Portunus trituberculatus isolate SZX2019 chromosome 40, 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\nCM030110.1.\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.
COORDINATES: polyA evidence [ECO:0006239]
similar to RNA sequence (same species):INSD:GFFJ01047440.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1135 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 964 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
neurogenic differentiation factor 1-like
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
probable serine/threonine-protein kinase nek3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 8 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: 1 long SRA read, 7 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial-like
neuropeptide CCHamide-1 receptor-like, transcript variant X3
neuropeptide CCHamide-1 receptor-like, transcript variant X1
neuropeptide CCHamide-1 receptor-like, transcript variant X2
uncharacterized LOC123516115, transcript variant X3
uncharacterized LOC123516115, transcript variant X5
uncharacterized LOC123516115, transcript variant X6
uncharacterized LOC123516115, transcript variant X7
uncharacterized LOC123516115, transcript variant X2
uncharacterized LOC123516115, transcript variant X4
uncharacterized LOC123516115, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 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: organic cation transporter protein-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 3 samples with support for all annotated introns
class A basic helix-loop-helix protein 15-like, transcript variant X2
class A basic helix-loop-helix protein 15-like, transcript variant X1
class A basic helix-loop-helix protein 15-like
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
myogenic factor 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
myogenic factor 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
integrator complex subunit 3-like, transcript variant X3
integrator complex subunit 3-like, transcript variant X2
integrator complex subunit 3-like, transcript variant X1
integrator complex subunit 3-like isoform X1
integrator complex subunit 3-like isoform X2
integrator complex subunit 3-like isoform 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 15 samples with support for all annotated introns
phospholipid-transporting ATPase ABCA3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
phospholipid-transporting ATPase ABCA3-like, transcript variant X1
phospholipid-transporting ATPase ABCA3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
phospholipid-transporting ATPase ABCA3-like, transcript variant X3
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 8 samples with support for all annotated introns
phospholipid-transporting ATPase ABCA3-like, transcript variant X5
phospholipid-transporting ATPase ABCA3-like
phospholipid-transporting ATPase ABCA1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phospholipid-transporting ATPase ABCA1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phospholipid-transporting ATPase ABCA1-like, transcript variant X3
phospholipid-transporting ATPase ABCA1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phospholipid-transporting ATPase ABCA1-like, transcript variant X5
phospholipid-transporting ATPase ABCA1-like, transcript variant X6
phospholipid-transporting ATPase ABCA1-like isoform X3
phospholipid-transporting ATPase ABCA1-like isoform X1
phospholipid-transporting ATPase ABCA1-like isoform X2
angiogenic factor with G patch and FHA domains 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC123516091, transcript variant X1
uncharacterized LOC123516091, transcript variant X2
uncharacterized protein LOC123516091 isoform X1
uncharacterized protein LOC123516091 isoform X2
uncharacterized LOC123516039, transcript variant X2
uncharacterized LOC123516039, transcript variant X1
uncharacterized LOC123516039, transcript variant X3
SUN domain-containing ossification factor-like, transcript variant X1
SUN domain-containing ossification factor-like, transcript variant X2
SUN domain-containing ossification factor-like, transcript variant X3
SUN domain-containing ossification factor-like isoform X1
SUN domain-containing ossification factor-like isoform 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 6 samples with support for all annotated introns
large proline-rich protein bag6-like, transcript variant X4
large proline-rich protein bag6-like, transcript variant X5
large proline-rich protein bag6-like, transcript variant X1
large proline-rich protein bag6-like, transcript variant X2
large proline-rich protein bag6-like, transcript variant X7
large proline-rich protein bag6-like, transcript variant X3
large proline-rich protein bag6-like, transcript variant X8
large proline-rich protein bag6-like, transcript variant X6
large proline-rich protein bag6-like, transcript variant X9
large proline-rich protein BAG6-like isoform X1
large proline-rich protein bag6-like isoform X7
large proline-rich protein BAG6-like isoform X3
large proline-rich protein BAG6-like isoform X8
large proline-rich protein bag6-like isoform X4
large proline-rich protein bag6-like isoform X5
large proline-rich protein BAG6-like isoform X6
large proline-rich protein BAG6-like isoform X9
large proline-rich protein BAG6-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
delta(24)-sterol reductase-like, transcript variant X5
delta(24)-sterol reductase-like, transcript variant X2
delta(24)-sterol reductase-like, transcript variant X4
delta(24)-sterol reductase-like, transcript variant X1
delta(24)-sterol reductase-like, transcript variant X3
rho GDP-dissociation inhibitor 1-like, transcript variant X1
rho GDP-dissociation inhibitor 1-like, transcript variant X2
rho GDP-dissociation inhibitor 1-like, transcript variant X4
rho GDP-dissociation inhibitor 1-like, transcript variant X3
uncharacterized LOC123516323, 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 1 sample with support for all annotated introns
uncharacterized LOC123516323, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123516323, transcript variant X1
uncharacterized protein LOC123516323 isoform X3
uncharacterized protein LOC123516323 isoform X2
uncharacterized protein LOC123516323 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
putative neural-cadherin 2, transcript variant X1
putative neural-cadherin 2, transcript variant X2
transfer RNA leucine (anticodon CAA); 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: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X8
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X3
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X5
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X4
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X7
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X6
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X9
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X10
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X2
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X1
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like isoform X5
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like isoform X4
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like isoform X3
flocculation protein FLO11-like isoform X2
flocculation protein FLO11-like isoform X1
flocculation protein FLO11-like isoform X6
apoptosis-inducing factor 1, mitochondrial-like
uncharacterized LOC123515812, transcript variant X2
uncharacterized LOC123515812, transcript variant X4
uncharacterized LOC123515812, transcript variant X3
uncharacterized LOC123515812, transcript variant X1
uncharacterized protein LOC123515812 isoform X3
uncharacterized protein LOC123515812 isoform X2
uncharacterized protein LOC123515812 isoform X1
uncharacterized LOC123515812, transcript variant X6
uncharacterized LOC123515812, 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 46 samples with support for all annotated introns
uncharacterized LOC123516354, transcript variant X4
uncharacterized LOC123516354, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 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
uncharacterized LOC123516354, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123516354, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC123516354 isoform X3
uncharacterized protein LOC123516354 isoform X1
uncharacterized LOC123516354, 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, including 11 samples with support for all annotated introns
uncharacterized protein LOC123516354 isoform X2
uncharacterized LOC123516356, transcript variant X4
uncharacterized LOC123516356, transcript variant X5
uncharacterized LOC123516356, transcript variant X2
uncharacterized LOC123516356, transcript variant X1
uncharacterized LOC123516356, transcript variant X3
uncharacterized protein LOC123516356 isoform X2
uncharacterized protein LOC123516356 isoform X1
uncharacterized protein LOC123516356 isoform X3
uncharacterized protein LOC123516356 isoform X4
uncharacterized LOC123516356, transcript variant X6
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 13 samples with support for all annotated introns
uncharacterized protein LOC123516356 isoform X6
uncharacterized protein LOC123516356 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
uncharacterized LOC123516144, transcript variant X2
uncharacterized LOC123516144, transcript variant X1
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); 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: 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
AT-rich interactive domain-containing protein 1B-like, transcript variant X2
AT-rich interactive domain-containing protein 1B-like, transcript variant X5
AT-rich interactive domain-containing protein 1B-like isoform X2
AT-rich interactive domain-containing protein 1B-like, transcript variant X6
AT-rich interactive domain-containing protein 1B-like, transcript variant X7
AT-rich interactive domain-containing protein 1B-like, transcript variant X3
AT-rich interactive domain-containing protein 1B-like, transcript variant X1
AT-rich interactive domain-containing protein 1B-like, transcript variant X4
lateral signaling target protein 2 homolog isoform X1
AT-rich interactive domain-containing protein 1B-like isoform 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 6 samples with support for all annotated introns
acyl-CoA dehydrogenase family member 11-like, transcript variant X1
acyl-CoA dehydrogenase family member 11-like isoform X1
acyl-CoA dehydrogenase family member 11-like, transcript variant X2
acyl-CoA dehydrogenase family member 11-like, transcript variant X3
acyl-CoA dehydrogenase family member 11-like, transcript variant X4
acyl-CoA dehydrogenase family member 11-like, transcript variant X5
acyl-CoA dehydrogenase family member 11-like isoform X2
acyl-CoA dehydrogenase family member 11-like isoform 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
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.
CD209 antigen-like, transcript variant X2
CD209 antigen-like, transcript variant X1
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
NT-3 growth factor receptor-like, transcript variant X1
NT-3 growth factor receptor-like, transcript variant X2
NT-3 growth factor receptor-like isoform X1
NT-3 growth factor receptor-like isoform 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
uncharacterized LOC123516167, transcript variant X1
uncharacterized LOC123516167, transcript variant X3
uncharacterized LOC123516167, transcript variant X2
uncharacterized LOC123516124, 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 LOC123516124, transcript variant X1
uncharacterized protein LOC123516124 isoform X1
uncharacterized protein LOC123516124 isoform X2
dual oxidase maturation factor 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
dual oxidase maturation factor 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dual oxidase maturation factor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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
dual oxidase maturation factor 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dual oxidase maturation factor 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
dual oxidase maturation factor 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
dual oxidase maturation factor 1-like isoform X1
dual oxidase maturation factor 1-like, transcript variant X7
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
uncharacterized protein LOC123516154 isoform X2
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like, transcript variant X4
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like isoform X2
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like, transcript variant X1
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like, transcript variant X3
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like, transcript variant X2
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like isoform X1
GA-binding protein subunit beta-2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 9 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
GA-binding protein subunit beta-2-like isoform X3
GA-binding protein subunit beta-2-like, transcript variant X1
GA-binding protein subunit beta-2-like, transcript variant X5
GA-binding protein subunit beta-2-like, transcript variant X4
poly [ADP-ribose] polymerase tankyrase-2-like isoform X1
GA-binding protein subunit beta-2-like isoform X4
GA-binding protein subunit beta-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase-2-like isoform X2
queuine tRNA-ribosyltransferase accessory subunit 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 32 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
LOW QUALITY PROTEIN: queuine tRNA-ribosyltransferase accessory subunit 2-like
methionine-R-sulfoxide reductase B1-like
peptidyl-prolyl cis-trans isomerase A1-like
ATPase family protein 2 homolog, transcript variant X2
ATPase family protein 2 homolog, transcript variant X5
ATPase family protein 2 homolog, transcript variant X1
ATPase family protein 2 homolog, transcript variant X4
ATPase family protein 2 homolog, transcript variant X3
ATPase family protein 2 homolog, transcript variant X6
ATPase family protein 2 homolog isoform X2
ATPase family protein 2 homolog isoform X1
CDK5 and ABL1 enzyme substrate 2-like, transcript variant X1
CDK5 and ABL1 enzyme substrate 2-like, transcript variant X2
CDK5 and ABL1 enzyme substrate 2-like isoform X2
CDK5 and ABL1 enzyme substrate 2-like isoform X1
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 14 samples with support for all annotated introns
uncharacterized LOC123515982, transcript variant X1
uncharacterized LOC123515982, transcript variant X2
neurogenic differentiation factor 4-like
uncharacterized LOC123515977, transcript variant X4
uncharacterized LOC123515977, transcript variant X3
uncharacterized LOC123515977, transcript variant X1
uncharacterized LOC123515977, transcript variant X2
uncharacterized LOC123515979, transcript variant X2
uncharacterized LOC123515979, transcript variant X1
uncharacterized PE-PGRS family protein PE_PGRS54-like
glucose dehydrogenase [FAD, quinone]-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X1
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 5 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like isoform X2
glucose dehydrogenase [FAD, quinone]-like isoform X1
uncharacterized LOC123516203, transcript variant X1
uncharacterized LOC123516203, transcript variant X2
uncharacterized LOC123516203, transcript variant X3
uncharacterized protein LOC123516203 isoform X1
uncharacterized protein LOC123516203 isoform X2
uncharacterized protein LOC123516203 isoform X3
von Willebrand factor A domain-containing protein 7-like
endoplasmic reticulum-Golgi intermediate compartment protein 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: endoplasmic reticulum-Golgi intermediate compartment protein 3-like
45 kDa calcium-binding protein-like, transcript variant X1
45 kDa calcium-binding protein-like, transcript variant X4
45 kDa calcium-binding protein-like, transcript variant X3
45 kDa calcium-binding protein-like, transcript variant X2
uncharacterized LOC123515832, transcript variant X4
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 5 samples with support for all annotated introns
uncharacterized LOC123515832, transcript variant X3
uncharacterized LOC123515832, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC123515832, transcript variant X5
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 7 samples with support for all annotated introns
uncharacterized LOC123515832, 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 10 samples with support for all annotated introns
uncharacterized LOC123515831, 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 17 samples with support for all annotated introns
uncharacterized LOC123515831, 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 16 samples with support for all annotated introns
uncharacterized LOC123516171, transcript variant X1
uncharacterized LOC123516171, 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 1 sample with support for all annotated introns
proton-coupled folate transporter-like, transcript variant X2
proton-coupled folate transporter-like, transcript variant X3
proton-coupled folate transporter-like, transcript variant X1
proton-coupled folate transporter-like isoform X1
proton-coupled folate transporter-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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123515819, transcript variant X1
uncharacterized LOC123515819, transcript variant X2
organic cation transporter protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
organic cation transporter protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
organic cation transporter protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
integrator complex subunit 8-like, 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, including 9 samples with support for all annotated introns
integrator complex subunit 8-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
integrator complex subunit 8-like, 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 17 samples with support for all annotated introns
integrator complex subunit 8-like, 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 27 samples with support for all annotated introns
integrator complex subunit 8-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 7 samples with support for all annotated introns
integrator complex subunit 8-like isoform X2
integrator complex subunit 8-like isoform X1
integrator complex subunit 8-like isoform X3
uncharacterized LOC123515818, transcript variant X1
uncharacterized LOC123515818, transcript variant X2
uncharacterized protein LOC123515818 isoform X1
uncharacterized protein LOC123515818 isoform X2
uncharacterized LOC123515818, transcript variant X3
uncharacterized LOC123515818, transcript variant X4
uncharacterized protein LOC123515818 isoform X3
proton-coupled folate transporter-like, transcript variant X4
proton-coupled folate transporter-like isoform X3
proton-coupled folate transporter-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
esterase FE4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
juvenile hormone esterase-like isoform X2
esterase FE4-like, transcript variant X1
esterase FE4-like, transcript variant X2
esterase FE4-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC123515836
uncharacterized LOC123516181, transcript variant X2
uncharacterized LOC123516181, transcript variant X1
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X12
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X18
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X2
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X5
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X4
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X1
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X6
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X3
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X13
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X16
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X17
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X15
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X14
voltage-dependent L-type calcium channel subunit beta-1-like isoform X10
voltage-dependent L-type calcium channel subunit beta-1-like isoform X8
voltage-dependent L-type calcium channel subunit beta-2-like isoform X5
voltage-dependent L-type calcium channel subunit beta-2-like isoform X6
voltage-dependent L-type calcium channel subunit beta-2-like isoform X3
voltage-dependent L-type calcium channel subunit beta-2-like isoform X4
voltage-dependent L-type calcium channel subunit beta-2-like isoform X2
voltage-dependent L-type calcium channel subunit beta-2-like isoform X1
voltage-dependent L-type calcium channel subunit beta-1-like isoform X9
voltage-dependent L-type calcium channel subunit beta-1-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 10 samples with support for all annotated introns
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X11
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
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X9
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
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
voltage-dependent L-type calcium channel subunit beta-1-like, transcript variant X10
uncharacterized protein LOC123516173 isoform X7
protein abrupt-like, transcript variant X3
protein abrupt-like, transcript variant X1
protein abrupt-like, transcript variant X2
uncharacterized protein LOC123516175 isoform X1
crustacean calcium-binding protein 23-like, transcript variant X2
crustacean calcium-binding protein 23-like, transcript variant X1
crustacean calcium-binding protein 23-like
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X3
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X1
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X5
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X4
guanine nucleotide-binding protein G(q) subunit alpha isoform X1
guanine nucleotide-binding protein G(q) subunit alpha isoform X3
guanine nucleotide-binding protein G(q) subunit alpha isoform X4
guanine nucleotide-binding protein G(q) subunit alpha isoform X2
peptidyl-prolyl cis-trans isomerase-like
S-adenosylmethionine mitochondrial carrier protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
spermatogenesis-associated protein 5-like protein 1
LOW QUALITY PROTEIN: spermatogenesis-associated protein 5-like protein 1
uncharacterized LOC123515987, transcript variant X1
uncharacterized LOC123515987, 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 9 samples with support for all annotated introns
adenylate cyclase type 8-like, transcript variant X1
adenylate cyclase type 8-like, transcript variant X4
adenylate cyclase type 8-like, transcript variant X6
adenylate cyclase type 8-like, transcript variant X5
adenylate cyclase type 8-like, transcript variant X7
adenylate cyclase type 8-like, transcript variant X2
adenylate cyclase type 8-like, transcript variant X3
adenylate cyclase type 8-like isoform X5
stromal interaction molecule homolog, transcript variant X3
stromal interaction molecule homolog, transcript variant X13
stromal interaction molecule homolog, transcript variant X17
stromal interaction molecule homolog, transcript variant X1
stromal interaction molecule homolog, transcript variant X6
stromal interaction molecule homolog, transcript variant X12
stromal interaction molecule homolog, transcript variant X15
stromal interaction molecule homolog, transcript variant X7
stromal interaction molecule homolog, transcript variant X16
stromal interaction molecule homolog, transcript variant X18
stromal interaction molecule homolog, transcript variant X8
stromal interaction molecule homolog, transcript variant X11
stromal interaction molecule homolog, transcript variant X2
stromal interaction molecule homolog, transcript variant X4
stromal interaction molecule homolog, transcript variant X9
stromal interaction molecule homolog, transcript variant X10
stromal interaction molecule homolog, transcript variant X5
stromal interaction molecule homolog, transcript variant X14
stromal interaction molecule homolog, transcript variant X20
stromal interaction molecule homolog, transcript variant X19
stromal interaction molecule 2-like isoform X3
stromal interaction molecule 2-like isoform X13
stromal interaction molecule 2-like isoform X17
stromal interaction molecule 2-like isoform X14
stromal interaction molecule homolog isoform X19
stromal interaction molecule 2-like isoform X6
stromal interaction molecule 2-like isoform X15
stromal interaction molecule 2-like isoform X18
stromal interaction molecule homolog isoform X20
stromal interaction molecule 2-like isoform X1
stromal interaction molecule 2-like isoform X12
stromal interaction molecule 2-like isoform X7
stromal interaction molecule 2-like isoform X16
stromal interaction molecule 2-like isoform X8
stromal interaction molecule 2-like isoform X11
stromal interaction molecule 2-like isoform X2
stromal interaction molecule 2-like isoform X4
stromal interaction molecule 2-like isoform X9
stromal interaction molecule 2-like isoform X10
stromal interaction molecule 2-like isoform X5
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123516253, transcript variant X2
uncharacterized LOC123516253, 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
E3 ubiquitin-protein ligase UBR2-like, transcript variant X2
E3 ubiquitin-protein ligase UBR2-like, transcript variant X1
E3 ubiquitin-protein ligase UBR2-like, transcript variant X6
E3 ubiquitin-protein ligase UBR2-like, transcript variant X4
E3 ubiquitin-protein ligase UBR2-like, transcript variant X5
E3 ubiquitin-protein ligase UBR2-like isoform X1
E3 ubiquitin-protein ligase UBR2-like isoform X3
E3 ubiquitin-protein ligase UBR2-like, transcript variant X3
E3 ubiquitin-protein ligase UBR2-like isoform X2
LOW QUALITY PROTEIN: endoribonuclease Dicer-like
GTPase-activating protein skywalker-like, transcript variant X3
GTPase-activating protein skywalker-like, transcript variant X5
GTPase-activating protein skywalker-like isoform X2
GTPase-activating protein skywalker-like isoform X4
GTPase-activating protein skywalker-like, transcript variant X4
GTPase-activating protein skywalker-like, transcript variant X1
GTPase-activating protein skywalker-like, transcript variant X2
GTPase-activating protein skywalker-like isoform X1
GTPase-activating protein skywalker-like isoform X3
uncharacterized LOC123516325, transcript variant X1
uncharacterized LOC123516325, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
leucine-rich repeat-containing protein 4C-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 6 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: lanC-like protein 2
uncharacterized LOC123516157, transcript variant X5
uncharacterized LOC123516157, transcript variant X1
uncharacterized LOC123516157, transcript variant X2
uncharacterized LOC123516157, transcript variant X4
uncharacterized LOC123516157, transcript variant X3
early endosome antigen 1-like, transcript variant X5
early endosome antigen 1-like, transcript variant X7
early endosome antigen 1-like, transcript variant X2
early endosome antigen 1-like, transcript variant X11
early endosome antigen 1-like, transcript variant X1
early endosome antigen 1-like, transcript variant X6
early endosome antigen 1-like, transcript variant X10
early endosome antigen 1-like, transcript variant X8
early endosome antigen 1-like, transcript variant X12
early endosome antigen 1-like, transcript variant X9
early endosome antigen 1-like, transcript variant X3
early endosome antigen 1-like, transcript variant X14
early endosome antigen 1-like, transcript variant X13
early endosome antigen 1-like, transcript variant X4
early endosome antigen 1-like, transcript variant X16
early endosome antigen 1-like, transcript variant X15
golgin subfamily A member 4-like isoform X10
early endosome antigen 1-like isoform X16
golgin subfamily A member 4-like isoform X13
golgin subfamily A member 4-like isoform X5
golgin subfamily A member 4-like isoform X8
early endosome antigen 1-like isoform X15
golgin subfamily A member 4-like isoform X12
golgin subfamily A member 4-like isoform X7
golgin subfamily A member 4-like isoform X9
golgin subfamily A member 4-like isoform X3
flagellar attachment zone protein 1-like isoform X11
golgin subfamily A member 4-like isoform X1
early endosome antigen 1-like isoform X14
golgin subfamily A member 4-like isoform X6
early endosome antigen 1-like, transcript variant X17
early endosome antigen 1-like isoform X17
mediator of RNA polymerase II transcription subunit 20-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog
LOW QUALITY PROTEIN: facilitated trehalose transporter Tret1-2 homolog
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine/threonine-protein kinase ste20-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
facilitated trehalose transporter Tret1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like, transcript variant X1
facilitated trehalose transporter Tret1-like, transcript variant X3
facilitated trehalose transporter Tret1-like
uncharacterized LOC123516037, transcript variant X2
uncharacterized LOC123516037, transcript variant X3
uncharacterized LOC123516037, transcript variant X1
LOW QUALITY PROTEIN: uncharacterized protein LOC123516034
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 98% 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: 1 long SRA read, 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
importin subunit beta-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
importin subunit beta-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
importin subunit beta-1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
importin subunit beta-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
importin subunit beta-1-like, transcript variant X4
importin subunit beta-1-like, transcript variant X6
acetyl-coenzyme A synthetase, cytoplasmic-like, transcript variant X1
acetyl-coenzyme A synthetase, cytoplasmic-like, transcript variant X2
acetyl-coenzyme A synthetase, cytoplasmic-like isoform X1
acetyl-coenzyme A synthetase, cytoplasmic-like isoform X2
alpha-crystallin B chain-like, transcript variant X1
alpha-crystallin B chain-like, transcript variant X2
alpha-crystallin B chain-like isoform X2
nuclear RNA export factor 1-like, transcript variant X1
nuclear RNA export factor 1-like, transcript variant X2
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
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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: AP-3 complex subunit delta-1-like
ras-related protein Rab-9A-like, transcript variant X5
ras-related protein Rab-9A-like, transcript variant X6
ras-related protein Rab-9A-like, transcript variant X3
ras-related protein Rab-9A-like, transcript variant X2
ras-related protein Rab-9A-like, transcript variant X10
ras-related protein Rab-9A-like, transcript variant X1
ras-related protein Rab-9A-like, transcript variant X12
ras-related protein Rab-9A-like, transcript variant X7
ras-related protein Rab-9A-like, transcript variant X8
ras-related protein Rab-9A-like, transcript variant X9
ras-related protein Rab-9A-like, transcript variant X11
ras-related protein Rab-9A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
ras-related protein Rab-9A-like, transcript variant X13
ras-related protein Rab-9A-like, transcript variant X14
protein inscuteable homolog, transcript variant X2
protein inscuteable homolog, transcript variant X1
WD repeat-containing protein 18-like, transcript variant X3
WD repeat-containing protein 18-like, transcript variant X1
WD repeat-containing protein 18-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
WD repeat-containing protein 18-like isoform X1
WD repeat-containing protein 18-like isoform X2
uncharacterized LOC123516024, transcript variant X1
uncharacterized LOC123516024, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123516133, transcript variant X3
uncharacterized LOC123516133, transcript variant X2
uncharacterized LOC123516133, transcript variant X8
uncharacterized LOC123516133, transcript variant X5
uncharacterized LOC123516133, transcript variant X1
uncharacterized LOC123516133, transcript variant X4
uncharacterized LOC123516133, transcript variant X6
uncharacterized protein LOC123516133 isoform X2
uncharacterized protein LOC123516133 isoform X1
uncharacterized protein LOC123516133 isoform X3
uncharacterized protein LOC123516133 isoform X6
uncharacterized LOC123516133, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC123516133 isoform X5
uncharacterized protein LOC123516133 isoform X4
uncharacterized LOC123516094, transcript variant X2
uncharacterized LOC123516094, transcript variant X1
uncharacterized protein LOC123516094 isoform X2
uncharacterized protein LOC123516094 isoform X1
basic proline-rich protein-like, transcript variant X1
basic proline-rich protein-like, transcript variant X2
basic proline-rich protein-like, transcript variant X3
basic proline-rich protein-like isoform X1
basic proline-rich protein-like isoform X2
basic proline-rich protein-like isoform X3
uncharacterized LOC123515940, transcript variant X3
uncharacterized LOC123515940, transcript variant X1
uncharacterized LOC123515940, transcript variant X2
dehydrogenase/reductase SDR family member 11-like, transcript variant X3
dehydrogenase/reductase SDR family member 11-like, transcript variant X2
dehydrogenase/reductase SDR family member 11-like, transcript variant X1
dehydrogenase/reductase SDR family member 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
trithorax group protein osa-like, transcript variant X2
trithorax group protein osa-like, transcript variant X1
trithorax group protein osa-like, transcript variant X3
uncharacterized LOC123516349, transcript variant X6
uncharacterized LOC123516349, transcript variant X2
uncharacterized LOC123516349, transcript variant X1
uncharacterized LOC123516349, transcript variant X3
uncharacterized LOC123516349, transcript variant X5
uncharacterized LOC123516349, transcript variant X4
uncharacterized protein LOC123516349 isoform X3
uncharacterized protein LOC123516349 isoform X1
uncharacterized protein LOC123516349 isoform X2
FGFR1 oncogene partner 2 homolog, transcript variant X4
FGFR1 oncogene partner 2 homolog, transcript variant X3
FGFR1 oncogene partner 2 homolog, transcript variant X5
FGFR1 oncogene partner 2 homolog, transcript variant X1
FGFR1 oncogene partner 2 homolog, transcript variant X2
FGFR1 oncogene partner 2 homolog isoform X3
FGFR1 oncogene partner 2 homolog isoform X2
FGFR1 oncogene partner 2 homolog isoform X4
FGFR1 oncogene partner 2 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated protein RP/EB family member 1-like, transcript variant X3
microtubule-associated protein RP/EB family member 1-like, transcript variant X2
microtubule-associated protein RP/EB family member 1-like, transcript variant X1
microtubule-associated protein RP/EB family member 1-like isoform X2
microtubule-associated protein RP/EB family member 1-like isoform X1
microtubule-associated protein RP/EB family member 1-like isoform X3
uncharacterized LOC123515971, transcript variant X1
uncharacterized LOC123515971, transcript variant X2
protein dopey-1 homolog, transcript variant X5
protein dopey-1 homolog, transcript variant X6
protein dopey-1 homolog, transcript variant X4
protein dopey-1 homolog, transcript variant X3
protein dopey-1 homolog, transcript variant X2
protein dopey-1 homolog, transcript variant X1
uncharacterized LOC123515973, transcript variant X1
uncharacterized LOC123515973, transcript variant X2
methyl-CpG-binding domain protein 4-like, transcript variant X2
methyl-CpG-binding domain protein 4-like, transcript variant X1
methyl-CpG-binding domain protein 4-like, transcript variant X3
methyl-CpG-binding domain protein 4-like isoform X2
methyl-CpG-binding domain protein 4-like isoform X1
methyl-CpG-binding domain protein 4-like isoform X3
gamma-tubulin complex component 3 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
beta-1,3-galactosyltransferase brn-like, transcript variant X1
beta-1,3-galactosyltransferase brn-like, transcript variant X2
lysosomal-associated transmembrane protein 4B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123516161, transcript variant X2
uncharacterized LOC123516161, transcript variant X3
uncharacterized LOC123516161, transcript variant X1
uncharacterized protein LOC123516161 isoform X3
uncharacterized protein LOC123516161 isoform X2
uncharacterized protein LOC123516161 isoform X1
uncharacterized LOC123516229, transcript variant X1
uncharacterized protein LOC123516229 isoform X1
uncharacterized LOC123516229, transcript variant X2
uncharacterized protein LOC123516229 isoform X2
basic helix-loop-helix transcription factor scleraxis-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123516147, transcript variant X2
uncharacterized LOC123516147, transcript variant X3
uncharacterized LOC123516147, transcript variant X4
uncharacterized LOC123516147, transcript variant X1
uncharacterized protein LOC123516147 isoform X2
uncharacterized protein LOC123516147 isoform X1
two pore potassium channel protein sup-9-like
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial, transcript variant X3
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial, transcript variant X4
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial, transcript variant X1
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial, transcript variant X2
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial isoform X2
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial isoform X3
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial isoform X1
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial isoform X4
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.
LOW QUALITY PROTEIN: solute carrier family 22 member 15-like
LOW QUALITY PROTEIN: uncharacterized protein LOC123516126
translation machinery-associated protein 16-like
uncharacterized LOC123516125, transcript variant X1
uncharacterized LOC123516125, transcript variant X2
uncharacterized protein LOC123516125 isoform X1
uncharacterized protein LOC123516125 isoform X2
carnitine O-palmitoyltransferase 2, mitochondrial-like, transcript variant X2
carnitine O-palmitoyltransferase 2, mitochondrial-like, transcript variant X3
carnitine O-palmitoyltransferase 2, mitochondrial-like, transcript variant X1
carnitine O-palmitoyltransferase 2, mitochondrial-like, transcript variant X4
carnitine O-palmitoyltransferase 2, mitochondrial-like isoform X3
carnitine O-palmitoyltransferase 2, mitochondrial-like isoform X2
carnitine O-palmitoyltransferase 2, mitochondrial-like isoform X1
proline-serine-threonine phosphatase-interacting protein 2-like, transcript variant X4
proline-serine-threonine phosphatase-interacting protein 2-like, transcript variant X3
proline-serine-threonine phosphatase-interacting protein 2-like, transcript variant X5
proline-serine-threonine phosphatase-interacting protein 2-like, transcript variant X2
proline-serine-threonine phosphatase-interacting protein 2-like, transcript variant X1
proline-serine-threonine phosphatase-interacting protein 2-like isoform X2
proline-serine-threonine phosphatase-interacting protein 2-like isoform X1
proline-serine-threonine phosphatase-interacting protein 2-like isoform X3
proline-serine-threonine phosphatase-interacting protein 2-like isoform X4
tetratricopeptide repeat protein 36-like
neuropeptide CCHamide-1 receptor-like, transcript variant X5
neuropeptide CCHamide-1 receptor-like, transcript variant X4
translocation protein SEC62-like isoform X5
translocation protein SEC62-like isoform X1
translocation protein SEC62-like isoform X4
translocation protein SEC62-like isoform X2
recQ-mediated genome instability protein 1-like, transcript variant X2
recQ-mediated genome instability protein 1-like, transcript variant X3
recQ-mediated genome instability protein 1-like, transcript variant X1
recQ-mediated genome instability protein 1-like isoform X1
recQ-mediated genome instability protein 1-like isoform X2
recQ-mediated genome instability protein 1-like isoform X3
LOW QUALITY PROTEIN: tonsoku-like protein
transient receptor potential channel pyrexia-like
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 30 samples with support for all annotated introns
uncharacterized LOC123516221, transcript variant X3
uncharacterized LOC123516221, transcript variant X1
uncharacterized LOC123516221, transcript variant X2
neuropeptide CCHamide-1 receptor-like isoform X3
pyrokinin-1 receptor-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 3 samples with support for all annotated introns
pyrokinin-1 receptor-like, transcript variant X1
low-density lipoprotein receptor-related protein 1B-like
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like, transcript variant X1
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like, transcript variant X2
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like
LOW QUALITY PROTEIN: AP-4 complex subunit beta-1-like
dual specificity protein phosphatase 3-like, transcript variant X1
dual specificity protein phosphatase 3-like, transcript variant X4
dual specificity protein phosphatase 3-like, transcript variant X2
uncharacterized protein LOC123515825 isoform X1
dual specificity protein phosphatase 3-like, transcript variant X3
dual specificity protein phosphatase 3-like, transcript variant X5
dual specificity protein phosphatase 3-like isoform X2
dual specificity protein phosphatase 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
major facilitator superfamily domain-containing protein 1-like, transcript variant X6
major facilitator superfamily domain-containing protein 1-like, transcript variant X8
major facilitator superfamily domain-containing protein 1-like, transcript variant X2
major facilitator superfamily domain-containing protein 1-like, transcript variant X1
major facilitator superfamily domain-containing protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 1-like, 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 9 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 17 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 1-like, transcript variant X4
major facilitator superfamily domain-containing protein 1-like isoform X3
major facilitator superfamily domain-containing protein 1-like isoform X1
major facilitator superfamily domain-containing protein 1-like isoform X4
major facilitator superfamily domain-containing protein 1-like isoform X2
major facilitator superfamily domain-containing protein 1-like isoform X5
lysM and putative peptidoglycan-binding domain-containing protein 3-like
ribosome biogenesis protein BMS1 homolog
L-2-hydroxyglutarate dehydrogenase, mitochondrial-like
bromodomain-containing protein 4-like, transcript variant X1
bromodomain-containing protein 4-like, transcript variant X2
bromodomain-containing protein 4-like isoform X1
transcription initiation factor TFIID subunit 4-like isoform X2
uncharacterized LOC123515992, transcript variant X5
uncharacterized LOC123515992, transcript variant X4
uncharacterized LOC123515992, transcript variant X3
uncharacterized LOC123515992, transcript variant X2
uncharacterized LOC123515992, transcript variant X1
uncharacterized protein LOC123515992 isoform X5
uncharacterized protein LOC123515992 isoform X4
uncharacterized protein LOC123515992 isoform X3
uncharacterized protein LOC123515992 isoform X2
uncharacterized protein LOC123515992 isoform X1
uncharacterized LOC123515992, transcript variant X11
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 LOC123515992, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123515992, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123515992, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123515992, transcript variant X9
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 5 samples with support for all annotated introns
uncharacterized LOC123515992, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC123515992 isoform X9
uncharacterized protein LOC123515992 isoform X8
uncharacterized protein LOC123515992 isoform X7
uncharacterized protein LOC123515992 isoform X6
uncharacterized protein DKFZp434B061-like, transcript variant X1
uncharacterized protein DKFZp434B061-like
uncharacterized protein DKFZp434B061-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 35 samples with support for all annotated introns
neuroendocrine convertase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
neuroendocrine convertase 1-like isoform X1
neuroendocrine convertase 1-like, transcript variant X3
neuroendocrine convertase 1-like isoform X3
neuroendocrine convertase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
neuroendocrine convertase 1-like isoform X2
essential MCU regulator, mitochondrial-like
coatomer subunit beta-like, transcript variant X1
coatomer subunit beta-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
twist-related protein-like, transcript variant X1
twist-related protein-like, transcript variant X3
twist-related protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tyrosine-protein kinase Dnt-like, transcript variant X1
tyrosine-protein kinase Dnt-like, transcript variant X2
tyrosine-protein kinase Dnt-like isoform X1
tyrosine-protein kinase Dnt-like isoform X2
sarcoplasmic calcium-binding protein, transcript variant X4
sarcoplasmic calcium-binding protein, transcript variant X3
sarcoplasmic calcium-binding protein, transcript variant X2
sarcoplasmic calcium-binding protein, transcript variant X1
sarcoplasmic calcium-binding protein isoform X2
sarcoplasmic calcium-binding protein isoform X1
sarcoplasmic calcium-binding protein isoform X4
sarcoplasmic calcium-binding protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123516194, transcript variant X1
uncharacterized protein LOC123516194 isoform X1
uncharacterized LOC123516194, transcript variant X3
uncharacterized LOC123516194, transcript variant X2
uncharacterized protein LOC123516194 isoform X2
uncharacterized LOC123516195, transcript variant X1
uncharacterized LOC123516195, transcript variant X2
uncharacterized protein LOC123516195 isoform X1
uncharacterized protein LOC123516195 isoform X2
uncharacterized LOC123516196, transcript variant X1
uncharacterized LOC123516196, transcript variant X2
uncharacterized LOC123516196, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123516197, transcript variant X3
uncharacterized LOC123516197, transcript variant X2
uncharacterized LOC123516197, transcript variant X1
uncharacterized protein LOC123516197 isoform X1
uncharacterized protein LOC123516197 isoform X2
similar to RNA sequence (same species):INSD:GFFJ01025846.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 176 bases not found in genome assembly; 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 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: added 176 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
major facilitator superfamily domain-containing protein 8-like
zinc finger BED domain-containing protein 5-like
uncharacterized LOC123516041, transcript variant X2
uncharacterized LOC123516041, transcript variant X1
uncharacterized protein LOC123516041 isoform X1
uncharacterized protein LOC123516041 isoform X2
uncharacterized LOC123516311, transcript variant X1
uncharacterized LOC123516311, 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
mpv17-like protein, 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 3 samples with support for all annotated introns
mpv17-like protein, 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 5 samples with support for all annotated introns
mpv17-like protein, 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 7 samples with support for all annotated introns
ADP-ribose glycohydrolase OARD1-like, transcript variant X1
ADP-ribose glycohydrolase OARD1-like, transcript variant X2
BCAS3 microtubule associated cell migration factor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
BCAS3 microtubule associated cell migration factor-like, 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 16 samples with support for all annotated introns
BCAS3 microtubule associated cell migration factor-like, transcript variant X1
BCAS3 microtubule associated cell migration factor-like isoform X2
BCAS3 microtubule associated cell migration factor-like isoform X1
BCAS3 microtubule associated cell migration factor-like isoform X3
ubiquitin-associated domain-containing protein 2-like
LOW QUALITY PROTEIN: ubiquitin-associated domain-containing protein 2-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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
putative uncharacterized protein DDB_G0271606, transcript variant X3
putative uncharacterized protein DDB_G0271606, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
putative uncharacterized protein DDB_G0271606, transcript variant X1
putative uncharacterized protein DDB_G0271606, transcript variant X4
putative uncharacterized protein DDB_G0271606
alpha-protein kinase 1-like, transcript variant X1
alpha-protein kinase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
AP2-associated protein kinase 1-like isoform X1
endoplasmic reticulum aminopeptidase 1-like, transcript variant X5
endoplasmic reticulum aminopeptidase 1-like, transcript variant X6
endoplasmic reticulum aminopeptidase 1-like, transcript variant X2
endoplasmic reticulum aminopeptidase 1-like, transcript variant X1
endoplasmic reticulum aminopeptidase 1-like, transcript variant X11
endoplasmic reticulum aminopeptidase 1-like, transcript variant X3
endoplasmic reticulum aminopeptidase 1-like, transcript variant X7
endoplasmic reticulum aminopeptidase 1-like, transcript variant X9
endoplasmic reticulum aminopeptidase 1-like, transcript variant X8
endoplasmic reticulum aminopeptidase 1-like, transcript variant X4
endoplasmic reticulum aminopeptidase 1-like, transcript variant X10
endoplasmic reticulum aminopeptidase 1-like isoform X6
endoplasmic reticulum aminopeptidase 1-like isoform X5
endoplasmic reticulum aminopeptidase 1-like isoform X2
endoplasmic reticulum aminopeptidase 1-like isoform X1
endoplasmic reticulum aminopeptidase 1-like isoform X8
endoplasmic reticulum aminopeptidase 1-like isoform X4
endoplasmic reticulum aminopeptidase 1-like isoform X3
endoplasmic reticulum aminopeptidase 1-like isoform X7
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: RNA-binding protein 25-like
gonadotropin-releasing hormone receptor-like
progestin and adipoQ receptor family member 4-like
uncharacterized LOC123516185, transcript variant X3
uncharacterized LOC123516185, transcript variant X2
uncharacterized protein LOC123516185 isoform X2
uncharacterized protein LOC123516185 isoform X3
uncharacterized LOC123516185, transcript variant X1
uncharacterized protein LOC123516185 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 16% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, delta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
E3 ubiquitin-protein transferase MAEA-like, transcript variant X1
E3 ubiquitin-protein transferase MAEA-like, transcript variant X2
E3 ubiquitin-protein transferase MAEA-like
uncharacterized LOC123516000, transcript variant X1
uncharacterized LOC123516000, transcript variant X2
uncharacterized protein LOC123516000 isoform X1
uncharacterized protein LOC123516000 isoform X2
synaptojanin-1-like, transcript variant X5
synaptojanin-1-like, transcript variant X4
synaptojanin-1-like, transcript variant X2
synaptojanin-1-like, transcript variant X3
synaptojanin-1-like, transcript variant X1
synaptojanin-1-like, transcript variant X6
uncharacterized LOC123516001, transcript variant X5
uncharacterized LOC123516001, transcript variant X8
uncharacterized LOC123516001, transcript variant X3
uncharacterized protein LOC123516001 isoform X3
uncharacterized LOC123516001, transcript variant X6
uncharacterized LOC123516001, transcript variant X4
uncharacterized LOC123516001, transcript variant X7
uncharacterized LOC123516001, transcript variant X2
uncharacterized protein LOC123516001 isoform X2
uncharacterized LOC123516001, transcript variant X1
uncharacterized protein LOC123516001 isoform X1
uncharacterized protein LOC123516001 isoform X4
uncharacterized LOC123516004, transcript variant X3
uncharacterized LOC123516004, transcript variant X2
uncharacterized LOC123516004, transcript variant X1
ATP-binding cassette sub-family C member 4-like, transcript variant X2
ATP-binding cassette sub-family C member 4-like, transcript variant X4
ATP-binding cassette sub-family C member 4-like, transcript variant X1
ATP-binding cassette sub-family C member 4-like isoform X1
ATP-binding cassette sub-family C member 4-like, transcript variant X3
ATP-binding cassette sub-family C member 4-like, transcript variant X5
ATP-binding cassette sub-family C member 4-like isoform X2
ATP-binding cassette sub-family C member 4-like isoform 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 7 samples with support for all annotated introns
putative tRNA (cytidine(32)/guanosine(34)-2'-O)-methyltransferase, transcript variant X2
putative tRNA (cytidine(32)/guanosine(34)-2'-O)-methyltransferase
putative tRNA (cytidine(32)/guanosine(34)-2'-O)-methyltransferase, 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 14 samples with support for all annotated introns
uncharacterized LOC123516056, transcript variant X1
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein LOC123516056 isoform X1
uncharacterized LOC123516056, transcript variant X2
uncharacterized protein LOC123516056 isoform 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 2 samples with support for all annotated introns
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
pyruvate carboxylase, mitochondrial-like, transcript variant X2
pyruvate carboxylase, mitochondrial-like, transcript variant X6
pyruvate carboxylase, mitochondrial-like, transcript variant X5
pyruvate carboxylase, mitochondrial-like, transcript variant X3
pyruvate carboxylase, mitochondrial-like, transcript variant X4
pyruvate carboxylase, mitochondrial-like, transcript variant X1
pyruvate carboxylase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATP-dependent RNA helicase abstrakt-like, transcript variant X3
ATP-dependent RNA helicase abstrakt-like, transcript variant X1
ATP-dependent RNA helicase abstrakt-like, transcript variant X4
ATP-dependent RNA helicase abstrakt-like, transcript variant X2
ATP-dependent RNA helicase abstrakt-like, transcript variant X5
ATP-dependent RNA helicase abstrakt-like
E3 ubiquitin-protein ligase parkin-like, transcript variant X2
E3 ubiquitin-protein ligase parkin-like, transcript variant X3
E3 ubiquitin-protein ligase parkin-like, transcript variant X1
E3 ubiquitin-protein ligase parkin-like isoform X1
E3 ubiquitin-protein ligase parkin-like isoform X2
uncharacterized LOC123516010, transcript variant X2
uncharacterized LOC123516010, transcript variant X1
protein TRACHEARY ELEMENT DIFFERENTIATION-RELATED 7A-like
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
histone acetyltransferase KAT7-like, transcript variant X5
histone acetyltransferase KAT7-like, transcript variant X4
histone acetyltransferase KAT7-like, transcript variant X3
histone acetyltransferase KAT7-like, transcript variant X2
histone acetyltransferase KAT7-like, transcript variant X1
histone acetyltransferase KAT7-like isoform X5
histone acetyltransferase KAT7-like isoform X4
histone acetyltransferase KAT7-like isoform X3
histone acetyltransferase KAT7-like isoform X2
histone acetyltransferase KAT7-like isoform X1
DNA replication licensing factor mcm5-like
LOW QUALITY PROTEIN: DNA replication licensing factor mcm5-like
uncharacterized LOC123516163, transcript variant X1
uncharacterized LOC123516163, transcript variant X2
protein rolling stone-like, transcript variant X2
protein rolling stone-like, transcript variant X1
LOW QUALITY PROTEIN: uncharacterized protein CG43867-like
uncharacterized LOC123515948, transcript variant X2
uncharacterized LOC123515948, transcript variant X3
uncharacterized LOC123515948, transcript variant X5
uncharacterized LOC123515948, transcript variant X1
uncharacterized LOC123515948, 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 8 samples with support for all annotated introns
lysosomal thioesterase PPT2-A-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 17 samples with support for all annotated introns
lysosomal thioesterase PPT2-A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
lysosomal thioesterase PPT2-A-like isoform X2
lysosomal thioesterase PPT2-A-like isoform X1
ankyrin repeat domain-containing protein 50-like, transcript variant X1
ankyrin repeat domain-containing protein 50-like, transcript variant X3
ankyrin repeat domain-containing protein 50-like, transcript variant X2
ankyrin repeat domain-containing protein 50-like isoform X1
transfer RNA isoleucine (anticodon GAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
eIF-2-alpha kinase GCN2-like, transcript variant X1
eIF-2-alpha kinase GCN2-like, transcript variant X4
eIF-2-alpha kinase GCN2-like, transcript variant X3
eIF-2-alpha kinase GCN2-like, transcript variant X2
eIF-2-alpha kinase GCN2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 8-like, transcript variant X3
major facilitator superfamily domain-containing protein 8-like, transcript variant X2
major facilitator superfamily domain-containing protein 8-like, transcript variant X1
major facilitator superfamily domain-containing protein 8-like isoform X1
major facilitator superfamily domain-containing protein 8-like isoform X2
cryptochrome DASH-like, transcript variant X3
cryptochrome DASH-like, transcript variant X4
cryptochrome DASH-like, transcript variant X2
cryptochrome DASH-like, transcript variant X1
uncharacterized LOC123515899, transcript variant X1
uncharacterized LOC123515899, transcript variant X2
uncharacterized LOC123515900, transcript variant X3
uncharacterized LOC123515900, transcript variant X2
uncharacterized LOC123515900, transcript variant X1
intraflagellar transport protein 88 homolog, transcript variant X1
intraflagellar transport protein 88 homolog, transcript variant X2
intraflagellar transport protein 88 homolog isoform X2
intraflagellar transport protein 88 homolog isoform X1
uncharacterized LOC123515897, transcript variant X2
uncharacterized LOC123515897, transcript variant X1
uncharacterized protein LOC123515897 isoform X1
uncharacterized protein LOC123515897 isoform X2
eukaryotic translation initiation factor 1A, Y-chromosomal-like
uncharacterized LOC123515903, 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 2 samples with support for all annotated introns
uncharacterized LOC123515903, transcript variant X1
uncharacterized LOC123515903, transcript variant X3
uncharacterized protein LOC123515903 isoform X1
uncharacterized protein LOC123515903 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCCH domain-containing protein 14-like
dnaJ homolog subfamily C member 21-like, transcript variant X3
dnaJ homolog subfamily C member 21-like, transcript variant X1
dnaJ homolog subfamily C member 21-like, transcript variant X4
dnaJ homolog subfamily C member 21-like, transcript variant X2
neural-cadherin-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 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
neural-cadherin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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
neural-cadherin-like, transcript variant X2
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 3 samples with support for all annotated introns
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transmembrane protein 211-like, transcript variant X2
transmembrane protein 211-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123515912, transcript variant X1
uncharacterized LOC123515912, transcript variant X2
uncharacterized LOC123515916, transcript variant X1
uncharacterized LOC123515916, transcript variant X2
uncharacterized protein LOC123515916 isoform X2
uncharacterized protein LOC123515916 isoform X1
glutamate [NMDA] receptor subunit 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glutamate [NMDA] receptor subunit 1-like, transcript variant X2
glutamate [NMDA] receptor subunit 1-like
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 20 samples with support for all annotated introns
2-aminomuconic semialdehyde dehydrogenase-like, transcript variant X2
2-aminomuconic semialdehyde dehydrogenase-like, transcript variant X7
2-aminomuconic semialdehyde dehydrogenase-like, transcript variant X5
2-aminomuconic semialdehyde dehydrogenase-like, transcript variant X3
2-aminomuconic semialdehyde dehydrogenase-like, transcript variant X1
2-aminomuconic semialdehyde dehydrogenase-like, transcript variant X6
2-aminomuconic semialdehyde dehydrogenase-like, transcript variant X4
2-aminomuconic semialdehyde dehydrogenase-like, transcript variant X9
2-aminomuconic semialdehyde dehydrogenase-like, transcript variant X10
2-aminomuconic semialdehyde dehydrogenase-like isoform X2
2-aminomuconic semialdehyde dehydrogenase-like isoform X1
2-aminomuconic semialdehyde dehydrogenase-like isoform X4
2-aminomuconic semialdehyde dehydrogenase-like isoform X5
2-aminomuconic semialdehyde dehydrogenase-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
2-aminomuconic semialdehyde dehydrogenase-like isoform X3
uncharacterized LOC123516069, 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 32 samples with support for all annotated introns
uncharacterized LOC123516069, 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 31 samples with support for all annotated introns
uncharacterized LOC123516069, transcript variant X1
uncharacterized LOC123516069, transcript variant X4
uncharacterized LOC123516071, transcript variant X1
uncharacterized LOC123516071, 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
uncharacterized protein LOC123516071 isoform X1
uncharacterized protein LOC123516071 isoform X2
protein fem-1 homolog C-like, transcript variant X2
protein fem-1 homolog C-like, transcript variant X1
protein fem-1 homolog C-like, transcript variant X3
protein fem-1 homolog C-like, transcript variant X4
active breakpoint cluster region-related protein-like, transcript variant X5
active breakpoint cluster region-related protein-like, transcript variant X4
active breakpoint cluster region-related protein-like, transcript variant X3
active breakpoint cluster region-related protein-like, transcript variant X1
active breakpoint cluster region-related protein-like, transcript variant X2
active breakpoint cluster region-related protein-like, transcript variant X7
active breakpoint cluster region-related protein-like, transcript variant X6
active breakpoint cluster region-related protein-like isoform X7
active breakpoint cluster region-related protein-like isoform X6
active breakpoint cluster region-related protein-like isoform X5
active breakpoint cluster region-related protein-like isoform X4
active breakpoint cluster region-related protein-like isoform X3
active breakpoint cluster region-related protein-like isoform X1
active breakpoint cluster region-related protein-like isoform X2
low density lipoprotein receptor adapter protein 1-like, transcript variant X2
low density lipoprotein receptor adapter protein 1-like, transcript variant X1
low density lipoprotein receptor adapter protein 1-like isoform X1
low density lipoprotein receptor adapter protein 1-like isoform X2
zinc metalloproteinase nas-4-like, transcript variant X1
zinc metalloproteinase nas-4-like, transcript variant X3
zinc metalloproteinase nas-4-like, transcript variant X2
zinc metalloproteinase nas-4-like isoform X3
zinc metalloproteinase nas-4-like isoform X2
zinc metalloproteinase nas-4-like isoform X1
proteasome adapter and scaffold protein ECM29-like
LOW QUALITY PROTEIN: proteasome adapter and scaffold protein ECM29-like
solute carrier family 12 member 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
solute carrier family 12 member 8-like, transcript variant X2
uncharacterized LOC123516143, transcript variant X1
uncharacterized LOC123516143, transcript variant X2
uncharacterized protein LOC123516143 isoform X1
uncharacterized protein LOC123516143 isoform X2
kinesin-like protein KIF13B, transcript variant X1
kinesin-like protein KIF13B, transcript variant X2
kinesin-like protein KIF13B, transcript variant X3
kinesin-like protein KIF13B, transcript variant X4
kinesin-like protein KIF13B, transcript variant X5
kinesin-like protein KIF13B, transcript variant X6
kinesin-like protein KIF13B, transcript variant X10
kinesin-like protein KIF13B, transcript variant X12
kinesin-like protein KIF13B, transcript variant X8
kinesin-like protein KIF13B, transcript variant X9
kinesin-like protein KIF13B, transcript variant X11
kinesin-like protein KIF13B, transcript variant X13
kinesin-like protein KIF13B, transcript variant X15
kinesin-like protein KIF13B, transcript variant X7
kinesin-like protein KIF13B, transcript variant X14
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 24 samples with support for all annotated introns
membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase-like
Ig-like and fibronectin type-III domain-containing protein 1
LOW QUALITY PROTEIN: Ig-like and fibronectin type-III domain-containing protein 1
glutamate receptor ionotropic, delta-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, delta-1-like, transcript variant X4
glutamate receptor ionotropic, delta-1-like, transcript variant X3
glutamate receptor ionotropic, delta-1-like, transcript variant X1
glutamate receptor ionotropic, delta-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RCC1-like G exchanging factor-like protein, 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 5 samples with support for all annotated introns
RCC1-like G exchanging factor-like protein, 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 15 samples with support for all annotated introns
RCC1-like G exchanging factor-like protein, transcript variant X1
RCC1-like G exchanging factor-like protein, transcript variant X2
RCC1-like G exchanging factor-like protein isoform X1
RCC1-like G exchanging factor-like protein isoform X2
RCC1-like G exchanging factor-like protein isoform X3
RCC1-like G exchanging factor-like protein isoform X4
Y-box factor homolog, transcript variant X2
Y-box factor homolog, transcript variant X6
Y-box factor homolog, transcript variant X1
Y-box factor homolog, transcript variant X4
Y-box factor homolog, transcript variant X3
Y-box factor homolog, transcript variant X5
WW domain-containing transcription regulator protein 1-like, transcript variant X7
WW domain-containing transcription regulator protein 1-like, transcript variant X2
WW domain-containing transcription regulator protein 1-like, transcript variant X3
WW domain-containing transcription regulator protein 1-like, transcript variant X1
WW domain-containing transcription regulator protein 1-like, transcript variant X9
WW domain-containing transcription regulator protein 1-like, transcript variant X5
WW domain-containing transcription regulator protein 1-like, transcript variant X4
WW domain-containing transcription regulator protein 1-like, transcript variant X6
WW domain-containing transcription regulator protein 1-like, transcript variant X8
WW domain-containing transcription regulator protein 1-like, transcript variant X11
WW domain-containing transcription regulator protein 1-like, transcript variant X10
transcriptional coactivator YAP1-like isoform X1
transcriptional coactivator YAP1-like isoform X6
transcriptional coactivator YAP1-like isoform X7
WW domain-containing transcription regulator protein 1-like isoform X3
WW domain-containing transcription regulator protein 1-like isoform X5
transcriptional coactivator YAP1-like isoform X8
transcriptional coactivator YAP1-like isoform X9
transcriptional coactivator YAP1-like isoform X10
transcriptional coactivator YAP1-like isoform X2
transcriptional coactivator YAP1-like isoform X4
mitochondrial RNA pseudouridine synthase RPUSD4-like
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 36 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LOW QUALITY PROTEIN: protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like
cytochrome P450 315a1, mitochondrial-like, transcript variant X1
cytochrome P450 315a1, mitochondrial-like, transcript variant X2
cytochrome P450 315a1, mitochondrial-like isoform X1
cytochrome P450 315a1, mitochondrial-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like isoform X3
cyclic AMP-dependent transcription factor ATF-1-like, transcript variant X4
cyclic AMP-dependent transcription factor ATF-1-like, transcript variant X7
cyclic AMP-dependent transcription factor ATF-1-like, transcript variant X1
cyclic AMP-dependent transcription factor ATF-1-like, transcript variant X2
cyclic AMP-dependent transcription factor ATF-1-like isoform X1
cyclic AMP-dependent transcription factor ATF-1-like isoform X2
cyclic AMP-dependent transcription factor ATF-1-like, transcript variant X8
cyclic AMP-dependent transcription factor ATF-1-like, transcript variant X6
cyclic AMP-dependent transcription factor ATF-1-like isoform X6
cyclic AMP-dependent transcription factor ATF-1-like, transcript variant X3
cyclic AMP-dependent transcription factor ATF-1-like isoform X3
cyclic AMP-dependent transcription factor ATF-1-like isoform X4
cyclic AMP-dependent transcription factor ATF-1-like isoform X7
cyclic AMP-dependent transcription factor ATF-1-like, transcript variant X5
cyclic AMP-dependent transcription factor ATF-1-like isoform X5
general transcription factor IIH subunit 2-like, transcript variant X1
general transcription factor IIH subunit 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
general transcription factor IIH subunit 2-like isoform X1
general transcription factor IIH subunit 2-like isoform X2
reactive oxygen species modulator 1-like
uncharacterized LOC123516275, transcript variant X8
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 6 samples with support for all annotated introns
uncharacterized LOC123516275, transcript variant X4
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 6 samples with support for all annotated introns
uncharacterized LOC123516275, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC123516275, transcript variant X9
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 18 samples with support for all annotated introns
uncharacterized LOC123516275, transcript variant X6
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 19 samples with support for all annotated introns
uncharacterized LOC123516275, transcript variant X10
uncharacterized LOC123516275, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized LOC123516275, transcript variant X3
uncharacterized LOC123516275, transcript variant X7
uncharacterized LOC123516275, transcript variant X5
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 12 samples with support for all annotated introns
uncharacterized LOC123516276, transcript variant X1
uncharacterized LOC123516276, transcript variant X2
uncharacterized protein LOC123516276 isoform X1
uncharacterized protein LOC123516276 isoform X2
tyrosine-protein phosphatase non-receptor type 2-like, transcript variant X3
tyrosine-protein phosphatase non-receptor type 2-like, transcript variant X2
tyrosine-protein phosphatase non-receptor type 2-like isoform X3
tyrosine-protein phosphatase non-receptor type 2-like isoform X2
tyrosine-protein phosphatase non-receptor type 2-like, transcript variant X4
tyrosine-protein phosphatase non-receptor type 2-like, transcript variant X1
tyrosine-protein phosphatase non-receptor type 2-like isoform X4
tyrosine-protein phosphatase non-receptor type 2-like isoform X1
serine/threonine-protein phosphatase 2A activator-like, transcript variant X1
serine/threonine-protein phosphatase 2A activator-like, transcript variant X3
serine/threonine-protein phosphatase 2A activator-like isoform X2
serine/threonine-protein phosphatase 2A activator-like, transcript variant X2
serine/threonine-protein phosphatase 2A activator-like isoform X1
uncharacterized LOC123516282, transcript variant X1
uncharacterized LOC123516282, transcript variant X2
uncharacterized protein LOC123516282 isoform X1
uncharacterized protein LOC123516282 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase SMYD3-like, transcript variant X1
histone-lysine N-methyltransferase SMYD3-like, transcript variant X3
histone-lysine N-methyltransferase SMYD3-like isoform X3
SET and MYND domain-containing protein DDB_G0292140-like isoform X1
histone-lysine N-methyltransferase SMYD3-like, transcript variant X2
uncharacterized protein LOC123516285 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
PDZ domain-containing protein 8-like, transcript variant X13
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 8 samples with support for all annotated introns
PDZ domain-containing protein 8-like, transcript variant X6
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 7 samples with support for all annotated introns
PDZ domain-containing protein 8-like, 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
PDZ domain-containing protein 8-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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
PDZ domain-containing protein 8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
PDZ domain-containing protein 8-like, transcript variant X3
PDZ domain-containing protein 8-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PDZ domain-containing protein 8-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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
PDZ domain-containing protein 8-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
PDZ domain-containing protein 8-like isoform X9
PDZ domain-containing protein 8-like isoform X2
PDZ domain-containing protein 8-like isoform X1
PDZ domain-containing protein 8-like isoform X3
PDZ domain-containing protein 8-like isoform X5
PDZ domain-containing protein 8-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
PDZ domain-containing protein 8-like isoform X4
PDZ domain-containing protein 8-like, transcript variant X14
PDZ domain-containing protein 8-like isoform X10
PDZ domain-containing protein 8-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PDZ domain-containing protein 8-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
PDZ domain-containing protein 8-like isoform X7
PDZ domain-containing protein 8-like isoform X6
PDZ domain-containing protein 8-like, transcript variant X12
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 9 samples with support for all annotated introns
PDZ domain-containing protein 8-like isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 5-like
uncharacterized LOC123516296, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized LOC123516296, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123516296, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC123516296, transcript variant X6
uncharacterized LOC123516296, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123516296, transcript variant X1
uncharacterized protein LOC123516296 isoform X4
uncharacterized protein LOC123516296 isoform X3
uncharacterized protein LOC123516296 isoform X1
uncharacterized protein LOC123516296 isoform X2
uncharacterized LOC123516296, transcript variant X8
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 LOC123516296, transcript variant X7
uncharacterized LOC123516299, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
uncharacterized LOC123516299, transcript variant X2
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 50 samples with support for all annotated introns
uncharacterized protein LOC123516299 isoform X1
uncharacterized protein LOC123516299 isoform 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 12 samples with support for all annotated introns
uncharacterized LOC123516302, transcript variant X1
uncharacterized LOC123516302, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123516302, transcript variant X2
uncharacterized protein LOC123516302 isoform X1
uncharacterized LOC123516302, transcript variant X5
uncharacterized protein LOC123516302 isoform X3
uncharacterized LOC123516302, transcript variant X4
uncharacterized protein LOC123516302 isoform X2
LOW QUALITY PROTEIN: xaa-Pro aminopeptidase 1-like
THO complex subunit 5 homolog, transcript variant X2
THO complex subunit 5 homolog, transcript variant X8
THO complex subunit 5 homolog, transcript variant X6
THO complex subunit 5 homolog, transcript variant X5
THO complex subunit 5 homolog, transcript variant X4
THO complex subunit 5 homolog, transcript variant X10
THO complex subunit 5 homolog, transcript variant X7
THO complex subunit 5 homolog, transcript variant X1
THO complex subunit 5 homolog, transcript variant X9
THO complex subunit 5 homolog, transcript variant X3
THO complex subunit 5 homolog isoform X3
THO complex subunit 5 homolog isoform X2
THO complex subunit 5 homolog isoform X4
THO complex subunit 5 homolog isoform X1
THO complex subunit 5 homolog isoform X5
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ecdysone receptor-like, transcript variant X1
ecdysone receptor-like, transcript variant X2
ecdysone receptor-like, transcript variant X4
ecdysone receptor-like, transcript variant X5
ecdysone receptor-like, transcript variant X3
ecdysone receptor-like, transcript variant X6
ecdysone receptor-like, transcript variant X7
ecdysone receptor-like, transcript variant X14
ecdysone receptor-like, transcript variant X8
ecdysone receptor-like, transcript variant X11
ecdysone receptor-like, transcript variant X10
ecdysone receptor-like, transcript variant X9
ecdysone receptor-like, transcript variant X13
ecdysone receptor-like, transcript variant X12
ecdysone receptor-like, transcript variant X15
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
high-affinity choline transporter 1-like, transcript variant X4
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 16 samples with support for all annotated introns
high-affinity choline transporter 1-like, transcript variant X5
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 15 samples with support for all annotated introns
high-affinity choline transporter 1-like, transcript variant X3
high-affinity choline transporter 1-like, transcript variant X1
high-affinity choline transporter 1-like, transcript variant X2
high-affinity choline transporter 1-like isoform X1
high-affinity choline transporter 1-like isoform X2
glutamate receptor ionotropic, delta-1-like isoform X1
glutamate receptor ionotropic, delta-1-like isoform 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 3 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 6 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 2 samples with support for all annotated introns
uncharacterized protein LOC123516083 isoform X8
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
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 LOC123516083 isoform X11
uncharacterized protein LOC123516083 isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC123516083 isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC123516083 isoform X12
uncharacterized protein LOC123516083 isoform X13
uncharacterized protein LOC123516083 isoform X14
uncharacterized protein LOC123516083 isoform X19
uncharacterized protein LOC123516083 isoform X20
uncharacterized protein LOC123516083 isoform X22
uncharacterized protein LOC123516083 isoform X1
uncharacterized protein LOC123516083 isoform X2
uncharacterized protein LOC123516083 isoform X4
uncharacterized protein LOC123516083 isoform X5
uncharacterized protein LOC123516083 isoform X3
uncharacterized protein LOC123516083 isoform X6
uncharacterized protein LOC123516083 isoform X7
uncharacterized protein LOC123516083 isoform X17
uncharacterized protein LOC123516083 isoform X18
uncharacterized protein LOC123516083 isoform X23
uncharacterized protein LOC123516083 isoform X24
uncharacterized protein LOC123516083 isoform X25
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
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
uncharacterized protein LOC123516083 isoform X15
uncharacterized protein LOC123516083 isoform X16
serine/arginine repetitive matrix protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC123516087, transcript variant X2
uncharacterized LOC123516087, transcript variant X1
protein Wnt-5b-like, transcript variant X1
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
F-box/LRR-repeat protein 14-like, transcript variant X1
F-box/LRR-repeat protein 14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein Wnt-5b-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
lysosome-associated membrane glycoprotein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123515920, transcript variant X1
uncharacterized LOC123515920, transcript variant X2
uncharacterized protein LOC123515920 isoform X1
uncharacterized protein LOC123515920 isoform X2
uroporphyrinogen-III synthase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
uroporphyrinogen-III synthase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC123515924, transcript variant X1
uncharacterized LOC123515924, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123515924, 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 42 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GFFJ01065121.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 274 bases not found in genome assembly; 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