for all annotated introns
glutathione S-transferase E14-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 3 samples with support for all annotated introns
glutathione S-transferase 1-like isoform X1
glutathione S-transferase E14-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cleavage and polyadenylation specificity factor 73
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
delta(24)-sterol reductase-like, transcript variant X2
delta(24)-sterol reductase-like, transcript variant X3
delta(24)-sterol reductase-like, transcript variant X1
delta(24)-sterol reductase-like isoform X1
delta(24)-sterol reductase-like isoform X2
uncharacterized LOC125234728, transcript variant X1
uncharacterized LOC125234728, transcript variant X2
general transcription factor IIH subunit 4
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
transfer RNA glycine (anticodon ACC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
glucose dehydrogenase [FAD, quinone]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 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: 75 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: 100 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: 39 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
general odorant-binding protein 1-like, transcript variant X1
general odorant-binding protein 1-like isoform X1
general odorant-binding protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
general odorant-binding protein 1-like isoform X2
transfer RNA alanine (anticodon UGC); 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: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
enhancer of mRNA-decapping protein 3, transcript variant X3
enhancer of mRNA-decapping protein 3, transcript variant X2
enhancer of mRNA-decapping protein 3, transcript variant X1
enhancer of mRNA-decapping protein 3 isoform X3
translation initiation factor IF-2 isoform X1
enhancer of mRNA-decapping protein 3 isoform X2
uncharacterized LOC125234673, transcript variant X2
uncharacterized LOC125234673, transcript variant X1
uncharacterized protein LOC125234673 isoform X1
uncharacterized protein LOC125234673 isoform X2
endoplasmic reticulum metallopeptidase 1-like, transcript variant X1
endoplasmic reticulum metallopeptidase 1-like, transcript variant X2
endoplasmic reticulum metallopeptidase 1-like, transcript variant X3
endoplasmic reticulum metallopeptidase 1-like isoform X1
endoplasmic reticulum metallopeptidase 1-like isoform X2
guanine nucleotide-binding protein subunit beta-5, transcript variant X2
guanine nucleotide-binding protein subunit beta-5, transcript variant X1
guanine nucleotide-binding protein subunit beta-5 isoform X2
guanine nucleotide-binding protein subunit beta-5 isoform X1