Portunus trituberculatus isolate SZX2019 chromosome 36, 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\nCM030106.1.\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: 2 Proteins
52 kDa repressor of the inhibitor of the protein kinase-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 12 samples with support for all annotated introns
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like isoform X1
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like isoform X2
complex I assembly factor ACAD9, mitochondrial-like, transcript variant X1
complex I assembly factor ACAD9, mitochondrial-like, transcript variant X2
complex I assembly factor ACAD9, mitochondrial-like isoform X1
uncharacterized protein LOC123513693 isoform 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 3 samples with support for all annotated introns
uncharacterized LOC123513695, transcript variant X3
uncharacterized LOC123513695, transcript variant X2
uncharacterized LOC123513695, transcript variant X10
uncharacterized LOC123513695, transcript variant X4
uncharacterized LOC123513695, transcript variant X6
uncharacterized LOC123513695, transcript variant X5
uncharacterized LOC123513695, transcript variant X8
uncharacterized LOC123513695, transcript variant X7
uncharacterized LOC123513695, transcript variant X9
uncharacterized LOC123513695, transcript variant X1
uncharacterized protein LOC123513695 isoform X1
uncharacterized protein LOC123513695 isoform X2
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
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
C2H2 type master regulator of conidiophore development brlA-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
C2H2 type master regulator of conidiophore development brlA-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
C2H2 type master regulator of conidiophore development brlA-like isoform X2
C2H2 type master regulator of conidiophore development brlA-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123513494, 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 LOC123513494, 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 9 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 1 Protein, and 86% 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 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine/threonine-protein kinase STY46-like
Y+L amino acid transporter 2-like, transcript variant X2
Y+L amino acid transporter 2-like, transcript variant X1
monocarboxylate transporter 9-like, transcript variant X2
monocarboxylate transporter 9-like, transcript variant X1
monocarboxylate transporter 9-like isoform X1
monocarboxylate transporter 14-like isoform X2
monocarboxylate transporter 2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
monocarboxylate transporter 2-like, transcript variant X5
monocarboxylate transporter 2-like, transcript variant X2
monocarboxylate transporter 2-like, transcript variant X3
monocarboxylate transporter 2-like, transcript variant X1
monocarboxylate transporter 2-like, transcript variant X6
monocarboxylate transporter 2-like, transcript variant X4
monocarboxylate transporter 2-like isoform X1
monocarboxylate transporter 2-like isoform X2
monocarboxylate transporter 2-like isoform X3
monocarboxylate transporter 2-like, transcript variant X8
monocarboxylate transporter 5-like isoform X4
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
endocuticle structural glycoprotein ABD-5-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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: innexin shaking-B-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
dynein axonemal heavy chain 2-like, transcript variant X1
dynein axonemal heavy chain 2-like, transcript variant X2
dynein axonemal heavy chain 2-like isoform X1
dynein axonemal heavy chain 2-like, transcript variant X3
dynein axonemal heavy chain 2-like isoform X2
uncharacterized protein B0416.5-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 4 samples with support for all annotated introns
uncharacterized protein B0416.5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized protein B0416.5-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein B0416.5-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein B0416.5-like, transcript variant X9
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 9 samples with support for all annotated introns
uncharacterized protein B0416.5-like, transcript variant X8
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 2 samples with support for all annotated introns
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 9 samples with support for all annotated introns
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 13 samples with support for all annotated introns
uncharacterized protein B0416.5-like, transcript variant X4
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 7 samples with support for all annotated introns
uncharacterized protein B0416.5-like, transcript variant X3
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 11 samples with support for all annotated introns
uncharacterized protein B0416.5-like, transcript variant X6
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
solute carrier family 49 member A3-like isoform X2
uncharacterized protein B0416.5-like isoform X1
eukaryotic translation initiation factor 3 subunit D-like, transcript variant X2
eukaryotic translation initiation factor 3 subunit D-like, transcript variant X1
eukaryotic translation initiation factor 3 subunit D-like isoform X1
eukaryotic translation initiation factor 3 subunit D-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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC123513531
charged multivesicular body protein 2a-like, transcript variant X1
charged multivesicular body protein 2a-like isoform X1
charged multivesicular body protein 2a-like, transcript variant X3
charged multivesicular body protein 2a-like, transcript variant X2
charged multivesicular body protein 2a-like isoform X2
charged multivesicular body protein 2a-like isoform X3
secreted frizzled-related protein 5-like, transcript variant X2
secreted frizzled-related protein 5-like, transcript variant X1
secreted frizzled-related protein 5-like isoform X1
secreted frizzled-related protein 5-like isoform X2
uncharacterized LOC123513505, transcript variant X1
uncharacterized LOC123513505, 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
putative uncharacterized protein FLJ46204
LOW QUALITY PROTEIN: HMG box-containing protein 1-like
uncharacterized LOC123513598, transcript variant X1
uncharacterized LOC123513598, transcript variant X5
uncharacterized LOC123513598, transcript variant X4
uncharacterized LOC123513598, transcript variant X7
uncharacterized LOC123513598, transcript variant X2
uncharacterized LOC123513598, transcript variant X6
uncharacterized LOC123513598, 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 15 samples with support for all annotated introns
BTB/POZ domain-containing protein 9-like, transcript variant X1
BTB/POZ domain-containing protein 9-like, transcript variant X2
BTB/POZ domain-containing protein 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule homolog, transcript variant X3
Down syndrome cell adhesion molecule homolog, transcript variant X2
Down syndrome cell adhesion molecule homolog, transcript variant X1
Down syndrome cell adhesion molecule homolog, transcript variant X4
Down syndrome cell adhesion molecule homolog
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
hemicentin-2-like, transcript variant X1
hemicentin-2-like, transcript variant X2
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
monocarboxylate transporter 9-like, transcript variant X5
monocarboxylate transporter 9-like, transcript variant X4
monocarboxylate transporter 9-like, transcript variant X3
monocarboxylate transporter 9-like, transcript variant X6
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
leucine-rich repeat extensin-like protein 3
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: toll-like receptor Tollo
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 5 samples with support for all annotated introns
28S ribosomal protein S18c, 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
LOW QUALITY PROTEIN: 28S ribosomal protein S18c, mitochondrial-like
peroxisome biogenesis protein 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 27 samples with support for all annotated introns
peroxisome biogenesis protein 1-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 34 samples with support for all annotated introns
uncharacterized LOC123513667, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123513667, transcript variant X1
ADP-ribosylation factor-like protein 16, transcript variant X1
ADP-ribosylation factor-like protein 16, transcript variant X3
ADP-ribosylation factor-like protein 16, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel subfamily A member 1-like, transcript variant X1
transient receptor potential cation channel subfamily A member 1-like, transcript variant X3
transient receptor potential cation channel subfamily A member 1-like, transcript variant X2
transient receptor potential cation channel subfamily A member 1-like
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine/threonine-protein kinase Nek7-like, transcript variant X4
serine/threonine-protein kinase Nek7-like, transcript variant X3
serine/threonine-protein kinase Nek7-like, transcript variant X2
serine/threonine-protein kinase Nek7-like, transcript variant X1
serine/threonine-protein kinase Nek7-like
LOW QUALITY PROTEIN: protein O-mannosyltransferase 1-like
NPC intracellular cholesterol transporter 1 homolog 1b-like
uncharacterized LOC123513498, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC123513498, 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 24 samples with support for all annotated introns
uncharacterized LOC123513498, 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
uncharacterized LOC123513497, transcript variant X2
uncharacterized LOC123513497, transcript variant X1
uncharacterized protein LOC123513497 isoform X1
uncharacterized protein LOC123513497 isoform X2
uncharacterized LOC123513541, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123513541, 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 9 samples with support for all annotated introns
E3 ubiquitin-protein ligase Siah1-like, transcript variant X1
E3 ubiquitin-protein ligase Siah1-like, transcript variant X6
E3 ubiquitin-protein ligase Siah1-like, transcript variant X5
E3 ubiquitin-protein ligase Siah1-like, transcript variant X3
E3 ubiquitin-protein ligase Siah1-like, transcript variant X2
E3 ubiquitin-protein ligase Siah1-like isoform X1
E3 ubiquitin-protein ligase Siah1-like isoform X2
E3 ubiquitin-protein ligase Siah1-like isoform X4
E3 ubiquitin-protein ligase Siah1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase Siah1-like isoform X3
serine/threonine-protein kinase par-1-like
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
lactoylglutathione lyase-like, transcript variant X1
lactoylglutathione lyase-like, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: protocadherin beta-4-like
neuronal-specific septin-3-like, transcript variant X1
neuronal-specific septin-3-like, transcript variant X2
neuronal-specific septin-3-like isoform X1
neuronal-specific septin-3-like isoform X2
protein piccolo-like, transcript variant X2
protein piccolo-like, transcript variant X3
protein piccolo-like, transcript variant X5
protein piccolo-like, transcript variant X1
protein piccolo-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 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, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123513603, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC123513603, 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 11 samples with support for all annotated introns
uncharacterized LOC123513603, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123513603, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized protein LOC123513603 isoform X1
uncharacterized protein LOC123513603 isoform X4
uncharacterized protein LOC123513603 isoform X2
uncharacterized protein LOC123513603 isoform X3
uncharacterized LOC123513684, transcript variant X1
uncharacterized LOC123513684, transcript variant X4
uncharacterized LOC123513684, transcript variant X2
uncharacterized LOC123513684, transcript variant X5
uncharacterized LOC123513684, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich repeat extensin-like protein 6
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X9
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X11
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X12
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X14
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X7
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X10
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X8
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X13
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 16-like isoform X6
ubiquitin carboxyl-terminal hydrolase 16-like isoform X8
ubiquitin carboxyl-terminal hydrolase 16-like isoform X3
ubiquitin carboxyl-terminal hydrolase 16-like isoform X11
ubiquitin carboxyl-terminal hydrolase 16-like isoform X9
ubiquitin carboxyl-terminal hydrolase 16-like isoform X4
ubiquitin carboxyl-terminal hydrolase 16-like isoform X7
ubiquitin carboxyl-terminal hydrolase 16-like isoform X2
ubiquitin carboxyl-terminal hydrolase 16-like isoform X5
ubiquitin carboxyl-terminal hydrolase 16-like isoform X10
ubiquitin carboxyl-terminal hydrolase 16-like isoform X1
vacuolar protein-sorting-associated protein 36-like
elongation factor G, mitochondrial-like, transcript variant X3
elongation factor G, mitochondrial-like, transcript variant X2
elongation factor G, mitochondrial-like, transcript variant X1
elongation factor G, mitochondrial-like isoform X1
elongation factor G, mitochondrial-like isoform X2
elongation factor G, mitochondrial-like isoform X3
proteoglycan 4-like, transcript variant X3
proteoglycan 4-like, transcript variant X1
proteoglycan 4-like, transcript variant X2
muscle M-line assembly protein unc-89-like isoform X3
pyruvate dehydrogenase E1 component subunit beta, mitochondrial-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 5 samples with support for all annotated introns
indolethylamine N-methyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
thioredoxin domain-containing protein 11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
thioredoxin domain-containing protein 11-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
thioredoxin domain-containing protein 11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
thioredoxin domain-containing protein 11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
thioredoxin domain-containing protein 11-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 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
thioredoxin domain-containing protein 11-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
thioredoxin domain-containing protein 11-like isoform X1
thioredoxin domain-containing protein 11-like isoform X6
thioredoxin domain-containing protein 11-like isoform X2
thioredoxin domain-containing protein 11-like isoform X3
thioredoxin domain-containing protein 11-like isoform X4
thioredoxin domain-containing protein 11-like isoform X5
uncharacterized LOC123513388, transcript variant X5
uncharacterized LOC123513388, transcript variant X3
uncharacterized LOC123513388, transcript variant X2
uncharacterized LOC123513388, transcript variant X1
uncharacterized LOC123513388, transcript variant X4
mediator of RNA polymerase II transcription subunit 13-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 13-like, transcript variant X3
mediator of RNA polymerase II transcription subunit 13-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 13-like, transcript variant X4
mediator of RNA polymerase II transcription subunit 13-like, transcript variant X5
mediator of RNA polymerase II transcription subunit 13-like isoform X3
mediator of RNA polymerase II transcription subunit 13-like isoform X2
mediator of RNA polymerase II transcription subunit 13-like isoform X1
mediator of RNA polymerase II transcription subunit 13-like isoform X4
mediator of RNA polymerase II transcription subunit 13-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123513396, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123513396, 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
xenotropic and polytropic retrovirus receptor 1-like
LOW QUALITY PROTEIN: xenotropic and polytropic retrovirus receptor 1-like
uncharacterized LOC123513399, transcript variant X4
uncharacterized LOC123513399, transcript variant X2
uncharacterized LOC123513399, transcript variant X3
uncharacterized LOC123513399, transcript variant X1
transcription factor HIVEP3-like, transcript variant X2
transcription factor HIVEP3-like, transcript variant X1
WD repeat-containing protein 48-like, transcript variant X2
WD repeat-containing protein 48-like, transcript variant X3
WD repeat-containing protein 48-like, transcript variant X1
WD repeat-containing protein 48-like isoform X2
WD repeat-containing protein 48-like isoform X1
armadillo repeat-containing protein 8-like, transcript variant X1
armadillo repeat-containing protein 8-like, transcript variant X2
armadillo repeat-containing protein 8-like isoform X1
armadillo repeat-containing protein 8-like isoform X2
armadillo repeat-containing protein 8-like, transcript variant X3
armadillo repeat-containing protein 8-like isoform X3
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 7 samples with support for all annotated introns
putative uncharacterized protein DDB_G0283051
homeobox protein extradenticle-like, transcript variant X5
homeobox protein extradenticle-like, transcript variant X2
homeobox protein extradenticle-like, transcript variant X6
homeobox protein extradenticle-like, transcript variant X7
homeobox protein extradenticle-like, transcript variant X4
homeobox protein extradenticle-like, transcript variant X3
homeobox protein extradenticle-like, transcript variant X1
homeobox protein extradenticle-like, transcript variant X8
homeobox protein extradenticle-like isoform X4
homeobox protein extradenticle-like isoform X5
homeobox protein extradenticle-like isoform X6
homeobox protein extradenticle-like isoform X1
homeobox protein extradenticle-like isoform X2
homeobox protein extradenticle-like isoform X3
uncharacterized LOC123513741, transcript variant X2
uncharacterized LOC123513741, transcript variant X3
uncharacterized LOC123513741, transcript variant X1
uncharacterized protein LOC123513741 isoform X2
uncharacterized protein LOC123513741 isoform X3
uncharacterized protein LOC123513741 isoform X1
uncharacterized LOC123513554, transcript variant X3
uncharacterized LOC123513554, transcript variant X2
uncharacterized LOC123513554, transcript variant X1
nucleolar complex protein 3 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 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
nucleolar complex protein 3 homolog, transcript variant X1
uncharacterized LOC123513705, transcript variant X1
uncharacterized LOC123513705, transcript variant X2
uncharacterized protein LOC123513705 isoform X1
uncharacterized protein LOC123513705 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
histone-lysine N-methyltransferase 2B-like
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fibroblast growth factor receptor-like 1
LOW QUALITY PROTEIN: fibroblast growth factor receptor-like 1
probable ATP-dependent DNA helicase HFM1
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
uncharacterized LOC123513407, transcript variant X1
uncharacterized LOC123513407, transcript variant X2
uncharacterized protein LOC123513407 isoform X1
uncharacterized protein LOC123513407 isoform X2
acyl-coenzyme A thioesterase 1-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 13 samples with support for all annotated introns
acyl-coenzyme A thioesterase 1-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 23 samples with support for all annotated introns
protein melted-like, transcript variant X2
protein melted-like, transcript variant X6
protein melted-like, transcript variant X5
protein melted-like, transcript variant X4
protein melted-like, transcript variant X1
protein melted-like, transcript variant X3
lysine-rich arabinogalactan protein 19-like
mitoferrin-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
mitoferrin-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
zinc finger protein 143-like, 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 1 sample with support for all annotated introns
zinc finger protein 143-like, transcript variant X5
zinc finger protein 143-like, transcript variant X4
zinc finger protein 143-like, transcript variant X3
zinc finger protein 143-like, transcript variant X1
lysophospholipid acyltransferase 5-like, transcript variant X2
lysophospholipid acyltransferase 5-like, transcript variant X1
lysophospholipid acyltransferase 5-like, transcript variant X3
lysophospholipid acyltransferase 5-like isoform X2
lysophospholipid acyltransferase 5-like isoform X1
lysophospholipid acyltransferase 5-like isoform X3
uncharacterized LOC123513565, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC123513565, transcript variant X3
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 10 samples with support for all annotated introns
uncharacterized LOC123513565, transcript variant X1
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 20 samples with support for all annotated introns
uncharacterized LOC123513565, transcript variant X4
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 4 samples with support for all annotated introns
arginine--tRNA ligase, cytoplasmic-like, transcript variant X1
arginine--tRNA ligase, cytoplasmic-like, transcript variant X2
arginine--tRNA ligase, cytoplasmic-like isoform X1
arginine--tRNA ligase, cytoplasmic-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
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.
tyrosine-protein kinase HTK16-like, transcript variant X2
tyrosine-protein kinase HTK16-like, transcript variant X1
sodium leak channel non-selective protein-like, transcript variant X1
sodium leak channel non-selective protein-like, transcript variant X4
sodium leak channel non-selective protein-like, transcript variant X2
sodium leak channel non-selective protein-like, transcript variant X3
sodium leak channel non-selective protein-like isoform X1
sodium leak channel non-selective protein-like isoform X2
thymidylate synthase-like, transcript variant X12
thymidylate synthase-like, transcript variant X10
thymidylate synthase-like, transcript variant X11
thymidylate synthase-like, transcript variant X13
thymidylate synthase-like, transcript variant X8
thymidylate synthase-like, transcript variant X9
thymidylate synthase-like, transcript variant X1
thymidylate synthase-like, transcript variant X7
thymidylate synthase-like, transcript variant X3
thymidylate synthase-like, transcript variant X4
thymidylate synthase-like, transcript variant X6
thymidylate synthase-like, transcript variant X5
thymidylate synthase-like, transcript variant X2
protein TRACHEARY ELEMENT DIFFERENTIATION-RELATED 7A-like
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
LOW QUALITY PROTEIN: uncharacterized protein LOC123513663
monocarboxylate transporter 14-like, transcript variant X1
monocarboxylate transporter 14-like, transcript variant X2
monocarboxylate transporter 14-like isoform X1
LOW QUALITY PROTEIN: alpha-1-inhibitor 3-like
serine/arginine repetitive matrix protein 1-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1-like, transcript variant X11
serine/arginine repetitive matrix protein 1-like, transcript variant X10
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
serine/arginine repetitive matrix protein 1-like, transcript variant X1
serine/arginine repetitive matrix protein 1-like, transcript variant X2
serine/arginine repetitive matrix protein 1-like, transcript variant X4
serine/arginine repetitive matrix protein 1-like, transcript variant X5
serine/arginine repetitive matrix protein 1-like, transcript variant X3
serine/arginine repetitive matrix protein 1-like, transcript variant X8
serine/arginine repetitive matrix protein 1-like, transcript variant X6
serine/arginine repetitive matrix protein 1-like, transcript variant X7
serine/arginine repetitive matrix protein 1-like
chorion peroxidase-like, transcript variant X2
chorion peroxidase-like, transcript variant X1
chorion peroxidase-like, transcript variant X3
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein singles bar-like, transcript variant X1
protein singles bar-like, transcript variant X2
elongation factor Ts, mitochondrial-like, transcript variant X1
elongation factor Ts, mitochondrial-like isoform X1
elongation factor Ts, mitochondrial-like, transcript variant X2
elongation factor Ts, mitochondrial-like isoform X2
RNA-binding protein pno1-like, transcript variant X2
RNA-binding protein pno1-like, transcript variant X1
RNA-binding protein pno1-like isoform X1
RNA-binding protein pno1-like isoform X2
flocculation protein FLO11-like, transcript variant X2
flocculation protein FLO11-like, transcript variant X1
flocculation protein FLO11-like isoform X2
uncharacterized protein LOC123513736 isoform X1
methylthioribose-1-phosphate isomerase-like, transcript variant X1
methylthioribose-1-phosphate isomerase-like, transcript variant X4
methylthioribose-1-phosphate isomerase-like, transcript variant X3
methylthioribose-1-phosphate isomerase-like, transcript variant X2
methylthioribose-1-phosphate isomerase-like
probable cationic amino acid transporter, 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 13 samples with support for all annotated introns
probable cationic amino acid transporter, 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 12 samples with support for all annotated introns
cationic amino acid transporter 2-like isoform X1
probable cationic amino acid transporter 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 40 samples with support for all annotated introns
28S ribosomal protein S9, mitochondrial-like
zinc finger protein 8-like, transcript variant X9
zinc finger protein 8-like, transcript variant X2
zinc finger protein 8-like, transcript variant X1
zinc finger protein 8-like, transcript variant X5
zinc finger protein 8-like, transcript variant X4
zinc finger and SCAN domain-containing protein 22-like isoform X1
zinc finger protein squeeze-like isoform X4
zinc finger protein 8-like, transcript variant X3
zinc finger protein 8-like, transcript variant X6
zinc finger protein 8-like, transcript variant X8
zinc finger protein 8-like, transcript variant X7
zinc finger protein 8-like, transcript variant X10
zinc finger and SCAN domain-containing protein 22-like isoform X3
zinc finger and SCAN domain-containing protein 22-like isoform X6
putative protein MSS51 homolog, mitochondrial, transcript variant X1
putative protein MSS51 homolog, mitochondrial isoform X1
putative protein MSS51 homolog, mitochondrial, transcript variant X2
putative protein MSS51 homolog, mitochondrial isoform X2
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial-like
QRFP-like peptide receptor, transcript variant X4
QRFP-like peptide receptor, transcript variant X6
QRFP-like peptide receptor, transcript variant X2
QRFP-like peptide receptor, transcript variant X3
QRFP-like peptide receptor, transcript variant X5
QRFP-like peptide receptor, transcript variant X1
general vesicular transport factor p115-like, transcript variant X2
general vesicular transport factor p115-like, transcript variant X1
general vesicular transport factor p115-like, transcript variant X3
general vesicular transport factor p115-like isoform X2
general vesicular transport factor p115-like isoform X1
general vesicular transport factor p115-like isoform X3
RISC-loading complex subunit tarbp2-like, transcript variant X2
RISC-loading complex subunit tarbp2-like, transcript variant X4
RISC-loading complex subunit tarbp2-like, transcript variant X5
RISC-loading complex subunit tarbp2-like, transcript variant X1
RISC-loading complex subunit tarbp2-like, transcript variant X3
RISC-loading complex subunit tarbp2-like isoform X1
RISC-loading complex subunit tarbp2-like isoform X2
RISC-loading complex subunit tarbp2-like isoform X3
transmembrane protein 184B-like, transcript variant X2
transmembrane protein 184B-like, transcript variant X3
transmembrane protein 184B-like, transcript variant X1
transmembrane protein 184B-like, transcript variant X4
transmembrane protein 184B-like, transcript variant X5
transmembrane protein 184B-like isoform X3
transmembrane protein 184B-like isoform X1
transmembrane protein 184B-like isoform X2
transfer RNA asparagine (anticodon GUU); 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
LOW QUALITY PROTEIN: nucleoporin GLE1-like
proline-rich receptor-like protein kinase PERK2
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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123513409, 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123513409, transcript variant X4
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 6 samples with support for all annotated introns
uncharacterized LOC123513409, transcript variant X3
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
uncharacterized LOC123513409, 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 3 samples with support for all annotated introns
uncharacterized LOC123513409, transcript variant X2
uncharacterized protein LOC123513409 isoform X3
uncharacterized protein LOC123513409 isoform X1
uncharacterized protein LOC123513409 isoform X2
uncharacterized protein LOC123513409 isoform X4
tyrosine-protein phosphatase 69D-like, transcript variant X4
tyrosine-protein phosphatase 69D-like, transcript variant X5
tyrosine-protein phosphatase 69D-like, transcript variant X2
tyrosine-protein phosphatase 69D-like, transcript variant X3
tyrosine-protein phosphatase 69D-like, transcript variant X1
tyrosine-protein phosphatase 69D-like, transcript variant X6
tyrosine-protein phosphatase 69D-like isoform X4
tyrosine-protein phosphatase 69D-like isoform X5
tyrosine-protein phosphatase 69D-like isoform X2
tyrosine-protein phosphatase 69D-like isoform X3
tyrosine-protein phosphatase 69D-like isoform X1
tyrosine-protein phosphatase 69D-like isoform X6
transcription initiation protein SPT3 homolog, transcript variant X1
transcription initiation protein SPT3 homolog, transcript variant X2
transcription initiation protein SPT3 homolog isoform X1
transcription initiation protein SPT3 homolog isoform X2
plasma membrane calcium-transporting ATPase 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 4-like, transcript variant X3
plasma membrane calcium-transporting ATPase 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 4-like
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase P-like
intraflagellar transport protein 57 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
ecdysone-induced protein 78C-like, transcript variant X5
ecdysone-induced protein 78C-like, transcript variant X3
ecdysone-induced protein 78C-like, transcript variant X4
ecdysone-induced protein 78C-like isoform X3
ecdysone-induced protein 78C-like, transcript variant X1
ecdysone-induced protein 78C-like, transcript variant X2
ecdysone-induced protein 78C-like isoform X1
ecdysone-induced protein 78C-like isoform X2
LOW QUALITY PROTEIN: uncharacterized protein C3orf38 homolog
uncharacterized LOC123513423, 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 25 samples with support for all annotated introns
uncharacterized LOC123513423, 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 23 samples with support for all annotated introns
uncharacterized LOC123513423, transcript variant X4
uncharacterized LOC123513423, 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 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC123513425, transcript variant X10
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 1 sample with support for all annotated introns
uncharacterized LOC123513425, transcript variant X1
uncharacterized LOC123513425, transcript variant X2
uncharacterized LOC123513425, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123513425, transcript variant X6
uncharacterized LOC123513425, transcript variant X8
uncharacterized LOC123513427, 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 3 samples with support for all annotated introns
uncharacterized LOC123513427, 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 5 samples with support for all annotated introns
uncharacterized LOC123513427, 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 6 samples with support for all annotated introns
uncharacterized LOC123513425, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123513425, transcript variant X3
uncharacterized LOC123513425, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123513425, 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 9 samples with support for all annotated introns
uncharacterized LOC123513429, 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 LOC123513429, transcript variant X2
uncharacterized LOC123513430, 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 2 samples with support for all annotated introns
uncharacterized LOC123513430, transcript variant X4
uncharacterized LOC123513430, transcript variant X1
uncharacterized LOC123513430, transcript variant X2
uncharacterized LOC123513426, transcript variant X3
uncharacterized LOC123513426, transcript variant X5
uncharacterized LOC123513426, transcript variant X7
uncharacterized LOC123513426, transcript variant X4
uncharacterized LOC123513426, transcript variant X8
uncharacterized LOC123513426, transcript variant X6
uncharacterized LOC123513426, transcript variant X2
uncharacterized LOC123513426, transcript variant X1
uncharacterized LOC123513436, transcript variant X2
uncharacterized LOC123513436, transcript variant X1
uncharacterized LOC123513435, transcript variant X2
uncharacterized LOC123513435, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC123513578
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
follicle-stimulating hormone receptor-like, transcript variant X3
follicle-stimulating hormone receptor-like, transcript variant X2
follicle-stimulating hormone receptor-like, transcript variant X1
follicle-stimulating hormone receptor-like, transcript variant X4
follicle-stimulating hormone receptor-like isoform X1
follicle-stimulating hormone receptor-like isoform X2
E3 ubiquitin-protein ligase RING1-like, transcript variant X2
E3 ubiquitin-protein ligase RING1-like, transcript variant X1
LOW QUALITY PROTEIN: 40S ribosomal protein S3a-like
hyaluronan mediated motility receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123513613, transcript variant X1
uncharacterized LOC123513613, transcript variant X3
uncharacterized LOC123513613, transcript variant X2
uncharacterized protein LOC123513613 isoform X1
uncharacterized protein LOC123513613 isoform X2
heat shock protein 67B1-like, transcript variant X2
heat shock protein 67B1-like, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: palmitoyltransferase ZDHHC17-like
heparan-alpha-glucosaminide N-acetyltransferase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
heparan-alpha-glucosaminide N-acetyltransferase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
heparan-alpha-glucosaminide N-acetyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
tubulin--tyrosine ligase-like protein 12
LOW QUALITY PROTEIN: tubulin--tyrosine ligase-like protein 12
LIM/homeobox protein Lhx9-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LIM/homeobox protein Lhx9-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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
LIM/homeobox protein Lhx9-like isoform X1
LIM/homeobox protein Lhx9-like isoform X2
LIM/homeobox protein Lhx9-like, transcript variant X3
uncharacterized LOC123513629, transcript variant X1
uncharacterized LOC123513629, transcript variant X2
bifunctional purine biosynthesis protein ATIC-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 21 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
CCR4-NOT transcription complex subunit 9-like
LOW QUALITY PROTEIN: CCR4-NOT transcription complex subunit 9-like
LOW QUALITY PROTEIN: ribonuclease 3-like
uncharacterized LOC123513638, transcript variant X2
uncharacterized LOC123513638, transcript variant X1
uncharacterized protein LOC123513638 isoform X2
uncharacterized protein LOC123513638 isoform X1
uncharacterized LOC123513639, transcript variant X8
uncharacterized LOC123513639, transcript variant X1
uncharacterized LOC123513639, transcript variant X3
uncharacterized LOC123513639, transcript variant X2
uncharacterized LOC123513639, transcript variant X7
uncharacterized LOC123513639, transcript variant X6
uncharacterized LOC123513639, transcript variant X4
uncharacterized protein LOC123513639 isoform X1
uncharacterized LOC123513639, transcript variant X5
uncharacterized protein LOC123513639 isoform X2
uncharacterized protein LOC123513639 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons
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: tyrosine-protein kinase Abl-like
rho GTPase-activating protein 1-like, transcript variant X3
rho GTPase-activating protein 1-like, transcript variant X1
rho GTPase-activating protein 1-like, transcript variant X4
rho GTPase-activating protein 1-like, transcript variant X2
rho GTPase-activating protein 1-like isoform X3
rho GTPase-activating protein 8-like isoform X1
rho GTPase-activating protein 1-like isoform X4
rho GTPase-activating protein 8-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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
vacuolar protein sorting-associated protein 41 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: venom serine carboxypeptidase-like
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 3 samples with support for all annotated introns
class E basic helix-loop-helix protein 22-like, transcript variant X3
class E basic helix-loop-helix protein 22-like, transcript variant X1
class E basic helix-loop-helix protein 22-like, transcript variant X2
class E basic helix-loop-helix protein 22-like isoform X1
class E basic helix-loop-helix protein 22-like, transcript variant X4
class E basic helix-loop-helix protein 22-like isoform X2
uncharacterized LOC123513645, transcript variant X2
uncharacterized LOC123513645, transcript variant X3
uncharacterized LOC123513645, transcript variant X1
uncharacterized protein LOC123513645 isoform X1
uncharacterized protein LOC123513645 isoform X2
uncharacterized protein LOC123513645 isoform X3
uncharacterized LOC123513648, transcript variant X1
uncharacterized LOC123513648, transcript variant X3
uncharacterized LOC123513648, transcript variant X2
uncharacterized protein LOC123513648 isoform X1
uncharacterized protein LOC123513648 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: Y+L amino acid transporter 2-like
dynein axonemal intermediate chain 4-like, transcript variant X1
dynein axonemal intermediate chain 4-like, transcript variant X2
dynein axonemal intermediate chain 4-like
LOW QUALITY PROTEIN: uncharacterized protein LOC123513653
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 78% coverage of the annotated genomic feature by RNAseq alignments
alpha-2-macroglobulin-like protein 1, transcript variant X6
alpha-2-macroglobulin-like protein 1, transcript variant X1
alpha-2-macroglobulin-like protein 1, transcript variant X4
alpha-2-macroglobulin-like protein 1, transcript variant X9
alpha-2-macroglobulin-like protein 1, transcript variant X5
alpha-2-macroglobulin-like protein 1, transcript variant X7
alpha-2-macroglobulin-like protein 1, transcript variant X2
alpha-2-macroglobulin-like protein 1, transcript variant X8
alpha-2-macroglobulin-like protein 1, transcript variant X3
alpha-2-macroglobulin-like protein 1 isoform X1
alpha-2-macroglobulin-like protein 1 isoform X4
alpha-2-macroglobulin-like protein 1 isoform X9
alpha-2-macroglobulin-like protein 1 isoform X5
alpha-2-macroglobulin-like protein 1 isoform X7
alpha-2-macroglobulin-like protein 1 isoform X2
alpha-2-macroglobulin-like protein 1 isoform X8
alpha-2-macroglobulin-like protein 1 isoform X3
WD repeat-containing protein 3-like, transcript variant X1
WD repeat-containing protein 3-like isoform X1
WD repeat-containing protein 3-like, transcript variant X2
WD repeat-containing protein 3-like isoform X2
protein hu-li tai shao-like, transcript variant X2
protein hu-li tai shao-like, transcript variant X12
protein hu-li tai shao-like, transcript variant X14
protein hu-li tai shao-like, transcript variant X18
protein hu-li tai shao-like, transcript variant X19
protein hu-li tai shao-like, transcript variant X1
protein hu-li tai shao-like, transcript variant X4
protein hu-li tai shao-like, transcript variant X6
protein hu-li tai shao-like, transcript variant X5
protein hu-li tai shao-like, transcript variant X7
protein hu-li tai shao-like, transcript variant X9
protein hu-li tai shao-like, transcript variant X10
protein hu-li tai shao-like, transcript variant X8
protein hu-li tai shao-like, transcript variant X11
protein hu-li tai shao-like, transcript variant X13
protein hu-li tai shao-like, transcript variant X16
protein hu-li tai shao-like, transcript variant X15
protein hu-li tai shao-like, transcript variant X17
protein hu-li tai shao-like, 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; deleted 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 1 base in 1 codon; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
regulator of G-protein signaling 20-like, transcript variant X1
regulator of G-protein signaling 20-like, transcript variant X2
regulator of G-protein signaling 17-like isoform X1
regulator of G-protein signaling 20-like, transcript variant X3
regulator of G-protein signaling 20-like isoform X2
zinc finger CCCH domain-containing protein 10-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, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC123513710
17-beta-hydroxysteroid dehydrogenase 13-like
transfer RNA valine (anticodon GAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
short-chain dehydrogenase/reductase family 16C member 6-like, transcript variant X2
short-chain dehydrogenase/reductase family 16C member 6-like, transcript variant X1
short-chain dehydrogenase/reductase family 16C member 6-like isoform X2
short-chain dehydrogenase/reductase family 16C member 6-like isoform X1
epidermal retinol dehydrogenase 2-like, transcript variant X2
epidermal retinol dehydrogenase 2-like, transcript variant X1
epidermal retinol dehydrogenase 2-like, transcript variant X3
epidermal retinol dehydrogenase 2-like isoform X2
N-acetylgalactosaminyltransferase 7-like, transcript variant X3
N-acetylgalactosaminyltransferase 7-like, transcript variant X1
N-acetylgalactosaminyltransferase 7-like, transcript variant X2
N-acetylgalactosaminyltransferase 7-like isoform X1
N-acetylgalactosaminyltransferase 7-like isoform X2
N-acetylgalactosaminyltransferase 7-like isoform X3
proline-rich protein 36-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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
proline-rich protein 36-like, transcript variant X1
RNA N6-adenosine-methyltransferase METTL16-like, transcript variant X2
RNA N6-adenosine-methyltransferase METTL16-like, transcript variant X1
RNA N6-adenosine-methyltransferase METTL16-like isoform X2
RNA N6-adenosine-methyltransferase METTL16-like isoform X1
cell division cycle 7-related protein kinase-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 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: cell division cycle 7-related protein kinase-like
zinc finger FYVE domain-containing protein 21-like, transcript variant X3
zinc finger FYVE domain-containing protein 21-like, transcript variant X1
zinc finger FYVE domain-containing protein 21-like, transcript variant X2
zinc finger FYVE domain-containing protein 21-like isoform X1
zinc finger FYVE domain-containing protein 21-like isoform X2
zinc finger FYVE domain-containing protein 21-like isoform X3
Y+L amino acid transporter 2-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Y+L amino acid transporter 2-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Y+L amino acid transporter 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Y+L amino acid transporter 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Y+L amino acid transporter 2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Y+L amino acid transporter 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC123513592
sodium-dependent noradrenaline transporter-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
fat-like cadherin-related tumor suppressor homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: fat-like cadherin-related tumor suppressor homolog
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon AGC); 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 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
LOW QUALITY PROTEIN: proline-rich extensin-like protein EPR1
N-sulphoglucosamine sulphohydrolase-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, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
LOW QUALITY PROTEIN: N-sulphoglucosamine sulphohydrolase-like
hairy/enhancer-of-split related with YRPW motif protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein LOC123513544 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123513748, transcript variant X1
uncharacterized LOC123513748, transcript variant X2
cancer-related nucleoside-triphosphatase homolog, transcript variant X2
cancer-related nucleoside-triphosphatase homolog, transcript variant X1
cancer-related nucleoside-triphosphatase homolog
NFX1-type zinc finger-containing protein 1-like, transcript variant X1
NFX1-type zinc finger-containing protein 1-like, transcript variant X4
NFX1-type zinc finger-containing protein 1-like, transcript variant X2
NFX1-type zinc finger-containing protein 1-like, transcript variant X5
NFX1-type zinc finger-containing protein 1-like, transcript variant X3
NFX1-type zinc finger-containing protein 1-like
uncharacterized LOC123513744, transcript variant X1
uncharacterized LOC123513744, transcript variant X2
uncharacterized protein LOC123513744 isoform X1
uncharacterized protein LOC123513744 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns