Portunus trituberculatus isolate SZX2019 chromosome 7, 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\nCM030077.1.\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: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
uncharacterized LOC123519676, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC123519676, transcript variant X2
deoxynucleoside triphosphate triphosphohydrolase SAMHD1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X3
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X2
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X4
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X5
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like isoform X1
uncharacterized protein LOC123519600 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
ankyrin repeat domain-containing protein 65-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 2 samples with support for all annotated introns
uncharacterized LOC123519625, transcript variant X1
uncharacterized LOC123519625, 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
uncharacterized protein LOC123519625 isoform X1
uncharacterized protein LOC123519625 isoform X2
vitellogenin receptor-like, transcript variant X2
vitellogenin receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
polycomb protein suz12-A-like, transcript variant X1
polycomb protein suz12-A-like, transcript variant X5
polycomb protein suz12-A-like, transcript variant X4
polycomb protein suz12-A-like, transcript variant X2
polycomb protein suz12-A-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 4 samples with support for all annotated introns
polycomb protein suz12-A-like, transcript variant X6
polycomb protein suz12-A-like isoform X2
polycomb protein suz12-A-like isoform X1
polycomb protein suz12-A-like isoform X5
polycomb protein suz12-A-like isoform X4
polycomb protein suz12-A-like isoform X3
polycomb protein suz12-A-like isoform X6
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X2
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X2
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X1
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X3
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X5
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X8
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X4
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X6
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X9
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X7
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X11
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X14
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X13
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X16
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X10
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X15
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X19
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X12
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X17
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X20
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X18
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X21
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X23
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X22
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X24
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X1
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X4
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X7
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X3
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X5
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X8
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X6
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X10
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X13
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X12
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X15
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X9
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X14
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X18
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X11
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X16
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X19
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X17
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X20
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X22
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X21
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X23
collagen alpha-5(IV) chain-like, transcript variant X6
collagen alpha-5(IV) chain-like, transcript variant X5
collagen alpha-5(IV) chain-like, transcript variant X4
collagen alpha-5(IV) chain-like, transcript variant X3
collagen alpha-5(IV) chain-like, transcript variant X2
collagen alpha-5(IV) chain-like, transcript variant X1
collagen alpha-5(IV) chain-like isoform X6
collagen alpha-5(IV) chain-like isoform X5
collagen alpha-5(IV) chain-like isoform X4
collagen alpha-5(IV) chain-like isoform X3
collagen alpha-5(IV) chain-like isoform X2
collagen alpha-5(IV) chain-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 11 samples with support for all annotated introns
biotin-dependent 3-methylcrotonyl-coenzyme A carboxylase beta1 subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123518930, transcript variant X1
uncharacterized LOC123518930, transcript variant X5
uncharacterized LOC123518930, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC123518930, transcript variant X2
uncharacterized LOC123518930, transcript variant X4
proline-rich receptor-like protein kinase PERK9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 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: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123520491, transcript variant X4
uncharacterized LOC123520491, transcript variant X3
uncharacterized LOC123520491, transcript variant X5
uncharacterized LOC123520491, transcript variant X1
uncharacterized LOC123520491, transcript variant X7
uncharacterized LOC123520491, transcript variant X8
uncharacterized LOC123520491, transcript variant X6
uncharacterized LOC123520491, transcript variant X9
uncharacterized LOC123520491, transcript variant X2
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: 2 long SRA reads, 1 Protein, and 56% 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: deleted 1 base in 1 codon; 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 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: uncharacterized protein LOC123520505
5'-3' exonuclease PLD3-like, transcript variant X2
5'-3' exonuclease PLD3-like, transcript variant X1
5'-3' exonuclease PLD3-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 6 samples with support for all annotated introns
solute carrier organic anion transporter family member 74D-like
protein GDAP2 homolog, transcript variant X3
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein GDAP2 homolog, transcript variant X1
protein GDAP2 homolog, transcript variant X2
protein GDAP2 homolog, transcript variant X4
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial-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
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: uncharacterized protein LOC123520561
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 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: 86% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: cuticle protein 18.6-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; 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 3 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC123520583
uncharacterized LOC123520664, transcript variant X2
uncharacterized LOC123520664, transcript variant X1
sepiapterin reductase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
sepiapterin reductase-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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
sepiapterin reductase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 7 Proteins, 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: 13 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sepiapterin reductase-like, transcript variant X4
coiled-coil and C2 domain-containing protein 1-like
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 40 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123498157, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123498157, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
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
uncharacterized LOC123498084, transcript variant X2
uncharacterized LOC123498084, transcript variant X1
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 12 samples with support for all annotated introns
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123520851, transcript variant X1
uncharacterized LOC123520851, transcript variant X2
Bardet-Biedl syndrome 10 protein homolog, transcript variant X1
Bardet-Biedl syndrome 10 protein homolog, transcript variant X5
Bardet-Biedl syndrome 10 protein homolog, transcript variant X2
Bardet-Biedl syndrome 10 protein homolog, transcript variant X4
Bardet-Biedl syndrome 10 protein homolog, transcript variant X3
Bardet-Biedl syndrome 10 protein homolog isoform X1
Bardet-Biedl syndrome 10 protein homolog isoform X2
Bardet-Biedl syndrome 10 protein homolog isoform X3
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like, transcript variant X6
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like, transcript variant X7
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like, transcript variant X5
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like, transcript variant X3
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like, transcript variant X1
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like, transcript variant X2
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like, transcript variant X4
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like isoform X5
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like isoform X3
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like isoform X1
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like isoform X2
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 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: 2 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC123498129
uncharacterized LOC123498074, transcript variant X2
uncharacterized LOC123498074, transcript variant X1
uncharacterized protein LOC123498074 isoform X2
uncharacterized protein LOC123498074 isoform X1
DNA ligase 4-like, transcript variant X2
DNA ligase 4-like, 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
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 LOC123520670
putative protein TPRXL, 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 14 samples with support for all annotated introns
putative protein TPRXL, transcript variant X2
cell wall integrity and stress response component 2-like isoform X2
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 26 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 1
myb-like protein X, transcript variant X1
myb-like protein X, transcript variant X2
activating signal cointegrator 1 complex subunit 2 homolog, transcript variant X2
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 3 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 2 homolog, transcript variant X3
activating signal cointegrator 1 complex subunit 2 homolog, transcript variant X1
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 15 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 2 homolog
uncharacterized LOC123498098, transcript variant X1
uncharacterized LOC123498098, transcript variant X4
uncharacterized LOC123498098, transcript variant X3
uncharacterized LOC123498098, transcript variant X2
ADP-ribosylation factor-like protein 8B-A
cytochrome c oxidase subunit 6A, mitochondrial-like
extracellular serine/threonine protein kinase four-jointed-like
LOW QUALITY PROTEIN: extracellular serine/threonine protein kinase four-jointed-like
ubiquitin-like modifier-activating enzyme 5
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: 10 long SRA reads, 36 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
LOW QUALITY PROTEIN: ubiquitin-like modifier-activating enzyme 5
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 40 samples with support for all annotated introns
tigger transposable element-derived protein 1-like, transcript variant X4
tigger transposable element-derived protein 1-like, transcript variant X3
tigger transposable element-derived protein 1-like, transcript variant X2
tigger transposable element-derived protein 1-like, transcript variant X1
tigger transposable element-derived protein 1-like isoform X1
tigger transposable element-derived protein 1-like isoform X2
uncharacterized LOC123498120, transcript variant X2
uncharacterized LOC123498120, 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 6 samples with support for all annotated introns
gamma-interferon-inducible lysosomal thiol reductase-like, transcript variant X4
gamma-interferon-inducible lysosomal thiol reductase-like, transcript variant X3
gamma-interferon-inducible lysosomal thiol reductase-like, transcript variant X5
gamma-interferon-inducible lysosomal thiol reductase-like, transcript variant X2
gamma-interferon-inducible lysosomal thiol reductase-like, transcript variant X1
gamma-interferon-inducible lysosomal thiol reductase-like isoform X4
gamma-interferon-inducible lysosomal thiol reductase-like isoform X3
gamma-interferon-inducible lysosomal thiol reductase-like isoform X2
gamma-interferon-inducible lysosomal thiol reductase-like isoform X1
gamma-interferon-inducible lysosomal thiol reductase-like isoform X5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 40 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: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: carbohydrate sulfotransferase 11-like
pancreatic lipase-related protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 73 long SRA reads, 15 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
carbohydrate-binding domain-containing protein C2E1P3.05c-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
EF-hand calcium-binding 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transcription initiation factor TFIID subunit 4-like, transcript variant X7
transcription initiation factor TFIID subunit 4-like, transcript variant X6
transcription initiation factor TFIID subunit 4-like, transcript variant X5
transcription initiation factor TFIID subunit 4-like, transcript variant X4
transcription initiation factor TFIID subunit 4-like, transcript variant X3
transcription initiation factor TFIID subunit 4-like, transcript variant X2
transcription initiation factor TFIID subunit 4-like, transcript variant X1
transcription initiation factor TFIID subunit 4-like isoform X4
transcription initiation factor TFIID subunit 4-like isoform X3
transcription initiation factor TFIID subunit 4-like isoform X2
transcription initiation factor TFIID subunit 4-like isoform X1
nudC domain-containing protein 3-like, transcript variant X1
nudC domain-containing protein 3-like, transcript variant X2
nudC domain-containing protein 3-like isoform X2
nudC domain-containing protein 3-like isoform X1
cilia- and flagella-associated protein 97-like
uncharacterized LOC123498493, transcript variant X2
uncharacterized LOC123498493, transcript variant X1
probable cysteine--tRNA ligase, mitochondrial
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 long SRA reads, 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable cysteine--tRNA ligase, mitochondrial
putative fatty acyl-CoA reductase CG5065
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: 10 long SRA reads, 18 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
LOW QUALITY PROTEIN: putative fatty acyl-CoA reductase CG5065
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 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
armadillo repeat-containing protein 2-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: 5 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: armadillo repeat-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 61% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123498556, transcript variant X2
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 11 samples with support for all annotated introns
uncharacterized LOC123498556, transcript variant X1
eukaryotic translation initiation factor 2 subunit 3, X-linked-like
putative helicase mov-10-B.1, transcript variant X2
putative helicase mov-10-B.1, transcript variant X3
putative helicase mov-10-B.1, transcript variant X1
putative helicase mov-10-B.1, transcript variant X5
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 39 samples with support for all annotated introns
putative helicase mov-10-B.1, transcript variant X6
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 36 samples with support for all annotated introns
putative helicase mov-10-B.1, transcript variant X4
putative helicase mov-10-B.1, transcript variant X7
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 28 samples with support for all annotated introns
putative helicase mov-10-B.1, transcript variant X8
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 18 samples with support for all annotated introns
translation initiation factor eIF-2B subunit gamma-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: translation initiation factor eIF-2B subunit gamma-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 30 samples with support for all annotated introns
Bardet-Biedl syndrome 1 protein homolog, transcript variant X1
Bardet-Biedl syndrome 1 protein homolog isoform X1
Bardet-Biedl syndrome 1 protein homolog, transcript variant X2
Bardet-Biedl syndrome 1 protein homolog isoform X2
N-acetylgalactosaminyltransferase 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase fray2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123498643, transcript variant X2
uncharacterized LOC123498643, transcript variant X1
RNA-binding protein Musashi homolog Rbp6-like, transcript variant X2
RNA-binding protein Musashi homolog Rbp6-like, transcript variant X1
RNA-binding protein Musashi homolog Rbp6-like isoform X2
RNA-binding protein Musashi homolog 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
oxysterol-binding protein 1-like, transcript variant X2
oxysterol-binding protein 1-like, transcript variant X1
oxysterol-binding protein 1-like, transcript variant X9
oxysterol-binding protein 1-like, transcript variant X6
oxysterol-binding protein 1-like, transcript variant X3
oxysterol-binding protein 1-like, transcript variant X7
oxysterol-binding protein 1-like, transcript variant X4
oxysterol-binding protein 1-like, transcript variant X5
oxysterol-binding protein 1-like, transcript variant X8
oxysterol-binding protein 1-like isoform X9
oxysterol-binding protein 1-like isoform X6
oxysterol-binding protein 1-like isoform X3
oxysterol-binding protein 1-like isoform X7
oxysterol-binding protein 1-like isoform X4
oxysterol-binding protein 1-like isoform X2
oxysterol-binding protein 1-like isoform X5
oxysterol-binding protein 1-like isoform X1
oxysterol-binding protein 1-like isoform X8
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: 25 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
LOW QUALITY PROTEIN: transmembrane protein 179-like
zinc finger protein OZF-like, transcript variant X1
zinc finger protein OZF-like, 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
LOW QUALITY PROTEIN: uncharacterized protein LOC123520341
LOW QUALITY PROTEIN: flap endonuclease 1-like
putative glutathione-specific gamma-glutamylcyclotransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 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: 3 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: delta-like protein B
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 8 bases in 4 codons; deleted 5 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 8 bases in 4 codons; deleted 5 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: F-actin-monooxygenase Mical-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; 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, 4 Proteins, and 99% 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; 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: uncharacterized protein LOC123519456
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
LOW QUALITY PROTEIN: transmembrane protein 208-like
uncharacterized LOC123519879, 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
uncharacterized LOC123519879, transcript variant X2
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
UTP--glucose-1-phosphate uridylyltransferase-like
uncharacterized LOC123519879, transcript variant X3
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 4 samples with support for all annotated introns
protein argonaute-1-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 9 samples with support for all annotated introns
protein argonaute-1-like, transcript variant X7
protein argonaute-1-like, transcript variant X8
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 5 samples with support for all annotated introns
protein argonaute-1-like, transcript variant X5
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 11 samples with support for all annotated introns
protein argonaute-1-like, transcript variant X4
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 10 samples with support for all annotated introns
protein argonaute-1-like, transcript variant X1
protein argonaute-1-like, transcript variant X2
protein argonaute-1-like, transcript variant X9
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 8 samples with support for all annotated introns
protein argonaute-1-like, transcript variant X6
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 8 samples with support for all annotated introns
mitotic apparatus protein p62-like, transcript variant X1
mitotic apparatus protein p62-like, transcript variant X2
mitotic apparatus protein p62-like isoform X1
uncharacterized protein LOC123519874 isoform X2
uncharacterized protein LOC123519887 isoform X1
tigger transposable element-derived protein 6-like
ATP-dependent RNA helicase A protein-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: 4 long SRA reads, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
LOW QUALITY PROTEIN: ATP-dependent RNA helicase A protein-like
uncharacterized LOC123519905, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123519905, transcript variant X3
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 1 sample with support for all annotated introns
uncharacterized LOC123519905, transcript variant X6
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
uncharacterized LOC123519905, transcript variant X1
uncharacterized LOC123519905, 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 6 samples with support for all annotated introns
uncharacterized protein LOC123519905 isoform X2
uncharacterized protein LOC123519905 isoform X1
uncharacterized protein LOC123519905 isoform X6
uncharacterized protein LOC123519905 isoform X4
uncharacterized protein LOC123519905 isoform X3
uncharacterized LOC123519905, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC123519905 isoform X5
uncharacterized LOC123519941, transcript variant X2
uncharacterized LOC123519941, transcript variant X1
uncharacterized LOC123519941, transcript variant X3
uncharacterized protein LOC123519941 isoform X3
uncharacterized protein LOC123519941 isoform X2
uncharacterized protein LOC123519941 isoform X1
uncharacterized LOC123519941, transcript variant X6
uncharacterized protein LOC123519941 isoform X5
uncharacterized LOC123519941, transcript variant X4
uncharacterized LOC123519941, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC123519941 isoform X4
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
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
sodium-dependent transporter bedraggled-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; deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sodium-dependent transporter bedraggled-like
COX assembly mitochondrial protein homolog, transcript variant X2
COX assembly mitochondrial protein homolog, transcript variant X1
COX assembly mitochondrial protein homolog isoform X2
COX assembly mitochondrial protein homolog isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: DNA-binding protein SMUBP-2-like
succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial-like
cytoplasmic dynein 1 light intermediate chain 2-like, transcript variant X1
cytoplasmic dynein 1 light intermediate chain 2-like, transcript variant X2
cytoplasmic dynein 1 light intermediate chain 2-like, transcript variant X3
cytoplasmic dynein 1 light intermediate chain 2-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
cytoplasmic dynein 1 light intermediate chain 2-like, transcript variant X4
cytoplasmic dynein 1 light intermediate chain 2-like, transcript variant X5
cytoplasmic dynein 1 light intermediate chain 2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
cytoplasmic dynein 1 light intermediate chain 2-like isoform X1
cytoplasmic dynein 1 light intermediate chain 2-like isoform X2
cytoplasmic dynein 1 light intermediate chain 2-like isoform X3
cytoplasmic dynein 1 light intermediate chain 2-like isoform X4
cytoplasmic dynein 1 light intermediate chain 2-like isoform X5
cytoplasmic dynein 1 light intermediate chain 2-like isoform X6
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: proteoglycan 4-like
serine/arginine-rich splicing factor 4-like, transcript variant X5
serine/arginine-rich splicing factor 4-like, transcript variant X7
serine/arginine-rich splicing factor 4-like, transcript variant X6
serine-arginine protein 55-like isoform X4
serine/arginine-rich splicing factor 4-like isoform X5
serine/arginine-rich splicing factor 4-like, transcript variant X2
serine/arginine-rich splicing factor 4-like, transcript variant X1
serine/arginine-rich splicing factor 4-like, transcript variant X3
serine/arginine-rich splicing factor 4-like, transcript variant X4
serine/arginine-rich splicing factor 6-like isoform X1
serine/arginine-rich splicing factor 4-like isoform X2
serine/arginine-rich splicing factor 6-like isoform X3
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: 4 long SRA reads, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: RNA-binding protein 25-like
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: uncharacterized protein LOC123519484
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 5 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 32 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 5 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC123520098, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC123520098, 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 93% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
uncharacterized protein LOC123520098 isoform X2
uncharacterized protein LOC123520098 isoform X1
28S ribosomal protein S18a, mitochondrial-like
transmembrane protein 209-like, transcript variant X5
transmembrane protein 209-like, transcript variant X3
transmembrane protein 209-like, transcript variant X4
transmembrane protein 209-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
transmembrane protein 209-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
cAMP-dependent protein kinase type II regulatory subunit-like
uncharacterized LOC123520157, transcript variant X1
uncharacterized LOC123520157, transcript variant X2
uncharacterized LOC123520165, transcript variant X2
uncharacterized LOC123520165, 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 4 samples with support for all annotated introns
serine/arginine repetitive matrix protein 2-like
tetraspanin-2A-like, transcript variant X5
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 2 samples with support for all annotated introns
tetraspanin-2A-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 11 samples with support for all annotated introns
tetraspanin-2A-like, transcript variant X3
tetraspanin-2A-like, transcript variant X1
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 12 samples with support for all annotated introns
tetraspanin-2A-like, transcript variant X4
uncharacterized LOC123520196, transcript variant X2
uncharacterized LOC123520196, transcript variant X3
uncharacterized LOC123520196, transcript variant X1
uncharacterized protein LOC123520196 isoform X2
uncharacterized protein LOC123520196 isoform 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 28 samples with support for all annotated introns
THO complex subunit 2-like, transcript variant X2
THO complex subunit 2-like, transcript variant X1
THO complex subunit 2-like, transcript variant X4
THO complex subunit 2-like, transcript variant X3
gonadotropin-releasing hormone II receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
membrane-bound alkaline phosphatase-like
proteoglycan 4-like, transcript variant X2
uncharacterized protein LOC123519545 isoform X2
proteoglycan 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
proteoglycan 4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized protein LOC123519545 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 12 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: UPF0764 protein C16orf89 homolog
innexin inx2-like, transcript variant X7
innexin inx2-like, transcript variant X9
innexin inx2-like, transcript variant X10
innexin inx2-like, transcript variant X5
innexin inx2-like, transcript variant X4
innexin inx2-like, transcript variant X2
innexin inx2-like, transcript variant X1
innexin inx2-like, transcript variant X8
innexin inx2-like, transcript variant X6
innexin inx2-like, transcript variant X3
cysteine-rich protein 2-binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
nucleolar and coiled-body phosphoprotein 1-like
cytochrome c oxidase subunit 7A1, mitochondrial-like
LOW QUALITY PROTEIN: cytochrome c oxidase subunit 7A1, mitochondrial-like
zinc finger protein 347-like, transcript variant X2
zinc finger protein 347-like, transcript variant X1
lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial-like
activator of 90 kDa heat shock protein ATPase homolog 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 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: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: 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
adult-specific cuticular protein ACP-20-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cuticle protein 7-like, transcript variant X2
cuticle protein 7-like, transcript variant X1
adult-specific cuticular protein ACP-22-like
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 3 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 86% coverage of the annotated genomic feature by RNAseq alignments, including 3 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: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: BRISC complex subunit Abraxas 2-like
terminal nucleotidyltransferase 5C-like, transcript variant X3
terminal nucleotidyltransferase 5C-like, transcript variant X2
terminal nucleotidyltransferase 5C-like, transcript variant X1
terminal nucleotidyltransferase 5C-like isoform X3
terminal nucleotidyltransferase 5C-like isoform X2
terminal nucleotidyltransferase 5C-like isoform X1
putative sodium-coupled neutral amino acid transporter 10
LOW QUALITY PROTEIN: putative sodium-coupled neutral amino acid transporter 10
probable arginine--tRNA ligase, mitochondrial
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 long SRA read, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: probable arginine--tRNA ligase, mitochondrial
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
uncharacterized LOC123498707, transcript variant X5
uncharacterized LOC123498707, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC123498707, 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 9 samples with support for all annotated introns
uncharacterized LOC123498707, transcript variant X3
uncharacterized LOC123498707, transcript variant X2
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 13 samples with support for all annotated introns
uncharacterized LOC123498707, transcript variant X4
uncharacterized protein LOC123498707 isoform X3
uncharacterized protein LOC123498707 isoform X1
uncharacterized protein LOC123498707 isoform X2
uncharacterized LOC123498695, transcript variant X2
uncharacterized LOC123498695, transcript variant 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC123498671
rhythmically expressed gene 5 protein-like
uncharacterized LOC123498678, 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
uncharacterized LOC123498678, transcript variant X1
uncharacterized protein LOC123498678 isoform X2
uncharacterized protein LOC123498678 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
transient receptor potential channel pyrexia-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
complement component 1 Q subcomponent-binding protein, mitochondrial-like
protein CLEC16A homolog, 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 10 samples with support for all annotated introns
protein CLEC16A homolog, transcript variant X1
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 15 samples with support for all annotated introns
protein CLEC16A homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123498423, transcript variant X3
uncharacterized LOC123498423, transcript variant X2
uncharacterized LOC123498423, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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: 4 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: drebrin-like protein B
acid phosphatase type 7-like, transcript variant X2
acid phosphatase type 7-like, transcript variant X1
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 95% 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: 100% 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns