Portunus trituberculatus isolate SZX2019 chromosome 26, 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\nCM030096.1.\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.
uncharacterized LOC123509051, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC123509051, transcript variant X7
uncharacterized LOC123509051, transcript variant X9
uncharacterized LOC123509051, transcript variant X5
uncharacterized LOC123509051, transcript variant X6
uncharacterized LOC123509051, transcript variant X4
uncharacterized protein LOC123509051 isoform X1
uncharacterized LOC123509051, transcript variant X2
uncharacterized LOC123509051, transcript variant X10
uncharacterized LOC123509051, transcript variant X8
uncharacterized protein LOC123509051 isoform X2
uncharacterized LOC123509052, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
uncharacterized LOC123509052, 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 50 samples with support for all annotated introns
uncharacterized LOC123509051, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein LOC123509051 isoform X3
uncharacterized LOC123509053, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
uncharacterized LOC123509053, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
uncharacterized LOC123509053, transcript variant X1
uncharacterized LOC123509053, 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 41 samples with support for all annotated introns
uncharacterized protein LOC123509053 isoform X1
uncharacterized protein LOC123509053 isoform X2
uncharacterized protein LOC123509053 isoform X3
general transcription factor II-I repeat domain-containing protein 2B-like
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: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 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 8 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 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 32 samples with support for all annotated introns
uncharacterized LOC123509058, transcript variant X3
uncharacterized LOC123509058, 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 4 samples with support for all annotated introns
uncharacterized protein LOC123509058 isoform X2
uncharacterized LOC123509058, 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 49 samples with support for all annotated introns
uncharacterized protein LOC123509058 isoform X1
uncharacterized LOC123509059, 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 2 samples with support for all annotated introns
uncharacterized LOC123509059, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC123509059, 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 11 samples with support for all annotated introns
uncharacterized LOC123509061, transcript variant X2
uncharacterized LOC123509061, transcript variant X1
uncharacterized LOC123509067, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123509067, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC123509065, transcript variant X2
uncharacterized LOC123509065, transcript variant X1
uncharacterized LOC123509063, 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 19 samples with support for all annotated introns
uncharacterized LOC123509063, 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 28 samples with support for all annotated introns
uncharacterized protein LOC123509063 isoform X2
uncharacterized protein LOC123509063 isoform X1
uncharacterized LOC123509071, transcript variant X1
uncharacterized protein LOC123509071 isoform X1
uncharacterized LOC123509071, transcript variant X2
uncharacterized protein LOC123509071 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable protein phosphatase CG10417
lethal(2) giant larvae protein homolog 1-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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: lethal(2) giant larvae protein homolog 1-like
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X3
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 16 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X2
histone-lysine N-methyltransferase SETD1A-like isoform X3
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X1
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 11 samples with support for all annotated introns
39S ribosomal protein L12, mitochondrial-like, transcript variant X1
39S ribosomal protein L12, mitochondrial-like, transcript variant X2
39S ribosomal protein L12, mitochondrial-like, transcript variant X4
39S ribosomal protein L12, mitochondrial-like, transcript variant X3
39S ribosomal protein L12, mitochondrial-like isoform X1
39S ribosomal protein L12, mitochondrial-like isoform X2
39S ribosomal protein L12, mitochondrial-like isoform X3
39S ribosomal protein L12, mitochondrial-like isoform X4
p53 and DNA damage-regulated protein 1-like, transcript variant X2
p53 and DNA damage-regulated protein 1-like, transcript variant X3
p53 and DNA damage-regulated protein 1-like, transcript variant X1
p53 and DNA damage-regulated protein 1-like isoform X2
p53 and DNA damage-regulated protein 1-like isoform X1
G patch domain and ankyrin repeat-containing protein 1 homolog
oocyte zinc finger protein XlCOF6-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like, transcript variant X5
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 4 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-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 7 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-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 12 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-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 4 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like isoform X3
oocyte zinc finger protein XlCOF6-like isoform X4
oocyte zinc finger protein XlCOF6-like isoform X1
oocyte zinc finger protein XlCOF6-like isoform X2
oocyte zinc finger protein XlCOF6-like, transcript variant X6
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 20 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like isoform X5
uncharacterized LOC123509112, transcript variant X2
uncharacterized LOC123509112, transcript variant X1
uncharacterized LOC123509112, transcript variant X4
uncharacterized LOC123509112, transcript variant X5
uncharacterized LOC123509112, transcript variant X3
U1 small nuclear ribonucleoprotein C-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 3 samples with support for all annotated introns
U1 small nuclear ribonucleoprotein C-like, transcript variant X1
U1 small nuclear ribonucleoprotein C-like
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon GAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
WW domain-containing oxidoreductase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
WW domain-containing oxidoreductase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
WW domain-containing oxidoreductase-like, transcript variant X1
WW domain-containing oxidoreductase-like
probable protein phosphatase CG10417, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
probable protein phosphatase CG10417, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
probable protein phosphatase CG10417 isoform X1
probable protein phosphatase CG10417 isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2-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
LOW QUALITY PROTEIN: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2-like
deubiquitinase DESI2-like, transcript variant X1
deubiquitinase DESI2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
BAH and coiled-coil domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 4 Proteins, and 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: 4 long SRA reads, 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA opal suppressor (anticodon UCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
delta-1-pyrroline-5-carboxylate synthase-like
regulator of G-protein signaling loco-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; deleted 1 base in 1 codon
protein TRACHEARY ELEMENT DIFFERENTIATION-RELATED 7A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: regulator of G-protein signaling loco-like
WAS/WASL-interacting protein family member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ELAV-like protein 1, transcript variant X5
ELAV-like protein 1, transcript variant X7
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ELAV-like protein 1, transcript variant X3
ELAV-like protein 1, transcript variant X6
ELAV-like protein 1, transcript variant X1
ELAV-like protein 1, transcript variant X2
ELAV-like protein 1, transcript variant X9
ELAV-like protein 1, transcript variant X11
ELAV-like protein 1, transcript variant X8
ELAV-like protein 1, transcript variant X13
ELAV-like protein 1, transcript variant X4
ELAV-like protein 1, transcript variant X12
ELAV-like protein 1, transcript variant X10
ELAV-like protein 1, transcript variant X14
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
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: RNA-binding protein 25-like
LIX1-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
LIX1-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein limb expression 1 homolog isoform X1
SR-related and CTD-associated factor 4-like, transcript variant X4
SR-related and CTD-associated factor 4-like, transcript variant X3
SR-related and CTD-associated factor 4-like, transcript variant X2
SR-related and CTD-associated factor 4-like, transcript variant X5
SR-related and CTD-associated factor 4-like, transcript variant X1
SR-related and CTD-associated factor 4-like isoform X4
SR-related and CTD-associated factor 4-like isoform X3
SR-related and CTD-associated factor 4-like isoform X2
SR-related and CTD-associated factor 4-like isoform X5
SR-related and CTD-associated factor 4-like isoform X1
peptidyl-prolyl cis-trans isomerase B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
DDB1- and CUL4-associated factor 12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
DDB1- and CUL4-associated factor 12-like, transcript variant X1
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 24 samples with support for all annotated introns
DDB1- and CUL4-associated factor 12-like
gastrula zinc finger protein XlCGF8.2DB-like
p53 and DNA damage-regulated protein 1-like, transcript variant X4
p53 and DNA damage-regulated protein 1-like, transcript variant X7
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 46 samples with support for all annotated introns
p53 and DNA damage-regulated protein 1-like, transcript variant X6
p53 and DNA damage-regulated protein 1-like, transcript variant X5
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 51 samples with support for all annotated introns
G patch domain and ankyrin repeat-containing protein 1-like isoform X1
p53 and DNA damage-regulated protein 1-like isoform X3
cleavage stimulation factor subunit 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 46 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 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: cleavage stimulation factor subunit 2-like
putative ATPase N2B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
putative ATPase N2B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
putative ATPase N2B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cystinosin homolog, transcript variant X1
cystinosin homolog, transcript variant X2
fibrous sheath CABYR-binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 5 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: 21 long SRA reads, 5 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: 21 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC123509147, transcript variant X2
uncharacterized LOC123509147, transcript variant X1
GDP-fucose transporter 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
GDP-fucose transporter 1-like, transcript variant X1
GDP-fucose transporter 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
GDP-fucose transporter 1-like isoform X1
GDP-fucose transporter 1-like isoform X2
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 10 samples with support for all annotated introns
uncharacterized LOC123509151, transcript variant X2
uncharacterized LOC123509151, transcript variant X1
U6 snRNA-associated Sm-like protein LSm8
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
LOW QUALITY PROTEIN: U6 snRNA-associated Sm-like protein LSm8
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC123509244
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
chromobox protein homolog 7-like, transcript variant X2
chromobox protein homolog 7-like, transcript variant X1
C-Jun-amino-terminal kinase-interacting protein 4-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: 11 long SRA reads, 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: C-Jun-amino-terminal kinase-interacting protein 4-like
MAM and LDL-receptor class A domain-containing protein 1-like, transcript variant X2
MAM and LDL-receptor class A domain-containing protein 1-like, transcript variant X1
MAM and LDL-receptor class A domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, 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: 3 long SRA reads, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
DNA-directed RNA polymerase I subunit RPA43-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
serine hydroxymethyltransferase-like, transcript variant X1
serine hydroxymethyltransferase-like, transcript variant X2
serine/threonine-protein kinase Nek8-like, transcript variant X1
serine/threonine-protein kinase Nek8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase Nek8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
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.
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: WW domain-binding protein 11-like
28S ribosomal protein S7, mitochondrial-like
LOW QUALITY PROTEIN: 28S ribosomal protein S7, mitochondrial-like
gastrula zinc finger protein XlCGF57.1-like, transcript variant X1
gastrula zinc finger protein XlCGF57.1-like, transcript variant X2
gastrula zinc finger protein XlCGF57.1-like, transcript variant X3
gastrula zinc finger protein XlCGF57.1-like isoform X1
gastrula zinc finger protein XlCGF57.1-like isoform X2
NEDD8-conjugating enzyme UBE2F-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
NEDD8-conjugating enzyme UBE2F-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 8 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
NEDD8-conjugating enzyme UBE2F-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 7 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
uncharacterized LOC123509175, transcript variant X1
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 12 samples with support for all annotated introns
uncharacterized LOC123509175, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
uncharacterized protein LOC123509175 isoform X2
uncharacterized protein LOC123509175 isoform X1
ubiquitin carboxyl-terminal hydrolase 36-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ubiquitin carboxyl-terminal hydrolase 36-like
peptidyl-prolyl cis-trans isomerase 6-like
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
cytosolic carboxypeptidase-like protein 5
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
vegetative cell wall protein gp1-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 6 samples with support for all annotated introns
vegetative cell wall protein gp1-like, transcript variant X2
vegetative cell wall protein gp1-like, transcript variant X1
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 39 samples with support for all annotated introns
leucine-rich repeat extensin-like protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 1-like
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein LOC123509172 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transcription initiation factor TFIID subunit 3-like isoform X2
muscle M-line assembly protein unc-89-like
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 15 samples with support for all annotated introns
ufm1-specific protease 2-like, transcript variant X3
ufm1-specific protease 2-like, transcript variant X2
ufm1-specific protease 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pentatricopeptide repeat-containing protein 2, mitochondrial-like
LOW QUALITY PROTEIN: pentatricopeptide repeat-containing protein 2, mitochondrial-like
very-long-chain 3-oxoacyl-CoA reductase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
probable serine/threonine-protein kinase dyrk2, transcript variant X1
probable serine/threonine-protein kinase dyrk2, transcript variant X2
probable serine/threonine-protein kinase dyrk2
cGMP-inhibited 3',5'-cyclic phosphodiesterase A-like, transcript variant X1
cGMP-inhibited 3',5'-cyclic phosphodiesterase A-like, transcript variant X2
cGMP-inhibited 3',5'-cyclic phosphodiesterase A-like isoform X1
cGMP-inhibited 3',5'-cyclic phosphodiesterase A-like isoform X2
mediator of DNA damage checkpoint protein 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: 5 long SRA reads, 1 Protein, 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: mediator of DNA damage checkpoint protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 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: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
equilibrative nucleoside transporter 1-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: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
LOW QUALITY PROTEIN: equilibrative nucleoside transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
hypoxia-inducible factor 1-alpha inhibitor-like, transcript variant X2
hypoxia-inducible factor 1-alpha inhibitor-like, transcript variant X1
hypoxia-inducible factor 1-alpha inhibitor-like, transcript variant X3
hypoxia-inducible factor 1-alpha inhibitor-like
uncharacterized LOC123509207, transcript variant X1
uncharacterized LOC123509207, transcript variant X2
uncharacterized protein LOC123509207 isoform X2
uncharacterized protein LOC123509207 isoform X1
uncharacterized LOC123509208, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123509208, transcript variant X1
uncharacterized LOC123509208, transcript variant X2
uncharacterized LOC123509208, transcript variant X6
uncharacterized LOC123509208, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized LOC123509208, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized protein LOC123509208 isoform X1
uncharacterized protein LOC123509208 isoform X3
uncharacterized protein LOC123509208 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized histidine-rich protein DDB_G0274557-like
uncharacterized LOC123509211, transcript variant X2
uncharacterized protein LOC123509211 isoform X2
uncharacterized LOC123509211, transcript variant X4
uncharacterized LOC123509211, transcript variant X3
uncharacterized LOC123509211, transcript variant X1
uncharacterized protein LOC123509211 isoform X3
uncharacterized protein LOC123509211 isoform X1
ATP-dependent RNA helicase WM6, transcript variant X4
ATP-dependent RNA helicase WM6, transcript variant X3
ATP-dependent RNA helicase WM6, transcript variant X2
ATP-dependent RNA helicase WM6, transcript variant X1
ATP-dependent RNA helicase WM6 isoform X2
ATP-dependent RNA helicase WM6 isoform X1
ATP-dependent RNA helicase WM6 isoform X3
ATP-dependent RNA helicase WM6 isoform X4
putative uncharacterized oxidoreductase C513.07
LOW QUALITY PROTEIN: transmembrane protein 132E-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 87% 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: 16 Proteins
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 6 samples with support for all annotated introns
methyltransferase-like protein 27, transcript variant X1
methyltransferase-like protein 27 isoform X1
methyltransferase-like protein 27, 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 15 samples with support for all annotated introns
methyltransferase-like protein 27 isoform X2
gamma-aminobutyric acid type B receptor subunit 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF123-like, transcript variant X1
E3 ubiquitin-protein ligase RNF123-like, transcript variant X2
E3 ubiquitin-protein ligase RNF123-like isoform X1
E3 ubiquitin-protein ligase RNF123-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons
LOW QUALITY PROTEIN: uncharacterized protein LOC123509268
gastrula zinc finger protein XlCGF57.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like, transcript variant X4
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-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 22 samples with support for all annotated introns
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like, transcript variant X5
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 11 samples with support for all annotated introns
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC123509335 isoform X3
uncharacterized protein LOC123509335 isoform X2
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like, transcript variant X1
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like isoform X1
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X1
putative leucine-rich repeat-containing protein DDB_G0290503 isoform X1
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X3
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X2
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X4
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X5
golgin subfamily A member 6-like protein 2 isoform X2
golgin subfamily A member 6-like protein 2 isoform X3
golgin subfamily A member 6-like protein 2 isoform 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: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: kynurenine formamidase-like
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 16 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 7-like
gastrula zinc finger protein XlCGF32.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like
methenyltetrahydrofolate synthase domain-containing 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: 3 long SRA reads, 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: methenyltetrahydrofolate synthase domain-containing protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ankyrin repeat and SOCS box protein 8-like, transcript variant X3
ankyrin repeat and SOCS box protein 8-like, transcript variant X1
ankyrin repeat and SOCS box protein 8-like, transcript variant X2
ankyrin repeat and SOCS box protein 8-like isoform X2
poly [ADP-ribose] polymerase tankyrase-2-like isoform X1
uncharacterized protein LOC123509287 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 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
LOW QUALITY PROTEIN: cell division cycle 5-like protein
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 16 samples with support for all annotated introns
probable sodium/potassium/calcium exchanger CG1090, transcript variant X1
probable sodium/potassium/calcium exchanger CG1090, transcript variant X2
probable sodium/potassium/calcium exchanger CG1090 isoform X1
probable sodium/potassium/calcium exchanger CG1090 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 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC123509314
peritrophin-48-like, transcript variant X1
peritrophin-48-like, transcript variant X2
peritrophin-48-like, transcript variant X3
uncharacterized LOC123509288, transcript variant X1
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 4 samples with support for all annotated introns
uncharacterized protein LOC123509288 isoform X1
uncharacterized LOC123509288, 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 23 samples with support for all annotated introns
uncharacterized protein LOC123509288 isoform X2
uncharacterized LOC123509292, transcript variant X2
uncharacterized LOC123509292, transcript variant X6
uncharacterized LOC123509292, transcript variant X5
uncharacterized LOC123509292, transcript variant X10
uncharacterized LOC123509292, transcript variant X4
uncharacterized LOC123509292, transcript variant X3
uncharacterized LOC123509292, transcript variant X7
uncharacterized LOC123509292, transcript variant X1
uncharacterized LOC123509292, transcript variant X9
uncharacterized LOC123509292, transcript variant X8
uncharacterized protein LOC123509292 isoform X10
uncharacterized protein LOC123509292 isoform X9
uncharacterized protein LOC123509292 isoform X4
uncharacterized protein LOC123509292 isoform X8
uncharacterized protein LOC123509292 isoform X3
uncharacterized protein LOC123509292 isoform X7
uncharacterized protein LOC123509292 isoform X1
uncharacterized protein LOC123509292 isoform X6
uncharacterized protein LOC123509292 isoform X2
uncharacterized protein LOC123509292 isoform X5
uncharacterized LOC123509295, transcript variant X1
uncharacterized LOC123509295, transcript variant X2
uncharacterized LOC123509300, transcript variant X1
uncharacterized LOC123509300, transcript variant X2
uncharacterized protein LOC123509300 isoform X1
uncharacterized protein LOC123509300 isoform X2
adhesive plaque matrix protein-like, transcript variant X3
adhesive plaque matrix protein-like, transcript variant X2
adhesive plaque matrix protein-like, transcript variant X1
adhesive plaque matrix protein-like isoform X2
adhesive plaque matrix protein-like isoform X3
adhesive plaque matrix protein-like isoform X1
gastrula zinc finger protein XlCGF46.1-like, transcript variant X4
gastrula zinc finger protein XlCGF46.1-like, transcript variant X6
gastrula zinc finger protein XlCGF46.1-like, transcript variant X3
gastrula zinc finger protein XlCGF46.1-like, transcript variant X2
gastrula zinc finger protein XlCGF46.1-like, transcript variant X1
gastrula zinc finger protein XlCGF46.1-like, transcript variant X5
gastrula zinc finger protein XlCGF46.1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: serine-protein kinase ATM-like
oocyte zinc finger protein XlCOF26-like, transcript variant X1
oocyte zinc finger protein XlCOF26-like, transcript variant X2
UPF0184 protein AAEL002161-like, transcript variant X2
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 18 samples with support for all annotated introns
UPF0184 protein AAEL002161-like, transcript variant X1
UPF0184 protein AAEL002161-like isoform X1
uncharacterized protein LOC123509305 isoform X2
mitochondrial import receptor subunit TOM22 homolog
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 31 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, 4 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
cGMP-specific 3',5'-cyclic phosphodiesterase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cGMP-specific 3',5'-cyclic phosphodiesterase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cGMP-specific 3',5'-cyclic phosphodiesterase-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 8 samples with support for all annotated introns
cGMP-specific 3',5'-cyclic phosphodiesterase-like isoform X2
cGMP-specific 3',5'-cyclic phosphodiesterase-like isoform X3
cGMP-specific 3',5'-cyclic phosphodiesterase-like isoform X1
zinc finger protein 652-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 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
zinc finger protein 652-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: GTP-binding nuclear protein Ran-like
DIS3-like exonuclease 2, transcript variant X2
DIS3-like exonuclease 2, transcript variant X1
DIS3-like exonuclease 2, transcript variant X3
DIS3-like exonuclease 2, transcript variant X4
LOW QUALITY PROTEIN: uncharacterized protein LOC123509075
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 50 samples with support for all annotated introns
melanopsin-B-like, transcript variant X5
melanopsin-B-like, transcript variant X4
melanopsin-B-like, transcript variant X1
melanopsin-B-like, transcript variant X2
melanopsin-B-like, transcript variant X3
uncharacterized protein LOC123509077 isoform X2
uncharacterized protein LOC123509077 isoform X1
uncharacterized protein LOC123509077 isoform X3
bestrophin-4-like, transcript variant X4
bestrophin-4-like, transcript variant X1
bestrophin-4-like, transcript variant X2
bestrophin-4-like, transcript variant X3
bestrophin-4-like, transcript variant X5
bestrophin-4-like, transcript variant X6
uncharacterized protein LOC123509082 isoform X1
uncharacterized protein LOC123509082 isoform X2
uncharacterized protein LOC123509082 isoform X4
bestrophin-4-like, transcript variant X7
uncharacterized protein LOC123509082 isoform X7
guanine nucleotide-binding protein subunit beta-2-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 11 samples with support for all annotated introns
guanine nucleotide-binding protein subunit beta-2-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 7 samples with support for all annotated introns
guanine nucleotide-binding protein subunit beta-2-like
procollagen-lysine,2-oxoglutarate 5-dioxygenase 2-like
LOW QUALITY PROTEIN: procollagen-lysine,2-oxoglutarate 5-dioxygenase 2-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 11 samples with support for all annotated introns
nitrilase and fragile histidine triad fusion protein NitFhit-like
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 27 samples with support for all annotated introns
uncharacterized protein LOC123509092 isoform X2
ankyrin repeat domain-containing protein 17-like, 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 4 samples with support for all annotated introns
uncharacterized LOC123509094, 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 18 samples with support for all annotated introns
uncharacterized LOC123509094, transcript variant X3
uncharacterized LOC123509094, transcript variant X4
uncharacterized LOC123509094, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain-containing protein 17-like, transcript variant X1
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 24 samples with support for all annotated introns
ankyrin repeat domain-containing protein 17-like isoform X2
ankyrin repeat domain-containing protein 17-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123509096, 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 16 samples with support for all annotated introns
uncharacterized LOC123509096, transcript variant X1
uncharacterized LOC123509096, transcript variant X3
uncharacterized LOC123509095, transcript variant X2
uncharacterized LOC123509095, transcript variant X1
uncharacterized LOC123509095, transcript variant X4
uncharacterized LOC123509095, transcript variant X3
uncharacterized protein LOC123509095 isoform X1
uncharacterized protein LOC123509095 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 87% coverage of the annotated genomic feature by RNAseq alignments
glucoside xylosyltransferase 2-like, transcript variant X3
glucoside xylosyltransferase 2-like, transcript variant X2
glucoside xylosyltransferase 2-like, transcript variant X1
glucoside xylosyltransferase 1-like isoform X1
glucoside xylosyltransferase 1-like isoform X3
glucoside xylosyltransferase 2-like isoform X2
ubiquitin carboxyl-terminal hydrolase 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 84% coverage of the annotated genomic feature by RNAseq alignments
piggyBac transposable element-derived protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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
uncharacterized LOC123509312, transcript variant X2
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 20 samples with support for all annotated introns
uncharacterized LOC123509312, transcript variant X1
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 19 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 79% coverage of the annotated genomic feature by RNAseq alignments