Plutella xylostella chromosome 6, 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\nOW026560.1.\nAssembly name: ilPluXylo3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/03/10. The original whole-genome shotgun project has the\naccession CAKNZZ000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Plutella xylostella Annotation\n Release 103\nAnnotation Version :: 103\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
collagen alpha chain CG42342, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
collagen alpha chain CG42342 isoform X12
collagen alpha chain CG42342, transcript variant X8
collagen alpha chain CG42342, transcript variant X10
collagen alpha chain CG42342, transcript variant X9
collagen alpha chain CG42342, transcript variant X3
collagen alpha chain CG42342, transcript variant X7
collagen alpha chain CG42342, transcript variant X5
collagen alpha chain CG42342, transcript variant X2
collagen alpha chain CG42342, transcript variant X13
collagen alpha chain CG42342, transcript variant X11
collagen alpha chain CG42342, transcript variant X6
collagen alpha chain CG42342, transcript variant X4
collagen alpha chain CG42342, transcript variant X1
collagen alpha chain CG42342, transcript variant X14
collagen alpha chain CG42342 isoform X10
collagen alpha chain CG42342 isoform X13
collagen alpha chain CG42342 isoform X11
collagen alpha chain CG42342 isoform X14
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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: 32 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48% 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, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
pyruvate dehydrogenase E1 component subunit beta, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
saccharopine dehydrogenase-like oxidoreductase, transcript variant X2
saccharopine dehydrogenase-like oxidoreductase, transcript variant X1
saccharopine dehydrogenase-like oxidoreductase isoform X2
saccharopine dehydrogenase-like oxidoreductase isoform X1
uncharacterized LOC119690619, transcript variant X5
uncharacterized LOC119690619, transcript variant X8
uncharacterized LOC119690619, transcript variant X3
uncharacterized LOC119690619, transcript variant X2
uncharacterized LOC119690619, transcript variant X1
uncharacterized LOC119690619, transcript variant X4
uncharacterized LOC119690619, transcript variant X6
uncharacterized LOC119690619, transcript variant X7
phenylalanine--tRNA ligase alpha subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 28 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
synaptic functional regulator FMR1, transcript variant X4
synaptic functional regulator FMR1, transcript variant X5
synaptic functional regulator FMR1, transcript variant X1
synaptic functional regulator FMR1, transcript variant X2
synaptic functional regulator FMR1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
synaptic functional regulator FMR1, 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 24 samples with support for all annotated introns
synaptic functional regulator FMR1, transcript variant X6
synaptic functional regulator FMR1, transcript variant X7
synaptic functional regulator FMR1, transcript variant X3
synaptic functional regulator FMR1 isoform X4
synaptic functional regulator FMR1 isoform X5
synaptic functional regulator FMR1 isoform X1
synaptic functional regulator FMR1 isoform X2
synaptic functional regulator FMR1 isoform X6
synaptic functional regulator FMR1 isoform X7
synaptic functional regulator FMR1 isoform X3
synaptic functional regulator FMR1 isoform X8
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 29 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 82 samples with support for all annotated introns
uncharacterized LOC105393968, transcript variant X2
uncharacterized LOC105393968, transcript variant X1
uncharacterized LOC105393970, 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 21 samples with support for all annotated introns
uncharacterized LOC105393970, 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 30 samples with support for all annotated introns
uncharacterized protein LOC105393970 isoform X2
uncharacterized protein LOC105393970 isoform X1
peripheral plasma membrane protein CASK, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
peripheral plasma membrane protein CASK, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
peripheral plasma membrane protein CASK, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
peripheral plasma membrane protein CASK, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
peripheral plasma membrane protein CASK, transcript variant X7
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 7 samples with support for all annotated introns
peripheral plasma membrane protein CASK, 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 13 samples with support for all annotated introns
peripheral plasma membrane protein CASK, 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 23 samples with support for all annotated introns
peripheral plasma membrane protein CASK isoform X2
peripheral plasma membrane protein CASK isoform X1
peripheral plasma membrane protein CASK isoform X3
peripheral plasma membrane protein CASK isoform X4
peripheral plasma membrane protein CASK-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerase I subunit RPA12, transcript variant X1
DNA-directed RNA polymerase I subunit RPA12, transcript variant X2
DNA-directed RNA polymerase I subunit RPA12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
glutathione S-transferase D7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glutathione S-transferase D7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 124 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glutathione S-transferase D7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized protein LOC105396319 isoform X1
uncharacterized LOC105381901, 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 27 samples with support for all annotated introns
uncharacterized LOC105381901, 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 9 samples with support for all annotated introns
glutathione S-transferase D7, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 126 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
glutathione S-transferase D7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 126 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
angiotensin-converting enzyme, transcript variant X1
angiotensin-converting enzyme, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
angiotensin-converting enzyme isoform X1
angiotensin-converting enzyme isoform X2
uncharacterized LOC105395636, transcript variant X1
uncharacterized LOC105395636, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125488634, 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 42 samples with support for all annotated introns
uncharacterized LOC125488634, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60% coverage of the annotated genomic feature by RNAseq alignments
vacuolar protein sorting-associated protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
U6 snRNA-associated Sm-like protein LSm8
probable mitochondrial glutathione transporter SLC25A40, transcript variant X3
probable mitochondrial glutathione transporter SLC25A40, transcript variant X2
probable mitochondrial glutathione transporter SLC25A40, transcript variant X1
probable mitochondrial glutathione transporter SLC25A40 isoform X1
probable mitochondrial glutathione transporter SLC25A40 isoform X2
NADP-dependent malic enzyme, transcript variant X7
NADP-dependent malic enzyme, transcript variant X1
NADP-dependent malic enzyme, transcript variant X2
NADP-dependent malic enzyme, transcript variant X4
NADP-dependent malic enzyme, transcript variant X5
NADP-dependent malic enzyme, transcript variant X3
NADP-dependent malic enzyme, transcript variant X6
suppressor of lurcher protein 1, transcript variant X1
suppressor of lurcher protein 1, transcript variant X2
suppressor of lurcher protein 1 isoform X1
suppressor of lurcher protein 1 isoform X2
uncharacterized protein DDB_G0271670 isoform X1
uncharacterized LOC125491485, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC125491485, 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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 25 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
tigger transposable element-derived protein 6
uncharacterized LOC125488684, transcript variant X3
uncharacterized LOC125488684, transcript variant X1
uncharacterized LOC125488684, transcript variant X2
uncharacterized protein LOC125488684 isoform X2
uncharacterized protein LOC125488684 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 samples with support for all annotated introns
mitochondrial transcription rescue factor 1
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 82 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 52 samples with support for all annotated introns
uncharacterized LOC105390657, 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 23 samples with support for all annotated introns
uncharacterized LOC105390657, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
protein held out wings, transcript variant X5
protein held out wings, transcript variant X4
protein held out wings, transcript variant X3
protein held out wings, transcript variant X1
protein held out wings, transcript variant X7
protein held out wings, transcript variant X8
protein held out wings, transcript variant X2
protein held out wings, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
non-structural maintenance of chromosomes element 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 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: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125488641, transcript variant X2
uncharacterized LOC125488641, transcript variant X1
probable ATP-dependent RNA helicase pitchoune, transcript variant X1
probable ATP-dependent RNA helicase pitchoune, transcript variant X2
probable ATP-dependent RNA helicase pitchoune isoform X1
probable ATP-dependent RNA helicase pitchoune isoform X2
probable ATP-dependent RNA helicase pitchoune
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
odorant receptor 94a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
odorant receptor 94a, transcript variant X1
WD repeat-containing protein 44, transcript variant X3
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
WD repeat-containing protein 44 isoform X3
WD repeat-containing protein 44, 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 27 samples with support for all annotated introns
WD repeat-containing protein 44, 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 21 samples with support for all annotated introns
WD repeat-containing protein 44 isoform X1
WD repeat-containing protein 44 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
trafficking protein particle complex subunit 1
mitochondrial import inner membrane translocase subunit Tim17-B
serine/threonine-protein kinase Warts, transcript variant X2
serine/threonine-protein kinase Warts, transcript variant X1
thioredoxin domain-containing protein 5 homolog
ADP-ribosylation factor-like protein 6-interacting protein 4
RING finger and transmembrane domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
alpha-2-macroglobulin receptor-associated protein, transcript variant X1
alpha-2-macroglobulin receptor-associated protein, transcript variant X2
alpha-2-macroglobulin receptor-associated protein isoform X1
alpha-2-macroglobulin receptor-associated protein isoform X2
ankyrin repeat domain-containing protein 17, transcript variant X2
ankyrin repeat domain-containing protein 17, transcript variant X4
ankyrin repeat domain-containing protein 17, transcript variant X7
ankyrin repeat domain-containing protein 17, transcript variant X3
ankyrin repeat domain-containing protein 17, transcript variant X1
ankyrin repeat domain-containing protein 17, transcript variant X8
ankyrin repeat domain-containing protein 17, transcript variant X5
ankyrin repeat domain-containing protein 17, transcript variant X9
ankyrin repeat domain-containing protein 17, transcript variant X6
ankyrin repeat domain-containing protein 17, transcript variant X10
ankyrin repeat domain-containing protein 17 isoform X2
ankyrin repeat and KH domain-containing protein 1 isoform X8
ankyrin repeat domain-containing protein 17 isoform X5
ankyrin repeat domain-containing protein 17 isoform X9
ankyrin repeat domain-containing protein 17 isoform X4
ankyrin repeat domain-containing protein 17 isoform X6
ankyrin repeat domain-containing protein 17 isoform X7
ankyrin repeat domain-containing protein 17 isoform X3
ankyrin repeat domain-containing protein 17 isoform X1
ankyrin repeat domain-containing protein 17 isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
glucose transporter type 1, transcript variant X2
glucose transporter type 1, transcript variant X3
glucose transporter type 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 92% 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 80 samples with support for all annotated introns
glutathione S-transferase 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
glutathione S-transferase 1, transcript variant X4
glutathione S-transferase 1, transcript variant X1
glutathione S-transferase 1, transcript variant X2
glutathione S-transferase 1, transcript variant X3
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305505.1
annotated by transcript or proteomic data
The RefSeq transcript has 8 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001292434.1
The RefSeq protein has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
glutathione S-transferase 1, isoform D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
putative inner dynein arm light chain, axonemal
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
mediator of RNA polymerase II transcription subunit 4
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 79 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC125488597, transcript variant X2
uncharacterized LOC125488597, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
trans-Golgi network integral membrane protein 2
vacuolar protein sorting-associated protein 72 homolog
uncharacterized LOC105386365, transcript variant X2
uncharacterized LOC105386365, transcript variant X1
uncharacterized protein LOC105386365 isoform X1
uncharacterized protein LOC105386365 isoform X2
glutathione S-transferase-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309132.1
The RefSeq transcript has 8 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.
C3 and PZP-like alpha-2-macroglobulin domain-containing protein 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium-transporting ATPase subunit beta-1
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 48 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 15 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 70% coverage of the annotated genomic feature by RNAseq alignments
probable 2-oxoglutarate dehydrogenase E1 component DHKTD1 homolog, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 491 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
transmembrane protein 135, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
transmembrane protein 135, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 6, transcript variant X1
CCR4-NOT transcription complex subunit 6, transcript variant X3
CCR4-NOT transcription complex subunit 6, transcript variant X2
CCR4-NOT transcription complex subunit 6 isoform X1
CCR4-NOT transcription complex subunit 6 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 55 samples with support for all annotated introns
28S ribosomal protein S24, mitochondrial, transcript variant X2
28S ribosomal protein S24, mitochondrial, transcript variant X1
28S ribosomal protein S24, mitochondrial isoform X2
28S ribosomal protein S24, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
tRNA (guanine(10)-N2)-methyltransferase homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
synaptic vesicle glycoprotein 2A, transcript variant X2
synaptic vesicle glycoprotein 2A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
synaptic vesicle 2-related protein isoform X1
synaptic vesicle glycoprotein 2A 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 67 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
cadherin-87A-like, transcript variant X1
cadherin-87A-like, transcript variant X2
lipid storage droplets surface-binding protein 1, transcript variant X7
lipid storage droplets surface-binding protein 1, transcript variant X8
lipid storage droplets surface-binding protein 1 isoform X7
lipid storage droplets surface-binding protein 1 isoform X8
lipid storage droplets surface-binding protein 1, transcript variant X6
lipid storage droplets surface-binding protein 1 isoform X6
lipid storage droplets surface-binding protein 1, transcript variant X1
lipid storage droplets surface-binding protein 1, transcript variant X5
lipid storage droplets surface-binding protein 1, transcript variant X3
lipid storage droplets surface-binding protein 1, transcript variant X2
lipid storage droplets surface-binding protein 1, transcript variant X4
lipid storage droplets surface-binding protein 1 isoform X1
lipid storage droplets surface-binding protein 1 isoform X3
lipid storage droplets surface-binding protein 1 isoform X5
lipid storage droplets surface-binding protein 1 isoform X2
lipid storage droplets surface-binding protein 1 isoform X4
diacylglycerol kinase theta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
diacylglycerol kinase theta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
diacylglycerol kinase theta, 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 30 samples with support for all annotated introns
diacylglycerol kinase theta, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
diacylglycerol kinase theta, transcript variant X6
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 74 samples with support for all annotated introns
diacylglycerol kinase theta, transcript variant X5
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 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 86% coverage of the annotated genomic feature by RNAseq alignments
F-box only protein 9, transcript variant X2
F-box only protein 9, transcript variant X1
AP-1 complex subunit sigma-2, transcript variant X1
AP-1 complex subunit sigma-2, transcript variant X2
lipid storage droplets surface-binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 83 samples with support for all annotated introns
cell division cycle protein 16 homolog, 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 11 samples with support for all annotated introns
cell division cycle protein 16 homolog, 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 15 samples with support for all annotated introns
cell division cycle protein 16 homolog isoform X1
cell division cycle protein 16 homolog isoform X2
cytoplasmic polyadenylation element-binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
nonsense-mediated mRNA decay factor SMG8, transcript variant X4
nonsense-mediated mRNA decay factor SMG8, transcript variant X5
nonsense-mediated mRNA decay factor SMG8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
nonsense-mediated mRNA decay factor SMG8, 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 9 samples with support for all annotated introns
nonsense-mediated mRNA decay factor SMG8, transcript variant X1
nonsense-mediated mRNA decay factor SMG8 isoform X3
nonsense-mediated mRNA decay factor SMG8 isoform X4
nonsense-mediated mRNA decay factor SMG8 isoform X5
nonsense-mediated mRNA decay factor SMG8 isoform X2
nonsense-mediated mRNA decay factor SMG8 isoform X1
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
eukaryotic translation initiation factor 4E type 2
uncharacterized LOC105390473, transcript variant X3
uncharacterized LOC105390473, transcript variant X1
uncharacterized LOC105390473, transcript variant X2
uncharacterized protein LOC105390473 isoform X2
uncharacterized protein LOC105390473 isoform X1
CDK5 regulatory subunit-associated protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119691138, transcript variant X3
uncharacterized LOC119691138, transcript variant X1
uncharacterized LOC119691138, transcript variant X2
uncharacterized protein LOC119691138 isoform X2
uncharacterized protein LOC119691138 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
uncharacterized LOC119694169, transcript variant X2
uncharacterized LOC119694169, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
uncharacterized LOC105381216, transcript variant X2
uncharacterized LOC105381216, transcript variant X1
uncharacterized LOC119694098, transcript variant X3
uncharacterized LOC119694098, transcript variant X2
uncharacterized LOC119694098, transcript variant X1
uncharacterized LOC105381219, transcript variant X1
uncharacterized LOC105381219, 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 49 samples with support for all annotated introns
glutathione S-transferase 1-1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
glutathione S-transferase 1-1, transcript variant X3
glutathione S-transferase 1-1, transcript variant X2
glutathione S-transferase 1-1, transcript variant X1
glutathione S-transferase 1-1, transcript variant X4
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309130.1
The RefSeq transcript has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
glutathione S-transferase 1-1 isoform X2
glutathione S-transferase 1-1 isoform X1
F-box/LRR-repeat protein fbxl-1, transcript variant X2
F-box/LRR-repeat protein fbxl-1, transcript variant X1
F-box/LRR-repeat protein fbxl-1 isoform X2
F-box/LRR-repeat protein fbxl-1 isoform X1
AN1-type zinc finger protein 5, transcript variant X3
AN1-type zinc finger protein 5, transcript variant X2
AN1-type zinc finger protein 5, transcript variant X5
AN1-type zinc finger protein 5, transcript variant X4
AN1-type zinc finger protein 5 isoform X2
AN1-type zinc finger protein 5 isoform X3
AN1-type zinc finger protein 5, transcript variant X1
zinc finger A20 and AN1 domain-containing stress-associated protein 6 isoform X1
progestin and adipoQ receptor family member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
trypsin CFT-1-like, transcript variant X1
trypsin CFT-1-like, transcript variant X2
dual specificity protein kinase CLK2, transcript variant X3
dual specificity protein kinase CLK2, transcript variant X4
dual specificity protein kinase CLK2 isoform X3
dual specificity protein kinase CLK2 isoform X4
dual specificity protein kinase CLK2, transcript variant X2
dual specificity protein kinase CLK2, transcript variant X1
dual specificity protein kinase KNS1 isoform X1
dual specificity protein kinase KNS1 isoform X2
translation initiation factor eIF-2B subunit alpha
tyrosine-protein kinase Fer, transcript variant X1
tyrosine-protein kinase Fer, transcript variant X2
tyrosine-protein kinase Fer, transcript variant X5
tyrosine-protein kinase Fer, transcript variant X3
tyrosine-protein kinase Fer, transcript variant X4
eukaryotic translation initiation factor 4B
uncharacterized LOC105397380, transcript variant X2
uncharacterized LOC105397380, transcript variant X1
transmembrane and ubiquitin-like domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
60S ribosomal protein L15; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309080.1
The RefSeq transcript has 6 substitutions, 1 non-frameshifting indel and aligns at 97% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
double-strand-break repair protein rad21 homolog, transcript variant X1
double-strand-break repair protein rad21 homolog, transcript variant X3
double-strand-break repair protein rad21 homolog, transcript variant X4
double-strand-break repair protein rad21 homolog, transcript variant X2
double-strand-break repair protein rad21 homolog isoform X1
double-strand-break repair protein rad21 homolog isoform X2
double-strand-break repair protein rad21 homolog isoform X3
ATP synthase lipid-binding protein, mitochondrial, transcript variant X1
ATP synthase lipid-binding protein, mitochondrial, transcript variant X2
ATP synthase lipid-binding protein, mitochondrial
juxtaposed with another zinc finger protein 1
vacuolar protein sorting-associated protein 16 homolog
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
single insulin-like growth factor-binding domain protein-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 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 53 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 34% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 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 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 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: 14 Proteins, 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: 53 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein 87F
heterogeneous nuclear ribonucleoprotein A1, A2/B1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
mannose-6-phosphate isomerase, transcript variant X2
mannose-6-phosphate isomerase, transcript variant X1
MATH and LRR domain-containing protein PFE0570w-like
ras-related C3 botulinum toxin substrate 1
leucine-rich repeat protein soc-2 homolog
cleavage stimulation factor subunit 2 tau variant, transcript variant X1
cleavage stimulation factor subunit 2 tau variant, transcript variant X2
cleavage stimulation factor subunit 2 tau variant isoform X1
cleavage stimulation factor subunit 2 tau variant 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 45 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 78 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 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
diencephalon/mesencephalon homeobox protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 57% 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 mRNA, 1 EST, 32 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC105386777, transcript variant X1
uncharacterized LOC105386777, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
homeotic protein antennapedia, transcript variant X1
homeotic protein antennapedia, transcript variant X2
homeotic protein antennapedia, transcript variant X3
homeotic protein ultrabithorax; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001316670.1
The RefSeq transcript has 9 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
homeobox protein abdominal-A homolog, transcript variant X4
homeobox protein abdominal-A homolog, transcript variant X2
homeobox protein abdominal-A homolog, transcript variant X3
homeobox protein abdominal-A homolog, transcript variant X1
homeobox protein abdominal-A homolog isoform X4
homeobox protein abdominal-A homolog isoform X3
homeobox protein abdominal-A homolog isoform X2
homeobox protein abdominal-A homolog isoform X1
homeobox protein abdominal-B, transcript variant X3
homeobox protein abdominal-B, transcript variant X1
homeobox protein abdominal-B, transcript variant X2
homeobox protein abdominal-B, transcript variant X4
uncharacterized LOC125488704, transcript variant X1
uncharacterized LOC125488704, transcript variant X2
protein wings apart-like, transcript variant X1
protein wings apart-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 samples with support for all annotated introns
IQ and ubiquitin-like domain-containing protein
sex determination protein fruitless, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sex determination protein fruitless, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sex determination protein fruitless, transcript variant X8
sex determination protein fruitless, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sex determination protein fruitless isoform X5
broad-complex core protein isoforms 1/2/3/4/5 isoform X3
broad-complex core protein isoforms 1/2/3/4/5 isoform X1
broad-complex core protein isoforms 1/2/3/4/5 isoform X2
sex determination protein fruitless, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sex determination protein fruitless, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
sex determination protein fruitless, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
sex determination protein fruitless, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
broad-complex core protein isoforms 1/2/3/4/5 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
RING finger protein 17, transcript variant X3
RING finger protein 17, transcript variant X2
RING finger protein 17, transcript variant X5
RING finger protein 17, transcript variant X1
RING finger protein 17, transcript variant X4
kynurenine formamidase, transcript variant X1
kynurenine formamidase, transcript variant X3
kynurenine formamidase, transcript variant X2
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L, transcript variant X1
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L isoform X1
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L isoform X2
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X2
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X4
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X3
LIM and senescent cell antigen-like-containing domain protein 1 isoform X2
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X1
LIM and senescent cell antigen-like-containing domain protein 1 isoform X1
LIM and senescent cell antigen-like-containing domain protein 1 isoform X3
ATPase H(+)-transporting accessory protein 2
protein N-lysine methyltransferase METTL21D
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
uncharacterized LOC105385830, transcript variant X1
uncharacterized LOC105385830, transcript variant X2
uncharacterized protein LOC105385830 isoform X1
uncharacterized protein LOC105385830 isoform X2
uncharacterized LOC105395304, transcript variant X1
uncharacterized LOC105395304, transcript variant X3
uncharacterized LOC105395304, transcript variant X2
uncharacterized protein LOC105395304 isoform X3
uncharacterized protein LOC105395304 isoform X2
uncharacterized protein LOC105395304 isoform X1
retinoid-inducible serine carboxypeptidase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
RUN and FYVE domain-containing protein 2, transcript variant X2
RUN and FYVE domain-containing protein 2, transcript variant X1
RUN and FYVE domain-containing protein 2 isoform X2
RUN and FYVE domain-containing protein 2 isoform X1
RUN and FYVE domain-containing protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
RUN and FYVE domain-containing protein 2, transcript variant X3
malate dehydrogenase 3, cytoplasmic, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
malate dehydrogenase 3, cytoplasmic, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
malate dehydrogenase 3, cytoplasmic, transcript variant X1
malate dehydrogenase 3, cytoplasmic isoform X1
uncharacterized protein LOC105385851 isoform X3
malate dehydrogenase 3, cytoplasmic, transcript variant X2
uncharacterized protein LOC105385851 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC105392135, transcript variant X1
uncharacterized LOC105392135, transcript variant X2
uncharacterized LOC105392135, 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 57 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
autophagy-related protein 16-1, 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 28 samples with support for all annotated introns
autophagy-related protein 16-1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
autophagy-related protein 16-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
autophagy-related protein 16-1 isoform X1
autophagy-related protein 16-1 isoform X2
autophagy-related protein 16-1 isoform X3
uncharacterized LOC105383883, transcript variant X3
uncharacterized LOC105383883, transcript variant X2
uncharacterized LOC105383883, transcript variant X1
transcription elongation factor B polypeptide 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
transmembrane emp24 domain-containing protein 3
uncharacterized LOC105383881, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
uncharacterized LOC105383881, 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 56 samples with support for all annotated introns
uncharacterized LOC105383881, transcript variant X3
uncharacterized protein LOC105383881 isoform X1
uncharacterized protein LOC105383881 isoform X2
uncharacterized protein LOC105383881 isoform X3
myosin light chain alkali, transcript variant X2
myosin light chain alkali, transcript variant X1
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
microtubule-associated protein tau, transcript variant X4
microtubule-associated protein tau, transcript variant X1
microtubule-associated protein tau, transcript variant X3
microtubule-associated protein tau, transcript variant X6
microtubule-associated protein tau, transcript variant X2
microtubule-associated protein tau, transcript variant X5
microtubule-associated protein tau, transcript variant X7
microtubule-associated protein tau isoform X1
microtubule-associated protein tau isoform X3
microtubule-associated protein tau isoform X2
microtubule-associated protein tau isoform X5
microtubule-associated protein tau isoform X7
microtubule-associated protein tau isoform X6
microtubule-associated protein tau isoform X4
uncharacterized LOC105383856, transcript variant X5
uncharacterized LOC105383856, transcript variant X6
uncharacterized LOC105383856, transcript variant X1
uncharacterized LOC105383856, transcript variant X2
uncharacterized LOC105383856, transcript variant X4
uncharacterized LOC105383856, transcript variant X8
uncharacterized LOC105383856, transcript variant X7
uncharacterized LOC105383856, transcript variant X3
uncharacterized LOC105383856, transcript variant X9
uncharacterized protein LOC105383856 isoform X5
uncharacterized protein LOC105383856 isoform X2
uncharacterized protein LOC105383856 isoform X6
uncharacterized protein LOC105383856 isoform X7
uncharacterized protein LOC105383856 isoform X4
uncharacterized protein LOC105383856 isoform X1
uncharacterized protein LOC105383856 isoform X3
uncharacterized protein LOC105383856 isoform X8
leukocyte receptor cluster member 8 homolog, transcript variant X5
leukocyte receptor cluster member 8 homolog, transcript variant X4
leukocyte receptor cluster member 8 homolog, transcript variant X1
leukocyte receptor cluster member 8 homolog, transcript variant X2
leukocyte receptor cluster member 8 homolog isoform X4
leukocyte receptor cluster member 8 homolog isoform X1
leukocyte receptor cluster member 8 homolog isoform X2
leukocyte receptor cluster member 8 homolog isoform X5
uncharacterized LOC119692958, transcript variant X2
uncharacterized LOC119692958, transcript variant X1
leukocyte receptor cluster member 8 homolog, transcript variant X3
sulfated surface glycoprotein 185-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% 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: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
tolloid-like protein 2, transcript variant X1
tolloid-like protein 2, transcript variant X2
tolloid-like protein 2, transcript variant X3
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 21 samples with support for all annotated introns
tolloid-like protein 2, transcript variant X4
heterogeneous nuclear ribonucleoprotein R, transcript variant X8
heterogeneous nuclear ribonucleoprotein R, transcript variant X10
heterogeneous nuclear ribonucleoprotein R, transcript variant X9
heterogeneous nuclear ribonucleoprotein R, transcript variant X12
heterogeneous nuclear ribonucleoprotein R, transcript variant X7
heterogeneous nuclear ribonucleoprotein R, transcript variant X4
heterogeneous nuclear ribonucleoprotein R, transcript variant X11
heterogeneous nuclear ribonucleoprotein R, transcript variant X6
heterogeneous nuclear ribonucleoprotein R, transcript variant X1
heterogeneous nuclear ribonucleoprotein R, transcript variant X3
heterogeneous nuclear ribonucleoprotein R, transcript variant X5
heterogeneous nuclear ribonucleoprotein R, transcript variant X2
heterogeneous nuclear ribonucleoprotein R isoform X4
heterogeneous nuclear ribonucleoprotein R isoform X1
heterogeneous nuclear ribonucleoprotein R isoform X3
heterogeneous nuclear ribonucleoprotein R isoform X6
heterogeneous nuclear ribonucleoprotein R, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein R, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein R isoform X5
heterogeneous nuclear ribonucleoprotein R isoform X2
heterogeneous nuclear ribonucleoprotein R isoform X8
heterogeneous nuclear ribonucleoprotein R isoform X7
ER membrane protein complex subunit 1, transcript variant X3
ER membrane protein complex subunit 1, transcript variant X1
ER membrane protein complex subunit 1, transcript variant X2
ER membrane protein complex subunit 1 isoform X1
ER membrane protein complex subunit 1 isoform X2
ER membrane protein complex subunit 1 isoform 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 21 samples with support for all annotated introns
uncharacterized LOC105383102, transcript variant X2
uncharacterized LOC105383102, transcript variant X1
uncharacterized protein LOC105383102 isoform X1
uncharacterized protein LOC105383102 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 94% 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 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 55 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
transmembrane protein 135, transcript variant X4
transmembrane protein 135, transcript variant X3
uncharacterized LOC105383076, transcript variant X2
uncharacterized LOC105383076, transcript variant X1
uncharacterized protein LOC105383076 isoform X2
uncharacterized protein LOC105383076 isoform X1
transfer RNA aspartic acid (anticodon GUC); 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 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
synaptic vesicle glycoprotein 2B-like, transcript variant X3
synaptic vesicle glycoprotein 2B-like, 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 17 samples with support for all annotated introns
synaptic vesicle glycoprotein 2B-like, transcript variant X2
synaptic vesicle glycoprotein 2B-like isoform X1
synaptic vesicle glycoprotein 2B-like isoform X2
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
TWiK family of potassium channels protein 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125488656, transcript variant X2
uncharacterized LOC125488656, transcript variant X1
chorion peroxidase, 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 3 samples with support for all annotated introns
chorion peroxidase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
synaptic vesicle glycoprotein 2C, transcript variant X1
synaptic vesicle glycoprotein 2C, transcript variant X2
synaptic vesicle glycoprotein 2C isoform X1
uncharacterized protein LOC119694174 isoform X2
plasminogen activator inhibitor 2, macrophage-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
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 61 samples with support for all annotated introns
heat shock protein 68, transcript variant X1
heat shock protein 68, transcript variant X2
heat shock protein 68, transcript variant X3
heat shock protein 68, transcript variant X4
ATP synthase mitochondrial F1 complex assembly factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105387846, transcript variant X1
uncharacterized LOC105387846, transcript variant X2
uncharacterized LOC105387846, transcript variant X3
uncharacterized protein LOC105387846 isoform X2
uncharacterized protein LOC105387846 isoform X3
uncharacterized protein LOC105387846 isoform X1
programmed cell death 6-interacting protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 4-like 2
uncharacterized LOC125488655, transcript variant X2
uncharacterized LOC125488655, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
splicing factor 1, transcript variant X2
splicing factor 1, transcript variant X3
splicing factor 1, transcript variant X1
ras GTPase-activating protein-binding protein 2, transcript variant X2
ras GTPase-activating protein-binding protein 2, transcript variant X3
ras GTPase-activating protein-binding protein 2, transcript variant X1
ras GTPase-activating protein-binding protein 2 isoform X2
ras GTPase-activating protein-binding protein 2 isoform X1
RNA-binding protein squid, transcript variant X1
RNA-binding protein squid, transcript variant X2
RNA-binding protein squid, transcript variant X3
RNA-binding protein squid, transcript variant X4
RNA-binding protein squid, transcript variant X5
RNA-binding protein squid, transcript variant X6
RNA-binding protein squid, transcript variant X7
RNA-binding protein squid, transcript variant X8
COORDINATES: nucleotide motif:Rfam:12.0:RF00476
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
vesicular acetylcholine transporter, 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 10 samples with support for all annotated introns
vesicular acetylcholine transporter, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
vesicular acetylcholine transporter isoform X2
vesicular acetylcholine transporter isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 4
uncharacterized LOC125488599, transcript variant X1
uncharacterized LOC125488599, transcript variant X2
uncharacterized protein DDB_G0283697-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 68% coverage of the annotated genomic feature by RNAseq alignments
scavenger receptor class B member 1, transcript variant X1
scavenger receptor class B member 1, transcript variant X4
scavenger receptor class B member 1, transcript variant X2
scavenger receptor class B member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
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
mothers against decapentaplegic homolog 6
heterogeneous nuclear ribonucleoprotein H
peptidyl-prolyl cis-trans isomerase G, transcript variant X1
peptidyl-prolyl cis-trans isomerase G, transcript variant X2
peptidyl-prolyl cis-trans isomerase G isoform X1
peptidyl-prolyl cis-trans isomerase G isoform X2
immunoglobulin superfamily DCC subclass member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105381054, transcript variant X2
uncharacterized protein LOC105381054 isoform X2
uncharacterized LOC105381054, 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 3 samples with support for all annotated introns
uncharacterized protein LOC105381054 isoform X1
uncharacterized LOC105381012, transcript variant X4
uncharacterized LOC105381012, transcript variant X3
uncharacterized LOC105381012, transcript variant X2
uncharacterized LOC105381012, transcript variant X1
uncharacterized LOC119694146, transcript variant X1
uncharacterized LOC119694146, transcript variant X2
leucine-rich repeat extensin-like protein 3, transcript variant X1
leucine-rich repeat extensin-like protein 3, transcript variant X3
leucine-rich repeat extensin-like protein 3 isoform X2
leucine-rich repeat extensin-like protein 3, transcript variant X2
leucine-rich repeat extensin-like protein 3 isoform X1
uncharacterized LOC105393567, 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 25 samples with support for all annotated introns
uncharacterized LOC105393567, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein CDV3 homolog, transcript variant X1
protein CDV3 homolog, transcript variant X2
protein CDV3 homolog, transcript variant X3
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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 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 76 samples with support for all annotated introns
putative transporter svop-1, transcript variant X2
putative transporter svop-1, transcript variant X1