Penaeus chinensis breed Huanghai No. 1 chromosome 6, 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\nCM032931.1.\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.
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
low-density lipoprotein receptor-related protein 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
thymidine phosphorylase-like, transcript variant X2
thymidine phosphorylase-like, transcript variant X1
thymidine phosphorylase-like, transcript variant X4
thymidine phosphorylase-like, transcript variant X3
thymidine phosphorylase-like, transcript variant X5
cell wall protein DAN4-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 3 samples with support for all annotated introns
cell wall protein DAN4-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 9 samples with support for all annotated introns
cell wall protein DAN4-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 8 samples with support for all annotated introns
cell wall protein DAN4-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 18 samples with support for all annotated introns
cell wall protein DAN4-like, transcript variant X3
mediator of RNA polymerase II transcription subunit 26-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 26-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 26-like isoform X2
mediator of RNA polymerase II transcription subunit 26-like isoform X1
iron-sulfur cluster assembly 1 homolog, mitochondrial-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
glycine, alanine and asparagine-rich protein-like
glycine-rich cell wall structural protein 2-like, transcript variant X1
glycine-rich cell wall structural protein 2-like, transcript variant X3
glycine-rich cell wall structural protein 2-like, transcript variant X2
glycine, alanine and asparagine-rich protein-like isoform X1
glycine, alanine and asparagine-rich protein-like isoform X2
glycine-rich cell wall structural protein 2-like isoform X3
probable cyclin-dependent serine/threonine-protein kinase DDB_G0292550
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 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, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 63% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125026546, 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 2 samples with support for all annotated introns
uncharacterized LOC125026546, transcript variant X1
uncharacterized protein LOC125026546 isoform X2
uncharacterized protein LOC125026546 isoform 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 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 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 89% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glucose-fructose oxidoreductase domain-containing protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: glucose-fructose oxidoreductase domain-containing protein 1-like
venom carboxylesterase-6-like, transcript variant X1
venom carboxylesterase-6-like, transcript variant X2
venom carboxylesterase-6-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
DNA polymerase beta-like, transcript variant X1
DNA polymerase beta-like, transcript variant X2
crustacyanin-A2 subunit-like, transcript variant X1
crustacyanin-A2 subunit-like, transcript variant X2
uncharacterized peptidase C1-like protein F26E4.3
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
vascular endothelial growth factor receptor 2-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: vascular endothelial growth factor receptor 2-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: 86% 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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
oxygen-dependent coproporphyrinogen-III oxidase-like, transcript variant X1
oxygen-dependent coproporphyrinogen-III oxidase-like, transcript variant X2
oxygen-dependent coproporphyrinogen-III oxidase-like
COP1-interactive protein 1-like, transcript variant X1
COP1-interactive protein 1-like, transcript variant X2
late secretory pathway protein AVL9 homolog, 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 28 samples with support for all annotated introns
late secretory pathway protein AVL9 homolog, 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 29 samples with support for all annotated introns
late secretory pathway protein AVL9 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
late secretory pathway protein AVL9 homolog isoform X1
late secretory pathway protein AVL9 homolog isoform X2
late secretory pathway protein AVL9 homolog isoform X3
structural maintenance of chromosomes protein 3-like, transcript variant X1
structural maintenance of chromosomes protein 3-like, transcript variant X3
structural maintenance of chromosomes protein 3-like, transcript variant X2
structural maintenance of chromosomes protein 3-like isoform X1
structural maintenance of chromosomes protein 3-like isoform X3
structural maintenance of chromosomes protein 3-like isoform X2
LOW QUALITY PROTEIN: uncharacterized protein LOC125026711
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
histone deacetylase complex subunit SAP130-A-like
LOW QUALITY PROTEIN: histone deacetylase complex subunit SAP130-A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
putative uncharacterized protein DDB_G0287265
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
venom peptide isomerase heavy chain-like, transcript variant X3
venom peptide isomerase heavy chain-like, transcript variant X1
venom peptide isomerase heavy chain-like, transcript variant X2
venom peptide isomerase heavy chain-like
probable ATP-dependent RNA helicase DDX23, transcript variant X1
probable ATP-dependent RNA helicase DDX23, transcript variant X2
probable ATP-dependent RNA helicase DDX23
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
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: 77 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: ABC transporter G family member 20-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 2 samples with support for all annotated introns
DDB1- and CUL4-associated factor 10-like
transcriptional activator cubitus interruptus-like
LOW QUALITY PROTEIN: transcriptional activator cubitus interruptus-like
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
solute carrier family 49 member 4 homolog
E3 ubiquitin-protein ligase KEG-like, transcript variant X1
E3 ubiquitin-protein ligase KEG-like, transcript variant X2
interferon alpha-inducible protein 27-like protein 2A, transcript variant X1
interferon alpha-inducible protein 27-like protein 2A, transcript variant X3
interferon alpha-inducible protein 27-like protein 2A, transcript variant X5
interferon alpha-inducible protein 27-like protein 2A, transcript variant X2
interferon alpha-inducible protein 27-like protein 2A, transcript variant X4
interferon alpha-inducible protein 27-like protein 2A isoform X1
interferon alpha-inducible protein 27-like protein 2A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
vascular endothelial growth factor receptor 1-like, transcript variant X1
vascular endothelial growth factor receptor 1-like, transcript variant X2
platelet-derived growth factor receptor alpha-like isoform X1
vascular endothelial growth factor receptor 1-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 17 samples with support for all annotated introns
uncharacterized protein DDB_G0274171-like, transcript variant X1
uncharacterized protein DDB_G0274171-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 5 samples with support for all annotated introns
uncharacterized protein DDB_G0274171-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein DDB_G0274171-like, transcript variant X2
uncharacterized protein LOC125026690 isoform X2
uncharacterized protein DDB_G0274171-like isoform X3
uncharacterized protein LOC125026690 isoform X1
uncharacterized LOC125026504, transcript variant X1
uncharacterized LOC125026504, transcript variant X2
protein pangolin, isoforms A/H/I/S-like, transcript variant X5
protein pangolin, isoforms A/H/I/S-like, transcript variant X1
protein pangolin, isoforms A/H/I/S-like, transcript variant X2
protein pangolin, isoforms A/H/I/S-like isoform X5
protein pangolin, isoforms A/H/I/S-like isoform X1
protein pangolin, isoforms A/H/I/S-like isoform X2
protein pangolin, isoforms A/H/I/S-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 6 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S-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 5 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S-like isoform X3
protein pangolin, isoforms A/H/I/S-like isoform X4
rab11 family-interacting protein 1-like, transcript variant X1
rab11 family-interacting protein 1-like, transcript variant X2
rab11 family-interacting protein 1-like isoform X1
rab11 family-interacting protein 1-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 37 samples with support for all annotated introns
inositol hexakisphosphate kinase 1-like, transcript variant X1
inositol hexakisphosphate kinase 1-like, transcript variant X3
inositol hexakisphosphate kinase 1-like, transcript variant X2
uncharacterized LOC125026563, transcript variant X2
uncharacterized LOC125026563, transcript variant X1
uncharacterized LOC125026562, transcript variant X2
uncharacterized LOC125026562, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
uncharacterized LOC125026562, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
protein still life, isoform SIF type 1-like
DNA-directed RNA polymerase II subunit RPB1-like
protein still life, isoforms C/SIF type 2-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
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
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
synaptonemal complex protein 1-like, transcript variant X3
synaptonemal complex protein 1-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 7 samples with support for all annotated introns
synaptonemal complex protein 1-like, transcript variant X5
synaptonemal complex protein 1-like, transcript variant X4
synaptonemal complex protein 1-like, transcript variant X2
similar to RNA sequence (same species):INSD:GHUY01007199.1
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 208 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 208 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
golgin subfamily A member 6-like protein 22
glycosyltransferase 25 family member-like
solute carrier family 49 member 4 homolog, transcript variant X2
solute carrier family 49 member 4 homolog, transcript variant X1
solute carrier family 49 member 4 homolog isoform X1
solute carrier family 49 member 4 homolog isoform X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
extracellular tyrosine-protein kinase PKDCC-like, transcript variant X1
extracellular tyrosine-protein kinase PKDCC-like, transcript variant X2
extracellular tyrosine-protein kinase PKDCC-like
protein broad-minded-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 13 samples with support for all annotated introns
protein broad-minded-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
protein broad-minded-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 10 samples with support for all annotated introns
venom protease-like, transcript variant X1
venom protease-like, transcript variant X2
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
venom protease-like, transcript variant X3
histone-lysine N-methyltransferase 2D-like
selenoprotein W-like, transcript variant X1
selenoprotein W-like, transcript variant X2
U4/U6 small nuclear ribonucleoprotein Prp3-like, transcript variant X1
U4/U6 small nuclear ribonucleoprotein Prp3-like, transcript variant X2
U4/U6 small nuclear ribonucleoprotein Prp3-like
nuclear hormone receptor E75-like, transcript variant X1
nuclear hormone receptor E75-like isoform X1
nuclear hormone receptor E75-like, transcript variant X2
nuclear hormone receptor E75-like isoform X2
nuclear hormone receptor E75-like, transcript variant X5
nuclear hormone receptor E75-like isoform X5
nuclear hormone receptor E75-like, transcript variant X3
nuclear hormone receptor E75-like isoform X3
nuclear hormone receptor E75-like, transcript variant X4
nuclear hormone receptor E75-like isoform X4
uncharacterized LOC125026712, transcript variant X2
uncharacterized LOC125026712, transcript variant X1
uncharacterized LOC125026712, transcript variant X3
uncharacterized LOC125026712, transcript variant X4
uncharacterized protein LOC125026712 isoform X1
uncharacterized protein LOC125026712 isoform X2
uncharacterized protein LOC125026712 isoform X3
cadherin-related tumor suppressor-like, transcript variant X3
cadherin-related tumor suppressor-like, transcript variant X5
cadherin-related tumor suppressor-like, transcript variant X2
cadherin-related tumor suppressor-like, transcript variant X4
cadherin-related tumor suppressor-like, transcript variant X1
cadherin-related tumor suppressor-like, transcript variant X12
cadherin-related tumor suppressor-like, transcript variant X11
cadherin-related tumor suppressor-like, transcript variant X10
cadherin-related tumor suppressor-like, transcript variant X9
cadherin-related tumor suppressor-like, transcript variant X8
cadherin-related tumor suppressor-like, transcript variant X6
cadherin-related tumor suppressor-like, transcript variant X7
cadherin-related tumor suppressor-like isoform X12
uncharacterized protein LOC125026297 isoform X11
uncharacterized protein LOC125026297 isoform X10
uncharacterized protein LOC125026297 isoform X3
uncharacterized protein LOC125026297 isoform X9
uncharacterized protein LOC125026297 isoform X8
uncharacterized protein LOC125026297 isoform X6
uncharacterized protein LOC125026297 isoform X5
uncharacterized protein LOC125026297 isoform X2
uncharacterized protein LOC125026297 isoform X7
uncharacterized protein LOC125026297 isoform X4
uncharacterized protein LOC125026297 isoform X1
inhibitor of nuclear factor kappa-B kinase subunit alpha-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 35 samples with support for all annotated introns
inhibitor of nuclear factor kappa-B kinase subunit alpha-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 11 samples with support for all annotated introns
inhibitor of nuclear factor kappa-B kinase subunit alpha-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 14 samples with support for all annotated introns
inhibitor of nuclear factor kappa-B kinase subunit alpha-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 30 samples with support for all annotated introns
inhibitor of nuclear factor kappa-B kinase subunit alpha-like, transcript variant X1
inhibitor of nuclear factor kappa-B kinase subunit alpha-like isoform X1
inhibitor of nuclear factor kappa-B kinase subunit alpha-like isoform X2
protein bric-a-brac 2-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 13 samples with support for all annotated introns
protein bric-a-brac 2-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 21 samples with support for all annotated introns
protein bric-a-brac 2-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 9 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X3
protein bric-a-brac 2-like, transcript variant X2
protein bric-a-brac 2-like, transcript variant X1
PAX-interacting protein 1-like isoform X1
PAX-interacting protein 1-like isoform X2
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 23-like, transcript variant X1
zinc finger protein 23-like, transcript variant X2
zinc finger protein 23-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 23 samples with support for all annotated introns
uncharacterized protein LOC125026336 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
uncharacterized LOC125026436, 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 LOC125026436, transcript variant X1
uncharacterized protein LOC125026436 isoform X1
uncharacterized protein LOC125026436 isoform X2
uncharacterized LOC125026436, transcript variant X3
uncharacterized protein LOC125026436 isoform X3
similar to RNA sequence (same species):INSD:GHUY01001099.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 804 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 790 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
WD repeat-containing protein 48 homolog, transcript variant X1
WD repeat-containing protein 48 homolog, transcript variant X2
myosin heavy chain kinase B-like isoform X1
WD repeat-containing protein 48 homolog isoform X2
uncharacterized LOC125026337, transcript variant X1
uncharacterized LOC125026337, transcript variant X2
diacylglycerol lipase-alpha-like, transcript variant X2
diacylglycerol lipase-alpha-like, transcript variant X1
diacylglycerol lipase-alpha-like isoform X2
diacylglycerol lipase-alpha-like isoform X1
7-dehydrocholesterol reductase-like, transcript variant X2
7-dehydrocholesterol reductase-like, transcript variant X1
toll-interacting protein B-like, transcript variant X2
toll-interacting protein B-like isoform X2
toll-interacting protein B-like, transcript variant X1
toll-interacting protein B-like, transcript variant X3
toll-interacting protein B-like isoform X1
toll-interacting protein B-like isoform X3
pectinesterase inhibitor 10-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
pectinesterase inhibitor 10-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 8 samples with support for all annotated introns
pectinesterase inhibitor 10-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 7 samples with support for all annotated introns
pectinesterase inhibitor 10-like, transcript variant X1
uncharacterized protein LOC125026505 isoform X2
uncharacterized protein LOC125026505 isoform X1
pectinesterase inhibitor 10-like isoform X3
uncharacterized serine-rich protein C215.13-like
similar to RNA sequence (same species):INSD:GHUY01004855.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 321 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 321 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
bifunctional peptidase and (3S)-lysyl hydroxylase Jmjd7-like
histone-lysine N-methyltransferase SETD1-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 16 samples with support for all annotated introns
histone-lysine N-methyltransferase SETD1-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 19 samples with support for all annotated introns
histone-lysine N-methyltransferase SETD1-like isoform X2
histone-lysine N-methyltransferase SETD1-like isoform X1
methylosome protein 50-like, transcript variant X1
methylosome protein 50-like, transcript variant X2
zinc finger and BTB domain-containing protein 24-like, transcript variant X1
zinc finger and BTB domain-containing protein 24-like, transcript variant X3
zinc finger and BTB domain-containing protein 24-like, transcript variant X2
zinc finger and BTB domain-containing protein 24-like isoform X2
zinc finger and BTB domain-containing protein 24-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44% coverage of the annotated genomic feature by RNAseq alignments
aminoacyl tRNA synthase complex-interacting multifunctional protein 1-like
CCAAT/enhancer-binding protein gamma-like, transcript variant X1
CCAAT/enhancer-binding protein gamma-like, transcript variant X2
CCAAT/enhancer-binding protein gamma-like, transcript variant X3
CCAAT/enhancer-binding protein gamma-like
ribonuclease H2 subunit B-like, transcript variant X1
ribonuclease H2 subunit B-like, transcript variant X2
ribonuclease H2 subunit B-like isoform X1
ribonuclease H2 subunit B-like isoform X2
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
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
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 31 samples with support for all annotated introns
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125026288, transcript variant X1
uncharacterized LOC125026288, transcript variant X2
uncharacterized LOC125026288, transcript variant X3
uncharacterized LOC125026288, transcript variant X4
uncharacterized LOC125026288, transcript variant X6
uncharacterized LOC125026288, transcript variant X5
uncharacterized protein LOC125026288 isoform X1
uncharacterized protein LOC125026288 isoform X2
uncharacterized LOC125026357, transcript variant X3
uncharacterized LOC125026357, 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 LOC125026357, transcript variant X6
uncharacterized LOC125026357, transcript variant X2
uncharacterized LOC125026357, transcript variant X5
uncharacterized LOC125026357, 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 12 samples with support for all annotated introns
uncharacterized LOC125026357, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 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 31 samples with support for all annotated introns
cartilage oligomeric matrix protein-like, transcript variant X7
cartilage oligomeric matrix protein-like, transcript variant X6
cartilage oligomeric matrix protein-like, transcript variant X3
cartilage oligomeric matrix protein-like, transcript variant X5
cartilage oligomeric matrix protein-like, transcript variant X4
cartilage oligomeric matrix protein-like, transcript variant X2
cartilage oligomeric matrix protein-like, transcript variant X1
cartilage oligomeric matrix protein-like isoform X7
cartilage oligomeric matrix protein-like isoform X6
cartilage oligomeric matrix protein-like isoform X3
cartilage oligomeric matrix protein-like isoform X5
cartilage oligomeric matrix protein-like isoform X4
cartilage oligomeric matrix protein-like isoform X2
cartilage oligomeric matrix protein-like isoform X1
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 37 samples with support for all annotated introns
transcriptional regulatory protein AlgP-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
putative mediator of RNA polymerase II transcription subunit 26
uncharacterized protein DDB_G0271670-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 17 samples with support for all annotated introns
protein lethal(2)essential for life-like, transcript variant X2
protein lethal(2)essential for life-like, transcript variant X1
protein lethal(2)essential for life-like isoform X1
protein lethal(2)essential for life-like isoform 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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
fibrous sheath CABYR-binding protein-like, transcript variant X7
fibrous sheath CABYR-binding protein-like, transcript variant X5
fibrous sheath CABYR-binding protein-like, transcript variant X4
fibrous sheath CABYR-binding protein-like, transcript variant X6
fibrous sheath CABYR-binding protein-like, transcript variant X1
fibrous sheath CABYR-binding protein-like, transcript variant X2
fibrous sheath CABYR-binding protein-like, transcript variant X3
fibrous sheath CABYR-binding protein-like isoform X6
fibrous sheath CABYR-binding protein-like isoform X4
cell surface glycoprotein 1-like isoform X3
fibrous sheath CABYR-binding protein-like isoform X1
fibrous sheath CABYR-binding protein-like isoform X7
neurofilament heavy polypeptide-like isoform X5
fibrous sheath CABYR-binding protein-like isoform X2
circadian locomoter output cycles protein kaput-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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
WAP four-disulfide core domain protein 5-like
WAP four-disulfide core domain protein 2-like
uncharacterized protein LOC125026615 isoform X3
eukaryotic translation initiation factor 3 subunit E-like
mannosyl-oligosaccharide 1,2-alpha-mannosidase IA-like, transcript variant X1
mannosyl-oligosaccharide 1,2-alpha-mannosidase IA-like, transcript variant X2
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 5 samples with support for all annotated introns
mannosyl-oligosaccharide 1,2-alpha-mannosidase IA-like isoform X2
mannosyl-oligosaccharide alpha-1,2-mannosidase IA-like isoform X1
neuropilin and tolloid-like protein 1, transcript variant X3
neuropilin and tolloid-like protein 1, transcript variant X2
neuropilin and tolloid-like protein 1, transcript variant X1
neuropilin and tolloid-like protein 1 isoform X3
neuropilin and tolloid-like protein 1 isoform X2
neuropilin and tolloid-like protein 1 isoform X1
OTU domain-containing protein 5-A-like, transcript variant X1
OTU domain-containing protein 5-A-like, transcript variant X2
OTU domain-containing protein 5-A-like isoform X2
OTU domain-containing protein 5-A-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
cholesterol 7-desaturase nvd-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 5 samples with support for all annotated introns
cholesterol 7-desaturase nvd-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 4 samples with support for all annotated introns
cholesterol 7-desaturase nvd-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 2 samples with support for all annotated introns
cholesterol 7-desaturase nvd-like isoform X1
cholesterol 7-desaturase nvd-like isoform X2
PITH domain-containing protein GA19395-like, transcript variant X1
PITH domain-containing protein GA19395-like, transcript variant X2
PITH domain-containing protein GA19395-like
phospholipid-transporting ATPase ABCA1-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 3 samples with support for all annotated introns
phospholipid-transporting ATPase ABCA1-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 2 samples with support for all annotated introns
phospholipid-transporting ATPase ABCA1-like
DNA (cytosine-5)-methyltransferase 3B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 78% 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:RF00007
dynein light chain 1, cytoplasmic, transcript variant X2
dynein light chain 1, cytoplasmic, transcript variant X1
dynein light chain 1, cytoplasmic isoform X1
dynein light chain 1, cytoplasmic isoform X2
ribonuclease Z, mitochondrial-like, transcript variant X3
ribonuclease Z, mitochondrial-like, transcript variant X2
ribonuclease Z, mitochondrial-like isoform X2
ribonuclease Z, mitochondrial-like, transcript variant X5
ribonuclease Z, mitochondrial-like, transcript variant X4
ribonuclease Z, mitochondrial-like, transcript variant X6
ribonuclease Z, mitochondrial-like, transcript variant X1
ribonuclease Z, mitochondrial-like isoform X1
ribonuclease Z, mitochondrial-like isoform X3
uncharacterized LOC125026311, 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
uncharacterized protein LOC125026311 isoform X2
uncharacterized LOC125026311, transcript variant X1
uncharacterized protein LOC125026311 isoform X1
proliferation-associated protein 2G4-like
N-alpha-acetyltransferase 10-like, transcript variant X2
N-alpha-acetyltransferase 10-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
N-alpha-acetyltransferase 10-like isoform X2
N-alpha-acetyltransferase 10-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
histone PARylation factor 1-like, transcript variant X1
histone PARylation factor 1-like, transcript variant X2
histone PARylation factor 1-like, transcript variant X3
histone PARylation factor 1-like, transcript variant X4
histone PARylation factor 1-like isoform X1
histone PARylation factor 1-like isoform X2
histone PARylation factor 1-like isoform X3
histone PARylation factor 1-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
deubiquitinase OTUD6B-like, transcript variant X4
deubiquitinase OTUD6B-like, transcript variant X6
deubiquitinase OTUD6B-like, transcript variant X5
deubiquitinase OTUD6B-like, transcript variant X2
deubiquitinase OTUD6B-like, transcript variant X3
deubiquitinase OTUD6B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-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 27 samples with support for all annotated introns
zinc finger CCCH domain-containing protein 13-like, transcript variant X1
zinc finger CCCH domain-containing protein 13-like, transcript variant X2
zinc finger CCCH domain-containing protein 13-like, transcript variant X6
zinc finger CCCH domain-containing protein 13-like, transcript variant X4
zinc finger CCCH domain-containing protein 13-like, transcript variant X3
zinc finger CCCH domain-containing protein 13-like, transcript variant X5
zinc finger CCCH domain-containing protein 13-like isoform X1
zinc finger CCCH domain-containing protein 13-like isoform X5
zinc finger CCCH domain-containing protein 13-like isoform X2
zinc finger CCCH domain-containing protein 13-like isoform X6
zinc finger CCCH domain-containing protein 13-like isoform X4
zinc finger CCCH domain-containing protein 13-like isoform X3
sorting nexin-18-like, transcript variant X2
sorting nexin-18-like, transcript variant X3
sorting nexin-18-like, transcript variant X1
sorting nexin lst-4-like, transcript variant X3
sorting nexin lst-4-like, transcript variant X2
sorting nexin lst-4-like, transcript variant X1
sorting nexin lst-4-like, transcript variant X4
probable H/ACA ribonucleoprotein complex subunit 1
acetyl-CoA acetyltransferase, mitochondrial-like
60S ribosomal protein L32-like, transcript variant X1
60S ribosomal protein L32-like, transcript variant X2
60S ribosomal protein L32-like, transcript variant X3
60S ribosomal protein L32-like isoform X1
60S ribosomal protein L32-like isoform X2
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
uncharacterized LOC125026359, transcript variant X2
uncharacterized LOC125026359, transcript variant X1
CD2 antigen cytoplasmic tail-binding protein 2 homolog
TWiK family of potassium channels protein 7-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 11 samples with support for all annotated introns
TWiK family of potassium channels protein 7-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 20 samples with support for all annotated introns
TWiK family of potassium channels protein 7-like, transcript variant X1
TWiK family of potassium channels protein 7-like isoform X1
TWiK family of potassium channels protein 7-like isoform X2
calmodulin-A-like, transcript variant X1
calmodulin-A-like, transcript variant X2
uncharacterized protein LOC125026375 isoform X2
vacuolar protein sorting-associated protein 54-like, transcript variant X2
vacuolar protein sorting-associated protein 54-like, transcript variant X1
vacuolar protein sorting-associated protein 54-like, transcript variant X3
vacuolar protein sorting-associated protein 54-like, transcript variant X4
vacuolar protein sorting-associated protein 54-like isoform X1
vacuolar protein sorting-associated protein 54-like isoform X2
vacuolar protein sorting-associated protein 54-like isoform X3
polypeptide N-acetylgalactosaminyltransferase 5-like, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 5-like, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 5-like, transcript variant X3
polypeptide N-acetylgalactosaminyltransferase 5-like isoform X2
polypeptide N-acetylgalactosaminyltransferase 5-like isoform X1
polypeptide N-acetylgalactosaminyltransferase 5-like isoform X3
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 5, mitochondrial-like
glutamate receptor ionotropic, delta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
SPRY domain-containing SOCS box protein 3-like
histone-lysine N-methyltransferase SETD2-like, transcript variant X1
histone-lysine N-methyltransferase SETD2-like, transcript variant X2
histone-lysine N-methyltransferase SETD2-like isoform X1
histone-lysine N-methyltransferase SETD2-like isoform X2
U-scoloptoxin(01)-Er1a-like, transcript variant X1
U-scoloptoxin(01)-Er1a-like, transcript variant X2
uncharacterized LOC125026564, transcript variant X3
uncharacterized LOC125026564, transcript variant X2
uncharacterized LOC125026564, 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
uncharacterized LOC125026564, transcript variant X4
uncharacterized protein LOC125026564 isoform X2
uncharacterized protein LOC125026564 isoform X1
uncharacterized protein LOC125026564 isoform X3
putative methyltransferase C9orf114 homolog, transcript variant X1
putative methyltransferase C9orf114 homolog, transcript variant X2
putative methyltransferase C9orf114 homolog
sarcosine dehydrogenase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 625-like, transcript variant X2
zinc finger protein 625-like, transcript variant X1
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, including 3 samples with support for all annotated introns
bromodomain-containing protein 8-like, transcript variant X1
bromodomain-containing protein 8-like, transcript variant X4
bromodomain-containing protein 8-like, transcript variant X2
bromodomain-containing protein 8-like, transcript variant X5
bromodomain-containing protein 8-like, transcript variant X3
bromodomain-containing protein 8-like isoform X1
bromodomain-containing protein 8-like isoform X4
bromodomain-containing protein 8-like isoform X2
bromodomain-containing protein 8-like isoform X5
bromodomain-containing protein 8-like isoform X3
TBC1 domain family member 5-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 26 samples with support for all annotated introns
TBC1 domain family member 5-like, transcript variant X2
TBC1 domain family member 5-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 21 samples with support for all annotated introns
TBC1 domain family member 5-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 28 samples with support for all annotated introns
TBC1 domain family member 5-like isoform X2
TBC1 domain family member 5-like isoform X4
TBC1 domain family member 5-like isoform X1
TBC1 domain family member 5-like isoform X3
solute carrier family 13 member 5-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 15 samples with support for all annotated introns
solute carrier family 13 member 5-like, transcript variant X1
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 10 samples with support for all annotated introns
solute carrier family 13 member 5-like, transcript variant X3
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 7 samples with support for all annotated introns
solute carrier family 13 member 5-like, transcript variant X4
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 17 samples with support for all annotated introns
solute carrier family 13 member 5-like isoform X2
solute carrier family 13 member 5-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
calcineurin B homologous protein 1-like, transcript variant X1
calcineurin B homologous protein 1-like, transcript variant X2
calcineurin B homologous protein 1-like isoform X1
calcineurin B homologous protein 1-like isoform X2
thioredoxin-dependent peroxide reductase, mitochondrial-like
activating signal cointegrator 1-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 38 samples with support for all annotated introns
activating signal cointegrator 1-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 13 samples with support for all annotated introns
serine/threonine-protein kinase PRP4 homolog
transcription factor Sox-2-like, transcript variant X4
transcription factor Sox-2-like, transcript variant X1
transcription factor Sox-2-like, transcript variant X6
transcription factor Sox-2-like, transcript variant X7
transcription factor Sox-2-like, transcript variant X5
transcription factor Sox-2-like, transcript variant X3
transcription factor Sox-2-like, transcript variant X2
transcription factor Sox-2-like isoform X4
transcription factor Sox-3-like isoform X1
transcription factor Sox-3-like isoform X6
transcription factor Sox-2-like isoform X7
transcription factor Sox-3-like isoform X5
transcription factor Sox-3-like isoform X3
transcription factor Sox-3-like isoform X2
transfer RNA methionine (anticodon CAU); 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: 12 Proteins, and 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
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 7 samples with support for all annotated introns
3-ketoacyl-CoA thiolase, mitochondrial-like
dehydrogenase/reductase SDR family member 12-like
triple QxxK/R motif-containing protein-like
39S ribosomal protein L46, mitochondrial-like
uncharacterized LOC125026541, transcript variant X1
uncharacterized protein LOC125026541 isoform X1
uncharacterized LOC125026541, transcript variant X2
uncharacterized protein LOC125026541 isoform X2
LOW QUALITY PROTEIN: hemocyanin D chain-like
platelet-activating factor acetylhydrolase-like, transcript variant X5
platelet-activating factor acetylhydrolase-like isoform X4
platelet-activating factor acetylhydrolase-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 12 samples with support for all annotated introns
platelet-activating factor acetylhydrolase-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 34 samples with support for all annotated introns
platelet-activating factor acetylhydrolase-like, transcript variant X4
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
platelet-activating factor acetylhydrolase-like, transcript variant X3
platelet-activating factor acetylhydrolase-like, transcript variant X7
platelet-activating factor acetylhydrolase-like, transcript variant X8
platelet-activating factor acetylhydrolase-like, transcript variant X6
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 3 samples with support for all annotated introns
platelet-activating factor acetylhydrolase-like isoform X3
platelet-activating factor acetylhydrolase-like isoform X1
platelet-activating factor acetylhydrolase-like isoform X2
platelet-activating factor acetylhydrolase-like isoform X5
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
uncharacterized LOC125026573, 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 1 sample with support for all annotated introns
uncharacterized LOC125026573, transcript variant X2
uncharacterized protein LOC125026573 isoform X1
uncharacterized protein LOC125026573 isoform X2
inosine triphosphate pyrophosphatase-like, transcript variant X1
inosine triphosphate pyrophosphatase-like, transcript variant X2
inosine triphosphate pyrophosphatase-like, transcript variant X3
inosine triphosphate pyrophosphatase-like, transcript variant X4
inosine triphosphate pyrophosphatase-like isoform X1
inosine triphosphate pyrophosphatase-like isoform X2
transcription initiation factor IIA subunit 1-like
ubiquitin conjugation factor E4 A-like, transcript variant X1
ubiquitin conjugation factor E4 A-like, transcript variant X2
similar to RNA sequence (same species):INSD:GHUY01000098.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 424 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 103 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
fibrous sheath CABYR-binding protein-like
similar to RNA sequence (same species):INSD:GIYE01016235.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 199 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 58 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
FERM and PDZ domain-containing protein 2-like, transcript variant X2
FERM and PDZ domain-containing protein 2-like, transcript variant X1
FERM and PDZ domain-containing protein 2-like, transcript variant X4
FERM and PDZ domain-containing protein 2-like, transcript variant X3
FERM and PDZ domain-containing protein 2-like isoform X1
FERM and PDZ domain-containing protein 2-like isoform X2
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like isoform X3
uncharacterized LOC125026341, 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
uncharacterized LOC125026341, transcript variant X1
phytanoyl-CoA dioxygenase, peroxisomal-like, transcript variant X3
phytanoyl-CoA dioxygenase, peroxisomal-like, transcript variant X4
phytanoyl-CoA dioxygenase, peroxisomal-like, transcript variant X2
phytanoyl-CoA dioxygenase, peroxisomal-like, transcript variant X1
phytanoyl-CoA dioxygenase, peroxisomal-like, transcript variant X5
phytanoyl-CoA dioxygenase, peroxisomal-like isoform X2
phytanoyl-CoA dioxygenase, peroxisomal-like isoform X1
phytanoyl-CoA dioxygenase, peroxisomal-like isoform X3
similar to RNA sequence (same species):INSD:GHUY01002417.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 578 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 336 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GIYE01007838.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 814 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 814 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
ribosomal protein S6 kinase delta-1-like, transcript variant X2
ribosomal protein S6 kinase delta-1-like, transcript variant X1
ribosomal protein S6 kinase delta-1-like isoform X2
ribosomal protein S6 kinase delta-1-like isoform X1
ribosomal protein S6 kinase delta-1-like, transcript variant X3
uncharacterized protein LOC125026379 isoform X3
dynactin subunit 1-like, transcript variant X11
dynactin subunit 1-like, transcript variant X8
dynactin subunit 1-like, transcript variant X4
dynactin subunit 1-like, transcript variant X3
dynactin subunit 1-like, transcript variant X1
dynactin subunit 1-like, transcript variant X6
dynactin subunit 1-like, transcript variant X10
dynactin subunit 1-like, transcript variant X7
dynactin subunit 1-like, transcript variant X9
dynactin subunit 1-like, transcript variant X5
dynactin subunit 1-like, transcript variant X2
interferon alpha-inducible protein 27-like protein 2A
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X1
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X4
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X3
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X5
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X2
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X1
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X3
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X2
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X4
protein lingerer-like, transcript variant X6
protein lingerer-like, transcript variant X4
protein lingerer-like, transcript variant X3
protein lingerer-like, transcript variant X5
protein lingerer-like, transcript variant X2
protein lingerer-like, transcript variant X1
ubiquitin-associated protein 2-like isoform X6
venom protease-like, transcript variant X4
histone-lysine N-methyltransferase SETDB1-like, transcript variant X3
histone-lysine N-methyltransferase SETDB1-like, transcript variant X4
histone-lysine N-methyltransferase SETDB1-like, transcript variant X1
histone-lysine N-methyltransferase SETDB1-like, transcript variant X5
histone-lysine N-methyltransferase SETDB1-like, transcript variant X6
histone-lysine N-methyltransferase SETDB1-like, transcript variant X2
histone-lysine N-methyltransferase SETDB1-like isoform X1
histone-lysine N-methyltransferase SETDB1-like isoform X3
histone-lysine N-methyltransferase SETDB1-like isoform X2
histone-lysine N-methyltransferase SETDB1-like isoform X4
histone-lysine N-methyltransferase SETDB1-like, transcript variant X7
histone-lysine N-methyltransferase SETDB1-like isoform X5
uncharacterized protein DDB_G0283357-like
proton-associated sugar transporter A-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 2 samples with support for all annotated introns
proton-associated sugar transporter A-like, transcript variant X1
proton-associated sugar transporter A-like isoform X2
proton-associated sugar transporter A-like isoform X1
coatomer subunit zeta-1-like, transcript variant X1
coatomer subunit zeta-1-like, transcript variant X3
coatomer subunit zeta-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
transcriptional repressor protein YY1-like
SH3 domain-containing protein Dlish-like, transcript variant X3
SH3 domain-containing protein Dlish-like, transcript variant X2
SH3 domain-containing protein Dlish-like, transcript variant X1
SH3 domain-containing protein Dlish-like isoform X3
SH3 domain-containing protein Dlish-like isoform X2
SH3 domain-containing protein Dlish-like isoform X1
uncharacterized LOC125026527, transcript variant X2
uncharacterized LOC125026527, transcript variant X1
uncharacterized protein LOC125026527 isoform X1
uncharacterized LOC125026527, 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
uncharacterized protein LOC125026527 isoform X2
venom phosphodiesterase 2-like, transcript variant X1
venom phosphodiesterase 2-like isoform X1
venom phosphodiesterase 2-like, transcript variant X2
venom phosphodiesterase 2-like isoform X2
zinc finger C4H2 domain-containing protein-like, transcript variant X4
zinc finger C4H2 domain-containing protein-like, transcript variant X3
zinc finger C4H2 domain-containing protein-like, transcript variant X2
zinc finger C4H2 domain-containing protein-like, transcript variant X1
zinc finger C4H2 domain-containing protein-like isoform X4
zinc finger C4H2 domain-containing protein-like isoform X3
zinc finger C4H2 domain-containing protein-like isoform X2
zinc finger C4H2 domain-containing protein-like isoform X1
threonine-rich protein-like, transcript variant X2
threonine-rich protein-like, transcript variant X1
threonine-rich protein-like, transcript variant X3
threonine-rich protein-like, transcript variant X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: G-protein coupled receptor GRL101-like
nascent polypeptide-associated complex subunit alpha, muscle-specific form-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 38 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-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 33 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X2
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X1
U-scoloptoxin(11)-Sm5a-like, transcript variant X1
U-scoloptoxin(11)-Sm5a-like, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: hemocyanin F chain-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
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: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC125026160
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
transcription initiation factor TFIID subunit 3-like
hemocyte protein-glutamine gamma-glutamyltransferase-like, transcript variant X1
hemocyte protein-glutamine gamma-glutamyltransferase-like, transcript variant X3
hemocyte protein-glutamine gamma-glutamyltransferase-like, transcript variant X2
hemocyte protein-glutamine gamma-glutamyltransferase-like isoform X1
hemocyte protein-glutamine gamma-glutamyltransferase-like isoform X3
hemocyte protein-glutamine gamma-glutamyltransferase-like isoform X2
cadherin-86C-like, transcript variant X2
cadherin-86C-like, transcript variant X1
protein krasavietz-like, transcript variant X1
protein krasavietz-like, transcript variant X2
leucine-rich repeat and WD repeat-containing protein 1-like, transcript variant X3
leucine-rich repeat and WD repeat-containing protein 1-like, transcript variant X1
leucine-rich repeat and WD repeat-containing protein 1-like, transcript variant X4
leucine-rich repeat and WD repeat-containing protein 1-like, transcript variant X2
leucine-rich repeat and WD repeat-containing protein 1-like isoform X2
leucine-rich repeat and WD repeat-containing protein 1-like isoform X1
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
probable serine/threonine-protein kinase dyrk2, transcript variant X2
probable serine/threonine-protein kinase dyrk2, transcript variant X1
probable serine/threonine-protein kinase dyrk2 isoform X2
uncharacterized protein LOC125026555 isoform X1
poly [ADP-ribose] polymerase tankyrase-2-like
LOW QUALITY PROTEIN: poly [ADP-ribose] polymerase tankyrase-2-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: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
LOW QUALITY PROTEIN: LETM1 domain-containing protein 1-like
uncharacterized LOC125026465, transcript variant X2
uncharacterized LOC125026465, transcript variant X1
uncharacterized LOC125026465, transcript variant X3
neuralized-like protein 2, transcript variant X1
neuralized-like protein 2, transcript variant X2
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
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized transmembrane protein DDB_G0289901-like
mediator of RNA polymerase II transcription subunit 6-like
dendritic arbor reduction protein 1-like
uncharacterized LOC125026168, 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 11 samples with support for all annotated introns
uncharacterized LOC125026168, 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 29 samples with support for all annotated introns
uncharacterized protein LOC125026168 isoform X1
uncharacterized protein LOC125026168 isoform X2
uncharacterized LOC125026168, 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 7 samples with support for all annotated introns
uncharacterized protein LOC125026168 isoform X3
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 14 samples with support for all annotated introns
lethal(3)malignant brain tumor-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
ribosome-recycling factor, mitochondrial-like
LOW QUALITY PROTEIN: toll-like receptor Tollo
lysine-rich arabinogalactan protein 19-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
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 18 samples with support for all annotated introns
probable cytochrome P450 49a1, 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 32 samples with support for all annotated introns
probable cytochrome P450 49a1, transcript variant X2
G-protein coupled receptor moody-like, transcript variant X5
G-protein coupled receptor moody-like, transcript variant X2
G-protein coupled receptor moody-like, transcript variant X1
G-protein coupled receptor moody-like, transcript variant X3
G-protein coupled receptor moody-like, transcript variant X4
Friend leukemia integration 1 transcription factor-like
adventurous-gliding motility protein Z-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125026560, transcript variant X2
uncharacterized LOC125026560, transcript variant X1
solute carrier family 49 member 4 homolog, transcript variant X3
solute carrier family 49 member 4 homolog, transcript variant X4
uncharacterized MFS-type transporter C09D4.1-like isoform X1
plasmanylethanolamine desaturase-like, transcript variant X2
plasmanylethanolamine desaturase-like, transcript variant X1
plasmanylethanolamine desaturase-like isoform X1
plasmanylethanolamine desaturase-like isoform X2
dual specificity tyrosine-phosphorylation-regulated kinase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
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 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
putative sodium-coupled neutral amino acid transporter 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial-like
progestin and adipoQ receptor family member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125026179, transcript variant X2
uncharacterized LOC125026179, transcript variant X1
uncharacterized protein LOC125026179 isoform X2
uncharacterized protein LOC125026179 isoform X1
similar to RNA sequence (same species):INSD:GIYE01046996.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 178 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 157 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
pre-mRNA 3'-end-processing factor FIP1-like
FUN14 domain-containing protein 1A-like, transcript variant X2
FUN14 domain-containing protein 1A-like, transcript variant X1
FUN14 domain-containing protein 1A-like isoform X2
FUN14 domain-containing protein 1A-like isoform X1
putative uncharacterized protein DDB_G0282499
serine/arginine repetitive matrix protein 1-like
F-box only protein 30-like, transcript variant X2
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 13 samples with support for all annotated introns
F-box only protein 30-like, transcript variant X1
SRR1-like protein, transcript variant X1
SRR1-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
glycoprotein 3-alpha-L-fucosyltransferase A-like
alpha-(1,3)-fucosyltransferase C-like, transcript variant X2
alpha-(1,3)-fucosyltransferase C-like, transcript variant X1
alpha-(1,3)-fucosyltransferase C-like, transcript variant X3
alpha-(1,3)-fucosyltransferase C-like isoform X1
alpha-(1,3)-fucosyltransferase C-like isoform X2
uncharacterized LOC125026420, transcript variant X1
uncharacterized LOC125026420, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 5B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
collagen alpha-1(I) chain-like, transcript variant X1
collagen alpha-1(I) chain-like, transcript variant X2
collagen alpha-1(I) chain-like, transcript variant X3
collagen alpha-1(I) chain-like, transcript variant X5
collagen alpha-1(I) chain-like, transcript variant X4
collagen alpha-1(I) chain-like isoform X1
collagen alpha-1(I) chain-like isoform X2
collagen alpha-1(I) chain-like isoform X3
collagen alpha-1(I) chain-like isoform X5
collagen alpha-1(I) chain-like isoform X4
carbohydrate sulfotransferase 11-like, transcript variant X2
carbohydrate sulfotransferase 11-like, transcript variant X1
carbohydrate sulfotransferase 11-like isoform X1
carbohydrate sulfotransferase 11-like isoform X2
very low-density lipoprotein receptor-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 39 samples with support for all annotated introns
phosphorylated adapter RNA export protein-like
probable rRNA-processing protein EBP2 homolog
uncharacterized LOC125026176, transcript variant X2
uncharacterized LOC125026176, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 69% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 306a1-like, transcript variant X1
cytochrome P450 306a1-like, transcript variant X2
far upstream element-binding protein 2-like, transcript variant X1
similar to RNA sequence (same species):INSD:GHUY01009494.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 179 bases not found in genome assembly; 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 24 samples with support for all annotated introns
far upstream element-binding protein 2-like, transcript variant X2
far upstream element-binding protein 2-like, transcript variant X3
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 160 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
far upstream element-binding protein 2-like isoform X1
far upstream element-binding protein 2-like isoform X2
far upstream element-binding protein 1-like isoform X3
far upstream element-binding protein 2-like, transcript variant X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 179 bases not found in genome assembly; 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
far upstream element-binding protein 2-like isoform X4