Penaeus chinensis breed Huanghai No. 1 chromosome 22, 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\nCM032947.1.\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.
small conductance calcium-activated potassium channel protein-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: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71% coverage of the annotated genomic feature by RNAseq alignments
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
COORDINATES: polyA evidence [ECO:0006239]
ras-related protein M-Ras-like, transcript variant X1
ras-related protein M-Ras-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 1 sample with support for all annotated introns
probable sodium/potassium/calcium exchanger CG1090, transcript variant X1
similar to RNA sequence (same species):INSD:GHUY01007559.1
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 527 bases not found in genome assembly; 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 18 samples with support for all annotated introns
probable sodium/potassium/calcium exchanger CG1090, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 527 bases not found in genome assembly; 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 15 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 394 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
probable sodium/potassium/calcium exchanger CG1090 isoform X1
probable sodium/potassium/calcium exchanger CG1090 isoform X2
probable sodium/potassium/calcium exchanger CG1090, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 527 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
probable sodium/potassium/calcium exchanger CG1090 isoform X3
pentatricopeptide repeat-containing protein 2, mitochondrial-like
peptidyl-prolyl cis-trans isomerase 5-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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein DKFZp434B061-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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC3-like
thioredoxin domain-containing protein 5-like
inositol monophosphatase 1-like, transcript variant X1
similar to RNA sequence (same species):INSD:GIYE01019055.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 419 bases not found in genome assembly
inositol monophosphatase 1-like isoform X1
inositol monophosphatase 1-like, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 419 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
inositol monophosphatase 1-like isoform X2
similar to RNA sequence (same species):INSD:GIYE01037454.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 562 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 562 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 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transformer-2 protein homolog alpha-like, transcript variant X7
transformer-2 protein homolog alpha-like, transcript variant X1
transformer-2 protein homolog alpha-like, transcript variant X2
transformer-2 protein homolog alpha-like, transcript variant X3
transformer-2 protein homolog alpha-like, transcript variant X4
transformer-2 protein homolog alpha-like, transcript variant X8
transformer-2 protein homolog alpha-like, transcript variant X6
transformer-2 protein homolog alpha-like, transcript variant X9
transformer-2 protein homolog alpha-like isoform X6
transformer-2 protein homolog alpha-like isoform X1
transformer-2 protein homolog alpha-like isoform X2
transformer-2 protein homolog alpha-like isoform X3
transformer-2 protein homolog alpha-like isoform X4
transformer-2 protein homolog alpha-like isoform X7
transformer-2 protein homolog alpha-like isoform X5
transformer-2 protein homolog alpha-like isoform X8
transformer-2 protein homolog alpha-like, transcript variant X5
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 12 samples with support for all annotated introns
hybrid signal transduction histidine kinase L-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
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 21 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase CYP95-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
nuclear receptor coactivator 5-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 26 samples with support for all annotated introns
nuclear receptor coactivator 5-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 36 samples with support for all annotated introns
nuclear receptor coactivator 5-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 9 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein A1-like isoform X2
DEAD-box ATP-dependent RNA helicase 9-like isoform X1
uncharacterized LOC125037065, transcript variant X1
uncharacterized LOC125037065, transcript variant X2
H(+)/Cl(-) exchange transporter 7-like, transcript variant X2
H(+)/Cl(-) exchange transporter 7-like, transcript variant X3
H(+)/Cl(-) exchange transporter 7-like, transcript variant X4
H(+)/Cl(-) exchange transporter 7-like, transcript variant X1
H(+)/Cl(-) exchange transporter 7-like isoform X2
H(+)/Cl(-) exchange transporter 7-like isoform X1
AP-3 complex subunit beta-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 7 samples with support for all annotated introns
AP-3 complex subunit beta-2-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 12 samples with support for all annotated introns
AP-3 complex subunit beta-2-like, transcript variant X4
AP-3 complex subunit beta-2-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 24 samples with support for all annotated introns
AP-3 complex subunit beta-1-like isoform X2
AP-3 complex subunit beta-1-like isoform X1
AP-3 complex subunit beta-2-like isoform X4
AP-3 complex subunit beta-2-like isoform X3
synaptic vesicle glycoprotein 2B-like, transcript variant X6
synaptic vesicle glycoprotein 2B-like, transcript variant X5
synaptic vesicle glycoprotein 2B-like isoform X4
synaptic vesicle glycoprotein 2B-like isoform X5
synaptic vesicle glycoprotein 2B-like, transcript variant X2
synaptic vesicle glycoprotein 2B-like isoform X2
synaptic vesicle glycoprotein 2B-like, transcript variant X1
synaptic vesicle glycoprotein 2B-like isoform X1
synaptic vesicle glycoprotein 2B-like, transcript variant X3
synaptic vesicle glycoprotein 2B-like, transcript variant X4
synaptic vesicle glycoprotein 2C-like isoform X3
similar to RNA sequence (same species):INSD:GHUY01004925.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 86 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 21 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6-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 9 samples with support for all annotated introns
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6-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 10 samples with support for all annotated introns
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6-like
eukaryotic translation initiation factor 3 subunit B-like, transcript variant X3
eukaryotic translation initiation factor 3 subunit B-like, transcript variant X1
eukaryotic translation initiation factor 3 subunit B-like, transcript variant X4
eukaryotic translation initiation factor 3 subunit B-like, transcript variant X2
eukaryotic translation initiation factor 3 subunit B-like isoform X4
eukaryotic translation initiation factor 3 subunit B-like isoform X2
eukaryotic translation initiation factor 3 subunit B-like isoform X3
eukaryotic translation initiation factor 3 subunit B-like isoform X1
tetraspanin-33-like, transcript variant X1
tetraspanin-33-like, transcript variant X3
tetraspanin-33-like, transcript variant X2
zinc finger protein 62-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 33 samples with support for all annotated introns
zinc finger protein 62-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 7 samples with support for all annotated introns
uncharacterized protein LOC125037044 isoform X2
oplophorus-luciferin 2-monooxygenase non-catalytic subunit-like
major facilitator superfamily domain-containing protein 12-like
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
location of vulva defective 1-like, transcript variant X1
location of vulva defective 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
location of vulva defective 1-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 24 samples with support for all annotated introns
location of vulva defective 1-like isoform X1
location of vulva defective 1-like isoform X2
location of vulva defective 1-like isoform X3
flocculation protein FLO11-like, 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 2 samples with support for all annotated introns
flocculation protein FLO11-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 4 samples with support for all annotated introns
flocculation protein FLO11-like, transcript variant X3
flocculation protein FLO11-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
flocculation protein FLO11-like, transcript variant X5
flocculation protein FLO11-like, transcript variant X6
flocculation protein FLO11-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 5 samples with support for all annotated introns
flocculation protein FLO11-like, transcript variant X9
flocculation protein FLO11-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
flocculation protein FLO11-like, transcript variant X10
flocculation protein FLO11-like isoform X3
flocculation protein FLO11-like isoform X1
flocculation protein FLO11-like isoform X2
flocculation protein FLO11-like isoform X4
flocculation protein FLO11-like isoform X5
methyl-CpG-binding domain protein 2-like
conserved oligomeric Golgi complex subunit 7-like
uncharacterized LOC125037037, transcript variant X1
uncharacterized LOC125037037, transcript variant X2
zinc finger and SCAN domain-containing protein 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
protein SCO1 homolog, mitochondrial-like
ETS domain-containing protein Elk-4-like, transcript variant X1
ETS domain-containing protein Elk-4-like, transcript variant X2
ETS domain-containing protein Elk-4-like, transcript variant X3
ETS domain-containing protein Elk-4-like isoform X1
ETS domain-containing protein Elk-4-like isoform X2
ETS domain-containing protein Elk-4-like isoform X3
poly(A) RNA polymerase, mitochondrial-like
diacylglycerol O-acyltransferase 1-like, transcript variant X1
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 29 samples with support for all annotated introns
diacylglycerol O-acyltransferase 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 25 samples with support for all annotated introns
diacylglycerol O-acyltransferase 1-like isoform X1
diacylglycerol O-acyltransferase 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized histidine-rich protein DDB_G0274557-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: 4 Proteins, and 80% 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125036921
phosphatidylinositol 4-phosphate 5-kinase 8-like
gamma-aminobutyric acid type B receptor subunit 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 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: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125037209
regulator of G-protein signaling 12-like, transcript variant X3
regulator of G-protein signaling 12-like, transcript variant X2
regulator of G-protein signaling 12-like, transcript variant X1
regulator of G-protein signaling 12-like isoform X3
regulator of G-protein signaling 12-like isoform X2
regulator of G-protein signaling 12-like isoform X1
regulator of G-protein signaling 12-like, transcript variant X5
regulator of G-protein signaling 12-like, transcript variant X4
uncharacterized protein LOC125036854 isoform X4
uncharacterized LOC125036857, 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 32 samples with support for all annotated introns
uncharacterized LOC125036857, 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 8 samples with support for all annotated introns
uncharacterized protein LOC125036857 isoform X2
uncharacterized protein LOC125036857 isoform X1
putative mediator of RNA polymerase II transcription subunit 26, transcript variant X1
putative mediator of RNA polymerase II transcription subunit 26, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26, 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 6 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26, 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 9 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26
chondroitin sulfate N-acetylgalactosaminyltransferase 1-like, transcript variant X4
chondroitin sulfate N-acetylgalactosaminyltransferase 1-like, transcript variant X1
chondroitin sulfate N-acetylgalactosaminyltransferase 1-like, transcript variant X3
chondroitin sulfate N-acetylgalactosaminyltransferase 1-like, transcript variant X2
chondroitin sulfate N-acetylgalactosaminyltransferase 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
chondroitin sulfate N-acetylgalactosaminyltransferase 1-like isoform X2
chondroitin sulfate N-acetylgalactosaminyltransferase 1-like isoform X1
chondroitin sulfate N-acetylgalactosaminyltransferase 2-like
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA opal suppressor (anticodon UCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
delta-1-pyrroline-5-carboxylate synthase-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 30 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 13 samples with support for all annotated introns
uncharacterized LOC125037023, transcript variant X1
uncharacterized LOC125037023, transcript variant X2
uncharacterized LOC125037225, transcript variant X3
uncharacterized protein LOC125037225 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 12 samples with support for all annotated introns
uncharacterized LOC125037225, 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 22 samples with support for all annotated introns
uncharacterized LOC125037225, transcript variant X2
uncharacterized protein LOC125037225 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
GDP-fucose transporter 1-like, transcript variant X1
GDP-fucose transporter 1-like, transcript variant X2
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
chromosome transmission fidelity protein 18 homolog, transcript variant X2
chromosome transmission fidelity protein 18 homolog, transcript variant X1
chromosome transmission fidelity protein 18 homolog, transcript variant X5
chromosome transmission fidelity protein 18 homolog, transcript variant X3
chromosome transmission fidelity protein 18 homolog, transcript variant X4
chromosome transmission fidelity protein 18 homolog isoform X2
chromosome transmission fidelity protein 18 homolog isoform X1
chromosome transmission fidelity protein 18 homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
probable ribonuclease ZC3H12C, transcript variant X3
probable ribonuclease ZC3H12C, transcript variant X2
probable ribonuclease ZC3H12C isoform X2
probable ribonuclease ZC3H12C, transcript variant X1
probable ribonuclease ZC3H12C isoform X1
probable ribonuclease ZC3H12C isoform X3
transcription elongation factor, mitochondrial-like, transcript variant X1
transcription elongation factor, mitochondrial-like, transcript variant X3
transcription elongation factor, mitochondrial-like, transcript variant X2
transcription elongation factor, mitochondrial-like isoform X1
transcription elongation factor, mitochondrial-like isoform X2
fibrous sheath CABYR-binding protein-like
clustered mitochondria protein homolog, transcript variant X1
clustered mitochondria protein homolog, transcript variant X2
clustered mitochondria protein homolog, transcript variant X3
clustered mitochondria protein homolog isoform X1
clustered mitochondria protein homolog isoform X2
clustered mitochondria protein homolog isoform X3
sphingomyelin phosphodiesterase 4-like, transcript variant X1
sphingomyelin phosphodiesterase 4-like, transcript variant X2
sphingomyelin phosphodiesterase 4-like isoform X2
sphingomyelin phosphodiesterase 4-like isoform X1
ankyrin repeat and KH domain-containing protein 1-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
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X2
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X1
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X1
ran-specific GTPase-activating protein-like, transcript variant X2
ran-specific GTPase-activating protein-like isoform X2
ran-specific GTPase-activating protein-like, transcript variant X1
ran-specific GTPase-activating protein-like, transcript variant X3
ran-specific GTPase-activating protein-like isoform X1
ran-specific GTPase-activating protein-like isoform X3
DDB1- and CUL4-associated factor 12 homolog, transcript variant X1
DDB1- and CUL4-associated factor 12 homolog, transcript variant X4
DDB1- and CUL4-associated factor 12 homolog, transcript variant X3
DDB1- and CUL4-associated factor 12 homolog, transcript variant X2
DDB1- and CUL4-associated factor 12 homolog
serine/threonine-protein kinase SIK2-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 8 samples with support for all annotated introns
serine/threonine-protein kinase meng-po-like
piggyBac transposable element-derived protein 4-like
collagen alpha-1(XI) chain-like, transcript variant X1
collagen alpha-1(XI) chain-like, transcript variant X2
collagen alpha-1(XI) chain-like, transcript variant X3
collagen alpha-1(XI) chain-like, transcript variant X4
collagen alpha-2(XI) chain-like isoform X1
collagen alpha-2(XI) chain-like isoform X2
collagen alpha-1(XI) chain-like isoform X3
collagen alpha-1(XI) chain-like isoform X4
uncharacterized protein DDB_G0271670-like
major facilitator superfamily domain-containing protein 4A-like, transcript variant X1
major facilitator superfamily domain-containing protein 4A-like, transcript variant X2
major facilitator superfamily domain-containing protein 4A-like
UDP-glucosyltransferase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
UDP-glucosyltransferase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
UDP-glucosyltransferase 2-like isoform X1
UDP-glucosyltransferase 2-like isoform X2
membrane-bound transcription factor site-2 protease-like, transcript variant X1
membrane-bound transcription factor site-2 protease-like, transcript variant X2
membrane-bound transcription factor site-2 protease-like, transcript variant X3
membrane-bound transcription factor site-2 protease-like isoform X1
membrane-bound transcription factor site-2 protease-like isoform X2
membrane-bound transcription factor site-2 protease-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 251-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
muscle M-line assembly protein unc-89-like
A disintegrin and metalloproteinase with thrombospondin motifs 9-like, transcript variant X2
A disintegrin and metalloproteinase with thrombospondin motifs 9-like, transcript variant X1
A disintegrin and metalloproteinase with thrombospondin motifs 9-like isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 9-like isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 1-like
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4-like, transcript variant X2
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4-like, transcript variant X1
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4-like isoform X2
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit wdr4-like isoform X1
basic proline-rich protein-like, transcript variant X1
basic proline-rich protein-like, transcript variant X2
ATP-binding cassette sub-family B member 6-like, transcript variant X3
ATP-binding cassette sub-family B member 6-like, transcript variant X2
ATP-binding cassette sub-family B member 6-like, transcript variant X1
ATP-binding cassette sub-family B member 6-like, transcript variant X4
ATP-binding cassette sub-family B member 6-like
ribosome-binding protein 1-like, 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 2 samples with support for all annotated introns
ribosome-binding protein 1-like, transcript variant X2
ribosome-binding protein 1-like, transcript variant X1
ribosome-binding protein 1-like, transcript variant X3
ribosome-binding protein 1-like, transcript variant X5
ribosome-binding protein 1-like, transcript variant X6
ribosome-binding protein 1-like isoform X3
ribosome-binding protein 1-like isoform X1
ribosome-binding protein 1-like isoform X4
ribosome-binding protein 1-like isoform X2
ribosome-binding protein 1-like isoform X5
E3 ubiquitin-protein ligase listerin-like
calcium-activated chloride channel regulator 1-like
calcium-activated chloride channel regulator 1-like, transcript variant X1
calcium-activated chloride channel regulator 1-like, transcript variant X3
calcium-activated chloride channel regulator 1-like, transcript variant X2
calcium-activated chloride channel regulator 1-like, transcript variant X4
protein FAM50 homolog, transcript variant X2
protein FAM50 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54% coverage of the annotated genomic feature by RNAseq alignments
proton channel OtopLc-like, transcript variant X10
proton channel OtopLc-like, transcript variant X8
proton channel OtopLc-like, transcript variant X1
proton channel OtopLc-like, transcript variant X3
proton channel OtopLc-like, transcript variant X5
proton channel OtopLc-like, transcript variant X6
proton channel OtopLc-like, transcript variant X2
proton channel OtopLc-like, transcript variant X4
proton channel OtopLc-like, transcript variant X7
proton channel OtopLc-like, transcript variant X9
bifunctional purine biosynthesis protein ATIC-like
U6 snRNA-associated Sm-like protein LSm8
ATP-dependent RNA helicase A-like, transcript variant X1
ATP-dependent RNA helicase A protein-like isoform X1
ATP-dependent RNA helicase A-like, transcript variant X2
ATP-dependent RNA helicase A-like isoform X2
ubiquitin carboxyl-terminal hydrolase 36-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 36-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 19 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 36-like isoform X1
ubiquitin carboxyl-terminal hydrolase 36-like isoform X2
failed axon connections homolog, transcript variant X1
failed axon connections homolog, transcript variant X3
failed axon connections homolog, transcript variant X2
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
failed axon connections homolog isoform X1
failed axon connections homolog isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: band 4.1-like protein 4
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like
methenyltetrahydrofolate synthase domain-containing protein-like, transcript variant X1
methenyltetrahydrofolate synthase domain-containing protein-like, transcript variant X5
methenyltetrahydrofolate synthase domain-containing protein-like, transcript variant X7
methenyltetrahydrofolate synthase domain-containing protein-like, transcript variant X8
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
methenyltetrahydrofolate synthase domain-containing protein-like, transcript variant X3
methenyltetrahydrofolate synthase domain-containing protein-like, transcript variant X4
methenyltetrahydrofolate synthase domain-containing protein-like, transcript variant X2
methenyltetrahydrofolate synthase domain-containing protein-like isoform X1
methenyltetrahydrofolate synthase domain-containing protein-like isoform X2
methenyltetrahydrofolate synthase domain-containing protein-like isoform X4
methenyltetrahydrofolate synthase domain-containing protein-like, transcript variant X6
methenyltetrahydrofolate synthase domain-containing protein-like isoform X3
uncharacterized LOC125037096, transcript variant X1
uncharacterized LOC125037096, transcript variant X2
uncharacterized LOC125037096, transcript variant X3
uncharacterized LOC125037235, transcript variant X4
uncharacterized LOC125037235, transcript variant 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, including 21 samples with support for all annotated introns
uncharacterized LOC125037235, transcript variant X2
uncharacterized LOC125037235, transcript variant X1
uncharacterized LOC125037235, transcript variant X6
uncharacterized LOC125037235, transcript variant X3
uncharacterized LOC125037235, transcript variant X8
uncharacterized LOC125037235, transcript variant X5
uncharacterized protein LOC125037235 isoform X2
uncharacterized protein LOC125037235 isoform X1
uncharacterized protein LOC125037235 isoform X3
ADP-sugar pyrophosphatase-like, transcript variant X1
ADP-sugar pyrophosphatase-like, transcript variant X6
ADP-sugar pyrophosphatase-like, transcript variant X3
ADP-sugar pyrophosphatase-like, transcript variant X7
ADP-sugar pyrophosphatase-like, transcript variant X4
ADP-sugar pyrophosphatase-like, transcript variant X2
ADP-sugar pyrophosphatase-like, transcript variant X5
ADP-sugar pyrophosphatase-like, transcript variant X8
ADP-sugar pyrophosphatase-like isoform X2
nucleoside diphosphate-linked moiety X motif 17-like, transcript variant X5
nucleoside diphosphate-linked moiety X motif 17-like, transcript variant X2
nucleoside diphosphate-linked moiety X motif 17-like, transcript variant X1
nucleoside diphosphate-linked moiety X motif 17-like, transcript variant X4
nucleoside diphosphate-linked moiety X motif 17-like, transcript variant X3
nucleoside diphosphate-linked moiety X motif 17-like isoform X2
nucleoside diphosphate-linked moiety X motif 17-like isoform X1
nucleoside diphosphate-linked moiety X motif 17-like isoform X3
nucleoside diphosphate-linked moiety X motif 17-like isoform X4
SR-related and CTD-associated factor 4-like, transcript variant X1
SR-related and CTD-associated factor 4-like, transcript variant X3
SR-related and CTD-associated factor 4-like, transcript variant X5
SR-related and CTD-associated factor 4-like, transcript variant X2
SR-related and CTD-associated factor 4-like, transcript variant X4
SR-related and CTD-associated factor 4-like isoform X1
SR-related and CTD-associated factor 4-like isoform X3
SR-related and CTD-associated factor 4-like isoform X5
SR-related and CTD-associated factor 4-like isoform X2
SR-related and CTD-associated factor 4-like isoform X4
protein limb expression 1 homolog, transcript variant X3
protein limb expression 1 homolog, transcript variant X1
protein limb expression 1 homolog, transcript variant X2
protein limb expression 1 homolog, transcript variant X4
protein limb expression 1 homolog, transcript variant X5
protein limb expression 1 homolog isoform X1
protein limb expression 1 homolog isoform X3
protein limb expression 1 homolog isoform X2
protein limb expression 1 homolog isoform X4
protein limb expression 1 homolog isoform X5
protein limb expression 1 homolog, transcript variant X6
protein limb expression 1 homolog, transcript variant X7
protein limb expression 1 homolog isoform X6
protein limb expression 1 homolog isoform X7
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 2 samples with support for all annotated introns
transmembrane 9 superfamily member 3-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
LOW QUALITY PROTEIN: transmembrane 9 superfamily member 3-like
2-aminoethanethiol dioxygenase-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 30 samples with support for all annotated introns
2-aminoethanethiol dioxygenase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
2-aminoethanethiol dioxygenase-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 5 samples with support for all annotated introns
2-aminoethanethiol dioxygenase-like isoform X1
2-aminoethanethiol dioxygenase-like isoform X2
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-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
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like isoform X1
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like isoform X2
uncharacterized LOC125037223, transcript variant X2
uncharacterized LOC125037223, transcript variant X3
uncharacterized LOC125037223, transcript variant X1
uncharacterized protein LOC125037223 isoform X1
uncharacterized protein LOC125037223 isoform X2
gastrula zinc finger protein XlCGF7.1-like, transcript variant X3
gastrula zinc finger protein XlCGF7.1-like, transcript variant X1
gastrula zinc finger protein XlCGF7.1-like, transcript variant X4
gastrula zinc finger protein XlCGF7.1-like, transcript variant X2
gastrula zinc finger protein XlCGF7.1-like
glutenin, high molecular weight subunit DX5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: lysosomal acid glucosylceramidase-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
similar to RNA sequence (same species):INSD:GIYE01040967.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 2747 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% 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 2747 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: 74% 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
glutamine synthetase-like, transcript variant X1
glutamine synthetase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
transfer RNA glutamine (anticodon CUG); 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: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
insulin-like growth factor-binding protein-related protein 1
galactose-3-O-sulfotransferase 4-like, transcript variant X1
galactose-3-O-sulfotransferase 4-like, transcript variant X2
galactosylceramide sulfotransferase-like isoform X1
galactose-3-O-sulfotransferase 4-like isoform X2
isopentenyl-diphosphate Delta-isomerase 1-like
FGGY carbohydrate kinase domain-containing protein-like
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
uncharacterized LOC125037161, 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 4 samples with support for all annotated introns
uncharacterized LOC125037161, 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 6 samples with support for all annotated introns
uncharacterized protein LOC125037161 isoform X2
uncharacterized protein LOC125037161 isoform X1
glycine receptor subunit alpha-2-like, transcript variant X1
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 3 samples with support for all annotated introns
glycine receptor subunit alpha-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glycine receptor subunit alpha-2-like isoform X1
glycine receptor subunit alpha-2-like isoform X2
protein downstream neighbor of son homolog, transcript variant X1
protein downstream neighbor of son homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein downstream neighbor of son homolog isoform X1
protein downstream neighbor of son homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
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: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
SUMO-interacting motif-containing protein 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 5 samples with support for all annotated introns
uncharacterized LOC125037165, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC125037165, transcript variant X1
uncharacterized LOC125037165, transcript variant X3
uncharacterized LOC125037165, transcript variant X4
uncharacterized protein LOC125037165 isoform X3
uncharacterized protein LOC125037165 isoform X1
uncharacterized protein LOC125037165 isoform X2
breast carcinoma-amplified sequence 1 homolog
von Willebrand factor D and EGF domain-containing protein-like
protein AAR2 homolog, transcript variant X1
protein AAR2 homolog, transcript variant X2
PWWP domain-containing protein 3-like, transcript variant X3
PWWP domain-containing protein 3-like, transcript variant X2
PWWP domain-containing protein 3-like isoform X3
PWWP domain-containing protein 3-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 34 samples with support for all annotated introns
uncharacterized protein LOC125037050 isoform X1
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 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 28 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 25 samples with support for all annotated introns
zinc finger protein 260-like, transcript variant X2
zinc finger protein 260-like, transcript variant X3
zinc finger protein 260-like, transcript variant X1
LOW QUALITY PROTEIN: uncharacterized protein LOC125036984
eukaryotic translation initiation factor 4 gamma-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
serine hydroxymethyltransferase-like, transcript variant X2
serine hydroxymethyltransferase-like, transcript variant X1
serine hydroxymethyltransferase-like isoform X1
serine hydroxymethyltransferase-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 34 samples with support for all annotated introns
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
uncharacterized LOC125037035, transcript variant X1
uncharacterized LOC125037035, transcript variant X2
uncharacterized LOC125037035, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
zinc finger protein castor homolog 1-like, transcript variant X3
zinc finger protein castor homolog 1-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 13 samples with support for all annotated introns
zinc finger protein castor homolog 1-like, transcript variant X1
zinc finger protein castor homolog 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 13 samples with support for all annotated introns
zinc finger protein castor homolog 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
zinc finger protein castor homolog 1-like isoform X4
zinc finger protein castor homolog 1-like isoform X2
zinc finger protein castor homolog 1-like isoform X3
zinc finger protein castor homolog 1-like isoform X1
zinc finger protein castor homolog 1-like isoform X5
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 26 samples with support for all annotated introns
C-type lectin domain family 17, member A-like
uncharacterized LOC125036871, 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 39 samples with support for all annotated introns
uncharacterized LOC125036871, 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 33 samples with support for all annotated introns
uncharacterized LOC125036871, 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 31 samples with support for all annotated introns
uncharacterized LOC125036871, 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 22 samples with support for all annotated introns
uncharacterized LOC125036909, transcript variant X1
uncharacterized LOC125036909, transcript variant X2
uncharacterized LOC125036909, transcript variant X3
ankyrin repeat domain-containing protein 65-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
proline-rich receptor-like protein kinase PERK2
sphingomyelin phosphodiesterase-like, transcript variant X2
sphingomyelin phosphodiesterase-like, transcript variant X1
sphingomyelin phosphodiesterase-like isoform X1
sphingomyelin phosphodiesterase-like isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00147
uncharacterized LOC125037034, 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 16 samples with support for all annotated introns
uncharacterized LOC125037034, transcript variant X1
uncharacterized protein LOC125037034 isoform X2
uncharacterized protein LOC125037034 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 29 samples with support for all annotated introns
thyrotropin-releasing hormone receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Kv channel-interacting protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Kv channel-interacting protein 1-like, transcript variant X5
Kv channel-interacting protein 1-like, transcript variant X3
Kv channel-interacting protein 1-like, transcript variant X2
Kv channel-interacting protein 1-like isoform X2
Kv channel-interacting protein 1-like, transcript variant X1
Kv channel-interacting protein 2-like isoform X1
Kv channel-interacting protein 1-like, transcript variant X6
Kv channel-interacting protein 1-like isoform X3
basic salivary proline-rich protein 4-like
capping protein inhibiting regulator of actin dynamics-like
cGMP-inhibited 3',5'-cyclic phosphodiesterase B-like, transcript variant X1
cGMP-inhibited 3',5'-cyclic phosphodiesterase B-like, transcript variant X2
cGMP-inhibited 3',5'-cyclic phosphodiesterase B-like, transcript variant X3
cGMP-inhibited 3',5'-cyclic phosphodiesterase B-like isoform X1
cGMP-inhibited 3',5'-cyclic phosphodiesterase B-like isoform X2
cGMP-inhibited 3',5'-cyclic phosphodiesterase B-like isoform X3
uncharacterized LOC125037072, transcript variant X1
uncharacterized protein LOC125037072 isoform X1
uncharacterized LOC125037072, transcript variant X2
uncharacterized protein LOC125037072 isoform X2
ras association domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
U11/U12 small nuclear ribonucleoprotein 25 kDa protein-like, transcript variant X1
U11/U12 small nuclear ribonucleoprotein 25 kDa protein-like
U11/U12 small nuclear ribonucleoprotein 25 kDa protein-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 37 samples with support for all annotated introns
U11/U12 small nuclear ribonucleoprotein 25 kDa protein-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 34 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 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: 87% coverage of the annotated genomic feature by RNAseq alignments
probable E3 ubiquitin-protein ligase HERC4, transcript variant 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 21 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase HERC4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase HERC4, transcript variant X4
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 14 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase HERC4, transcript variant X5
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 5 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase HERC4, 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 13 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase HERC4 isoform X1
probable E3 ubiquitin-protein ligase HERC4 isoform X2
probable E3 ubiquitin-protein ligase HERC4 isoform X3
calcitonin gene-related peptide type 1 receptor-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: calcitonin gene-related peptide type 1 receptor-like
uncharacterized LOC125037080, transcript variant X6
uncharacterized LOC125037080, transcript variant X3
uncharacterized LOC125037080, transcript variant X4
uncharacterized LOC125037080, transcript variant X1
uncharacterized LOC125037080, 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 1 sample with support for all annotated introns
uncharacterized LOC125037080, transcript variant X5
uncharacterized protein LOC125037080 isoform X1
uncharacterized protein LOC125037080 isoform X2
uncharacterized protein LOC125037080 isoform X3
zinc finger protein OZF-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger protein OZF-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 12 samples with support for all annotated introns
zinc finger protein OZF-like, transcript variant X5
zinc finger protein OZF-like, transcript variant X4
zinc finger protein OZF-like, transcript variant X2
zinc finger protein OZF-like, transcript variant X1
zinc finger protein 583-like, transcript variant X2
zinc finger protein 583-like, transcript variant X1
zinc finger protein 583-like, transcript variant X4
zinc finger protein 583-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
pollen-specific leucine-rich repeat extensin-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 87% 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 44% coverage of the annotated genomic feature by RNAseq alignments
transmembrane ascorbate-dependent reductase CYB561-like, transcript variant X2
transmembrane ascorbate-dependent reductase CYB561-like isoform X2
transmembrane ascorbate-dependent reductase CYB561-like, transcript variant X3
transmembrane ascorbate-dependent reductase CYB561-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 14 samples with support for all annotated introns
transmembrane ascorbate-dependent reductase CYB561-like isoform X3
transmembrane ascorbate-dependent reductase CYB561-like isoform X1
mitochondrial import receptor subunit TOM22 homolog
protein Gawky-like, transcript variant X5
protein Gawky-like, transcript variant X2
protein Gawky-like, transcript variant X3
protein Gawky-like, transcript variant X1
protein Gawky-like, transcript variant X4
decapping and exoribonuclease protein-like, transcript variant X1
decapping and exoribonuclease protein-like isoform X1
decapping and exoribonuclease protein-like, transcript variant X2
decapping and exoribonuclease protein-like isoform X2
protein SYS1 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
protein SYS1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC125036881, transcript variant X1
uncharacterized LOC125036881, transcript variant X2
ubiquitin carboxyl-terminal hydrolase calypso-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase calypso-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase calypso-like isoform X1
ubiquitin carboxyl-terminal hydrolase calypso-like isoform X2
uncharacterized LOC125037085, 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 39 samples with support for all annotated introns
uncharacterized LOC125037085, transcript variant X2
uncharacterized protein LOC125037085 isoform X1
uncharacterized protein LOC125037085 isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2-like, transcript variant X4
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2-like, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2-like, transcript variant X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2-like, transcript variant X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2-like, transcript variant X5
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2-like, transcript variant X6
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-4-like isoform X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2-like isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-4-like isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-4-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
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 28 samples with support for all annotated introns
neurogenic differentiation factor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC125036875 isoform X1
uncharacterized protein LOC125036875 isoform X4
uncharacterized protein LOC125036875 isoform X2
uncharacterized protein LOC125036875 isoform X3
uncharacterized protein LOC125036875 isoform X5
uncharacterized protein LOC125036875 isoform X6
uncharacterized protein LOC125036875 isoform X7
trithorax group protein osa-like, transcript variant X1
trithorax group protein osa-like, transcript variant X2
trithorax group protein osa-like, transcript variant X3
trithorax group protein osa-like, transcript variant X4
trithorax group protein osa-like, transcript variant X5
trithorax group protein osa-like, transcript variant X7
trithorax group protein osa-like, transcript variant X6
trithorax group protein osa-like isoform X1
trithorax group protein osa-like isoform X2
trithorax group protein osa-like isoform X3
trithorax group protein osa-like isoform X4
trithorax group protein osa-like isoform X5
trithorax group protein osa-like isoform X7
histone acetyltransferase KAT6A-like isoform X6
similar to RNA sequence (same species):INSD:GIYE01030788.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 419 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% 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 391 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
cGMP-specific 3',5'-cyclic phosphodiesterase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phospholipid phosphatase 2-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
phospholipid phosphatase 2-like isoform X2
phospholipid phosphatase 2-like, transcript variant X1
phospholipid phosphatase 2-like isoform X1
WW domain-containing oxidoreductase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
lethal(2) giant larvae protein homolog 1-like, transcript variant X2
lethal(2) giant larvae protein homolog 1-like, transcript variant X1
lethal(2) giant larvae protein homolog 1-like, transcript variant X3
lethal(2) giant larvae protein homolog 1-like, transcript variant X4
lethal(2) giant larvae protein homolog 1-like, transcript variant X5
lethal(2) giant larvae protein homolog 1-like isoform X1
lethal(2) giant larvae protein homolog 1-like isoform X3
lethal(2) giant larvae protein homolog 1-like isoform X2
lethal(2) giant larvae protein homolog 1-like isoform X4
NEDD8-conjugating enzyme UBE2F-like, transcript variant X1
NEDD8-conjugating enzyme UBE2F-like, transcript variant X2
CUB and sushi domain-containing protein 3-like
serine/threonine-protein kinase fused-like, transcript variant X1
serine/threonine-protein kinase fused-like, transcript variant X2
serine/threonine-protein kinase fused-like