Plutella xylostella chromosome 20, 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\nOW026575.1.\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]
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
retrovirus-related Pol polyprotein from type-1 retrotransposable element R1
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
prolow-density lipoprotein receptor-related protein 1
prolow-density lipoprotein receptor-related protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3
non-canonical poly(A) RNA polymerase protein Trf4-1
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
uncharacterized LOC105383202, 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 3 samples with support for all annotated introns
uncharacterized protein LOC105383202 isoform X1
uncharacterized LOC105383202, 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 2 samples with support for all annotated introns
uncharacterized protein LOC105383202 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 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 71% coverage of the annotated genomic feature by RNAseq alignments
replication stress response regulator SDE2
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 76 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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 31 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 9 samples with support for all annotated introns
vacuolar protein sorting-associated protein 28 homolog, transcript variant X2
vacuolar protein sorting-associated protein 28 homolog, transcript variant X1
vacuolar protein sorting-associated protein 28 homolog
protein 4.1 homolog, transcript variant X10
protein 4.1 homolog, transcript variant X7
protein 4.1 homolog, transcript variant X6
protein 4.1 homolog, transcript variant X1
protein 4.1 homolog, transcript variant X2
protein 4.1 homolog, transcript variant X4
protein 4.1 homolog, transcript variant X5
protein 4.1 homolog, transcript variant X3
protein 4.1 homolog, transcript variant X8
protein 4.1 homolog, transcript variant X9
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 28 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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
oxidative stress-induced growth inhibitor 1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
trafficking protein particle complex subunit 2-like protein
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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
cilia- and flagella-associated protein 45
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
S-adenosylmethionine mitochondrial carrier protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
pancreatic lipase-related protein 2, transcript variant X1
pancreatic lipase-related protein 2 isoform X1
pancreatic lipase-related protein 2, transcript variant X2
pancreatic lipase-related protein 2 isoform X2
uncharacterized LOC125490143, transcript variant X1
uncharacterized LOC125490143, transcript variant X2
uncharacterized protein LOC125490143 isoform X1
uncharacterized protein LOC125490143 isoform X2
oxysterol-binding protein-related protein 3
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
probable aminopeptidase NPEPL1, transcript variant X3
probable aminopeptidase NPEPL1, transcript variant X1
probable aminopeptidase NPEPL1, transcript variant X2
probable aminopeptidase NPEPL1 isoform X1
probable aminopeptidase NPEPL1 isoform X2
probable aminopeptidase NPEPL1 isoform X3
coactosin-like protein, transcript variant X2
coactosin-like protein, transcript variant X1
39S ribosomal protein L39, 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 81 samples with support for all annotated introns
gastrulation defective protein 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 82 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
uncharacterized LOC125490092, transcript variant X2
uncharacterized LOC125490092, transcript variant X1
lipase member H-B, 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 22 samples with support for all annotated introns
lipase member H-B, 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 20 samples with support for all annotated introns
lipase member H-B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
lipase member H-B, transcript variant X2
lipase member H-B, 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 56 samples with support for all annotated introns
mannosylglucosyl-3-phosphoglycerate phosphatase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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: 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 83 samples with support for all annotated introns
uncharacterized LOC125490093, transcript variant X1
uncharacterized LOC125490093, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
histone-arginine methyltransferase CARMER
trafficking protein particle complex subunit 12
vacuolar protein sorting-associated protein 35
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 65% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 2, transcript variant X1
KH domain-containing, RNA-binding, signal transduction-associated protein 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 2, transcript variant X7
KH domain-containing, RNA-binding, signal transduction-associated protein 2, transcript variant X5
KH domain-containing, RNA-binding, signal transduction-associated protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 2 isoform X4
KH domain-containing, RNA-binding, signal transduction-associated protein 2 isoform X2
KH domain-containing, RNA-binding, signal transduction-associated protein 2 isoform X5
KH domain-containing, RNA-binding, signal transduction-associated protein 2 isoform X3
uncharacterized LOC125490129, 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 43 samples with support for all annotated introns
uncharacterized LOC125490129, 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 20 samples with support for all annotated introns
transient receptor potential channel pyrexia, transcript variant X2
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 52 samples with support for all annotated introns
transient receptor potential channel pyrexia, 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 30 samples with support for all annotated introns
transient receptor potential channel pyrexia, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
transient receptor potential channel pyrexia isoform X2
transient receptor potential channel pyrexia isoform X1
transient receptor potential channel pyrexia isoform X3
dynein light chain roadblock-type 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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
probable ATP-dependent RNA helicase DDX27
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
trifunctional enzyme subunit beta, mitochondrial, transcript variant X2
trifunctional enzyme subunit beta, mitochondrial, transcript variant X1
trifunctional enzyme subunit beta, mitochondrial
MTOR-associated protein MEAK7, transcript variant X4
MTOR-associated protein MEAK7, transcript variant X2
MTOR-associated protein MEAK7, transcript variant X3
MTOR-associated protein MEAK7, transcript variant X1
MTOR-associated protein MEAK7 isoform X2
MTOR-associated protein MEAK7 isoform X1
MTOR-associated protein MEAK7 isoform X3
MTOR-associated protein MEAK7 isoform X4
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 16 samples with support for all annotated introns
coiled-coil domain-containing protein 102A
snRNA-activating protein complex subunit 1
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 67 samples with support for all annotated introns
dolichol-phosphate mannosyltransferase subunit 1
NF-kappa-B inhibitor-interacting Ras-like protein, 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 43 samples with support for all annotated introns
NF-kappa-B inhibitor-interacting Ras-like protein, 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 76 samples with support for all annotated introns
NF-kappa-B inhibitor-interacting Ras-like protein isoform X1
NF-kappa-B inhibitor-interacting Ras-like protein isoform X2
sodium-dependent neutral amino acid transporter B(0)AT3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
cytochrome c oxidase subunit 5B, mitochondrial
heparan-alpha-glucosaminide N-acetyltransferase
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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 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 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC105383426, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
uncharacterized LOC105383426, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC105383426, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
uncharacterized LOC105383426, transcript variant X4
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 50 samples with support for all annotated introns
uncharacterized protein LOC105383426 isoform X3
uncharacterized protein LOC105383426 isoform X2
uncharacterized protein LOC105383426 isoform X4
uncharacterized protein LOC105383426 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 9 samples with support for all annotated introns
EARP and GARP complex-interacting protein 1, transcript variant X1
EARP and GARP complex-interacting protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
EARP and GARP complex-interacting protein 1 isoform X1
EARP and GARP complex-interacting protein 1 isoform X2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial
glutathione synthetase, transcript variant X2
glutathione synthetase, transcript variant X1
glutathione synthetase, transcript variant X3
glutathione synthetase, transcript variant X4
glutathione synthetase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 84% 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 46 samples with support for all annotated introns
uncharacterized LOC105385363, 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 50 samples with support for all annotated introns
uncharacterized LOC105385363, transcript variant X2
uncharacterized protein LOC105385363 isoform X1
uncharacterized protein LOC105385363 isoform X2
uncharacterized LOC119691633, 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 4 samples with support for all annotated introns
uncharacterized LOC119691633, transcript variant X2
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
uncharacterized LOC105386764, transcript variant X4
uncharacterized LOC105386764, transcript variant X5
uncharacterized LOC105386764, transcript variant X6
uncharacterized LOC105386764, 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 17 samples with support for all annotated introns
uncharacterized LOC105386764, transcript variant X3
uncharacterized LOC105386764, 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
uncharacterized protein LOC105386764 isoform X2
uncharacterized protein LOC105386764 isoform X3
uncharacterized protein LOC105386764 isoform X4
uncharacterized protein LOC105386764 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
putative nuclease HARBI1, transcript variant X1
putative nuclease HARBI1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
probable basic-leucine zipper transcription factor N, 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 22 samples with support for all annotated introns
probable basic-leucine zipper transcription factor N, 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 83 samples with support for all annotated introns
probable basic-leucine zipper transcription factor N, 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 67 samples with support for all annotated introns
probable basic-leucine zipper transcription factor N
uncharacterized LOC125490134, 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 56 samples with support for all annotated introns
uncharacterized LOC125490134, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
guanine nucleotide-binding protein G(s) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(s) subunit alpha, transcript variant X1
guanine nucleotide-binding protein G(s) subunit alpha
RNA-binding protein fusilli, transcript variant X1
RNA-binding protein fusilli, transcript variant X2
RNA-binding protein fusilli, transcript variant X4
RNA-binding protein fusilli, transcript variant X3
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 57 samples with support for all annotated introns
nuclear transcription factor Y subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
PHAF1 protein CG7083, transcript variant X1
PHAF1 protein CG7083, transcript variant X2
G patch domain-containing protein 1 homolog, transcript variant X2
G patch domain-containing protein 1 homolog, transcript variant X1
G patch domain-containing protein 1 homolog isoform X2
G patch domain-containing protein 1 homolog isoform X1
mediator of RNA polymerase II transcription subunit 25, transcript variant X2
mediator of RNA polymerase II transcription subunit 25, transcript variant X1
mediator of RNA polymerase II transcription subunit 25, transcript variant X4
mediator of RNA polymerase II transcription subunit 25, transcript variant X3
mediator of RNA polymerase II transcription subunit 25 isoform X1
mediator of RNA polymerase II transcription subunit 25 isoform X3
mediator of RNA polymerase II transcription subunit 25 isoform X2
mediator of RNA polymerase II transcription subunit 25 isoform X4
transmembrane protein 68, transcript variant X2
transmembrane protein 68, transcript variant X3
transmembrane protein 68, transcript variant X1
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein, transcript variant X1
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein, transcript variant X3
uncharacterized protein LOC105388873 isoform X2
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein isoform X1
malonate--CoA ligase ACSF3, mitochondrial
probable sodium-coupled neutral amino acid transporter 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
thyroid transcription factor 1-associated protein 26
ornithine decarboxylase 1, transcript variant X2
ornithine decarboxylase 1, transcript variant X1
ornithine decarboxylase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
origin recognition complex subunit 6, transcript variant X1
origin recognition complex subunit 6, transcript variant X2
origin recognition complex subunit 6 isoform X1
origin recognition complex subunit 6 isoform 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 42 samples with support for all annotated introns
uncharacterized LOC119691363, transcript variant X2
uncharacterized LOC119691363, transcript variant X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sodium/hydrogen exchanger 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 72% 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 6 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
uncharacterized LOC105396748, transcript variant X2
uncharacterized LOC105396748, transcript variant X1
uncharacterized protein LOC105396748 isoform X1
uncharacterized protein LOC105396748 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
uncharacterized LOC119691725, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC119691725, transcript variant X1
uncharacterized LOC119691716, transcript variant X1
uncharacterized LOC119691716, 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
putative odorant receptor 71a, transcript variant X2
putative odorant receptor 71a, transcript variant X3
putative odorant receptor 71a, transcript variant X1
uncharacterized protein LOC119694057 isoform X3
putative odorant receptor 71a isoform X1
odorant receptor Or2-like, transcript variant X2
odorant receptor Or2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
odorant receptor Or2-like, transcript variant X3
uncharacterized LOC119691684, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC119691684, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase domain-containing protein 1, transcript variant X1
protein tyrosine phosphatase domain-containing protein 1, transcript variant X2
protein tyrosine phosphatase domain-containing protein 1 isoform X1
protein tyrosine phosphatase domain-containing protein 1 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
LOW QUALITY PROTEIN: ornithine decarboxylase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 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 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
phosphoenolpyruvate carboxykinase [GTP], transcript variant X2
phosphoenolpyruvate carboxykinase [GTP], transcript variant X4
phosphoenolpyruvate carboxykinase [GTP], transcript variant X3
phosphoenolpyruvate carboxykinase [GTP] isoform X2
phosphoenolpyruvate carboxykinase [GTP], transcript variant X1
phosphoenolpyruvate carboxykinase [GTP] isoform 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 74 samples with support for all annotated introns
mitochondrial import inner membrane translocase subunit Tim23
stromal membrane-associated protein 1, transcript variant X2
stromal membrane-associated protein 1, transcript variant X1
stromal membrane-associated protein 1 isoform X2
stromal membrane-associated protein 1 isoform X1
phosphoinositide 3-kinase regulatory subunit 4
serine/arginine repetitive matrix protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase Fkbp12
uncharacterized LOC105380951, transcript variant X1
uncharacterized LOC105380951, transcript variant X2
cytochrome b-c1 complex subunit 1, mitochondrial-like
uncharacterized LOC105380983, transcript variant X1
uncharacterized LOC105380983, transcript variant X3
uncharacterized LOC105380983, transcript variant X2
uncharacterized LOC105380983, transcript variant X6
uncharacterized LOC105380983, transcript variant X7
uncharacterized LOC105380983, transcript variant X5
uncharacterized LOC105380983, transcript variant X4
uncharacterized protein LOC105380983 isoform X1
uncharacterized protein LOC105380983 isoform X3
uncharacterized protein LOC105380983 isoform X2
uncharacterized protein LOC105380983 isoform X6
uncharacterized protein LOC105380983 isoform X7
uncharacterized protein LOC105380983 isoform X5
uncharacterized protein LOC105380983 isoform X4
uncharacterized LOC105380983, transcript variant X8
uncharacterized protein LOC105380983 isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 2 subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
probable phenylalanine--tRNA ligase, mitochondrial, transcript variant X1
probable phenylalanine--tRNA ligase, mitochondrial, transcript variant X2
probable phenylalanine--tRNA ligase, mitochondrial, transcript variant X3
probable phenylalanine--tRNA ligase, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC105385997
far upstream element-binding protein 3, transcript variant X8
far upstream element-binding protein 3, transcript variant X7
far upstream element-binding protein 3, transcript variant X5
far upstream element-binding protein 3, transcript variant X4
far upstream element-binding protein 3, transcript variant X2
far upstream element-binding protein 3, transcript variant X6
far upstream element-binding protein 3, transcript variant X3
far upstream element-binding protein 3, transcript variant X1
far upstream element-binding protein 3 isoform X8
far upstream element-binding protein 3 isoform X7
far upstream element-binding protein 3 isoform X5
far upstream element-binding protein 3 isoform X4
far upstream element-binding protein 3 isoform X2
far upstream element-binding protein 3 isoform X6
far upstream element-binding protein 3 isoform X3
far upstream element-binding protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125490081, transcript variant X2
uncharacterized LOC125490081, transcript variant X1
uncharacterized protein LOC125490081 isoform X2
uncharacterized protein LOC125490081 isoform X1
uncharacterized LOC105393821, transcript variant X4
uncharacterized LOC105393821, transcript variant X3
uncharacterized LOC105393821, transcript variant X1
uncharacterized LOC105393821, 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 25 samples with support for all annotated introns
uncharacterized protein LOC105393821 isoform X4
uncharacterized protein LOC105393821 isoform X3
uncharacterized protein LOC105393821 isoform X1
uncharacterized protein LOC105393821 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
sodium-dependent noradrenaline transporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 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 99% coverage of the annotated genomic feature by RNAseq alignments
bifunctional peptidase and (3S)-lysyl hydroxylase Jmjd7
transmembrane protein 165, transcript variant X2
transmembrane protein 165, transcript variant X3
transmembrane protein 165, 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 31 samples with support for all annotated introns
UDP-glucose 4-epimerase, transcript variant X1
UDP-glucose 4-epimerase, transcript variant X2
40S ribosomal protein S7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305503.1
annotated by transcript or proteomic data
The RefSeq transcript has 6 substitutions and aligns at 97% coverage 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.
probable peroxisomal membrane protein PEX13
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 85 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 33, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 33, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 33 isoform X1
ubiquitin carboxyl-terminal hydrolase 33 isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 1, transcript variant X2
A disintegrin and metalloproteinase with thrombospondin motifs 1, transcript variant X1
A disintegrin and metalloproteinase with thrombospondin motifs 1, transcript variant X3
A disintegrin and metalloproteinase with thrombospondin motifs 1 isoform X3
A disintegrin and metalloproteinase with thrombospondin motifs 1 isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 1 isoform X1
tRNA N(3)-methylcytidine methyltransferase METTL6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
small nucleolar RNA snR60/Z15/Z230/Z193/J17
COORDINATES: nucleotide motif:Rfam:12.0:RF00309
tRNA N(3)-methylcytidine methyltransferase METTL6
glutamate--cysteine ligase regulatory subunit
uncharacterized LOC119690310, 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 30 samples with support for all annotated introns
uncharacterized LOC119690310, transcript variant X2
uncharacterized protein LOC119690310 isoform X1
uncharacterized protein LOC119690310 isoform X2
BSD domain-containing protein 1-B, transcript variant X2
BSD domain-containing protein 1-B, transcript variant X1
BSD domain-containing protein 1-B isoform X1
BSD domain-containing protein 1-B isoform X2
vesicular inhibitory amino acid transporter
DNA polymerase interacting tetratricopeptide repeat-containing, protein of 47 kDa
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9
N6-adenosine-methyltransferase subunit METTL3
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 24 samples with support for all annotated introns
dual specificity protein phosphatase CDC14AB, transcript variant X1
dual specificity protein phosphatase CDC14AB, transcript variant X3
dual specificity protein phosphatase CDC14AB, transcript variant X5
dual specificity protein phosphatase CDC14AB, transcript variant X4
dual specificity protein phosphatase CDC14AB isoform X1
dual specificity protein phosphatase CDC14AB isoform X2
dual specificity protein phosphatase CDC14AB isoform X3
dual specificity protein phosphatase CDC14AB, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
dual specificity protein phosphatase CDC14AB, transcript variant X6
40S ribosomal protein S12; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
40S ribosomal protein S12, transcript variant X1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305530.1
The RefSeq transcript has 6 substitutions, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
zinc finger MYND domain-containing protein 10
transcription factor AP-2-epsilon, transcript variant X1
transcription factor AP-2-epsilon, transcript variant X2
transcription factor AP-2-epsilon, transcript variant X3
transcription factor AP-2-epsilon isoform X2
transcription factor AP-2-epsilon isoform X1
transcription factor AP-2-epsilon isoform X3
proteasome subunit beta type-5, transcript variant X2
proteasome subunit beta type-5, transcript variant X1
proteasome subunit beta type-5 isoform X2
proteasome subunit beta type-5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
retinaldehyde-binding protein 1-like, transcript variant X1
retinaldehyde-binding protein 1-like, transcript variant X2
sister chromatid cohesion protein PDS5 homolog B
solute carrier family 2, facilitated glucose transporter member 8
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 32 samples with support for all annotated introns
mannose-1-phosphate guanyltransferase alpha-B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
uncharacterized LOC105384668, transcript variant X1
uncharacterized LOC105384668, transcript variant X2
uncharacterized LOC105384683, 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 10 samples with support for all annotated introns
uncharacterized LOC105384683, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC105384683 isoform X1
uncharacterized protein LOC105384683 isoform X2
nuclear inhibitor of protein phosphatase 1
MRG/MORF4L-binding protein, 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 39 samples with support for all annotated introns
MRG/MORF4L-binding protein, 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 63 samples with support for all annotated introns
MRG/MORF4L-binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
MRG/MORF4L-binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125490142, transcript variant X1
uncharacterized LOC125490142, transcript variant X2
nucleolar protein 4, transcript variant X1
nucleolar protein 4, transcript variant X4
nucleolar protein 4, transcript variant X5
nucleolar protein 4, transcript variant X6
nucleolar protein 4, transcript variant X3
nucleolar protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
intraflagellar transport protein 52 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
stress-associated endoplasmic reticulum protein 2, transcript variant X1
stress-associated endoplasmic reticulum protein 2, transcript variant X2
stress-associated endoplasmic reticulum protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit gamma
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 28 samples with support for all annotated introns
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
tRNA (cytosine(34)-C(5))-methyltransferase
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 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
organic cation transporter 1, transcript variant X2
organic cation transporter 1, transcript variant X1
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC105380782, transcript variant X2
uncharacterized LOC105380782, transcript variant X1
uncharacterized protein LOC105380782 isoform X1
uncharacterized protein LOC105380782 isoform X2
uncharacterized protein F54H12.2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
uncharacterized protein F54H12.2-like, transcript variant X3
uncharacterized protein F54H12.2-like, transcript variant X1
uncharacterized protein F54H12.2-like, transcript variant X2
uncharacterized protein LOC105386391 isoform X1
uncharacterized protein LOC105386391 isoform X2
uncharacterized protein F54H12.2-like isoform X3
facilitated trehalose transporter Tret1-1
long-chain fatty acid transport protein 1
glycosylphosphatidylinositol anchor attachment 1 protein, transcript variant X2
glycosylphosphatidylinositol anchor attachment 1 protein, transcript variant X1
glycosylphosphatidylinositol anchor attachment 1 protein isoform X2
glycosylphosphatidylinositol anchor attachment 1 protein 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 58 samples with support for all annotated introns
serine protease inhibitor dipetalogastin
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 61 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 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 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 2 samples with support for all annotated introns
reticulon-4-interacting protein 1, mitochondrial
uncharacterized LOC105392188, transcript variant X1
uncharacterized LOC105392188, transcript variant X3
uncharacterized LOC105392188, transcript variant X2
uncharacterized protein LOC105392188 isoform X1
uncharacterized protein LOC105392188 isoform X2
facilitated trehalose transporter Tret1-2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized peptidase C1-like protein F26E4.3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
uncharacterized peptidase C1-like protein F26E4.3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized peptidase C1-like protein F26E4.3 isoform X2
uncharacterized peptidase C1-like protein F26E4.3 isoform X1
coiled-coil-helix-coiled-coil-helix domain-containing protein 7
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 44 samples with support for all annotated introns
partitioning defective 6 homolog beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
partitioning defective 6 homolog beta, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
partitioning defective 6 homolog beta, transcript variant X1
partitioning defective 6 homolog beta, transcript variant X3
partitioning defective protein 6 isoform X1
partitioning defective 6 homolog beta isoform X2
partitioning defective protein 6 isoform X3
partitioning defective protein 6 isoform X4
dual specificity protein phosphatase 23, transcript variant X2
dual specificity protein phosphatase 23 isoform X2
dual specificity protein phosphatase 23, transcript variant X1
dual specificity protein phosphatase 23 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 9
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: 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 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 4 samples with support for all annotated introns
ecdysone oxidase-like, transcript variant X1
ecdysone oxidase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% 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 79 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 26
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 59 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
RB-associated KRAB zinc finger protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
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: 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
guanine nucleotide exchange factor MSS4 homolog
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 85 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 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: 1 Protein, 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125490085, transcript variant X2
uncharacterized LOC125490085, transcript variant X1
transmembrane protein 234 homolog, transcript variant X1
transmembrane protein 234 homolog, transcript variant X2
transmembrane protein 234 homolog isoform X2
transmembrane protein 234 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
cytochrome c oxidase subunit 4 isoform 1, mitochondrial, transcript variant X3
cytochrome c oxidase subunit 4 isoform 1, mitochondrial, transcript variant X2
cytochrome c oxidase subunit 4 isoform 1, mitochondrial, transcript variant X1
cytochrome c oxidase subunit 4 isoform 1, mitochondrial isoform X2
cytochrome c oxidase subunit 4 isoform 1, mitochondrial isoform X1
cytochrome c oxidase subunit 4 isoform 1, mitochondrial isoform X3
cytochrome c oxidase subunit 4 isoform 1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 45% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylation factor-like protein 6, transcript variant X2
ADP-ribosylation factor-like protein 6, transcript variant X1
chondroitin sulfate glucuronyltransferase
influenza virus NS1A-binding protein homolog A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns