Plutella xylostella chromosome 30, 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\nOW026581.1.\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.
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
COORDINATES: polyA evidence [ECO:0006239]
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 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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 EST, 44 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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: 8 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon AGG); 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 97% coverage of the annotated genomic feature by RNAseq alignments
ribosomal RNA processing protein 1 homolog
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
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 26 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 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 12 samples with support for all annotated introns
zinc finger protein 664, 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 33 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
zinc finger protein OZF, transcript variant X1
zinc finger protein OZF, transcript variant X2
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: 1 EST, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
scavenger receptor class B member 1, transcript variant X2
scavenger receptor class B member 1 isoform X2
scavenger receptor class B member 1, transcript variant X1
scavenger receptor class B member 1 isoform X1
uncharacterized LOC105392437, transcript variant X2
uncharacterized LOC105392437, transcript variant X1
uncharacterized protein LOC105392437 isoform X2
uncharacterized protein LOC105392437 isoform X1
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
uncharacterized LOC105392431, transcript variant X1
uncharacterized LOC105392431, transcript variant X3
uncharacterized LOC105392431, transcript variant X2
uncharacterized protein LOC105392431 isoform X1
uncharacterized protein LOC105392431 isoform X2
fatty acyl-CoA reductase wat, transcript variant X2
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 50 samples with support for all annotated introns
fatty acyl-CoA reductase wat, transcript variant X1
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 3 samples with support for all annotated introns
zinc transporter ZIP9, transcript variant X2
zinc transporter ZIP9, transcript variant X1
putative fatty acyl-CoA reductase CG5065
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fatty acyl-CoA reductase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
fatty acyl-CoA reductase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 54% 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 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 4 samples with support for all annotated introns
stress response protein NST1, transcript variant X2
stress response protein NST1, transcript variant X1
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 23 samples with support for all annotated introns
putative fatty acyl-CoA reductase CG5065, transcript variant X2
putative fatty acyl-CoA reductase CG5065, transcript variant X3
putative fatty acyl-CoA reductase CG5065, transcript variant X4
putative fatty acyl-CoA reductase CG5065, transcript variant X1
putative fatty acyl-CoA reductase CG5065 isoform X2
putative fatty acyl-CoA reductase CG5065 isoform X1
putative fatty acyl-CoA reductase CG5065, transcript variant X5
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 32 samples with support for all annotated introns
putative fatty acyl-CoA reductase CG5065 isoform X3
zinc finger protein 436, 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 40 samples with support for all annotated introns
zinc finger protein 436, transcript variant X1
zinc finger protein 436, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
protein suppressor of forked, 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 2 samples with support for all annotated introns
protein suppressor of forked, transcript variant X4
protein suppressor of forked, 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 2 samples with support for all annotated introns
protein suppressor of forked, 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
protein suppressor of forked, 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 2 samples with support for all annotated introns
mitogen-activated protein kinase-binding protein 1
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
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
extracellular serine/threonine protein kinase four-jointed
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
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
peroxisomal biogenesis factor 19, transcript variant X2
peroxisomal biogenesis factor 19, transcript variant X1
peroxisomal biogenesis factor 19 isoform X1
peroxisomal biogenesis factor 19 isoform X2
ubiquitin-fold modifier-conjugating enzyme 1
NADH-ubiquinone oxidoreductase 49 kDa subunit, transcript variant X2
NADH-ubiquinone oxidoreductase 49 kDa subunit, transcript variant X1
NADH-ubiquinone oxidoreductase 49 kDa subunit isoform X2
NADH-ubiquinone oxidoreductase 49 kDa subunit isoform X1
U6 snRNA-associated Sm-like protein LSm2
leucine-rich repeat neuronal protein 3, 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 36 samples with support for all annotated introns
leucine-rich repeat neuronal protein 3, 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 42 samples with support for all annotated introns
leucine-rich repeat neuronal protein 3, transcript variant X4
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 39 samples with support for all annotated introns
leucine-rich repeat neuronal protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
leucine-rich repeat neuronal protein 3 isoform X2
leucine-rich repeat neuronal protein 3 isoform X1
acidic fibroblast growth factor intracellular-binding protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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 2 samples with support for all annotated introns
lysosome membrane protein 2, transcript variant X1
lysosome membrane protein 2, transcript variant X2
sphingolipid delta(4)-desaturase DES1, transcript variant X2
sphingolipid delta(4)-desaturase DES1 isoform X2
sphingolipid delta(4)-desaturase DES1, 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 71 samples with support for all annotated introns
sphingolipid delta(4)-desaturase DES1 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 28 samples with support for all annotated introns
cysteine and glycine-rich protein 3, transcript variant X1
cysteine and glycine-rich protein 3, transcript variant X2
uncharacterized protein LOC105385493 isoform X1
cysteine and glycine-rich protein 3 isoform X2
43 kDa receptor-associated protein of the synapse homolog
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
myoblast determination protein 1 homolog
isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial, transcript variant X2
isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial, transcript variant X3
isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial, transcript variant X1
isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial isoform X2
isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial isoform X3
isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial isoform X1
transcriptional repressor protein YY1, transcript variant X1
transcriptional repressor protein YY1, transcript variant X2
transcriptional repressor protein YY1, transcript variant X4
transcriptional repressor protein YY1, transcript variant X5
transcriptional repressor protein YY1, transcript variant X3
transcriptional repressor protein YY1, transcript variant X6
transcriptional repressor protein YY1 isoform X1
transcriptional repressor protein YY1 isoform X5
transcriptional repressor protein YY1 isoform X3
transcriptional repressor protein YY1 isoform X6
transcriptional repressor protein YY1 isoform X2
transcriptional repressor protein YY1 isoform X4
transcriptional repressor protein YY1, transcript variant X7
transcriptional repressor protein YY1 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
scavenger receptor class B member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
scavenger receptor class B member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
scavenger receptor class B member 1-like isoform X1
scavenger receptor class B member 1-like isoform 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 18 samples with support for all annotated introns
transfer RNA leucine (anticodon UAG); 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: 1 Protein, 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC125491072, transcript variant X4
uncharacterized LOC125491072, transcript variant X3
uncharacterized LOC125491072, transcript variant X1
uncharacterized LOC125491072, transcript variant X2
zinc finger protein 709, transcript variant X1
zinc finger protein 709, 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 57 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
vacuolar protein sorting-associated protein 37A
uncharacterized LOC105381513, transcript variant X2
uncharacterized LOC105381513, transcript variant X1
uncharacterized protein LOC105381513 isoform X1
uncharacterized protein LOC105381513 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 18 samples with support for all annotated introns
putative nuclease HARBI1, transcript variant X1
putative nuclease HARBI1, transcript variant X2
arginine-hydroxylase NDUFAF5, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC105381494, transcript variant X2
uncharacterized LOC105381494, transcript variant X1
uncharacterized LOC105381494, transcript variant X4
uncharacterized LOC105381494, transcript variant X5
uncharacterized LOC105381494, transcript variant X3
uncharacterized protein LOC105381494 isoform X2
uncharacterized protein LOC105381494 isoform X3
uncharacterized protein LOC105381494 isoform X1
putative fatty acyl-CoA reductase CG8306, transcript variant X2
putative fatty acyl-CoA reductase CG8306, 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 10 samples with support for all annotated introns
putative fatty acyl-CoA reductase CG8306
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 79 samples with support for all annotated introns
uncharacterized LOC105381502, transcript variant X2
uncharacterized LOC105381502, transcript variant X1
uncharacterized protein LOC105381502 isoform X1
uncharacterized protein LOC105381502 isoform X2
probable U3 small nucleolar RNA-associated protein 11
uncharacterized LOC125491045, transcript variant X1
uncharacterized LOC125491045, 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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
nitrilase and fragile histidine triad fusion protein NitFhit, transcript variant X1
nitrilase and fragile histidine triad fusion protein NitFhit, transcript variant X2
nitrilase and fragile histidine triad fusion protein NitFhit isoform X1
nitrilase and fragile histidine triad fusion protein NitFhit isoform X2
uncharacterized LOC125491038, transcript variant X2
uncharacterized LOC125491038, transcript variant X3
uncharacterized LOC125491038, transcript variant X1
uncharacterized protein LOC125491038 isoform X2
uncharacterized protein LOC125491038 isoform X1
uncharacterized LOC125491038, 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 37 samples with support for all annotated introns
uncharacterized protein LOC125491038 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 86% 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 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC125491040, transcript variant X2
uncharacterized LOC125491040, transcript variant X1
nitrilase and fragile histidine triad fusion protein NitFhit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 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: 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: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 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 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 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
tau-tubulin kinase homolog Asator, transcript variant X6
tau-tubulin kinase homolog Asator, transcript variant X3
tau-tubulin kinase homolog Asator, transcript variant X5
tau-tubulin kinase homolog Asator, transcript variant X4
tau-tubulin kinase homolog Asator, transcript variant X2
tau-tubulin kinase homolog Asator, transcript variant X1
tau-tubulin kinase homolog Asator, transcript variant X7
serine/arginine repetitive matrix protein 1 isoform X5
serine/arginine repetitive matrix protein 1 isoform X4
serine/arginine repetitive matrix protein 1 isoform X3
serine/arginine repetitive matrix protein 1 isoform X2
serine/arginine repetitive matrix protein 1 isoform X1
tau-tubulin kinase homolog Asator isoform X6
piggyBac transposable element-derived protein 4
zinc finger protein 729, transcript variant X1
zinc finger protein 729, transcript variant X3
zinc finger protein 729, transcript variant X2
DENN domain-containing protein 2A, transcript variant X1
uncharacterized protein LOC105393138 isoform X1
DENN domain-containing protein 2A, transcript variant X2
DENN domain-containing protein 2A 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
choline/ethanolamine kinase, transcript variant X2
choline/ethanolamine kinase, transcript variant X4
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 47 samples with support for all annotated introns
choline/ethanolamine kinase, 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 51 samples with support for all annotated introns
choline/ethanolamine kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 21 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
leucine-rich repeat-containing protein 34
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
GTPase-activating protein CdGAPr, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
GTPase-activating protein CdGAPr, transcript variant X6
GTPase-activating protein CdGAPr, transcript variant X1
GTPase-activating protein CdGAPr, transcript variant X2
GTPase-activating protein CdGAPr isoform X1
GTPase-activating protein CdGAPr isoform X6
GTPase-activating protein CdGAPr isoform X2
GTPase-activating protein CdGAPr isoform X3
GTPase-activating protein CdGAPr, transcript variant X5
GTPase-activating protein CdGAPr, transcript variant X4
GTPase-activating protein CdGAPr isoform X5
GTPase-activating protein CdGAPr 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
uncharacterized LOC105383173, transcript variant X2
uncharacterized LOC105383173, transcript variant X1
uncharacterized protein C1orf198 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 80 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 40 samples with support for all annotated introns
breast cancer type 2 susceptibility protein homolog
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
glycogen [starch] synthase, transcript variant X2
glycogen [starch] synthase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60% 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 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 6 samples with support for all annotated introns
carcinine transporter, transcript variant X2
carcinine transporter, transcript variant X4
carcinine transporter, transcript variant X3
carcinine transporter, 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
sorting and assembly machinery component 50 homolog A
putative tRNA pseudouridine synthase Pus10
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 25 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 94% coverage of the annotated genomic feature by RNAseq alignments
toll-like receptor 6, transcript variant X2
toll-like receptor 6, transcript variant X4
toll-like receptor 6, transcript variant X3
toll-like receptor 6, transcript variant X1
toll-like receptor 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
leucine-rich repeat-containing G-protein coupled receptor 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
protein PAT1 homolog 1, transcript variant X1
protein PAT1 homolog 1, transcript variant X2
protein PAT1 homolog 1, transcript variant X3
uncharacterized LOC119690408, transcript variant X1
uncharacterized LOC119690408, transcript variant X2
uncharacterized protein LOC119690408 isoform X1
uncharacterized protein LOC119690408 isoform X2
juvenile hormone esterase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 EST, 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
juvenile hormone esterase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 EST, 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
juvenile hormone esterase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 EST, 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
juvenile hormone esterase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 EST, 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
uncharacterized LOC105397166, transcript variant X2
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, including 32 samples with support for all annotated introns
uncharacterized LOC105397166, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized protein LOC105397166 isoform X2
uncharacterized protein LOC105397166 isoform X1
probable multidrug resistance-associated protein lethal(2)03659
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 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: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
TBC1 domain family member 1, transcript variant X3
TBC1 domain family member 1, transcript variant X1
TBC1 domain family member 1, transcript variant X2
TBC1 domain family member 1, transcript variant X4
TBC1 domain family member 1, transcript variant X5
TBC1 domain family member 1, transcript variant X6
scavenger receptor class B member 1, transcript variant X3
scavenger receptor class B member 1 isoform X3
uncharacterized LOC105395237, transcript variant X1
uncharacterized protein LOC105395237 isoform X1
uncharacterized LOC105395237, transcript variant X3
uncharacterized LOC105395237, transcript variant X2
uncharacterized protein LOC105395237 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 20 samples with support for all annotated introns
organic cation transporter protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
organic cation transporter protein isoform X2
organic cation transporter protein, transcript variant X1
organic cation transporter protein isoform X1
ubiquitin carboxyl-terminal hydrolase 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 80 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
uncharacterized LOC105389016, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC105389016, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC105389016, 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 6 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 13
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 67 samples with support for all annotated introns
serine/threonine-protein kinase SIK3, transcript variant X2
serine/threonine-protein kinase SIK3, transcript variant X4
serine/threonine-protein kinase SIK3, transcript variant X1
serine/threonine-protein kinase SIK3, transcript variant X3
serine/threonine-protein kinase par-1 isoform X2
serine/threonine-protein kinase SIK3 isoform X4
serine/threonine-protein kinase par-1 isoform X1
serine/threonine-protein kinase par-1 isoform X3
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC105391040, transcript variant X1
uncharacterized LOC105391040, transcript variant X2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3
uncharacterized LOC105389552, transcript variant X3
uncharacterized LOC105389552, transcript variant X4
uncharacterized LOC105389552, transcript variant X2
uncharacterized protein LOC105389552 isoform X2
uncharacterized LOC105389552, transcript variant X1
uncharacterized protein LOC105389552 isoform X1
transposon Tf2-1 polyprotein, transcript variant X4
transposon Tf2-1 polyprotein, transcript variant X3
transposon Tf2-1 polyprotein, transcript variant X2
transposon Tf2-1 polyprotein, transcript variant X1
uncharacterized protein LOC105383898 isoform X4
uncharacterized protein LOC105383898 isoform X2
uncharacterized protein LOC105383898 isoform X1
uncharacterized protein LOC105383898 isoform X3