Penaeus chinensis breed Huanghai No. 1 chromosome 28, 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\nCM032953.1.\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.
calcium-activated chloride channel regulator 3A-1-like
COORDINATES: polyA evidence [ECO:0006239]
calcium-activated chloride channel regulator 1-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 30 samples with support for all annotated introns
oxysterol-binding protein-related protein 9-like
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 19 samples with support for all annotated introns
carboxypeptidase B-like, transcript variant X2
carboxypeptidase B-like, transcript variant X1
uncharacterized LOC125039916, transcript variant X1
uncharacterized LOC125039916, transcript variant X3
uncharacterized LOC125039916, transcript variant X2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial-like
uncharacterized LOC125039943, 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 7 samples with support for all annotated introns
uncharacterized protein LOC125039943 isoform X3
uncharacterized LOC125039943, 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 4 samples with support for all annotated introns
uncharacterized LOC125039943, transcript variant X2
uncharacterized LOC125039943, 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 28 samples with support for all annotated introns
uncharacterized protein LOC125039943 isoform X2
uncharacterized protein LOC125039943 isoform X1
uncharacterized LOC125040015, transcript variant X3
uncharacterized LOC125040015, transcript variant X2
uncharacterized LOC125040015, 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 6 samples with support for all annotated introns
uncharacterized LOC125040250, 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 21 samples with support for all annotated introns
uncharacterized LOC125040250, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized LOC125040250, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125040250, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC125040250, transcript variant 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 17 samples with support for all annotated introns
uncharacterized LOC125040250, transcript variant X4
uncharacterized LOC125040250, 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 26 samples with support for all annotated introns
uncharacterized LOC125040250, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC125040250, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
uncharacterized LOC125040250, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC125040250, transcript variant X11
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 16 samples with support for all annotated introns
uncharacterized protein LOC125040250 isoform X1
uncharacterized protein LOC125040250 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ragulator complex protein LAMTOR4-like, transcript variant X1
ragulator complex protein LAMTOR4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% 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
DNA-directed primase/polymerase protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
beta-mannosidase-like, transcript variant X3
beta-mannosidase-like, transcript variant X4
beta-mannosidase-like, transcript variant X2
beta-mannosidase-like, transcript variant X1
high affinity copper uptake protein 1-like
similar to RNA sequence (same species):INSD:GHUY01002151.1
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 703 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 548 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC125039865, transcript variant X1
uncharacterized LOC125039865, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LIM/homeobox protein Lhx1-like, transcript variant X1
LIM/homeobox protein Lhx1-like, transcript variant X3
LIM/homeobox protein Lhx1-like, transcript variant X2
LIM/homeobox protein Lhx1-like isoform X1
uncharacterized protein LOC125040122 isoform X3
LIM/homeobox protein Lhx1-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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
sodium- and chloride-dependent glycine transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
inositol polyphosphate-4-phosphatase type I A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase isozyme L3-like
cadherin-like and PC-esterase domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized LOC125039929, transcript variant X1
uncharacterized LOC125039929, 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 15 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 1-like
UPF0538 protein C2orf76 homolog, transcript variant X1
UPF0538 protein C2orf76 homolog, transcript variant X2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: kinesin heavy chain-like
guanine nucleotide-binding protein-like 3 homolog, transcript variant X1
guanine nucleotide-binding protein-like 3 homolog, transcript variant X2
guanine nucleotide-binding protein-like 3 homolog isoform X1
guanine nucleotide-binding protein-like 3 homolog isoform X2
conserved oligomeric Golgi complex subunit 3-like
alpha- and gamma-adaptin-binding protein p34-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 38 samples with support for all annotated introns
uncharacterized LOC125040060, transcript variant X1
uncharacterized LOC125040060, transcript variant X2
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 99% 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: 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 2-like, transcript variant X2
glutamate receptor ionotropic, kainate 2-like, transcript variant X3
glutamate receptor ionotropic, kainate 2-like, transcript variant X1
glutamate receptor ionotropic, kainate 2-like isoform X2
glutamate receptor ionotropic, kainate 2-like isoform X3
glutamate receptor ionotropic, kainate 2-like isoform X1
probable U3 small nucleolar RNA-associated protein 11
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: probable U3 small nucleolar RNA-associated protein 11
SH3 domain-binding glutamic acid-rich protein homolog
similar to RNA sequence (same species):INSD:GHUY01003693.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 160 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 45 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125039935, transcript variant X2
uncharacterized LOC125039935, transcript variant X1
uncharacterized LOC125039935, transcript variant X3
uncharacterized protein LOC125039935 isoform X2
uncharacterized protein LOC125039935 isoform X1
uncharacterized protein LOC125039935 isoform 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
protein ABHD11-like, transcript variant X2
protein ABHD11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
sequestosome-1-like, transcript variant X1
sequestosome-1-like, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 1-like, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 1-like, transcript variant X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 1-like isoform X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 1-like isoform X1
general transcription factor 3C polypeptide 5-like, transcript variant X2
general transcription factor 3C polypeptide 5-like, transcript variant X1
general transcription factor 3C polypeptide 5-like
transcriptional regulator GZF3-like, transcript variant X1
similar to RNA sequence (same species):INSD:GHUY01009826.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 293 bases not found in genome assembly
transcriptional regulator GZF3-like, transcript variant X4
transcriptional regulator GZF3-like, transcript variant X3
transcriptional regulator GZF3-like, transcript variant X5
transcriptional regulator GZF3-like, transcript variant X2
transcriptional regulator GZF3-like, transcript variant X6
uncharacterized protein LOC125040111 isoform X1
putative GPI-anchored protein pfl2 isoform X4
transcriptional regulator GZF3-like isoform X3
uncharacterized serine-rich protein C215.13-like isoform X5
uncharacterized protein LOC125040111 isoform X2
uncharacterized protein LOC125040111 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GIYE01034671.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 96 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 3 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GHUY01002531.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 46 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 1 sample with support for all annotated introns
general transcription factor 3C polypeptide 1-like, transcript variant X3
general transcription factor 3C polypeptide 1-like, transcript variant X2
general transcription factor 3C polypeptide 1-like, transcript variant X1
general transcription factor 3C polypeptide 1-like isoform X3
general transcription factor 3C polypeptide 1-like isoform X2
general transcription factor 3C polypeptide 1-like isoform X1
arginine-glutamic acid dipeptide repeats protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
transmembrane and coiled-coil domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel subfamily A member 1 homolog, transcript variant X1
transient receptor potential cation channel subfamily A member 1 homolog, transcript variant X2
transient receptor potential cation channel subfamily A member 1 homolog, transcript variant X5
transient receptor potential cation channel subfamily A member 1 homolog, transcript variant X4
transient receptor potential cation channel subfamily A member 1 homolog, transcript variant X3
transient receptor potential cation channel subfamily A member 1 homolog, transcript variant X6
transient receptor potential cation channel subfamily A member 1 homolog isoform X1
transient receptor potential cation channel subfamily A member 1 homolog isoform X3
transient receptor potential cation channel subfamily A member 1 homolog isoform X2
transient receptor potential cation channel subfamily A member 1 homolog isoform X4
transient receptor potential cation channel subfamily A member 1 homolog isoform X5
dual specificity testis-specific protein kinase 1-like
hydroxyacylglutathione hydrolase, mitochondrial-like, transcript variant X1
hydroxyacylglutathione hydrolase, mitochondrial-like, transcript variant X4
hydroxyacylglutathione hydrolase, mitochondrial-like, transcript variant X3
hydroxyacylglutathione hydrolase, mitochondrial-like, transcript variant X2
hydroxyacylglutathione hydrolase, mitochondrial-like isoform X1
hydroxyacylglutathione hydrolase, mitochondrial-like isoform 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 35 samples with support for all annotated introns
uncharacterized LOC125040220, transcript variant X1
uncharacterized LOC125040220, transcript variant X2
uncharacterized LOC125040220, transcript variant X4
uncharacterized LOC125040220, transcript variant X3
uncharacterized LOC125040220, transcript variant X9
uncharacterized LOC125040220, transcript variant X8
uncharacterized LOC125040220, transcript variant X7
uncharacterized LOC125040220, transcript variant X6
uncharacterized LOC125040220, transcript variant X5
uncharacterized protein LOC125040220 isoform X6
uncharacterized protein LOC125040220 isoform X5
uncharacterized protein LOC125040220 isoform X4
uncharacterized protein LOC125040220 isoform X3
uncharacterized protein LOC125040220 isoform X2
uncharacterized protein LOC125040220 isoform X1
epidermal growth factor receptor substrate 15-like 1, transcript variant X2
epidermal growth factor receptor substrate 15-like 1, transcript variant X3
epidermal growth factor receptor substrate 15-like 1, transcript variant X1
epidermal growth factor receptor substrate 15-like 1 isoform X2
epidermal growth factor receptor substrate 15-like 1 isoform X3
epidermal growth factor receptor substrate 15-like 1 isoform X1
epidermal growth factor receptor substrate 15-like 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
epidermal growth factor receptor substrate 15-like 1 isoform X4
peptide methionine sulfoxide reductase B1, chloroplastic-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
cholinesterase 1-like, transcript variant X2
cholinesterase 1-like, transcript variant X1
cholinesterase 1-like, transcript variant X4
cholinesterase 1-like, transcript variant X3
cholinesterase 1-like, transcript variant X5
cholinesterase 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
two pore potassium channel protein sup-9-like
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
trans-Golgi network integral membrane protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
ubiquitin carboxyl-terminal hydrolase 31-like
N-acylneuraminate cytidylyltransferase A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
N-acylneuraminate cytidylyltransferase A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
N-acylneuraminate cytidylyltransferase A-like isoform X1
N-acylneuraminate cytidylyltransferase A-like isoform X2
protein diaphanous-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 5 samples with support for all annotated introns
protein diaphanous-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein diaphanous-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
protein diaphanous-like, transcript variant X4
uncharacterized LOC125039932, transcript variant X1
uncharacterized LOC125039932, transcript variant X2
uncharacterized LOC125039932, transcript variant X4
uncharacterized LOC125039932, transcript variant X3
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.
homeobox protein unc-4 homolog, transcript variant X1
homeobox protein unc-4 homolog, transcript variant X2
homeobox protein unc-4 homolog isoform X1
homeobox protein unc-4 homolog isoform X2
homeobox protein unc-4 homolog, transcript variant X3
homeobox protein unc-4 homolog isoform X3
transient receptor potential cation channel subfamily A member 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125040231, 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 3 samples with support for all annotated introns
uncharacterized LOC125040231, transcript variant X2
uncharacterized LOC125040231, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
CDAN1-interacting nuclease 1-like, transcript variant X3
CDAN1-interacting nuclease 1-like, transcript variant X2
CDAN1-interacting nuclease 1-like, transcript variant X1
CDAN1-interacting nuclease 1-like, transcript variant X4
CDAN1-interacting nuclease 1-like, transcript variant X5
TBC1 domain family member 2B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
TBC1 domain family member 2B-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 26 samples with support for all annotated introns
TBC1 domain family member 2B-like isoform X2
TBC1 domain family member 2B-like isoform X1
similar to RNA sequence (same species):INSD:GHUY01007098.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 91 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 91 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
vacuolar ATPase assembly integral membrane protein vma21-like, transcript variant X1
vacuolar ATPase assembly integral membrane protein vma21-like, transcript variant X3
vacuolar ATPase assembly integral membrane protein vma21-like, transcript variant X2
vacuolar ATPase assembly integral membrane protein vma21-like
neurofilament heavy polypeptide-like, transcript variant X8
neurofilament heavy polypeptide-like, transcript variant X6
neurofilament heavy polypeptide-like, transcript variant X1
neurofilament heavy polypeptide-like, transcript variant X2
neurofilament heavy polypeptide-like, transcript variant X4
neurofilament heavy polypeptide-like, transcript variant X3
neurofilament heavy polypeptide-like, transcript variant X5
neurofilament heavy polypeptide-like, transcript variant X7
neurofilament heavy polypeptide-like isoform X1
neurofilament heavy polypeptide-like isoform X6
neurofilament heavy polypeptide-like isoform X8
neurofilament heavy polypeptide-like isoform X5
neurofilament heavy polypeptide-like isoform X3
neurofilament heavy polypeptide-like isoform X2
neurofilament heavy polypeptide-like isoform X4
neurofilament heavy polypeptide-like isoform X7
sperm-associated antigen 1-like, transcript variant X1
sperm-associated antigen 1-like, transcript variant X3
sperm-associated antigen 1-like, transcript variant X2
glycoprotein 3-alpha-L-fucosyltransferase A-like, transcript variant X1
glycoprotein 3-alpha-L-fucosyltransferase A-like, transcript variant X2
glycoprotein 3-alpha-L-fucosyltransferase A-like
alpha-(1,3)-fucosyltransferase 7-like, transcript variant X3
alpha-(1,3)-fucosyltransferase 7-like, transcript variant X4
alpha-(1,3)-fucosyltransferase 7-like, transcript variant X2
alpha-(1,3)-fucosyltransferase 7-like, transcript variant X1
alpha-(1,3)-fucosyltransferase 7-like isoform X1
alpha-(1,3)-fucosyltransferase 7-like isoform X2
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT6-like, transcript variant X2
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT6-like isoform X2
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT6-like, transcript variant X1
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT6-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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 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: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin-like protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
ubiquitin-like protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
dnaJ homolog subfamily B member 9-like, transcript variant X1
dnaJ homolog subfamily B member 9-like, transcript variant X3
dnaJ homolog subfamily B member 9-like, transcript variant X2
protein N-terminal asparagine amidohydrolase-like isoform X1
dnaJ homolog subfamily B member 9-like isoform X2
dnaJ homolog subfamily B member 9-like isoform X3
vacuolar protein sorting-associated protein 13B-like, transcript variant X5
vacuolar protein sorting-associated protein 13B-like, transcript variant X4
vacuolar protein sorting-associated protein 13B-like, transcript variant X3
vacuolar protein sorting-associated protein 13B-like, transcript variant X1
vacuolar protein sorting-associated protein 13B-like, transcript variant X2
vacuolar protein sorting-associated protein 13B-like isoform X4
vacuolar protein sorting-associated protein 13B-like isoform X3
vacuolar protein sorting-associated protein 13B-like isoform X2
vacuolar protein sorting-associated protein 13B-like isoform X1
MTOR-associated protein MEAK7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
MTOR-associated protein MEAK7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
early endosome antigen 1-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 34 samples with support for all annotated introns
early endosome antigen 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 38 samples with support for all annotated introns
early endosome antigen 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 29 samples with support for all annotated introns
early endosome antigen 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
early endosome antigen 1-like isoform X3
early endosome antigen 1-like isoform X2
early endosome antigen 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
heat shock 70 kDa protein cognate 4-like
5'-nucleotidase domain-containing protein 2-like, transcript variant X1
5'-nucleotidase domain-containing protein 2-like, transcript variant X3
5'-nucleotidase domain-containing protein 2-like, transcript variant X2
5'-nucleotidase domain-containing protein 2-like, transcript variant X4
5'-nucleotidase domain-containing protein 2-like isoform X1
5'-nucleotidase domain-containing protein 2-like isoform X3
5'-nucleotidase domain-containing protein 2-like isoform X2
5'-nucleotidase domain-containing protein 2-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
sodium-coupled monocarboxylate transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
sodium-coupled monocarboxylate transporter 1-like
serine/arginine repetitive matrix protein 1-like
death-associated protein kinase related-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
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
uncharacterized LOC125040193, transcript variant X3
uncharacterized LOC125040193, transcript variant X1
uncharacterized LOC125040193, transcript variant X2
uncharacterized protein LOC125040193 isoform X1
uncharacterized protein LOC125040193 isoform X3
uncharacterized protein LOC125040193 isoform X2
acidic mammalian chitinase-like, transcript variant X3
acidic mammalian chitinase-like, transcript variant X1
acidic mammalian chitinase-like, transcript variant X2
acidic mammalian chitinase-like isoform X2
acidic mammalian chitinase-like isoform X3
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like, transcript variant X2
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like, transcript variant X3
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like, transcript variant X1
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like
probable serine/threonine-protein kinase kinX
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: beta-1,4-galactosyltransferase 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 22 samples with support for all annotated introns
multiple epidermal growth factor-like domains protein 6, transcript variant X8
multiple epidermal growth factor-like domains protein 6, transcript variant X1
multiple epidermal growth factor-like domains protein 6, transcript variant X5
multiple epidermal growth factor-like domains protein 6, transcript variant X7
multiple epidermal growth factor-like domains protein 6, transcript variant X11
multiple epidermal growth factor-like domains protein 6, transcript variant X9
multiple epidermal growth factor-like domains protein 6, transcript variant X12
multiple epidermal growth factor-like domains protein 6, transcript variant X6
multiple epidermal growth factor-like domains protein 6, transcript variant X4
multiple epidermal growth factor-like domains protein 6, transcript variant X10
multiple epidermal growth factor-like domains protein 6, transcript variant X3
multiple epidermal growth factor-like domains protein 6, transcript variant X2
multiple epidermal growth factor-like domains protein 6 isoform X1
multiple epidermal growth factor-like domains protein 6 isoform X3
multiple epidermal growth factor-like domains protein 6 isoform X6
multiple epidermal growth factor-like domains protein 6 isoform X5
multiple epidermal growth factor-like domains protein 6 isoform X9
multiple epidermal growth factor-like domains protein 6 isoform X7
multiple epidermal growth factor-like domains protein 6 isoform X10
multiple epidermal growth factor-like domains protein 6 isoform X4
multiple epidermal growth factor-like domains protein 6 isoform X2
multiple epidermal growth factor-like domains protein 6 isoform X8
proprotein convertase subtilisin/kexin type 5-like isoform X1
proprotein convertase subtilisin/kexin type 5-like isoform X4
proprotein convertase subtilisin/kexin type 5-like isoform X7
proprotein convertase subtilisin/kexin type 5-like isoform X6
cell death abnormality protein 1-like isoform X1
chorion class high-cysteine HCB protein 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein subunit gamma 4-like, transcript variant X2
guanine nucleotide-binding protein subunit gamma 4-like, transcript variant X1
guanine nucleotide-binding protein subunit gamma 4-like isoform X2
guanine nucleotide-binding protein subunit gamma 4-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
cold shock domain-containing protein CG9705-like, transcript variant X1
cold shock domain-containing protein CG9705-like, transcript variant X2
cold shock domain-containing protein CG9705-like, transcript variant X3
cold shock domain-containing protein CG9705-like
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125039940, transcript variant X1
uncharacterized LOC125039940, transcript variant X2
uncharacterized LOC125039885, transcript variant X2
uncharacterized LOC125039885, transcript variant X1
uncharacterized protein LOC125039885 isoform X1
uncharacterized protein LOC125039885 isoform X2
tubulin-specific chaperone cofactor E-like protein, transcript variant X2
tubulin-specific chaperone cofactor E-like protein, transcript variant X3
tubulin-specific chaperone cofactor E-like protein, transcript variant X1
tubulin-specific chaperone cofactor E-like protein
nuclear factor related to kappa-B-binding protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
nuclear factor related to kappa-B-binding protein-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 23 samples with support for all annotated introns
nuclear factor related to kappa-B-binding protein-like
ribitol-5-phosphate transferase FKTN-like, transcript variant X2
ribitol-5-phosphate transferase FKTN-like, transcript variant X1
ribitol-5-phosphate transferase FKTN-like isoform X1
ribitol-5-phosphate transferase FKTN-like isoform X2
probable methylthioribulose-1-phosphate dehydratase, transcript variant X2
probable methylthioribulose-1-phosphate dehydratase, transcript variant X1
probable methylthioribulose-1-phosphate dehydratase isoform X2
probable methylthioribulose-1-phosphate dehydratase isoform X1
solute carrier family 66 member 2-like, transcript variant X2
solute carrier family 66 member 2-like, transcript variant X1
solute carrier family 66 member 2-like isoform X1
solute carrier family 66 member 2-like isoform X2
GDNF-inducible zinc finger protein 1-like
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X1
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X2
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like isoform X1
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like isoform X2
uncharacterized LOC125040029, transcript variant X1
uncharacterized LOC125040029, transcript variant X3
uncharacterized LOC125040029, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24% coverage of the annotated genomic feature by RNAseq alignments
protein IMPACT-B-like, transcript variant X2
protein IMPACT-B-like, transcript variant X3
protein IMPACT-B-like, transcript variant X1
protein IMPACT-B-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
doublesex- and mab-3-related transcription factor 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
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: doublesex- and mab-3-related transcription factor 1-like
nucleolar complex protein 4 homolog A-like, transcript variant X2
nucleolar complex protein 4 homolog A-like, transcript variant X1
nucleolar complex protein 4 homolog A-like isoform X2
nucleolar complex protein 4 homolog A-like isoform X1
potassium voltage-gated channel protein eag-like, transcript variant X3
potassium voltage-gated channel protein eag-like, transcript variant X2
potassium voltage-gated channel protein eag-like, transcript variant X1
potassium voltage-gated channel protein eag-like isoform X1
potassium voltage-gated channel protein eag-like isoform X3
potassium voltage-gated channel protein eag-like isoform X2
spermatogenesis-associated protein 20-like, transcript variant X4
spermatogenesis-associated protein 20-like, transcript variant X5
spermatogenesis-associated protein 20-like, transcript variant X1
spermatogenesis-associated protein 20-like, transcript variant X2
spermatogenesis-associated protein 20-like, transcript variant X3
spermatogenesis-associated protein 20-like isoform X3
spermatogenesis-associated protein 20-like isoform X4
spermatogenesis-associated protein 20-like isoform X1
spermatogenesis-associated protein 20-like isoform X2
inward rectifier potassium channel 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
inward rectifier potassium channel 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
inward rectifier potassium channel 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
inward rectifier potassium channel 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
inward rectifier potassium channel 2-like, transcript variant X4
inward rectifier potassium channel 2-like isoform X1
inward rectifier potassium channel 2-like isoform X2
pyrroline-5-carboxylate reductase-like, transcript variant X1
pyrroline-5-carboxylate reductase-like, transcript variant X2
pyrroline-5-carboxylate reductase-like isoform X1
pyrroline-5-carboxylate reductase-like isoform X2
pyrroline-5-carboxylate reductase-like, transcript variant X3
pyrroline-5-carboxylate reductase-like, transcript variant X4
pyrroline-5-carboxylate reductase-like isoform X3
pyrroline-5-carboxylate reductase-like isoform X4
polyribonucleotide nucleotidyltransferase 1, mitochondrial-like, transcript variant X2
polyribonucleotide nucleotidyltransferase 1, mitochondrial-like, transcript variant X1
polyribonucleotide nucleotidyltransferase 1, mitochondrial-like, transcript variant X3
polyribonucleotide nucleotidyltransferase 1, mitochondrial-like isoform X3
polyribonucleotide nucleotidyltransferase 1, mitochondrial-like isoform X2
polyribonucleotide nucleotidyltransferase 1, mitochondrial-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
meiotic recombination protein SPO11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
monocarboxylate transporter 12-like, transcript variant X2
monocarboxylate transporter 12-like, transcript variant X3
monocarboxylate transporter 12-like, transcript variant X1
monocarboxylate transporter 12-like isoform X2
monocarboxylate transporter 12-like isoform X1
pollen-specific leucine-rich repeat extensin-like protein 3
uncharacterized LOC125039863, transcript variant X1
uncharacterized LOC125039863, transcript variant X8
uncharacterized LOC125039863, transcript variant X6
uncharacterized LOC125039863, transcript variant X2
uncharacterized LOC125039863, transcript variant X4
uncharacterized LOC125039863, transcript variant X3
uncharacterized LOC125039863, transcript variant X5
uncharacterized LOC125039863, transcript variant X7
uncharacterized protein LOC125039863 isoform X1
uncharacterized protein LOC125039863 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATP-binding cassette sub-family C member 5-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ATP-binding cassette sub-family C member 5-like
similar to RNA sequence (same species):INSD:GIYE01022063.1
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; added 111 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: deleted 1 base in 1 codon; added 74 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
disintegrin and metalloproteinase domain-containing protein 10-like, transcript variant X3
disintegrin and metalloproteinase domain-containing protein 10-like, transcript variant X2
disintegrin and metalloproteinase domain-containing protein 10-like, transcript variant X1
disintegrin and metalloproteinase domain-containing protein 10-like isoform X2
disintegrin and metalloproteinase domain-containing protein 10-like isoform X3
disintegrin and metalloproteinase domain-containing protein 10-like isoform X1
E3 SUMO-protein ligase RanBP2-like, transcript variant X2
E3 SUMO-protein ligase RanBP2-like, transcript variant X7
E3 SUMO-protein ligase RanBP2-like, transcript variant X5
E3 SUMO-protein ligase RanBP2-like, transcript variant X3
E3 SUMO-protein ligase RanBP2-like, transcript variant X4
E3 SUMO-protein ligase RanBP2-like, transcript variant X9
E3 SUMO-protein ligase RanBP2-like, transcript variant X8
E3 SUMO-protein ligase RanBP2-like, transcript variant X6
E3 SUMO-protein ligase RanBP2-like, transcript variant X1
E3 SUMO-protein ligase RanBP2-like isoform X2
E3 SUMO-protein ligase RanBP2-like isoform X7
E3 SUMO-protein ligase RanBP2-like isoform X5
E3 SUMO-protein ligase RanBP2-like isoform X3
E3 SUMO-protein ligase RanBP2-like isoform X4
E3 SUMO-protein ligase RanBP2-like isoform X9
E3 SUMO-protein ligase RanBP2-like isoform X8
E3 SUMO-protein ligase RanBP2-like isoform X6
E3 SUMO-protein ligase RanBP2-like isoform X1
E3 SUMO-protein ligase RanBP2-like, transcript variant X10
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 30 samples with support for all annotated introns
NADH-cytochrome b5 reductase-like, transcript variant X2
NADH-cytochrome b5 reductase-like, transcript variant X7
NADH-cytochrome b5 reductase-like, transcript variant X4
NADH-cytochrome b5 reductase-like, transcript variant X10
NADH-cytochrome b5 reductase-like, transcript variant X1
NADH-cytochrome b5 reductase-like, transcript variant X6
NADH-cytochrome b5 reductase-like, transcript variant X5
NADH-cytochrome b5 reductase-like, transcript variant X9
NADH-cytochrome b5 reductase-like, transcript variant X3
NADH-cytochrome b5 reductase-like, transcript variant X8
actin-2, muscle-specific-like, transcript variant X2
actin-2, muscle-specific-like, transcript variant X1
actin-2, muscle-specific-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 331 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: 337 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 763 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 263 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 776 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
actin-5, muscle-specific-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 707 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
actin-5, muscle-specific-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 712 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
actin-5, muscle-specific-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 707 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: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
actin, muscle-like, transcript variant X2
actin, muscle-like, transcript variant X1
actin-3, muscle-specific-like, transcript variant X1
actin-3, muscle-specific-like, transcript variant X2
uncharacterized LOC125040036, transcript variant X1
uncharacterized LOC125040036, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 678 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
actin-2, muscle-specific-like isoform X2
actin-2, muscle-specific-like isoform X1
rapamycin-insensitive companion of mTOR-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
rapamycin-insensitive companion of mTOR-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 37 samples with support for all annotated introns
rapamycin-insensitive companion of mTOR-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
rapamycin-insensitive companion of mTOR-like isoform X3
rapamycin-insensitive companion of mTOR-like isoform X1
rapamycin-insensitive companion of mTOR-like isoform X2
glucose-6-phosphate 1-dehydrogenase-like
LOW QUALITY PROTEIN: glucose-6-phosphate 1-dehydrogenase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125039906, transcript variant X2
uncharacterized LOC125039906, transcript variant X1
uncharacterized LOC125039906, transcript variant X3
uncharacterized protein LOC125039906 isoform X2
uncharacterized protein LOC125039906 isoform X1
succinate--CoA ligase [GDP-forming] subunit beta, mitochondrial-like
28S ribosomal protein S5, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125040138, transcript variant X2
uncharacterized LOC125040138, transcript variant X1
uncharacterized protein LOC125040138 isoform X1
uncharacterized protein LOC125040138 isoform X2
ubiquitin carboxyl-terminal hydrolase 1-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 1-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 1-like isoform X2
ubiquitin carboxyl-terminal hydrolase 1-like isoform X1
uncharacterized LOC125040147, transcript variant X1
uncharacterized LOC125040147, transcript variant X2
uncharacterized LOC125040147, transcript variant X3
uncharacterized protein LOC125040147 isoform X1
uncharacterized protein LOC125040147 isoform X2
uncharacterized protein LOC125040147 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125040090, transcript variant X2
uncharacterized LOC125040090, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
suppressor protein of bem1/bed5 double mutants-like
uncharacterized protein LOC125040068 isoform X1
guanine nucleotide-binding protein subunit alpha-11-like
serine/threonine-protein kinase tousled-like 2, 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 4 samples with support for all annotated introns
serine/threonine-protein kinase tousled-like 2, 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 10 samples with support for all annotated introns
serine/threonine-protein kinase tousled-like 2, 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 8 samples with support for all annotated introns
serine/threonine-protein kinase tousled-like 2, 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 9 samples with support for all annotated introns
serine/threonine-protein kinase tousled-like 2, transcript variant X5
serine/threonine-protein kinase tousled-like 2, transcript variant X7
serine/threonine-protein kinase tousled-like 2, transcript variant X6
serine/threonine-protein kinase tousled-like 2 isoform X7
serine/threonine-protein kinase tousled-like 2 isoform X4
serine/threonine-protein kinase tousled-like 2 isoform X6
serine/threonine-protein kinase tousled-like 2 isoform X2
serine/threonine-protein kinase tousled-like 2 isoform X5
serine/threonine-protein kinase tousled-like 2 isoform X3
serine/threonine-protein kinase tousled-like 2 isoform X1
vicilin-like seed storage protein At2g18540
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
U-scoloptoxin(01)-Cw1a-like, transcript variant X2
U-scoloptoxin(01)-Cw1a-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 63% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
structural maintenance of chromosomes protein 2-like
gamma-aminobutyric acid receptor subunit rho-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% 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 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
putative polypeptide N-acetylgalactosaminyltransferase 9
similar to RNA sequence (same species):INSD:GHUY01000542.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 170 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 170 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
phenylalanine--tRNA ligase beta subunit-like
transformation/transcription domain-associated protein-like
LOW QUALITY PROTEIN: transformation/transcription domain-associated protein-like
uncharacterized LOC125039882, transcript variant X1
uncharacterized LOC125039882, transcript variant X2
uncharacterized LOC125039882, transcript variant X3
uncharacterized protein LOC125039882 isoform X1
uncharacterized protein LOC125039882 isoform X2
uncharacterized protein LOC125039882 isoform X3
uncharacterized LOC125039882, transcript variant X4
uncharacterized protein LOC125039882 isoform X4
homeobox protein onecut-like, transcript variant X1
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
homeobox protein onecut-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
uncharacterized abhydrolase domain-containing protein DDB_G0269086-like
similar to RNA sequence (same species):INSD:GIYE01000623.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 550 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 476 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
beta-1-syntrophin-like, transcript variant X1
beta-1-syntrophin-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
histone-arginine methyltransferase CARMER-like, transcript variant X2
histone-arginine methyltransferase CARMER-like, transcript variant X1
histone-arginine methyltransferase CARMER-like isoform X2
probable histone-arginine methyltransferase CARMER isoform X1
histone-arginine methyltransferase CARMER-like, transcript variant X3
histone-arginine methyltransferase CARMER-like isoform X3
Down syndrome cell adhesion molecule-like protein Dscam2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 83% 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
solute carrier family 25 member 45-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 25 member 45-like, 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 1 sample with support for all annotated introns
solute carrier family 25 member 45-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
solute carrier family 25 member 45-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 2 samples with support for all annotated introns
solute carrier family 25 member 45-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 25 member 45-like, transcript variant X6
solute carrier family 25 member 45-like isoform X2
solute carrier family 25 member 45-like isoform X1
solute carrier family 25 member 45-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transcription factor ets-4-like, transcript variant X2
transcription factor ets-4-like, transcript variant X3
transcription factor ets-4-like isoform X3
transcription factor ets-4-like, transcript variant X4
transcription factor ets-4-like isoform X2
transcription factor ets-4-like, transcript variant X5
transcription factor ets-4-like, transcript variant X1
transcription factor ets-4-like isoform X1
transcription factor ets-4-like, transcript variant X6
transcription factor ets-4-like isoform X4
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 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: 25 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
sec1 family domain-containing protein 2-like, transcript variant X2
sec1 family domain-containing protein 2-like, transcript variant X3
sec1 family domain-containing protein 2-like, transcript variant X1
sec1 family domain-containing protein 2-like
succinate dehydrogenase cytochrome b560 subunit, mitochondrial-like
LOW QUALITY PROTEIN: succinate dehydrogenase cytochrome b560 subunit, mitochondrial-like
FMRFamide receptor-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 25 samples with support for all annotated introns
FMRFamide receptor-like, transcript variant X6
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 9 samples with support for all annotated introns
FMRFamide receptor-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
FMRFamide receptor-like, transcript variant X4
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
FMRFamide receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
FMRFamide receptor-like, transcript variant X5
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 18 samples with support for all annotated introns
FMRFamide receptor-like, transcript variant X7
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 5 samples with support for all annotated introns