Leguminivora glycinivorella isolate SPB_JAAS2020 chromosome 12, 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\nCM041132.1.\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: 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125232166, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC125232166, transcript variant X1
uncharacterized protein LOC125232166 isoform X2
uncharacterized protein LOC125232166 isoform X1
protein lifeguard 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein lifeguard 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein lifeguard 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein lifeguard 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 178 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
dynein axonemal assembly factor 4-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 1 sample 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
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: probable cytosolic oligopeptidase A
dynein axonemal assembly factor 4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dynein axonemal assembly factor 4-like, transcript variant 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: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 7 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: phosphotriesterase-related protein
zinc finger CCCH domain-containing protein 15 homolog, transcript variant X1
zinc finger CCCH domain-containing protein 15 homolog isoform X1
zinc finger CCCH domain-containing protein 15 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCCH domain-containing protein 15 homolog isoform X2
transmembrane protein 64, transcript variant X1
transmembrane protein 64, transcript variant X4
transmembrane protein 64, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transmembrane protein 64, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% coverage of the annotated genomic feature by RNAseq alignments
putative 1-phosphatidylinositol 3-phosphate 5-kinase
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: putative 1-phosphatidylinositol 3-phosphate 5-kinase
uncharacterized LOC125232068, transcript variant X2
uncharacterized LOC125232068, transcript variant X1
uncharacterized LOC125232067, transcript variant X2
uncharacterized LOC125232067, 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 9 samples with support for all annotated introns
ER membrane protein complex subunit 8/9 homolog
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
alanine--glyoxylate aminotransferase 2, mitochondrial
translocon-associated protein subunit alpha
LOW QUALITY PROTEIN: translocon-associated protein subunit alpha
sodium-dependent neutral amino acid transporter B(0)AT3
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
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
lysophosphatidylcholine acyltransferase, 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 2 samples with support for all annotated introns
lysophosphatidylcholine acyltransferase, 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 7 samples with support for all annotated introns
lysophosphatidylcholine acyltransferase isoform X1
lysophosphatidylcholine acyltransferase isoform X2
uncharacterized LOC125232132, transcript variant X2
uncharacterized protein LOC125232132 isoform X2
uncharacterized LOC125232132, transcript variant X1
uncharacterized protein LOC125232132 isoform X1
uncharacterized LOC125232131, transcript variant X1
uncharacterized LOC125232131, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125231620, transcript variant X2
uncharacterized protein LOC125231620 isoform X2
uncharacterized LOC125231620, transcript variant X1
uncharacterized protein LOC125231620 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA asparagine (anticodon AUU); 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: 68% coverage of the annotated genomic feature by RNAseq alignments
N-acetylneuraminate 9-O-acetyltransferase
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 95% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: N-acetylneuraminate 9-O-acetyltransferase
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 11 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
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 12 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: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ATP-dependent RNA helicase dbp2-like
protein trapped in endoderm-1, 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
protein trapped in endoderm-1, transcript variant X1
protein trapped in endoderm-1, transcript variant X3
protein trapped in endoderm-1 isoform X2
protein trapped in endoderm-1 isoform X1
protein trapped in endoderm-1 isoform X3
threonylcarbamoyladenosine tRNA methylthiotransferase
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
LOW QUALITY PROTEIN: threonylcarbamoyladenosine tRNA methylthiotransferase
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: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: uridine-cytidine kinase-like 1
xylose isomerase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
xylose isomerase-like, transcript variant X1
xylose isomerase-like, transcript variant X2
xylose isomerase-like, transcript variant X4
pancreatic lipase-related protein 2-like
LOW QUALITY PROTEIN: pancreatic lipase-related protein 2-like
uncharacterized LOC125232224, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125232224, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC125232224, transcript variant X3
guanine nucleotide-binding protein subunit gamma 4-like
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
DNA topoisomerase 2, transcript variant X3
DNA topoisomerase 2, transcript variant X2
DNA topoisomerase 2, transcript variant X1
E3 ubiquitin-protein ligase RNF144A, 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 12 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF144A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF144A, 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 8 samples with support for all annotated introns
uncharacterized protein LOC125232221 isoform X1
E3 ubiquitin-protein ligase RNF144A isoform X2
activating transcription factor 7-interacting protein 1, transcript variant X1
activating transcription factor 7-interacting protein 1, transcript variant X2
activating transcription factor 7-interacting protein 1
transcription elongation factor, mitochondrial
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
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
NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial
calcium-transporting ATPase type 2C member 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: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: calcium-transporting ATPase type 2C member 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: 48 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: beta-1,3-glucan-binding protein-like
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L52, mitochondrial
protein lifeguard 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
protein lifeguard 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein lifeguard 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 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: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125231676, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC125231676 isoform X3
uncharacterized LOC125231676, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125231676, transcript variant X1
uncharacterized LOC125231676, transcript variant X3
uncharacterized protein LOC125231676 isoform X1
uncharacterized protein LOC125231676 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
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: 4 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
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
alanine aminotransferase 1, transcript variant X2
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 10 samples with support for all annotated introns
alanine aminotransferase 1, transcript variant X3
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 8 samples with support for all annotated introns
alanine aminotransferase 1, 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 9 samples with support for all annotated introns
alanine aminotransferase 1, transcript variant X4
alanine aminotransferase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
low-density lipoprotein receptor-related protein 2, transcript variant X1
low-density lipoprotein receptor-related protein 2, transcript variant X2
low-density lipoprotein receptor-related protein 2 isoform X2
low-density lipoprotein receptor-related protein 2 isoform X1
uncharacterized LOC125231595, transcript variant X1
uncharacterized LOC125231595, transcript variant X2
uncharacterized protein LOC125231595 isoform X2
uncharacterized protein LOC125231595 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC125231822, transcript variant X2
uncharacterized LOC125231822, transcript variant X1
uncharacterized LOC125231822, transcript variant X3
uncharacterized protein LOC125231822 isoform X1
uncharacterized protein LOC125231822 isoform X2
uncharacterized Golgi apparatus membrane protein-like protein CG5021
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: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized Golgi apparatus membrane protein-like protein CG5021
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: TATA element modulatory factor
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: serine/threonine-protein kinase SMG1
uncharacterized LOC125231626, transcript variant X2
uncharacterized LOC125231626, transcript variant X1
uncharacterized LOC125231626, transcript variant X4
uncharacterized protein LOC125231626 isoform X2
uncharacterized protein LOC125231626 isoform X1
uncharacterized protein LOC125231626 isoform X4
uncharacterized LOC125231626, transcript variant X3
uncharacterized protein LOC125231626 isoform X3
ribosomal RNA-processing protein 7 homolog A
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
cleavage and polyadenylation specificity factor subunit 4
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: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: cleavage and polyadenylation specificity factor subunit 4
chitobiosyldiphosphodolichol beta-mannosyltransferase
LOW QUALITY PROTEIN: chitobiosyldiphosphodolichol beta-mannosyltransferase
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: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: regulator of MON1-CCZ1 complex
coiled-coil and C2 domain-containing protein 2A
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: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: coiled-coil and C2 domain-containing protein 2A
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
diphosphoinositol polyphosphate phosphohydrolase 2, transcript variant X1
diphosphoinositol polyphosphate phosphohydrolase 2, 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 13 samples with support for all annotated introns
diphosphoinositol polyphosphate phosphohydrolase 1 isoform X1
diphosphoinositol polyphosphate phosphohydrolase 2 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: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA threonine (anticodon CGU); 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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125231795, transcript variant X1
uncharacterized LOC125231795, transcript variant X2
uncharacterized LOC125231795, 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 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phospholipase A1-like, transcript variant X2
phospholipase A1-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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phospholipase A1 member A-like, transcript variant X2
phospholipase A1 member A-like, transcript variant X1
phospholipase A1 member A-like isoform X1
phospholipase A1 member A-like isoform X2
lipase member H-like, transcript variant X4
lipase member H-like, transcript variant X3
lipase member H-like, transcript variant X7
lipase member H-like, transcript variant X6
lipase member H-like, transcript variant X1
lipase member H-like, transcript variant X5
lipase member H-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase SETMAR-like
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: 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: cmsearch.
small nucleolar RNA SNORA16B/SNORA16A family
COORDINATES: nucleotide motif:Rfam:12.0:RF00190
transfer RNA valine (anticodon CAC); 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: 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
cytochrome c1-2, heme protein, mitochondrial
protein arginine N-methyltransferase 7, 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 12 samples with support for all annotated introns
protein arginine N-methyltransferase 7, transcript variant X2
protein arginine N-methyltransferase 7 isoform X1
protein arginine N-methyltransferase 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
kelch-like protein 10, transcript variant X2
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
kelch-like 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 1 sample with support for all annotated introns
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like
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 9 samples with support for all annotated introns
LOW QUALITY PROTEIN: protein LSM14 homolog B-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: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: maternal protein tudor
tRNA (cytosine(38)-C(5))-methyltransferase
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
ankyrin repeat domain-containing protein 54
LOW QUALITY PROTEIN: ankyrin repeat domain-containing protein 54
armadillo repeat-containing protein 8-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
liver carboxylesterase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
liver carboxylesterase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cyclin-dependent kinase 14, transcript variant X1
cyclin-dependent kinase 14, transcript variant X3
cyclin-dependent kinase 14, transcript variant X2
uncharacterized LOC125232207, transcript variant X1
uncharacterized LOC125232207, transcript variant X2
uncharacterized LOC125232207, transcript variant X3
uncharacterized protein LOC125232207 isoform X2
uncharacterized protein LOC125232207 isoform X1
85/88 kDa calcium-independent phospholipase A2, transcript variant X2
85/88 kDa calcium-independent phospholipase A2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2 isoform X1
85/88 kDa calcium-independent phospholipase A2 isoform X2
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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
uncharacterized LOC125231840, transcript variant X2
uncharacterized LOC125231840, transcript variant X1
uncharacterized protein LOC125231840 isoform X2
uncharacterized protein LOC125231840 isoform X1
LOW QUALITY PROTEIN: uncharacterized protein LOC125231690
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
LOW QUALITY PROTEIN: clumping factor B-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 10-A
uncharacterized LOC125232243, transcript variant X1
uncharacterized LOC125232243, transcript variant X2
uncharacterized protein LOC125232243 isoform X1
uncharacterized protein LOC125232243 isoform X2
macrophage mannose receptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
macrophage mannose receptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC125231664 isoform X2
macrophage mannose receptor 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC125231650
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
nuclear envelope phosphatase-regulatory subunit 1
enoyl-CoA delta isomerase 1, mitochondrial-like, transcript variant X1
enoyl-CoA delta isomerase 1, mitochondrial-like, transcript variant X2
enoyl-CoA delta isomerase 1, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
dynein regulatory complex subunit 3-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 2 samples with support for all annotated introns
methyltransferase-like protein 22, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
methyltransferase-like protein 22, 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 13 samples with support for all annotated introns
methyltransferase-like protein 22, transcript variant X5
methyltransferase-like protein 22 isoform X2
methyltransferase-like protein 22 isoform X5
methyltransferase-like protein 22, transcript variant X4
methyltransferase-like protein 22, transcript variant X1
methyltransferase-like protein 22 isoform X1
methyltransferase-like protein 22 isoform X4
methyltransferase-like protein 22 isoform X3
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: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: polycomb protein suz12-B
ubiquitin domain-containing protein UBFD1-like, transcript variant X2
ubiquitin domain-containing protein UBFD1-like, transcript variant X1
ubiquitin domain-containing protein UBFD1-like isoform X2
ubiquitin domain-containing protein UBFD1-like isoform X1
rab11 family-interacting protein 4, transcript variant X4
rab11 family-interacting protein 4, transcript variant X2
rab11 family-interacting protein 4, transcript variant X3
rab11 family-interacting protein 4, transcript variant X1
rab11 family-interacting protein 4, transcript variant X5
rab11 family-interacting protein 4, transcript variant X6
rab11 family-interacting protein 4 isoform X2
rab11 family-interacting protein 4 isoform X3
rab11 family-interacting protein 4 isoform X1
rab11 family-interacting protein 4 isoform X4
mpv17-like protein, transcript variant X3
mpv17-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
mpv17-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125232254, transcript variant X2
uncharacterized LOC125232254, transcript variant X1
uncharacterized protein LOC125232254 isoform X2
uncharacterized protein LOC125232254 isoform X1
MAPK regulated corepressor interacting protein 2, 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
MAPK regulated corepressor interacting protein 2, transcript variant X1
MAPK regulated corepressor interacting protein 2
chitooligosaccharidolytic beta-N-acetylglucosaminidase, 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 11 samples with support for all annotated introns
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
chitooligosaccharidolytic beta-N-acetylglucosaminidase
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
palmitoyl-protein thioesterase 1-like, transcript variant X2
palmitoyl-protein thioesterase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
palmitoyl-protein thioesterase 1-like isoform X2
palmitoyl-protein thioesterase 1-like isoform X1
protein phosphatase 1 regulatory subunit 16A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein phosphatase 1 regulatory subunit 16A, transcript variant X1
protein phosphatase 1 regulatory subunit 16A, transcript variant X3
protein phosphatase 1 regulatory subunit 16A isoform X2
protein phosphatase 1 regulatory subunit 16A isoform X1
protein phosphatase 1 regulatory subunit 16A isoform X3
probable Na(+)/H(+) antiporter nhx-3, transcript variant X1
probable Na(+)/H(+) antiporter nhx-3, transcript variant X3
probable Na(+)/H(+) antiporter nhx-3, transcript variant X2
probable Na(+)/H(+) antiporter nhx-3 isoform 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 3 samples with support for all annotated introns
mpv17-like protein 2, transcript variant X2
mpv17-like protein 2, transcript variant X1
mpv17-like protein 2, transcript variant X3
nuclear receptor coactivator 5, transcript variant X2
nuclear receptor coactivator 5, transcript variant X1
nuclear receptor coactivator 5 isoform X2
nuclear receptor coactivator 5 isoform X1
transmembrane protein 184B, transcript variant X2
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
transmembrane protein 184B, transcript variant X1
dual specificity protein phosphatase 22-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125232082, transcript variant X3
uncharacterized LOC125232082, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125232082, 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
uncharacterized protein LOC125232082 isoform X2
uncharacterized protein LOC125232082 isoform X1
BTB/POZ domain-containing protein 6-B, transcript variant X1
BTB/POZ domain-containing protein 6-B, transcript variant X2
N-alpha-acetyltransferase 11, transcript variant X1
N-alpha-acetyltransferase 11, transcript variant X3
N-alpha-acetyltransferase 11, transcript variant X2
breast cancer anti-estrogen resistance protein 1, transcript variant X2
breast cancer anti-estrogen resistance protein 1, transcript variant X3
breast cancer anti-estrogen resistance protein 1, transcript variant X5
breast cancer anti-estrogen resistance protein 1, transcript variant X4
breast cancer anti-estrogen resistance protein 1, transcript variant X1
breast cancer anti-estrogen resistance protein 1 isoform X2
breast cancer anti-estrogen resistance protein 1 isoform X3
breast cancer anti-estrogen resistance protein 1 isoform X1
breast cancer anti-estrogen resistance protein 1 isoform X4
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
RAB11-binding protein RELCH homolog, transcript variant X2
RAB11-binding protein RELCH homolog, transcript variant X1
RAB11-binding protein RELCH homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC125231671 isoform X2
uncharacterized protein LOC125231671 isoform X1
RAB11-binding protein RELCH homolog isoform X3
pyrimidodiazepine synthase-like, transcript variant X1
pyrimidodiazepine synthase-like, transcript variant X2
pyrimidodiazepine synthase-like, transcript variant X3
pyrimidodiazepine synthase-like isoform X3
pyrimidodiazepine synthase-like isoform X2
pyrimidodiazepine synthase-like isoform X1
divergent protein kinase domain 1C, transcript variant X2
divergent protein kinase domain 1C, transcript variant X1
glycogen-binding subunit 76A, transcript variant X3
glycogen-binding subunit 76A, transcript variant X4
glycogen-binding subunit 76A, transcript variant X2
glycogen-binding subunit 76A, transcript variant X1
glycogen-binding subunit 76A, transcript variant X5
heparan sulfate 2-O-sulfotransferase pipe, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
heparan sulfate 2-O-sulfotransferase pipe, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
heparan sulfate 2-O-sulfotransferase pipe isoform X1
heparan sulfate 2-O-sulfotransferase pipe 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
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 11 samples with support for all annotated introns
ethanolamine-phosphate cytidylyltransferase, 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 7 samples with support for all annotated introns
ethanolamine-phosphate cytidylyltransferase, transcript variant X1
ethanolamine-phosphate cytidylyltransferase, 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 11 samples with support for all annotated introns
ethanolamine-phosphate cytidylyltransferase, transcript variant X3
ethanolamine-phosphate cytidylyltransferase isoform X4
ethanolamine-phosphate cytidylyltransferase isoform X3
ethanolamine-phosphate cytidylyltransferase isoform X2
ethanolamine-phosphate cytidylyltransferase isoform X1
meiotic recombination protein DMC1/LIM15 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: meiotic recombination protein DMC1/LIM15 homolog
zinc finger CCCH domain-containing protein 18-like, transcript variant X3
zinc finger CCCH domain-containing protein 18-like, transcript variant X1
zinc finger CCCH domain-containing protein 18-like, transcript variant X4
zinc finger CCCH domain-containing protein 18-like, transcript variant X5
zinc finger CCCH domain-containing protein 18-like, transcript variant X2
zinc finger CCCH domain-containing protein 18-like, transcript variant X6
zinc finger CCCH domain-containing protein 18-like, transcript variant X7
zinc finger CCCH domain-containing protein 18-like isoform X1
zinc finger CCCH domain-containing protein 18-like isoform X2
zinc finger CCCH domain-containing protein 18-like isoform X3
ribonucleases P/MRP protein subunit POP1
uncharacterized LOC125231721, transcript variant X1
uncharacterized LOC125231721, transcript variant X2
uncharacterized protein LOC125231721 isoform X1
uncharacterized protein LOC125231721 isoform X2
uncharacterized LOC125231722, transcript variant X1
uncharacterized LOC125231722, transcript variant X2
uncharacterized protein LOC125231722 isoform X1
uncharacterized protein LOC125231722 isoform X2
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
N-alpha-acetyltransferase 60, transcript variant X2
N-alpha-acetyltransferase 60, 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 10 samples with support for all annotated introns
potassium voltage-gated channel protein Shab, transcript variant X3
potassium voltage-gated channel protein Shab, transcript variant X6
potassium voltage-gated channel protein Shab, transcript variant X5
potassium voltage-gated channel protein Shab, transcript variant X1
potassium voltage-gated channel protein Shab, transcript variant X4
potassium voltage-gated channel protein Shab, transcript variant X7
potassium voltage-gated channel protein Shab, transcript variant X2
potassium voltage-gated channel protein Shab isoform X4
potassium voltage-gated channel protein Shab isoform X7
potassium voltage-gated channel protein Shab isoform X2
potassium voltage-gated channel protein Shab isoform X6
potassium voltage-gated channel protein Shab isoform X5
potassium voltage-gated channel protein Shab isoform X3
potassium voltage-gated channel protein Shab isoform X1
potassium voltage-gated channel protein Shab, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium voltage-gated channel protein Shab isoform X8
uncharacterized LOC125231707, transcript variant X3
uncharacterized LOC125231707, transcript variant X2
uncharacterized LOC125231707, transcript variant X1
uncharacterized protein LOC125231707 isoform X2
uncharacterized protein LOC125231707 isoform X1
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 1 sample with support for all annotated introns
regulator of nonsense transcripts 1 homolog
ubiquitin carboxyl-terminal hydrolase 36-like
ubiquitin-conjugating enzyme E2 variant 2
SNF-related serine/threonine-protein kinase, transcript variant X2
SNF-related serine/threonine-protein kinase, transcript variant X1
SNF-related serine/threonine-protein kinase
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
LOW QUALITY PROTEIN: F-box/LRR-repeat protein 16
uncharacterized LOC125232145, transcript variant X1
uncharacterized LOC125232145, transcript variant X2
uncharacterized protein LOC125232145 isoform X1
uncharacterized protein LOC125232145 isoform X2
nuclear pore complex protein Nup160 homolog
leukocyte receptor cluster member 1 homolog
uncharacterized LOC125231541, 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 10 samples with support for all annotated introns
uncharacterized LOC125231541, transcript variant X1
uncharacterized LOC125231541, transcript variant X3
uncharacterized protein LOC125231541 isoform X1
uncharacterized protein LOC125231541 isoform X2
chromosome transmission fidelity protein 8 homolog
general transcription and DNA repair factor IIH helicase subunit XPB
LOW QUALITY PROTEIN: general transcription and DNA repair factor IIH helicase subunit XPB
uncharacterized LOC125231697, transcript variant X1
uncharacterized LOC125231697, transcript variant X2
uncharacterized LOC125231638, transcript variant X3
uncharacterized protein LOC125231638 isoform X3
uncharacterized LOC125231638, transcript variant X2
uncharacterized protein LOC125231638 isoform X2
uncharacterized LOC125231638, transcript variant X1
uncharacterized protein LOC125231638 isoform X1
U3 small nucleolar RNA-associated protein 4 homolog, transcript variant X1
U3 small nucleolar RNA-associated protein 4 homolog, transcript variant X2
U3 small nucleolar RNA-associated protein 4 homolog isoform X1
U3 small nucleolar RNA-associated protein 4 homolog isoform X2
type 2 phosphatidylinositol 4,5-bisphosphate 4-phosphatase
tubulin polymerization-promoting protein homolog, transcript variant X2
tubulin polymerization-promoting protein homolog, transcript variant X1
tubulin polymerization-promoting protein homolog isoform X2
tubulin polymerization-promoting protein homolog isoform X1
sodium/potassium-transporting ATPase subunit alpha-like
uncharacterized LOC125232201, transcript variant X1
uncharacterized LOC125232201, transcript variant X3
uncharacterized protein LOC125232201 isoform X1
uncharacterized protein LOC125232201 isoform X3
uncharacterized LOC125232201, transcript variant X2
uncharacterized protein LOC125232201 isoform X2
uncharacterized LOC125232230, transcript variant X1
uncharacterized LOC125232230, transcript variant X2
uncharacterized protein LOC125232230 isoform X1
uncharacterized protein LOC125232230 isoform X2
uncharacterized protein C16orf52 homolog A
leukocyte receptor cluster member 8 homolog
LOW QUALITY PROTEIN: leukocyte receptor cluster member 8 homolog
vacuolar protein sorting-associated protein 8 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: vacuolar protein sorting-associated protein 8 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ganglioside-induced differentiation-associated protein 1
glutamate receptor ionotropic, NMDA 2B-like
uncharacterized LOC125231623, transcript variant X4
uncharacterized LOC125231623, transcript variant X3
uncharacterized LOC125231623, transcript variant X1
uncharacterized LOC125231623, transcript variant X2
uncharacterized protein LOC125231623 isoform X1
uncharacterized protein LOC125231623 isoform X2
LOW QUALITY PROTEIN: glutamate receptor ionotropic, NMDA 2B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
xylosyltransferase oxt, 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 12 samples with support for all annotated introns
xylosyltransferase oxt, transcript variant X2
cAMP-dependent protein kinase type I regulatory subunit
LOW QUALITY PROTEIN: nucleoprotein TPR-like
gamma-aminobutyric acid receptor-associated protein
transcription elongation factor spt5-like
E3 ubiquitin-protein ligase RNF146-A, transcript variant X2
E3 ubiquitin-protein ligase RNF146-A, transcript variant X1
E3 ubiquitin-protein ligase RNF146-A isoform X1
E3 ubiquitin-protein ligase RNF146-A isoform X2
2-iminobutanoate/2-iminopropanoate deaminase-like, transcript variant X2
2-iminobutanoate/2-iminopropanoate deaminase-like, transcript variant X3
2-iminobutanoate/2-iminopropanoate deaminase-like
2-iminobutanoate/2-iminopropanoate deaminase-like, transcript variant X1
2-iminobutanoate/2-iminopropanoate deaminase-like, transcript variant X4
uncharacterized protein LOC125231694 isoform X1
2-iminobutanoate/2-iminopropanoate deaminase-like isoform X3
uncharacterized protein LOC125231694 isoform X2
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: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC125231903
uncharacterized LOC125231590, transcript variant X2
uncharacterized LOC125231590, transcript variant X1
uncharacterized LOC125231590, transcript variant X3
uncharacterized protein LOC125231590 isoform X1
uncharacterized protein LOC125231590 isoform X2
uncharacterized protein LOC125231590 isoform X3
tRNA-splicing endonuclease subunit Sen34
purine nucleoside phosphorylase-like, transcript variant X2
purine nucleoside phosphorylase-like, transcript variant X1
purine nucleoside phosphorylase-like isoform X2
purine nucleoside phosphorylase-like isoform X1
farnesoate epoxidase-like, transcript variant X3
farnesoate epoxidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
farnesoate epoxidase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATPase family AAA domain-containing protein 5
cytochrome b-c1 complex subunit 2, mitochondrial
uncharacterized LOC125231928, transcript variant X2
uncharacterized LOC125231928, transcript variant X4
uncharacterized LOC125231928, transcript variant X3
uncharacterized LOC125231928, transcript variant X1
multifunctional methyltransferase subunit TRM112-like protein
COP9 signalosome complex subunit 1, transcript variant X1
COP9 signalosome complex subunit 1, transcript variant X2
gamma-glutamyl hydrolase A-like, transcript variant X1
gamma-glutamyl hydrolase A-like, transcript variant X2
gamma-glutamyl hydrolase A-like, transcript variant X7
gamma-glutamyl hydrolase A-like, transcript variant X6
gamma-glutamyl hydrolase A-like isoform X1
gamma-glutamyl hydrolase A-like isoform X2
gamma-glutamyl hydrolase A-like, transcript variant X3
gamma-glutamyl hydrolase A-like isoform X3
gamma-glutamyl hydrolase A-like, transcript variant X4
gamma-glutamyl hydrolase A-like, transcript variant X5
gamma-glutamyl hydrolase A-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
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: 6 Proteins
SH3 domain-containing protein C23A1.17-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
cuticle protein 70, isoforms A and B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125231610, transcript variant X1
uncharacterized LOC125231610, transcript variant X2
uncharacterized protein LOC125231610 isoform X1
uncharacterized protein LOC125231610 isoform X2
3-phosphoinositide-dependent protein kinase 1, transcript variant X2
3-phosphoinositide-dependent protein kinase 1, transcript variant X1
3-phosphoinositide-dependent protein kinase 1, transcript variant X3
3-phosphoinositide-dependent protein kinase 1 isoform X1
3-phosphoinositide-dependent protein kinase 1 isoform X2
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
ATP-dependent RNA helicase dbp2-like, transcript variant X2
ATP-dependent RNA helicase dbp2-like, transcript variant X1
ATP-dependent RNA helicase dbp2-like isoform X2
ATP-dependent RNA helicase dbp2-like isoform X1
ecto-NOX disulfide-thiol exchanger 2-like
LOW QUALITY PROTEIN: ecto-NOX disulfide-thiol exchanger 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
meiosis-specific with OB domain-containing protein, transcript variant X1
meiosis-specific with OB domain-containing protein isoform X1
meiosis-specific with OB domain-containing protein, transcript variant X2
meiosis-specific with OB domain-containing protein isoform X2
integral membrane protein GPR155, 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 1 sample with support for all annotated introns
integral membrane protein GPR155, 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 2 samples with support for all annotated introns
integral membrane protein GPR155, transcript variant X4
integral membrane protein GPR155, transcript variant X5
integral membrane protein GPR155, transcript variant X3
integral membrane protein GPR155 isoform X1
integral membrane protein GPR155 isoform X2
integral membrane protein GPR155 isoform X4
integral membrane protein GPR155 isoform X3
integral membrane protein GPR155 isoform X5
DNA-directed RNA polymerase III subunit RPC8
activating transcription factor of chaperone, transcript variant X1
activating transcription factor of chaperone isoform X1
activating transcription factor of chaperone, transcript variant X2
activating transcription factor of chaperone isoform X2
regulating synaptic membrane exocytosis protein 1
transcription initiation factor IIA subunit 1
LOW QUALITY PROTEIN: regulating synaptic membrane exocytosis protein 1
intraflagellar transport protein 172 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125232155, transcript variant X2
uncharacterized LOC125232155, transcript variant X1
sperm-associated antigen 6-like, transcript variant X2
sperm-associated antigen 6-like, transcript variant X1
sperm-associated antigen 6-like isoform X2
sperm-associated antigen 6-like isoform X1
DNA-directed RNA polymerase III subunit RPC7-like
coiled-coil domain-containing protein 93
ubiquinone biosynthesis protein COQ9, mitochondrial-like, transcript variant X1
ubiquinone biosynthesis protein COQ9, mitochondrial-like, transcript variant X2
ubiquinone biosynthesis protein COQ9, mitochondrial-like isoform X2
F-actin-uncapping protein LRRC16A, transcript variant X3
F-actin-uncapping protein LRRC16A, transcript variant X1
F-actin-uncapping protein LRRC16A, transcript variant X4
F-actin-uncapping protein LRRC16A, transcript variant X6
F-actin-uncapping protein LRRC16A, transcript variant X5
F-actin-uncapping protein LRRC16A, transcript variant X7
F-actin-uncapping protein LRRC16A, transcript variant X2
F-actin-uncapping protein LRRC16A isoform X1
F-actin-uncapping protein LRRC16A isoform X3
F-actin-uncapping protein LRRC16A isoform X4
F-actin-uncapping protein LRRC16A isoform X5
F-actin-uncapping protein LRRC16A isoform X2
ATP-dependent RNA helicase p62, transcript variant X2
ATP-dependent RNA helicase p62, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 18% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylation factor-like protein 4C, transcript variant X2
ADP-ribosylation factor-like protein 4C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
cysteine and histidine-rich protein 1-like, transcript variant X1
cysteine and histidine-rich protein 1-like, transcript variant X2
cysteine and histidine-rich protein 1-like isoform X1
cysteine and histidine-rich protein 1-like 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 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein K02A2.6-like
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, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fatty acid synthase-like, transcript variant X2
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 1 sample with support for all annotated introns
fatty acid synthase-like, 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
sodium-coupled monocarboxylate transporter 2-like, transcript variant X2
sodium-coupled monocarboxylate transporter 2-like, transcript variant X1
sodium-coupled monocarboxylate transporter 2-like isoform X2
sodium-coupled monocarboxylate transporter 2-like isoform X1
LOW QUALITY PROTEIN: zinc finger homeobox protein 4
uncharacterized LOC125232205, transcript variant X1
uncharacterized LOC125232205, transcript variant X2
uncharacterized LOC125232206, transcript variant X1
uncharacterized LOC125232206, transcript variant X2
protein-L-histidine N-pros-methyltransferase
LOW QUALITY PROTEIN: protein-L-histidine N-pros-methyltransferase
p21-activated protein kinase-interacting 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 5 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
uncharacterized LOC125232042, transcript variant X2
uncharacterized LOC125232042, 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; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: WW domain-binding protein 2
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 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: mismatch repair endonuclease PMS2
glutamate-rich WD repeat-containing protein 1
pentatricopeptide repeat-containing protein 1, mitochondrial
LOW QUALITY PROTEIN: pentatricopeptide repeat-containing protein 1, mitochondrial
eukaryotic translation initiation factor 3 subunit L
uncharacterized LOC125231659, transcript variant X2
uncharacterized LOC125231659, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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
histone-lysine N-methyltransferase, H3 lysine-79 specific-like, transcript variant X1
histone-lysine N-methyltransferase, H3 lysine-79 specific-like, transcript variant X3
histone-lysine N-methyltransferase, H3 lysine-79 specific-like, transcript variant X2
histone-lysine N-methyltransferase, H3 lysine-79 specific-like isoform X1
histone-lysine N-methyltransferase, H3 lysine-79 specific-like isoform X2
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 62% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: sucrose-6-phosphate hydrolase-like
LOW QUALITY PROTEIN: splicing factor 3B subunit 3
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: putative inactive cysteine synthase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
10 kDa heat shock protein, mitochondrial-like
glucose-fructose oxidoreductase domain-containing protein 1
arf-GAP with dual PH domain-containing protein 1-like
LOW QUALITY PROTEIN: WW domain-binding protein 11
ATP-binding cassette sub-family G member 4
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: 4 Proteins
cysteine sulfinic acid decarboxylase-like
LOW QUALITY PROTEIN: cysteine sulfinic acid decarboxylase-like
multiple C2 and transmembrane domain-containing protein-like, transcript variant X2
multiple C2 and transmembrane domain-containing protein-like, transcript variant X1
multiple C2 and transmembrane domain-containing protein-like, transcript variant X3
multiple C2 and transmembrane domain-containing protein-like isoform X2
multiple C2 and transmembrane domain-containing protein-like isoform X1
multiple C2 and transmembrane domain-containing protein-like isoform X3
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: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: collagen alpha-1(IX) chain-like
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
hemolymph lipopolysaccharide-binding protein-like, transcript variant X1
hemolymph lipopolysaccharide-binding protein-like, transcript variant X2
secretory phospholipase A2 receptor-like isoform X1
hemolymph lipopolysaccharide-binding protein-like isoform X2
collagen alpha-1(I) chain-like, transcript variant X1
collagen alpha-1(I) chain-like, transcript variant X2
collagen alpha-1(I) chain-like, transcript variant X5
collagen alpha-1(I) chain-like, transcript variant X8
collagen alpha-1(I) chain-like, transcript variant X3
collagen alpha-1(I) chain-like, transcript variant X4
collagen alpha-1(I) chain-like, transcript variant X7
collagen alpha-1(I) chain-like, transcript variant X6
collagen alpha-1(I) chain-like, transcript variant X9
collagen alpha-2(XI) chain-like isoform X1
collagen alpha-2(XI) chain-like isoform X2
collagen alpha-2(XI) chain-like isoform X5
collagen alpha-1(XVIII) chain-like isoform X8
collagen alpha-1(XVIII) chain-like isoform X3
collagen alpha-1(XVIII) chain-like isoform X4
collagen alpha-1(XVIII) chain-like isoform X7
collagen alpha-1(XVIII) chain-like isoform X6
collagen alpha-1(I) chain-like, transcript variant X10
collagen alpha-1(I) chain-like isoform X9
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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC125232181
U3 small nucleolar RNA-associated protein 6 homolog
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
tyrosine-protein kinase Src64B, transcript variant X2
tyrosine-protein kinase Src64B, transcript variant X1
tyrosine-protein kinase Src64B, transcript variant X3
tyrosine-protein kinase Src64B, transcript variant X4
tyrosine-protein kinase Src64B isoform X1
tyrosine-protein kinase Src64B isoform X2
tyrosine-protein kinase Src64B isoform X3
adenosine 3'-phospho 5'-phosphosulfate transporter 2
E3 ubiquitin-protein ligase MARCHF6, transcript variant X1
E3 ubiquitin-protein ligase MARCHF6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
unconventional myosin-IXAa, 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
unconventional myosin-IXAa, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC125232128
probable small nuclear ribonucleoprotein E
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125231894, transcript variant X1
uncharacterized LOC125231894, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X4
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X1
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X5
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X3
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X2
longitudinals lacking protein, isoforms A/B/D/L-like isoform X4
longitudinals lacking protein, isoforms F/I/K/T-like isoform X1
longitudinals lacking protein, isoforms A/B/D/L-like isoform X2
cytochrome c oxidase assembly protein COX11, mitochondrial
cytosolic Fe-S cluster assembly factor NUBP1 homolog
serine/arginine repetitive matrix protein 2
aprataxin and PNK-like factor, transcript variant X1
aprataxin and PNK-like factor isoform X1
aprataxin and PNK-like factor, transcript variant X3
aprataxin and PNK-like factor, transcript variant X2
aprataxin and PNK-like factor isoform X3
aprataxin and PNK-like factor isoform X2
oxysterol-binding protein-related protein 11
actin-related protein 2/3 complex subunit 1A-B
brefeldin A-inhibited guanine nucleotide-exchange protein 1
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: brefeldin A-inhibited guanine nucleotide-exchange protein 1
LOW QUALITY PROTEIN: mitotic checkpoint protein BUB3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
SWR1-complex protein 4-like, transcript variant X2
SWR1-complex protein 4-like, transcript variant X1
SWR1-complex protein 4-like, transcript variant X3
putative uncharacterized protein DDB_G0282133 isoform X1
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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 91% 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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: adenylate cyclase type 2
E3 ubiquitin-protein ligase SIAH2-like, transcript variant X2
uncharacterized protein LOC125231604 isoform X2
E3 ubiquitin-protein ligase SIAH2-like, transcript variant X1
E3 ubiquitin-protein ligase SIAH2-like, transcript variant X4
uncharacterized protein LOC125231604 isoform X1
E3 ubiquitin-protein ligase SIAH2-like isoform X4
E3 ubiquitin-protein ligase SIAH2-like, transcript variant X3
uncharacterized protein LOC125231604 isoform X3
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16
LOW QUALITY PROTEIN: pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16
uncharacterized LOC125231726, transcript variant X1
uncharacterized LOC125231726, transcript variant X2
uncharacterized protein LOC125231726 isoform X1
uncharacterized LOC125231726, transcript variant X3
uncharacterized protein LOC125231726 isoform X2
uncharacterized LOC125231726, transcript variant X4
uncharacterized protein LOC125231726 isoform X3
uncharacterized LOC125231727, transcript variant X2
uncharacterized LOC125231727, transcript variant X1
lipid droplet-regulating VLDL assembly factor AUP1-like
facilitated trehalose transporter Tret1, transcript variant X5
facilitated trehalose transporter Tret1, transcript variant X2
facilitated trehalose transporter Tret1, transcript variant X4
facilitated trehalose transporter Tret1, transcript variant X6
facilitated trehalose transporter Tret1, transcript variant X1
facilitated trehalose transporter Tret1, transcript variant X3
facilitated trehalose transporter Tret1 isoform X5
facilitated trehalose transporter Tret1 isoform X2
facilitated trehalose transporter Tret1 isoform X4
facilitated trehalose transporter Tret1 isoform X1
facilitated trehalose transporter Tret1 isoform X3
facilitated trehalose transporter Tret1 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% 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: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 10
mitochondrial cardiolipin hydrolase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
tyrosine-protein phosphatase Lar, transcript variant X5
tyrosine-protein phosphatase Lar, transcript variant X3
tyrosine-protein phosphatase Lar, transcript variant X2
tyrosine-protein phosphatase Lar, transcript variant X4
tyrosine-protein phosphatase Lar, transcript variant X1
tyrosine-protein phosphatase Lar isoform X5
tyrosine-protein phosphatase Lar isoform X3
tyrosine-protein phosphatase Lar isoform X2
tyrosine-protein phosphatase Lar isoform X4
tyrosine-protein phosphatase Lar isoform X1
probable tRNA N6-adenosine threonylcarbamoyltransferase
proline-, glutamic acid- and leucine-rich protein 1-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
transfer RNA methionine (anticodon CAU); 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: 66% coverage of the annotated genomic feature by RNAseq alignments
prolactin-releasing peptide receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
prolactin-releasing peptide receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
prolactin-releasing peptide receptor-like
transfer RNA alanine (anticodon GGC); 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: 22 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
probable WRKY transcription factor protein 1
mitochondrial thiamine pyrophosphate carrier-like
zinc finger protein 135-like, transcript variant X4
zinc finger protein 135-like, transcript variant X1
zinc finger protein 135-like, transcript variant X2
zinc finger protein 135-like, transcript variant X3
F-box only protein 25, transcript variant X2
F-box only protein 25, transcript variant X1
cytochrome c oxidase assembly factor 3, mitochondrial
dimethyladenosine transferase 1, mitochondrial
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
myc proto-oncogene protein, transcript variant X1
myc proto-oncogene protein, transcript variant X2
transfer RNA threonine (anticodon GGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125231666, transcript variant X2
uncharacterized LOC125231666, transcript variant X3
uncharacterized LOC125231666, transcript variant X4
uncharacterized LOC125231665, transcript variant X1
uncharacterized protein LOC125231665 isoform X1
uncharacterized LOC125231665, transcript variant X2
uncharacterized LOC125231665, transcript variant X3
uncharacterized protein LOC125231665 isoform X2
uncharacterized protein LOC125231665 isoform X3
uncharacterized LOC125231666, transcript variant X1
lysosomal alpha-glucosidase-like, transcript variant X1
lysosomal alpha-glucosidase-like isoform X1
lysosomal alpha-glucosidase-like, transcript variant X2
lysosomal alpha-glucosidase-like isoform X2
glycine cleavage system H protein, mitochondrial, transcript variant X2
glycine cleavage system H protein, mitochondrial, transcript variant X1
glycine cleavage system H protein, mitochondrial
zinc finger protein 62 homolog, transcript variant X2
zinc finger protein 62 homolog, transcript variant X3
zinc finger protein 62 homolog, transcript variant X1
zinc finger protein 62 homolog isoform X2
zinc finger protein 62 homolog isoform X1
serine/threonine-protein kinase ICK, transcript variant X1
serine/threonine-protein kinase ICK, transcript variant X3
serine/threonine-protein kinase ICK, transcript variant X2
serine/threonine-protein kinase ICK isoform X3
serine/threonine-protein kinase ICK isoform X2
serine/threonine-protein kinase ICK isoform X1
protein N-terminal asparagine amidohydrolase, transcript variant X4
protein N-terminal asparagine amidohydrolase, transcript variant X2
protein N-terminal asparagine amidohydrolase, transcript variant X3
protein N-terminal asparagine amidohydrolase, transcript variant X5
protein N-terminal asparagine amidohydrolase, transcript variant X1
protein N-terminal asparagine amidohydrolase, transcript variant X6
protein N-terminal asparagine amidohydrolase isoform X1
protein N-terminal asparagine amidohydrolase isoform X2
protein N-terminal asparagine amidohydrolase isoform X3
serine/threonine-protein kinase SBK1, 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
serine/threonine-protein kinase SBK1, transcript variant X1
serine/threonine-protein kinase SBK1, transcript variant X3
serine/threonine-protein kinase SBK1, transcript variant X4
serine/threonine-protein kinase meng-po isoform X1
serine/threonine-protein kinase SBK1 isoform X2
serine/threonine-protein kinase SBK1 isoform X3
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
putative sodium-coupled neutral amino acid transporter 10
mini-chromosome maintenance complex-binding protein
fatty acid synthase, transcript variant X2
fatty acid synthase, transcript variant X3
fatty acid synthase, transcript variant X1
reticulon-4-interacting protein 1, mitochondrial, transcript variant X1
reticulon-4-interacting protein 1, mitochondrial, transcript variant X2
reticulon-4-interacting protein 1, mitochondrial
transfer RNA serine (anticodon GGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
GTP-binding protein Rhes, 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 1 sample with support for all annotated introns
GTP-binding protein Rhes, transcript variant X2