Penaeus chinensis breed Huanghai No. 1 chromosome 23, ASM1920278v2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea; Malacostraca; Eumalacostraca; Eucarida; Decapoda; Dendrobranchiata; Penaeoidea; Penaeidae; Penaeus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM032948.1.\nAssembly name: ASM1920278v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Yellow Sea Fisheries Research\nInstitute, Chinese Academy of Fishery Sciences on 2021/07/13. The\noriginal whole-genome shotgun project has the accession\nJAGKSU000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Yellow Sea Fisheries Research Institute,\n Chinese Academy of Fishery Sciences\nAssembly Date :: 2020\nAssembly Method :: FALCON-Unzip v. MAY-2020\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 150.0x\nSequencing Technology :: PacBio Sequel\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Penaeus chinensis Annotation Release\n 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##
conservation base of Haifeng Aquaculture Co., Ltd.
Derived by automated computational analysis using gene prediction method: Gnomon.
insulin-like growth factor-binding protein complex acid labile subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
RNA cytidine acetyltransferase-like, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
RNA cytidine acetyltransferase-like, transcript variant X2
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial-like, transcript variant X2
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial-like, transcript variant X1
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial-like isoform X1
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial-like isoform X2
vesicular inhibitory amino acid transporter-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
serine/arginine repetitive matrix protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 94% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GIYE01037258.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 874 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 363 bases not found in genome assembly; 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
serine/threonine-protein phosphatase 6 regulatory subunit 3-like, transcript variant X1
serine/threonine-protein phosphatase 6 regulatory subunit 3-like, transcript variant X5
serine/threonine-protein phosphatase 6 regulatory subunit 3-like, transcript variant X3
serine/threonine-protein phosphatase 6 regulatory subunit 3-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 36 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory subunit 3-like, transcript variant X7
serine/threonine-protein phosphatase 6 regulatory subunit 3-like, transcript variant X2
serine/threonine-protein phosphatase 6 regulatory subunit 3-like, transcript variant X4
serine/threonine-protein phosphatase 6 regulatory subunit 3-like isoform X1
serine/threonine-protein phosphatase 6 regulatory subunit 3-like isoform X4
serine/threonine-protein phosphatase 6 regulatory subunit 3-like isoform X2
serine/threonine-protein phosphatase 6 regulatory subunit 3-A-like isoform X3
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
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: succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial-like
RNA-binding protein 39-like, transcript variant X2
RNA-binding protein 39-like, transcript variant X5
RNA-binding protein 39-like, transcript variant X3
RNA-binding protein 39-like, transcript variant X4
RNA-binding protein 39-like, transcript variant X1
RNA-binding protein 39-like, transcript variant X6
RNA-binding protein 39-like, transcript variant X8
RNA-binding protein 39-like, transcript variant X7
mitochondrial proton/calcium exchanger protein-like
pre-rRNA-processing protein TSR1 homolog, transcript variant X2
pre-rRNA-processing protein TSR1 homolog, transcript variant X3
pre-rRNA-processing protein TSR1 homolog, transcript variant X1
pre-rRNA-processing protein TSR1 homolog isoform X3
pre-rRNA-processing protein TSR1 homolog isoform X2
pre-rRNA-processing protein TSR1 homolog isoform X1
similar to RNA sequence (same species):INSD:GHUY01009327.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 945 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 939 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor A domain-containing protein 5A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GIYE01002211.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 375 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 375 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC125037363, transcript variant X1
uncharacterized LOC125037363, transcript variant X2
leucine-rich repeat-containing protein AAC1-like
RNA polymerase II degradation factor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
uncharacterized protein LOC125037630 isoform X2
LOW QUALITY PROTEIN: gamma-tubulin complex component 2-like
sodium-dependent serotonin transporter-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
cell cycle checkpoint protein RAD17-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
cell cycle checkpoint protein RAD17-like isoform X2
cell cycle checkpoint protein RAD17-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
cell cycle checkpoint protein RAD17-like isoform X1
growth hormone-regulated TBC protein 1-A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
DNA ligase 1-like, transcript variant X2
DNA ligase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: superoxide dismutase [Cu-Zn]-like
D-threo-3-hydroxyaspartate dehydratase-like
similar to RNA sequence (same species):INSD:GHUY01001493.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 501 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 317 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
39S ribosomal protein L48, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
protein tramtrack, beta isoform-like, transcript variant X12
protein tramtrack, beta isoform-like, transcript variant X2
protein tramtrack, beta isoform-like, transcript variant X1
protein tramtrack, beta isoform-like, transcript variant X7
protein tramtrack, beta isoform-like, transcript variant X5
protein tramtrack, beta isoform-like, transcript variant X6
protein tramtrack, beta isoform-like, transcript variant X10
protein tramtrack, beta isoform-like, transcript variant X9
protein tramtrack, beta isoform-like, transcript variant X3
protein tramtrack, beta isoform-like, transcript variant X8
protein tramtrack, beta isoform-like, transcript variant X4
protein tramtrack, beta isoform-like isoform X1
protein tramtrack, beta isoform-like isoform X2
protein tramtrack, beta isoform-like, transcript variant X11
protein tramtrack, beta isoform-like isoform X3
phosphatidylinositol N-acetylglucosaminyltransferase subunit A-like
TBC1 domain family member 16-like, transcript variant X4
TBC1 domain family member 16-like, transcript variant X5
TBC1 domain family member 16-like, transcript variant X1
TBC1 domain family member 16-like, transcript variant X2
TBC1 domain family member 16-like, transcript variant X3
TBC1 domain family member 16-like, transcript variant X6
TBC1 domain family member 16-like isoform X2
TBC1 domain family member 16-like isoform X3
TBC1 domain family member 16-like isoform X1
TBC1 domain family member 16-like isoform X4
target of rapamycin complex subunit lst8-like, transcript variant X1
target of rapamycin complex subunit lst8-like, transcript variant X2
target of rapamycin complex subunit lst8-like isoform X1
target of rapamycin complex subunit lst8-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 1 sample with support for all annotated introns
uncharacterized LOC125037584, 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 10 samples with support for all annotated introns
uncharacterized LOC125037585, transcript variant X2
uncharacterized LOC125037585, transcript variant X1
uncharacterized protein LOC125037585 isoform X2
uncharacterized protein LOC125037585 isoform X1
uncharacterized LOC125037584, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
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 LOC125037508, transcript variant X1
uncharacterized LOC125037508, transcript variant X2
uncharacterized LOC125037538, transcript variant X1
uncharacterized protein LOC125037538 isoform X1
uncharacterized LOC125037538, 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 LOC125037538, transcript variant X3
uncharacterized protein LOC125037538 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
puromycin-sensitive aminopeptidase-like, transcript variant X2
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 28 samples with support for all annotated introns
puromycin-sensitive aminopeptidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
puromycin-sensitive aminopeptidase-like, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fructose-bisphosphate aldolase-like, transcript variant X2
fructose-bisphosphate aldolase-like, transcript variant X1
fructose-bisphosphate aldolase-like isoform X1
fructose-bisphosphate aldolase-like isoform X2
protein LZIC-like, transcript variant X1
protein LZIC-like, transcript variant X2
double-strand-break repair protein rad21 homolog, transcript variant X3
double-strand-break repair protein rad21 homolog, transcript variant X4
double-strand-break repair protein rad21 homolog, transcript variant X1
double-strand-break repair protein rad21 homolog, transcript variant X2
double-strand-break repair protein rad21 homolog isoform X2
double-strand-break repair protein rad21 homolog isoform X3
double-strand-break repair protein rad21 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
pyrimidodiazepine synthase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
pyrimidodiazepine synthase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
pyrimidodiazepine synthase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
pyrimidodiazepine synthase-like, transcript variant X1
pyrimidodiazepine synthase-like, transcript variant X5
pyrimidodiazepine synthase-like isoform X1
pyrimidodiazepine synthase-like isoform X2
putative inorganic phosphate cotransporter, transcript variant X1
putative inorganic phosphate cotransporter, transcript variant X3
putative inorganic phosphate cotransporter, transcript variant X2
putative inorganic phosphate cotransporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
uncharacterized LOC125037271, transcript variant X2
uncharacterized LOC125037271, transcript variant X1
uncharacterized protein LOC125037271 isoform X2
uncharacterized protein LOC125037271 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 73% 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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125037455
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: phosphatidylinositol 3-kinase 2-like
store-operated calcium entry regulator STIMATE-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, including 28 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC125037576
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
saccharopine dehydrogenase-like oxidoreductase
procyclic form-specific polypeptide B-alpha-like
zinc finger CCCH domain-containing protein 4-like
guanine nucleotide exchange factor MSS4 homolog
U11/U12 small nuclear ribonucleoprotein 35 kDa protein-like
two pore channel protein 1-like, transcript variant X3
two pore channel protein 1-like isoform X3
two pore channel protein 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
two pore channel protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
two pore channel protein 1-like, transcript variant X2
two pore channel protein 1-like isoform X1
two pore channel protein 1-like isoform X2
two pore channel protein 1-like, transcript variant X4
two pore channel protein 1-like isoform X4
two pore channel protein 1-like isoform 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 1 sample with support for all annotated introns
E3 SUMO-protein ligase PIAS2-like, transcript variant X1
E3 SUMO-protein ligase PIAS2-like, transcript variant X4
E3 SUMO-protein ligase PIAS2-like, transcript variant X2
E3 SUMO-protein ligase PIAS2-like, transcript variant X3
E3 SUMO-protein ligase PIAS2-like isoform X1
E3 SUMO-protein ligase PIAS2-like isoform X4
E3 SUMO-protein ligase PIAS2-like isoform X2
E3 SUMO-protein ligase PIAS2-like isoform X3
FACT complex subunit Ssrp1-like, transcript variant X2
FACT complex subunit Ssrp1-like, transcript variant X1
FACT complex subunit Ssrp1-like isoform X2
FACT complex subunit Ssrp1-like isoform X1
uncharacterized LOC125037557, transcript variant X4
uncharacterized LOC125037557, transcript variant X7
uncharacterized LOC125037557, transcript variant X5
uncharacterized LOC125037557, transcript variant X3
uncharacterized LOC125037557, transcript variant X1
uncharacterized LOC125037557, transcript variant X2
uncharacterized protein LOC125037557 isoform X4
uncharacterized protein LOC125037557 isoform X3
uncharacterized protein LOC125037557 isoform X2
uncharacterized protein LOC125037557 isoform X7
uncharacterized protein LOC125037557 isoform X5
uncharacterized protein LOC125037557 isoform X1
uncharacterized LOC125037557, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
uncharacterized protein LOC125037557 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
potassium channel subfamily K member 18-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pyridoxal phosphate phosphatase PHOSPHO2-like, transcript variant X2
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 3 samples with support for all annotated introns
pyridoxal phosphate phosphatase PHOSPHO2-like isoform X2
pyridoxal phosphate phosphatase PHOSPHO2-like, 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 32 samples with support for all annotated introns
pyridoxal phosphate phosphatase PHOSPHO2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
pyridoxal phosphate phosphatase PHOSPHO2-like isoform X1
pyridoxal phosphate phosphatase PHOSPHO2-like isoform X3
dehydrogenase/reductase SDR family protein 7-like, transcript variant X2
dehydrogenase/reductase SDR family protein 7-like, transcript variant X1
dehydrogenase/reductase SDR family protein 7-like, transcript variant X3
dehydrogenase/reductase SDR family protein 7-like isoform X1
dehydrogenase/reductase SDR family protein 7-like isoform X2
dehydrogenase/reductase SDR family protein 7-like isoform X3
probable methyltransferase-like protein 24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
methionine aminopeptidase 1D, mitochondrial-like, transcript variant X2
methionine aminopeptidase 1D, mitochondrial-like isoform X2
methionine aminopeptidase 1D, mitochondrial-like, transcript variant X1
methionine aminopeptidase 1D, mitochondrial-like isoform X1
nuclear receptor coactivator 6-like, transcript variant X4
nuclear receptor coactivator 6-like, transcript variant X2
nuclear receptor coactivator 6-like, transcript variant X3
nuclear receptor coactivator 6-like, transcript variant X1
nuclear receptor coactivator 6-like isoform X2
nuclear receptor coactivator 6-like isoform X1
N(6)-adenine-specific methyltransferase METTL4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
N(6)-adenine-specific methyltransferase METTL4-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
N(6)-adenine-specific methyltransferase METTL4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
N(6)-adenine-specific methyltransferase METTL4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
N(6)-adenine-specific methyltransferase METTL4-like
cleavage and polyadenylation specificity factor subunit 5-like
RING finger protein 44-like, transcript variant X2
RING finger protein 44-like, transcript variant X1
RING finger protein 44-like, transcript variant X4
RING finger protein 44-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
RING finger protein 44-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
39S ribosomal protein L55, mitochondrial-like
NADPH oxidase 4-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 6 samples with support for all annotated introns
NADPH oxidase 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
NADPH oxidase 4-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 14 samples with support for all annotated introns
polyisoprenoid diphosphate/phosphate phosphohydrolase PLPP6-like, transcript variant X1
polyisoprenoid diphosphate/phosphate phosphohydrolase PLPP6-like, transcript variant X2
polyisoprenoid diphosphate/phosphate phosphohydrolase PLPP6-like, transcript variant X3
polyisoprenoid diphosphate/phosphate phosphohydrolase PLPP6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
KAT8 regulatory NSL complex subunit 2-like
similar to RNA sequence (same species):INSD:GHUY01001712.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 139 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 99 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2-like
LOW QUALITY PROTEIN: dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2-like
uncharacterized LOC125037352, transcript variant X1
uncharacterized LOC125037352, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
uncharacterized LOC125037352, transcript variant X3
uncharacterized LOC125037352, transcript variant X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: ionotropic receptor 93a-like
ionotropic receptor 25a-like, transcript variant X2
ionotropic receptor 25a-like, transcript variant X3
ionotropic receptor 25a-like, transcript variant X1
ionotropic receptor 25a-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable G-protein coupled receptor B0563.6
uncharacterized LOC125037577, transcript variant X2
uncharacterized LOC125037577, transcript variant X1
uncharacterized protein LOC125037577 isoform X1
uncharacterized protein LOC125037577 isoform X2
ATP synthase subunit alpha, mitochondrial-like
inositol monophosphatase 3-like, transcript variant X1
inositol monophosphatase 3-like, transcript variant X2
inositol monophosphatase 3-like, transcript variant X3
inositol monophosphatase 3-like isoform X1
inositol monophosphatase 3-like isoform X2
similar to RNA sequence (same species):INSD:GHUY01003732.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 230 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 74 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
stomatin-like protein 1, transcript variant X2
stomatin-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
stomatin-like protein 1, transcript variant X4
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 27 samples with support for all annotated introns
stomatin-like protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
stomatin-like protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
unconventional myosin-Va-like, transcript variant X1
unconventional myosin-Va-like, transcript variant X3
unconventional myosin-Va-like, transcript variant X2
unconventional myosin-Va-like isoform X3
unconventional myosin-Va-like isoform X2
unconventional myosin-Va-like isoform X1
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X2
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X1
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X2
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
cardioactive peptide-like, transcript variant X1
cardioactive peptide-like, transcript variant X2
cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2-like, transcript variant X1
cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2-like, transcript variant X2
cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2-like, transcript variant X4
cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2-like, transcript variant X3
cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2-like
similar to RNA sequence, mRNA (same species):INSD:MN765110.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 285 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 285 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
neprilysin-2-like, transcript variant X5
neprilysin-2-like, transcript variant X7
neprilysin-2-like, transcript variant X1
neprilysin-2-like, transcript variant X2
neprilysin-2-like, transcript variant X6
neprilysin-2-like, transcript variant X4
neprilysin-2-like, transcript variant X3
small proline-rich protein 2G-like, transcript variant X2
small proline-rich protein 2G-like isoform X2
small proline-rich protein 2G-like, transcript variant X1
small proline-rich protein 2G-like isoform X1
sperm mitochondrial-associated cysteine-rich protein-like
meiosis-specific nuclear structural protein 1-like
vang-like protein 2, transcript variant X1
vang-like protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
procollagen C-endopeptidase enhancer 1-like
fatty acid hydroxylase domain-containing protein 2-like
sodium- and chloride-dependent glycine transporter 2-like
LOW QUALITY PROTEIN: sodium- and chloride-dependent glycine transporter 2-like
sodium- and chloride-dependent glycine transporter 1-like
sodium- and chloride-dependent betaine transporter-like, transcript variant X1
sodium- and chloride-dependent betaine transporter-like, transcript variant X2
sodium- and chloride-dependent betaine transporter-like isoform X1
sodium- and chloride-dependent betaine transporter-like isoform X2
sodium- and chloride-dependent glycine transporter 1-like, transcript variant X1
sodium- and chloride-dependent glycine transporter 1-like, transcript variant X2
sodium- and chloride-dependent glycine transporter 1-like, transcript variant X3
hydroxysteroid dehydrogenase-like protein 1, transcript variant X2
hydroxysteroid dehydrogenase-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
hydroxysteroid dehydrogenase-like protein 1
similar to RNA sequence (same species):INSD:GHUY01001219.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 661 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 303 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
protein polybromo-1-like, transcript variant X2
protein polybromo-1-like, transcript variant X1
protein polybromo-1-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 27 samples with support for all annotated introns
protein polybromo-1-like, transcript variant X4
protein polybromo-1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
cytochrome c oxidase assembly protein COX18, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
ERI1 exoribonuclease 3-like, transcript variant X2
ERI1 exoribonuclease 3-like, transcript variant X3
ERI1 exoribonuclease 3-like, transcript variant X1
ERI1 exoribonuclease 3-like, transcript variant X4
ERI1 exoribonuclease 3-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125037342, transcript variant X3
uncharacterized LOC125037342, transcript variant X4
uncharacterized LOC125037342, transcript variant X2
uncharacterized LOC125037342, transcript variant X1
uncharacterized LOC125037342, transcript variant X6
uncharacterized LOC125037342, transcript variant X5
uncharacterized protein LOC125037342 isoform X1
uncharacterized protein LOC125037342 isoform X2
uncharacterized protein LOC125037342 isoform X3
TAF6-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 6L, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SHC SH2 domain-binding protein 1 homolog B-like, transcript variant X2
SHC SH2 domain-binding protein 1 homolog B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
SHC SH2 domain-binding protein 1 homolog B-like
TAF6-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 6L, transcript variant X1
TAF6-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 6L isoform X1
uncharacterized protein LOC125037339 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125037530, transcript variant X2
uncharacterized LOC125037530, transcript variant X1
uncharacterized protein LOC125037530 isoform X2
uncharacterized protein LOC125037530 isoform X1
uncharacterized LOC125037277, transcript variant X3
uncharacterized protein LOC125037277 isoform X3
uncharacterized LOC125037277, transcript variant X1
uncharacterized LOC125037277, transcript variant X2
uncharacterized protein LOC125037277 isoform X1
uncharacterized protein LOC125037277 isoform X2
uncharacterized LOC125037276, transcript variant X4
uncharacterized LOC125037276, transcript variant X1
uncharacterized protein LOC125037276 isoform X2
uncharacterized LOC125037276, transcript variant X3
uncharacterized LOC125037276, transcript variant X2
uncharacterized protein LOC125037276 isoform X1
serine/arginine repetitive matrix protein 5-like
pseudouridine-5'-phosphate glycosidase-like, transcript variant X1
pseudouridine-5'-phosphate glycosidase-like, transcript variant X2
pseudouridine-5'-phosphate glycosidase-like
threonine synthase-like 2, 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 7 samples with support for all annotated introns
threonine synthase-like 2, transcript variant X1
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 26 samples with support for all annotated introns
threonine synthase-like 2, transcript variant X4
threonine synthase-like 2, transcript variant X3
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 11 samples with support for all annotated introns
N-acetylgalactosaminyltransferase 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
cytochrome c oxidase assembly protein COX15 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cytochrome c oxidase assembly protein COX15 homolog, transcript variant X1
cytochrome c oxidase assembly protein COX15 homolog
4-hydroxyphenylpyruvate dioxygenase-like protein
phosphatidylinositol 4-kinase type 2-alpha-like, transcript variant X1
similar to RNA sequence (same species):INSD:GIYE01007142.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1354 bases not found in genome assembly
phosphatidylinositol 4-kinase type 2-alpha-like, transcript variant X2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 319 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
phosphatidylinositol 4-kinase type 2-alpha-like isoform X1
phosphatidylinositol 4-kinase type 2-alpha-like isoform X2
ankyrin repeat domain-containing protein 50-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: ankyrin repeat domain-containing protein 50-like
fatty acid hydroxylase domain-containing protein 2-like, transcript variant X2
fatty acid hydroxylase domain-containing protein 2-like, transcript variant X3
fatty acid hydroxylase domain-containing protein 2-like, transcript variant X1
fatty acid hydroxylase domain-containing protein 2-like isoform X1
fatty acid hydroxylase domain-containing protein 2-like isoform X2
enhancer of polycomb homolog 1-like, transcript variant X2
enhancer of polycomb homolog 1-like, transcript variant X1
enhancer of polycomb homolog 1-like isoform X2
enhancer of polycomb homolog 1-like isoform X1
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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
zinc finger BED domain-containing protein 5-like
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
polyamine-transporting ATPase 13A3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
polyamine-transporting ATPase 13A3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
polyamine-transporting ATPase 13A3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
polyamine-transporting ATPase 13A3-like isoform X2
polyamine-transporting ATPase 13A3-like isoform X3
polyamine-transporting ATPase 13A3-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125037345, transcript variant X3
uncharacterized LOC125037345, transcript variant X1
uncharacterized LOC125037345, transcript variant X2
uncharacterized protein LOC125037345 isoform X1
uncharacterized protein LOC125037345 isoform X2
uncharacterized protein LOC125037345 isoform X3
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
calcium-dependent protein kinase 14-like
uncharacterized LOC125037580, transcript variant X1
uncharacterized LOC125037580, transcript variant X2
uncharacterized protein LOC125037580 isoform X1
uncharacterized protein LOC125037580 isoform X2
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X31
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X29
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X22
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X30
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X20
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X33
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X28
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X27
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X21
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X12
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X5
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X2
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X19
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X15
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X18
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X17
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X14
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X26
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X13
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X7
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X9
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X11
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X8
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X25
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X10
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X23
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X3
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X1
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X24
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X16
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X6
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X4
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X32
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X31
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X29
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X22
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X30
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X20
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X33
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X28
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X27
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X21
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X12
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X5
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X2
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X19
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X15
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X18
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X17
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X14
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X26
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X13
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X7
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X9
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X11
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X8
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X25
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X10
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X23
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X3
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X1
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X24
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X16
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X6
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X4
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X32
choline-phosphate cytidylyltransferase B-like, transcript variant X2
choline-phosphate cytidylyltransferase B-like, transcript variant X6
choline-phosphate cytidylyltransferase B-like, transcript variant X1
choline-phosphate cytidylyltransferase B-like, transcript variant X8
choline-phosphate cytidylyltransferase B-like, transcript variant X7
choline-phosphate cytidylyltransferase B-like, transcript variant X3
choline-phosphate cytidylyltransferase B-like, transcript variant X4
choline-phosphate cytidylyltransferase B-like, transcript variant X5
choline-phosphate cytidylyltransferase B-like isoform X3
choline-phosphate cytidylyltransferase B-like isoform X2
choline-phosphate cytidylyltransferase B-like isoform X1
altered inheritance of mitochondria protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 54% coverage of the annotated genomic feature by RNAseq alignments
heavy metal-associated isoprenylated plant protein 32-like
uncharacterized protein DDB_G0271670-like
bifunctional coenzyme A synthase-like, transcript variant X2
bifunctional coenzyme A synthase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
carbohydrate sulfotransferase 10-like, transcript variant X1
carbohydrate sulfotransferase 10-like, transcript variant X2
carbohydrate sulfotransferase 10-like isoform X1
carbohydrate sulfotransferase 10-like isoform X2
cytochrome P450 2L1-like, transcript variant X1
cytochrome P450 2L1-like, transcript variant X2
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X3
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X2
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X4
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X1
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X6
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X5
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like isoform X1
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like isoform X3
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
probable L-asparaginase 4, transcript variant X2
probable L-asparaginase 4, transcript variant X1
uncharacterized protein LOC125037548 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
LOW QUALITY PROTEIN: flocculation protein FLO11-like
furin-like protease 1, transcript variant X1
furin-like protease 1, transcript variant X2
furin-like protease 1, transcript variant X3
furin-like protease 1, transcript variant X4
furin-like protease 1, isoforms 1/1-X/2 isoform X1
furin-like protease 1, isoforms 1/1-X/2 isoform X2
furin-like protease 1, isoforms 1/1-X/2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
probable RNA-binding protein 18, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
probable RNA-binding protein 18, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
probable RNA-binding protein 18 isoform X1
probable RNA-binding protein 18 isoform X2
transcription initiation factor TFIID subunit 10-like, transcript variant X1
chloride intracellular channel exl-1-like, transcript variant X2
chloride intracellular channel exl-1-like, transcript variant X1
chloride intracellular channel exl-1-like, transcript variant X3
chloride intracellular channel exl-1-like
transcription initiation factor TFIID subunit 10-like, transcript variant X2
transcription initiation factor TFIID subunit 10-like
calcium-activated chloride channel regulator 4A-like
presenilins-associated rhomboid-like protein, mitochondrial, transcript variant X2
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 12 samples with support for all annotated introns
presenilins-associated rhomboid-like protein, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
presenilins-associated rhomboid-like protein, mitochondrial
sec1 family domain-containing protein 1-like
selenocysteine-specific elongation factor-like, transcript variant X1
selenocysteine-specific elongation factor-like, transcript variant X2
selenocysteine-specific elongation factor-like
uncharacterized LOC125037380, transcript variant X2
uncharacterized protein LOC125037380 isoform X2
uncharacterized LOC125037380, transcript variant X1
uncharacterized protein LOC125037380 isoform X1
uncharacterized LOC125037503, transcript variant X3
uncharacterized LOC125037503, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC125037503, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
hemicentin-1-like, transcript variant X1
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 27 samples with support for all annotated introns
hemicentin-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC125037389, transcript variant X2
uncharacterized LOC125037389, transcript variant X1
uncharacterized LOC125037389, transcript variant X3
uncharacterized protein LOC125037389 isoform X1
uncharacterized protein LOC125037389 isoform X2
uncharacterized LOC125037400, transcript variant X2
uncharacterized LOC125037400, transcript variant X1
insulin-like growth factor-binding protein 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
protein pigeon-like, transcript variant X1
protein pigeon-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
protein prune homolog 2-like, transcript variant X4
protein prune homolog 2-like, transcript variant X3
protein prune homolog 2-like, transcript variant X6
protein prune homolog 2-like, transcript variant X2
protein prune homolog 2-like, transcript variant X1
protein prune homolog 2-like, transcript variant X5
rab-like protein 6, transcript variant X2
rab-like protein 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
rab-like protein 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 92% coverage of the annotated genomic feature by RNAseq alignments
thrombospondin type-1 domain-containing protein 7B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DNA topoisomerase 2-binding protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: DNA topoisomerase 2-binding protein 1-like
ribosomal oxygenase 1-like, transcript variant X2
ribosomal oxygenase 1-like, transcript variant X1
mitogen-activated protein kinase kinase kinase 13-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 13-like, transcript variant X1
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 13 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 13-like, 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 15 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 13-like isoform X1
mitogen-activated protein kinase kinase kinase 13-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
adipocyte plasma membrane-associated protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
adipocyte plasma membrane-associated protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
adipocyte plasma membrane-associated protein-like
splicing factor U2af 38 kDa subunit, transcript variant X1
splicing factor U2AF 26 kDa subunit isoform X1
splicing factor U2af 38 kDa subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
splicing factor U2af 38 kDa subunit isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
piggyBac transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
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 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
adhesion G protein-coupled receptor E1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
putative N-acetylated-alpha-linked acidic dipeptidase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns