Plutella xylostella chromosome 29, 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\nOW026564.1.\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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
alanine aminotransferase 1, transcript variant X1
alanine aminotransferase 1, transcript variant X2
alanine aminotransferase 1, transcript variant X3
low-density lipoprotein receptor-related protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
protein virilizer, 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 42 samples with support for all annotated introns
protein virilizer, 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 30 samples with support for all annotated introns
protein virilizer, 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 8 samples with support for all annotated introns
protein virilizer, transcript variant X4
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 21 samples with support for all annotated introns
uncharacterized LOC119692992, transcript variant X6
uncharacterized LOC119692992, transcript variant X5
uncharacterized LOC119692992, transcript variant X4
uncharacterized LOC119692992, transcript variant X3
uncharacterized LOC119692992, transcript variant X2
uncharacterized LOC119692992, transcript variant X1
uncharacterized protein LOC119692992 isoform X2
uncharacterized protein LOC119692992 isoform X1
uncharacterized protein LOC119692992 isoform X3
E3 ubiquitin-protein ligase znrf2, transcript variant X1
E3 ubiquitin-protein ligase znrf2, transcript variant X2
E3 ubiquitin-protein ligase ZNRF2 isoform X1
E3 ubiquitin-protein ligase znrf2 isoform X2
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
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
uncharacterized Golgi apparatus membrane protein-like protein CG5021, 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 85 samples with support for all annotated introns
uncharacterized Golgi apparatus membrane protein-like protein CG5021, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
uncharacterized Golgi apparatus membrane protein-like protein CG5021, 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 60 samples with support for all annotated introns
uncharacterized Golgi apparatus membrane protein-like protein CG5021, transcript variant X4
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 60 samples with support for all annotated introns
uncharacterized Golgi apparatus membrane protein-like protein CG5021 isoform X1
uncharacterized Golgi apparatus membrane protein-like protein CG5021 isoform X2
uncharacterized Golgi apparatus membrane protein-like protein CG5021 isoform X3
uncharacterized Golgi apparatus membrane protein-like protein CG5021 isoform X4
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
serine/threonine-protein kinase SMG1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
ribosomal RNA-processing protein 7 homolog A
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 70 samples with support for all annotated introns
cleavage and polyadenylation specificity factor subunit 4
chitobiosyldiphosphodolichol beta-mannosyltransferase
nuclear envelope phosphatase-regulatory subunit 1
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 73 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
C-type lectin 37Db, transcript variant X1
C-type lectin 37Db, transcript variant X4
C-type lectin 37Db, transcript variant X3
C-type lectin 37Db, transcript variant X2
C-type lectin 37Db, transcript variant X5
low affinity immunoglobulin epsilon Fc receptor isoform X1
regulation of nuclear pre-mRNA domain-containing protein 1B
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 52 samples with support for all annotated introns
sodium-dependent noradrenaline transporter
proline-rich extensin-like protein EPR1, transcript variant X3
proline-rich extensin-like protein EPR1, transcript variant X2
proline-rich extensin-like protein EPR1, transcript variant X1
proline-rich extensin-like protein EPR1, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 10 isoform X2
proline-rich extensin-like protein EPR1 isoform X3
proline-rich extensin-like protein EPR1 isoform X1
proline-rich extensin-like protein EPR1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
sarcoplasmic reticulum histidine-rich calcium-binding protein
serine/arginine repetitive matrix protein 2, transcript variant X2
serine/arginine repetitive matrix protein 2, transcript variant X3
serine/arginine repetitive matrix protein 2, transcript variant X1
serine/arginine repetitive matrix protein 2, transcript variant X4
serine/arginine repetitive matrix protein 2, transcript variant X5
serine/arginine repetitive matrix protein 2 isoform X2
serine/arginine repetitive matrix protein 2 isoform X3
serine/arginine repetitive matrix protein 2 isoform X1
serine/arginine repetitive matrix protein 2 isoform X4
uncharacterized protein LOC105386276 isoform X5
uncharacterized LOC105386255, transcript variant X3
uncharacterized protein LOC105386255 isoform X3
uncharacterized LOC105386255, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
uncharacterized LOC105386255, 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 58 samples with support for all annotated introns
uncharacterized protein LOC105386255 isoform X2
uncharacterized protein LOC105386255 isoform X1
85/88 kDa calcium-independent phospholipase A2
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
trypsin, alkaline B, transcript variant X1
trypsin, alkaline B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
cyclin-dependent kinase 14, transcript variant X2
cyclin-dependent kinase 14, transcript variant X7
cyclin-dependent kinase 14, transcript variant X1
cyclin-dependent kinase 14, transcript variant X4
cyclin-dependent kinase 14, transcript variant X5
cyclin-dependent kinase 14, transcript variant X8
cyclin-dependent kinase 14, transcript variant X10
cyclin-dependent kinase 14, transcript variant X3
cyclin-dependent kinase 14, transcript variant X6
cyclin-dependent kinase 14, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
sodium-independent sulfate anion transporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
ankyrin repeat domain-containing protein 54
tRNA (cytosine(38)-C(5))-methyltransferase
maternal protein tudor, transcript variant X1
maternal protein tudor, transcript variant X2
maternal protein tudor, transcript variant X3
protein LSM14 homolog B, transcript variant X4
protein LSM14 homolog B, transcript variant X1
protein LSM14 homolog B, transcript variant X6
protein LSM14 homolog B, transcript variant X5
protein LSM14 homolog B, transcript variant X3
protein LSM14 homolog B, transcript variant X2
15-hydroxyprostaglandin dehydrogenase [NAD(+)]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
cytochrome c1, heme protein, mitochondrial
protein arginine N-methyltransferase 7, transcript variant X1
protein arginine N-methyltransferase 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein arginine N-methyltransferase 7, 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
protein arginine N-methyltransferase 7 isoform X1
protein arginine N-methyltransferase 7 isoform X3
protein arginine N-methyltransferase 7 isoform X2
uncharacterized LOC119693680, transcript variant X2
uncharacterized LOC119693680, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
small nucleolar RNA SNORA16B/SNORA16A family
COORDINATES: nucleotide motif:Rfam:12.0:RF00190
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 7 samples with support for all annotated introns
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
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
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
DNA topoisomerase 2, transcript variant X2
DNA topoisomerase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1, transcript variant X2
activating transcription factor 7-interacting protein 1, transcript variant X1
activating transcription factor 7-interacting protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
uncharacterized LOC105391529, 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 45 samples with support for all annotated introns
uncharacterized LOC105391529, 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 68 samples with support for all annotated introns
uncharacterized protein LOC105391529 isoform X1
uncharacterized protein LOC105391529 isoform X2
zinc finger protein 250, transcript variant X2
zinc finger protein 250, transcript variant X1
probable NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial
calcium-transporting ATPase type 2C member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119693541, transcript variant X3
uncharacterized LOC119693541, transcript variant X1
uncharacterized LOC119693541, transcript variant X2
beta-1,3-glucan-binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
beta-1,3-glucan-binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
beta-1,3-glucan-binding protein, transcript variant X2
beta-1,3-glucan-binding protein isoform X2
beta-1,3-glucan-binding protein isoform X3
beta-1,3-glucan-binding protein isoform X1
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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein lifeguard 1, transcript variant X4
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 64 samples with support for all annotated introns
protein lifeguard 1, 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 71 samples with support for all annotated introns
protein lifeguard 1, 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 68 samples with support for all annotated introns
protein lifeguard 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 samples with support for all annotated introns
39S ribosomal protein L52, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 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 9 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 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger CCCH domain-containing protein 15 homolog
transmembrane protein 64, transcript variant X1
transmembrane protein 64, transcript variant X2
putative 1-phosphatidylinositol 3-phosphate 5-kinase
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: 99% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105383566, transcript variant X3
uncharacterized LOC105383566, transcript variant X1
uncharacterized protein LOC105383566 isoform X1
uncharacterized protein LOC105383566 isoform X3
uncharacterized LOC105383566, 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 36 samples with support for all annotated introns
uncharacterized protein LOC105383566 isoform X2
ER membrane protein complex subunit 8/9 homolog
alanine--glyoxylate aminotransferase 2, mitochondrial
translocon-associated protein subunit alpha
sodium-dependent neutral amino acid transporter B(0)AT3
sperm-associated antigen 7 homolog, transcript variant X2
sperm-associated antigen 7 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105384198, transcript variant X2
uncharacterized LOC105384198, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
N-acetylneuraminate 9-O-acetyltransferase
uncharacterized LOC105381929, transcript variant X1
uncharacterized LOC105381929, transcript variant X3
uncharacterized LOC105381929, transcript variant X2
ubiquitin-conjugating enzyme E2 W, 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 84 samples with support for all annotated introns
ubiquitin-conjugating enzyme E2 W, transcript variant X2
ubiquitin-conjugating enzyme E2 W isoform X2
ubiquitin-conjugating enzyme E2 W isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
ATP-dependent RNA helicase dbp2, transcript variant X1
ATP-dependent RNA helicase dbp2, transcript variant X2
ATP-dependent RNA helicase dbp2 isoform X1
ATP-dependent RNA helicase dbp2 isoform X2
ATP synthase subunit d, mitochondrial; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305492.1
annotated by transcript or proteomic data
The RefSeq transcript has 16 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.
protein trapped in endoderm-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
protein trapped in endoderm-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
protein trapped in endoderm-1 isoform X2
protein trapped in endoderm-1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
threonylcarbamoyladenosine tRNA methylthiotransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 15 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: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
thialysine N-epsilon-acetyltransferase, transcript variant X6
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
thialysine N-epsilon-acetyltransferase, transcript variant X7
thialysine N-epsilon-acetyltransferase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
thialysine N-epsilon-acetyltransferase, 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 23 samples with support for all annotated introns
thialysine N-epsilon-acetyltransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
thialysine N-epsilon-acetyltransferase, 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 33 samples with support for all annotated introns
thialysine N-epsilon-acetyltransferase isoform X4
thialysine N-epsilon-acetyltransferase isoform X7
thialysine N-epsilon-acetyltransferase isoform X3
thialysine N-epsilon-acetyltransferase isoform X2
thialysine N-epsilon-acetyltransferase isoform X6
thialysine N-epsilon-acetyltransferase isoform X5
thialysine N-epsilon-acetyltransferase, transcript variant X8
thialysine N-epsilon-acetyltransferase isoform X8
thialysine N-epsilon-acetyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
thialysine N-epsilon-acetyltransferase isoform X1
diphosphoinositol polyphosphate phosphohydrolase 2
coiled-coil and C2 domain-containing protein 2A
cold shock domain-containing protein 3-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 28 samples with support for all annotated introns
enoyl-CoA delta isomerase 1, mitochondrial
dynein regulatory complex subunit 3-like
target of Myb protein 1, transcript variant X1
target of Myb protein 1, transcript variant X4
target of Myb protein 1, transcript variant X2
target of Myb protein 1, transcript variant X3
tubulin polymerization-promoting protein homolog
histone-lysine N-methyltransferase SETD1B
ubiquitin domain-containing protein UBFD1
rab11 family-interacting protein 4A, transcript variant X4
rab11 family-interacting protein 4A, transcript variant X5
rab11 family-interacting protein 4A, transcript variant X3
rab11 family-interacting protein 4A, transcript variant X2
rab11 family-interacting protein 4A, transcript variant X1
rab11 family-interacting protein 4A isoform X3
rab11 family-interacting protein 4A isoform X2
rab11 family-interacting protein 4A isoform X1
rab11 family-interacting protein 4A isoform X4
mpv17-like protein, transcript variant X3
mpv17-like protein, transcript variant X2
mpv17-like protein, transcript variant X1
transfer RNA leucine (anticodon AAG); 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 EST, 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
MAPK regulated corepressor interacting protein 2
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X2
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X1
chitooligosaccharidolytic beta-N-acetylglucosaminidase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 15 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 16A, transcript variant X6
protein phosphatase 1 regulatory subunit 16A, transcript variant X3
protein phosphatase 1 regulatory subunit 16A, transcript variant X1
protein phosphatase 1 regulatory subunit 16A, transcript variant X2
protein phosphatase 1 regulatory subunit 16A, transcript variant X5
protein phosphatase 1 regulatory subunit 16A, transcript variant X4
protein phosphatase 1 regulatory subunit 16A isoform X5
protein phosphatase 1 regulatory subunit 16A isoform X2
protein phosphatase 1 regulatory subunit 16A isoform X1
protein phosphatase 1 regulatory subunit 16A isoform X4
protein phosphatase 1 regulatory subunit 16A isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105393800, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC105393800 isoform X2
uncharacterized LOC105393800, 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 5 samples with support for all annotated introns
uncharacterized protein LOC105393800 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
uncharacterized LOC119692503, transcript variant X2
uncharacterized LOC119692503, transcript variant X1
uncharacterized protein LOC119692503 isoform X1
uncharacterized protein LOC119692503 isoform X2
transmembrane protein 184B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
transmembrane protein 184B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
transmembrane protein 184B, 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 72 samples with support for all annotated introns
transmembrane protein 184B, transcript variant X2
transmembrane protein 184B, transcript variant X5
transmembrane protein 184B, transcript variant X6
dual specificity protein phosphatase 22, transcript variant X1
dual specificity protein phosphatase 22, transcript variant X2
dual specificity protein phosphatase 22, transcript variant X3
dual specificity protein phosphatase 22 isoform X2
dual specificity protein phosphatase 22 isoform X1
uncharacterized protein ZK757.2 isoform 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 80 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
N-alpha-acetyltransferase 10, transcript variant X1
N-alpha-acetyltransferase 10, transcript variant X2
N-alpha-acetyltransferase 10, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105393985, 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 LOC105393985, transcript variant X2
uncharacterized protein LOC105393985 isoform X1
uncharacterized protein LOC105393985 isoform X2
breast cancer anti-estrogen resistance protein 1, 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 46 samples with support for all annotated introns
breast cancer anti-estrogen resistance protein 1, transcript variant X2
breast cancer anti-estrogen resistance protein 1 isoform X1
breast cancer anti-estrogen resistance protein 1 isoform 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 83 samples with support for all annotated introns
SNF-related serine/threonine-protein kinase
ubiquitin-conjugating enzyme E2 variant 2
ubiquitin carboxyl-terminal hydrolase 36, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 36, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 36 isoform X1
ubiquitin carboxyl-terminal hydrolase 36 isoform X2
potassium voltage-gated channel protein Shab, transcript variant X6
potassium voltage-gated channel protein Shab, transcript variant X4
potassium voltage-gated channel protein Shab, transcript variant X11
potassium voltage-gated channel protein Shab, transcript variant X1
potassium voltage-gated channel protein Shab, transcript variant X5
potassium voltage-gated channel protein Shab, transcript variant X7
potassium voltage-gated channel protein Shab, transcript variant X8
potassium voltage-gated channel protein Shab, transcript variant X9
potassium voltage-gated channel protein Shab, transcript variant X10
potassium voltage-gated channel protein Shab, transcript variant X2
potassium voltage-gated channel protein Shab, transcript variant X3
potassium voltage-gated channel protein Shab isoform X1
potassium voltage-gated channel protein Shab isoform X3
potassium voltage-gated channel protein Shab isoform X4
potassium voltage-gated channel protein Shab isoform X5
potassium voltage-gated channel protein Shab isoform X6
potassium voltage-gated channel protein Shab isoform X7
potassium voltage-gated channel protein Shab isoform X2
potassium voltage-gated channel protein Shab isoform X8
potassium voltage-gated channel protein Shab isoform X9
potassium voltage-gated channel protein Shab, transcript variant X12
potassium voltage-gated channel protein Shab, transcript variant X13
potassium voltage-gated channel protein Shab isoform X10
N-alpha-acetyltransferase 60, transcript variant X2
N-alpha-acetyltransferase 60, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 56 samples with support for all annotated introns
ribonucleases P/MRP protein subunit POP1
zinc finger CCCH domain-containing protein 18, transcript variant X4
zinc finger CCCH domain-containing protein 18, transcript variant X3
zinc finger CCCH domain-containing protein 18, transcript variant X1
zinc finger CCCH domain-containing protein 18, transcript variant X2
zinc finger CCCH domain-containing protein 18 isoform X3
zinc finger CCCH domain-containing protein 18 isoform X2
zinc finger CCCH domain-containing protein 18 isoform X1
meiotic recombination protein DMC1/LIM15 homolog
ethanolamine-phosphate cytidylyltransferase
proline-rich protein 36, 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 7 samples with support for all annotated introns
proline-rich protein 36, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
proline-rich protein 36, transcript variant X1
actin cytoskeleton-regulatory complex protein pan1 isoform X4
proline-rich protein 36, transcript variant X3
actin cytoskeleton-regulatory complex protein pan1 isoform X3
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
heparan sulfate 2-O-sulfotransferase pipe
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 10 samples with support for all annotated introns
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
glycogen-binding subunit 76A, transcript variant X3
glycogen-binding subunit 76A, transcript variant X2
glycogen-binding subunit 76A, transcript variant X1
probable ATP-dependent RNA helicase DDX20
mediator of RNA polymerase II transcription subunit 15
gamma-aminobutyric acid receptor-associated protein
cAMP-dependent protein kinase type I regulatory subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 4
zinc finger CCCH domain-containing protein 3
glutamate receptor ionotropic, NMDA 2B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
glutamate receptor ionotropic, NMDA 2B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ganglioside-induced differentiation-associated protein 1, transcript variant X2
ganglioside-induced differentiation-associated protein 1, transcript variant X1
ganglioside-induced differentiation-associated protein 1 isoform X1
ganglioside-induced differentiation-associated protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
vacuolar protein sorting-associated protein 8 homolog
WW domain-binding protein 11, transcript variant X2
WW domain-binding protein 11, transcript variant X1
WW domain-binding protein 11, transcript variant X3
uncharacterized protein LOC105393473 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
tRNA-splicing endonuclease subunit Sen34
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
purine nucleoside phosphorylase, transcript variant X1
purine nucleoside phosphorylase, transcript variant X2
purine nucleoside phosphorylase isoform X2
purine nucleoside phosphorylase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
equilibrative nucleoside transporter 4, 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 8 samples with support for all annotated introns
equilibrative nucleoside transporter 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 16 samples with support for all annotated introns
equilibrative nucleoside transporter 4 isoform X1
equilibrative nucleoside transporter 4 isoform X2
ATPase family AAA domain-containing protein 5, 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 26 samples with support for all annotated introns
ATPase family AAA domain-containing protein 5, 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 59 samples with support for all annotated introns
ATPase family AAA domain-containing protein 5 isoform X1
ATPase family AAA domain-containing protein 5 isoform X2
cytochrome b-c1 complex subunit 2, mitochondrial, transcript variant X1
cytochrome b-c1 complex subunit 2, mitochondrial, transcript variant X2
cytochrome b-c1 complex subunit 2, mitochondrial isoform X1
cytochrome b-c1 complex subunit 2, mitochondrial isoform X2
multifunctional methyltransferase subunit TRM112-like protein
COP9 signalosome complex subunit 1, transcript variant X1
COP9 signalosome complex subunit 1, transcript variant X2
cyclin-dependent kinase inhibitor 1C-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 37 samples with support for all annotated introns
pupal cuticle protein C1B-like, transcript variant X2
pupal cuticle protein C1B-like, transcript variant X4
pupal cuticle protein C1B-like, transcript variant X1
pupal cuticle protein C1B-like isoform X4
pupal cuticle protein C1B-like isoform X1
pupal cuticle protein C1B-like isoform X2
pupal cuticle protein C1B-like, transcript variant X3
pupal cuticle protein C1B-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
glutaconyl-CoA decarboxylase subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105381678, transcript variant X1
uncharacterized LOC105381678, transcript variant X2
uncharacterized protein LOC105381678 isoform X1
uncharacterized protein LOC105381678 isoform X2
3-phosphoinositide-dependent protein kinase 1, transcript variant X1
3-phosphoinositide-dependent protein kinase 1, transcript variant X2
3-phosphoinositide-dependent protein kinase 1, transcript variant X4
3-phosphoinositide-dependent protein kinase 1, transcript variant X5
3-phosphoinositide-dependent protein kinase 1, transcript variant X3
3-phosphoinositide-dependent protein kinase 1 isoform X4
3-phosphoinositide-dependent protein kinase 1 isoform X2
3-phosphoinositide-dependent protein kinase 1 isoform X1
3-phosphoinositide-dependent protein kinase 1 isoform X3
3-phosphoinositide-dependent protein kinase 1 isoform X5
DNA-directed RNA polymerase III subunit RPC8
nuclear pore complex protein Nup160 homolog
leukocyte receptor cluster member 1 homolog
general transcriptional corepressor trfA
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 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 42 samples with support for all annotated introns
chromosome transmission fidelity protein 8 homolog
general transcription and DNA repair factor IIH helicase subunit XPB
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
proline-rich protein HaeIII subfamily 1, transcript variant X2
proline-rich protein HaeIII subfamily 1, transcript variant X3
proline-rich protein HaeIII subfamily 1, transcript variant X1
proline-rich protein HaeIII subfamily 1 isoform X2
uncharacterized protein LOC105381708 isoform X1
proline-rich protein HaeIII subfamily 1 isoform X3
U3 small nucleolar RNA-associated protein 4 homolog
type 1 phosphatidylinositol 4,5-bisphosphate 4-phosphatase
tubulin polymerization-promoting protein homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tubulin polymerization-promoting protein homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
enoyl-CoA delta isomerase 3, peroxisomal
sodium/potassium-transporting ATPase subunit alpha-B
uncharacterized LOC105384739, 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 63 samples with support for all annotated introns
uncharacterized LOC105384739, transcript variant X2
uncharacterized protein LOC105384739 isoform X1
uncharacterized protein LOC105384739 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C16orf52 homolog A
leukocyte receptor cluster member 8 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
meiosis-specific with OB domain-containing protein
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 9 samples with support for all annotated introns
activating transcription factor of chaperone, transcript variant X1
activating transcription factor of chaperone isoform X1
activating transcription factor of chaperone, transcript variant X2
activating transcription factor of chaperone isoform X2
regulating synaptic membrane exocytosis protein 1, 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
regulating synaptic membrane exocytosis protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulating synaptic membrane exocytosis protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulating synaptic membrane exocytosis protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulating synaptic membrane exocytosis protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription initiation factor IIA subunit 1
regulating synaptic membrane exocytosis protein 1 isoform X1
regulating synaptic membrane exocytosis protein 1 isoform X3
regulating synaptic membrane exocytosis protein 1 isoform X2
regulating synaptic membrane exocytosis protein 1 isoform X4
intraflagellar transport protein 172 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00089
DNA-directed RNA polymerase III subunit RPC7-like
coiled-coil domain-containing protein 93
ubiquinone biosynthesis protein COQ9, mitochondrial
F-actin-uncapping protein LRRC16A, transcript variant X2
F-actin-uncapping protein LRRC16A, transcript variant X1
F-actin-uncapping protein LRRC16A, transcript variant X4
F-actin-uncapping protein LRRC16A, transcript variant X6
F-actin-uncapping protein LRRC16A, transcript variant X5
F-actin-uncapping protein LRRC16A, transcript variant X8
F-actin-uncapping protein LRRC16A, transcript variant X3
F-actin-uncapping protein LRRC16A isoform X1
F-actin-uncapping protein LRRC16A isoform X3
F-actin-uncapping protein LRRC16A isoform X4
F-actin-uncapping protein LRRC16A isoform X6
F-actin-uncapping protein LRRC16A isoform X2
F-actin-uncapping protein LRRC16A, transcript variant X7
F-actin-uncapping protein LRRC16A isoform X5
ATP-dependent RNA helicase p62-like, transcript variant X1
ATP-dependent RNA helicase p62-like, transcript variant X2
uncharacterized LOC105394774, 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
uncharacterized LOC105394774, transcript variant X2
uncharacterized protein LOC105394774 isoform X1
uncharacterized protein LOC105394774 isoform X2
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
methanethiol oxidase, transcript variant X1
methanethiol oxidase, transcript variant X2
E3 ubiquitin-protein ligase SINA-like 11, transcript variant X1
E3 ubiquitin-protein ligase SINA-like 11 isoform X1
E3 ubiquitin-protein ligase SINA-like 11, transcript variant X2
E3 ubiquitin-protein ligase SINA-like 11 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 81 samples with support for all annotated introns
sodium-coupled monocarboxylate transporter 2
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
uncharacterized LOC119691062, transcript variant X2
uncharacterized LOC119691062, transcript variant X1
uncharacterized LOC125491016, transcript variant X2
uncharacterized LOC125491016, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
zinc finger homeobox protein 3, transcript variant X2
zinc finger homeobox protein 3, transcript variant X1
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
protein-L-histidine N-pros-methyltransferase, 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 75 samples with support for all annotated introns
protein-L-histidine N-pros-methyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
protein-L-histidine N-pros-methyltransferase isoform X2
protein-L-histidine N-pros-methyltransferase, 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 83 samples with support for all annotated introns
protein-L-histidine N-pros-methyltransferase isoform X1
uncharacterized LOC105392072, transcript variant X2
uncharacterized LOC105392072, transcript variant X1
uncharacterized protein LOC105392072 isoform X2
uncharacterized protein LOC105392072 isoform X1
p21-activated protein kinase-interacting protein 1-like
uncharacterized LOC105392075, 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
uncharacterized LOC105392075, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
uncharacterized LOC105392075, transcript variant X4
uncharacterized LOC105392075, transcript variant X6
uncharacterized LOC105392075, 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 44 samples with support for all annotated introns
uncharacterized LOC105392075, transcript variant X1
uncharacterized LOC105392075, transcript variant X5
uncharacterized LOC105392075, transcript variant X10
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
uncharacterized protein LOC105392075 isoform X4
uncharacterized protein LOC105392075 isoform X3
uncharacterized protein LOC105392075 isoform X5
uncharacterized protein LOC105392075 isoform X1
uncharacterized protein LOC105392075 isoform X2
uncharacterized protein LOC105392075 isoform X6
uncharacterized LOC105392075, transcript variant X9
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
uncharacterized LOC105392075, transcript variant X8
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X2
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X1
nucleolar and coiled-body phosphoprotein 1-like isoform X1
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
nucleolar and coiled-body phosphoprotein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
uncharacterized protein LOC125488474 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
glutamate-rich WD repeat-containing protein 1
pentatricopeptide repeat-containing protein 1, mitochondrial
eukaryotic translation initiation factor 3 subunit L, transcript variant X2
eukaryotic translation initiation factor 3 subunit L, transcript variant X1
eukaryotic translation initiation factor 3 subunit L isoform X2
eukaryotic translation initiation factor 3 subunit L isoform X1
histone-lysine N-methyltransferase, H3 lysine-79 specific, transcript variant X1
histone-lysine N-methyltransferase, H3 lysine-79 specific, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
histone-lysine N-methyltransferase, H3 lysine-79 specific isoform X1
histone-lysine N-methyltransferase, H3 lysine-79 specific isoform X2
splicing factor 3B subunit 3, transcript variant X1
splicing factor 3B subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 83 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
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon UGU); 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, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 samples with support for all annotated introns
10 kDa heat shock protein, mitochondrial
glucose-fructose oxidoreductase domain-containing protein 1
basic helix-loop-helix transcription factor scleraxis
arf-GAP with dual PH domain-containing protein 1, transcript variant X2
arf-GAP with dual PH domain-containing protein 1, transcript variant X1
arf-GAP with dual PH domain-containing protein 1, transcript variant X3
arf-GAP with dual PH domain-containing protein 1
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 62 samples with support for all annotated introns
large subunit GTPase 1 homolog, transcript variant X3
large subunit GTPase 1 homolog, transcript variant X2
large subunit GTPase 1 homolog, transcript variant X1
large subunit GTPase 1 homolog isoform X3
large subunit GTPase 1 homolog isoform X2
large subunit GTPase 1 homolog isoform X1
mini-chromosome maintenance complex-binding protein
tRNA N6-adenosine threonylcarbamoyltransferase
proline-, glutamic acid- and leucine-rich protein 1
prolactin-releasing peptide receptor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
uncharacterized LOC105382375, transcript variant X1
uncharacterized LOC105382375, transcript variant X2
uncharacterized LOC105382375, transcript variant X4
uncharacterized LOC105382375, transcript variant X3
uncharacterized protein LOC105382375 isoform X1
uncharacterized protein LOC105382375 isoform X2
uncharacterized protein LOC105382375 isoform X3
uncharacterized protein LOC105382375 isoform X4
prolactin-releasing peptide receptor, transcript variant X2
prolactin-releasing peptide receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
transfer RNA phenylalanine (anticodon GAA); 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 EST, 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: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
trimethylguanosine synthase, transcript variant X2
trimethylguanosine synthase, transcript variant X1
lipid droplet-regulating VLDL assembly factor AUP1
facilitated trehalose transporter Tret1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
facilitated trehalose transporter Tret1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
facilitated trehalose transporter Tret1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
facilitated trehalose transporter Tret1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 77 samples with support for all annotated introns
facilitated trehalose transporter Tret1, transcript variant X1
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 77 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog isoform X4
facilitated trehalose transporter Tret1-2 homolog isoform X3
facilitated trehalose transporter Tret1-2 homolog isoform X2
facilitated trehalose transporter Tret1-2 homolog isoform X1
facilitated trehalose transporter Tret1 isoform X5
TBC1 domain family member 12, transcript variant X1
TBC1 domain family member 12, transcript variant X2
retinol dehydrogenase 11, transcript variant X2
retinol dehydrogenase 11, transcript variant X1
glycine cleavage system H protein, mitochondrial, transcript variant X2
glycine cleavage system H protein, mitochondrial, transcript variant X1
glycine cleavage system H protein, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial cardiolipin hydrolase-like, transcript variant X2
mitochondrial cardiolipin hydrolase-like, transcript variant X1
mitochondrial cardiolipin hydrolase-like, transcript variant X3
mitochondrial cardiolipin hydrolase-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 13 samples with support for all annotated introns
myc proto-oncogene protein, transcript variant X1
myc proto-oncogene protein, transcript variant X2
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
dimethyladenosine transferase 1, mitochondrial
cytochrome c oxidase assembly factor 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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, 19 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16
uncharacterized LOC105385762, transcript variant X2
uncharacterized LOC105385762, transcript variant X1
uncharacterized protein LOC105385762 isoform X1
uncharacterized protein LOC105385762 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
uncharacterized LOC105385463, 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 LOC105385463, transcript variant X1
brefeldin A-inhibited guanine nucleotide-exchange protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 samples with support for all annotated introns
actin-related protein 2/3 complex subunit 1A-B
uncharacterized LOC105392797, 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 15 samples with support for all annotated introns
uncharacterized LOC105392797, transcript variant X4
uncharacterized LOC105392797, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized LOC105392797, 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 20 samples with support for all annotated introns
uncharacterized protein LOC105392797 isoform X4
uncharacterized protein LOC105392797 isoform X3
uncharacterized protein LOC105392797 isoform X2
uncharacterized protein LOC105392797 isoform X1
reticulon-4-interacting protein 1 homolog, mitochondrial
fatty acid synthase, transcript variant X5
fatty acid synthase, transcript variant X4
fatty acid synthase, transcript variant X3
fatty acid synthase, transcript variant X1
fatty acid synthase, transcript variant X2
unconventional myosin-IXa, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
unconventional myosin-IXa, 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 15 samples with support for all annotated introns
unconventional myosin-IXa, 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 12 samples with support for all annotated introns
putative sodium-coupled neutral amino acid transporter 10
zinc finger protein 34, transcript variant X4
zinc finger protein 34, transcript variant X3
zinc finger protein 34, transcript variant X2
zinc finger protein 34, 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 24 samples with support for all annotated introns
mitochondrial thiamine pyrophosphate carrier
mediator of RNA polymerase II transcription subunit 10
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 4 samples with support for all annotated introns
ATP-binding cassette sub-family G member 4
multiple C2 and transmembrane domain-containing protein, transcript variant X2
multiple C2 and transmembrane domain-containing protein, transcript variant X1
multiple C2 and transmembrane domain-containing protein isoform X2
multiple C2 and transmembrane domain-containing protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 84 Proteins, and 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
facilitated trehalose transporter Tret1 isoform X1
facilitated trehalose transporter Tret1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 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 46 samples with support for all annotated introns
collagen alpha-1(XV) chain-like, transcript variant X1
collagen alpha-1(XV) chain-like, transcript variant X3
collagen alpha-1(XV) chain-like, transcript variant X2
collagen alpha-1(XV) chain-like isoform X1
collagen alpha-1(XV) chain-like isoform X2
uncharacterized LOC105387211, transcript variant X1
uncharacterized LOC105387211, transcript variant X2
U3 small nucleolar RNA-associated protein 6 homolog
tonsoku-like protein, transcript variant X1
tonsoku-like protein, transcript variant X2
tyrosine-protein kinase Src64B, transcript variant X1
tyrosine-protein kinase Src64B, transcript variant X2
tyrosine-protein kinase Src64B isoform X1
tyrosine-protein kinase Src64B isoform X2
adenosine 3'-phospho 5'-phosphosulfate transporter 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase MARCHF6, transcript variant X2
E3 ubiquitin-protein ligase MARCHF6, transcript variant X1
E3 ubiquitin-protein ligase MARCHF6 isoform X1
E3 ubiquitin-protein ligase MARCHF6 isoform X2
GTP-binding protein Rhes, 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 4 samples with support for all annotated introns
GTP-binding protein Rhes, transcript variant X3
GTP-binding protein Rhes, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein N-terminal asparagine amidohydrolase, transcript variant X3
protein N-terminal asparagine amidohydrolase, 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 73 samples with support for all annotated introns
protein N-terminal asparagine amidohydrolase, 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 73 samples with support for all annotated introns
protein N-terminal asparagine amidohydrolase, 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 25 samples with support for all annotated introns
protein N-terminal asparagine amidohydrolase, 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 8 samples with support for all annotated introns
protein N-terminal asparagine amidohydrolase, 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 46 samples with support for all annotated introns
protein N-terminal asparagine amidohydrolase
serine/threonine-protein kinase meng-po, transcript variant X2
serine/threonine-protein kinase meng-po, transcript variant X1
cohesin subunit SA-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 24 samples with support for all annotated introns
cohesin subunit SA-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 40 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
BTB/POZ domain-containing protein 19, 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 27 samples with support for all annotated introns
BTB/POZ domain-containing protein 19, 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 44 samples with support for all annotated introns
BTB/POZ domain-containing protein 19, 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 23 samples with support for all annotated introns
BTB/POZ domain-containing protein 19 isoform X1
uncharacterized protein LOC105389031 isoform X2
uncharacterized protein LOC105389031 isoform X3
probable small nuclear ribonucleoprotein E
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
longitudinals lacking protein, transcript variant X3
longitudinals lacking protein, transcript variant X2
longitudinals lacking protein, transcript variant X1
longitudinals lacking protein isoform X2
longitudinals lacking protein isoform X1
cytochrome c oxidase assembly protein COX11, mitochondrial
cytosolic Fe-S cluster assembly factor NUBP1 homolog
histone-lysine N-methyltransferase E(z), transcript variant X2
histone-lysine N-methyltransferase E(z), transcript variant X1
histone-lysine N-methyltransferase E(z) isoform X2
histone-lysine N-methyltransferase E(z) isoform X1
cytochrome c oxidase subunit 6b-2, transcript variant X1
cytochrome c oxidase subunit 6b-2, transcript variant X2
cytochrome c oxidase subunit 6b-2 isoform X2
oxysterol-binding protein-related protein 11
aprataxin and PNK-like factor, transcript variant X1
aprataxin and PNK-like factor, transcript variant X2
aprataxin and PNK-like factor, transcript variant X4
aprataxin and PNK-like factor, transcript variant X3
aprataxin and PNK-like factor isoform X1
aprataxin and PNK-like factor isoform X2
aprataxin and PNK-like factor isoform X3
aprataxin and PNK-like factor isoform X4
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
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
COORDINATES: nucleotide motif:Rfam:12.0:RF02543
COORDINATES: nucleotide motif:Rfam:12.0:RF01960