Plutella xylostella chromosome 22, 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\nOW026556.1.\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.
glycogen debranching enzyme, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
glycogen debranching enzyme, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
glycogen debranching enzyme, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
radial spoke head protein 3 homolog B, 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 6 samples with support for all annotated introns
radial spoke head protein 3 homolog B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
radial spoke head protein 3 homolog B isoform X2
radial spoke head protein 3 homolog B 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 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC105382134, transcript variant X3
uncharacterized LOC105382134, transcript variant X2
uncharacterized LOC105382134, transcript variant X4
uncharacterized LOC105382134, transcript variant X1
uncharacterized LOC105382132, transcript variant X1
uncharacterized LOC105382132, transcript variant X3
uncharacterized LOC105382132, transcript variant X2
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, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119693454, transcript variant X1
uncharacterized LOC119693454, transcript variant X2
uncharacterized protein LOC119693454 isoform X1
uncharacterized protein LOC119693454 isoform X2
glutenin, high molecular weight subunit DX5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% 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 32 samples with support for all annotated introns
probable basic-leucine zipper transcription factor I
glutenin, high molecular weight subunit 12
transposon Ty3-I Gag-Pol polyprotein, 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 17 samples with support for all annotated introns
transposon Ty3-I Gag-Pol polyprotein, transcript variant X2
transposon Ty3-I Gag-Pol polyprotein, 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 7 samples with support for all annotated introns
uncharacterized protein LOC119693540 isoform X2
uncharacterized protein LOC119693540 isoform X1
uncharacterized LOC105382126, 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 41 samples with support for all annotated introns
uncharacterized LOC105382126, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA Delta(11) desaturase, transcript variant X2
acyl-CoA Delta(11) desaturase, transcript variant X4
acyl-CoA Delta(11) desaturase, transcript variant X3
acyl-CoA Delta(11) desaturase, transcript variant X1
acyl-CoA Delta(11) desaturase, transcript variant X6
acyl-CoA Delta(11) desaturase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
elongation of very long chain fatty acids protein 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 134 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: 72% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
glutamate receptor-interacting protein 2
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
piggyBac transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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
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
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 39 samples with support for all annotated introns
odorant receptor Or2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
odorant receptor Or2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
dual specificity protein kinase splB, 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 25 samples with support for all annotated introns
dual specificity protein kinase splB, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
dual specificity protein kinase splB isoform X1
dual specificity protein kinase splB isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
MATH and LRR domain-containing protein PFE0570w
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
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 27 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 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: 5 Proteins
basic helix-loop-helix neural transcription factor TAP
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
uncharacterized protein ZK1073.1, 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 30 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X7
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 30 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X6
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 23 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X5
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 29 samples with support for all annotated introns
uncharacterized protein ZK1073.1, 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 10 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X3
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 83 samples with support for all annotated introns
uncharacterized protein ZK1073.1 isoform X7
uncharacterized protein ZK1073.1 isoform X6
uncharacterized protein ZK1073.1 isoform X5
uncharacterized protein ZK1073.1 isoform X4
uncharacterized protein ZK1073.1 isoform X2
uncharacterized protein ZK1073.1 isoform X8
uncharacterized protein ZK1073.1 isoform X3
uncharacterized protein ZK1073.1 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
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
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
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 15 samples with support for all annotated introns
rap1 GTPase-GDP dissociation stimulator 1-B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
cAMP-specific 3',5'-cyclic phosphodiesterase, isoforms N/G, transcript variant X1
cAMP-specific 3',5'-cyclic phosphodiesterase, isoforms N/G, transcript variant X3
cAMP-specific 3',5'-cyclic phosphodiesterase, isoforms N/G, transcript variant X2
cAMP-specific 3',5'-cyclic phosphodiesterase, isoforms N/G, transcript variant X4
cAMP-specific 3',5'-cyclic phosphodiesterase isoform X3
cAMP-specific 3',5'-cyclic phosphodiesterase isoform X2
cAMP-specific 3',5'-cyclic phosphodiesterase isoform X1
cAMP-specific 3',5'-cyclic phosphodiesterase, isoforms N/G isoform X4
cAMP-specific 3',5'-cyclic phosphodiesterase-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
cAMP-specific 3',5'-cyclic phosphodiesterase-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 9 samples with support for all annotated introns
cAMP-specific 3',5'-cyclic phosphodiesterase-like isoform X2
cAMP-specific 3',5'-cyclic phosphodiesterase-like, transcript variant X1
cAMP-specific 3',5'-cyclic phosphodiesterase-like 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 11 samples with support for all annotated introns
cAMP-specific 3',5'-cyclic phosphodiesterase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
uncharacterized LOC125490333, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized LOC125490333, 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 10 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 7
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 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 75 samples with support for all annotated introns
prothoracicotropic hormone-like, transcript variant X1
prothoracicotropic hormone-like, transcript variant X3
prothoracicotropic hormone-like isoform X1
prothoracicotropic hormone-like isoform X3
prothoracicotropic hormone-like, transcript variant X2
prothoracicotropic hormone-like isoform X2
zinc finger protein 84, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
zinc finger protein 84, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 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 96% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 484, transcript variant X2
zinc finger protein 484, transcript variant X1
zinc finger protein 484, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
zinc finger protein 484, 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 48 samples with support for all annotated introns
putative ATPase N2B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 82 samples with support for all annotated introns
putative ATPase N2B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
putative ATPase N2B, transcript variant X3
putative ATPase N2B, transcript variant X4
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 81 samples with support for all annotated introns
general transcription factor IIE subunit 1, transcript variant X1
general transcription factor IIE subunit 1, transcript variant X2
general transcription factor IIE subunit 1 isoform X2
general transcription factor IIE subunit 1 isoform X1
tyrosine-protein kinase transmembrane receptor Ror2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 ESTs, 131 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial
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 26 samples with support for all annotated introns
polyamine-transporting ATPase 13A3, transcript variant X1
polyamine-transporting ATPase 13A3, transcript variant X5
polyamine-transporting ATPase 13A3, transcript variant X6
polyamine-transporting ATPase 13A3, transcript variant X2
polyamine-transporting ATPase 13A3, transcript variant X3
polyamine-transporting ATPase 13A3, transcript variant X4
polyamine-transporting ATPase 13A3, transcript variant X7
polyamine-transporting ATPase 13A3, transcript variant X8
polyamine-transporting ATPase 13A3 isoform X1
polyamine-transporting ATPase 13A3 isoform X5
polyamine-transporting ATPase 13A3 isoform X6
polyamine-transporting ATPase 13A3 isoform X2
polyamine-transporting ATPase 13A3 isoform X3
polyamine-transporting ATPase 13A3 isoform X4
polyamine-transporting ATPase 13A3 isoform X7
polyamine-transporting ATPase 13A3 isoform X8
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 17 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit G, transcript variant X1
eukaryotic translation initiation factor 3 subunit G, transcript variant X2
eukaryotic translation initiation factor 3 subunit G
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB1
protein lethal(3)malignant blood neoplasm 1
endocuticle structural glycoprotein SgAbd-5-like
endocuticle structural glycoprotein SgAbd-5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
endocuticle structural glycoprotein SgAbd-5-like, transcript variant X2
endocuticle structural glycoprotein SgAbd-5-like, transcript variant X1
endocuticle structural glycoprotein SgAbd-5-like isoform X2
endocuticle structural glycoprotein SgAbd-5-like isoform X1
endocuticle structural glycoprotein SgAbd-5, transcript variant X1
endocuticle structural glycoprotein SgAbd-5, transcript variant X2
endocuticle structural glycoprotein SgAbd-5 isoform X1
endocuticle structural glycoprotein SgAbd-5 isoform X2
uncharacterized LOC125490324, transcript variant X1
uncharacterized protein LOC125490324 isoform X1
uncharacterized LOC125490324, transcript variant X3
uncharacterized protein LOC125490324 isoform X3
uncharacterized LOC125490324, transcript variant X2
uncharacterized protein LOC125490324 isoform X2
endocuticle structural glycoprotein SgAbd-2
endocuticle structural glycoprotein ABD-4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
probable dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 3
magnesium transporter protein 1, 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
magnesium transporter protein 1, 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 14 samples with support for all annotated introns
magnesium transporter protein 1 isoform X1
probable inactive protein kinase DDB_G0270444
endocuticle structural glycoprotein SgAbd-8-like
endocuticle structural glycoprotein ABD-4-like
coiled-coil domain-containing protein 6, transcript variant X2
coiled-coil domain-containing protein 6, transcript variant X1
coiled-coil domain-containing protein 6 isoform X2
coiled-coil domain-containing protein 6 isoform X1
serine/arginine repetitive matrix protein 1, transcript variant X1
serine/arginine repetitive matrix protein 1, transcript variant X3
serine/arginine repetitive matrix protein 1, transcript variant X4
serine/arginine repetitive matrix protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 81 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1 isoform X1
serine/arginine repetitive matrix protein 1 isoform X2
serine/arginine repetitive matrix protein 1 isoform X3
serine/arginine repetitive matrix protein 1, transcript variant X5
peptidyl-prolyl cis-trans isomerase G isoform X4
pupal cuticle protein Edg-91, transcript variant X1
pupal cuticle protein Edg-91, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105384182, transcript variant X3
uncharacterized LOC105384182, transcript variant X2
uncharacterized LOC105384182, transcript variant X1
uncharacterized protein LOC105384182 isoform X3
uncharacterized protein LOC105384182 isoform X2
uncharacterized protein LOC105384182 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, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 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: 5 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: 2 Proteins
protein odr-4 homolog, transcript variant X2
protein odr-4 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 80 samples with support for all annotated introns
protein still life, isoform SIF type 1, transcript variant X9
protein still life, isoform SIF type 1, transcript variant X10
protein still life, isoform SIF type 1 isoform X7
protein still life, isoforms C/SIF type 2 isoform X8
protein still life, isoform SIF type 1, transcript variant X8
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 15 samples with support for all annotated introns
protein still life, isoform SIF type 1, 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 5 samples with support for all annotated introns
protein still life, isoform SIF type 1, transcript variant X2
protein still life, isoform SIF type 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein still life, isoform SIF type 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein still life, isoform SIF type 1, transcript variant X5
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
protein still life, isoform SIF type 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein still life, isoform SIF type 1, 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 4 samples with support for all annotated introns
protein still life, isoform SIF type 1 isoform X6
protein still life, isoforms C/SIF type 2 isoform X4
protein still life, isoforms C/SIF type 2 isoform X2
protein still life, isoforms C/SIF type 2 isoform X3
protein still life, isoforms C/SIF type 2 isoform X5
protein still life, isoforms C/SIF type 2 isoform X1
protein lin-28 homolog, transcript variant X1
protein lin-28 homolog, transcript variant X2
PR domain zinc finger protein 1, transcript variant X1
PR domain zinc finger protein 1, transcript variant X3
PR domain zinc finger protein 1, transcript variant X2
PR domain zinc finger protein 1 isoform X1
PR domain zinc finger protein 1 isoform X2
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
uncharacterized tRNA-dihydrouridine synthase-like protein C45G9.2
phosphoribosylformylglycinamidine synthase
glycine dehydrogenase (decarboxylating), mitochondrial
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 8 samples with support for all annotated introns
uncharacterized LOC105391863, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
uncharacterized LOC105391863, 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
uncharacterized protein LOC105391863 isoform X1
uncharacterized protein LOC105391863 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 10 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 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
uncharacterized LOC119693710, transcript variant X6
uncharacterized LOC119693710, transcript variant X1
uncharacterized LOC119693710, transcript variant X2
uncharacterized LOC119693710, transcript variant X5
uncharacterized LOC119693710, transcript variant X4
uncharacterized LOC119693710, transcript variant X3
uncharacterized protein LOC119693710 isoform X1
uncharacterized protein LOC119693710 isoform X2
uncharacterized protein LOC119693710 isoform X3
uncharacterized protein LOC119693710 isoform X4
metalloproteinase inhibitor 3, transcript variant X1
metalloproteinase inhibitor 3, transcript variant X2
uncharacterized LOC105394215, 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 22 samples with support for all annotated introns
uncharacterized LOC105394215, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 samples with support for all annotated introns
glutamate receptor ionotropic, delta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 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: 13 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
doublesex- and mab-3-related transcription factor A2
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 8 samples with support for all annotated introns
uncharacterized LOC105388499, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC105388499, 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 64 samples with support for all annotated introns
D-2-hydroxyglutarate dehydrogenase, mitochondrial
polyadenylate-binding protein-interacting protein 1
iron-sulfur cluster assembly 1 homolog, mitochondrial
PDZ and LIM domain protein Zasp, transcript variant X4
PDZ and LIM domain protein Zasp, transcript variant X3
PDZ and LIM domain protein Zasp, transcript variant X7
PDZ and LIM domain protein Zasp, transcript variant X5
PDZ and LIM domain protein Zasp, transcript variant X6
PDZ and LIM domain protein Zasp isoform X4
PDZ and LIM domain protein Zasp isoform X7
PDZ and LIM domain protein Zasp isoform X5
PDZ and LIM domain protein Zasp isoform X6
PDZ and LIM domain protein Zasp isoform X3
uncharacterized LOC125490338, 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 53 samples with support for all annotated introns
uncharacterized LOC125490338, transcript variant X4
uncharacterized LOC125490338, 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 41 samples with support for all annotated introns
uncharacterized LOC125490338, transcript variant X1
PDZ and LIM domain protein Zasp, transcript variant X1
PDZ and LIM domain protein Zasp, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
PDZ and LIM domain protein Zasp isoform X1
PDZ and LIM domain protein Zasp isoform X2
ceramide phosphoethanolamine synthase-like
poly [ADP-ribose] polymerase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
poly [ADP-ribose] polymerase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
poly [ADP-ribose] polymerase-like isoform X2
poly [ADP-ribose] polymerase-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 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 79 samples with support for all annotated introns
uncharacterized LOC105387844, transcript variant X1
uncharacterized protein LOC105387844 isoform X1
uncharacterized LOC105387844, transcript variant X2
uncharacterized protein LOC105387844 isoform X2
uncharacterized LOC105395418, 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 63 samples with support for all annotated introns
uncharacterized LOC105395418, transcript variant X2
uncharacterized protein LOC105395418 isoform X2
uncharacterized protein LOC105395418 isoform X1
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: 6 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: 4 Proteins, 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: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
polypyrimidine tract-binding protein 1, transcript variant X5
polypyrimidine tract-binding protein 1, transcript variant X8
polypyrimidine tract-binding protein 1 isoform X5
polypyrimidine tract-binding protein 1 isoform X8
polypyrimidine tract-binding protein 1, transcript variant X10
polypyrimidine tract-binding protein 1, transcript variant X13
polypyrimidine tract-binding protein 1 isoform X10
polypyrimidine tract-binding protein 1 isoform X13
polypyrimidine tract-binding protein 1, transcript variant X12
polypyrimidine tract-binding protein 1, transcript variant X14
polypyrimidine tract-binding protein 1 isoform X12
polypyrimidine tract-binding protein 1 isoform X14
polypyrimidine tract-binding protein 1, transcript variant X9
polypyrimidine tract-binding protein 1, transcript variant X1
polypyrimidine tract-binding protein 1, transcript variant X3
polypyrimidine tract-binding protein 1, transcript variant X4
polypyrimidine tract-binding protein 1, transcript variant X2
polypyrimidine tract-binding protein 1, transcript variant X6
polypyrimidine tract-binding protein 1, transcript variant X7
polypyrimidine tract-binding protein 1 isoform X9
polypyrimidine tract-binding protein 1 isoform X1
polypyrimidine tract-binding protein 2 isoform X3
polypyrimidine tract-binding protein 1 isoform X4
polypyrimidine tract-binding protein 1 isoform X2
polypyrimidine tract-binding protein 2 isoform X6
polypyrimidine tract-binding protein 1 isoform X7
polypyrimidine tract-binding protein 1, transcript variant X11
polypyrimidine tract-binding protein 1 isoform X11
proline-rich receptor-like protein kinase PERK9
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 23 samples with support for all annotated introns
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
uncharacterized LOC105395552, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized protein LOC105395552 isoform X1
uncharacterized LOC105395552, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized protein LOC105395552 isoform X2
uncharacterized LOC105395150, transcript variant X2
uncharacterized LOC105395150, transcript variant X1
uncharacterized protein LOC105395150 isoform X1
uncharacterized protein LOC105395150 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 39 samples with support for all annotated introns
uncharacterized LOC119693466, transcript variant X5
uncharacterized LOC119693466, transcript variant X6
uncharacterized LOC119693466, transcript variant X3
uncharacterized LOC119693466, transcript variant X4
uncharacterized LOC119693466, transcript variant X1
uncharacterized LOC119693466, transcript variant X2
uncharacterized protein LOC119693466 isoform X2
uncharacterized protein LOC119693466 isoform X3
uncharacterized protein LOC119693466 isoform X4
uncharacterized protein LOC119693466 isoform X1
uncharacterized LOC125490347, transcript variant X1
uncharacterized LOC125490347, transcript variant X2
antichymotrypsin-2-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305514.1
annotated by transcript or proteomic data
The RefSeq transcript has 11 substitutions, 3 non-frameshifting indels and aligns at 97% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001292443.1
The RefSeq protein has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
COORDINATES: ab initio prediction:SignalP:4.0
2-oxoglutarate dehydrogenase complex component E1
calcium uptake protein 1 homolog, mitochondrial, transcript variant X3
calcium uptake protein 1 homolog, mitochondrial, transcript variant X2
calcium uptake protein 1 homolog, mitochondrial, transcript variant X5
calcium uptake protein 1 homolog, mitochondrial, transcript variant X1
calcium uptake protein 1 homolog, mitochondrial, transcript variant X4
calcium uptake protein 1 homolog, mitochondrial isoform X1
calcium uptake protein 1 homolog, mitochondrial isoform X2
calcium uptake protein 1 homolog, mitochondrial isoform X4
calcium uptake protein 1 homolog, mitochondrial isoform X3
calcium uptake protein 1 homolog, mitochondrial isoform X5
PDZ and LIM domain protein 3, transcript variant X2
uncharacterized protein LOC105395010 isoform X2
PDZ and LIM domain protein 3, transcript variant X1
PDZ and LIM domain protein 3, transcript variant X3
PDZ and LIM domain protein 3, transcript variant X4
PDZ and LIM domain protein 3, transcript variant X5
PDZ and LIM domain protein 3, transcript variant X6
PDZ and LIM domain protein 3, transcript variant X7
E3 ubiquitin-protein ligase MARCHF8, transcript variant X2
E3 ubiquitin-protein ligase MARCHF8, transcript variant X1
E3 ubiquitin-protein ligase MARCHF8 isoform X2
E3 ubiquitin-protein ligase MARCHF8 isoform X1
nucleolar protein dao-5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
nucleolar protein dao-5, transcript variant X1
nucleolar protein dao-5, transcript variant X3
SH3 domain-binding glutamic acid-rich protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
uncharacterized LOC105383011, transcript variant X3
uncharacterized LOC105383011, transcript variant X1
uncharacterized LOC105383011, transcript variant X2
uncharacterized protein LOC105383011 isoform X2
uncharacterized protein LOC105383011 isoform X1
vacuolar protein sorting-associated protein VTA1 homolog
NADH-cytochrome b5 reductase-like, transcript variant X3
NADH-cytochrome b5 reductase-like, transcript variant X2
NADH-cytochrome b5 reductase-like, transcript variant X1
NADH-cytochrome b5 reductase-like, transcript variant X4
high mobility group protein HMGI-C, transcript variant X1
high mobility group protein HMGI-C, transcript variant X2
uncharacterized protein LOC105383043 isoform X1
uncharacterized protein LOC105383043 isoform X4
uncharacterized protein LOC105383043 isoform X3
uncharacterized protein LOC105383043 isoform X2
uncharacterized protein LOC105383043 isoform X5
uncharacterized protein LOC105383043 isoform X6
dual specificity protein phosphatase Mpk3, transcript variant X1
dual specificity protein phosphatase Mpk3, 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 74 samples with support for all annotated introns
dual specificity protein phosphatase Mpk3 isoform X1
dual specificity protein phosphatase Mpk3 isoform X2
uncharacterized protein DDB_G0283697, transcript variant X1
uncharacterized protein DDB_G0283697, transcript variant X2
uncharacterized protein DDB_G0283697 isoform X1
uncharacterized protein DDB_G0283697 isoform X2
kelch-like ECH-associated protein 1B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
kelch-like ECH-associated protein 1B, transcript variant X1
kelch-like ECH-associated protein 1B, transcript variant X2
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 56 samples with support for all annotated introns
kelch-like ECH-associated protein 1B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
kelch-like ECH-associated protein 1B isoform X2
kelch-like ECH-associated protein 1B isoform X1
kelch-like ECH-associated protein 1B isoform X3
kelch-like ECH-associated protein 1B, transcript variant X5
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 28 samples with support for all annotated introns
kelch-like ECH-associated protein 1B isoform X4
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 2 samples with support for all annotated introns
putative protein kinase C delta type homolog, transcript variant X5
putative protein kinase C delta type homolog isoform X5
putative protein kinase C delta type homolog, transcript variant X6
putative protein kinase C delta type homolog isoform X6
putative protein kinase C delta type homolog, transcript variant X1
putative protein kinase C delta type homolog, transcript variant X3
putative protein kinase C delta type homolog, transcript variant X4
putative protein kinase C delta type homolog, transcript variant X2
uncharacterized protein LOC105383046 isoform X1
uncharacterized protein LOC105383046 isoform X3
uncharacterized protein LOC105383046 isoform X4
uncharacterized protein LOC105383046 isoform X2
pre-mRNA-splicing factor ISY1 homolog, transcript variant X2
pre-mRNA-splicing factor ISY1 homolog isoform X2
pre-mRNA-splicing factor ISY1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized protein LOC125488475 isoform X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase NRDP1
eukaryotic translation initiation factor 5B, transcript variant X2
eukaryotic translation initiation factor 5B, transcript variant X3
eukaryotic translation initiation factor 5B, transcript variant X1
eukaryotic translation initiation factor 5B isoform X2
uncharacterized protein LOC105383027 isoform X1
proteasome-associated protein ECM29 homolog, transcript variant X1
proteasome-associated protein ECM29 homolog, transcript variant X3
proteasome-associated protein ECM29 homolog, transcript variant X2
proteasome-associated protein ECM29 homolog isoform X1
proteasome adapter and scaffold protein ECM29 isoform X3
proteasome-associated protein ECM29 homolog isoform X2
LMBR1 domain-containing protein 2 homolog, transcript variant X2
LMBR1 domain-containing protein 2 homolog, transcript variant X1
LMBR1 domain-containing protein 2 homolog isoform X2
LMBR1 domain-containing protein 2 homolog isoform X1
uncharacterized LOC105380181, 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
uncharacterized LOC105380181, 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
uncharacterized protein LOC105380181 isoform X1
uncharacterized protein LOC105380181 isoform X2
vesicular glutamate transporter 1, transcript variant X2
vesicular glutamate transporter 1, transcript variant X1
vesicular glutamate transporter 2.1 isoform X2
vesicular glutamate transporter 1 isoform X1
UDP-N-acetylglucosamine 1-carboxyvinyltransferase 2
cardioacceleratory peptide receptor-like, transcript variant X1
cardioacceleratory peptide receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
cardioacceleratory peptide receptor-like isoform X1
cardioacceleratory peptide receptor-like isoform X2
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: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 1, 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 7 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 1, 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 27 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X2
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X1
sporozoite surface protein 2, transcript variant X1
sporozoite surface protein 2, 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
uncharacterized LOC119690403, transcript variant X2
uncharacterized LOC119690403, transcript variant X1
uncharacterized LOC105382734, transcript variant X1
uncharacterized LOC105382734, transcript variant X3
uncharacterized LOC105382734, transcript variant X5
uncharacterized LOC105382734, transcript variant X2
uncharacterized LOC105382734, transcript variant X4
uncharacterized LOC105382734, transcript variant X6
uncharacterized protein LOC105382734 isoform X1
uncharacterized protein LOC105382734 isoform X3
uncharacterized protein LOC105382734 isoform X5
uncharacterized protein LOC105382734 isoform X2
uncharacterized protein LOC105382734 isoform X4
uncharacterized protein LOC105382734 isoform X6
peroxisomal targeting signal 2 receptor, transcript variant X1
peroxisomal targeting signal 2 receptor, transcript variant X2
altered inheritance of mitochondria protein 21, transcript variant X2
altered inheritance of mitochondria protein 21, transcript variant X1
uncharacterized protein LOC105382767 isoform X2
altered inheritance of mitochondria protein 21 isoform X1
activating signal cointegrator 1 complex subunit 2 homolog
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 43 samples with support for all annotated introns
uncharacterized LOC105382730, transcript variant X2
uncharacterized LOC105382730, transcript variant X1
uncharacterized protein LOC105382730 isoform X2
uncharacterized protein LOC105382730 isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004
uncharacterized LOC119694927, transcript variant X2
uncharacterized LOC119694927, transcript variant X1
elongation of very long chain fatty acids protein 7, transcript variant X1
elongation of very long chain fatty acids protein 7, transcript variant X2
elongation of very long chain fatty acids protein 7, transcript variant X3
elongation of very long chain fatty acids protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
elongation of very long chain fatty acids protein 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 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 25 samples with support for all annotated introns
dual specificity testis-specific protein kinase 1
cyclic GMP-AMP synthase-like receptor, transcript variant X1
cyclic GMP-AMP synthase-like receptor, transcript variant X2
rhodanese domain-containing protein CG4456
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
transcription factor cwo, transcript variant X2
transcription factor cwo, transcript variant X1
transcription factor cwo, 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 43 samples with support for all annotated introns
hairy/enhancer-of-split related with YRPW motif protein isoform X3
uncharacterized LOC105392796, transcript variant X2
uncharacterized LOC105392796, transcript variant X1
uncharacterized protein LOC105392796 isoform X2
uncharacterized protein LOC105392796 isoform X1
probable rRNA-processing protein EBP2 homolog
signal recognition particle subunit SRP72
kinesin-like protein KIF18A, transcript variant X3
kinesin-like protein KIF18A, transcript variant X2
kinesin-like protein KIF18A, transcript variant X4
kinesin-like protein KIF18A, 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 30 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
proton-coupled folate transporter, transcript variant X3
proton-coupled folate transporter, transcript variant X2
proton-coupled folate transporter, transcript variant X4
proton-coupled folate transporter, transcript variant X1
proton-coupled folate transporter isoform X1
proton-coupled folate transporter isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
elongation of very long chain fatty acids protein 7-like
MAP kinase-interacting serine/threonine-protein kinase 1, transcript variant X1
MAP kinase-interacting serine/threonine-protein kinase 1, transcript variant X2
MAP kinase-interacting serine/threonine-protein kinase 1 isoform X1
MAP kinase-interacting serine/threonine-protein kinase 1 isoform X2
zinc finger and BTB domain-containing protein 17, 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 12 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 17, 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 9 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 17, 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 18 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 17, transcript variant X4
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
zinc finger and BTB domain-containing protein 17 isoform X2
zinc finger and BTB domain-containing protein 42 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
peroxisome biogenesis factor 2, transcript variant X1
peroxisome biogenesis factor 2, transcript variant X2
chromatin modification-related protein MEAF6
osteopetrosis-associated transmembrane protein 1
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 68 samples with support for all annotated introns
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma
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 68 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
traB domain-containing protein, transcript variant X2
traB domain-containing protein, transcript variant X1
traB domain-containing protein isoform X1
traB domain-containing protein isoform X2
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 85 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004, transcript variant X3
elongation of very long chain fatty acids protein AAEL008004, transcript variant X1
elongation of very long chain fatty acids protein AAEL008004, transcript variant X2
elongation of very long chain fatty acids protein AAEL008004 isoform X1
elongation of very long chain fatty acids protein AAEL008004 isoform X2
elongation of very long chain fatty acids protein, transcript variant X3
elongation of very long chain fatty acids protein, transcript variant X2
elongation of very long chain fatty acids protein, transcript variant X1
elongation of very long chain fatty acids protein
bromodomain-containing protein DDB_G0280777, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
bromodomain-containing protein DDB_G0280777, 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 25 samples with support for all annotated introns
bromodomain-containing protein DDB_G0280777 isoform X2
bromodomain-containing protein DDB_G0280777 isoform X1
serine/threonine-protein kinase STK11, transcript variant X3
serine/threonine-protein kinase STK11, transcript variant X1
serine/threonine-protein kinase STK11, 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 27 samples with support for all annotated introns
serine/threonine-protein kinase STK11 isoform X3
serine/threonine-protein kinase STK11 isoform X1
serine/threonine-protein kinase STK11 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
histone-lysine N-methyltransferase 2C, transcript variant X2
histone-lysine N-methyltransferase 2C, transcript variant X1
histone-lysine N-methyltransferase 2C, transcript variant X3
histone-lysine N-methyltransferase 2C isoform X2
histone-lysine N-methyltransferase 2C isoform X1
histone-lysine N-methyltransferase 2C isoform X3
THUMP domain-containing protein 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X4
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X2
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X1
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X3
calcium/calmodulin-dependent protein kinase type II alpha chain
uncharacterized LOC105391165, transcript variant X2
uncharacterized LOC105391165, transcript variant X1
uncharacterized protein LOC105391165 isoform X2
uncharacterized protein LOC105391165 isoform X1
uncharacterized LOC105391174, transcript variant X3
uncharacterized protein LOC105391174 isoform X3
uncharacterized LOC105391174, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC105391174 isoform X1
uncharacterized LOC105391174, transcript variant X2
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 7 samples with support for all annotated introns
uncharacterized protein LOC105391174 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 76 samples with support for all annotated introns
ras-related protein Rab-3, transcript variant X3
ras-related protein Rab-3, transcript variant X4
ras-related protein Rab-3, transcript variant X1
ras-related protein Rab-3, transcript variant X2
ras-related protein Rab-3, transcript variant X5
multiple inositol polyphosphate phosphatase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
translation initiation factor eIF-2B subunit gamma
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 82 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L20, mitochondrial, transcript variant X1
39S ribosomal protein L20, mitochondrial, transcript variant X2
39S ribosomal protein L20, mitochondrial
succinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial, transcript variant X1
succinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial, transcript variant X2
succinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial
rod outer segment membrane protein 1, transcript variant X1
rod outer segment membrane protein 1, transcript variant X2
photoreceptor outer segment membrane glycoprotein 2 isoform X1
rod outer segment membrane protein 1 isoform X2
rod outer segment membrane protein 1, transcript variant X3
rod outer segment membrane protein 1 isoform X3
constitutive coactivator of PPAR-gamma-like protein 1
GPN-loop GTPase 2, transcript variant X1
GPN-loop GTPase 2, transcript variant X2
GPN-loop GTPase 2, transcript variant X3
ribosome biogenesis protein BRX1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L55, mitochondrial
BRISC and BRCA1-A complex member 2, transcript variant X2
BRISC and BRCA1-A complex member 2, transcript variant X1
tRNA (guanine(37)-N1)-methyltransferase, 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 74 samples with support for all annotated introns
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X3
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X2
tRNA (guanine(37)-N1)-methyltransferase isoform X1
GPN-loop GTPase 1, transcript variant X1
GPN-loop GTPase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 83 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 59 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
adult-specific cuticular protein ACP-22-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
cuticle protein 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
cuticle protein 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
cuticle protein 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 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: 91 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC105396081, transcript variant X2
uncharacterized LOC105396081, 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 20 samples with support for all annotated introns
putative nuclease HARBI1, transcript variant X2
putative nuclease HARBI1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105391850, transcript variant X1
uncharacterized LOC105391850, transcript variant X2
uncharacterized protein LOC105391850 isoform X1
uncharacterized protein LOC105391850 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
band 7 protein AGAP004871, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
band 7 protein AGAP004871, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
band 7 protein AGAP004871, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
band 7 protein AGAP004871, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
band 7 protein AGAP004871, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cuticle protein 8, transcript variant X2
cuticle protein 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
cuticle protein 8-like, transcript variant X2
cuticle protein 8-like, transcript variant X1
uncharacterized LOC105391266, transcript variant X1
uncharacterized LOC105391266, transcript variant X2
uncharacterized protein LOC105391266 isoform X1
uncharacterized protein LOC105391266 isoform X2
39S ribosomal protein L47, mitochondrial
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase
COORDINATES: nucleotide motif:Rfam:12.0:RF00007
uncharacterized LOC105383070, transcript variant X5
uncharacterized LOC105383070, transcript variant X4
uncharacterized LOC105383070, transcript variant X2
uncharacterized LOC105383070, transcript variant X3
uncharacterized LOC105383070, transcript variant X1
uncharacterized protein LOC105383070 isoform X2
uncharacterized protein LOC105383070 isoform X4
uncharacterized protein LOC105383070 isoform X3
uncharacterized protein LOC105383070 isoform X1
uro-adherence factor A, transcript variant X1
uro-adherence factor A, transcript variant X3
uro-adherence factor A, transcript variant X2
calcium homeostasis endoplasmic reticulum protein
vesicle-fusing ATPase 1, transcript variant X1
vesicle-fusing ATPase 1, transcript variant X2
vesicle-fusing ATPase 1, transcript variant X3
transcription elongation factor 1 homolog
GATA-binding factor C, transcript variant X2
GATA-binding factor C, transcript variant X1
GATA-binding factor C, transcript variant X3
glucose-induced degradation protein 8 homolog
eukaryotic translation initiation factor 4E
X-linked retinitis pigmentosa GTPase regulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
four and a half LIM domains protein 2, transcript variant X9
prickle planar cell polarity protein 3-A isoform X7
four and a half LIM domains protein 2, transcript variant X2
four and a half LIM domains protein 2, transcript variant X1
prickle planar cell polarity protein 3-A isoform X1
prickle planar cell polarity protein 3-A isoform X2
four and a half LIM domains protein 2, transcript variant X7
four and a half LIM domains protein 2, transcript variant X6
four and a half LIM domains protein 2, transcript variant X8
four and a half LIM domains protein 2, transcript variant X12
prickle planar cell polarity protein 3 isoform X6
four and a half LIM domains protein 2, transcript variant X3
four and a half LIM domains protein 2, transcript variant X4
four and a half LIM domains protein 2, transcript variant X5
four and a half LIM domains protein 2, transcript variant X10
four and a half LIM domains protein 2 isoform X8
four and a half LIM domains protein 2, transcript variant X11
four and a half LIM domains protein 2 isoform X9
uracil phosphoribosyltransferase homolog
uncharacterized LOC119692677, transcript variant X1
uncharacterized protein LOC119692677 isoform X1
uncharacterized LOC119692677, transcript variant X2
uncharacterized protein LOC119692677 isoform X2
elongation of very long chain fatty acids protein 6
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
glutamate synthase [NADH], amyloplastic, transcript variant X2
glutamate synthase [NADH], amyloplastic, transcript variant X1
glutamate synthase [NADH], amyloplastic isoform X2
glutamate synthase [NADH], amyloplastic isoform X1
all trans-polyprenyl-diphosphate synthase PDSS2, transcript variant X2
all trans-polyprenyl-diphosphate synthase PDSS2, transcript variant X1
all trans-polyprenyl-diphosphate synthase PDSS2 isoform X2
all trans-polyprenyl-diphosphate synthase PDSS2 isoform X1
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
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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: DNA N6-methyl adenine demethylase
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 27 samples with support for all annotated introns
uncharacterized LOC119691947, transcript variant X2
uncharacterized LOC119691947, transcript variant X1
phosphatidate cytidylyltransferase, photoreceptor-specific, transcript variant X2
phosphatidate cytidylyltransferase, photoreceptor-specific, transcript variant X1
phosphatidate cytidylyltransferase, photoreceptor-specific isoform X2
phosphatidate cytidylyltransferase, photoreceptor-specific isoform X1
putative uncharacterized protein DDB_G0282133, transcript variant X3
putative uncharacterized protein DDB_G0282133, transcript variant X2
putative uncharacterized protein DDB_G0282133, transcript variant X1
putative uncharacterized protein DDB_G0282133 isoform X3
putative uncharacterized protein DDB_G0282133 isoform X2
putative uncharacterized protein DDB_G0282133 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
pre-rRNA-processing protein TSR1 homolog
protein transport protein Sec61 subunit alpha
ATP-binding cassette sub-family D member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
calreticulin; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305516.1
The RefSeq transcript has 24 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: BestRefSeq.
guanine nucleotide-binding protein-like 3 homolog
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 47 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
5'-3' exoribonuclease 1, transcript variant X2
5'-3' exoribonuclease 1, transcript variant X3
5'-3' exoribonuclease 1, transcript variant X1
nuclear transcription factor Y subunit B-1
ATP-binding cassette sub-family G member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette sub-family G member 8
spermatogenesis-associated protein 6, transcript variant X2
spermatogenesis-associated protein 6, transcript variant X1
spermatogenesis-associated protein 6 isoform X2
spermatogenesis-associated protein 6 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 80 samples with support for all annotated introns
cystinosin homolog, transcript variant X2
cystinosin homolog, transcript variant X1
cystinosin homolog, transcript variant X4
cystinosin homolog, transcript variant X3
V-type proton ATPase 21 kDa proteolipid subunit c''
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
collagen alpha-1(I) chain, transcript variant X1
collagen alpha-1(I) chain, transcript variant X2
calcium uniporter protein, mitochondrial, transcript variant X1
calcium uniporter protein, mitochondrial, transcript variant X2
calcium uniporter protein, mitochondrial isoform X2
calcium uniporter protein, mitochondrial isoform X1
protocadherin-like wing polarity protein stan
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
calcyphosin-like protein, transcript variant X1
calcyphosin-like protein, transcript variant X2
calcyphosin-like protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
calcyphosin-like protein, transcript variant X4
calcyphosin-like protein, transcript variant X5
calcyphosin-like protein, transcript variant X6
calcyphosin-like protein, transcript variant X9
calcyphosin-like protein, transcript variant X7
calcyphosin-like protein, transcript variant X8
27 kDa glycoprotein, transcript variant X1
27 kDa glycoprotein, transcript variant X2
27 kDa hemolymph protein, transcript variant X2
27 kDa hemolymph protein, 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 29 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase, transcript variant X2
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase isoform X2
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase, transcript variant X1
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase isoform X1
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase, transcript variant X3
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase isoform X3
isovaleryl-CoA dehydrogenase, mitochondrial
bifunctional peptidase and arginyl-hydroxylase JMJD5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transcription factor RFX3, 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 14 samples with support for all annotated introns
transcription factor RFX3, 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 5 samples with support for all annotated introns
transcription factor RFX3, 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 3 samples with support for all annotated introns
transcription factor RFX3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
transcription factor RFX3, transcript variant X5
interferon-related developmental regulator 1, transcript variant X2
interferon-related developmental regulator 1, transcript variant X1
interferon-related developmental regulator 1 isoform X2
interferon-related developmental regulator 1 isoform X1
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
netrin receptor UNC5B, transcript variant X3
netrin receptor UNC5B, transcript variant X7
netrin receptor UNC5B, transcript variant X6
netrin receptor UNC5B, transcript variant X5
netrin receptor UNC5B, transcript variant X4
netrin receptor UNC5B, transcript variant X1
netrin receptor UNC5B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
mitotic spindle assembly checkpoint protein MAD2A
iron-sulfur clusters transporter ABCB7, mitochondrial, transcript variant X1
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 71 samples with support for all annotated introns
iron-sulfur clusters transporter ABCB7, mitochondrial, transcript variant X2
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 51 samples with support for all annotated introns
iron-sulfur clusters transporter ABCB7, mitochondrial, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
iron-sulfur clusters transporter ABCB7, mitochondrial isoform X1
iron-sulfur clusters transporter ABCB7, mitochondrial isoform X2
iron-sulfur clusters transporter ABCB7, mitochondrial isoform X3
lebercilin-like protein, transcript variant X1
lebercilin-like protein, transcript variant X2
neuropeptide FF receptor 1, 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
neuropeptide FF receptor 1, 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
transfer RNA valine (anticodon CAC); 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 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: 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: 60 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA valine (anticodon AAC); 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC119694922, transcript variant X1
uncharacterized LOC119694922, transcript variant X2
solute carrier family 35 member E1 homolog