Plutella xylostella chromosome 18, 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\nOW026566.1.\nAssembly name: ilPluXylo3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/03/10. The original whole-genome shotgun project has the\naccession CAKNZZ000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Plutella xylostella Annotation\n Release 103\nAnnotation Version :: 103\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
UPF0692 protein CG33108, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
UPF0692 protein CG33108, 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 75 samples with support for all annotated introns
uncharacterized LOC105385269, 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 1 sample with support for all annotated introns
uncharacterized protein LOC105385269 isoform X3
uncharacterized LOC105385269, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC105385269, transcript variant X2
uncharacterized protein LOC105385269 isoform X1
uncharacterized protein LOC105385269 isoform X2
MD-2-related lipid-recognition protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 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 27 samples with support for all annotated introns
uncharacterized LOC105389948, 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 22 samples with support for all annotated introns
uncharacterized LOC105389948, 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 15 samples with support for all annotated introns
uncharacterized protein LOC105389948 isoform X2
uncharacterized protein LOC105389948 isoform X1
vasodilator-stimulated phosphoprotein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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 5 samples with support for all annotated introns
uncharacterized LOC105385959, transcript variant X1
uncharacterized LOC105385959, 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 79 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 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
26S proteasome non-ATPase regulatory subunit 8
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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 24 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 18 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 72 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
cyclin-dependent kinase inhibitor 1C-like
uncharacterized LOC119692681, transcript variant X5
uncharacterized LOC119692681, transcript variant X7
uncharacterized LOC119692681, transcript variant X4
uncharacterized LOC119692681, transcript variant X3
uncharacterized LOC119692681, transcript variant X2
uncharacterized LOC119692681, transcript variant X1
uncharacterized LOC119692681, transcript variant X8
uncharacterized LOC119692681, transcript variant X6
uncharacterized protein LOC119692681 isoform X5
uncharacterized protein LOC119692681 isoform X3
uncharacterized protein LOC119692681 isoform X2
uncharacterized protein LOC119692681 isoform X1
uncharacterized protein LOC119692681 isoform X4
probable serine/threonine-protein kinase DDB_G0272282, transcript variant X1
probable serine/threonine-protein kinase DDB_G0272282, transcript variant X2
probable serine/threonine-protein kinase DDB_G0272282
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
forkhead box protein N3, transcript variant X1
forkhead box protein N3, transcript variant X2
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 19 samples with support for all annotated introns
uncharacterized LOC119692749, transcript variant X1
uncharacterized LOC119692749, transcript variant X3
uncharacterized LOC119692749, transcript variant X2
uncharacterized LOC119692749, transcript variant X4
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
uncharacterized LOC105393423, transcript variant X2
uncharacterized LOC105393423, 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 75 samples with support for all annotated introns
echinoderm microtubule-associated protein-like 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
echinoderm microtubule-associated protein-like 2, 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 44 samples with support for all annotated introns
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein K02A2.6-like, transcript variant X2
uncharacterized protein LOC119691270 isoform X2
uncharacterized protein K02A2.6-like isoform X1
echinoderm microtubule-associated protein-like 2 isoform X3
echinoderm microtubule-associated protein-like 2 isoform X4
echinoderm microtubule-associated protein-like 2, 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 21 samples with support for all annotated introns
echinoderm microtubule-associated protein-like 2, 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 18 samples with support for all annotated introns
echinoderm microtubule-associated protein-like 2, 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 21 samples with support for all annotated introns
echinoderm microtubule-associated protein-like 2, transcript variant X6
echinoderm microtubule-associated protein-like 2 isoform X1
echinoderm microtubule-associated protein-like 2 isoform X5
echinoderm microtubule-associated protein-like 2 isoform X2
echinoderm microtubule-associated protein-like 2 isoform X6
mitochondrial import inner membrane translocase subunit TIM44
eukaryotic translation initiation factor 5, transcript variant X1
eukaryotic translation initiation factor 5, transcript variant X2
eukaryotic translation initiation factor 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
thyroid adenoma-associated protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
ribosome-recycling factor, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
interferon regulatory factor 2-binding protein-like A
speckle targeted PIP5K1A-regulated poly(A) polymerase
uncharacterized LOC105392250, transcript variant X1
uncharacterized protein LOC105392250 isoform X1
uncharacterized LOC105392250, transcript variant X2
uncharacterized protein LOC105392250 isoform X2
speckle targeted PIP5K1A-regulated poly(A) polymerase, transcript variant X4
speckle targeted PIP5K1A-regulated poly(A) polymerase, transcript variant X3
speckle targeted PIP5K1A-regulated poly(A) polymerase, transcript variant X2
speckle targeted PIP5K1A-regulated poly(A) polymerase, transcript variant X1
uncharacterized protein LOC105392321 isoform X4
uncharacterized protein LOC105392321 isoform X3
speckle targeted PIP5K1A-regulated poly(A) polymerase isoform X2
speckle targeted PIP5K1A-regulated poly(A) polymerase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
V-type proton ATPase catalytic subunit A, transcript variant X1
V-type proton ATPase catalytic subunit A, transcript variant X2
V-type proton ATPase catalytic subunit A, transcript variant X3
V-type proton ATPase catalytic subunit A isoform X1
V-type proton ATPase catalytic subunit A isoform X2
V-type proton ATPase catalytic subunit A, transcript variant X4
V-type proton ATPase catalytic subunit A, transcript variant X6
V-type proton ATPase catalytic subunit A, transcript variant X5
V-type proton ATPase catalytic subunit A isoform X3
V-type proton ATPase catalytic subunit A isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 81 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 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 97% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L14, mitochondrial
calcineurin subunit B type 2, transcript variant X2
calcineurin subunit B type 2, transcript variant X1
serine/arginine repetitive matrix protein 1, 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 5 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1 isoform X2
serine/arginine repetitive matrix protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel protein eag, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
potassium voltage-gated channel protein eag, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
potassium voltage-gated channel protein eag, 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 12 samples with support for all annotated introns
potassium voltage-gated channel protein eag isoform X2
potassium voltage-gated channel protein eag isoform X3
potassium voltage-gated channel protein eag isoform X1
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
acyl-CoA:lysophosphatidylglycerol acyltransferase 1
acyl-CoA:lysophosphatidylglycerol acyltransferase 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 8 samples with support for all annotated introns
acyl-CoA:lysophosphatidylglycerol acyltransferase 1 isoform X2
acyl-CoA:lysophosphatidylglycerol acyltransferase 1, transcript variant X1
fumarate hydratase, mitochondrial, transcript variant X1
fumarate hydratase, mitochondrial, transcript variant X2
fumarate hydratase, mitochondrial isoform X1
fumarate hydratase, mitochondrial isoform X2
fumarate hydratase, mitochondrial, transcript variant X4
fumarate hydratase, mitochondrial isoform X4
fumarate hydratase, mitochondrial, transcript variant X3
fumarate hydratase, mitochondrial isoform X3
PAXIP1-associated glutamate-rich protein 1
tubulin-specific chaperone cofactor E-like protein
persulfide dioxygenase ETHE1, mitochondrial, transcript variant X2
persulfide dioxygenase ETHE1, mitochondrial, transcript variant X3
persulfide dioxygenase ETHE1, mitochondrial, transcript variant X1
persulfide dioxygenase ETHE1, mitochondrial
amyloid-beta-like protein, transcript variant X1
amyloid-beta-like protein, transcript variant X2
amyloid-beta-like protein, transcript variant X3
uncharacterized LOC105388839, 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 67 samples with support for all annotated introns
uncharacterized LOC105388839, 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 78 samples with support for all annotated introns
uncharacterized protein LOC105388839 isoform X1
uncharacterized protein LOC105388839 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
spectrin beta chain, transcript variant X2
spectrin beta chain, transcript variant X1
fasciculation and elongation protein zeta-2
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 83 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 59 samples with support for all annotated introns
arylalkylamine N-acetyltransferase 1-like
zinc finger CCCH domain-containing protein 14
G-protein coupled receptor moody, transcript variant X1
G-protein coupled receptor moody isoform X1
G-protein coupled receptor moody, transcript variant X3
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 67 samples with support for all annotated introns
G-protein coupled receptor moody, 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 31 samples with support for all annotated introns
G-protein coupled receptor moody isoform X2
uncharacterized LOC125489862, transcript variant X2
uncharacterized LOC125489862, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
elongation of very long chain fatty acids protein 7
elongation of very long chain fatty acids protein F
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 36 samples with support for all annotated introns
hormone-sensitive lipase, 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 10 samples with support for all annotated introns
hormone-sensitive lipase, 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 47 samples with support for all annotated introns
hormone-sensitive lipase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial
protein lin-52 homolog, transcript variant X2
protein lin-52 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 46 samples with support for all annotated introns
sortilin-related receptor, transcript variant X1
sortilin-related receptor, transcript variant X5
sortilin-related receptor, transcript variant X4
sortilin-related receptor, transcript variant X3
sortilin-related receptor, transcript variant X2
sortilin-related receptor, transcript variant X6
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
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 20 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 94% 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: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase I
uncharacterized LOC105380439, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC105380439 isoform X1
uncharacterized LOC105380439, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC105380439 isoform X2
alpha-actinin, sarcomeric, transcript variant X1
alpha-actinin, sarcomeric, transcript variant X2
uncharacterized monothiol glutaredoxin ycf64-like
serine/threonine-protein phosphatase 4 regulatory subunit 2
probable 4-coumarate--CoA ligase 1, transcript variant X1
probable 4-coumarate--CoA ligase 1, transcript variant X3
probable 4-coumarate--CoA ligase 1, transcript variant X2
probable 4-coumarate--CoA ligase 1 isoform X1
probable 4-coumarate--CoA ligase 1 isoform X2
ATP-binding cassette sub-family B member 10, mitochondrial
motile sperm domain-containing protein 1
arp2/3 complex-activating protein rickA-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
organic solute transporter alpha-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
early endosome antigen 1, 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 6 samples with support for all annotated introns
early endosome antigen 1, 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 49 samples with support for all annotated introns
putative uncharacterized protein DDB_G0282133, transcript variant X2
putative uncharacterized protein DDB_G0282133, transcript variant X1
uncharacterized protein LOC105390308 isoform X1
putative uncharacterized protein DDB_G0282133 isoform X2
uncharacterized LOC105390307, transcript variant X1
uncharacterized LOC105390307, transcript variant X2
uncharacterized protein LOC105390307 isoform X1
uncharacterized protein LOC105390307 isoform X2
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: 5 ESTs, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105380074, transcript variant X1
uncharacterized LOC105380074, transcript variant X2
uncharacterized protein LOC105380074 isoform X1
uncharacterized protein LOC105380074 isoform X2
histone acetyltransferase Tip60, transcript variant X6
histone acetyltransferase Tip60, transcript variant X4
histone acetyltransferase Tip60, transcript variant X5
histone acetyltransferase Tip60, transcript variant X3
histone acetyltransferase Tip60, transcript variant X2
histone acetyltransferase Tip60, transcript variant X1
histone acetyltransferase Tip60 isoform X2
histone acetyltransferase Tip60 isoform X6
histone acetyltransferase Tip60 isoform X4
histone acetyltransferase Tip60 isoform X5
histone acetyltransferase Tip60 isoform X3
histone acetyltransferase Tip60 isoform X1
mitochondrial import inner membrane translocase subunit Tim9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 43 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: 13 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
chymotrypsin-like protease CTRL-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
chymotrypsin-like protease CTRL-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 74 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 56 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
leucine-rich repeat-containing protein 58
glycogen synthase kinase-3 beta, transcript variant X3
glycogen synthase kinase-3 beta, transcript variant X4
glycogen synthase kinase-3 beta, transcript variant X5
glycogen synthase kinase-3 beta, transcript variant X7
glycogen synthase kinase-3 beta isoform X3
glycogen synthase kinase-3 beta isoform X4
glycogen synthase kinase-3 beta isoform X5
glycogen synthase kinase-3 beta isoform X7
glycogen synthase kinase-3 beta, transcript variant X6
glycogen synthase kinase-3 beta isoform X6
glycogen synthase kinase-3 beta, transcript variant X1
glycogen synthase kinase-3 beta, transcript variant X2
glycogen synthase kinase-3 beta isoform X1
glycogen synthase kinase-3 beta isoform 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
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
homeobox protein vnd, transcript variant X1
homeobox protein vnd, transcript variant X2
uncharacterized LOC105384358, transcript variant X1
uncharacterized LOC105384358, transcript variant X3
uncharacterized LOC105384358, transcript variant X4
uncharacterized LOC105384358, transcript variant X5
uncharacterized LOC105384358, transcript variant X6
uncharacterized LOC105384358, transcript variant X7
uncharacterized LOC105384358, transcript variant X2
uncharacterized protein LOC105384358 isoform X2
uncharacterized protein LOC105384358 isoform X5
uncharacterized protein LOC105384358 isoform X1
uncharacterized protein LOC105384358 isoform X3
uncharacterized protein LOC105384358 isoform X4
uncharacterized protein LOC105384358 isoform X6
serine/threonine-protein phosphatase PP1-beta catalytic subunit, transcript variant X1
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X1
serine/threonine-protein phosphatase PP1-beta catalytic subunit, transcript variant X2
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X2
nuclear factor related to kappa-B-binding protein
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
uncharacterized LOC125489869, transcript variant X2
uncharacterized LOC125489869, transcript variant X1
uncharacterized protein LOC125489869 isoform X1
uncharacterized protein LOC125489869 isoform X2
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial
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: deoxyribonuclease-2-beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC105385703, transcript variant X1
uncharacterized LOC105385703, transcript variant X4
uncharacterized LOC105385703, transcript variant X2
uncharacterized LOC105385703, transcript variant X3
uncharacterized protein LOC105385703 isoform X1
uncharacterized protein LOC105385703 isoform X2
transcription initiation factor TFIID subunit 8
mitochondrial tRNA-specific 2-thiouridylase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 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: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 185A, transcript variant X1
transmembrane protein 185A, transcript variant X2
NEDD8-activating enzyme E1 regulatory subunit
cytochrome c oxidase assembly factor 6 homolog, transcript variant X1
cytochrome c oxidase assembly factor 6 homolog, transcript variant X3
cytochrome c oxidase assembly factor 6 homolog isoform X2
cytochrome c oxidase assembly factor 6 homolog, transcript variant X2
uncharacterized protein LOC105388245 isoform X1
N-alpha-acetyltransferase 38-B, NatC auxiliary subunit
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 77 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 95% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
odorant receptor 85b-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 2 samples with support for all annotated introns
odorant receptor 85b-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
apoptosis-stimulating of p53 protein 1, transcript variant X10
apoptosis-stimulating of p53 protein 1, transcript variant X8
apoptosis-stimulating of p53 protein 1, transcript variant X12
apoptosis-stimulating of p53 protein 1, transcript variant X11
apoptosis-stimulating of p53 protein 1, transcript variant X7
apoptosis-stimulating of p53 protein 1, transcript variant X6
apoptosis-stimulating of p53 protein 1, transcript variant X5
apoptosis-stimulating of p53 protein 1, transcript variant X3
apoptosis-stimulating of p53 protein 1, transcript variant X2
apoptosis-stimulating of p53 protein 1, transcript variant X1
apoptosis-stimulating of p53 protein 1, transcript variant X9
apoptosis-stimulating of p53 protein 1, transcript variant X4
apoptosis-stimulating of p53 protein 1 isoform X6
apoptosis-stimulating of p53 protein 1 isoform X4
apoptosis-stimulating of p53 protein 1 isoform X8
apoptosis-stimulating of p53 protein 1 isoform X7
apoptosis-stimulating of p53 protein 1 isoform X3
apoptosis-stimulating of p53 protein 1 isoform X5
apoptosis-stimulating of p53 protein 1 isoform X2
apoptosis-stimulating of p53 protein 1 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 67 samples with support for all annotated introns
CLK4-associating serine/arginine rich protein, transcript variant X1
CLK4-associating serine/arginine rich protein, 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 56 samples with support for all annotated introns
CLK4-associating serine/arginine rich protein
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: 4 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: 4 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
general transcriptional corepressor trfA, transcript variant X3
uncharacterized LOC105387975, transcript variant X1
uncharacterized LOC105387975, transcript variant X3
uncharacterized LOC105387975, transcript variant X2
uncharacterized LOC105387975, transcript variant X4
uncharacterized protein LOC105387975 isoform X1
uncharacterized protein LOC105387975 isoform X3
uncharacterized protein LOC105387975 isoform X2
uncharacterized protein LOC105387975 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 61% coverage of the annotated genomic feature by RNAseq alignments
general transcriptional corepressor trfA, transcript variant X1
uncharacterized protein DDB_G0284459 isoform X1
general transcriptional corepressor trfA, transcript variant X2
general transcriptional corepressor trfA 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 4 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26
39S ribosomal protein L17, mitochondrial
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
NPC intracellular cholesterol transporter 1 homolog 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 1 Protein, 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized protein LOC105387984 isoform X1
nonsense-mediated mRNA decay factor SMG9
uncharacterized LOC105387985, transcript variant X1
uncharacterized LOC105387985, transcript variant X2
uncharacterized LOC105387985, transcript variant X3
uncharacterized protein LOC105387985 isoform X1
uncharacterized protein LOC105387985 isoform X2
uncharacterized LOC105387986, transcript variant X2
uncharacterized LOC105387986, transcript variant X1
uncharacterized protein LOC105387986 isoform X1
uncharacterized protein LOC105387986 isoform X2
general odorant-binding protein 72-like, transcript variant X1
general odorant-binding protein 72-like, transcript variant X2
general odorant-binding protein 72-like isoform X1
general odorant-binding protein 72-like isoform X2
general odorant-binding protein lush-like, transcript variant X1
general odorant-binding protein lush-like, transcript variant X2
general odorant-binding protein lush-like isoform X1
general odorant-binding protein lush-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105388000, 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 11 samples with support for all annotated introns
uncharacterized LOC105388000, transcript variant X2
uncharacterized protein LOC105388000 isoform X1
uncharacterized protein LOC105388000 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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 96% coverage of the annotated genomic feature by RNAseq alignments
gamma-interferon-inducible lysosomal thiol reductase, transcript variant X5
gamma-interferon-inducible lysosomal thiol reductase, transcript variant X1
gamma-interferon-inducible lysosomal thiol reductase, transcript variant X3
gamma-interferon-inducible lysosomal thiol reductase, transcript variant X2
gamma-interferon-inducible lysosomal thiol reductase, transcript variant X4
gamma-interferon-inducible lysosomal thiol reductase isoform X1
gamma-interferon-inducible lysosomal thiol reductase isoform X2
CLIP domain-containing serine protease 14D, 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 16 samples with support for all annotated introns
CLIP domain-containing serine protease 14D, 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 11 samples with support for all annotated introns
CLIP domain-containing serine protease 14D, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
CLIP domain-containing serine protease 14D isoform X2
CLIP domain-containing serine protease 14D isoform X1
CLIP domain-containing serine protease 14D isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 58% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105381378, transcript variant X1
uncharacterized LOC105381378, transcript variant X5
uncharacterized LOC105381378, transcript variant X2
uncharacterized LOC105381378, transcript variant X3
uncharacterized LOC105381378, transcript variant X4
uncharacterized LOC105381378, transcript variant X7
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 23 samples with support for all annotated introns
uncharacterized LOC105381378, transcript variant X8
uncharacterized LOC105381378, transcript variant X9
uncharacterized LOC105381378, transcript variant X10
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 22 samples with support for all annotated introns
uncharacterized protein LOC105381378 isoform X1
uncharacterized protein LOC105381378 isoform X5
uncharacterized protein LOC105381378 isoform X2
uncharacterized protein LOC105381378 isoform X3
uncharacterized protein LOC105381378 isoform X4
uncharacterized protein LOC105381378 isoform X7
uncharacterized protein LOC105381378 isoform X8
uncharacterized LOC105381378, transcript variant X6
uncharacterized protein LOC105381378 isoform X6
cilia- and flagella-associated protein 61
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ras guanine nucleotide exchange factor P
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
mitochondrial ribonuclease P catalytic subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
mitochondrial ribonuclease P catalytic subunit, transcript variant X2
mitochondrial ribonuclease P catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
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 50 samples with support for all annotated introns
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
multiple coagulation factor deficiency protein 2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105381411, transcript variant X1
uncharacterized LOC105381411, transcript variant X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
upstream stimulatory factor 2, transcript variant X2
upstream stimulatory factor 2, transcript variant X4
upstream stimulatory factor 2, transcript variant X3
upstream stimulatory factor 2, transcript variant X1
upstream stimulatory factor 2 isoform X1
upstream stimulatory factor 2 isoform X2
upstream stimulatory factor 2 isoform X4
upstream stimulatory factor 2 isoform X3
zinc finger protein with KRAB and SCAN domains 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
putative ATP-dependent RNA helicase DHX57
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
inositol-trisphosphate 3-kinase A, transcript variant X2
inositol-trisphosphate 3-kinase A, transcript variant X1
inositol-trisphosphate 3-kinase B isoform X2
inositol-trisphosphate 3-kinase A isoform X1
serine/threonine-protein kinase minibrain, 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 68 samples with support for all annotated introns
serine/threonine-protein kinase minibrain, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
serine/threonine-protein kinase minibrain, transcript variant X3
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 69 samples with support for all annotated introns
serine/threonine-protein kinase minibrain isoform X1
serine/threonine-protein kinase minibrain isoform X2
serine/threonine-protein kinase minibrain isoform X3
serine/threonine-protein kinase minibrain, transcript variant X4
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 31 samples with support for all annotated introns
serine/threonine-protein kinase minibrain isoform X4
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125489836, transcript variant X2
uncharacterized LOC125489836, transcript variant X1
uncharacterized protein LOC125489836 isoform X1
uncharacterized protein LOC125489836 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 45 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
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 68 samples with support for all annotated introns
uncharacterized LOC105390507, transcript variant X3
uncharacterized LOC105390507, 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 20 samples with support for all annotated introns
uncharacterized LOC105390507, 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 50 samples with support for all annotated introns
uncharacterized protein LOC105390507 isoform X3
uncharacterized protein LOC105390507 isoform X1
uncharacterized protein LOC105390507 isoform X2
pyruvate carboxylase, mitochondrial, transcript variant X2
pyruvate carboxylase, mitochondrial, transcript variant X4
pyruvate carboxylase, mitochondrial, transcript variant X5
pyruvate carboxylase, mitochondrial, transcript variant X3
pyruvate carboxylase, mitochondrial, transcript variant X1
pyruvate carboxylase, mitochondrial, transcript variant X6
pyruvate carboxylase, mitochondrial, transcript variant X7
pyruvate carboxylase, mitochondrial isoform X3
pyruvate carboxylase, mitochondrial isoform X4
pyruvate carboxylase, mitochondrial isoform X2
pyruvate carboxylase, mitochondrial isoform X1
pyruvate carboxylase, mitochondrial isoform X5
pyruvate carboxylase, mitochondrial isoform X6
zinc finger protein 660, 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 22 samples with support for all annotated introns
zinc finger protein 660, 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 26 samples with support for all annotated introns
zinc finger protein 660, 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 45 samples with support for all annotated introns
zinc finger protein 660, 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 48 samples with support for all annotated introns
UDP-glucosyltransferase 2, transcript variant X1
UDP-glucosyltransferase 2, transcript variant X2
phospholipase A1 VesT1.02, transcript variant X2
phospholipase A1 VesT1.02, transcript variant X1
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
disheveled-associated activator of morphogenesis 1, transcript variant X5
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 9 samples with support for all annotated introns
disheveled-associated activator of morphogenesis 1, transcript variant X4
disheveled-associated activator of morphogenesis 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 6 samples with support for all annotated introns
disheveled-associated activator of morphogenesis 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
disheveled-associated activator of morphogenesis 1, transcript variant X2
disheveled-associated activator of morphogenesis 1, transcript variant X6
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
disheveled-associated activator of morphogenesis 1, transcript variant X7
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
disheveled-associated activator of morphogenesis 1 isoform X3
disheveled-associated activator of morphogenesis 1 isoform X1
disheveled-associated activator of morphogenesis 1 isoform X2
disheveled-associated activator of morphogenesis 1 isoform X4
disheveled-associated activator of morphogenesis 1 isoform X5
disheveled-associated activator of morphogenesis 2 isoform X6
pollen-specific leucine-rich repeat extensin-like protein 1, transcript variant X2
pollen-specific leucine-rich repeat extensin-like protein 1, transcript variant X1
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X2
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
GDP-mannose 4,6 dehydratase, transcript variant X1
GDP-mannose 4,6 dehydratase, transcript variant X2
probable tubulin polyglutamylase ttll-15
uncharacterized LOC105396272, transcript variant X2
uncharacterized LOC105396272, transcript variant X1
uncharacterized LOC105396272, transcript variant X3
uncharacterized protein LOC105396272 isoform X1
uncharacterized protein LOC105396272 isoform X2
uncharacterized LOC105396233, transcript variant X1
uncharacterized LOC105396233, transcript variant X2
inhibitor of nuclear factor kappa-B kinase subunit alpha
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
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
nuclear nucleic acid-binding protein C1D
26S proteasome non-ATPase regulatory subunit 1
signal recognition particle receptor subunit alpha homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 83 samples with support for all annotated introns
alpha-(1,6)-fucosyltransferase, 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 14 samples with support for all annotated introns
alpha-(1,6)-fucosyltransferase, 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 20 samples with support for all annotated introns
alpha-(1,6)-fucosyltransferase isoform X1
alpha-(1,6)-fucosyltransferase isoform X2
endothelin-converting enzyme 2, transcript variant X2
endothelin-converting enzyme 2, transcript variant X1
endothelin-converting enzyme 2 isoform X2
endothelin-converting enzyme 2 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, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 83% 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 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 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 82 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105386862, transcript variant X2
uncharacterized LOC105386862, transcript variant X1
uncharacterized protein LOC105386862 isoform X2
uncharacterized protein LOC105386862 isoform X1
rho GTPase-activating 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 26 samples with support for all annotated introns
rho GTPase-activating protein 4, 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 37 samples with support for all annotated introns
rho GTPase-activating protein 4, transcript variant X1
rho GTPase-activating protein 4, 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 35 samples with support for all annotated introns
rho GTPase-activating protein 4 isoform X2
rho GTPase-activating protein 4 isoform X3
rho GTPase-activating protein 4 isoform X1
rho GTPase-activating protein 4 isoform X4
rho GTPase-activating protein 4, transcript variant X6
rho GTPase-activating protein 4, transcript variant X5
ribosome biogenesis protein BOP1 homolog
eukaryotic translation initiation factor 3 subunit F
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 14 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 8 ESTs, 14 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: 14 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: 4 ESTs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
NADH-cytochrome b5 reductase-like protein alnC isoform X2
probable methyltransferase-like protein 25
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 83 samples with support for all annotated introns
uncharacterized LOC105388067, transcript variant X1
uncharacterized LOC105388067, transcript variant X2
mitochondrial 2-oxodicarboxylate carrier
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
thioredoxin, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 80 samples with support for all annotated introns
thioredoxin, mitochondrial, 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 71 samples with support for all annotated introns
thioredoxin, mitochondrial, transcript variant X1
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 77 samples with support for all annotated introns
kinesin light chain, transcript variant X3
kinesin light chain, transcript variant X5
kinesin light chain, transcript variant X4
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 28 samples with support for all annotated introns
kinesin light chain, transcript variant X6
kinesin light chain, transcript variant X1
kinesin light chain, transcript variant X2
kinesin light chain, transcript variant X7
probable 39S ribosomal protein L49, mitochondrial
breast cancer metastasis-suppressor 1-like protein
uncharacterized LOC119692415, transcript variant X2
uncharacterized LOC119692415, transcript variant X1
uncharacterized LOC119692415, transcript variant X3
putative nuclease HARBI1, transcript variant X2
putative nuclease HARBI1, transcript variant X1
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
mitogen-activated protein kinase kinase kinase 11, transcript variant X1
mitogen-activated protein kinase kinase kinase 11, transcript variant X3
mitogen-activated protein kinase kinase kinase 11, transcript variant X2
mitogen-activated protein kinase kinase kinase 11, transcript variant X4
mitogen-activated protein kinase kinase kinase 11 isoform X1
mitogen-activated protein kinase kinase kinase 11 isoform X3
mitogen-activated protein kinase kinase kinase 11 isoform X2
mitogen-activated protein kinase kinase kinase 11 isoform X4
39S ribosomal protein L33, mitochondrial
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50% 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 80% coverage of the annotated genomic feature by RNAseq alignments
anaphase-promoting complex subunit 1-like
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 32 samples with support for all annotated introns
glycerophosphodiester phosphodiesterase GDPD6-like
glycerophosphodiester phosphodiesterase GDPD6
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
uncharacterized LOC119692904, transcript variant X1
uncharacterized LOC119692904, transcript variant X2
uncharacterized protein LOC119692904 isoform X1
uncharacterized protein LOC119692904 isoform X2
uncharacterized LOC119692733, transcript variant X1
uncharacterized LOC119692733, transcript variant X5
uncharacterized LOC119692733, transcript variant X4
uncharacterized LOC119692733, transcript variant X3
uncharacterized protein LOC119692733 isoform X1
uncharacterized LOC119692733, transcript variant X2
uncharacterized protein LOC119692733 isoform X2
uncharacterized LOC119692737, 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 18 samples with support for all annotated introns
uncharacterized LOC119692737, 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 9 samples with support for all annotated introns
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 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: 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
probable RNA-directed DNA polymerase from transposon BS
uncharacterized LOC119692738, transcript variant X2
uncharacterized LOC119692738, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
40S ribosomal protein S12, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 58% 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 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
uncharacterized LOC105380866, transcript variant X2
uncharacterized protein LOC105380866 isoform X2
uncharacterized LOC105380866, transcript variant X1
uncharacterized protein LOC105380866 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
xanthine dehydrogenase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
xanthine dehydrogenase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
xanthine dehydrogenase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
xanthine dehydrogenase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
protein charlatan, transcript variant X1
protein charlatan, transcript variant X2
protein charlatan, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119692795, transcript variant X2
uncharacterized LOC119692795, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC119692795 isoform X1
uncharacterized protein LOC119692795 isoform X2