Portunus trituberculatus isolate SZX2019 chromosome 3, 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\nCM030073.1.\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 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
tripartite motif containing 13-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
tripartite motif containing 13-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
tripartite motif containing 13-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
tripartite motif containing 13-like, transcript variant 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 47 samples with support for all annotated introns
tripartite motif containing 13-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
spindle assembly checkpoint component MAD1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
uncharacterized LOC123508107, 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 14 samples with support for all annotated introns
uncharacterized LOC123508107, 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 15 samples with support for all annotated introns
uncharacterized LOC123508107, transcript variant X3
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 6 samples with support for all annotated introns
RING finger protein 224-like, transcript variant X1
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 20 samples with support for all annotated introns
RING finger protein 224-like, 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 27 samples with support for all annotated introns
RING finger protein 224-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
RING finger protein 224-like, transcript variant X4
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
tripartite motif-containing protein 65-like
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
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 52 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 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
putative tripartite motif-containing protein 64B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
collagen alpha-1(XV) chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
collagen alpha-1(XV) chain-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 10 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 5 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 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123508155, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123508155, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 97% 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: 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
tripartite motif-containing protein 65-like, transcript variant X2
tripartite motif-containing protein 65-like, 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 12 samples with support for all annotated introns
tripartite motif-containing protein 65-like, 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 13 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM32-like isoform X1
tripartite motif-containing protein 65-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
deubiquitinase OTUD6B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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
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
zinc finger protein 771-like, transcript variant X1
zinc finger protein 771-like, transcript variant X2
deubiquitinase OTUD6B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
deubiquitinase OTUD6B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
deubiquitinase OTUD6B-like, transcript variant X4
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 41 samples with support for all annotated introns
deubiquitinase OTUD6B-like, transcript variant X6
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 33 samples with support for all annotated introns
deubiquitinase OTUD6B-like, transcript variant X5
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 34 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 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 57% coverage of the annotated genomic feature by RNAseq alignments
iron-sulfur cluster assembly 1 homolog, mitochondrial-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 21 samples with support for all annotated introns
uncharacterized LOC123510034, transcript variant X2
uncharacterized LOC123510034, transcript variant X3
uncharacterized LOC123510034, transcript variant X4
uncharacterized LOC123510034, transcript variant X1
uncharacterized protein LOC123510034 isoform X2
uncharacterized protein LOC123510034 isoform X1
uncharacterized LOC123510034, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC123510034 isoform X3
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: uncharacterized protein LOC123510044
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: 1 Protein, 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 4 samples with support for all annotated introns
uncharacterized LOC123509143, transcript variant X3
uncharacterized LOC123509143, transcript variant X4
uncharacterized LOC123509143, transcript variant X1
uncharacterized LOC123509143, transcript variant X2
uncharacterized protein LOC123509143 isoform X2
uncharacterized protein LOC123509143 isoform X3
uncharacterized protein LOC123509143 isoform X1
putative tripartite motif-containing protein 64B, 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 5 samples with support for all annotated introns
putative tripartite motif-containing protein 64B, 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
putative tripartite motif-containing protein 64B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123509181, transcript variant X1
uncharacterized LOC123509181, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
beta-1,3-galactosyltransferase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
beta-1,3-galactosyltransferase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
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, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 95% 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: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 19% 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: putative nuclease HARBI1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
probable ATP-dependent RNA helicase DDX23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 4 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable ATP-dependent RNA helicase DDX23
dendritic arbor reduction protein 1-like
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: junctional adhesion molecule 2A-like
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: diacylglycerol lipase-alpha-like
zinc finger protein OZF-like, transcript variant X3
zinc finger protein OZF-like, transcript variant X2
zinc finger protein OZF-like, transcript variant X1
zinc finger protein OZF-like, transcript variant X4
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, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: GPI inositol-deacylase-like
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
LIM domain-binding protein 2-like, transcript variant X1
LIM domain-binding protein 2-like, transcript variant X3
LIM domain-binding protein 2-like, transcript variant X5
LIM domain-binding protein 2-like, transcript variant X2
LIM domain-binding protein 2-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
LIM domain-binding protein 2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
LIM domain-binding protein 2-like, transcript variant X4
LIM domain-binding protein 2-like isoform X1
LIM domain-binding protein 2-like isoform X2
LIM domain-binding protein 2-like isoform X3
LIM domain-binding protein 2-like isoform X4
LIM domain-binding protein 2-like isoform X5
probable histone-lysine N-methyltransferase CG1716, transcript variant X1
probable histone-lysine N-methyltransferase CG1716, transcript variant X3
probable histone-lysine N-methyltransferase CG1716, transcript variant X4
probable histone-lysine N-methyltransferase CG1716, transcript variant X5
probable histone-lysine N-methyltransferase CG1716, transcript variant X2
probable histone-lysine N-methyltransferase CG1716 isoform X1
histone-lysine N-methyltransferase SETD2-like isoform X2
probable histone-lysine N-methyltransferase CG1716 isoform X3
probable histone-lysine N-methyltransferase CG1716 isoform X4
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: sushi domain-containing protein 4-like
F-box/WD repeat-containing protein 7-like, transcript variant X1
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 14 samples with support for all annotated introns
F-box/WD repeat-containing protein 7-like, 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 4 samples with support for all annotated introns
F-box/WD repeat-containing protein 7-like
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 5, mitochondrial-like
CCAAT/enhancer-binding protein gamma-like, transcript variant X3
CCAAT/enhancer-binding protein gamma-like, transcript variant X2
CCAAT/enhancer-binding protein gamma-like, transcript variant X1
CCAAT/enhancer-binding protein gamma-like
aminoacyl tRNA synthase complex-interacting multifunctional protein 1-like
spermidine synthase-like, transcript variant X1
spermidine synthase-like, transcript variant X2
solute carrier family 49 member 4 homolog
plasmanylethanolamine desaturase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
plasmanylethanolamine desaturase-like, transcript variant X2
plasmanylethanolamine desaturase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
dual specificity tyrosine-phosphorylation-regulated kinase 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
LOW QUALITY PROTEIN: dual specificity tyrosine-phosphorylation-regulated kinase 2-like
far upstream element-binding protein 3-like, transcript variant X6
far upstream element-binding protein 3-like, transcript variant X1
far upstream element-binding protein 3-like, transcript variant X2
far upstream element-binding protein 3-like, transcript variant X10
far upstream element-binding protein 3-like, transcript variant X3
far upstream element-binding protein 3-like, transcript variant X4
far upstream element-binding protein 3-like, transcript variant X13
far upstream element-binding protein 3-like, transcript variant X8
far upstream element-binding protein 3-like, transcript variant X9
far upstream element-binding protein 3-like, transcript variant X14
far upstream element-binding protein 3-like, transcript variant X11
far upstream element-binding protein 3-like, transcript variant X7
far upstream element-binding protein 3-like, transcript variant X15
far upstream element-binding protein 3-like, transcript variant X5
far upstream element-binding protein 3-like, transcript variant X12
far upstream element-binding protein 2-like isoform X1
far upstream element-binding protein 3-like isoform X9
far upstream element-binding protein 2-like isoform X5
far upstream element-binding protein 3-like isoform X13
far upstream element-binding protein 2-like isoform X2
far upstream element-binding protein 3-like isoform X10
far upstream element-binding protein 3-like isoform X3
far upstream element-binding protein 2-like isoform X6
far upstream element-binding protein 3-like isoform X14
far upstream element-binding protein 3-like isoform X4
far upstream element-binding protein 3-like isoform X11
far upstream element-binding protein 3-like isoform X12
far upstream element-binding protein 3-like isoform X7
far upstream element-binding protein 3-like isoform X8
protein krasavietz-like, transcript variant X2
protein krasavietz-like, transcript variant X4
protein krasavietz-like, transcript variant X5
protein krasavietz-like, transcript variant X1
protein krasavietz-like, transcript variant X3
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
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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
60S ribosomal protein L32-like, transcript variant X1
60S ribosomal protein L32-like, transcript variant X2
zinc finger protein 423-like, transcript variant X4
zinc finger protein 423-like, transcript variant X6
zinc finger protein 423-like, transcript variant X3
zinc finger protein 423-like, transcript variant X2
zinc finger protein 423-like, transcript variant X1
zinc finger protein 423-like, transcript variant X5
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: solute carrier family 13 member 2-like
galanin receptor 2a-like, transcript variant X2
galanin receptor 2a-like, transcript variant X1
cholecystokinin receptor type A-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein ecdysoneless homolog
GATA zinc finger domain-containing protein 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
GATA zinc finger domain-containing protein 8-like, transcript variant X2
GATA zinc finger domain-containing protein 8-like isoform X2
thymidine phosphorylase-like, transcript variant X1
thymidine phosphorylase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC123509901, transcript variant X11
uncharacterized LOC123509901, transcript variant X3
uncharacterized LOC123509901, transcript variant X14
uncharacterized LOC123509901, transcript variant X19
uncharacterized LOC123509901, transcript variant X9
uncharacterized LOC123509901, transcript variant X17
uncharacterized LOC123509901, transcript variant X12
uncharacterized LOC123509901, transcript variant X13
uncharacterized LOC123509901, transcript variant X10
uncharacterized LOC123509901, transcript variant X6
uncharacterized LOC123509901, transcript variant X8
uncharacterized LOC123509901, transcript variant X1
uncharacterized LOC123509901, transcript variant X2
uncharacterized LOC123509901, transcript variant X5
uncharacterized LOC123509901, transcript variant X18
uncharacterized LOC123509901, transcript variant X15
uncharacterized LOC123509901, transcript variant X4
uncharacterized LOC123509901, transcript variant X16
uncharacterized LOC123509901, transcript variant X7
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, 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
LOW QUALITY PROTEIN: 7-dehydrocholesterol reductase-like
bifunctional peptidase and (3S)-lysyl hydroxylase Jmjd7-like, transcript variant X3
bifunctional peptidase and (3S)-lysyl hydroxylase Jmjd7-like, transcript variant X1
bifunctional peptidase and (3S)-lysyl hydroxylase Jmjd7-like, transcript variant X2
bifunctional peptidase and (3S)-lysyl hydroxylase Jmjd7-like isoform X1
bifunctional peptidase and (3S)-lysyl hydroxylase Jmjd7-like isoform X3
bifunctional peptidase and (3S)-lysyl hydroxylase Jmjd7-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; 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 2 bases in 2 codons; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC123508640
sterol O-acyltransferase 1-like, transcript variant X1
sterol O-acyltransferase 1-like, transcript variant X2
sterol O-acyltransferase 1-like isoform X1
sterol O-acyltransferase 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
sterol O-acyltransferase 1-like, transcript variant X3
sterol O-acyltransferase 1-like isoform X3
myeloid leukemia factor-like, transcript variant X1
myeloid leukemia factor-like, transcript variant X3
myeloid leukemia factor-like, transcript variant X2
myeloid leukemia factor-like, transcript variant X4
myeloid leukemia factor-like, transcript variant X5
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 22 samples with support for all annotated introns
ribosome-recycling factor, 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: ribosome-recycling factor, mitochondrial-like
ras-related GTP-binding protein C-like, transcript variant X3
ras-related GTP-binding protein C-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
ras-related GTP-binding protein C-like, transcript variant X1
ras-related GTP-binding protein C-like isoform X3
ras-related GTP-binding protein C-like isoform X1
ras-related GTP-binding protein C-like isoform X2
uncharacterized LOC123510341, transcript variant X2
uncharacterized LOC123510341, transcript variant X1
uncharacterized protein LOC123510341 isoform X2
uncharacterized protein LOC123510341 isoform X1
uncharacterized LOC123510341, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: collagen alpha-1(I) chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
UBA-like domain-containing protein 2-B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
UBA-like domain-containing protein 2-B, 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 7 samples with support for all annotated introns
UBA-like domain-containing protein 2-B isoform X2
UBA-like domain-containing protein 2-B isoform X1
leucine-rich repeat and WD repeat-containing protein 1-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
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: leucine-rich repeat and WD repeat-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
protein lethal(2)essential for life-like, transcript variant X2
protein lethal(2)essential for life-like, transcript variant X1
protein lethal(2)essential for life-like, transcript variant X3
protein lethal(2)essential for life-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
glycine, alanine and asparagine-rich protein-like
uncharacterized LOC123507738, transcript variant X1
uncharacterized LOC123507738, transcript variant X2
LOW QUALITY PROTEIN: ATP-dependent RNA helicase DHX30-like
uncharacterized LOC123508771, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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 LOC123508779, transcript variant X1
uncharacterized LOC123508779, transcript variant X3
uncharacterized protein LOC123508779 isoform X1
uncharacterized LOC123508779, transcript variant X2
uncharacterized protein LOC123508779 isoform X3
uncharacterized protein LOC123508779 isoform X2
uncharacterized LOC123508771, transcript variant X1
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123508921, transcript variant X2
uncharacterized LOC123508921, transcript variant X1
MOXD1 homolog 2-like, transcript variant X1
MOXD1 homolog 2-like, transcript variant X2
uncharacterized LOC123508888, transcript variant X1
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 5 samples with support for all annotated introns
uncharacterized LOC123508888, transcript variant X4
uncharacterized LOC123508888, transcript variant X2
uncharacterized LOC123508888, transcript variant X3
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 10 samples with support for all annotated introns
uncharacterized LOC123508880, transcript variant X2
uncharacterized LOC123508880, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123509508, transcript variant 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 2 samples with support for all annotated introns
uncharacterized LOC123509508, transcript variant X1
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 6 samples with support for all annotated introns
uncharacterized protein LOC123509508 isoform X2
uncharacterized protein LOC123509508 isoform X1
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: 16 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: toll-like receptor 7
mediator of RNA polymerase II transcription subunit 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123510275, 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 23 samples with support for all annotated introns
uncharacterized LOC123510275, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized protein LOC123510275 isoform X1
uncharacterized protein LOC123510275 isoform X2
neuralized-like protein 2, transcript variant X1
neuralized-like protein 2, transcript variant X2
mediator of RNA polymerase II transcription subunit 12-like, transcript variant X3
mediator of RNA polymerase II transcription subunit 12-like, transcript variant X4
mediator of RNA polymerase II transcription subunit 12-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 12-like, transcript variant X2
histone-lysine N-methyltransferase 2D-like isoform X4
mediator of RNA polymerase II transcription subunit 12-like isoform X1
mediator of RNA polymerase II transcription subunit 12-like isoform X2
transcriptional repressor protein YY1-like, transcript variant X1
transcriptional repressor protein YY1-like, transcript variant X2
transcriptional repressor protein YY1-like isoform X2
transcriptional repressor protein YY1-like isoform X1
uncharacterized LOC123508863, transcript variant X1
uncharacterized LOC123508863, transcript variant X2
SH3 domain-containing protein Dlish-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 7 samples with support for all annotated introns
histone-lysine N-methyltransferase eggless-like, transcript variant X6
histone-lysine N-methyltransferase eggless-like, transcript variant X5
histone-lysine N-methyltransferase eggless-like, transcript variant X3
histone-lysine N-methyltransferase eggless-like, transcript variant X2
histone-lysine N-methyltransferase eggless-like, transcript variant X1
histone-lysine N-methyltransferase eggless-like, transcript variant X4
histone-lysine N-methyltransferase eggless-like isoform X3
histone-lysine N-methyltransferase eggless-like isoform X2
histone-lysine N-methyltransferase eggless-like isoform X1
histone-lysine N-methyltransferase eggless-like isoform X5
histone-lysine N-methyltransferase eggless-like isoform X4
uncharacterized protein C3orf18 homolog, transcript variant X1
uncharacterized protein C3orf18 homolog, transcript variant X2
mediator of RNA polymerase II transcription subunit 26-like, transcript variant X3
mediator of RNA polymerase II transcription subunit 26-like isoform X3
mediator of RNA polymerase II transcription subunit 26-like, transcript variant X7
mediator of RNA polymerase II transcription subunit 26-like, transcript variant X8
mediator of RNA polymerase II transcription subunit 26-like, transcript variant X6
mediator of RNA polymerase II transcription subunit 26-like isoform X6
mediator of RNA polymerase II transcription subunit 26-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 26-like isoform X1
mediator of RNA polymerase II transcription subunit 26-like, transcript variant X5
mediator of RNA polymerase II transcription subunit 26-like isoform X5
mediator of RNA polymerase II transcription subunit 26-like, transcript variant X4
mediator of RNA polymerase II transcription subunit 26-like isoform X4
mediator of RNA polymerase II transcription subunit 26-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 26-like isoform X2
mediator of RNA polymerase II transcription subunit 26-like isoform X7
methylosome protein 50-like, transcript variant X3
methylosome protein 50-like, transcript variant X1
methylosome protein 50-like, transcript variant X2
histone-lysine N-methyltransferase SETD1B-like
toll-interacting protein B-like, transcript variant X9
toll-interacting protein B-like isoform X2
toll-interacting protein B-like, transcript variant X7
toll-interacting protein B-like, transcript variant X1
toll-interacting protein B-like, transcript variant X2
toll-interacting protein B-like, transcript variant X5
toll-interacting protein B-like, transcript variant X8
toll-interacting protein B-like, transcript variant X6
toll-interacting protein B-like, transcript variant X3
toll-interacting protein B-like, transcript variant X4
toll-interacting protein B-like isoform X1
uncharacterized LOC123510246, transcript variant X2
uncharacterized LOC123510246, transcript variant X1
uncharacterized protein LOC123510246 isoform X1
uncharacterized protein LOC123510246 isoform X2
uncharacterized PE-PGRS family protein PE_PGRS54-like, transcript variant X1
uncharacterized PE-PGRS family protein PE_PGRS54-like, transcript variant X3
uncharacterized PE-PGRS family protein PE_PGRS54-like, transcript variant X2
uncharacterized PE-PGRS family protein PE_PGRS54-like, transcript variant X4
uncharacterized PE-PGRS family protein PE_PGRS54-like isoform X1
uncharacterized PE-PGRS family protein PE_PGRS54-like isoform X3
uncharacterized PE-PGRS family protein PE_PGRS54-like isoform X2
uncharacterized PE-PGRS family protein PE_PGRS54-like isoform X4
G8 domain-containing protein DDB_G0286311-like
uncharacterized LOC123510252, transcript variant X2
uncharacterized LOC123510252, transcript variant X1
hemicentin-2-like, transcript variant X2
hemicentin-2-like, transcript variant X1
uncharacterized protein DDB_G0271670-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 21 samples with support for all annotated introns
glutamate-gated chloride channel-like, transcript variant X2
glutamate-gated chloride channel-like, transcript variant X1
glutamate-gated chloride channel-like isoform X2
glutamate-gated chloride channel-like isoform X1
oxygen-dependent coproporphyrinogen-III oxidase-like, transcript variant X5
oxygen-dependent coproporphyrinogen-III oxidase-like, transcript variant X1
oxygen-dependent coproporphyrinogen-III oxidase-like, transcript variant X3
oxygen-dependent coproporphyrinogen-III oxidase-like, transcript variant X2
oxygen-dependent coproporphyrinogen-III oxidase-like, transcript variant X4
oxygen-dependent coproporphyrinogen-III oxidase-like
LOW QUALITY PROTEIN: uncharacterized protein LOC123508500
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: serine-rich adhesin for platelets-like
glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial-like
centrosomal protein of 55 kDa-like, transcript variant X1
centrosomal protein of 55 kDa-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
centrosomal protein of 55 kDa-like isoform X2
uncharacterized LOC123510003, transcript variant X2
uncharacterized protein LOC123510003 isoform X2
uncharacterized LOC123510003, transcript variant X1
uncharacterized LOC123510003, transcript variant X3
uncharacterized protein LOC123510003 isoform X1
uncharacterized protein LOC123510003 isoform X3
uncharacterized LOC123508602, transcript variant X1
uncharacterized LOC123508602, transcript variant X4
uncharacterized protein LOC123508602 isoform X1
uncharacterized protein LOC123508602 isoform X4
uncharacterized LOC123508602, transcript variant X3
uncharacterized protein LOC123508602 isoform X3
uncharacterized LOC123508602, transcript variant X2
uncharacterized protein LOC123508602 isoform X2
uncharacterized LOC123509599, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123509599, 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 4 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
LOW QUALITY PROTEIN: zygotic gap protein knirps-like
LOW QUALITY PROTEIN: knirps-related protein-like
uncharacterized LOC123509581, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123509581, transcript variant X2
uncharacterized protein LOC123509581 isoform X1
uncharacterized protein LOC123509581 isoform X2
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: uncharacterized protein LOC123510296
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
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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
fibrous sheath CABYR-binding protein-like
uncharacterized LOC123510097, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123510097, 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 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: deleted 2 bases 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 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC123508975
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
dynein light chain 1, cytoplasmic, transcript variant X1
dynein light chain 1, cytoplasmic isoform X1
dynein light chain 1, cytoplasmic, transcript variant X2
dynein light chain 1, cytoplasmic isoform X2
LOW QUALITY PROTEIN: protein BCCIP homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
solute carrier family 35 member F6-like, transcript variant X1
solute carrier family 35 member F6-like isoform X1
solute carrier family 35 member F6-like, transcript variant X2
solute carrier family 35 member F6-like isoform X2
LOW QUALITY PROTEIN: uncharacterized protein LOC123507699
uncharacterized LOC123510263, transcript variant X1
uncharacterized protein LOC123510263 isoform X1
uncharacterized LOC123510263, transcript variant X2
uncharacterized protein LOC123510263 isoform X2
transcription termination factor, mitochondrial-like, transcript variant X1
transcription termination factor, mitochondrial-like, transcript variant X6
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 1 sample with support for all annotated introns
transcription termination factor, mitochondrial-like, transcript variant X4
transcription termination factor, mitochondrial-like, transcript variant X5
transcription termination factor, mitochondrial-like, transcript variant X3
transcription termination factor, mitochondrial-like, transcript variant X2
uncharacterized protein LOC123510360 isoform X2
transcription termination factor, mitochondrial-like isoform X1
dehydrogenase/reductase SDR family member 12-like, transcript variant X1
dehydrogenase/reductase SDR family member 12-like, transcript variant X2
dehydrogenase/reductase SDR family member 12-like
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable chitinase 10
uncharacterized LOC123509476, transcript variant X3
uncharacterized LOC123509476, transcript variant X1
uncharacterized LOC123509476, transcript variant X2
venom phosphodiesterase-like, transcript variant X1
venom phosphodiesterase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00007
thioredoxin-dependent peroxide reductase, mitochondrial-like
spermidine synthase-like, transcript variant X3
uncharacterized LOC123507497, transcript variant X2
uncharacterized LOC123507497, transcript variant X1
uncharacterized protein LOC123507497 isoform X1
uncharacterized protein LOC123507497 isoform X2
lethal(3)malignant brain tumor-like protein 3
LOW QUALITY PROTEIN: lethal(3)malignant brain tumor-like protein 3
LOW QUALITY PROTEIN: OTU domain-containing protein 5-B-like
LOW QUALITY PROTEIN: uncharacterized protein LOC123509792
platelet-activating factor acetylhydrolase-like, transcript variant X13
platelet-activating factor acetylhydrolase-like, transcript variant X9
platelet-activating factor acetylhydrolase-like, transcript variant X10
platelet-activating factor acetylhydrolase-like, transcript variant X7
platelet-activating factor acetylhydrolase-like, transcript variant X4
platelet-activating factor acetylhydrolase-like, transcript variant X2
platelet-activating factor acetylhydrolase-like, transcript variant X11
platelet-activating factor acetylhydrolase-like, transcript variant X1
platelet-activating factor acetylhydrolase-like, transcript variant X3
platelet-activating factor acetylhydrolase-like, transcript variant X12
platelet-activating factor acetylhydrolase-like, transcript variant X8
platelet-activating factor acetylhydrolase-like, transcript variant X6
platelet-activating factor acetylhydrolase-like, transcript variant X5
platelet-activating factor acetylhydrolase-like isoform X2
platelet-activating factor acetylhydrolase-like isoform X1
lysine-specific demethylase 6A-like, transcript variant X2
lysine-specific demethylase 6A-like, transcript variant X1
lysine-specific demethylase 6A-like, transcript variant X4
lysine-specific demethylase 6A-like, transcript variant X3
lysine-specific demethylase 6A-like isoform X2
lysine-specific demethylase 6A-like isoform X1
lysine-specific demethylase 6A-like isoform X3
lysine-specific demethylase 6A-like isoform X4
FUN14 domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
FUN14 domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
FUN14 domain-containing protein 1-like, transcript variant X3
progestin and adipoQ receptor family member 3-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 1 sample with support for all annotated introns
progestin and adipoQ receptor family member 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
progestin and adipoQ receptor family member 3-like, transcript variant X1
progestin and adipoQ receptor family member 3-like, transcript variant X2
progestin and adipoQ receptor family member 3-like isoform X1
progestin and adipoQ receptor family member 3-like isoform X4
progestin and adipoQ receptor family member 3-like, transcript variant X7
progestin and adipoQ receptor family member 3-like, transcript variant X5
progestin and adipoQ receptor family member 3-like, transcript variant X4
progestin and adipoQ receptor family member 3-like isoform X5
progestin and adipoQ receptor family member 3-like isoform X2
progestin and adipoQ receptor family member 3-like isoform X3
3-ketoacyl-CoA thiolase, mitochondrial-like
uncharacterized LOC123507659, 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 8 samples with support for all annotated introns
uncharacterized LOC123507659, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
LOW QUALITY PROTEIN: transcription factor Sox-2-like
uncharacterized LOC123507688, transcript variant X2
uncharacterized LOC123507688, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123509357, transcript variant X1
uncharacterized LOC123509357, transcript variant X2
LOW QUALITY PROTEIN: uncharacterized protein LOC123509881
uncharacterized LOC123508516, 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 1 sample with support for all annotated introns
uncharacterized LOC123508516, transcript variant X1
myelin transcription factor 1-like, transcript variant X1
myelin transcription factor 1-like, transcript variant X2
myelin transcription factor 1-like isoform X1
myelin transcription factor 1-like isoform X2
proton-associated sugar transporter A-like
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
low-density lipoprotein receptor-related protein 6-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 4 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 31 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 4 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: low-density lipoprotein receptor-related protein 6-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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 15 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
acetyl-CoA acetyltransferase, mitochondrial-like, transcript variant X2
acetyl-CoA acetyltransferase, mitochondrial-like, transcript variant X1
acetyl-CoA acetyltransferase, mitochondrial-like isoform X1
acetyl-CoA acetyltransferase, mitochondrial-like isoform X2
protein still life, isoform SIF type 1-like, transcript variant X4
protein still life, isoform SIF type 1-like, transcript variant X3
protein still life, isoform SIF type 1-like, transcript variant X2
protein still life, isoform SIF type 1-like, transcript variant X7
protein still life, isoform SIF type 1-like, transcript variant X8
protein still life, isoform SIF type 1-like, transcript variant X6
protein still life, isoform SIF type 1-like, transcript variant X9
protein still life, isoform SIF type 1-like, transcript variant X1
protein still life, isoform SIF type 1-like, transcript variant X5
protein still life, isoform SIF type 1-like, transcript variant X11
protein still life, isoform SIF type 1-like, transcript variant X15
protein still life, isoform SIF type 1-like, transcript variant X12
protein still life, isoform SIF type 1-like, transcript variant X10
protein still life, isoform SIF type 1-like isoform X12
protein still life, isoform SIF type 1-like isoform X4
protein still life, isoform SIF type 1-like isoform X5
protein still life, isoform SIF type 1-like isoform X3
protein still life, isoform SIF type 1-like isoform X6
protein still life, isoform SIF type 1-like isoform X2
protein still life, isoform SIF type 1-like isoform X1
protein still life, isoform SIF type 1-like isoform X8
protein still life, isoforms C/SIF type 2-like isoform X9
protein still life, isoforms C/SIF type 2-like isoform X7
protein still life, isoform SIF type 1-like, transcript variant X13
protein still life, isoform SIF type 1-like, transcript variant X14
protein still life, isoform SIF type 1-like isoform X11
protein still life, isoform SIF type 1-like isoform X10
protein still life, isoform SIF type 1-like, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
protein still life, isoform SIF type 1-like isoform X13
protein still life, isoform SIF type 1-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: 1 Protein, and 23% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: protein still life, isoform SIF type 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC123509083
biorientation of chromosomes in cell division protein 1-like 1