Plutella xylostella chromosome 2, 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\nOW026580.1.\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.
uncharacterized LOC119691921, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC119691921, transcript variant X1
zinc finger CCCH domain-containing protein 13, transcript variant X3
zinc finger CCCH domain-containing protein 13, transcript variant X1
zinc finger CCCH domain-containing protein 13, transcript variant X2
zinc finger CCCH domain-containing protein 13 isoform X3
zinc finger CCCH domain-containing protein 13 isoform X1
zinc finger CCCH domain-containing protein 13 isoform X2
vacuolar protein sorting-associated protein 53 homolog
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.
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
polypeptide N-acetylgalactosaminyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
polypeptide N-acetylgalactosaminyltransferase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 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: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 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 13 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 1
polypeptide N-acetylgalactosaminyltransferase 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 59 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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC105393776, transcript variant X3
uncharacterized LOC105393776, transcript variant X2
uncharacterized LOC105393776, transcript variant X1
uncharacterized protein LOC105393776 isoform X1
uncharacterized protein LOC105393776 isoform 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 24 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 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105382316, transcript variant X2
uncharacterized LOC105382316, transcript variant X1
uncharacterized protein LOC105382316 isoform X2
uncharacterized protein LOC105382316 isoform X1
uncharacterized LOC105390395, 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 27 samples with support for all annotated introns
uncharacterized LOC105390395, 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 27 samples with support for all annotated introns
uncharacterized protein LOC105390395 isoform X1
uncharacterized protein LOC105390395 isoform X2
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
aldo-keto reductase AKR2E4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
aldo-keto reductase AKR2E4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
beta-1,3-galactosyltransferase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
beta-1,3-galactosyltransferase 2, 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 16 samples with support for all annotated introns
beta-1,3-galactosyltransferase 2, transcript variant X1
beta-1,3-galactosyltransferase 2 isoform X2
beta-1,3-galactosyltransferase 2 isoform X1
beta-1,3-galactosyltransferase 2 isoform X3
uncharacterized LOC105382256, transcript variant X2
uncharacterized LOC105382256, transcript variant X1
uncharacterized protein LOC105382256 isoform X2
uncharacterized protein LOC105382256 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 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 38 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF113A-like
E3 ubiquitin-protein ligase RNF113A, 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 40 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF113A isoform X1
E3 ubiquitin-protein ligase RNF113A, 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 82 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF113A isoform X2
cysteine dioxygenase type 1, transcript variant X2
cysteine dioxygenase type 1, transcript variant X1
uncharacterized LOC105392891, transcript variant X1
uncharacterized LOC105392891, transcript variant X2
uncharacterized LOC105392891, transcript variant X3
uncharacterized LOC105392891, transcript variant X4
uncharacterized protein LOC105392891 isoform X1
uncharacterized protein LOC105392891 isoform X2
uncharacterized protein LOC105392891 isoform X3
uncharacterized protein LOC105392891 isoform X4
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 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 99% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA proline (anticodon CGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
uncharacterized LOC105389915, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC105389915, transcript variant X1
uncharacterized LOC105389915, transcript variant X2
uncharacterized protein LOC105389915 isoform X1
uncharacterized protein LOC105389915 isoform X2
uncharacterized protein LOC105389915 isoform X4
uncharacterized LOC105389915, transcript variant X3
uncharacterized protein LOC105389915 isoform X3
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105389913, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
uncharacterized LOC105389913, 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 50 samples with support for all annotated introns
uncharacterized LOC105389913, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein LOC105389913 isoform X2
uncharacterized protein LOC105389913 isoform X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: adenosylhomocysteinase-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
differentially expressed in FDCP 8 homolog
uncharacterized LOC105389921, 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 9 samples with support for all annotated introns
uncharacterized LOC105389921, 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
beta-1,3-galactosyltransferase 5, transcript variant X6
beta-1,3-galactosyltransferase 5, transcript variant X4
beta-1,3-galactosyltransferase 5, transcript variant X5
beta-1,3-galactosyltransferase 5, transcript variant X3
beta-1,3-galactosyltransferase 5, transcript variant X10
beta-1,3-galactosyltransferase 5, transcript variant X13
beta-1,3-galactosyltransferase 5, transcript variant X9
beta-1,3-galactosyltransferase 5, transcript variant X7
beta-1,3-galactosyltransferase 5, transcript variant X11
beta-1,3-galactosyltransferase 5, transcript variant X14
beta-1,3-galactosyltransferase 5, transcript variant X12
beta-1,3-galactosyltransferase 5, transcript variant X8
uncharacterized protein LOC105389906 isoform X5
uncharacterized protein LOC105389906 isoform X3
uncharacterized protein LOC105389906 isoform X4
uncharacterized protein LOC105389906 isoform X2
uncharacterized protein LOC105389906 isoform X8
uncharacterized protein LOC105389906 isoform X6
uncharacterized protein LOC105389906 isoform X7
uncharacterized protein LOC105389906 isoform X10
uncharacterized protein LOC105389906 isoform X9
beta-1,3-galactosyltransferase 5, transcript variant X1
beta-1,3-galactosyltransferase 5, transcript variant X2
beta-1,3-galactosyltransferase 5 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 78 samples with support for all annotated introns
homeobox protein invected, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
homeobox protein invected, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
segmentation polarity homeobox protein engrailed
zinc transporter foi, transcript variant X1
zinc transporter foi, transcript variant X2
zinc transporter foi, transcript variant X3
aspartate--tRNA ligase, cytoplasmic, transcript variant X3
aspartate--tRNA ligase, cytoplasmic, transcript variant X2
aspartate--tRNA ligase, cytoplasmic, transcript variant X1
aspartate--tRNA ligase, cytoplasmic isoform X2
aspartate--tRNA ligase, cytoplasmic isoform X1
uncharacterized LOC105393924, transcript variant X2
uncharacterized LOC105393924, transcript variant X1
uncharacterized protein LOC105393924 isoform X1
uncharacterized protein LOC105393924 isoform X2
steroidogenic acute regulatory protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61% coverage of the annotated genomic feature by RNAseq alignments
steroidogenic acute regulatory protein-like, transcript variant X1
steroidogenic acute regulatory protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 23 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
mothers against decapentaplegic homolog 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
transcription factor CP2-like protein 1, transcript variant X4
transcription factor CP2-like protein 1, transcript variant X3
transcription factor CP2-like protein 1, transcript variant X7
transcription factor CP2-like protein 1, transcript variant X1
transcription factor CP2-like protein 1, transcript variant X2
transcription factor CP2-like protein 1, transcript variant X5
transcription factor CP2-like protein 1, transcript variant X6
transcription factor CP2-like protein 1 isoform X6
probable inactive tRNA-specific adenosine deaminase-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
guanine nucleotide-binding protein G(f) subunit alpha
LHFPL tetraspan subfamily member 2a protein
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 25 samples with support for all annotated introns
homeotic protein distal-less, transcript variant X2
homeotic protein distal-less, transcript variant X4
homeotic protein distal-less, transcript variant X3
homeotic protein distal-less, transcript variant X6
homeotic protein distal-less, transcript variant X1
homeotic protein distal-less, transcript variant X7
homeotic protein distal-less, transcript variant X5
isochorismatase domain-containing protein 1, transcript variant X1
isochorismatase domain-containing protein 1, transcript variant X2
isochorismatase domain-containing protein 1 isoform X2
isochorismatase domain-containing protein 1 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105393867, transcript variant X1
uncharacterized LOC105393867, transcript variant X2
uncharacterized protein LOC105393867 isoform X1
uncharacterized protein LOC105393867 isoform X2
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
translation machinery-associated protein 7 homolog
PC4 and SFRS1-interacting protein, transcript variant X2
PC4 and SFRS1-interacting protein, transcript variant X3
PC4 and SFRS1-interacting protein, transcript variant X1
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, transcript variant X7
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, 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 20 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, transcript variant X9
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 35 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, 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 13 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, transcript variant X11
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
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, transcript variant X6
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, 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 40 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, 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 39 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha isoform X7
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha isoform X4
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha isoform X8
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha isoform X9
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha isoform X5
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha isoform X10
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha isoform X11
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha isoform X6
phosphatidylinositol 4-phosphate 5-kinase type-1 beta isoform X1
phosphatidylinositol 4-phosphate 5-kinase type-1 beta isoform X3
phosphatidylinositol 4-phosphate 5-kinase type-1 beta isoform X2
phosphatidylinositol 4-phosphate 5-kinase type-1 alpha, transcript variant X12
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 45 samples with support for all annotated introns
uncharacterized protein LOC105388794 isoform X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
PTB domain-containing adapter protein ced-6, transcript variant X4
PTB domain-containing adapter protein ced-6, transcript variant X3
PTB domain-containing adapter protein ced-6, transcript variant X5
PTB domain-containing adapter protein ced-6, transcript variant X1
PTB domain-containing adapter protein ced-6 isoform X1
PTB domain-containing adapter protein ced-6, transcript variant X2
PTB domain-containing adapter protein ced-6 isoform X2
PTB domain-containing adapter protein ced-6 isoform X3
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC105388772, transcript variant X2
uncharacterized protein LOC105388772 isoform X2
uncharacterized LOC105388772, transcript variant X1
uncharacterized protein LOC105388772 isoform X1
KAT8 regulatory NSL complex subunit 2, transcript variant X3
KAT8 regulatory NSL complex subunit 2, transcript variant X1
KAT8 regulatory NSL complex subunit 2, transcript variant X2
KAT8 regulatory NSL complex subunit 2 isoform X1
KAT8 regulatory NSL complex subunit 2 isoform X2
KAT8 regulatory NSL complex subunit 2 isoform X3
uncharacterized LOC105390485, transcript variant X1
uncharacterized LOC105390485, transcript variant X2
putative ATP-dependent RNA helicase TDRD12
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 50 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 13
LIM and SH3 domain protein Lasp, transcript variant X1
LIM and SH3 domain protein Lasp, transcript variant X2
LIM and SH3 domain protein Lasp, transcript variant X3
LIM and SH3 domain protein Lasp, transcript variant X4
LIM and SH3 domain protein Lasp isoform X1
LIM and SH3 domain protein Lasp isoform X2
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
uncharacterized LOC105391821, transcript variant X3
uncharacterized LOC105391821, transcript variant X1
uncharacterized LOC105391821, transcript variant X2
uncharacterized protein LOC105391821 isoform X1
uncharacterized protein LOC105391821 isoform X3
uncharacterized protein LOC105391821 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 16 samples with support for all annotated introns
endoplasmic reticulum junction formation protein lunapark-B, transcript variant X1
endoplasmic reticulum junction formation protein lunapark-B, transcript variant X2
endoplasmic reticulum junction formation protein lunapark-B, transcript variant X3
endoplasmic reticulum junction formation protein lunapark-B isoform X2
endoplasmic reticulum junction formation protein lunapark-B isoform X1
60S ribosomal protein L23; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
60S ribosomal protein L23, transcript variant X1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305533.1
annotated by transcript or proteomic data
The RefSeq transcript has 3 substitutions, 1 non-frameshifting indel 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.
COORDINATES: nucleotide motif:Rfam:12.0:RF00325
proteasome subunit beta type-4, transcript variant X1
proteasome subunit beta type-4, transcript variant X2
proteasome subunit beta type-4 isoform X1
proteasome subunit beta type-4 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
RNA-binding protein 34, transcript variant X1
RNA-binding protein 34, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125488706, transcript variant X2
uncharacterized LOC125488706, transcript variant X1
probable nuclear hormone receptor HR3, transcript variant X7
probable nuclear hormone receptor HR3 isoform X6
probable nuclear hormone receptor HR3, transcript variant X1
probable nuclear hormone receptor HR3, transcript variant X9
probable nuclear hormone receptor HR3 isoform X1
probable nuclear hormone receptor HR3 isoform X8
probable nuclear hormone receptor HR3, transcript variant X4
probable nuclear hormone receptor HR3, transcript variant X5
probable nuclear hormone receptor HR3, transcript variant X6
probable nuclear hormone receptor HR3, transcript variant X8
probable nuclear hormone receptor HR3, transcript variant X12
probable nuclear hormone receptor HR3, transcript variant X11
probable nuclear hormone receptor HR3 isoform X5
probable nuclear hormone receptor HR3 isoform X7
probable nuclear hormone receptor HR3 isoform X3
probable nuclear hormone receptor HR3 isoform X11
probable nuclear hormone receptor HR3 isoform X4
probable nuclear hormone receptor HR3 isoform X10
probable nuclear hormone receptor HR3, transcript variant X3
probable nuclear hormone receptor HR3, transcript variant X2
probable nuclear hormone receptor HR3, transcript variant X10
probable nuclear hormone receptor HR3 isoform X2
probable nuclear hormone receptor HR3 isoform X9
uncharacterized LOC105394373, transcript variant X1
uncharacterized LOC105394373, transcript variant X2
androgen-dependent TFPI-regulating protein
all trans-polyprenyl-diphosphate synthase PDSS2
histidine decarboxylase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 714 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
histidine decarboxylase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 715 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
histidine decarboxylase, transcript variant X2
histidine decarboxylase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 715 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: 418 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 ESTs, 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
spliceosome-associated protein CWC27 homolog, transcript variant X2
spliceosome-associated protein CWC27 homolog isoform X2
spliceosome-associated protein CWC27 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
spliceosome-associated protein CWC27 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC105381319, transcript variant X1
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 6 samples with support for all annotated introns
uncharacterized LOC105381319, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized protein LOC105381319 isoform X2
uncharacterized protein LOC105381319 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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 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: 1 EST, 22 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
carnosine N-methyltransferase, 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 57 samples with support for all annotated introns
carnosine N-methyltransferase, 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 60 samples with support for all annotated introns
acyl-CoA-binding domain-containing protein 5
nascent polypeptide-associated complex subunit alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
cytochrome c oxidase subunit 7C, mitochondrial, transcript variant X1
cytochrome c oxidase subunit 7C, mitochondrial, transcript variant X2
cytochrome c oxidase subunit 7C, mitochondrial
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
alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase, 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 13 samples with support for all annotated introns
alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase isoform X2
alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase isoform X1
dihydrofolate reductase, transcript variant X1
dihydrofolate reductase, transcript variant X2
dihydrofolate reductase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
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 35 samples with support for all annotated introns
uncharacterized LOC105394839, transcript variant X1
uncharacterized LOC105394839, transcript variant X2
uncharacterized protein LOC105394839 isoform X2
uncharacterized protein LOC105394839 isoform X1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ornithine decarboxylase antizyme 2
putative mediator of RNA polymerase II transcription subunit 15
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 35 samples with support for all annotated introns
probable cyclin-dependent serine/threonine-protein kinase DDB_G0292550
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: chorion class A protein L11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 62% 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, including 36 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC105393590, transcript variant X2
uncharacterized LOC105393590, transcript variant X1
uncharacterized protein LOC105393590 isoform X2
uncharacterized protein LOC105393590 isoform 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
uncharacterized LOC105393590, transcript variant X3
uncharacterized protein LOC105393590 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 84 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 65% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
putative uncharacterized protein DDB_G0286901
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
probable NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
probable NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 81 samples with support for all annotated introns
probable NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12
putative gamma-glutamylcyclotransferase CG2811, transcript variant X3
putative gamma-glutamylcyclotransferase CG2811, transcript variant X1
putative gamma-glutamylcyclotransferase CG2811, transcript variant X2
putative gamma-glutamylcyclotransferase CG2811 isoform X1
putative gamma-glutamylcyclotransferase CG2811 isoform X3
putative gamma-glutamylcyclotransferase CG2811 isoform X2
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial, transcript variant X2
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial, transcript variant X1
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial isoform X1
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial isoform X2
coiled-coil domain-containing protein 113
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC105398588, transcript variant X2
uncharacterized LOC105398588, transcript variant X4
uncharacterized LOC105398588, transcript variant X3
uncharacterized LOC105398588, transcript variant X1
uncharacterized protein LOC105398588 isoform X1
uncharacterized protein LOC105398588 isoform X2
UBX domain-containing protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
UBX domain-containing protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
UBX domain-containing protein 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
UBX domain-containing protein 4 isoform X2
UBX domain-containing protein 4 isoform X1
UBX domain-containing protein 4 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
ras-related protein RABF2b, 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 21 samples with support for all annotated introns
ras-related protein RABF2b, 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 64 samples with support for all annotated introns
ras-related protein RABF2b, transcript variant X6
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 26 samples with support for all annotated introns
ras-related protein RABF2b, transcript variant X2
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 54 samples with support for all annotated introns
ras-related protein RABF2b, transcript variant X5
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 53 samples with support for all annotated introns
ras-related protein RABF2b, transcript variant X4
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 23 samples with support for all annotated introns
paired amphipathic helix protein Sin3b, transcript variant X10
paired amphipathic helix protein Sin3b, transcript variant X3
paired amphipathic helix protein Sin3b, transcript variant X9
paired amphipathic helix protein Sin3b, transcript variant X8
paired amphipathic helix protein Sin3b, transcript variant X1
paired amphipathic helix protein Sin3b, transcript variant X4
paired amphipathic helix protein Sin3b, transcript variant X6
paired amphipathic helix protein Sin3b, transcript variant X11
paired amphipathic helix protein Sin3b, transcript variant X2
paired amphipathic helix protein Sin3b, transcript variant X12
paired amphipathic helix protein Sin3b, transcript variant X5
paired amphipathic helix protein Sin3b, transcript variant X7
paired amphipathic helix protein Sin3a isoform X6
paired amphipathic helix protein Sin3a isoform X8
paired amphipathic helix protein Sin3a isoform X7
paired amphipathic helix protein Sin3a isoform X3
paired amphipathic helix protein Sin3a isoform X5
paired amphipathic helix protein Sin3a isoform X2
paired amphipathic helix protein Sin3b isoform X4
paired amphipathic helix protein Sin3a isoform X1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
uncharacterized LOC105398319, transcript variant X3
uncharacterized LOC105398319, transcript variant X5
uncharacterized LOC105398319, transcript variant X1
uncharacterized LOC105398319, transcript variant X4
uncharacterized LOC105398319, transcript variant X2
uncharacterized protein LOC105398319 isoform X3
uncharacterized protein LOC105398319 isoform X1
uncharacterized protein LOC105398319 isoform X2
uncharacterized protein LOC105398319 isoform X5
uncharacterized protein LOC105398319 isoform X4
uncharacterized LOC105398319, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized protein LOC105398319 isoform X6
uncharacterized LOC105398319, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC105398319, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized protein LOC105398319 isoform X7
uncharacterized protein LOC105398319 isoform X8
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 18 samples with support for all annotated introns
androgen-dependent TFPI-regulating protein, transcript variant X4
uncharacterized protein LOC105381231 isoform X4
androgen-dependent TFPI-regulating protein, transcript variant X6
uncharacterized protein LOC105381231 isoform X6
androgen-dependent TFPI-regulating protein, transcript variant X1
androgen-dependent TFPI-regulating protein, transcript variant X2
uncharacterized protein LOC105381231 isoform X1
uncharacterized protein LOC105381231 isoform X2
androgen-dependent TFPI-regulating protein, transcript variant X5
androgen-dependent TFPI-regulating protein isoform X5
androgen-dependent TFPI-regulating protein, transcript variant X3
androgen-dependent TFPI-regulating protein isoform 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 10 samples with support for all annotated introns
low density lipoprotein receptor adapter protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein daughterless, transcript variant X9
protein daughterless, transcript variant X10
protein daughterless, transcript variant X4
protein daughterless, transcript variant X6
protein daughterless, transcript variant X7
protein daughterless, transcript variant X3
protein daughterless, transcript variant X1
protein daughterless, transcript variant X8
protein daughterless, transcript variant X5
protein daughterless, transcript variant X2
ATP-dependent zinc metalloprotease YME1L, transcript variant X2
ATP-dependent zinc metalloprotease YME1L, transcript variant X1
ATP-dependent zinc metalloprotease YME1L, transcript variant X3
ATP-dependent zinc metalloprotease YME1L, transcript variant X4
ATP-dependent zinc metalloprotease YME1L isoform X1
ATP-dependent zinc metalloprotease YME1L isoform X2
ATP-dependent zinc metalloprotease YME1L isoform X3
ATP-dependent zinc metalloprotease YME1L isoform 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 72 samples with support for all annotated introns
endothelial zinc finger protein induced by tumor necrosis factor alpha
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 53 samples with support for all annotated introns
glutamate decarboxylase, transcript variant X3
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
glutamate decarboxylase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
glutamate decarboxylase, transcript variant X2
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 25 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 95% coverage of the annotated genomic feature by RNAseq alignments
DAZ-associated protein 2, transcript variant X2
DAZ-associated protein 2, transcript variant X1
mediator of RNA polymerase II transcription subunit 16
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein K02A2.6-like isoform X1
uncharacterized protein K02A2.6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized protein LOC119692412 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 18 samples with support for all annotated introns
4-hydroxybenzoate polyprenyltransferase, mitochondrial, transcript variant X1
4-hydroxybenzoate polyprenyltransferase, mitochondrial, transcript variant X2
4-hydroxybenzoate polyprenyltransferase, mitochondrial
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 63 samples with support for all annotated introns