Plutella xylostella chromosome 3, 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\nOW026569.1.\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.
COORDINATES: polyA evidence [ECO:0006239]
membrane-bound alkaline phosphatase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
membrane-bound alkaline phosphatase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
membrane-bound alkaline phosphatase isoform X1
membrane-bound alkaline phosphatase 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 20 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: 15 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: 2 Proteins
meiosis-specific nuclear structural protein 1
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
protein phosphatase inhibitor 2, transcript variant X1
protein phosphatase inhibitor 2, transcript variant X2
protein phosphatase inhibitor 2 isoform X1
protein phosphatase inhibitor 2 isoform 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
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
SET domain-containing protein SmydA-8, transcript variant X1
SET domain-containing protein SmydA-8 isoform X1
SET domain-containing protein SmydA-8, transcript variant X2
SET domain-containing protein SmydA-8 isoform X2
toll-like receptor 3, transcript variant X1
toll-like receptor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
nucleosomal histone kinase 1, transcript variant X2
nucleosomal histone kinase 1, transcript variant X1
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
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: disks large homolog 5
uncharacterized LOC119693499, transcript variant X1
uncharacterized LOC119693499, transcript variant X2
uncharacterized protein LOC119693499 isoform X1
uncharacterized protein LOC119693499 isoform X2
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
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
potassium voltage-gated channel protein Shaw, transcript variant X1
potassium voltage-gated channel protein Shaw isoform X1
potassium voltage-gated channel protein Shaw, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
potassium voltage-gated channel protein Shaw, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
potassium voltage-gated channel protein Shaw, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel protein Shaw isoform X3
potassium voltage-gated channel protein Shaw, transcript variant X2
potassium voltage-gated channel protein Shaw isoform X2
potassium voltage-gated channel protein Shaw, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium voltage-gated channel protein Shaw, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
potassium voltage-gated channel protein Shaw isoform X4
potassium voltage-gated channel protein Shaw isoform X5
uncharacterized LOC119691286, 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 46 samples with support for all annotated introns
uncharacterized LOC119691286, 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 52 samples with support for all annotated introns
uncharacterized protein LOC119691286 isoform X1
uncharacterized protein LOC119691286 isoform X2
potassium voltage-gated channel protein Shaw
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC105383819, transcript variant X1
uncharacterized LOC105383819, transcript variant X2
uncharacterized protein LOC105383819 isoform X1
uncharacterized protein LOC105383819 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine protease inhibitor dipetalogastin-like
serine protease inhibitor dipetalogastin
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
uncharacterized LOC105387425, transcript variant X2
uncharacterized protein LOC105387425 isoform X2
uncharacterized LOC105387425, transcript variant X1
uncharacterized protein LOC105387425 isoform X1
uncharacterized LOC119692373, 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 75 samples with support for all annotated introns
uncharacterized LOC119692373, 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 76 samples with support for all annotated introns
uncharacterized protein LOC119692373 isoform X2
uncharacterized protein LOC119692373 isoform X3
uncharacterized LOC119692373, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 83 samples with support for all annotated introns
uncharacterized protein LOC119692373 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 7 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
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1
G patch domain and ankyrin repeat-containing protein 1 homolog
uncharacterized LOC105385747, transcript variant X3
uncharacterized LOC105385747, transcript variant X2
uncharacterized LOC105385747, transcript variant X1
uncharacterized protein LOC105385747 isoform X2
uncharacterized protein LOC105385747 isoform X1
uncharacterized protein LOC105385747 isoform X3
NPC intracellular cholesterol transporter 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: NPC intracellular cholesterol transporter 1
sarcoplasmic calcium-binding protein, alpha-B and -A chains, transcript variant X1
sarcoplasmic calcium-binding protein, alpha-B and -A chains, transcript variant X2
sarcoplasmic calcium-binding protein, alpha-B and -A chains isoform X2
sarcoplasmic calcium-binding protein 1 isoform X1
thioredoxin domain-containing protein 15
glyoxylate reductase/hydroxypyruvate reductase
uncharacterized LOC125489672, 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 30 samples with support for all annotated introns
uncharacterized LOC125489672, transcript variant X1
SH2 domain-containing protein 4B, transcript variant X3
SH2 domain-containing protein 4B, transcript variant X1
SH2 domain-containing protein 4B, transcript variant X2
cyclin-dependent kinase-like 1, transcript variant X1
cyclin-dependent kinase-like 1, transcript variant X2
zinc finger CCHC domain-containing protein 24, 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 61 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 24, 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 70 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 24 isoform X1
zinc finger CCHC domain-containing protein 24 isoform X2
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 55 samples with support for all annotated introns
glutathione S-transferase 2-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309076.1
annotated by transcript or proteomic data
The RefSeq transcript has 15 substitutions, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001296005.1
The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SET and MYND domain-containing protein 4, transcript variant X1
SET and MYND domain-containing protein 4, transcript variant X3
SET and MYND domain-containing protein 4, transcript variant X2
SET and MYND domain-containing protein 4 isoform X1
SET and MYND domain-containing protein 4 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 85 samples with support for all annotated introns
SET and MYND domain-containing protein 4
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 27 samples with support for all annotated introns
mitochondrial 2-oxoglutarate/malate carrier protein, transcript variant X2
mitochondrial 2-oxoglutarate/malate carrier protein, transcript variant X3
mitochondrial 2-oxoglutarate/malate carrier protein, transcript variant X1
mitochondrial 2-oxoglutarate/malate carrier protein isoform X2
mitochondrial 2-oxoglutarate/malate carrier protein isoform X3
mitochondrial 2-oxoglutarate/malate carrier protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial 2-oxoglutarate/malate carrier protein
uncharacterized LOC105391658, 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 LOC105391658, transcript variant X1
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 85 samples with support for all annotated introns
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
bromodomain-containing protein DDB_G0280777
myeloid leukemia factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 68 samples with support for all annotated introns
myeloid leukemia factor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
myeloid leukemia factor, 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 68 samples with support for all annotated introns
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC105382543, 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 43 samples with support for all annotated introns
uncharacterized protein LOC105382543 isoform X1
uncharacterized LOC105382543, 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 4 samples with support for all annotated introns
uncharacterized protein LOC105382543 isoform X2
uncharacterized LOC105382514, 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 23 samples with support for all annotated introns
uncharacterized LOC105382514, 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 30 samples with support for all annotated introns
uncharacterized LOC105382514, transcript variant X4
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 12 samples with support for all annotated introns
uncharacterized LOC105382514, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
outer mitochondrial transmembrane helix translocase, transcript variant X2
outer mitochondrial transmembrane helix translocase, transcript variant X1
outer mitochondrial transmembrane helix translocase isoform X2
outer mitochondrial transmembrane helix translocase isoform X1
outer mitochondrial transmembrane helix translocase, transcript variant X3
outer mitochondrial transmembrane helix translocase isoform X3
nucleolar MIF4G domain-containing protein 1 homolog
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nucleolar MIF4G domain-containing protein 1 homolog
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN, transcript variant X1
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN, transcript variant X2
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN, transcript variant X3
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN isoform X3
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN isoform X2
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN isoform X1
N6-adenosine-methyltransferase non-catalytic subunit
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 80 samples with support for all annotated introns
serine protease inhibitor dipetalogastin, transcript variant X2
serine protease inhibitor dipetalogastin, transcript variant X1
serine protease inhibitor dipetalogastin isoform X2
serine protease inhibitor dipetalogastin isoform X1
uncharacterized LOC119691428, transcript variant X2
uncharacterized LOC119691428, transcript variant X1
mitochondrial coenzyme A diphosphatase NUDT8
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
chloride intracellular channel exc-4, transcript variant X1
chloride intracellular channel exc-4, transcript variant X2
chloride intracellular channel exc-4 isoform X2
chloride intracellular channel exc-4 isoform X1
TGF-beta-activated kinase 1 and MAP3K7-binding protein 2, 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
TGF-beta-activated kinase 1 and MAP3K7-binding protein 2 isoform X2
TGF-beta-activated kinase 1 and MAP3K7-binding protein 2, 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 80 samples with support for all annotated introns
TGF-beta-activated kinase 1 and MAP3K7-binding protein 2 isoform X1
ragulator complex protein LAMTOR3 homolog
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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glyoxylate reductase/hydroxypyruvate reductase, transcript variant X1
glyoxylate reductase/hydroxypyruvate reductase isoform X1
glyoxylate reductase/hydroxypyruvate reductase, transcript variant X2
glyoxylate reductase/hydroxypyruvate reductase 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 69 samples with support for all annotated introns
zinc finger HIT domain-containing protein 1
general transcription factor IIH subunit 5
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 85 samples with support for all annotated introns
meiotic nuclear division protein 1 homolog
uncharacterized LOC105381752, transcript variant X3
uncharacterized LOC105381752, transcript variant X2
uncharacterized LOC105381752, transcript variant X1
uncharacterized protein LOC105381752 isoform X3
uncharacterized protein LOC105381752 isoform X1
uncharacterized protein LOC105381752 isoform X2
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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
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: 4 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: 9 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: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
protein jim lovell, transcript variant X1
protein jim lovell, transcript variant X2
ATPase family AAA domain-containing protein 2
monocyte to macrophage differentiation factor
DNA-directed RNA polymerase, mitochondrial, transcript variant X2
DNA-directed RNA polymerase, mitochondrial, transcript variant X3
DNA-directed RNA polymerase, mitochondrial, transcript variant X1
DNA-directed RNA polymerase, mitochondrial isoform X2
DNA-directed RNA polymerase, mitochondrial isoform X3
DNA-directed RNA polymerase, mitochondrial isoform X1
DNA-directed RNA polymerase, mitochondrial, 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 21 samples with support for all annotated introns
transmembrane inner ear expressed protein
probable actin-related protein 2/3 complex subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
ubiA prenyltransferase domain-containing protein 1 homolog
uncharacterized LOC105390781, transcript variant X3
uncharacterized LOC105390781, transcript variant X2
uncharacterized LOC105390781, transcript variant X1
zinc finger CCHC domain-containing protein 9
voltage-dependent anion-selective channel, transcript variant X1
voltage-dependent anion-selective channel isoform X1
voltage-dependent anion-selective channel, transcript variant X2
voltage-dependent anion-selective channel 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 11 samples with support for all annotated introns
elongation factor 1-beta'; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309138.1
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.
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X1
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X2
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X3
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial
reversion-inducing cysteine-rich protein with Kazal motifs
brefeldin A-inhibited guanine nucleotide-exchange protein 3
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 5, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
pancreatic lipase-related protein 2, transcript variant X2
pancreatic lipase-related protein 2, transcript variant X3
pancreatic lipase-related protein 2, transcript variant X1
pancreatic lipase-related protein 2 isoform X1
pancreatic lipase-related protein 2 isoform X2
malate dehydrogenase, mitochondrial, transcript variant X3
malate dehydrogenase, mitochondrial, transcript variant X1
uncharacterized protein LOC105387887 isoform X3
malate dehydrogenase, mitochondrial isoform X1
malate dehydrogenase, mitochondrial, transcript variant X2
malate dehydrogenase, mitochondrial isoform X2
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC105398351, transcript variant X1
uncharacterized LOC105398351, 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 79 samples with support for all annotated introns
farnesol dehydrogenase, transcript variant X1
farnesol dehydrogenase, transcript variant X2
probable ATP-dependent RNA helicase DDX46, transcript variant X4
probable ATP-dependent RNA helicase DDX46, transcript variant X3
probable ATP-dependent RNA helicase DDX46, transcript variant X2
probable ATP-dependent RNA helicase DDX46, transcript variant X1
probable ATP-dependent RNA helicase DDX46 isoform X4
probable ATP-dependent RNA helicase DDX46 isoform X3
probable ATP-dependent RNA helicase DDX46 isoform X2
probable ATP-dependent RNA helicase DDX46 isoform X1
U6 snRNA-associated Sm-like protein LSm3
U3 small nucleolar RNA-associated protein 14 homolog A
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
probable ribonuclease ZC3H12B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 77 samples with support for all annotated introns
probable ribonuclease ZC3H12D isoform X1
probable ribonuclease ZC3H12B, transcript variant X2
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 74 samples with support for all annotated introns
probable ribonuclease ZC3H12B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pre-mRNA-processing factor 6, transcript variant 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, including 46 samples with support for all annotated introns
pre-mRNA-processing factor 6, transcript variant X1
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 63 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, including 27 samples with support for all annotated introns
carboxypeptidase B, transcript variant X1
carboxypeptidase B, transcript variant X2
pre-mRNA-splicing regulator female-lethal(2)D
runt-related transcription factor 3, transcript variant X2
runt-related transcription factor 3, transcript variant X1
runt-related transcription factor 3 isoform X2
runt-related transcription factor 3 isoform X1
segmentation protein Runt, transcript variant X1
segmentation protein Runt, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-prolyl cis-trans isomerase sig-7
putative neuropeptide precursor protein, transcript variant X2
putative neuropeptide precursor protein, transcript variant X1
putative neuropeptide precursor protein isoform X1
putative neuropeptide precursor protein isoform X2
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B, 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 32 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B, 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 63 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B, transcript variant X1
ankyrin repeat domain-containing protein 7 isoform X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X2
mitogen-activated protein kinase kinase kinase 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 5
60S ribosomal protein L37a; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305531.2
The RefSeq transcript has 2 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X1
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X4
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X2
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X3
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X1
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X4
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X2
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X3
phosphatidylinositol 4-phosphate 5-kinase 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 22 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase 2, 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 21 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase 2
short-chain dehydrogenase/reductase family 16C member 6
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 21 samples with support for all annotated introns
U6 snRNA-associated Sm-like protein LSm7
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 65 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 60 samples with support for all annotated introns
uncharacterized LOC105380058, 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 4 samples with support for all annotated introns
uncharacterized LOC105380058, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC105380058 isoform X1
uncharacterized protein LOC105380058 isoform X2
histone-lysine N-methyltransferase PRDM16, transcript variant X2
histone-lysine N-methyltransferase PRDM16, 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 6 samples with support for all annotated introns
histone-lysine N-methyltransferase PRDM16 isoform X1
histone-lysine N-methyltransferase PRDM16 isoform X2
histone-lysine N-methyltransferase PRDM16, transcript variant X4
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 48 samples with support for all annotated introns
histone-lysine N-methyltransferase PRDM16 isoform X4
histone-lysine N-methyltransferase PRDM16, 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 26 samples with support for all annotated introns
histone-lysine N-methyltransferase PRDM16 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105384472, transcript variant X1
uncharacterized LOC105384472, transcript variant X2
uncharacterized protein LOC105384472 isoform X1
uncharacterized protein LOC105384472 isoform X2
polypeptide N-acetylgalactosaminyltransferase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
enoyl-CoA hydratase domain-containing protein 3, mitochondrial
putative uncharacterized protein DDB_G0277255, transcript variant X6
putative uncharacterized protein DDB_G0277255, transcript variant X8
putative uncharacterized protein DDB_G0277255, transcript variant X9
putative uncharacterized protein DDB_G0287457 isoform X6
putative mediator of RNA polymerase II transcription subunit 26 isoform X8
putative mediator of RNA polymerase II transcription subunit 26 isoform X9
putative uncharacterized protein DDB_G0277255, transcript variant X1
putative uncharacterized protein DDB_G0277255, transcript variant X3
putative uncharacterized protein DDB_G0277255, transcript variant X5
putative uncharacterized protein DDB_G0277255, transcript variant X7
putative uncharacterized protein DDB_G0277255, transcript variant X2
putative uncharacterized protein DDB_G0287457 isoform X1
putative uncharacterized protein DDB_G0277255 isoform X2
putative uncharacterized protein DDB_G0287457 isoform X3
putative uncharacterized protein DDB_G0287457 isoform X5
putative uncharacterized protein DDB_G0287457 isoform X7
putative uncharacterized protein DDB_G0277255, transcript variant X4
putative uncharacterized protein DDB_G0287457 isoform X4
MATH and LRR domain-containing protein PFE0570w-like
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
transcription initiation factor TFIID subunit 11
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 79 samples with support for all annotated introns
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial, transcript variant X1
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial, transcript variant X2
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial isoform X1
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial isoform X2
iron-sulfur cluster assembly 2 homolog, mitochondrial
protein split ends, transcript variant X1
protein split ends, transcript variant X2
protein split ends, transcript variant X3
uncharacterized LOC125489030, transcript variant X1
uncharacterized LOC125489030, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105390638, transcript variant X1
uncharacterized LOC105390638, transcript variant X2
protein quick-to-court, transcript variant X3
protein quick-to-court, transcript variant X2
protein quick-to-court, transcript variant X4
protein quick-to-court, transcript variant X1
protein quick-to-court, transcript variant X6
protein quick-to-court, transcript variant X5
protein smoothened, transcript variant X4
protein smoothened, transcript variant X5
protein smoothened, transcript variant X2
protein smoothened, transcript variant X3
protein smoothened, transcript variant X1
pre-mRNA 3' end processing protein WDR33 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X11
zinc finger protein OZF, transcript variant X10
zinc finger protein OZF, transcript variant X6
zinc finger protein OZF, transcript variant X5
zinc finger protein OZF, transcript variant X4
zinc finger protein OZF, transcript variant X12
zinc finger protein OZF, transcript variant X3
zinc finger protein OZF, transcript variant X8
zinc finger protein OZF, transcript variant X1
zinc finger protein OZF, transcript variant X23
zinc finger protein OZF, transcript variant X20
zinc finger protein OZF, transcript variant X17
zinc finger protein OZF, transcript variant X19
zinc finger protein OZF, transcript variant X14
zinc finger protein OZF, transcript variant X22
zinc finger protein OZF, transcript variant X16
zinc finger protein OZF, transcript variant X9
zinc finger protein OZF, transcript variant X21
zinc finger protein OZF, transcript variant X18
zinc finger protein OZF, transcript variant X13
zinc finger protein OZF, transcript variant X15
zinc finger protein OZF, transcript variant X7
zinc finger protein OZF, transcript variant X2
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
V-type proton ATPase subunit H, transcript variant X2
V-type proton ATPase subunit H, transcript variant X3
V-type proton ATPase subunit H, transcript variant X1
V-type proton ATPase subunit H, transcript variant X4
V-type proton ATPase subunit H isoform X4
V-type proton ATPase subunit H isoform X2
V-type proton ATPase subunit H isoform X3
V-type proton ATPase subunit H isoform X1
tRNA-splicing endonuclease subunit SEN2, transcript variant X1
tRNA-splicing endonuclease subunit SEN2, transcript variant X2
tRNA-splicing endonuclease subunit SEN2 isoform X1
uncharacterized protein LOC105380109 isoform X2
COX assembly mitochondrial protein homolog
26S proteasome non-ATPase regulatory subunit 14
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cytochrome c; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305479.1
The RefSeq transcript has 4 substitutions, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
cytochrome b5 reductase 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 47 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
cytochrome b5 reductase 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 39 samples with support for all annotated introns
cytochrome b5 reductase 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
cytochrome b5 reductase 4, 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 17 samples with support for all annotated introns
FAS-associated factor 2, 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 33 samples with support for all annotated introns
FAS-associated factor 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 41 samples with support for all annotated introns
enoyl-[acyl-carrier-protein] reductase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 25 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 63 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
glutathione S-transferase C-terminal domain-containing protein homolog
39S ribosomal protein L41, mitochondrial
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 59 samples with support for all annotated introns
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase
glyceraldehyde-3-phosphate dehydrogenase; Derived by automated computational analysis using gene prediction method: BestRefSeq.
glyceraldehyde-3-phosphate dehydrogenase
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309122.1
The RefSeq transcript has 13 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ralBP1-associated Eps domain-containing protein 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 64 samples with support for all annotated introns
uncharacterized LOC105386069, transcript variant X3
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
uncharacterized protein LOC105386069 isoform X3
uncharacterized LOC105386069, 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 8 samples with support for all annotated introns
uncharacterized protein LOC105386069 isoform X2
uncharacterized LOC105386069, 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 3 samples with support for all annotated introns
uncharacterized protein LOC105386069 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 26 samples with support for all annotated introns
SET and MYND domain-containing protein 4-like
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 44 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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
neuropeptide CCHamide-2 receptor, transcript variant X3
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
neuropeptide CCHamide-2 receptor, 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 38 samples with support for all annotated introns
neuropeptide CCHamide-2 receptor, transcript variant X2
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 44 samples with support for all annotated introns
neuropeptide CCHamide-2 receptor isoform X3
neuropeptide CCHamide-2 receptor isoform X1
neuropeptide CCHamide-2 receptor isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105391812, transcript variant X1
uncharacterized LOC105391812, transcript variant X2
uncharacterized protein LOC105391812 isoform X1
uncharacterized protein LOC105391812 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
putative uncharacterized protein DDB_G0286901
uncharacterized LOC105386277, transcript variant X1
uncharacterized LOC105386277, transcript variant X2
uncharacterized protein LOC105386277 isoform X1
uncharacterized protein LOC105386277 isoform X2
uncharacterized LOC125488943, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC125488943, 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 49 samples with support for all annotated introns
uncharacterized LOC119690295, 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 8 samples with support for all annotated introns
uncharacterized LOC119690295, transcript variant X2
protein drumstick, transcript variant X1
protein drumstick, transcript variant X3
protein drumstick, transcript variant X2
piwi-like protein Ago3, transcript variant X1
piwi-like protein Ago3, 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 75 samples with support for all annotated introns
NFU1 iron-sulfur cluster scaffold homolog, mitochondrial
mitochondrial ribosome-associated GTPase 2
probable G-protein coupled receptor CG31760, transcript variant X2
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 1 sample with support for all annotated introns
probable G-protein coupled receptor CG31760, transcript variant X4
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 3 samples with support for all annotated introns
probable G-protein coupled receptor CG31760, 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 4 samples with support for all annotated introns
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like
probable G-protein coupled receptor CG31760 isoform X1
probable G-protein coupled receptor CG31760, transcript variant X3
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 9 samples with support for all annotated introns
probable G-protein coupled receptor CG31760 isoform X2
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
uncharacterized LOC105389461, 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 26 samples with support for all annotated introns
uncharacterized LOC105389461, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized LOC105389461, 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 47 samples with support for all annotated introns
uncharacterized LOC105389461, 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 77 samples with support for all annotated introns
uncharacterized protein LOC105389461 isoform X1
uncharacterized protein LOC105389461 isoform X2
uncharacterized protein LOC105389461 isoform X3
uncharacterized protein LOC105389461 isoform X4
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X1
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X2
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X4
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X5
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X3
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X6
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X7
uncharacterized LOC119693669, transcript variant X2
uncharacterized protein LOC119693669 isoform X2
uncharacterized LOC119693669, transcript variant X1
uncharacterized protein LOC119693669 isoform X1
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X4
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X1
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X2
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X3
long-chain-fatty-acid--CoA ligase 1, transcript variant X4
long-chain-fatty-acid--CoA ligase 1, transcript variant X6
long-chain-fatty-acid--CoA ligase 1, transcript variant X7
long-chain-fatty-acid--CoA ligase 1, transcript variant X5
long-chain-fatty-acid--CoA ligase 5 isoform X3
long-chain-fatty-acid--CoA ligase 1, transcript variant X2
long-chain-fatty-acid--CoA ligase 1, transcript variant X1
long-chain-fatty-acid--CoA ligase 1, transcript variant X3
long-chain-fatty-acid--CoA ligase 5 isoform X1
long-chain-fatty-acid--CoA ligase 5 isoform X2
long-chain-fatty-acid--CoA ligase 1, transcript variant X8
long-chain-fatty-acid--CoA ligase 1, transcript variant X9
long-chain-fatty-acid--CoA ligase 1 isoform X4
long-chain-fatty-acid--CoA ligase 1 isoform X5
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X2
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X3
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B isoform X2
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X4
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B isoform X3
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X1
cGMP-dependent protein kinase, isozyme 2 forms cD5/T2 isoform X1
rap1 GTPase-activating protein 1, transcript variant X7
rap1 GTPase-activating protein 1 isoform X7
rap1 GTPase-activating protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rap1 GTPase-activating protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
rap1 GTPase-activating protein 1, transcript variant X8
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
rap1 GTPase-activating protein 1, transcript variant X10
rap1 GTPase-activating protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rap1 GTPase-activating protein 1, transcript variant X4
rap1 GTPase-activating protein 1 isoform X10
rap1 GTPase-activating protein 1 isoform X1
rap1 GTPase-activating protein 1 isoform X3
rap1 GTPase-activating protein 1 isoform X2
rap1 GTPase-activating protein 1 isoform X4
rap1 GTPase-activating protein 1 isoform X8
rap1 GTPase-activating protein 1, transcript variant X5
rap1 GTPase-activating protein 1, transcript variant X6
rap1 GTPase-activating protein 1, transcript variant X9
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 54 samples with support for all annotated introns
rap1 GTPase-activating protein 1 isoform X5
rap1 GTPase-activating protein 1 isoform X6
rap1 GTPase-activating protein 1 isoform X9
rap1 GTPase-activating protein 1, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
rap1 GTPase-activating protein 1, transcript variant X12
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 55 samples with support for all annotated introns
rap1 GTPase-activating protein 1, transcript variant X14
rap1 GTPase-activating protein 1 isoform X11
rap1 GTPase-activating protein 1 isoform X12
rap1 GTPase-activating protein 1 isoform X14
rap1 GTPase-activating protein 1, transcript variant X15
rap1 GTPase-activating protein 1, transcript variant X16
rap1 GTPase-activating protein 1 isoform X15
rap1 GTPase-activating protein 1 isoform X16
rap1 GTPase-activating protein 1, transcript variant X13
rap1 GTPase-activating protein 1 isoform X13
basic juvenile hormone-suppressible protein 2
basic juvenile hormone-suppressible protein 2-like
basic juvenile hormone-suppressible protein 2-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309096.2
The RefSeq transcript has 51 substitutions, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001296025.2
The RefSeq protein has 5 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
basic juvenile hormone-suppressible protein 2-like precursor
COORDINATES: ab initio prediction:SignalP:4.0
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: 95% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
arylphorin subunit alpha, transcript variant X1
arylphorin subunit alpha, transcript variant X2
arylphorin subunit beta-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305497.1
The RefSeq transcript has 27 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001292426.1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305496.1
The RefSeq transcript has 20 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC125489314, 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 85 samples with support for all annotated introns
uncharacterized LOC125489314, 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 35 samples with support for all annotated introns
uncharacterized LOC125489314, 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 14 samples with support for all annotated introns
uncharacterized LOC125489314, transcript variant X2
uncharacterized LOC125489314, 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 29 samples with support for all annotated introns
uncharacterized LOC125489314, 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 44 samples with support for all annotated introns
acidic juvenile hormone-suppressible protein 1, transcript variant X1
acidic juvenile hormone-suppressible protein 1, transcript variant X2
acidic juvenile hormone-suppressible protein 1 isoform X1
acidic juvenile hormone-suppressible protein 1 isoform X2
protein gooseberry, transcript variant X1
protein gooseberry, transcript variant X3
protein gooseberry, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
protein gooseberry-neuro, transcript variant X2
protein gooseberry-neuro, transcript variant X1
protein gooseberry-neuro, transcript variant X3
ice-structuring glycoprotein, transcript variant X3
ice-structuring glycoprotein, transcript variant X7
ice-structuring glycoprotein, transcript variant X2
ice-structuring glycoprotein, transcript variant X5
ice-structuring glycoprotein, transcript variant X6
ice-structuring glycoprotein, transcript variant X4
ice-structuring glycoprotein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
EF-hand domain-containing protein D2 homolog
guided entry of tail-anchored proteins factor 1
mitochondrial carrier protein Rim2, transcript variant X2
mitochondrial carrier protein Rim2, transcript variant X1
mitochondrial carrier protein Rim2, transcript variant X4
mitochondrial carrier protein Rim2, transcript variant X3
mitochondrial carrier protein Rim2 isoform X2
mitochondrial carrier protein Rim2 isoform X1
mitochondrial carrier protein Rim2 isoform X4
mitochondrial carrier protein Rim2 isoform X3
superoxide dismutase [Mn], mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
vacuolar protein sorting-associated protein 11 homolog, transcript variant X3
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
vacuolar protein sorting-associated protein 11 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 29 samples with support for all annotated introns
vacuolar protein sorting-associated protein 11 homolog, 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 40 samples with support for all annotated introns
vacuolar protein sorting-associated protein 11 homolog isoform X3
vacuolar protein sorting-associated protein 11 homolog isoform X1
vacuolar protein sorting-associated protein 11 homolog isoform X2
beta-1,4-N-acetylgalactosaminyltransferase bre-4
beta-1,4-N-acetylgalactosaminyltransferase bre-4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 EST, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
PAT complex subunit CCDC47, transcript variant X2
PAT complex subunit CCDC47, transcript variant X1
PAT complex subunit CCDC47, transcript variant X3
invertebrate-type lysozyme 3, 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 82 samples with support for all annotated introns
invertebrate-type lysozyme 3, transcript variant X1
invertebrate-type lysozyme 3, 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 62 samples with support for all annotated introns
low density lipoprotein receptor adapter protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
wiskott-Aldrich syndrome protein family member 2
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
guanine nucleotide-binding protein subunit beta-like protein; Derived by automated computational analysis using gene prediction method: BestRefSeq.
guanine nucleotide-binding protein subunit beta-like protein
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305507.2
The RefSeq transcript has 11 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
serine/threonine-protein phosphatase 2A catalytic subunit; Derived by automated computational analysis using gene prediction method: BestRefSeq.
serine/threonine-protein phosphatase 2A catalytic subunit
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309105.1
The RefSeq transcript has 22 substitutions, 6 non-frameshifting indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001296034.1
The RefSeq protein has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
serine/threonine-protein phosphatase 2A catalytic subunit beta isoform
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
5-methylcytosine rRNA methyltransferase nsun-4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
tudor and KH domain-containing protein homolog, transcript variant X2
tudor and KH domain-containing protein homolog, transcript variant X1
tudor and KH domain-containing protein homolog isoform X2
tudor and KH domain-containing protein homolog isoform X1
tudor and KH domain-containing protein homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tudor and KH domain-containing protein homolog isoform X3
uncharacterized LOC105394452, transcript variant X2
uncharacterized protein LOC105394452 isoform X2
uncharacterized LOC105394452, transcript variant X1
uncharacterized protein LOC105394452 isoform X1
X-ray repair cross-complementing protein 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
X-ray repair cross-complementing protein 5, transcript variant X2
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 67 samples with support for all annotated introns
X-ray repair cross-complementing protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 samples with support for all annotated introns
eukaryotic translation initiation factor 4E-binding protein
neutral and basic amino acid transport protein rBAT, transcript variant X1
neutral and basic amino acid transport protein rBAT, transcript variant X2
uncharacterized protein LOC105383450 isoform X1
uncharacterized protein LOC105383450 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 77 samples with support for all annotated introns
neutral and basic amino acid transport protein rBAT, transcript variant X3
neutral and basic amino acid transport protein rBAT isoform X3
zinc finger C2HC domain-containing protein 1B
chromosome transmission fidelity protein 18 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 54% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 5A, transcript variant X2
eukaryotic translation initiation factor 5A, transcript variant X1
eukaryotic translation initiation factor 5A
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, including 48 samples with support for all annotated introns
F-actin-capping protein subunit beta, transcript variant X2
F-actin-capping protein subunit beta, transcript variant X1
F-actin-capping protein subunit beta isoform X2
F-actin-capping protein subunit beta isoform X1
atypical protein kinase C, transcript variant X7
atypical protein kinase C, transcript variant X5
atypical protein kinase C, transcript variant X6
atypical protein kinase C, transcript variant X1
atypical protein kinase C, transcript variant X3
atypical protein kinase C, transcript variant X2
atypical protein kinase C, transcript variant X4
atypical protein kinase C, transcript variant X10
atypical protein kinase C, transcript variant X9
atypical protein kinase C, transcript variant X8
zinc finger and BTB domain-containing protein 49, transcript variant X1
zinc finger and BTB domain-containing protein 49, transcript variant X3
zinc finger and BTB domain-containing protein 49, transcript variant X2
zinc finger and BTB domain-containing protein 2 isoform X1
zinc finger and BTB domain-containing protein 2 isoform X3
zinc finger and BTB domain-containing protein 49 isoform X2
H/ACA ribonucleoprotein complex non-core subunit NAF1
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 70 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 7, transcript variant X1
protein phosphatase 1 regulatory subunit 7, transcript variant X2
protein phosphatase 1 regulatory subunit 7 isoform X1
protein phosphatase 1 regulatory subunit 7 isoform X2
protein phosphatase 1 regulatory subunit 7, transcript variant X3
protein phosphatase 1 regulatory subunit 7 isoform X3
GMP synthase [glutamine-hydrolyzing], transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
GMP synthase [glutamine-hydrolyzing], transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
GMP synthase [glutamine-hydrolyzing], transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
GMP synthase [glutamine-hydrolyzing], transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
GMP synthase [glutamine-hydrolyzing] isoform X2
GMP synthase [glutamine-hydrolyzing] isoform X1
GMP synthase [glutamine-hydrolyzing] isoform X3
transcriptional adapter 2A, transcript variant X2
transcriptional adapter 2A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 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: 3 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: 2 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
rho-related GTP-binding protein RhoN, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial import receptor subunit TOM40 homolog
rho-related GTP-binding protein RhoN isoform X2
rho-related GTP-binding protein RhoN, transcript variant X1
rho-related GTP-binding protein RhoN isoform X1
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger-containing ubiquitin peptidase 1
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
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 69 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 66 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
fatty-acid amide hydrolase 2-A, transcript variant X1
fatty-acid amide hydrolase 2-A, transcript variant X2
fatty-acid amide hydrolase 2-A isoform X1
fatty-acid amide hydrolase 2-A isoform X2
sodium-coupled neutral amino acid transporter 9 homolog
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
phosphoglucomutase, transcript variant X3
phosphoglucomutase, transcript variant X2
phosphoglucomutase, transcript variant X1
fatty-acid amide hydrolase 2, transcript variant 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, including 20 samples with support for all annotated introns
fatty-acid amide hydrolase 2, transcript variant X1
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 19 samples with support for all annotated introns
fatty-acid amide hydrolase 2, transcript variant X4
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 11 samples with support for all annotated introns
fatty-acid amide hydrolase 2, transcript variant X2
fatty-acid amide hydrolase 2, transcript variant X5
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 13 samples with support for all annotated introns
S-adenosylmethionine decarboxylase proenzyme, transcript variant X3
S-adenosylmethionine decarboxylase proenzyme, transcript variant X2
S-adenosylmethionine decarboxylase proenzyme, transcript variant X5
S-adenosylmethionine decarboxylase proenzyme, transcript variant X4
S-adenosylmethionine decarboxylase proenzyme, transcript variant X1
S-adenosylmethionine decarboxylase proenzyme
activating signal cointegrator 1 complex subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1, transcript variant X2
Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1, transcript variant X1
Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1 isoform X2
Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1 isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
ubiquitin carboxyl-terminal hydrolase 45, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 45, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 45, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 45 isoform X1
ubiquitin carboxyl-terminal hydrolase 16 isoform X3
ubiquitin carboxyl-terminal hydrolase 45 isoform X2
recQ-mediated genome instability protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
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 5 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Ig-like and fibronectin type-III domain-containing protein 1
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 80 samples with support for all annotated introns
histone acetyltransferase KAT6A, transcript variant X2
histone acetyltransferase KAT6A, transcript variant X6
histone acetyltransferase KAT6A, transcript variant X5
histone acetyltransferase KAT6A, transcript variant X4
histone acetyltransferase KAT6A, transcript variant X3
histone acetyltransferase KAT6A, transcript variant X1
histone acetyltransferase KAT6A isoform X2
histone acetyltransferase KAT6A isoform X6
histone acetyltransferase KAT6A isoform X5
histone acetyltransferase KAT6A isoform X4
histone acetyltransferase KAT6A isoform X3
histone acetyltransferase KAT6A isoform X1
60 kDa heat shock protein, mitochondrial-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
60 kDa heat shock protein, mitochondrial-like
similar to RNA sequence, mRNA (same species):RefSeq:NM_001320024.1
The RefSeq transcript has 53 substitutions, 2 non-frameshifting indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
tyrosine-protein phosphatase non-receptor type 13
vesicle transport through interaction with t-SNAREs homolog 1A, 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 58 samples with support for all annotated introns
vesicle transport through interaction with t-SNAREs homolog 1A, 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 53 samples with support for all annotated introns
vesicle transport through interaction with t-SNAREs homolog 1A isoform X2
vesicle transport through interaction with t-SNAREs homolog 1A isoform 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 67 samples with support for all annotated introns
bone morphogenetic protein receptor type-1B, transcript variant X2
bone morphogenetic protein receptor type-1B isoform X2
bone morphogenetic protein receptor type-1B, transcript variant X1
bone morphogenetic protein receptor type-1B isoform X1
RNA-binding protein lark, transcript variant X2
RNA-binding protein lark, transcript variant X1
stress-activated protein kinase JNK, transcript variant X1
stress-activated protein kinase JNK, transcript variant X3
stress-activated protein kinase JNK, transcript variant X4
stress-activated protein kinase JNK, transcript variant X5
stress-activated protein kinase JNK, transcript variant X2
stress-activated protein kinase JNK isoform X1
stress-activated protein kinase JNK isoform X2
stress-activated protein kinase JNK, transcript variant X6
stress-activated protein kinase JNK, transcript variant X7
stress-activated protein kinase JNK isoform X3
stress-activated protein kinase JNK isoform X4
transcription initiation factor TFIID subunit 9
hydroxyacyl-coenzyme A dehydrogenase, mitochondrial
probable 3-hydroxyacyl-CoA dehydrogenase B0272.3, transcript variant 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, including 80 samples with support for all annotated introns
probable 3-hydroxyacyl-CoA dehydrogenase B0272.3, transcript variant X1
probable 3-hydroxyacyl-CoA dehydrogenase B0272.3 isoform X2
probable 3-hydroxyacyl-CoA dehydrogenase B0272.3 isoform X1
AN1-type zinc finger protein 4, transcript variant X1
AN1-type zinc finger protein 4, transcript variant X2
AN1-type zinc finger protein 4 isoform X2
AN1-type zinc finger protein 4 isoform X1
40S ribosomal protein S26; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309128.1
The RefSeq transcript has 4 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
PEST proteolytic signal-containing nuclear protein
mitochondrial tRNA methylthiotransferase CDK5RAP1
uncharacterized LOC105384971, transcript variant X2
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 5 samples with support for all annotated introns
uncharacterized LOC105384971, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57% coverage of the annotated genomic feature by RNAseq alignments
microsomal triacylglycerol transfer protein
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: 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: 99% coverage of the annotated genomic feature by RNAseq alignments
kelch-like protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 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 81 samples with support for all annotated introns
kelch-like protein 3, 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 60 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 76 samples with support for all annotated introns
uncharacterized LOC105387752, transcript variant X5
uncharacterized LOC105387752, transcript variant X4
uncharacterized LOC105387752, transcript variant X3
uncharacterized LOC105387752, transcript variant X2
uncharacterized LOC105387752, transcript variant X1
uncharacterized protein LOC105387752 isoform X4
uncharacterized protein LOC105387752 isoform X1
uncharacterized protein LOC105387752 isoform X3
uncharacterized protein LOC105387752 isoform X2
uncharacterized protein LOC105387752 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
U5 small nuclear ribonucleoprotein 40 kDa protein
stimulator of interferon genes protein homolog
LOW QUALITY PROTEIN: uncharacterized protein LOC119693506