Portunus trituberculatus isolate SZX2019 chromosome 1, ASM1759143v1, whole genome shotgun sequence.
Portunus trituberculatus (swimming crab)
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea; Malacostraca; Eumalacostraca; Eucarida; Decapoda; Pleocyemata; Brachyura; Eubrachyura; Portunoidea; Portunidae; Portunus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM030071.1.\nAssembly name: ASM1759143v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Center for Ecological and\nEnvironmental Sciences on 2021/03/30. The original whole-genome\nshotgun project has the accession JAGGDN000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Center for Ecological and Environmental\n Sciences\nAssembly Method :: Wtdbg v. 2.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 54.74x\nSequencing Technology :: Oxford Nanopore; Illumina\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Portunus trituberculatus Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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: zinc finger MYM-type protein 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
general transcription factor II-I repeat domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123507346, transcript variant X1
uncharacterized LOC123507346, transcript variant X2
uncharacterized protein LOC123507346 isoform X1
uncharacterized protein LOC123507346 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
electron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrial-like
uncharacterized LOC123507580, 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 5 samples with support for all annotated introns
uncharacterized LOC123507580, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized protein LOC123507580 isoform X2
uncharacterized protein LOC123507580 isoform X1
lipid droplet-associated hydrolase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
lipid droplet-associated hydrolase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
lipid droplet-associated hydrolase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
lipid droplet-associated hydrolase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lipid droplet-associated hydrolase-like isoform X1
lipid droplet-associated hydrolase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like, transcript variant X3
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like, transcript variant X1
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like, transcript variant X4
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like, transcript variant X2
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like isoform X2
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like isoform X1
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like isoform X3
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like isoform X4
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like, transcript variant X5
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like, transcript variant X6
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like isoform X6
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1-like isoform X5
metabotropic glutamate receptor 7-like, transcript variant X1
metabotropic glutamate receptor 7-like, transcript variant X3
metabotropic glutamate receptor 7-like, transcript variant X4
metabotropic glutamate receptor 7-like, transcript variant X5
metabotropic glutamate receptor 7-like, transcript variant X2
metabotropic glutamate receptor 7-like isoform X4
protein bride of sevenless-like isoform X3
metabotropic glutamate receptor 7-like isoform X2
uncharacterized protein LOC123508037 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: broad-complex core protein-like
mini-chromosome maintenance complex-binding protein-like
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 long SRA reads, 2 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: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: mini-chromosome maintenance complex-binding protein-like
basement membrane-specific heparan sulfate proteoglycan core protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 2 Proteins, and 89% 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: tRNAscan-SE.
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ATP-dependent zinc metalloprotease YME1L-like
zinc finger protein OZF-like, transcript variant X1
zinc finger protein OZF-like, transcript variant X2
uncharacterized protein LOC123505111 isoform X2
FYVE, RhoGEF and PH domain-containing protein 4-like, transcript variant X3
FYVE, RhoGEF and PH domain-containing protein 4-like, transcript variant X1
FYVE, RhoGEF and PH domain-containing protein 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
FYVE, RhoGEF and PH domain-containing protein 4-like isoform X2
FYVE, RhoGEF and PH domain-containing protein 4-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 20 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
probable G-protein coupled receptor CG31760
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
nose resistant to fluoxetine protein 6-like, transcript variant X1
nose resistant to fluoxetine protein 6-like, transcript variant X3
nose resistant to fluoxetine protein 6-like, transcript variant X2
nose resistant to fluoxetine protein 6-like isoform X1
nose resistant to fluoxetine protein 6-like isoform X2
nose resistant to fluoxetine protein 6-like isoform X3
nose resistant to fluoxetine protein 6-like, transcript variant X5
nose resistant to fluoxetine protein 6-like, transcript variant X6
nose resistant to fluoxetine protein 6-like, transcript variant X4
nose resistant to fluoxetine protein 6-like isoform X4
vesicle transport through interaction with t-SNAREs homolog 1A-like, transcript variant X3
vesicle transport through interaction with t-SNAREs homolog 1A-like, transcript variant X5
vesicle transport through interaction with t-SNAREs homolog 1A-like, transcript variant X4
uncharacterized LOC123505856, transcript variant X1
uncharacterized LOC123505856, 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
ADP-ribosylation factor-like protein 2-binding protein, transcript variant X2
ADP-ribosylation factor-like protein 2-binding protein, transcript variant X4
ADP-ribosylation factor-like protein 2-binding protein, transcript variant X3
ADP-ribosylation factor-like protein 2-binding protein, transcript variant X5
ADP-ribosylation factor-like protein 2-binding protein, transcript variant X1
ADP-ribosylation factor-like protein 2-binding protein isoform X2
ADP-ribosylation factor-like protein 2-binding protein isoform X4
ADP-ribosylation factor-like protein 2-binding protein isoform X3
ADP-ribosylation factor-like protein 2-binding protein isoform X1
vesicle transport through interaction with t-SNAREs homolog 1A-like, transcript variant X1
vesicle transport through interaction with t-SNAREs homolog 1A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
vesicle transport through interaction with t-SNAREs homolog 1A-like isoform X1
vesicle transport through interaction with t-SNAREs homolog 1A-like isoform X2
vesicle transport through interaction with t-SNAREs homolog 1A-like isoform X3
nose resistant to fluoxetine protein 6-like
nucleolysin TIAR-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
nucleolysin TIAR-like, transcript variant X1
nucleolysin TIAR-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
nucleolysin TIAR-like, transcript variant X4
FGGY carbohydrate kinase domain-containing protein-like, transcript variant X4
FGGY carbohydrate kinase domain-containing protein-like, transcript variant X5
FGGY carbohydrate kinase domain-containing protein-like, transcript variant X1
FGGY carbohydrate kinase domain-containing protein-like, transcript variant X3
FGGY carbohydrate kinase domain-containing protein-like, transcript variant X2
FGGY carbohydrate kinase domain-containing protein-like, transcript variant X6
FGGY carbohydrate kinase domain-containing protein-like isoform X2
FGGY carbohydrate kinase domain-containing protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
serine/threonine-protein kinase mig-15-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: serine/threonine-protein kinase mig-15-like
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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: 9 long SRA reads, 1 Protein, and 92% 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC123519192
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123504618, transcript variant X1
uncharacterized LOC123504618, transcript variant X2
uncharacterized protein LOC123504618 isoform X1
uncharacterized protein LOC123504618 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
troponin T, skeletal muscle-like, transcript variant X4
troponin T, skeletal muscle-like, transcript variant X5
troponin T, skeletal muscle-like, transcript variant X3
troponin T, skeletal muscle-like, transcript variant X1
troponin T, skeletal muscle-like, transcript variant X2
troponin T, skeletal muscle-like isoform X3
troponin T, skeletal muscle-like isoform X1
troponin T, skeletal muscle-like isoform X2
troponin T, skeletal muscle-like isoform X4
troponin T, skeletal muscle-like isoform X5
potassium channel subfamily K member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium channel subfamily K member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium channel subfamily K member 1-like
galactoside alpha-(1,2)-fucosyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
galactoside 2-alpha-L-fucosyltransferase SEC1-like
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: galactoside 2-alpha-L-fucosyltransferase SEC1-like
galactoside 2-alpha-L-fucosyltransferase SEC1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
galactoside 2-alpha-L-fucosyltransferase SEC1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
galactoside 2-alpha-L-fucosyltransferase SEC1-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 5 samples with support for all annotated introns
galactoside alpha-(1,2)-fucosyltransferase 1-like, transcript variant X1
galactoside alpha-(1,2)-fucosyltransferase 1-like, transcript variant X2
galactoside alpha-(1,2)-fucosyltransferase 1-like, transcript variant X3
galactoside alpha-(1,2)-fucosyltransferase 1-like, transcript variant X5
galactoside alpha-(1,2)-fucosyltransferase 1-like, transcript variant X4
galactoside alpha-(1,2)-fucosyltransferase 2-like isoform X2
galactoside alpha-(1,2)-fucosyltransferase 2-like isoform X1
galactoside alpha-(1,2)-fucosyltransferase 1-like isoform X4
galactoside alpha-(1,2)-fucosyltransferase 1-like isoform X3
limbic system-associated membrane protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123501035, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123501035, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123501035, transcript variant X2
uncharacterized LOC123501035, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
tectonin beta-propeller repeat-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
tectonin beta-propeller repeat-containing protein 2-like isoform X1
tectonin beta-propeller repeat-containing protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
tectonin beta-propeller repeat-containing protein 2-like isoform X2
crustacean hyperglycemic hormones B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
palmitoyltransferase ZDHHC20-B-like, transcript variant X3
palmitoyltransferase ZDHHC20-B-like, transcript variant X2
palmitoyltransferase ZDHHC20-B-like, transcript variant X1
palmitoyltransferase ZDHHC20-B-like isoform X2
palmitoyltransferase ZDHHC20-B-like isoform X3
palmitoyltransferase ZDHHC20-B-like isoform X1
uncharacterized protein LOC123508632 isoform X1
uncharacterized protein LOC123508632 isoform X5
uncharacterized protein LOC123508632 isoform X4
uncharacterized protein LOC123508632 isoform X2
uncharacterized protein LOC123508632 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog, transcript variant X2
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog, transcript variant X6
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog, transcript variant X3
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog, transcript variant X1
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog, transcript variant X5
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog, transcript variant X4
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog, transcript variant X7
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog, transcript variant X8
heterogeneous nuclear ribonucleoprotein 87F-like isoform X7
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog isoform X5
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog isoform X6
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog isoform X4
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog isoform X2
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog isoform X3
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 8 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
novel acetylcholine receptor chaperone-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
5'-AMP-activated protein kinase subunit gamma-2-like, transcript variant X3
5'-AMP-activated protein kinase subunit gamma-2-like, transcript variant X2
5'-AMP-activated protein kinase subunit gamma-2-like, transcript variant X8
5'-AMP-activated protein kinase subunit gamma-2-like, transcript variant X6
5'-AMP-activated protein kinase subunit gamma-2-like, transcript variant X4
5'-AMP-activated protein kinase subunit gamma-2-like, transcript variant X1
5'-AMP-activated protein kinase subunit gamma-2-like, transcript variant X5
5'-AMP-activated protein kinase subunit gamma-2-like, transcript variant X7
5'-AMP-activated protein kinase subunit gamma-2-like, transcript variant X9
uncharacterized protein LOC123509003 isoform X7
uncharacterized protein LOC123509003 isoform X5
uncharacterized protein LOC123509003 isoform X3
uncharacterized protein LOC123509003 isoform X2
uncharacterized protein LOC123509003 isoform X1
uncharacterized protein LOC123509003 isoform X4
uncharacterized protein LOC123509003 isoform X6
5'-AMP-activated protein kinase subunit gamma-2-like isoform X8
N-acetyltransferase 9-like, transcript variant X2
N-acetyltransferase 9-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
protein Hook homolog 3-like, transcript variant X2
protein Hook homolog 3-like, transcript variant X1
GATA zinc finger domain-containing protein 14-like
aldehyde dehydrogenase family 3 member A2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123510533, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123510533, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
DNA damage-inducible transcript 4-like protein, transcript variant X3
DNA damage-inducible transcript 4-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DNA damage-inducible transcript 4-like protein, transcript variant X1
uncharacterized protein LOC123510755 isoform X3
uncharacterized protein LOC123510755 isoform X2
DNA damage-inducible transcript 4-like protein isoform X1
ribosome biogenesis protein WDR12 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit epsilon isoform-like
pyruvate kinase-like, transcript variant X2
pyruvate kinase-like, transcript variant X3
pyruvate kinase-like, transcript variant X7
pyruvate kinase-like, transcript variant X1
pyruvate kinase-like, transcript variant X4
pyruvate kinase-like, transcript variant X6
pyruvate kinase-like, transcript variant X5
LOW QUALITY PROTEIN: adenylate cyclase type 6-like
uncharacterized LOC123512124, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123512124, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123512124, transcript variant X3
uncharacterized LOC123512124, transcript variant X1
uncharacterized protein LOC123512124 isoform X1
uncharacterized protein LOC123512124 isoform X2
uncharacterized LOC123511743, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123511743, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123511743, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC123511743 isoform X1
uncharacterized protein LOC123511743 isoform X2
TBC1 domain family member 22B-like, transcript variant X1
TBC1 domain family member 22B-like, transcript variant X3
TBC1 domain family member 22B-like, transcript variant X2
TBC1 domain family member 22B-like, transcript variant X4
TBC1 domain family member 22B-like isoform X1
TBC1 domain family member 22B-like isoform X3
TBC1 domain family member 22B-like isoform X2
TBC1 domain family member 22B-like isoform X4
uncharacterized LOC123511596, transcript variant X1
uncharacterized LOC123511596, transcript variant X2
uncharacterized protein LOC123511596 isoform X1
uncharacterized protein LOC123511596 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
calcium-activated chloride channel regulator family member 3-like
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
uncharacterized LOC123512725, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC123512725 isoform X5
uncharacterized LOC123512725, transcript variant X1
uncharacterized LOC123512725, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123512725, transcript variant X4
uncharacterized LOC123512725, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein LOC123512725 isoform X1
uncharacterized protein LOC123512725 isoform X2
uncharacterized protein LOC123512725 isoform X4
uncharacterized protein LOC123512725 isoform X3
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
mitochondrial E3 ubiquitin protein ligase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
aminoacyl tRNA synthase complex-interacting multifunctional protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
aminoacyl tRNA synthase complex-interacting multifunctional protein 2-like, transcript variant X1
aminoacyl tRNA synthase complex-interacting multifunctional protein 2-like, transcript variant X3
aminoacyl tRNA synthase complex-interacting multifunctional protein 2-like
uncharacterized LOC123513140, transcript variant X2
uncharacterized LOC123513140, transcript variant X1
uncharacterized LOC123513140, transcript variant X3
uncharacterized LOC123513140, transcript variant X4
uncharacterized protein LOC123513140 isoform X1
uncharacterized protein LOC123513140 isoform X2
eEF1A lysine and N-terminal methyltransferase-like
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: 32 Proteins, and 89% 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: eEF1A lysine and N-terminal methyltransferase-like
NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 6 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 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ADP-dependent glucokinase-like
AT-rich interactive domain-containing protein 1B-like
major facilitator superfamily domain-containing protein 10-like
LOW QUALITY PROTEIN: major facilitator superfamily domain-containing protein 10-like
brain tumor protein-like, transcript variant X2
brain tumor protein-like, transcript variant X1
nucleosome-remodeling factor subunit NURF301-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
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: nucleosome-remodeling factor subunit NURF301-like
probable asparagine--tRNA ligase, mitochondrial, transcript variant X1
probable asparagine--tRNA ligase, mitochondrial, transcript variant X3
probable asparagine--tRNA ligase, mitochondrial, transcript variant X2
probable asparagine--tRNA ligase, mitochondrial isoform X1
probable asparagine--tRNA ligase, mitochondrial isoform X2
probable asparagine--tRNA ligase, mitochondrial isoform X3
phospholipid-transporting ATPase ID-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
phospholipid-transporting ATPase ID-like isoform X2
phospholipid-transporting ATPase ID-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
phospholipid-transporting ATPase ID-like isoform X1
phospholipid-transporting ATPase ID-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
phospholipid-transporting ATPase ID-like isoform X3
probable phospholipid-transporting ATPase IM
RNA-binding protein squid-like, transcript variant X1
RNA-binding protein squid-like, transcript variant X4
RNA-binding protein squid-like, transcript variant X12
RNA-binding protein squid-like, transcript variant X2
RNA-binding protein squid-like, transcript variant X5
RNA-binding protein squid-like, transcript variant X3
RNA-binding protein squid-like, transcript variant X13
RNA-binding protein squid-like, transcript variant X7
RNA-binding protein squid-like, transcript variant X6
RNA-binding protein squid-like, transcript variant X10
RNA-binding protein squid-like, transcript variant X9
RNA-binding protein squid-like, transcript variant X8
RNA-binding protein squid-like, transcript variant X11
RNA-binding protein squid-like, transcript variant X15
RNA-binding protein squid-like, transcript variant X14
RNA-binding protein squid-like isoform X1
RNA-binding protein squid-like isoform X2
RNA-binding protein squid-like isoform X3
RNA-binding protein squid-like isoform X4
RNA-binding protein squid-like isoform X8
RNA-binding protein squid-like isoform X5
RNA-binding protein squid-like isoform X9
RNA-binding protein squid-like isoform X6
RNA-binding protein squid-like isoform X7
RNA-binding protein squid-like isoform X10
single-minded homolog 2-like, transcript variant X2
single-minded homolog 2-like, transcript variant X1
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 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: protein single-minded-like
anaphase-promoting complex subunit 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
epidermal retinol dehydrogenase 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
epidermal retinol dehydrogenase 2-like, transcript variant X1
epidermal retinol dehydrogenase 2-like, transcript variant X2
epidermal retinol dehydrogenase 2-like isoform X2
epidermal retinol dehydrogenase 2-like 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 1 codon
LOW QUALITY PROTEIN: twinkle protein, mitochondrial-like
actin-binding Rho-activating protein-like, transcript variant X1
actin-binding Rho-activating protein-like, transcript variant X2
actin-binding Rho-activating protein-like isoform X2
actin-binding Rho-activating protein-like isoform X1
plexin domain-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 31 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
plexin domain-containing protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
plexin domain-containing protein 2-like isoform X1
plexin domain-containing protein 2-like isoform X2
adult-specific cuticular protein ACP-20-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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: 6 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase TRIM32-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM32-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase TRIM32-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM32-like isoform X1
uncharacterized LOC123516761, transcript variant X2
uncharacterized LOC123516761, transcript variant X1
uncharacterized LOC123516761, transcript variant X4
uncharacterized LOC123516761, transcript variant X3
uncharacterized protein LOC123516761 isoform X2
uncharacterized protein LOC123516761 isoform X1
uncharacterized protein LOC123516761 isoform X4
uncharacterized protein LOC123516761 isoform X3
LOW QUALITY PROTEIN: piwi-like protein 1
LOW QUALITY PROTEIN: melanotransferrin-like
constitutive coactivator of peroxisome proliferator-activated receptor gamma-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: constitutive coactivator of peroxisome proliferator-activated receptor gamma-like
beta-1,4-glucuronyltransferase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
beta-1,4-glucuronyltransferase 1-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 7 samples with support for all annotated introns
beta-1,4-glucuronyltransferase 1-like isoform X1
beta-1,4-glucuronyltransferase 1-like isoform X2
uncharacterized LOC123517317, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC123517317 isoform X3
uncharacterized LOC123517317, transcript variant X2
uncharacterized LOC123517317, transcript variant X1
uncharacterized protein LOC123517317 isoform X1
uncharacterized protein LOC123517317 isoform X2
alpha-aspartyl dipeptidase-like, transcript variant X1
alpha-aspartyl dipeptidase-like, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: protein couch potato-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
LOW QUALITY PROTEIN: DDRGK domain-containing protein 1-like
uncharacterized LOC123517746, transcript variant X1
uncharacterized LOC123517746, transcript variant X2
uncharacterized protein LOC123517746 isoform X1
uncharacterized protein LOC123517746 isoform X2
LOW QUALITY PROTEIN: uncharacterized protein LOC123517949
uncharacterized LOC123518027, 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 20 samples with support for all annotated introns
uncharacterized LOC123518027, 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 30 samples with support for all annotated introns
uncharacterized LOC123518027, 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 42 samples with support for all annotated introns
uncharacterized LOC123518027, 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 26 samples with support for all annotated introns
uncharacterized LOC123518118, transcript variant X1
uncharacterized LOC123518118, transcript variant X2
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 long SRA reads, 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 long SRA reads, 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 long SRA reads, 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 long SRA reads, 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 long SRA reads, 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 long SRA reads, 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like isoform X4
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like isoform X3
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like isoform X2
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like isoform X1
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase-like isoform X5
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1-like isoform X6
thioredoxin reductase 1, cytoplasmic-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
LOW QUALITY PROTEIN: thioredoxin reductase 1, cytoplasmic-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 3 bases in 2 codons
charged multivesicular body protein 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: charged multivesicular body protein 7-like
LOW QUALITY PROTEIN: WD repeat-containing protein 26-like
DNA damage-regulated autophagy modulator protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DNA damage-regulated autophagy modulator protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
DNA damage-regulated autophagy modulator protein 2-like, transcript variant X5
DNA damage-regulated autophagy modulator protein 2-like, transcript variant X3
DNA damage-regulated autophagy modulator protein 2-like, transcript variant X4
DNA damage-regulated autophagy modulator protein 2-like isoform X3
DNA damage-regulated autophagy modulator protein 2-like isoform X2
DNA damage-regulated autophagy modulator protein 2-like isoform X1
transformer-2 protein homolog alpha-like, transcript variant X3
transformer-2 protein homolog alpha-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
transformer-2 protein homolog alpha-like, transcript variant X2
transformer-2 protein homolog alpha-like isoform X3
transformer-2 protein homolog alpha-like isoform X1
transformer-2 protein homolog alpha-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons
LOW QUALITY PROTEIN: splicing factor 3B subunit 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
SH3 domain-containing protein C23A1.17-like, transcript variant X2
SH3 domain-containing protein C23A1.17-like, transcript variant X1
uncharacterized protein LOC123519571 isoform X2
SH3 domain-containing protein C23A1.17-like isoform X1
28S ribosomal protein S15, mitochondrial-like
protein tyrosine phosphatase domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
glucose-6-phosphate exchanger SLC37A4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57% coverage of the annotated genomic feature by RNAseq alignments
probable 28S rRNA (cytosine(4447)-C(5))-methyltransferase
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
LOW QUALITY PROTEIN: liprin-alpha-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
ankyrin repeat domain-containing protein 27-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
LOW QUALITY PROTEIN: ankyrin repeat domain-containing protein 27-like
LOW QUALITY PROTEIN: integrator complex subunit 10-like
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial-like
cytochrome P450 9e2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 64 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
cytochrome P450 9e2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
LOW QUALITY PROTEIN: kelch-like protein 26
chromodomain-helicase-DNA-binding protein 7-like
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: 5 long SRA reads, 11 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
LOW QUALITY PROTEIN: trithorax group protein osa-like
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 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: DENN domain-containing protein 11-like
LOW QUALITY PROTEIN: serine/threonine-protein kinase H1-like
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: serine-rich adhesin for platelets-like
uncharacterized LOC123498322, transcript variant X1
uncharacterized LOC123498322, transcript variant X2
uncharacterized LOC123498161, transcript variant X2
uncharacterized LOC123498161, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized protein LOC123498161 isoform X2
uncharacterized protein LOC123498161 isoform X1
protein TRACHEARY ELEMENT DIFFERENTIATION-RELATED 7A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
putative inorganic phosphate cotransporter, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
putative inorganic phosphate cotransporter, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
putative inorganic phosphate cotransporter isoform X2
putative inorganic phosphate cotransporter isoform X1
uncharacterized LOC123498656, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC123498656 isoform X2
uncharacterized LOC123498656, transcript variant X1
uncharacterized LOC123498656, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123498656, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC123498656 isoform X1
uncharacterized protein LOC123498656 isoform X3
uncharacterized protein LOC123498656 isoform X4
vacuolar protein-sorting-associated protein 25-like
uncharacterized LOC123499310, 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 17 samples with support for all annotated introns
uncharacterized protein LOC123499310 isoform X2
uncharacterized LOC123499310, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123499310, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized protein LOC123499310 isoform X1
glutathione S-transferase C-terminal domain-containing protein homolog
LOW QUALITY PROTEIN: glutathione S-transferase C-terminal domain-containing protein homolog
probable transcriptional regulatory protein TTE1135
LOW QUALITY PROTEIN: probable transcriptional regulatory protein TTE1135
probable pyruvate dehydrogenase E1 component subunit alpha, mitochondrial, transcript variant X2
probable pyruvate dehydrogenase E1 component subunit alpha, mitochondrial isoform X2
probable pyruvate dehydrogenase E1 component subunit alpha, mitochondrial, transcript variant X1
probable pyruvate dehydrogenase E1 component subunit alpha, mitochondrial isoform X1
transmembrane protein adipocyte-associated 1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
transmembrane protein adipocyte-associated 1 homolog, transcript variant X2
transmembrane protein adipocyte-associated 1 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
transmembrane protein adipocyte-associated 1 homolog isoform X1
transmembrane protein adipocyte-associated 1 homolog isoform X2
STAM-binding protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
STAM-binding protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
STAM-binding protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
cytochrome c oxidase assembly protein COX11, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial-like
CD109 antigen-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 11 samples with support for all annotated introns
CD109 antigen-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 16 samples with support for all annotated introns
C-type lectin domain family 2 member L-like
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 3 samples with support for all annotated introns
C-type lectin 9a-like, transcript variant X2
C-type lectin 9a-like, transcript variant X1