Penaeus chinensis breed Huanghai No. 1 chromosome 16, 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\nCM032941.1.\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.
cuticle protein CP14.6-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 9 samples with support for all annotated introns
cuticle protein CP14.6-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 15 samples with support for all annotated introns
cuticle protein CP14.6-like, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GIYE01032999.1
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 117 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 15 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
acetylcholine receptor subunit beta-like 1
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
flavin-containing monooxygenase FMO GS-OX-like 2, transcript variant X1
flavin-containing monooxygenase FMO GS-OX-like 2, transcript variant X2
flavin-containing monooxygenase FMO GS-OX5-like isoform X1
flavin-containing monooxygenase FMO GS-OX5-like isoform X2
flavin-containing monooxygenase FMO GS-OX-like 2, 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 11 samples with support for all annotated introns
flavin-containing monooxygenase FMO GS-OX-like 2 isoform X5
flavin-containing monooxygenase FMO GS-OX-like 2, transcript variant X6
flavin-containing monooxygenase FMO GS-OX-like 2, transcript variant X3
flavin-containing monooxygenase FMO GS-OX-like 2 isoform X6
flavin-containing monooxygenase FMO GS-OX-like 2 isoform X3
flavin-containing monooxygenase FMO GS-OX-like 2, transcript variant X4
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 33 samples with support for all annotated introns
flavin-containing monooxygenase FMO GS-OX5-like isoform X4
hydroxysteroid dehydrogenase-like protein 2, transcript variant X1
hydroxysteroid dehydrogenase-like protein 2 isoform X1
hydroxysteroid dehydrogenase-like protein 2, transcript variant X2
hydroxysteroid dehydrogenase-like protein 2 isoform X2
integrin alpha-5-like, transcript variant X2
integrin alpha-5-like, transcript variant X4
integrin alpha-5-like, transcript variant X1
integrin alpha-5-like, transcript variant X3
integrin alpha-5-like, transcript variant X6
integrin alpha-5-like, transcript variant X5
zinc finger protein 32-like, transcript variant X1
zinc finger protein 32-like, transcript variant X2
zinc finger protein 32-like, transcript variant X3
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 5 samples with support for all annotated introns
U6 snRNA-associated Sm-like protein LSm2
zinc finger protein 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 23 samples with support for all annotated introns
zinc finger protein 2-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 18 samples with support for all annotated introns
peroxidasin homolog pxn-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peroxidasin homolog pxn-1-like, transcript variant X1
peroxidasin homolog pxn-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit alpha-6-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 32 samples with support for all annotated introns
vitelline membrane outer layer protein 1-like, transcript variant X2
similar to RNA sequence (same species):INSD:GIYE01047678.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 247 bases not found in genome assembly; 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
vitelline membrane outer layer protein 1-like, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 247 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 200 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
vitelline membrane outer layer protein 1-like isoform X1
vitelline membrane outer layer protein 1-like isoform X2
vitelline membrane outer layer protein 1-like
vitelline membrane outer layer protein 1 homolog
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
sucrase-isomaltase, intestinal-like, transcript variant X1
sucrase-isomaltase, intestinal-like isoform X1
sucrase-isomaltase, intestinal-like, transcript variant X2
sucrase-isomaltase, intestinal-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 15 samples with support for all annotated introns
adipokinetic hormone/corazonin-related peptide receptor variant I-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 82% 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
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: NADPH oxidase 5-like
alanine--tRNA ligase, cytoplasmic-like, transcript variant X2
alanine--tRNA ligase, cytoplasmic-like, transcript variant X1
alanine--tRNA ligase, cytoplasmic-like isoform X1
alanine--tRNA ligase, cytoplasmic-like isoform X2
nucleoside diphosphate kinase 7-like, transcript variant X2
nucleoside diphosphate kinase 7-like, transcript variant X1
nucleoside diphosphate kinase 7-like isoform X2
nucleoside diphosphate kinase 7-like isoform X1
semaphorin-1A-like, transcript variant X1
semaphorin-1A-like, transcript variant X3
semaphorin-1A-like, transcript variant X5
semaphorin-1A-like, transcript variant X2
semaphorin-1A-like, transcript variant X4
semaphorin-1A-like, transcript variant X6
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like
elongation factor 1-delta-like, transcript variant X1
elongation factor 1-delta-like, transcript variant X2
elongation factor 1-delta-like, transcript variant X3
elongation factor 1-delta-like, transcript variant X4
probable elongation factor 1-delta isoform X1
elongation factor 1-beta'-like isoform X2
probable elongation factor 1-delta isoform X3
elongation factor 1-delta-like isoform X4
uncharacterized LOC125033522, transcript variant X3
uncharacterized LOC125033522, transcript variant X1
uncharacterized LOC125033522, transcript variant X5
uncharacterized LOC125033522, transcript variant X2
uncharacterized protein LOC125033522 isoform X2
uncharacterized protein LOC125033522 isoform X1
uncharacterized protein LOC125033522 isoform X4
uncharacterized LOC125033522, 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 9 samples with support for all annotated introns
uncharacterized protein LOC125033522 isoform X3
uncharacterized LOC125033522, transcript variant X6
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 14 samples with support for all annotated introns
uncharacterized protein LOC125033522 isoform X5
probable phosphorylase b kinase regulatory subunit beta, transcript variant X2
probable phosphorylase b kinase regulatory subunit beta, transcript variant X1
probable phosphorylase b kinase regulatory subunit beta, transcript variant X3
probable phosphorylase b kinase regulatory subunit beta isoform X2
probable phosphorylase b kinase regulatory subunit beta isoform X1
probable phosphorylase b kinase regulatory subunit beta isoform X3
ecotropic viral integration site 5 ortholog-like, transcript variant X5
ecotropic viral integration site 5 ortholog-like, transcript variant X4
ecotropic viral integration site 5 ortholog-like, transcript variant X2
ecotropic viral integration site 5 ortholog-like, transcript variant X3
ecotropic viral integration site 5 ortholog-like, transcript variant X1
ecotropic viral integration site 5 ortholog-like, transcript variant X8
ecotropic viral integration site 5 ortholog-like, transcript variant X9
ecotropic viral integration site 5 ortholog-like, transcript variant X7
ecotropic viral integration site 5 ortholog-like, transcript variant X6
ecotropic viral integration site 5 ortholog-like isoform X5
ecotropic viral integration site 5 ortholog-like isoform X4
ecotropic viral integration site 5 ortholog-like isoform X2
ecotropic viral integration site 5 ortholog-like isoform X3
ecotropic viral integration site 5 ortholog-like isoform X1
ecotropic viral integration site 5 ortholog-like isoform X8
ecotropic viral integration site 5 ortholog-like isoform X9
ecotropic viral integration site 5 ortholog-like isoform X7
ecotropic viral integration site 5 ortholog-like isoform X6
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
cleavage and polyadenylation specificity factor subunit 1-like
uncharacterized LOC125033404, transcript variant X1
uncharacterized LOC125033404, transcript variant X2
uncharacterized protein LOC125033404 isoform X1
uncharacterized protein LOC125033404 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
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: uncharacterized protein LOC125033622
galactosylceramide sulfotransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
proton myo-inositol cotransporter-like, transcript variant X3
proton myo-inositol cotransporter-like, transcript variant X2
proton myo-inositol cotransporter-like, transcript variant X1
proton myo-inositol cotransporter-like, transcript variant X4
proton myo-inositol cotransporter-like, transcript variant X5
proton myo-inositol cotransporter-like isoform X2
proton myo-inositol cotransporter-like isoform X1
proton myo-inositol cotransporter-like isoform X3
proton myo-inositol cotransporter-like isoform 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 39 samples with support for all annotated introns
transcription elongation factor 1 homolog
eukaryotic translation initiation factor 4E-binding protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 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: rac GTPase-activating protein 1-like
tripeptidyl-peptidase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
tripeptidyl-peptidase 2-like, transcript variant X4
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 39 samples with support for all annotated introns
tripeptidyl-peptidase 2-like, transcript variant X2
tripeptidyl-peptidase 2-like, transcript variant X3
uncharacterized LOC125033580, transcript variant X2
uncharacterized LOC125033580, transcript variant X1
uncharacterized protein LOC125033580 isoform X2
uncharacterized protein LOC125033580 isoform X1
uncharacterized PPE family protein PPE24-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein amalgam-like, transcript variant X2
protein amalgam-like, transcript variant X1
protein amalgam-like, transcript variant X3
histone H3.v1-like, transcript variant X2
histone H3.v1-like, transcript variant X1
60S ribosomal protein L44-like, transcript variant X1
60S ribosomal protein L44-like isoform X1
60S ribosomal protein L44-like, transcript variant X2
60S ribosomal protein L44-like isoform X2
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
neuropeptide F-like, transcript variant X2
neuropeptide F-like, transcript variant X1
uncharacterized protein LOC125033601 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
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
basement membrane-specific heparan sulfate proteoglycan core protein-like
flagellar attachment zone protein 1-like, transcript variant X2
flagellar attachment zone protein 1-like, transcript variant X1
flagellar attachment zone protein 1-like
LOW QUALITY PROTEIN: uncharacterized protein LOC125033206
5-phosphohydroxy-L-lysine phospho-lyase-like, transcript variant X6
5-phosphohydroxy-L-lysine phospho-lyase-like, transcript variant X7
5-phosphohydroxy-L-lysine phospho-lyase-like, transcript variant X3
5-phosphohydroxy-L-lysine phospho-lyase-like isoform X3
5-phosphohydroxy-L-lysine phospho-lyase-like isoform X2
5-phosphohydroxy-L-lysine phospho-lyase-like, transcript variant X2
5-phosphohydroxy-L-lysine phospho-lyase-like, transcript variant X1
5-phosphohydroxy-L-lysine phospho-lyase-like, transcript variant X5
5-phosphohydroxy-L-lysine phospho-lyase-like, transcript variant X4
5-phosphohydroxy-L-lysine phospho-lyase-like isoform X1
X-ray repair cross-complementing protein 5-like
GPI ethanolamine phosphate transferase 3-like, transcript variant X2
GPI ethanolamine phosphate transferase 3-like, transcript variant X1
GPI ethanolamine phosphate transferase 3-like, transcript variant X3
GPI ethanolamine phosphate transferase 3-like isoform X1
GPI ethanolamine phosphate transferase 3-like isoform X2
leucine-rich repeat protein soc-2 homolog, transcript variant X1
leucine-rich repeat protein soc-2 homolog, transcript variant X2
leucine-rich repeat protein soc-2 homolog isoform X2
leucine-rich repeat protein SHOC-2-like isoform X1
probable Dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
nuclear protein localization protein 4 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
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: nuclear protein localization protein 4 homolog
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
SLIT-ROBO Rho GTPase-activating protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: SLIT-ROBO Rho GTPase-activating protein 1-like
ras-associated and pleckstrin homology domains-containing protein 1-like
uncharacterized LOC125033420, transcript variant X1
uncharacterized LOC125033420, transcript variant X2
uncharacterized LOC125033420, transcript variant X3
uncharacterized protein LOC125033420 isoform X1
uncharacterized protein LOC125033420 isoform X2
proton-coupled folate transporter-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
proton-coupled folate transporter-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
proton-coupled folate transporter-like isoform X1
proton-coupled folate transporter-like isoform X2
solute carrier family 46 member 3-like, transcript variant X2
solute carrier family 46 member 3-like, transcript variant X1
solute carrier family 46 member 3-like, transcript variant X3
transfer RNA valine (anticodon AAC); 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.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125033520, transcript variant X1
uncharacterized LOC125033520, transcript variant X2
transfer RNA aspartic acid (anticodon GUC); 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: AF4/FMR2 family member lilli-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
transfer RNA glycine (anticodon ACC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein TRACHEARY ELEMENT DIFFERENTIATION-RELATED 7A-like
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125033560, transcript variant X1
uncharacterized LOC125033560, transcript variant X2
uncharacterized protein LOC125033560 isoform X1
uncharacterized protein LOC125033560 isoform X2
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B-like, transcript variant X3
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B-like, transcript variant X2
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B-like, transcript variant X1
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B-like isoform X3
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B-like isoform X2
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B-like isoform X1
schwannomin-interacting protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
schwannomin-interacting protein 1-like, transcript variant X4
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
schwannomin-interacting protein 1-like, transcript variant X1
schwannomin-interacting protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
schwannomin-interacting protein 1-like isoform X1
schwannomin-interacting protein 1-like isoform X3
schwannomin-interacting protein 1-like isoform X2
schwannomin-interacting protein 1-like isoform X4
WD repeat and FYVE domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
LOW QUALITY PROTEIN: dynein heavy chain, cytoplasmic-like
kinesin-like protein KIF3B, transcript variant X4
kinesin-like protein KIF3B, transcript variant X6
kinesin-like protein KIF3B, transcript variant X1
kinesin-like protein KIF3B, transcript variant X2
kinesin-like protein KIF3B, transcript variant X3
kinesin-like protein KIF3B, transcript variant X5
similar to RNA sequence (same species):INSD:GIYE01034043.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 284 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 284 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
probable maleylacetoacetate isomerase 2, transcript variant X1
probable maleylacetoacetate isomerase 2, transcript variant X2
probable maleylacetoacetate isomerase 2 isoform X1
probable maleylacetoacetate isomerase 2 isoform X2
glutamate receptor ionotropic, delta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
receptor-type tyrosine-protein phosphatase T-like
uncharacterized LOC125033391, 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 LOC125033391, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
uncharacterized LOC125033391, 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 24 samples with support for all annotated introns
uncharacterized LOC125033391, transcript variant X1
uncharacterized protein LOC125033391 isoform X1
uncharacterized protein LOC125033391 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 27 samples with support for all annotated introns
protein O-mannosyl-transferase TMTC1-like
uncharacterized LOC125033320, 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 21 samples with support for all annotated introns
uncharacterized LOC125033320, 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 8 samples with support for all annotated introns
uncharacterized LOC125033320, 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 7 samples with support for all annotated introns
uncharacterized LOC125033320, transcript variant X4
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
protein O-mannosyl-transferase TMTC2-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 26 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
chorion peroxidase-like, transcript variant X2
similar to RNA sequence (same species):INSD:GHUY01008481.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 232 bases not found in genome assembly
chorion peroxidase-like, transcript variant X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 168 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: 10 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
integrin-linked protein kinase homolog pat-4-like, transcript variant X1
integrin-linked protein kinase homolog pat-4-like, transcript variant X2
integrin-linked protein kinase homolog pat-4-like, transcript variant X4
integrin-linked protein kinase homolog pat-4-like, transcript variant X3
integrin-linked protein kinase homolog pat-4-like
zinc finger protein 407-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 31 samples with support for all annotated introns
zinc finger protein 407-like, transcript variant X3
zinc finger protein 407-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
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, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitochondrial 2-oxodicarboxylate carrier-like, transcript variant X1
mitochondrial 2-oxodicarboxylate carrier-like, transcript variant X3
mitochondrial 2-oxodicarboxylate carrier-like, transcript variant X2
mitochondrial 2-oxodicarboxylate carrier-like isoform X1
mitochondrial 2-oxodicarboxylate carrier-like isoform X2
poly(A)-specific ribonuclease PARN-like, transcript variant X2
similar to RNA sequence (same species):INSD:GHUY01009539.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1219 bases not found in genome assembly
poly(A)-specific ribonuclease PARN-like, transcript variant X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 1219 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
poly(A)-specific ribonuclease PARN-like isoform X2
poly(A)-specific ribonuclease PARN-like isoform X1
similar to RNA sequence (same species):INSD:GHUY01004828.1
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
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 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 58 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC125033503, transcript variant X2
uncharacterized LOC125033503, transcript variant X1
uncharacterized protein LOC125033503 isoform X1
uncharacterized protein LOC125033503 isoform X2
ras-related and estrogen-regulated growth inhibitor-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 6 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor-like isoform X2
ras-related and estrogen-regulated growth inhibitor-like isoform X1
hydroxysteroid dehydrogenase-like protein 2
irregular chiasm C-roughest protein-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: 426 Proteins
lanC-like protein 2, transcript variant X2
lanC-like protein 2, transcript variant X1
SET and MYND domain-containing protein 4-like
echinoderm microtubule-associated protein-like 5
PR domain zinc finger protein 10-like, transcript variant X2
PR domain zinc finger protein 10-like, transcript variant X1
PR domain zinc finger protein 10-like, transcript variant X3
PR domain zinc finger protein 10-like isoform X2
PR domain zinc finger protein 10-like isoform X1
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like, transcript variant X2
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like, transcript variant X5
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like, transcript variant X4
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like isoform X2
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like isoform X4
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like isoform X5
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like isoform X1
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like isoform X3
protein-L-isoaspartate(D-aspartate) O-methyltransferase-like isoform X6
SANT and BTB domain regulator of class switch recombination-like
complement C1q tumor necrosis factor-related protein 4-like, transcript variant X2
complement C1q tumor necrosis factor-related protein 4-like, transcript variant X1
complement C1q tumor necrosis factor-related protein 4-like isoform X2
complement C1q tumor necrosis factor-related protein 4-like isoform X1
uncharacterized LOC125033483, transcript variant X2
uncharacterized LOC125033483, transcript variant X1
uncharacterized protein LOC125033483 isoform X2
uncharacterized protein LOC125033483 isoform X1
uncharacterized LOC125033367, 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
uncharacterized LOC125033367, 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 19 samples with support for all annotated introns
uncharacterized LOC125033367, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein madd-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein madd-4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein madd-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 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: 75% 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 2 samples with support for all annotated introns
FMRFamide-activated amiloride-sensitive sodium channel-like
chromodomain-helicase-DNA-binding protein Mi-2 homolog
LOW QUALITY PROTEIN: chromodomain-helicase-DNA-binding protein Mi-2 homolog
CCR4-NOT transcription complex subunit 10-A-like, transcript variant X3
CCR4-NOT transcription complex subunit 10-A-like, transcript variant X2
CCR4-NOT transcription complex subunit 10-A-like, transcript variant X1
CCR4-NOT transcription complex subunit 10-A-like isoform X1
CCR4-NOT transcription complex subunit 10-A-like isoform X2
JNK1/MAPK8-associated membrane protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
JNK1/MAPK8-associated membrane protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
JNK1/MAPK8-associated membrane protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
JNK1/MAPK8-associated membrane protein-like, transcript variant X1
JNK1/MAPK8-associated membrane protein-like
hybrid signal transduction histidine kinase I-like
p21-activated protein kinase-interacting protein 1-like
F-box/LRR-repeat protein 4-like, transcript variant X2
F-box/LRR-repeat protein 4-like, transcript variant X1
uncharacterized LOC125033186, transcript variant X1
uncharacterized LOC125033186, transcript variant X4
uncharacterized LOC125033186, transcript variant X2
uncharacterized LOC125033186, transcript variant X5
uncharacterized LOC125033186, transcript variant X3
muscle M-line assembly protein unc-89-like
calsequestrin-1-like, transcript variant X1
calsequestrin-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 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: 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: 97% coverage of the annotated genomic feature by RNAseq alignments
NPC intracellular cholesterol transporter 2 homolog a-like
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 1 sample with support for all annotated introns
cytosolic Fe-S cluster assembly factor nubp1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 90% 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 EST, and 75% coverage of the annotated genomic feature by RNAseq alignments
tetratricopeptide repeat protein 19, mitochondrial-like
ribosomal L1 domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
UDP-glucose 4-epimerase-like, transcript variant X2
UDP-glucose 4-epimerase-like, transcript variant X1
UDP-glucose 4-epimerase-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
protein suppressor of white apricot-like
aurora kinase A-like, transcript variant X1
aurora kinase A-like, transcript variant X3
aurora kinase A-like, transcript variant X4
aurora kinase A-like, transcript variant X2
protein unc-13 homolog A-like, transcript variant X7
protein unc-13 homolog A-like, transcript variant X2
protein unc-13 homolog A-like, transcript variant X4
protein unc-13 homolog A-like, transcript variant X1
protein unc-13 homolog A-like, transcript variant X3
protein unc-13 homolog A-like, transcript variant X5
protein unc-13 homolog A-like isoform X7
protein unc-13 homolog A-like isoform X4
protein unc-13 homolog A-like isoform X3
uncharacterized protein LOC125033350 isoform X2
uncharacterized protein LOC125033350 isoform X5
uncharacterized protein LOC125033350 isoform X1
protein unc-13 homolog A-like, transcript variant X6
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
uncharacterized protein LOC125033350 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
histidine--tRNA ligase-like, transcript variant X1
histidine--tRNA ligase-like, transcript variant X2
histidine--tRNA ligase-like, transcript variant X4
histidine--tRNA ligase-like, transcript variant X5
histidine--tRNA ligase-like, transcript variant X3
uncharacterized protein C1orf50 homolog, transcript variant X1
uncharacterized protein C1orf50 homolog, transcript variant X2
uncharacterized protein C1orf50 homolog isoform X2
uncharacterized protein C1orf50 homolog isoform X1
TATA-binding protein-associated factor 2N-like, transcript variant X2
TATA-binding protein-associated factor 2N-like, transcript variant X3
TATA-binding protein-associated factor 2N-like, transcript variant X1
TATA-binding protein-associated factor 2N-like isoform X1
peptidyl-glycine alpha-amidating monooxygenase B-like
beta-hexosaminidase subunit alpha-like, transcript variant X1
beta-hexosaminidase subunit alpha-like, transcript variant X2
beta-hexosaminidase subunit alpha-like, transcript variant X3
beta-hexosaminidase subunit alpha-like isoform X2
beta-hexosaminidase subunit alpha-like isoform X1
beta-hexosaminidase subunit alpha-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
alanine racemase-like, transcript variant X1
alanine racemase-like, transcript variant X2
alanine racemase-like, transcript variant X4
alanine racemase-like, transcript variant X3
probable antibacterial peptide polyprotein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 76% coverage of the annotated genomic feature by RNAseq alignments
SAFB-like transcription modulator, transcript variant X2
SAFB-like transcription modulator, transcript variant X8
SAFB-like transcription modulator isoform X2
SAFB-like transcription modulator isoform X8
SAFB-like transcription modulator, transcript variant X3
SAFB-like transcription modulator, transcript variant X4
SAFB-like transcription modulator, transcript variant X1
SAFB-like transcription modulator, transcript variant X10
SAFB-like transcription modulator, transcript variant X6
SAFB-like transcription modulator, transcript variant X9
SAFB-like transcription modulator, transcript variant X5
SAFB-like transcription modulator, transcript variant X7
SAFB-like transcription modulator isoform X1
SAFB-like transcription modulator isoform X10
SAFB-like transcription modulator isoform X6
SAFB-like transcription modulator isoform X3
SAFB-like transcription modulator isoform X4
SAFB-like transcription modulator isoform X5
SAFB-like transcription modulator isoform X9
SAFB-like transcription modulator isoform X7
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
succinate-semialdehyde dehydrogenase, mitochondrial-like
betaine--homocysteine S-methyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
alpha-2-macroglobulin receptor-associated protein-like
organic solute transporter subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125033409, transcript variant X1
uncharacterized LOC125033409, transcript variant X2
probable RNA-binding protein 46, transcript variant X3
probable RNA-binding protein 46, transcript variant X4
probable RNA-binding protein 46, transcript variant X1
probable RNA-binding protein 46, transcript variant X2
probable RNA-binding protein 46 isoform X3
probable RNA-binding protein 46 isoform X2
probable RNA-binding protein 46 isoform 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 3 samples with support for all annotated introns
electron transfer flavoprotein beta subunit lysine methyltransferase-like, transcript variant X2
electron transfer flavoprotein beta subunit lysine methyltransferase-like, transcript variant X3
electron transfer flavoprotein beta subunit lysine methyltransferase-like, transcript variant X1
electron transfer flavoprotein beta subunit lysine methyltransferase-like, transcript variant X4
electron transfer flavoprotein beta subunit lysine methyltransferase-like isoform X1
electron transfer flavoprotein beta subunit lysine methyltransferase-like isoform X2
electron transfer flavoprotein beta subunit lysine methyltransferase-like isoform X3
nuclear mitotic apparatus protein 1-like, transcript variant X1
nuclear mitotic apparatus protein 1-like, transcript variant X2
nuclear mitotic apparatus protein 1-like, transcript variant X3
nuclear mitotic apparatus protein 1-like isoform X1
nuclear mitotic apparatus protein 1-like isoform X3
nuclear mitotic apparatus protein 1-like isoform X2
uncharacterized LOC125033435, 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 7 samples with support for all annotated introns
uncharacterized LOC125033435, transcript variant X3
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 9 samples with support for all annotated introns
uncharacterized LOC125033435, transcript variant X1
uncharacterized protein LOC125033435 isoform X2
uncharacterized protein LOC125033435 isoform X1
uncharacterized LOC125033554, transcript variant X1
uncharacterized protein LOC125033554 isoform X1
uncharacterized LOC125033554, transcript variant X2
uncharacterized protein LOC125033554 isoform X2
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X1
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X2
acyl-coenzyme A synthetase ACSM3, mitochondrial-like
E3 ubiquitin-protein ligase TRIM33-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 31 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X3
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X4
E3 ubiquitin-protein ligase TRIM33-like isoform X1
transcription intermediary factor 1-alpha-like isoform X2
E3 ubiquitin-protein ligase TRIM33-like isoform X3
MAP7 domain-containing protein 2-like, transcript variant X13
MAP7 domain-containing protein 2-like isoform X13
MAP7 domain-containing protein 2-like, transcript variant X4
MAP7 domain-containing protein 2-like, transcript variant X1
MAP7 domain-containing protein 2-like, transcript variant X7
MAP7 domain-containing protein 2-like, transcript variant X11
MAP7 domain-containing protein 2-like, transcript variant X14
MAP7 domain-containing protein 2-like, transcript variant X6
MAP7 domain-containing protein 2-like, transcript variant X2
MAP7 domain-containing protein 2-like, transcript variant X5
MAP7 domain-containing protein 2-like, transcript variant X8
neurofilament heavy polypeptide-like isoform X4
serine/arginine repetitive matrix protein 2-like isoform X1
MAP7 domain-containing protein 2-like isoform X7
neurofilament heavy polypeptide-like isoform X6
MAP7 domain-containing protein 2-like isoform X5
MAP7 domain-containing protein 2-like isoform X8
MAP7 domain-containing protein 2-like, transcript variant X10
MAP7 domain-containing protein 2-like isoform X10
MAP7 domain-containing protein 2-like, transcript variant X12
MAP7 domain-containing protein 2-like isoform X12
MAP7 domain-containing protein 2-like, transcript variant X3
MAP7 domain-containing protein 2-like isoform X3
MAP7 domain-containing protein 2-like, transcript variant X9
MAP7 domain-containing protein 2-like isoform X9
nuclear pore glycoprotein p62-like, transcript variant X4
nuclear pore glycoprotein p62-like, transcript variant X1
nuclear pore glycoprotein p62-like, transcript variant X3
nuclear pore glycoprotein p62-like, transcript variant X2
nuclear pore glycoprotein p62-like isoform X2
nuclear pore glycoprotein p62-like isoform X1
potassium channel subfamily K member 1-like, transcript variant X7
potassium channel subfamily K member 1-like isoform X2
potassium channel subfamily K member 1-like, transcript variant X5
potassium channel subfamily K member 1-like, transcript variant X4
potassium channel subfamily K member 1-like, transcript variant X1
potassium channel subfamily K member 1-like, transcript variant X3
potassium channel subfamily K member 1-like, transcript variant X6
potassium channel subfamily K member 1-like, transcript variant X2
potassium channel subfamily K member 1-like isoform X1
28S ribosomal protein S28, mitochondrial-like
5'-deoxynucleotidase HDDC2-like, transcript variant X1
5'-deoxynucleotidase HDDC2-like, transcript variant X2
beta-arrestin-1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
beta-arrestin-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
beta-arrestin-1-like, transcript variant X3
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 35 samples with support for all annotated introns
beta-arrestin-1-like, 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 33 samples with support for all annotated introns
cysteine-rich and transmembrane domain-containing protein WIH2-like
serine/threonine-protein kinase DCLK1-like, transcript variant X2
serine/threonine-protein kinase DCLK1-like, transcript variant X4
serine/threonine-protein kinase DCLK1-like, transcript variant X1
serine/threonine-protein kinase DCLK1-like, transcript variant X3
serine/threonine-protein kinase DCLK1-like, transcript variant X5
serine/threonine-protein kinase DCLK1-like, transcript variant X6
serine/threonine-protein kinase DCLK1-like isoform X2
serine/threonine-protein kinase DCLK1-like isoform X3
serine/threonine-protein kinase DCLK1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
protein phosphatase 1K, 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 19 samples with support for all annotated introns
trans-Golgi network integral membrane protein 2-like
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
26S proteasome non-ATPase regulatory subunit 12-like
LOW QUALITY PROTEIN: 26S proteasome non-ATPase regulatory subunit 12-like
regulator of G-protein signaling 9-like, transcript variant X3
regulator of G-protein signaling 9-like, transcript variant X2
regulator of G-protein signaling 9-like, transcript variant X4
regulator of G-protein signaling 9-like, transcript variant X5
regulator of G-protein signaling 9-like, transcript variant X1
regulator of G-protein signaling 9-like, transcript variant X6
regulator of G-protein signaling 9-like, transcript variant X8
regulator of G-protein signaling 9-like isoform X1
regulator of G-protein signaling 9-like isoform X3
regulator of G-protein signaling 9-like isoform X5
regulator of G-protein signaling 9-like isoform X2
regulator of G-protein signaling 9-like, transcript variant X7
regulator of G-protein signaling 9-like isoform X4
acetyl-CoA acetyltransferase, cytosolic-like
probable isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial
E3 ubiquitin-protein ligase Mdm2-like, transcript variant X3
E3 ubiquitin-protein ligase Mdm2-like, transcript variant X4
E3 ubiquitin-protein ligase Mdm2-like, transcript variant X1
E3 ubiquitin-protein ligase Mdm2-like, transcript variant X6
E3 ubiquitin-protein ligase Mdm2-like isoform X1
E3 ubiquitin-protein ligase Mdm2-like, transcript variant X2
E3 ubiquitin-protein ligase Mdm2-like isoform X2
E3 ubiquitin-protein ligase Mdm2-like isoform X3
E3 ubiquitin-protein ligase Mdm2-like, transcript variant X5
E3 ubiquitin-protein ligase Mdm2-like isoform X4
protein yippee-like 2, transcript variant X3
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 8 samples with support for all annotated introns
protein yippee-like 2, 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 37 samples with support for all annotated introns
protein yippee-like 2, transcript variant X1
uncharacterized protein DDB_G0271670-like
DNA-directed RNA polymerase II subunit RPB1-like
small nuclear ribonucleoprotein Sm D1-like
RING-type E3 ubiquitin-protein ligase PPIL2-like
NADH-ubiquinone oxidoreductase 49 kDa subunit-like
LOW QUALITY PROTEIN: betaine--homocysteine S-methyltransferase 1-like
type-1 angiotensin II receptor-associated protein-like, 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 31 samples with support for all annotated introns
type-1 angiotensin II receptor-associated protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
type-1 angiotensin II receptor-associated protein-like, transcript variant X1
type-1 angiotensin II receptor-associated protein-like isoform X2
type-1 angiotensin II receptor-associated protein-like isoform X1
type-1 angiotensin II receptor-associated protein-like isoform X3
PH domain-containing protein DDB_G0287875-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
TRAF3-interacting protein 1-like, transcript variant X1
TRAF3-interacting protein 1-like, transcript variant X2
TRAF3-interacting protein 1-like isoform X1
TRAF3-interacting protein 1-like isoform X2
uncharacterized LOC125033541, 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 11 samples with support for all annotated introns
uncharacterized LOC125033541, transcript variant X1
uncharacterized protein LOC125033541 isoform X1
uncharacterized protein LOC125033541 isoform X2
uncharacterized LOC125033612, transcript variant X2
uncharacterized LOC125033612, transcript variant X1
uncharacterized LOC125033473, transcript variant X2
uncharacterized LOC125033473, transcript variant X1
ras GTPase-activating protein nGAP-like, transcript variant X3
ras GTPase-activating protein nGAP-like, transcript variant X2
ras GTPase-activating protein nGAP-like, transcript variant X1
ras GTPase-activating protein nGAP-like isoform X3
ras GTPase-activating protein nGAP-like isoform X2
ras GTPase-activating protein nGAP-like isoform X1
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 34 samples with support for all annotated introns
proline-rich receptor-like protein kinase PERK10, transcript variant X1
proline-rich receptor-like protein kinase PERK10, 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 9 samples with support for all annotated introns
proline-rich receptor-like protein kinase PERK10, transcript variant X4
proline-rich receptor-like protein kinase PERK10, transcript variant X2
proline-rich receptor-like protein kinase PERK10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
regulator of G-protein signaling 2-like, transcript variant X2
regulator of G-protein signaling 2-like isoform X2
regulator of G-protein signaling 2-like, transcript variant X1
regulator of G-protein signaling 21-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 24 samples with support for all annotated introns
chitobiosyldiphosphodolichol beta-mannosyltransferase-like
ras-related and estrogen-regulated growth inhibitor-like
flavin-containing monooxygenase FMO GS-OX-like 2
alkylated DNA repair protein alkB homolog 8-like
putative cell division cycle ATPase, transcript variant X2
putative cell division cycle ATPase, transcript variant X1
abasic site processing protein HMCES-like
origin recognition complex subunit 1-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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-prolyl cis-trans isomerase FKBP62-like
retinol dehydrogenase 11-like, transcript variant X3
retinol dehydrogenase 11-like, transcript variant X6
retinol dehydrogenase 11-like, transcript variant X1
retinol dehydrogenase 11-like, transcript variant X7
retinol dehydrogenase 11-like, transcript variant X5
retinol dehydrogenase 11-like, transcript variant X4
retinol dehydrogenase 11-like, transcript variant X2
dehydrogenase/reductase SDR family member 13-like isoform X2
retinol dehydrogenase 11-like isoform X3
dehydrogenase/reductase SDR family member 13-like isoform X1
piggyBac transposable element-derived protein 4-like, transcript variant X2
piggyBac transposable element-derived protein 4-like, transcript variant X1
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 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GIYE01020786.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 378 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 217 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC125033590, transcript variant X1
uncharacterized LOC125033590, transcript variant X3
uncharacterized LOC125033590, transcript variant X5
uncharacterized LOC125033590, transcript variant X6
uncharacterized protein LOC125033590 isoform X1
uncharacterized protein LOC125033590 isoform X3
uncharacterized protein LOC125033590 isoform X5
uncharacterized protein LOC125033590 isoform X6
uncharacterized LOC125033590, transcript variant X2
uncharacterized LOC125033590, transcript variant X4
uncharacterized protein LOC125033590 isoform X2
uncharacterized protein LOC125033590 isoform X4
zinc finger protein 568-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 36 samples with support for all annotated introns
zinc finger protein 568-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
thioredoxin-related transmembrane protein 2 homolog
similar to RNA sequence (same species):INSD:GIYE01046688.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 548 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 501 bases not found in genome assembly; 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: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: venom phosphodiesterase 2-like
DNA cross-link repair protein SNM1-like, transcript variant X4
DNA cross-link repair protein SNM1-like, transcript variant X3
DNA cross-link repair protein SNM1-like, transcript variant X6
DNA cross-link repair protein SNM1-like, transcript variant X1
DNA cross-link repair protein SNM1-like, transcript variant X5
DNA cross-link repair protein SNM1-like, transcript variant X2
DNA cross-link repair 1A protein-like isoform X3
DNA cross-link repair 1A protein-like isoform X1
DNA cross-link repair 1A protein-like isoform X2
DNA cross-link repair 1A protein-like isoform X5
DNA cross-link repair 1A protein-like isoform X4
DNA cross-link repair protein SNM1-like, transcript variant X7
DNA cross-link repair protein SNM1-like, transcript variant X8
DNA cross-link repair 1A protein-like isoform X6
DNA cross-link repair protein SNM1-like isoform X7
uncharacterized LOC125033700, transcript variant X2
uncharacterized LOC125033700, transcript variant X5
uncharacterized LOC125033700, transcript variant X1
uncharacterized LOC125033700, transcript variant X4
uncharacterized LOC125033700, transcript variant X3
uncharacterized protein LOC125033700 isoform X2
uncharacterized protein LOC125033700 isoform X1
uncharacterized protein LOC125033700 isoform X3
uncharacterized LOC125033699, transcript variant X1
uncharacterized LOC125033699, 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 13 samples with support for all annotated introns
uncharacterized LOC125033699, transcript variant X4
uncharacterized LOC125033699, transcript variant X3
uncharacterized protein LOC125033699 isoform X1
uncharacterized protein LOC125033699 isoform X2
uncharacterized LOC125033171, transcript variant X4
uncharacterized LOC125033171, transcript variant X3
uncharacterized LOC125033171, transcript variant X2
uncharacterized LOC125033171, transcript variant X1
uncharacterized LOC125033635, transcript variant X1
uncharacterized LOC125033635, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
polycystic kidney disease protein 1-like 3
soluble scavenger receptor cysteine-rich domain-containing protein SSC5D-like
mitochondrial coenzyme A diphosphatase NUDT8-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 9 samples with support for all annotated introns
mitochondrial coenzyme A diphosphatase NUDT8-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 37 samples with support for all annotated introns
mitochondrial coenzyme A diphosphatase NUDT8-like isoform X1
mitochondrial coenzyme A diphosphatase NUDT8-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35% coverage of the annotated genomic feature by RNAseq alignments
serine/arginine-rich splicing factor 4-like
enhancer of mRNA-decapping protein 3-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 34 samples with support for all annotated introns
telomere length and silencing protein 1 homolog
SAGA-associated factor 29-like, transcript variant X1
SAGA-associated factor 29-like, transcript variant X2
SAGA-associated factor 29-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 67% 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 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: 17 Proteins, 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: 16 Proteins, and 56% 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 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pigment-dispersing hormone type 1-like, transcript variant X1
pigment-dispersing hormone type 1-like, transcript variant X2
pigment-dispersing hormone type 1, transcript variant X1
pigment-dispersing hormone type 1, transcript variant X2
pigment-dispersing hormone type 1 isoform X1
pigment-dispersing hormone type 1 isoform X2
leucine-rich repeat neuronal protein 3-like
WD repeat-containing protein 61-like, transcript variant X1
WD repeat-containing protein 61-like, transcript variant X2
WD repeat-containing protein 61-like isoform X1
WD repeat-containing protein 61-like isoform X2
protein HIRA-like, transcript variant X1
protein HIRA-like, transcript variant X2
protein HIRA-like, transcript variant X3
mitochondrial import inner membrane translocase subunit TIM44-like
RNA polymerase-associated protein Rtf1-like
zinc finger protein 2-like, transcript variant X3
zinc finger protein 2-like, transcript variant X4
zinc finger protein 2-like, transcript variant X6
zinc finger protein 2-like, transcript variant X8
zinc finger protein 2-like, transcript variant X7
zinc finger protein 2-like, transcript variant X13
zinc finger protein 2-like, transcript variant X11
zinc finger protein 2-like, transcript variant X5
zinc finger protein 2-like, transcript variant X9
zinc finger protein 2-like, transcript variant X12
zinc finger protein 2-like, transcript variant X10
monocarboxylate transporter 9-like, transcript variant X13
monocarboxylate transporter 9-like, transcript variant X12
monocarboxylate transporter 9-like, transcript variant X11
monocarboxylate transporter 9-like, transcript variant X9
monocarboxylate transporter 9-like, transcript variant X3
monocarboxylate transporter 9-like, transcript variant X4
monocarboxylate transporter 9-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 14 samples with support for all annotated introns
monocarboxylate transporter 9-like, transcript variant X7
monocarboxylate transporter 9-like, transcript variant X2
monocarboxylate transporter 9-like, transcript variant X6
monocarboxylate transporter 9-like, transcript variant X1
monocarboxylate transporter 9-like, transcript variant X10
monocarboxylate transporter 9-like, transcript variant X8
uncharacterized protein LOC125033549 isoform X2
monocarboxylate transporter 9-like isoform X1
uncharacterized protein LOC125033549 isoform X3
monocarboxylate transporter 9-like, transcript variant X15
monocarboxylate transporter 9-like, transcript variant X14
uncharacterized protein LOC125033549 isoform X5
uncharacterized protein LOC125033549 isoform X4
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like, transcript variant X3
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like, transcript variant X2
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like, transcript variant X1
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like, transcript variant X4
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like
MAP kinase-activated protein kinase 2-like
sulfotransferase 1B1-like, transcript variant X1
sulfotransferase 1B1-like, transcript variant X2
ubiquitin-conjugating enzyme E2 W-like, transcript variant X4
ubiquitin-conjugating enzyme E2 W-like, transcript variant X3
ubiquitin-conjugating enzyme E2 W-like, transcript variant X2
ubiquitin-conjugating enzyme E2 W-like, transcript variant X1
ubiquitin-conjugating enzyme E2 W-like, transcript variant X5
ubiquitin-conjugating enzyme E2 W-like isoform X4
ubiquitin-conjugating enzyme E2 W-like isoform X3
ubiquitin-conjugating enzyme E2 W-like isoform X2
ubiquitin-conjugating enzyme E2 W-like isoform X1
ubiquitin-conjugating enzyme E2 W-like isoform X5
ubiquinone biosynthesis monooxygenase COQ6, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
serine/arginine repetitive matrix protein 1-like
uncharacterized LOC125033453, transcript variant X3
uncharacterized LOC125033453, transcript variant X4
uncharacterized LOC125033453, transcript variant X1
uncharacterized LOC125033453, transcript variant X2
uncharacterized LOC125033330, transcript variant X1
uncharacterized LOC125033330, 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 26 samples with support for all annotated introns
mevalonyl-coenzyme A hydratase sidH-like
uncharacterized LOC125033436, transcript variant X9
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 5 samples with support for all annotated introns
uncharacterized LOC125033436, transcript variant X7
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 6 samples with support for all annotated introns
uncharacterized LOC125033436, transcript variant X1
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 11 samples with support for all annotated introns
uncharacterized LOC125033436, transcript variant X5
uncharacterized LOC125033436, 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 31 samples with support for all annotated introns
uncharacterized LOC125033436, 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 17 samples with support for all annotated introns
uncharacterized LOC125033436, transcript variant X13
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 9 samples with support for all annotated introns
uncharacterized LOC125033436, transcript variant X10
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 2 samples with support for all annotated introns
uncharacterized LOC125033436, transcript variant X11
uncharacterized LOC125033436, transcript variant X4
uncharacterized LOC125033436, transcript variant X8
uncharacterized LOC125033436, transcript variant X12
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 4 samples with support for all annotated introns
uncharacterized LOC125033436, transcript variant X6
probable bifunctional dTTP/UTP pyrophosphatase/methyltransferase protein
ribosomal protein S6 kinase beta-1-like, transcript variant X2
ribosomal protein S6 kinase beta-1-like, transcript variant X1
uncharacterized LOC125033632, transcript variant X1
uncharacterized LOC125033632, transcript variant X3
uncharacterized LOC125033632, transcript variant X4
uncharacterized LOC125033632, transcript variant X5
uncharacterized LOC125033632, transcript variant X2
vacuolar protein sorting-associated protein 26C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
putative tricarboxylate transport protein, mitochondrial
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 34 samples with support for all annotated introns
VWFA and cache domain-containing protein 1-like, transcript variant X2
VWFA and cache domain-containing protein 1-like, transcript variant X1
VWFA and cache domain-containing protein 1-like, transcript variant X4
VWFA and cache domain-containing protein 1-like, transcript variant X3
VWFA and cache domain-containing protein 1-like isoform X1
VWFA and cache domain-containing protein 1-like, transcript variant X5
VWFA and cache domain-containing protein 1-like isoform X2
long-chain-fatty-acid--CoA ligase 6-like, transcript variant X5
long-chain-fatty-acid--CoA ligase 6-like, transcript variant X2
long-chain-fatty-acid--CoA ligase 6-like, transcript variant X3
long-chain-fatty-acid--CoA ligase 6-like, transcript variant X4
long-chain-fatty-acid--CoA ligase 6-like, transcript variant X1
long-chain-fatty-acid--CoA ligase 6-like, transcript variant X6
long-chain-fatty-acid--CoA ligase 1-like isoform X2
long-chain-fatty-acid--CoA ligase 1-like isoform X1
long-chain-fatty-acid--CoA ligase 6-like isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC125033308
U6 snRNA-associated Sm-like protein LSm3, transcript variant X2
U6 snRNA-associated Sm-like protein LSm3 isoform X2
U6 snRNA-associated Sm-like protein LSm3, transcript variant X1
chromatin accessibility complex protein 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
nuclear pore complex protein Nup153-like
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 10 samples with support for all annotated introns
beta-1,4-glucuronyltransferase 1-like, transcript variant X1
beta-1,4-glucuronyltransferase 1-like, transcript variant X3
beta-1,4-glucuronyltransferase 1-like, transcript variant X2
uncharacterized LOC125033566, transcript variant X2
uncharacterized LOC125033566, transcript variant X1
uncharacterized protein LOC125033566 isoform X2
uncharacterized protein LOC125033566 isoform X1
histone-lysine N-methyltransferase SMYD3-like, transcript variant X2
similar to RNA sequence (same species):INSD:GIYE01044337.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 153 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 149 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
histone-lysine N-methyltransferase SMYD3-like isoform X2
histone-lysine N-methyltransferase SMYD3-like, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 153 bases not found in genome assembly; 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
histone-lysine N-methyltransferase SMYD3-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 72% coverage of the annotated genomic feature by RNAseq alignments
proteasome activator complex subunit 3-like, transcript variant X2
proteasome activator complex subunit 3-like, transcript variant X1
proteasome activator complex subunit 3-like isoform X2
proteasome activator complex subunit 3-like isoform X1
2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase-like, transcript variant X1
2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase-like, transcript variant X2
2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase-like isoform X2
2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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: 2 Proteins, and 100% 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: 84% coverage of the annotated genomic feature by RNAseq alignments
platelet glycoprotein Ib alpha chain-like
leucine-rich repeat-containing G-protein coupled receptor 4-like
regulator of nonsense transcripts 3B-like