Plutella xylostella chromosome 19, ilPluXylo3.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Yponomeutoidea; Plutellidae; Plutella.
REFSEQ INFORMATION: The reference sequence is identical to\nOW026570.1.\nAssembly name: ilPluXylo3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/03/10. The original whole-genome shotgun project has the\naccession CAKNZZ000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Plutella xylostella Annotation\n Release 103\nAnnotation Version :: 103\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##
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
guanine nucleotide-binding protein subunit beta-5
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 79 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
chromatin assembly factor 1 subunit rlf2
endoplasmic reticulum metallopeptidase 1
enhancer of mRNA-decapping protein 3, transcript variant X1
enhancer of mRNA-decapping protein 3, transcript variant X2
enhancer of mRNA-decapping protein 3 isoform X1
enhancer of mRNA-decapping protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein prickle-like, transcript variant X3
protein prickle-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
uncharacterized LOC105391019, transcript variant X1
uncharacterized LOC105391019, transcript variant X2
uncharacterized LOC105391019, transcript variant X3
uncharacterized protein LOC105391019 isoform X1
uncharacterized protein LOC105391019 isoform X2
uncharacterized protein LOC105391019 isoform X3
protein prickle-like, transcript variant X5
general odorant-binding protein 1, transcript variant X1
general odorant-binding protein 1, transcript variant X2
general odorant-binding protein 1 isoform X1
general odorant-binding protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
protein prickle-like, transcript variant X1
protein prickle-like, transcript variant X2
DNA-directed RNA polymerase III subunit RPC1, transcript variant X1
DNA-directed RNA polymerase III subunit RPC1, transcript variant X2
DNA-directed RNA polymerase III subunit RPC1 isoform X1
DNA-directed RNA polymerase III subunit RPC1 isoform X2
DNA-directed RNA polymerase III subunit RPC1, 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 27 samples with support for all annotated introns
uncharacterized protein LOC105384028 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: 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.
general transcription factor IIH subunit 4
cleavage and polyadenylation specificity factor 73
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
40S ribosomal protein S9; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309100.2
annotated by transcript or proteomic data
The RefSeq transcript has 10 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC105384034, transcript variant X3
uncharacterized LOC105384034, transcript variant X2
uncharacterized LOC105384034, transcript variant X1
uncharacterized protein LOC105384034 isoform X3
uncharacterized protein LOC105384034 isoform X2
uncharacterized protein LOC105384034 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
coiled-coil domain-containing protein 50
glutathione S-transferase 1-like; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
glutathione S-transferase 1-like, transcript variant X2
glutathione S-transferase 1-like, transcript variant X1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305502.1
The RefSeq transcript has 6 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
glutathione S-transferase 1-like isoform X1
similar to AA sequence (same species):RefSeq:NP_001292431.1
The RefSeq protein has 5 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
glutathione S-transferase 1-like isoform X2
epidermal growth factor receptor substrate 15-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
nose resistant to fluoxetine protein 6, transcript variant X2
nose resistant to fluoxetine protein 6, transcript variant X1
nose resistant to fluoxetine protein 6 isoform X2
nose resistant to fluoxetine protein 6 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA-binding domain-containing protein 6
histone-arginine methyltransferase METTL23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
3-ketoacyl-CoA thiolase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
probable protein BRICK1-B, transcript variant X2
probable protein BRICK1-B, 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 46 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 83% coverage of the annotated genomic feature by RNAseq alignments
resistance to inhibitors of cholinesterase protein 3, transcript variant X7
resistance to inhibitors of cholinesterase protein 3, transcript variant X3
resistance to inhibitors of cholinesterase protein 3, transcript variant X5
resistance to inhibitors of cholinesterase protein 3, transcript variant X1
resistance to inhibitors of cholinesterase protein 3, transcript variant X2
resistance to inhibitors of cholinesterase protein 3, transcript variant X6
resistance to inhibitors of cholinesterase protein 3, transcript variant X4
muscle M-line assembly protein unc-89 isoform X1
muscle M-line assembly protein unc-89 isoform X6
muscle M-line assembly protein unc-89 isoform X2
muscle M-line assembly protein unc-89 isoform X3
muscle M-line assembly protein unc-89 isoform X4
muscle M-line assembly protein unc-89 isoform X5
resistance to inhibitors of cholinesterase protein 3 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
uncharacterized LOC119691049, 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 4 samples with support for all annotated introns
uncharacterized LOC119691049, 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 27 samples with support for all annotated introns
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zwei Ig domain protein zig-8, transcript variant X1
zwei Ig domain protein zig-8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70% coverage of the annotated genomic feature by RNAseq alignments
RNA polymerase II-associated protein 3, transcript variant X2
RNA polymerase II-associated protein 3, transcript variant X1
RNA polymerase II-associated protein 3 isoform X1
RNA polymerase II-associated protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized protein DDB_G0284671-like
GRIP domain-containing protein RUD3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 18, 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 7 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 18, transcript variant X2
uncharacterized protein LOC105380191 isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 18 isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 16-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
phospholipid phosphatase 2, transcript variant X1
phospholipid phosphatase 2, transcript variant X2
phospholipid phosphatase 2, 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 40 samples with support for all annotated introns
phospholipid phosphatase 3, transcript variant X1
phospholipid phosphatase 3, 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 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
threonine--tRNA ligase 1, cytoplasmic, transcript variant X5
threonine--tRNA ligase 1, cytoplasmic, transcript variant X3
threonine--tRNA ligase 1, cytoplasmic, transcript variant X4
threonine--tRNA ligase 1, cytoplasmic, transcript variant X2
threonine--tRNA ligase 1, cytoplasmic, transcript variant X1
threonine--tRNA ligase 1, cytoplasmic isoform X5
threonine--tRNA ligase 1, cytoplasmic isoform X3
threonine--tRNA ligase 1, cytoplasmic isoform X4
threonine--tRNA ligase 1, cytoplasmic isoform X2
threonine--tRNA ligase 1, cytoplasmic isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
hemocyte protein-glutamine gamma-glutamyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 71 samples with support for all annotated introns
sodium/potassium/calcium exchanger Nckx30C, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sodium/potassium/calcium exchanger Nckx30C, 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 16 samples with support for all annotated introns
sodium/potassium/calcium exchanger Nckx30C, 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 14 samples with support for all annotated introns
sodium/potassium/calcium exchanger Nckx30C, 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
sodium/potassium/calcium exchanger Nckx30C isoform X1
sodium/potassium/calcium exchanger Nckx30C isoform X2
sodium/potassium/calcium exchanger Nckx30C isoform X3
sodium/potassium/calcium exchanger Nckx30C isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger SWIM domain-containing protein 4
antichymotrypsin-1, transcript variant X6
antichymotrypsin-1, transcript variant X2
antichymotrypsin-1, transcript variant X7
antichymotrypsin-1, transcript variant X9
antichymotrypsin-1, transcript variant X5
antichymotrypsin-1, transcript variant X8
antichymotrypsin-1, transcript variant X1
antichymotrypsin-1, transcript variant X4
antichymotrypsin-1, transcript variant X3
leucine-rich repeat-containing protein 49
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 3 Proteins, and 91% 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 85 samples with support for all annotated introns
glutathione S-transferase 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305482.1
The RefSeq transcript has 11 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
zinc finger protein 664, 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 20 samples with support for all annotated introns
zinc finger protein 664, 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 68 samples with support for all annotated introns
zinc finger protein 664, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
cyclin-dependent kinases regulatory subunit
adipokinetic hormone/corazonin-related peptide receptor variant I
speckle-type POZ protein, transcript variant X2
speckle-type POZ protein, transcript variant X1
uncharacterized protein LOC105380341 isoform X1
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 94% 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: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ionotropic receptor 75a
transient receptor potential cation channel trpm, transcript variant X11
transient receptor potential cation channel trpm, transcript variant X24
transient receptor potential cation channel trpm, transcript variant X14
transient receptor potential cation channel trpm, transcript variant X23
transient receptor potential cation channel trpm, transcript variant X12
transient receptor potential cation channel trpm, transcript variant X20
transient receptor potential cation channel trpm, transcript variant X8
transient receptor potential cation channel trpm, transcript variant X13
transient receptor potential cation channel trpm, transcript variant X5
transient receptor potential cation channel trpm, transcript variant X4
transient receptor potential cation channel trpm, transcript variant X6
transient receptor potential cation channel trpm, transcript variant X17
transient receptor potential cation channel trpm, transcript variant X1
transient receptor potential cation channel trpm, transcript variant X22
transient receptor potential cation channel trpm, transcript variant X18
transient receptor potential cation channel trpm, transcript variant X16
transient receptor potential cation channel trpm, transcript variant X7
transient receptor potential cation channel trpm, transcript variant X3
transient receptor potential cation channel trpm, transcript variant X15
transient receptor potential cation channel trpm, transcript variant X21
transient receptor potential cation channel trpm, transcript variant X2
transient receptor potential cation channel trpm, transcript variant X9
transient receptor potential cation channel trpm, transcript variant X10
transient receptor potential cation channel trpm, transcript variant X19
transient receptor potential cation channel trpm isoform X16
transient receptor potential cation channel trpm isoform X10
transient receptor potential cation channel trpm isoform X23
transient receptor potential cation channel trpm isoform X13
transient receptor potential cation channel trpm isoform X14
transient receptor potential cation channel trpm isoform X22
transient receptor potential cation channel trpm isoform X11
transient receptor potential cation channel trpm isoform X19
transient receptor potential cation channel trpm isoform X21
transient receptor potential cation channel trpm isoform X8
transient receptor potential cation channel trpm isoform X17
transient receptor potential cation channel trpm isoform X15
transient receptor potential cation channel trpm isoform X12
transient receptor potential cation channel trpm isoform X5
transient receptor potential cation channel trpm isoform X4
transient receptor potential cation channel trpm isoform X7
transient receptor potential cation channel trpm isoform X6
transient receptor potential cation channel trpm isoform X3
transient receptor potential cation channel trpm isoform X1
transient receptor potential cation channel trpm isoform X20
transient receptor potential cation channel trpm isoform X2
transient receptor potential cation channel trpm isoform X9
transient receptor potential cation channel trpm isoform X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 182 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
5-formyltetrahydrofolate cyclo-ligase, transcript variant X2
5-formyltetrahydrofolate cyclo-ligase, transcript variant X1
pollen-specific leucine-rich repeat extensin-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X4
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X5
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X3
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X6
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X4
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X5
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X3
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X6
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X2
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X1
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X7
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X7
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X2
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 14
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
BAG family molecular chaperone regulator 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 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 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125489945, transcript variant X3
uncharacterized LOC125489945, transcript variant X2
uncharacterized LOC125489945, transcript variant X1
protein bicaudal D, transcript variant X1
protein bicaudal D, transcript variant X2
guanine nucleotide exchange factor subunit Rich
uncharacterized LOC105396305, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
uncharacterized LOC105396305, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
uncharacterized protein LOC105396305 isoform X1
uncharacterized protein LOC105396305 isoform X2
PX domain-containing protein kinase-like protein
ATP synthase subunit alpha, mitochondrial
ras-like GTP-binding protein Rho1, transcript variant X2
ras-like GTP-binding protein Rho1, transcript variant X1
ras-like GTP-binding protein Rho1 isoform X1
ras-like GTP-binding protein Rho1 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
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: 96% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
putative uncharacterized protein DDB_G0286901
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase kappa, 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
receptor-type tyrosine-protein phosphatase kappa, 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 26 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase kappa, 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 16 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase kappa isoform X2
receptor-type tyrosine-protein phosphatase kappa isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X3
aldehyde dehydrogenase, dimeric NADP-preferring isoform X3
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X2
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X1
aldehyde dehydrogenase, dimeric NADP-preferring isoform X2
aldehyde dehydrogenase, dimeric NADP-preferring isoform X1
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X4
aldehyde dehydrogenase, dimeric NADP-preferring isoform X4
repetitive proline-rich cell wall protein, transcript variant X2
repetitive proline-rich cell wall protein, transcript variant X10
repetitive proline-rich cell wall protein, transcript variant X3
repetitive proline-rich cell wall protein, transcript variant X22
repetitive proline-rich cell wall protein, transcript variant X15
repetitive proline-rich cell wall protein, transcript variant X1
repetitive proline-rich cell wall protein, transcript variant X14
repetitive proline-rich cell wall protein, transcript variant X5
repetitive proline-rich cell wall protein, transcript variant X24
repetitive proline-rich cell wall protein, transcript variant X31
repetitive proline-rich cell wall protein, transcript variant X6
repetitive proline-rich cell wall protein, transcript variant X8
repetitive proline-rich cell wall protein, transcript variant X19
repetitive proline-rich cell wall protein, transcript variant X7
repetitive proline-rich cell wall protein, transcript variant X18
repetitive proline-rich cell wall protein, transcript variant X4
repetitive proline-rich cell wall protein, transcript variant X16
repetitive proline-rich cell wall protein, transcript variant X17
repetitive proline-rich cell wall protein, transcript variant X25
repetitive proline-rich cell wall protein, transcript variant X12
repetitive proline-rich cell wall protein, transcript variant X9
repetitive proline-rich cell wall protein, transcript variant X20
repetitive proline-rich cell wall protein, transcript variant X21
repetitive proline-rich cell wall protein, transcript variant X11
repetitive proline-rich cell wall protein, transcript variant X28
repetitive proline-rich cell wall protein, transcript variant X23
repetitive proline-rich cell wall protein, transcript variant X33
repetitive proline-rich cell wall protein, transcript variant X34
repetitive proline-rich cell wall protein, transcript variant X29
repetitive proline-rich cell wall protein, transcript variant X26
repetitive proline-rich cell wall protein, transcript variant X30
repetitive proline-rich cell wall protein, transcript variant X27
repetitive proline-rich cell wall protein, transcript variant X32
repetitive proline-rich cell wall protein 1 isoform X3
repetitive proline-rich cell wall protein 1 isoform X22
splicing factor 3A subunit 2 isoform X15
repetitive proline-rich cell wall protein 1 isoform X1
repetitive proline-rich cell wall protein 1 isoform X14
repetitive proline-rich cell wall protein isoform X5
repetitive proline-rich cell wall protein isoform X24
repetitive proline-rich cell wall protein isoform X31
repetitive proline-rich cell wall protein isoform X8
repetitive proline-rich cell wall protein isoform X19
splicing factor 3A subunit 2 isoform X18
repetitive proline-rich cell wall protein isoform X4
splicing factor 3A subunit 2 isoform X16
repetitive proline-rich cell wall protein isoform X25
splicing factor 3A subunit 2 isoform X20
repetitive proline-rich cell wall protein isoform X27
repetitive proline-rich cell wall protein 1 isoform X32
repetitive proline-rich cell wall protein 1 isoform X11
repetitive proline-rich cell wall protein, transcript variant X13
keratin, type I cytoskeletal 9, transcript variant X2
keratin, type I cytoskeletal 9, transcript variant X1
keratin, type I cytoskeletal 9 isoform X2
keratin, type I cytoskeletal 9 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105382863, transcript variant X2
uncharacterized LOC105382863, transcript variant X1
uncharacterized LOC105382863, transcript variant X3
uncharacterized protein LOC105382863 isoform X1
uncharacterized protein LOC105382863 isoform X2
calcium and integrin-binding family member 2
dentin sialophosphoprotein, transcript variant X2
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 38 samples with support for all annotated introns
dentin sialophosphoprotein, transcript variant X1
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 24 samples with support for all annotated introns
trimeric intracellular cation channel type 1B.1
transfer RNA proline (anticodon CGG); 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
G-protein coupled receptor dmsr-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
G-protein coupled receptor dmsr-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
G-protein coupled receptor dmsr-1 isoform X2
G-protein coupled receptor dmsr-1 isoform X1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology domain-containing family F member 2, transcript variant X1
pleckstrin homology domain-containing family F member 2, transcript variant X2
pleckstrin homology domain-containing family F member 2 isoform X1
pleckstrin homology domain-containing family F member 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
testis-specific serine/threonine-protein kinase 3, transcript variant X1
testis-specific serine/threonine-protein kinase 3, transcript variant X2
testis-specific serine/threonine-protein kinase 3 isoform X2
testis-specific serine/threonine-protein kinase 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
polyadenylate-binding protein 2-B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
polyadenylate-binding protein 2-B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
putative ribosome-binding factor A, mitochondrial
synaptic vesicle membrane protein VAT-1 homolog-like, transcript variant X1
synaptic vesicle membrane protein VAT-1 homolog-like, transcript variant X2
synaptic vesicle membrane protein VAT-1 homolog-like, transcript variant X3
synaptic vesicle membrane protein VAT-1 homolog-like isoform X1
synaptic vesicle membrane protein VAT-1 homolog-like isoform X2
synaptic vesicle membrane protein VAT-1 homolog-like isoform 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 17 samples with support for all annotated introns
transcription factor HNF-4 homolog, transcript variant X4
transcription factor HNF-4 homolog, transcript variant X3
transcription factor HNF-4 homolog, transcript variant X5
transcription factor HNF-4 homolog, transcript variant X2
transcription factor HNF-4 homolog, transcript variant X1
transcription factor HNF-4 homolog isoform X4
hepatocyte nuclear factor 4-gamma isoform X3
transcription factor HNF-4 homolog isoform X5
hepatocyte nuclear factor 4-gamma isoform X2
hepatocyte nuclear factor 4-gamma isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 75 samples with support for all annotated introns
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105388799, transcript variant X3
uncharacterized LOC105388799, transcript variant X2
uncharacterized LOC105388799, transcript variant X1
uncharacterized protein LOC105388799 isoform X2
uncharacterized protein LOC105388799 isoform X1
GPI ethanolamine phosphate transferase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC105380212, transcript variant X1
uncharacterized protein LOC105380212 isoform X1
uncharacterized LOC105380212, transcript variant X3
uncharacterized LOC105380212, transcript variant X2
uncharacterized protein LOC105380212 isoform X2
uncharacterized protein LOC105380212 isoform X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X6
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X5
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X7
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X8
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X5
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X6
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X7
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X15
uncharacterized LOC125489964, transcript variant X1
uncharacterized LOC125489964, transcript variant X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X17
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X11
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X12
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X16
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X14
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X18
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X9
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X8
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X13
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2, transcript variant X10
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X9
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X10
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 isoform X11
tRNA selenocysteine 1-associated protein 1
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 55 samples with support for all annotated introns
angiogenic factor with G patch and FHA domains 1, 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 24 samples with support for all annotated introns
angiogenic factor with G patch and FHA domains 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
angiogenic factor with G patch and FHA domains 1 isoform X2
angiogenic factor with G patch and FHA domains 1 isoform X1
mitotic spindle assembly checkpoint protein MAD1
probable protein arginine N-methyltransferase 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
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 40 samples with support for all annotated introns
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
growth arrest-specific protein 1, transcript variant X2
growth arrest-specific protein 1, transcript variant X1
peroxisomal multifunctional enzyme type 2, transcript variant X1
peroxisomal multifunctional enzyme type 2, transcript variant X2
peroxisomal multifunctional enzyme type 2, transcript variant X3
peroxisomal multifunctional enzyme type 2 isoform X2
peroxisomal multifunctional enzyme type 2 isoform X3
peroxisomal multifunctional enzyme type 2 isoform X1
thioredoxin domain-containing protein 9, transcript variant X1
thioredoxin domain-containing protein 9, transcript variant X2
uncharacterized LOC105391373, transcript variant X2
uncharacterized LOC105391373, transcript variant X1
uncharacterized LOC105391373, transcript variant X3
uncharacterized LOC105391373, transcript variant X5
uncharacterized LOC105391373, transcript variant X4
uncharacterized protein LOC105391373 isoform X1
uncharacterized protein LOC105391373 isoform X2
uncharacterized protein LOC105391373 isoform X4
uncharacterized protein LOC105391373 isoform X3
CWF19-like protein 1, 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 67 samples with support for all annotated introns
CWF19-like protein 1, 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 76 samples with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
leptin receptor gene-related protein, transcript variant X1
leptin receptor gene-related protein, transcript variant X2
leptin receptor gene-related protein isoform X1
leptin receptor gene-related protein isoform X2
DNA-directed RNA polymerases I, II, and III subunit RPABC1
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
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); 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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
carbohydrate sulfotransferase 11, transcript variant X3
carbohydrate sulfotransferase 11, transcript variant X4
carbohydrate sulfotransferase 11, transcript variant X1
carbohydrate sulfotransferase 11, transcript variant X2
carbohydrate sulfotransferase 11 isoform X1
carbohydrate sulfotransferase 11 isoform X2
carbohydrate sulfotransferase 11 isoform X3
uncharacterized LOC105395948, transcript variant X2
uncharacterized LOC105395948, transcript variant X1
uncharacterized protein LOC105395948 isoform X1
uncharacterized protein LOC105395948 isoform X2
peptidyl-alpha-hydroxyglycine alpha-amidating lyase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119690288, transcript variant X3
uncharacterized protein LOC119690288 isoform X3
uncharacterized LOC119690288, transcript variant X1
uncharacterized protein LOC119690288 isoform X1
uncharacterized LOC119690288, transcript variant X2
uncharacterized protein LOC119690288 isoform X2
diuretic hormone receptor, transcript variant X2
diuretic hormone receptor, transcript variant X1
diuretic hormone receptor, transcript variant X4
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 9 samples with support for all annotated introns
diuretic hormone receptor, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
diuretic hormone receptor, transcript variant X5
diuretic hormone receptor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
pentatricopeptide repeat-containing protein 2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
serine/threonine-protein kinase PRP4 homolog, transcript variant X2
serine/threonine-protein kinase PRP4 homolog, transcript variant X6
serine/threonine-protein kinase PRP4 homolog, transcript variant X11
serine/threonine-protein kinase PRP4 homolog, transcript variant X8
serine/threonine-protein kinase PRP4 homolog, transcript variant X3
serine/threonine-protein kinase PRP4 homolog, transcript variant X7
serine/threonine-protein kinase PRP4 homolog, transcript variant X14
serine/threonine-protein kinase PRP4 homolog, transcript variant X10
serine/threonine-protein kinase PRP4 homolog, transcript variant X13
serine/threonine-protein kinase PRP4 homolog, transcript variant X1
serine/threonine-protein kinase PRP4 homolog, transcript variant X4
serine/threonine-protein kinase PRP4 homolog, transcript variant X5
serine/threonine-protein kinase PRP4 homolog, transcript variant X9
serine/threonine-protein kinase PRP4 homolog, transcript variant X15
serine/threonine-protein kinase PRP4 homolog, transcript variant X16
serine/threonine-protein kinase PRP4 homolog, transcript variant X12
serine/threonine-protein kinase PRP4 homolog
transmembrane protein adipocyte-associated 1 homolog
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 69 samples with support for all annotated introns
probable splicing factor, arginine/serine-rich 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 68 samples with support for all annotated introns
probable splicing factor, arginine/serine-rich 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
probable splicing factor, arginine/serine-rich 7 isoform X2
probable splicing factor, arginine/serine-rich 7 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
store-operated calcium entry regulator STIMATE
heterogeneous nuclear ribonucleoprotein K, transcript variant X3
heterogeneous nuclear ribonucleoprotein K, transcript variant X1
heterogeneous nuclear ribonucleoprotein K, transcript variant X2
heterogeneous nuclear ribonucleoprotein K isoform X1
heterogeneous nuclear ribonucleoprotein K isoform X2
lysM and putative peptidoglycan-binding domain-containing protein 4
N(6)-adenine-specific methyltransferase METTL4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 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 16 samples with support for all annotated introns
G-protein coupled receptor dmsr-1, transcript variant X3
G-protein coupled receptor dmsr-1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
tyrosine-protein kinase Src42A, transcript variant X3
tyrosine-protein kinase Src42A, transcript variant X4
tyrosine-protein kinase Src42A isoform X3
tyrosine-protein kinase Src42A isoform X4
tyrosine-protein kinase Src42A, transcript variant X2
tyrosine-protein kinase Src42A, transcript variant X1
uncharacterized protein LOC105398073 isoform X1
uncharacterized protein C1orf112 homolog
ATP-dependent RNA helicase vasa, transcript variant X1
ATP-dependent RNA helicase vasa, transcript variant X2
ATP-dependent RNA helicase vasa isoform X1
ATP-dependent RNA helicase vasa isoform X2
microtubule-associated protein RP/EB family member 1, transcript variant X1
microtubule-associated protein RP/EB family member 1, transcript variant X2
microtubule-associated protein RP/EB family member 1 isoform X1
microtubule-associated protein RP/EB family member 1 isoform X2
probable serine/threonine-protein kinase DDB_G0282963
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 44 samples with support for all annotated introns
probable RNA-binding protein CG14230, transcript variant X2
probable RNA-binding protein CG14230, transcript variant X1
probable RNA-binding protein CG14230 isoform X2
probable RNA-binding protein CG14230 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 33 samples with support for all annotated introns
eukaryotic translation elongation factor 1 epsilon-1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
glycine-rich cell wall structural protein
glycine-rich cell wall structural protein-like
uncharacterized LOC105398088, transcript variant X2
uncharacterized LOC105398088, transcript variant X1
uncharacterized LOC105392900, transcript variant X4
uncharacterized LOC105392900, transcript variant X2
uncharacterized LOC105392900, transcript variant X5
uncharacterized LOC105392900, transcript variant X3
uncharacterized LOC105392900, transcript variant X1
uncharacterized protein LOC105392900 isoform X4
uncharacterized protein LOC105392900 isoform X2
uncharacterized protein LOC105392900 isoform X5
uncharacterized protein LOC105392900 isoform X3
uncharacterized protein LOC105392900 isoform 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 33 samples with support for all annotated introns
ejaculatory bulb-specific protein 3, transcript variant X2
ejaculatory bulb-specific protein 3, transcript variant X1
ejaculatory bulb-specific protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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
EF-hand domain-containing family member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
ejaculatory bulb-specific protein 3-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305480.1
The RefSeq transcript has 7 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ejaculatory bulb-specific protein 3-like precursor
COORDINATES: ab initio prediction:SignalP:4.0
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309094.1
The RefSeq transcript has 10 substitutions, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305499.1
The RefSeq transcript has 8 substitutions, 3 non-frameshifting indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC105398103, 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
uncharacterized protein LOC105398103 isoform X2
uncharacterized LOC105398103, transcript variant X3
uncharacterized LOC105398103, transcript variant X1
uncharacterized protein LOC105398103 isoform X3
uncharacterized protein LOC105398103 isoform X1
similar to AA sequence (same species):RefSeq:NP_001292428.1
The RefSeq protein has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
caseinolytic peptidase B protein homolog
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial
uncharacterized LOC105398107, transcript variant X1
uncharacterized LOC105398107, transcript variant X2
uncharacterized protein LOC105398107 isoform X1
uncharacterized protein LOC105398107 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, including 37 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 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: 2 ESTs, 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
CREB-regulated transcription coactivator 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
CREB-regulated transcription coactivator 1, transcript variant X1
CREB-regulated transcription coactivator 1, transcript variant X3
CREB-regulated transcription coactivator 1, transcript variant X2
CREB-regulated transcription coactivator 1, transcript variant X4
CREB-regulated transcription coactivator 1, transcript variant X5
CREB-regulated transcription coactivator 3 isoform X1
CREB-regulated transcription coactivator 3 isoform X2
CREB-regulated transcription coactivator 3 isoform X4
CREB-regulated transcription coactivator 1 isoform X5
CREB-regulated transcription coactivator 3 isoform X3
CREB-regulated transcription coactivator 1 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
coiled-coil domain-containing protein 112-like
tetratricopeptide repeat protein 19 homolog, mitochondrial
nematocyst expressed protein 3-like, transcript variant X3
nematocyst expressed protein 3-like, transcript variant X2
nematocyst expressed protein 3-like, transcript variant X1
nematocyst expressed protein 3-like isoform X3
nematocyst expressed protein 3-like isoform X2
nematocyst expressed protein 3-like isoform X1
cilia- and flagella-associated protein 20-like
cilia- and flagella-associated protein 20
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 46 samples with support for all annotated introns
X-ray repair cross-complementing protein 6
guanine nucleotide-binding protein G(o) subunit alpha, transcript variant X4
guanine nucleotide-binding protein G(o) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(o) subunit alpha isoform X2
guanine nucleotide-binding protein G(o) subunit alpha isoform X4
guanine nucleotide-binding protein G(o) subunit alpha, transcript variant X1
guanine nucleotide-binding protein G(o) subunit alpha, transcript variant X3
guanine nucleotide-binding protein G(o) subunit alpha isoform X1
guanine nucleotide-binding protein G(o) subunit alpha isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cAMP-dependent protein kinase type II regulatory subunit, transcript variant X2
cAMP-dependent protein kinase type II regulatory subunit, transcript variant X1
cAMP-dependent protein kinase type II regulatory subunit isoform X2
cAMP-dependent protein kinase type II regulatory subunit isoform X1
uncharacterized LOC105383319, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
uncharacterized LOC105383319, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
uncharacterized LOC105383319, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
uncharacterized LOC105383319, transcript variant X1
uncharacterized protein LOC105383319 isoform X4
uncharacterized protein LOC105383319 isoform X3
uncharacterized protein LOC105383319 isoform X2
uncharacterized protein LOC105383319 isoform X1
DNA replication complex GINS protein PSF3, 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 26 samples with support for all annotated introns
DNA replication complex GINS protein PSF3, transcript variant X1
DNA replication complex GINS protein PSF3
cyclin-dependent-like kinase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
cyclin-dependent-like kinase 5, 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 70 samples with support for all annotated introns
cyclin-dependent-like kinase 5 isoform X2
cyclin-dependent-like kinase 5 isoform X1
peptidyl-prolyl cis-trans isomerase FKBP8
GPI ethanolamine phosphate transferase 2, transcript variant X3
GPI ethanolamine phosphate transferase 2, transcript variant X1
GPI ethanolamine phosphate transferase 2, transcript variant X2
GPI ethanolamine phosphate transferase 2 isoform X2
GPI ethanolamine phosphate transferase 2 isoform X1
protein lethal(2)essential for life-like
protein dead ringer, transcript variant X5
protein dead ringer, transcript variant X4
protein dead ringer, transcript variant X2
protein dead ringer, transcript variant X1
protein dead ringer, transcript variant X3
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X5
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X5
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X8
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X8
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X7
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X7
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X6
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X6
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X3
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X2
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X1
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X4
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8, transcript variant X9
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X2
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X1
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X4
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X3
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8 isoform X9
RNA polymerase II subunit A C-terminal domain phosphatase
28S ribosomal protein S17, mitochondrial
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 85 samples with support for all annotated introns
leukotriene A-4 hydrolase, transcript variant X1
leukotriene A-4 hydrolase, transcript variant X2
leukotriene A-4 hydrolase, transcript variant X4
leukotriene A-4 hydrolase, transcript variant X3
39S ribosomal protein L13, mitochondrial
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 85 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
foot protein 1 variant 1-like isoform X3
sodium channel protein 60E-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium channel protein 60E-like, transcript variant X2
sodium channel protein 60E-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
sodium channel protein 60E-like, transcript variant X5
sodium channel protein 60E-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
sodium channel protein 60E-like isoform X1
sodium channel protein 60E-like isoform X2
sodium channel protein 60E-like isoform X3
sodium channel protein 60E-like isoform X5
sodium channel protein 60E-like isoform X4
NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial
ankyrin repeat and LEM domain-containing protein 1
zinc finger protein 608, transcript variant X1
zinc finger protein 608, transcript variant X3
zinc finger protein 608, transcript variant X2
zinc finger protein 608, transcript variant X4
E3 SUMO-protein ligase PIAS3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
E3 SUMO-protein ligase PIAS3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
E3 SUMO-protein ligase PIAS3, transcript variant X2
E3 SUMO-protein ligase PIAS3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
E3 SUMO-protein ligase PIAS3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
phosphorylated adapter RNA export protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
bis(5'-nucleosyl)-tetraphosphatase [asymmetrical]
probable beta-hexosaminidase fdl, 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 62 samples with support for all annotated introns
probable beta-hexosaminidase fdl, transcript variant X2
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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC119690639, transcript variant X1
uncharacterized LOC119690639, transcript variant X2
uncharacterized protein LOC119690639 isoform X1
uncharacterized protein LOC119690639 isoform X2
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 69 samples with support for all annotated introns
uncharacterized oxidoreductase YjmC, transcript variant X2
uncharacterized oxidoreductase YjmC, 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 7 samples with support for all annotated introns
transitional endoplasmic reticulum ATPase TER94, transcript variant X2
transitional endoplasmic reticulum ATPase TER94, transcript variant X1
transitional endoplasmic reticulum ATPase TER94, transcript variant X3
transitional endoplasmic reticulum ATPase TER94 isoform X2
transitional endoplasmic reticulum ATPase TER94 isoform X1
transitional endoplasmic reticulum ATPase TER94 isoform X3
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: 15 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 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 81 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
NADH dehydrogenase [ubiquinone] iron-sulfur protein 5
NADH dehydrogenase [ubiquinone] iron-sulfur protein 5-like
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1
activating signal cointegrator 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
activating signal cointegrator 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
activating signal cointegrator 1 isoform X1
activating signal cointegrator 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
inactive selenide, water dikinase-like protein
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 14 samples with support for all annotated introns
transfer RNA serine (anticodon AGA); 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
probable methylcrotonoyl-CoA carboxylase beta chain, mitochondrial
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 43 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 55 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
uncharacterized LOC105398333, 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 5 samples with support for all annotated introns
uncharacterized LOC105398333, transcript variant X2
uncharacterized LOC125488548, transcript variant X2
uncharacterized LOC125488548, transcript variant X1
uncharacterized protein LOC125488548 isoform X1
uncharacterized protein LOC125488548 isoform X2
mitochondrial potassium channel ATP-binding subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 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: 8 Proteins, 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 7 samples with support for all annotated introns
synaptic vesicle glycoprotein 2A, transcript variant X1
synaptic vesicle glycoprotein 2A, 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 13 samples with support for all annotated introns
synaptic vesicle glycoprotein 2A, transcript variant X3
synaptic vesicle glycoprotein 2A, 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 16 samples with support for all annotated introns
synaptic vesicle glycoprotein 2A isoform X1
synaptic vesicle glycoprotein 2A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105390970, transcript variant X1
uncharacterized LOC105390970, transcript variant X2
uncharacterized protein LOC105390970 isoform X1
uncharacterized protein LOC105390970 isoform X2
uncharacterized LOC105390971, transcript variant X2
uncharacterized LOC105390971, transcript variant X1
eukaryotic translation initiation factor 3 subunit J
oxysterol-binding protein-related protein 9, transcript variant X1
oxysterol-binding protein-related protein 9, transcript variant X2
oxysterol-binding protein-related protein 9 isoform X1
oxysterol-binding protein-related protein 9 isoform X2
oxysterol-binding protein-related protein 9, transcript variant X3
oxysterol-binding protein-related protein 9 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
RING finger and CHY zinc finger domain-containing protein 1, transcript variant X1
RING finger and CHY zinc finger domain-containing protein 1, transcript variant X2
RING finger and CHY zinc finger domain-containing protein 1 isoform X1
RING finger and CHY zinc finger domain-containing protein 1 isoform 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 75 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 2 Proteins, and 99% 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 90% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 11
peroxisomal leader peptide-processing protease-like
neurofilament medium polypeptide, transcript variant X1
neurofilament medium polypeptide, transcript variant X3
neurofilament medium polypeptide, transcript variant X2
capping protein-inhibiting regulator of actin dynamics isoform X1
neurofilament medium polypeptide isoform X3
neurofilament medium polypeptide isoform X2
ATP-binding cassette sub-family A member 2
LOW QUALITY PROTEIN: ATP-binding cassette sub-family A member 2
peptidylprolyl isomerase domain and WD repeat-containing protein 1, transcript variant X2
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 31 samples with support for all annotated introns
peptidylprolyl isomerase domain and WD repeat-containing protein 1, transcript variant X1
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 58 samples with support for all annotated introns
peptidylprolyl isomerase domain and WD repeat-containing protein 1
CCHC-type zinc finger nucleic acid binding protein, transcript variant X1
CCHC-type zinc finger nucleic acid binding protein, transcript variant X2
CCHC-type zinc finger nucleic acid binding protein
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 44 samples with support for all annotated introns
minor histocompatibility antigen H13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
minor histocompatibility antigen H13, transcript variant X1
minor histocompatibility antigen H13 isoform X1
minor histocompatibility antigen H13 isoform X2
actin cytoskeleton-regulatory complex protein PAN1, transcript variant X2
actin cytoskeleton-regulatory complex protein PAN1, transcript variant X1
actin cytoskeleton-regulatory complex protein PAN1 isoform X1
actin cytoskeleton-regulatory complex protein PAN1 isoform X2
homeobox protein homothorax, transcript variant X4
homeobox protein homothorax, transcript variant X2
homeobox protein homothorax, transcript variant X1
homeobox protein homothorax, transcript variant X3
iroquois-class homeodomain protein IRX-6 isoform X3
iroquois-class homeodomain protein IRX-6 isoform X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 4, transcript variant X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 4, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 4
uncharacterized LOC105389905, transcript variant X1
uncharacterized LOC105389905, transcript variant X3
uncharacterized LOC105389905, transcript variant X2
uncharacterized LOC125488552, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 68 samples with support for all annotated introns
uncharacterized LOC125488552, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
uncharacterized LOC125488552, transcript variant X2
uncharacterized protein LOC125488552 isoform X2
uncharacterized protein LOC125488552 isoform X3
uncharacterized protein LOC125488552 isoform X1
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
cholinesterase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
cholinesterase 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
cholinesterase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ran-binding protein 9, transcript variant X1
ran-binding protein 9, transcript variant X3
ran-binding protein 9, transcript variant X2
translin-associated factor X-interacting protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 71 samples with support for all annotated introns
cysteine and histidine-rich protein 1 homolog, transcript variant X1
cysteine and histidine-rich protein 1 homolog, transcript variant X2
cysteine and histidine-rich protein 1 homolog isoform X2
cysteine and histidine-rich protein 1 homolog isoform X1
trafficking protein particle complex subunit 11
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit DAD1
E3 ubiquitin-protein ligase AMFR, transcript variant X1
E3 ubiquitin-protein ligase AMFR, transcript variant X2
E3 ubiquitin-protein ligase AMFR isoform X2
E3 ubiquitin-protein ligase AMFR isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 52 samples with support for all annotated introns
transcription initiation factor TFIID subunit 7
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.
NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial
uncharacterized protein K02A2.6-like, transcript variant X2
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein LOC119692713 isoform X2
uncharacterized protein K02A2.6-like isoform X1
uncharacterized LOC119692573, transcript variant X1
uncharacterized LOC119692573, transcript variant X2
beta-hexosaminidase subunit beta, transcript variant X1
beta-hexosaminidase subunit beta, transcript variant X2