Portunus trituberculatus isolate SZX2019 chromosome 15, 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\nCM030085.1.\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.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC123504184
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
COORDINATES: polyA evidence [ECO:0006239]
RAC-beta serine/threonine-protein kinase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 99% 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 Protein, and 48% coverage of the annotated genomic feature by RNAseq alignments
glycerate kinase-like, transcript variant X1
glycerate kinase-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
structural maintenance of chromosomes protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
respirasome Complex Assembly Factor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
respirasome Complex Assembly Factor 1-like, transcript variant X2
respirasome Complex Assembly Factor 1-like isoform X2
respirasome Complex Assembly Factor 1-like isoform X1
WD and tetratricopeptide repeats protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
WD and tetratricopeptide repeats protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
WD and tetratricopeptide repeats protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
WD and tetratricopeptide repeats protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
WD and tetratricopeptide repeats protein 1-like isoform X3
WD and tetratricopeptide repeats protein 1-like isoform X1
WD and tetratricopeptide repeats protein 1-like isoform X2
uncharacterized LOC123504012, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC123504012, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
putative uncharacterized protein DDB_G0268364
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123504182, transcript variant X2
uncharacterized LOC123504182, transcript variant X1
uncharacterized LOC123504177, transcript variant X2
uncharacterized LOC123504177, transcript variant X1
uncharacterized protein LOC123504177 isoform X2
uncharacterized protein LOC123504177 isoform X1
AN1-type zinc finger protein 2A-like, transcript variant X1
AN1-type zinc finger protein 2A-like isoform X1
AN1-type zinc finger protein 2A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
AN1-type zinc finger protein 2A-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 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 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123504144, transcript variant X2
uncharacterized LOC123504144, transcript variant X1
uncharacterized protein LOC123504144 isoform X2
uncharacterized protein LOC123504144 isoform X1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123504131, transcript variant X3
uncharacterized LOC123504131, transcript variant X1
uncharacterized LOC123504131, transcript variant X2
uncharacterized protein LOC123504131 isoform X1
uncharacterized LOC123504131, transcript variant X4
uncharacterized protein LOC123504131 isoform X2
heparan sulfate glucosamine 3-O-sulfotransferase 6-like, transcript variant X1
heparan sulfate glucosamine 3-O-sulfotransferase 6-like, transcript variant X2
heparan sulfate glucosamine 3-O-sulfotransferase 6-like, transcript variant X3
heparan sulfate glucosamine 3-O-sulfotransferase 6-like isoform X1
heparan sulfate glucosamine 3-O-sulfotransferase 6-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 3A1-like isoform X2
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: 8 Proteins
LIM and SH3 domain protein 1-like, transcript variant X1
LIM and SH3 domain protein 1-like, transcript variant X3
LIM and SH3 domain protein 1-like, transcript variant X4
LIM and SH3 domain protein Lasp-like isoform X1
LIM and SH3 domain protein 1-like isoform X3
LIM and SH3 domain protein 1-like isoform X4
LIM and SH3 domain protein 1-like, transcript variant X2
LIM and SH3 domain protein Lasp-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transfer RNA isoleucine (anticodon GAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine/threonine-protein kinase SMG1-like
uncharacterized LOC123504311, transcript variant X1
uncharacterized LOC123504311, transcript variant X3
uncharacterized LOC123504311, transcript variant X2
uncharacterized LOC123504311, transcript variant X4
uncharacterized protein LOC123504311 isoform X2
uncharacterized protein LOC123504311 isoform X1
uncharacterized protein LOC123504311 isoform X4
uncharacterized protein LOC123504311 isoform X3
multiple inositol polyphosphate phosphatase 1-like, transcript variant X16
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 3 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1-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 3 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1-like, transcript variant X15
multiple inositol polyphosphate phosphatase 1-like, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1-like, transcript variant X9
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 4 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1-like, transcript variant X6
multiple inositol polyphosphate phosphatase 1-like, transcript variant X22
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
multiple inositol polyphosphate phosphatase 1-like, transcript variant X10
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
multiple inositol polyphosphate phosphatase 1-like, transcript variant X13
multiple inositol polyphosphate phosphatase 1-like, transcript variant X11
multiple inositol polyphosphate phosphatase 1-like, transcript variant X14
multiple inositol polyphosphate phosphatase 1-like, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1-like, transcript variant X12
multiple inositol polyphosphate phosphatase 1-like, transcript variant X2
multiple inositol polyphosphate phosphatase 1-like, transcript variant X7
multiple inositol polyphosphate phosphatase 1-like, transcript variant X5
multiple inositol polyphosphate phosphatase 1-like, transcript variant X3
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 9 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1-like, transcript variant X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1-like, 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 5 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1-like, transcript variant X19
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 5 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1-like, transcript variant X21
multiple inositol polyphosphate phosphatase 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
multiple inositol polyphosphate phosphatase 1-like isoform X1
multiple inositol polyphosphate phosphatase 1-like isoform X2
multiple inositol polyphosphate phosphatase 1-like isoform X3
uncharacterized LOC123504026, transcript variant X1
uncharacterized LOC123504026, transcript variant X2
paired box protein Pax-5-like, transcript variant X6
paired box protein Pax-5-like, transcript variant X5
paired box protein Pax-5-like, transcript variant X8
paired box protein Pax-5-like, transcript variant X7
paired box protein Pax-5-like, transcript variant X4
paired box protein Pax-5-like, transcript variant X1
paired box protein Pax-5-like, transcript variant X3
paired box protein Pax-5-like, transcript variant X16
paired box protein Pax-5-like, transcript variant X12
paired box protein Pax-5-like, transcript variant X15
paired box protein Pax-5-like, transcript variant X2
paired box protein Pax-5-like, transcript variant X9
paired box protein Pax-5-like, transcript variant X13
paired box protein Pax-5-like, transcript variant X11
paired box protein Pax-5-like, transcript variant X10
paired box protein Pax-5-like isoform X6
paired box protein Pax-5-like isoform X5
paired box protein Pax-5-like isoform X8
paired box protein Pax-5-like isoform X7
paired box protein Pax-5-like isoform X4
paired box protein Pax-5-like isoform X1
paired box protein Pax-5-like isoform X3
paired box protein Pax-5-like isoform X16
paired box protein Pax-5-like isoform X12
paired box protein Pax-5-like isoform X15
paired box protein Pax-5-like isoform X2
paired box protein Pax-5-like isoform X9
paired box protein Pax-5-like isoform X13
paired box protein Pax-5-like isoform X11
paired box protein Pax-5-like isoform X10
paired box protein Pax-5-like, transcript variant X14
paired box protein Pax-5-like isoform X14
uncharacterized LOC123504028, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123504028, 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 3 samples with support for all annotated introns
uncharacterized LOC123504028, transcript variant X4
uncharacterized LOC123504028, transcript variant X3
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon UAC); 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 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger MYND domain-containing protein 19-like, transcript variant X1
zinc finger MYND domain-containing protein 19-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
zinc finger MYND domain-containing protein 19-like isoform X1
zinc finger MYND domain-containing protein 19-like isoform X2
zinc finger MYND domain-containing protein 11-like, transcript variant X5
zinc finger MYND domain-containing protein 11-like, transcript variant X3
zinc finger MYND domain-containing protein 11-like, transcript variant X1
zinc finger MYND domain-containing protein 11-like, transcript variant X2
zinc finger MYND domain-containing protein 11-like, transcript variant X4
zinc finger MYND domain-containing protein 11-like isoform X3
zinc finger MYND domain-containing protein 11-like isoform X2
zinc finger MYND domain-containing protein 11-like isoform X1
glutamate receptor U1-like, transcript variant X3
glutamate receptor U1-like, transcript variant X6
glutamate receptor U1-like, transcript variant X4
glutamate receptor U1-like, transcript variant X5
glutamate receptor U1-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 1 sample with support for all annotated introns
glutamate receptor U1-like, transcript variant X1
glutamate receptor ionotropic, kainate 3-like isoform X4
tyrosine--tRNA ligase, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
LOW QUALITY PROTEIN: tyrosine--tRNA ligase, mitochondrial-like
tigger transposable element-derived protein 1-like
rab3 GTPase-activating protein catalytic subunit-like, transcript variant X1
rab3 GTPase-activating protein catalytic subunit-like, transcript variant X2
rab3 GTPase-activating protein catalytic subunit-like isoform X1
rab3 GTPase-activating protein catalytic subunit-like isoform 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 10 samples with support for all annotated introns
golgin subfamily B member 1-like, transcript variant X4
golgin subfamily B member 1-like, transcript variant X3
golgin subfamily B member 1-like, transcript variant X2
golgin subfamily B member 1-like, transcript variant X1
uncharacterized LOC123504138, transcript variant X2
uncharacterized LOC123504138, transcript variant X1
uncharacterized LOC123504138, transcript variant X3
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein LOC123504138 isoform X1
uncharacterized protein LOC123504138 isoform X2
transfer RNA tyrosine (anticodon GUA); 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123504018, transcript variant X2
uncharacterized LOC123504018, transcript variant X1
leucine zipper putative tumor suppressor 2 homolog, transcript variant X3
leucine zipper putative tumor suppressor 2 homolog, transcript variant X4
leucine zipper putative tumor suppressor 2 homolog, transcript variant X1
leucine zipper putative tumor suppressor 2 homolog, transcript variant X2
leucine zipper putative tumor suppressor 1-like isoform X2
leucine zipper putative tumor suppressor 2 homolog isoform X1
LOW QUALITY PROTEIN: fatty acid-binding protein-like
uncharacterized LOC123504046, transcript variant X1
uncharacterized LOC123504046, transcript variant X2
uncharacterized LOC123504046, transcript variant X3
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon GCA); 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 LOC123504105, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123504105, transcript variant X1
uncharacterized LOC123504105, transcript variant X4
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
uncharacterized LOC123504105, transcript variant X3
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 10 samples with support for all annotated introns
uncharacterized protein LOC123504105 isoform X1
uncharacterized protein LOC123504105 isoform X2
uncharacterized protein LOC123504105 isoform X3
pulmonary surfactant-associated protein D-like
LOW QUALITY PROTEIN: uncharacterized protein LOC123504088
uncharacterized LOC123504087, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123504087, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123504087, transcript variant X3
uncharacterized protein LOC123504087 isoform X3
uncharacterized protein LOC123504087 isoform X2
uncharacterized protein LOC123504087 isoform X1
uncharacterized LOC123504290, transcript variant X2
uncharacterized LOC123504290, transcript variant X4
uncharacterized LOC123504290, transcript variant X3
uncharacterized LOC123504290, transcript variant X1
uncharacterized LOC123504204, transcript variant X1
uncharacterized LOC123504204, transcript variant X5
uncharacterized LOC123504204, transcript variant X3
uncharacterized LOC123504204, transcript variant X4
uncharacterized LOC123504204, transcript variant X2
uncharacterized LOC123504204, transcript variant X6
uncharacterized LOC123504276, transcript variant X2
uncharacterized LOC123504276, transcript variant X1
eyes absent homolog 2-like, transcript variant X1
eyes absent homolog 2-like, transcript variant X2
uncharacterized LOC123504275, transcript variant X2
uncharacterized LOC123504275, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
signal peptidase complex catalytic subunit SEC11A-like
uncharacterized LOC123504097, transcript variant X1
uncharacterized LOC123504097, transcript variant X2
cell adhesion molecule 2-like, transcript variant X2
cell adhesion molecule 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
cell adhesion molecule 2-like, transcript variant X1
cell adhesion molecule 2-like isoform X1
cell adhesion molecule 2-like isoform X2
cell adhesion molecule 2-like isoform X3
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
peptide methionine sulfoxide reductase MsrB-like, transcript variant X3
peptide methionine sulfoxide reductase MsrB-like, transcript variant X1
peptide methionine sulfoxide reductase MsrB-like, transcript variant X2
peptide methionine sulfoxide reductase MsrB-like
uncharacterized LOC123504220, transcript variant X2
uncharacterized LOC123504220, transcript variant X1
uncharacterized LOC123504221, transcript variant X5
uncharacterized LOC123504221, transcript variant X2
uncharacterized LOC123504221, transcript variant X7
uncharacterized LOC123504221, transcript variant X4
uncharacterized LOC123504221, transcript variant X3
uncharacterized LOC123504221, transcript variant X6
uncharacterized LOC123504221, transcript variant X1
protein piccolo-like, transcript variant X1
protein piccolo-like, transcript variant X2
protein piccolo-like, transcript variant X3
protein piccolo-like, transcript variant X4
heparan-sulfate 6-O-sulfotransferase 2-like
dihydropyrimidinase-like, transcript variant X4
dihydropyrimidinase-like, transcript variant X6
dihydropyrimidinase-like, transcript variant X3
dihydropyrimidinase-like, transcript variant X5
dihydropyrimidinase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
dihydropyrimidinase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
dihydropyrimidinase-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dihydropyrimidinase-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
dihydropyrimidinase-like, transcript variant X10
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
dihydropyrimidinase-like, transcript variant X9
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 6 samples with support for all annotated introns
trafficking protein particle complex subunit 3-like
armadillo segment polarity protein-like, transcript variant X1
armadillo segment polarity protein-like isoform X1
armadillo segment polarity protein-like, transcript variant X2
armadillo segment polarity protein-like, transcript variant X3
armadillo segment polarity protein-like isoform X2
armadillo segment polarity protein-like isoform X3
DET1- and DDB1-associated protein 1-like, transcript variant X1
DET1- and DDB1-associated protein 1-like isoform X1
DET1- and DDB1-associated protein 1-like, transcript variant X2
DET1- and DDB1-associated protein 1-like, transcript variant X3
DET1- and DDB1-associated protein 1-like isoform X3
DET1- and DDB1-associated protein 1-like isoform X2
uncharacterized LOC123504231, transcript variant X2
uncharacterized LOC123504231, transcript variant X3
uncharacterized LOC123504230, transcript variant X2
uncharacterized LOC123504230, transcript variant X1
uncharacterized protein LOC123504230 isoform X2
uncharacterized protein LOC123504230 isoform X1
uncharacterized LOC123504231, transcript variant X1
uncharacterized LOC123504235, transcript variant X2
uncharacterized LOC123504235, transcript variant X3
uncharacterized LOC123504235, transcript variant X1
uncharacterized protein LOC123504235 isoform X2
uncharacterized protein LOC123504235 isoform X3
uncharacterized protein LOC123504235 isoform X1
sphingomyelin phosphodiesterase-like, transcript variant X2
sphingomyelin phosphodiesterase-like, transcript variant X1
sphingomyelin phosphodiesterase-like isoform X2
sphingomyelin phosphodiesterase-like isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
von Willebrand factor D and EGF domain-containing protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
von Willebrand factor D and EGF domain-containing protein-like, 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 5 samples with support for all annotated introns
uncharacterized protein LOC123504238 isoform X1
uncharacterized LOC123504242, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC123504242 isoform X2
uncharacterized LOC123504242, transcript variant X1
uncharacterized protein LOC123504242 isoform X1
uncharacterized LOC123504241, transcript variant X3
uncharacterized LOC123504241, transcript variant X2
uncharacterized protein LOC123504241 isoform X3
uncharacterized protein LOC123504241 isoform X2
uncharacterized LOC123504241, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein LOC123504241 isoform X1
uncharacterized LOC123504239, transcript variant X1
uncharacterized LOC123504239, transcript variant X2
uncharacterized protein LOC123504239 isoform X2
uncharacterized protein LOC123504239 isoform X1
von Willebrand factor D and EGF domain-containing protein-like, transcript variant X3
von Willebrand factor D and EGF domain-containing protein-like isoform 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 3 samples with support for all annotated introns
uncharacterized LOC123504250, transcript variant X5
uncharacterized LOC123504250, transcript variant X1
uncharacterized LOC123504250, transcript variant X2
uncharacterized LOC123504250, transcript variant X3
uncharacterized LOC123504250, transcript variant X4
uncharacterized protein LOC123504250 isoform X4
uncharacterized protein LOC123504250 isoform X2
uncharacterized protein LOC123504250 isoform X1
uncharacterized protein LOC123504250 isoform 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123504253, transcript variant X2
uncharacterized LOC123504253, transcript variant X3
uncharacterized LOC123504253, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
peroxidasin homolog, transcript variant X2
peroxidasin homolog, transcript variant X1
uncharacterized LOC123504257, transcript variant X1
uncharacterized LOC123504257, transcript variant X2
uncharacterized LOC123504257, 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 11 samples with support for all annotated introns
uncharacterized LOC123504257, transcript variant X3
uncharacterized LOC123504257, transcript variant X4
uncharacterized protein LOC123504257 isoform X1
uncharacterized protein LOC123504257 isoform X2
uncharacterized protein LOC123504257 isoform X3
uncharacterized protein LOC123504257 isoform X4
uncharacterized protein LOC123504257 isoform X5
uncharacterized LOC123504257, transcript variant X6
uncharacterized protein LOC123504257 isoform X6
uncharacterized LOC123504259, transcript variant X2
uncharacterized LOC123504259, transcript variant X1
uncharacterized LOC123504259, transcript variant X4
uncharacterized LOC123504259, transcript variant X3
uncharacterized LOC123504259, transcript variant X5
uncharacterized protein LOC123504259 isoform X3
uncharacterized protein LOC123504259 isoform X2
uncharacterized protein LOC123504259 isoform X5
uncharacterized protein LOC123504259 isoform X1
uncharacterized protein LOC123504259 isoform X4
potassium channel subfamily K member 13-like, transcript variant X2
potassium channel subfamily K member 13-like, transcript variant X1
potassium channel subfamily K member 13-like, transcript variant X3
potassium channel subfamily K member 13-like isoform X1
potassium channel subfamily K member 13-like isoform X2
uncharacterized LOC123504263, 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 26 samples with support for all annotated introns
uncharacterized LOC123504263, 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
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: POC1 centriolar protein homolog A-like
tuftelin-interacting protein 11-like, transcript variant X1
tuftelin-interacting protein 11-like, transcript variant X2
myosin heavy chain, non-muscle-like, transcript variant X5
myosin heavy chain, non-muscle-like, transcript variant X4
myosin heavy chain, non-muscle-like, transcript variant X1
myosin heavy chain, non-muscle-like, transcript variant X3
myosin heavy chain, non-muscle-like, transcript variant X2
myosin heavy chain, non-muscle-like isoform X5
uncharacterized protein LOC123504266 isoform X4
myosin heavy chain, non-muscle-like isoform X1
uncharacterized protein LOC123504266 isoform X3
myosin heavy chain, non-muscle-like isoform X2
LOW QUALITY PROTEIN: uncharacterized protein LOC123504267
transmembrane protein 70 homolog, mitochondrial-like, transcript variant X6
transmembrane protein 70 homolog, mitochondrial-like, transcript variant X7
transmembrane protein 70 homolog, mitochondrial-like, transcript variant X1
transmembrane protein 70 homolog, mitochondrial-like, transcript variant X5
transmembrane protein 70 homolog, mitochondrial-like, transcript variant X4
transmembrane protein 70 homolog, mitochondrial-like, transcript variant X2
transmembrane protein 70 homolog, mitochondrial-like, transcript variant X3
transmembrane protein 70 homolog, mitochondrial-like isoform X2
transmembrane protein 70 homolog, mitochondrial-like isoform X1
paternally-expressed gene 3 protein-like
activating signal cointegrator 1 complex subunit 2 homolog
thiopurine S-methyltransferase-like, transcript variant X2
probable thiopurine S-methyltransferase isoform X2
thiopurine S-methyltransferase-like, transcript variant X4
thiopurine S-methyltransferase-like, transcript variant X1
probable thiopurine S-methyltransferase isoform X1
thiopurine S-methyltransferase-like, transcript variant X3
thiopurine S-methyltransferase-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
thiopurine S-methyltransferase-like isoform X2
uncharacterized LOC123504044, transcript variant X1
uncharacterized LOC123504044, transcript variant X2
alpha-ketoglutarate-dependent 2,4-dichlorophenoxyacetate dioxygenase-like
zinc finger protein 628-like, transcript variant X3
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 8 samples with support for all annotated introns
zinc finger protein 628-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 6 samples with support for all annotated introns
zinc finger protein 628-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 15 samples with support for all annotated introns
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X1
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X3
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X11
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X7
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X8
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X4
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X5
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X6
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X9
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X2
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X13
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X14
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X10
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X15
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X17
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X12
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X18
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X19
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X16
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X20
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X21
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X24
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X22
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X25
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X23
voltage-dependent calcium channel subunit alpha-2/delta-3-like, transcript variant X26
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X1
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X5
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X11
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X13
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X6
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X7
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X3
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X8
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X9
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X10
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X12
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X14
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X15
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X16
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X17
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X18
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X19
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X20
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X4
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X2
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X24
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X21
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X22
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X25
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X23
voltage-dependent calcium channel subunit alpha-2/delta-3-like isoform X26
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 LOC123504136, transcript variant X1
uncharacterized LOC123504136, transcript variant X3
uncharacterized LOC123504136, transcript variant X5
uncharacterized LOC123504136, transcript variant X2
uncharacterized LOC123504136, transcript variant X4
sodium channel protein 60E-like, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein 60E-like isoform X12
sodium channel protein 60E-like, transcript variant X11
sodium channel protein 60E-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein 60E-like, transcript variant X3
sodium channel protein 60E-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein 60E-like, transcript variant X5
sodium channel protein 60E-like, transcript variant X9
sodium channel protein 60E-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein 60E-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein 60E-like, transcript variant X4
sodium channel protein 60E-like, transcript variant X8
sodium channel protein 60E-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium channel protein 60E-like isoform X1
sodium channel protein 60E-like isoform X6
sodium channel protein 60E-like isoform X3
sodium channel protein 60E-like isoform X7
sodium channel protein 60E-like isoform X4
sodium channel protein 60E-like isoform X5
sodium channel protein 60E-like isoform X8
sodium channel protein 60E-like isoform X9
sodium channel protein 60E-like isoform X10
sodium channel protein 60E-like isoform X2
sodium channel protein 60E-like isoform X11
potassium channel subfamily K member 15-like
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
uncharacterized LOC123504287, transcript variant X1
uncharacterized LOC123504287, transcript variant X2
autism susceptibility gene 2 protein homolog
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123504321, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123504321, transcript variant X2
LIM homeobox transcription factor 1-alpha-like, transcript variant X1
LIM homeobox transcription factor 1-alpha-like, transcript variant X2
LIM homeobox transcription factor 1-alpha-like, transcript variant X3
LIM homeobox transcription factor 1-alpha-like, transcript variant X4
LIM homeobox transcription factor 1-alpha-like isoform X3
LIM homeobox transcription factor 1-beta-like isoform X4
LIM homeobox transcription factor 1-alpha-like isoform X1
LIM homeobox transcription factor 1-beta-like isoform X2
uncharacterized LOC123504325, transcript variant X1
uncharacterized LOC123504325, transcript variant X2
uncharacterized LOC123504325, transcript variant X3
uncharacterized LOC123504323, transcript variant X2
uncharacterized LOC123504323, transcript variant X1
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123504326, transcript variant X11
uncharacterized LOC123504326, 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 4 samples with support for all annotated introns
uncharacterized LOC123504326, transcript variant X8
uncharacterized LOC123504326, 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 13 samples with support for all annotated introns
uncharacterized LOC123504326, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC123504326, transcript variant X10
uncharacterized LOC123504326, transcript variant X9
uncharacterized LOC123504326, transcript variant X4
uncharacterized LOC123504326, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123504326, transcript variant X5
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 2 samples with support for all annotated introns
uncharacterized LOC123504326, transcript variant X7
uncharacterized protein LOC123504326 isoform X4
uncharacterized protein LOC123504326 isoform X3
uncharacterized protein LOC123504326 isoform X1
uncharacterized protein LOC123504326 isoform X2
facilitated trehalose transporter Tret1-like
LOW QUALITY PROTEIN: facilitated trehalose transporter Tret1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123504330, transcript variant X2
uncharacterized LOC123504330, transcript variant X3
uncharacterized LOC123504330, transcript variant X1
uncharacterized protein LOC123504330 isoform X1
uncharacterized protein LOC123504330 isoform X2
calcineurin subunit B type 2, transcript variant X7
calcineurin subunit B type 2, transcript variant X12
calcineurin subunit B type 2, transcript variant X5
calcineurin subunit B type 2, transcript variant X6
calcineurin subunit B type 2, transcript variant X11
calcineurin subunit B type 2, transcript variant X13
calcineurin subunit B type 2, transcript variant X8
calcineurin subunit B type 2, transcript variant X1
calcineurin subunit B type 2, transcript variant X3
calcineurin subunit B type 2, transcript variant X2
calcineurin subunit B type 2, transcript variant X4
calcineurin subunit B type 2 isoform X10
calcineurin subunit B type 2, transcript variant X9
calcineurin subunit B type 2, transcript variant X14
calcineurin subunit B type 2, transcript variant X15
calcineurin subunit B type 2, transcript variant X10
calcineurin subunit B type 2 isoform X11
calcineurin subunit B type 2 isoform X12
dual specificity tyrosine-phosphorylation-regulated kinase 1A-like, transcript variant X1
dual specificity tyrosine-phosphorylation-regulated kinase 1A-like, transcript variant X2
dual specificity tyrosine-phosphorylation-regulated kinase 1A-like isoform X1
dual specificity tyrosine-phosphorylation-regulated kinase 1A-like isoform X2
adenylate kinase isoenzyme 1-like, transcript variant X2
adenylate kinase isoenzyme 1-like, transcript variant X1
adenylate kinase isoenzyme 1-like, transcript variant X3
adenylate kinase isoenzyme 1-like isoform X2
adenylate kinase isoenzyme 1-like isoform X1
adenylate kinase isoenzyme 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized LOC123504336, transcript variant X3
uncharacterized LOC123504336, transcript variant X2
uncharacterized protein LOC123504336 isoform X2
uncharacterized LOC123504336, transcript variant X4
uncharacterized LOC123504336, transcript variant X1
uncharacterized protein LOC123504336 isoform X1
zinc transporter 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc transporter 2-like, transcript variant X1
myosuppressin-like, transcript variant X2
myosuppressin-like, transcript variant X1
solute carrier family 12 member 9-like, transcript variant X1
solute carrier family 12 member 9-like, transcript variant X2
solute carrier family 12 member 9-like isoform X2
solute carrier family 12 member 9-like isoform X1
S-adenosylmethionine decarboxylase proenzyme-like
kinesin light chain-like, transcript variant X6
kinesin light chain-like, transcript variant X8
kinesin light chain-like, transcript variant X9
kinesin light chain-like, transcript variant X7
kinesin light chain-like, transcript variant X3
kinesin light chain-like, transcript variant X1
kinesin light chain-like, transcript variant X2
kinesin light chain-like, transcript variant X16
kinesin light chain-like, transcript variant X13
kinesin light chain-like, transcript variant X5
kinesin light chain-like, transcript variant X4
kinesin light chain-like, transcript variant X17
kinesin light chain-like, transcript variant X14
kinesin light chain-like, transcript variant X10
kinesin light chain-like, transcript variant X11
kinesin light chain-like, transcript variant X15
kinesin light chain-like, transcript variant X12
kinesin light chain-like, transcript variant X18
protein arginine methyltransferase NDUFAF7 homolog, mitochondrial-like
LOW QUALITY PROTEIN: uncharacterized protein LOC123504352
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine/arginine repetitive matrix protein 1-like, transcript variant X2
serine/arginine repetitive matrix protein 1-like, transcript variant X1
serine/arginine repetitive matrix protein 1-like isoform X2
serine/arginine repetitive matrix protein 1-like isoform 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 1 sample with support for all annotated introns
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like isoform X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X2
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like isoform X2
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X4
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X5
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X3
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like isoform X3
chromatin assembly factor 1 subunit B-like, transcript variant X2
chromatin assembly factor 1 subunit B-like, transcript variant X1
chromatin assembly factor 1 subunit B-like
protein ST7 homolog, transcript variant X1
protein ST7 homolog, transcript variant X3
protein ST7 homolog, transcript variant X2
DNA-(apurinic or apyrimidinic site) endonuclease-like
uncharacterized LOC123504295, transcript variant X1
uncharacterized LOC123504295, transcript variant X2
uncharacterized protein LOC123504295 isoform X1
uncharacterized protein LOC123504295 isoform X2
uncharacterized LOC123503960, transcript variant X5
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 LOC123503960, 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 9 samples with support for all annotated introns
uncharacterized LOC123503960, 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 33 samples with support for all annotated introns
uncharacterized LOC123503960, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
uncharacterized LOC123503960, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
lysocardiolipin acyltransferase 1-like, transcript variant X1
lysocardiolipin acyltransferase 1-like, transcript variant X4
lysocardiolipin acyltransferase 1-like, transcript variant X2
lysocardiolipin acyltransferase 1-like, transcript variant X3
coiled-coil domain-containing protein 6-like, transcript variant X4
coiled-coil domain-containing protein 6-like, transcript variant X3
coiled-coil domain-containing protein 6-like, transcript variant X1
coiled-coil domain-containing protein 6-like, transcript variant X2
coiled-coil domain-containing protein 6-like isoform X4
coiled-coil domain-containing protein 6-like isoform X1
coiled-coil domain-containing protein 6-like isoform X2
coiled-coil domain-containing protein 6-like isoform X3
arginine/serine-rich coiled-coil protein 2-like
uncharacterized LOC123503969, transcript variant X2
uncharacterized LOC123503969, transcript variant X1
uncharacterized protein LOC123503969 isoform X2
uncharacterized protein LOC123503969 isoform X1
tRNA pseudouridine synthase A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
tRNA pseudouridine synthase A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 3 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
tRNA pseudouridine synthase A-like, transcript variant X2
tRNA pseudouridine synthase A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 3 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
tRNA pseudouridine synthase A-like isoform X1
tRNA pseudouridine synthase A-like isoform X2
uncharacterized LOC123503982, transcript variant X4
uncharacterized LOC123503982, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC123503982, transcript variant X3
uncharacterized LOC123503982, transcript variant X2
ankyrin repeat domain-containing protein 10-like, transcript variant X6
ankyrin repeat domain-containing protein 10-like isoform X4
ankyrin repeat domain-containing protein 10-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
ankyrin repeat domain-containing protein 10-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 14 samples with support for all annotated introns
ankyrin repeat domain-containing protein 10-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 10 samples with support for all annotated introns
uncharacterized protein LOC123503974 isoform X1
ankyrin repeat domain-containing protein 12-like isoform X2
ankyrin repeat domain-containing protein 10-like, transcript variant X5
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 24 samples with support for all annotated introns
ankyrin repeat domain-containing protein 10-like, transcript variant X4
ankyrin repeat domain-containing protein 10-like isoform X3
uncharacterized LOC123503982, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uridine-cytidine kinase 2-like, transcript variant X2
uridine-cytidine kinase 2-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 11 samples with support for all annotated introns
uridine-cytidine kinase 2-like, transcript variant X5
uridine-cytidine kinase 2-like, transcript variant X1
uridine-cytidine kinase 2-like isoform X1
uridine-cytidine kinase 2-like isoform X3
uridine-cytidine kinase 2-like, transcript variant X4
uridine-cytidine kinase 2-A-like isoform X2
MARVEL domain-containing protein 1-like, transcript variant X1
MARVEL domain-containing protein 1-like, transcript variant X4
MARVEL domain-containing protein 1-like, transcript variant X3
MARVEL domain-containing protein 1-like, transcript variant X5
MARVEL domain-containing protein 1-like, transcript variant X6
MARVEL domain-containing protein 1-like, transcript variant X2
MARVEL domain-containing protein 1-like isoform X6
uncharacterized protein LOC123503979 isoform X5
uncharacterized protein LOC123503979 isoform X3
uncharacterized protein LOC123503979 isoform X4
uncharacterized protein LOC123503979 isoform X1
uncharacterized protein LOC123503979 isoform X2
WD repeat-containing protein 35-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WD repeat-containing protein 35-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
WD repeat-containing protein 35-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
WD repeat-containing protein 35-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
WD repeat-containing protein 35-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable 28S ribosomal protein S6, mitochondrial
uncharacterized LOC123503973, transcript variant X2
uncharacterized LOC123503973, transcript variant X1
uncharacterized protein LOC123503973 isoform X1
uncharacterized protein LOC123503973 isoform X2
UNC93-like protein, transcript variant X2
UNC93-like protein, transcript variant X1
UNC93-like protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123504014, transcript variant X1
uncharacterized LOC123504014, transcript variant X2
uncharacterized protein LOC123504014 isoform X1
uncharacterized protein LOC123504014 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 51% 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
uncharacterized LOC123504171, 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 8 samples with support for all annotated introns
uncharacterized LOC123504171, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
platelet binding protein GspB-like isoform X8
platelet binding protein GspB-like isoform X7
platelet binding protein GspB-like isoform X6
platelet binding protein GspB-like isoform X5
platelet binding protein GspB-like isoform X3
platelet binding protein GspB-like isoform X1
platelet binding protein GspB-like isoform X4
platelet binding protein GspB-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
platelet binding protein GspB-like isoform X11
platelet binding protein GspB-like isoform X9
platelet binding protein GspB-like isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
platelet binding protein GspB-like isoform X12
tRNA pseudouridine synthase A-like isoform X3
acetyl-coenzyme A synthetase 2-like, mitochondrial
G protein-coupled receptor kinase 1-like
protein lifeguard 3-like, transcript variant X3
protein lifeguard 3-like, transcript variant X1
protein lifeguard 3-like, transcript variant X2
protein lifeguard 3-like, transcript variant X4
protein lifeguard 3-like, transcript variant X5
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 9 samples with support for all annotated introns
triokinase/FMN cyclase-like, transcript variant X1
triokinase/FMN cyclase-like, transcript variant X2
gamma-butyrobetaine dioxygenase-like, transcript variant X1
gamma-butyrobetaine dioxygenase-like, transcript variant X2
gamma-butyrobetaine dioxygenase-like isoform X2
gamma-butyrobetaine dioxygenase-like isoform X1
endochitinase A-like, transcript variant X1
endochitinase A-like, transcript variant X2
endochitinase A-like, transcript variant X3
endochitinase A-like, transcript variant X4
28S ribosomal protein S11, mitochondrial-like
chromodomain-helicase-DNA-binding protein 1-like, transcript variant X1
chromodomain-helicase-DNA-binding protein 1-like, transcript variant X2
chromodomain-helicase-DNA-binding protein 1-like, transcript variant X3
chromodomain-helicase-DNA-binding protein 1-like isoform X1
chromodomain-helicase-DNA-binding protein 1-like isoform X2
chromodomain-helicase-DNA-binding protein 1-like isoform X3
L-galactose dehydrogenase-like, transcript variant X1
L-galactose dehydrogenase-like, transcript variant X2
excitatory amino acid transporter-like, transcript variant X3
excitatory amino acid transporter-like, transcript variant X1
excitatory amino acid transporter-like, transcript variant X2
excitatory amino acid transporter-like isoform X3
excitatory amino acid transporter-like isoform X2
excitatory amino acid transporter-like isoform X1
major facilitator superfamily domain-containing protein 6-like
major facilitator superfamily domain-containing protein 6-like, transcript variant X3
major facilitator superfamily domain-containing protein 6-like, transcript variant X2
major facilitator superfamily domain-containing protein 6-like, transcript variant X1
major facilitator superfamily domain-containing protein 6-like isoform X1
major facilitator superfamily domain-containing protein 6-like isoform X2
solute carrier family 15 member 1-like, transcript variant X4
solute carrier family 15 member 1-like, transcript variant X2
solute carrier family 15 member 1-like, transcript variant X3
solute carrier family 15 member 1-like, transcript variant X1
solute carrier family 15 member 1-like isoform X2
solute carrier family 15 member 1-like isoform X3
solute carrier family 15 member 1-like isoform X1
solute carrier family 15 member 1-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
putative aldolase class 2 protein CC_1201
putative thiamine transporter SLC35F3, transcript variant X2
putative thiamine transporter SLC35F3, transcript variant X1
putative thiamine transporter SLC35F3, transcript variant X3
putative thiamine transporter SLC35F3 isoform X1
putative thiamine transporter SLC35F3 isoform X2
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ras-related protein Rab-43-like, transcript variant X2
ras-related protein Rab-43-like, transcript variant X1
neurochondrin homolog, transcript variant X4
neurochondrin homolog, transcript variant X2
neurochondrin homolog, transcript variant X3
N-acylneuraminate-9-phosphatase-like isoform X3
neurochondrin homolog, transcript variant X1
dynein assembly factor with WDR repeat domains 1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dynein assembly factor with WDR repeat domains 1-like, transcript variant X3
dynein assembly factor with WDR repeat domains 1-like, transcript variant X5
dynein assembly factor with WDR repeat domains 1-like, transcript variant X4
dynein assembly factor with WDR repeat domains 1-like, transcript variant X8
dynein assembly factor with WDR repeat domains 1-like, transcript variant X1
dynein assembly factor with WDR repeat domains 1-like, transcript variant X11
dynein assembly factor with WDR repeat domains 1-like, transcript variant X2
dynein assembly factor with WDR repeat domains 1-like, transcript variant X10
dynein assembly factor with WDR repeat domains 1-like, transcript variant X9
dynein assembly factor with WDR repeat domains 1-like, transcript variant X6
dynein assembly factor with WDR repeat domains 1-like
uncharacterized LOC123503984, transcript variant X8
uncharacterized LOC123503984, transcript variant X7
uncharacterized protein LOC123503984 isoform X3
uncharacterized protein LOC123503984 isoform X4
uncharacterized LOC123503984, transcript variant X1
uncharacterized LOC123503984, transcript variant X5
uncharacterized LOC123503984, transcript variant X6
uncharacterized LOC123503984, transcript variant X4
uncharacterized LOC123503984, transcript variant X2
uncharacterized LOC123503984, transcript variant X3
uncharacterized protein LOC123503984 isoform X1
uncharacterized protein LOC123503984 isoform X2
uncharacterized LOC123503984, transcript variant X9
uncharacterized protein LOC123503984 isoform X5
uncharacterized LOC123503984, transcript variant X10
uncharacterized protein LOC123503984 isoform X6
uncharacterized LOC123504203, transcript variant X2
uncharacterized LOC123504203, transcript variant X1
uncharacterized LOC123504203, transcript variant X3
uncharacterized LOC123504316, transcript variant X3
uncharacterized LOC123504316, transcript variant X5
uncharacterized LOC123504316, transcript variant X4
uncharacterized LOC123504316, transcript variant X7
uncharacterized LOC123504316, transcript variant X1
uncharacterized LOC123504316, transcript variant X2
uncharacterized LOC123504316, transcript variant X6
uncharacterized LOC123504316, transcript variant X8
uncharacterized protein LOC123504316 isoform X1
uncharacterized LOC123504316, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC123504316 isoform X2
uncharacterized LOC123503923, transcript variant X2
uncharacterized protein LOC123503923 isoform X2
uncharacterized LOC123503923, transcript variant X1
uncharacterized protein LOC123503923 isoform X1
lysM and putative peptidoglycan-binding domain-containing protein 2-like
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial-like, transcript variant X1
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial-like, transcript variant X2
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial-like
uncharacterized LOC123504314, transcript variant X4
uncharacterized LOC123504314, transcript variant X3
uncharacterized LOC123504314, transcript variant X1
uncharacterized LOC123504314, transcript variant X2
semaphorin-2A-like, transcript variant X2
semaphorin-2A-like, transcript variant X1
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 34 samples with support for all annotated introns
semaphorin-2A-like, transcript variant X3
uncharacterized LOC123503930, transcript variant X5
uncharacterized LOC123503930, 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 9 samples with support for all annotated introns
uncharacterized LOC123503930, transcript variant X3
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 LOC123503930, 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 12 samples with support for all annotated introns
uncharacterized LOC123503930, transcript variant X6
uncharacterized LOC123503930, 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 3 samples with support for all annotated introns
exocyst complex component 1-like, transcript variant X1
exocyst complex component 1-like, transcript variant X2
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like, transcript variant X2
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like, transcript variant X1
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like, transcript variant X3
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like, transcript variant X4
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like isoform X1
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like isoform X4
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like isoform X2
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: gamma-butyrobetaine dioxygenase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
dynein axonemal assembly factor 11-like, transcript variant X2
dynein axonemal assembly factor 11-like, transcript variant X1
dynein axonemal assembly factor 11-like isoform X2
dynein axonemal assembly factor 11-like isoform X1
uncharacterized LOC123503995, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123503995, transcript variant X2
uridine-cytidine kinase-like 1, transcript variant X1
uridine-cytidine kinase-like 1 isoform X1
uridine-cytidine kinase-like 1, transcript variant X2
uridine-cytidine kinase-like 1 isoform X2
AT-rich interactive domain-containing protein 3B-like
LOW QUALITY PROTEIN: AT-rich interactive domain-containing protein 3B-like
uncharacterized LOC123504306, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123504306, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
protein dead ringer homolog, transcript variant X3
protein dead ringer homolog, transcript variant X2
protein dead ringer homolog, transcript variant X1
protein dead ringer homolog, transcript variant X4
AT-rich interactive domain-containing protein 3B-like isoform X3
AT-rich interactive domain-containing protein 3B-like isoform X1
AT-rich interactive domain-containing protein 3A-like isoform X4
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: cryptochrome-1-like
protein bowel-like, transcript variant X3
protein bowel-like, transcript variant X4
protein bowel-like, transcript variant X2
protein bowel-like, transcript variant X1
uncharacterized LOC123504082, transcript variant X1
uncharacterized LOC123504082, transcript variant X2
uncharacterized LOC123504082, transcript variant X3
uncharacterized protein LOC123504082 isoform X1
uncharacterized protein LOC123504082 isoform X2
uncharacterized LOC123504077, transcript variant X1
uncharacterized LOC123504077, transcript variant X2
uncharacterized LOC123504077, transcript variant X3
retinol dehydrogenase 13-like, transcript variant X4
retinol dehydrogenase 13-like, transcript variant X3
retinol dehydrogenase 13-like, transcript variant X2
retinol dehydrogenase 13-like, transcript variant X1
retinol dehydrogenase 13-like isoform X1
retinol dehydrogenase 13-like isoform X2
retinol dehydrogenase 13-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase epsilon-like
acidic amino acid decarboxylase GADL1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
uncharacterized LOC123504081, transcript variant X3
uncharacterized LOC123504081, transcript variant X2
uncharacterized LOC123504081, transcript variant X1
uncharacterized protein LOC123504081 isoform X3
uncharacterized protein LOC123504081 isoform X2
uncharacterized protein LOC123504081 isoform X1
histone-lysine N-methyltransferase 2D-like
glucosamine-6-phosphate isomerase-like, transcript variant X1
glucosamine-6-phosphate isomerase-like, transcript variant X3
glucosamine-6-phosphate isomerase-like, transcript variant X2
glucosamine-6-phosphate isomerase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
glucosamine-6-phosphate isomerase-like isoform X2
glucosamine-6-phosphate isomerase-like isoform X1
glucosamine-6-phosphate isomerase-like isoform X3
DNA-directed RNA polymerase III subunit RPC10-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC10-like, transcript variant X6
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 27 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC10-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC10-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 6 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC10-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC10-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC10-like, transcript variant X5
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 30 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC10-like isoform X1
DNA-directed RNA polymerase III subunit RPC10-like isoform X2
yrdC domain-containing protein, mitochondrial-like
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
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like
uncharacterized LOC123504195, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123504195, transcript variant X4
uncharacterized LOC123504195, transcript variant X1
uncharacterized LOC123504195, transcript variant X2
uncharacterized LOC123504096, transcript variant X1
uncharacterized LOC123504096, transcript variant X2
uncharacterized LOC123504134, transcript variant X6
uncharacterized LOC123504134, transcript variant X4
uncharacterized LOC123504134, transcript variant X5
uncharacterized LOC123504134, transcript variant X2
uncharacterized LOC123504134, transcript variant X7
uncharacterized LOC123504134, transcript variant X3
uncharacterized LOC123504134, 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 18 samples with support for all annotated introns
EF-hand domain-containing family member C2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: EF-hand domain-containing family member C2-like
protein trapped in endoderm-1-like, transcript variant X2
protein trapped in endoderm-1-like, transcript variant X1
LOW QUALITY PROTEIN: uncharacterized protein LOC123504132
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
atrial natriuretic peptide-converting enzyme-like
LOW QUALITY PROTEIN: atrial natriuretic peptide-converting enzyme-like
uncharacterized LOC123504033, transcript variant X10
uncharacterized LOC123504033, transcript variant X7
uncharacterized LOC123504033, transcript variant X3
uncharacterized LOC123504033, transcript variant X2
uncharacterized LOC123504033, transcript variant X1
uncharacterized LOC123504033, transcript variant X8
uncharacterized LOC123504033, transcript variant X6
uncharacterized LOC123504033, transcript variant X4
uncharacterized LOC123504033, transcript variant X5
uncharacterized LOC123504033, transcript variant X11
uncharacterized LOC123504033, transcript variant X9
uncharacterized protein LOC123504033 isoform X9
uncharacterized protein LOC123504033 isoform X6
uncharacterized protein LOC123504033 isoform X2
uncharacterized protein LOC123504033 isoform X7
uncharacterized protein LOC123504033 isoform X5
uncharacterized protein LOC123504033 isoform X3
uncharacterized protein LOC123504033 isoform X4
uncharacterized protein LOC123504033 isoform X1
uncharacterized protein LOC123504033 isoform X8
uncharacterized protein LOC123504033 isoform X10
retinoblastoma-binding protein 5 homolog, transcript variant X2
retinoblastoma-binding protein 5 homolog, transcript variant X1
retinoblastoma-binding protein 5 homolog isoform X2
retinoblastoma-binding protein 5 homolog isoform X1
uncharacterized LOC123504308, transcript variant X2
uncharacterized LOC123504308, transcript variant X1
pre-mRNA-processing factor 17-like, transcript variant X1
pre-mRNA-processing factor 17-like, transcript variant X2
pre-mRNA-processing factor 17-like isoform X1
pre-mRNA-processing factor 17-like isoform X2
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X2
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X6
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X1
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X8
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X10
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X7
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X9
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X4
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X3
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X5
wiskott-Aldrich syndrome protein family member 2-like isoform X1
wiskott-Aldrich syndrome protein family member 2-like isoform X2
wiskott-Aldrich syndrome protein family member 2-like isoform X4
wiskott-Aldrich syndrome protein family member 2-like isoform X3
wiskott-Aldrich syndrome protein family member 2-like isoform X5
wiskott-Aldrich syndrome protein family member 2-like isoform X6
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X11
wiskott-Aldrich syndrome protein family member 2-like isoform X7
CDP-diacylglycerol--inositol 3-phosphatidyltransferase-like
tubulin polyglutamylase complex subunit 2-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 2 samples with support for all annotated introns
tubulin polyglutamylase complex subunit 2-like, transcript variant X2
tubulin polyglutamylase complex subunit 2-like, transcript variant X3
tubulin polyglutamylase complex subunit 2-like isoform X1
tubulin polyglutamylase complex subunit 2-like isoform X2
tubulin polyglutamylase complex subunit 2-like isoform X3
zinc transporter ZIP1-like, transcript variant X2
zinc transporter ZIP1-like, transcript variant X3
zinc transporter ZIP1-like, transcript variant X1
uncharacterized LOC123504145, transcript variant X2
uncharacterized LOC123504145, transcript variant X1
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 52 samples with support for all annotated introns
uncharacterized LOC123504146, transcript variant X2
uncharacterized LOC123504146, transcript variant X3
uncharacterized LOC123504146, transcript variant X4
uncharacterized LOC123504146, transcript variant X1
oplophorus-luciferin 2-monooxygenase non-catalytic subunit-like
uncharacterized protein DDB_G0287625-like
uncharacterized LOC123504201, transcript variant X2
uncharacterized LOC123504201, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns