Vanessa cardui chromosome 14, ilVanCard2.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Nymphalidae; Nymphalinae; Vanessa.
REFSEQ INFORMATION: The reference sequence is identical to\nLR999938.1.\nAssembly name: ilVanCard2.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/02/16. The original whole-genome shotgun project has the\naccession CAJMZP000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Vanessa cardui Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
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 52 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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: 15 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC124535236, transcript variant X1
uncharacterized LOC124535236, 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
uncharacterized LOC124535236, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC124535236 isoform X1
uncharacterized protein LOC124535236 isoform X2
uncharacterized protein LOC124535236 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
pyruvate dehydrogenase E1 component subunit beta, mitochondrial
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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
saccharopine dehydrogenase-like oxidoreductase
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phenylalanine--tRNA ligase alpha subunit
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 70 samples with support for all annotated introns
fragile X mental retardation syndrome-related protein 1
D-aspartate oxidase, 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 11 samples with support for all annotated introns
D-aspartate oxidase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 68 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
mitochondrial import inner membrane translocase subunit Tim17-B, transcript variant X1
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 84 samples with support for all annotated introns
mitochondrial import inner membrane translocase subunit Tim17-B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
mitochondrial import inner membrane translocase subunit Tim17-B
trafficking protein particle complex subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: WD repeat-containing protein 44
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
glutathione S-transferase 1-1-like, transcript variant X1
glutathione S-transferase 1-1-like, 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 82 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
mitochondrial pyruvate carrier 1, transcript variant X1
mitochondrial pyruvate carrier 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
transmembrane protein 135-like, transcript variant X2
transmembrane protein 135-like, transcript variant X3
transmembrane protein 135-like, transcript variant X1
BPTI/Kunitz domain-containing protein-like
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
TELO2-interacting protein 1 homolog, transcript variant X1
TELO2-interacting protein 1 homolog, transcript variant X2
TELO2-interacting protein 1 homolog isoform X1
TELO2-interacting protein 1 homolog isoform X2
TELO2-interacting protein 1 homolog, transcript variant X3
TELO2-interacting protein 1 homolog isoform X3
ER membrane protein complex subunit 1, transcript variant X2
ER membrane protein complex subunit 1, transcript variant X1
ER membrane protein complex subunit 1 isoform X2
ER membrane protein complex subunit 1 isoform X1
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X8
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X5
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X7
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X6
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X10
heterogeneous nuclear ribonucleoprotein R-like, transcript variant X11
heterogeneous nuclear ribonucleoprotein R-like isoform X1
heterogeneous nuclear ribonucleoprotein R-like isoform X6
heterogeneous nuclear ribonucleoprotein R-like isoform X3
heterogeneous nuclear ribonucleoprotein R-like isoform X4
heterogeneous nuclear ribonucleoprotein R-like isoform X2
heterogeneous nuclear ribonucleoprotein R-like isoform X5
heterogeneous nuclear ribonucleoprotein R-like isoform X8
heterogeneous nuclear ribonucleoprotein R-like isoform X9
heterogeneous nuclear ribonucleoprotein R-like isoform X7
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
thioredoxin domain-containing protein 5 homolog
ADP-ribosylation factor-like protein 6-interacting protein 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 45 samples with support for all annotated introns
RING finger and transmembrane domain-containing protein 2
E3 ubiquitin-protein ligase RNF19B-like, 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 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF19B-like, 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 8 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF19B-like isoform X1
E3 ubiquitin-protein ligase RNF19B-like isoform X2
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 and KH domain-containing protein mask, transcript variant X6
ankyrin repeat and KH domain-containing protein mask, transcript variant X5
ankyrin repeat and KH domain-containing protein mask, transcript variant X13
ankyrin repeat and KH domain-containing protein mask, transcript variant X4
ankyrin repeat and KH domain-containing protein mask, transcript variant X11
ankyrin repeat and KH domain-containing protein mask, transcript variant X10
ankyrin repeat and KH domain-containing protein mask, transcript variant X8
ankyrin repeat and KH domain-containing protein mask, transcript variant X9
ankyrin repeat and KH domain-containing protein mask, transcript variant X12
ankyrin repeat and KH domain-containing protein mask, transcript variant X7
ankyrin repeat and KH domain-containing protein mask, transcript variant X3
ankyrin repeat and KH domain-containing protein mask, transcript variant X2
ankyrin repeat and KH domain-containing protein mask, transcript variant X1
ankyrin repeat domain-containing protein 17 isoform X6
ankyrin repeat domain-containing protein 17 isoform X5
ankyrin repeat domain-containing protein 17 isoform X13
ankyrin repeat domain-containing protein 17 isoform X4
ankyrin repeat and KH domain-containing protein mask isoform X11
ankyrin repeat domain-containing protein 17 isoform X10
ankyrin repeat domain-containing protein 17 isoform X8
ankyrin repeat domain-containing protein 17 isoform X9
ankyrin repeat domain-containing protein 17 isoform X12
ankyrin repeat domain-containing protein 17 isoform X7
ankyrin repeat domain-containing protein 17 isoform X3
ankyrin repeat domain-containing protein 17 isoform X2
ankyrin repeat domain-containing protein 17 isoform X1
putative thiamine transporter SLC35F3, transcript variant X1
putative thiamine transporter SLC35F3, transcript variant X2
putative thiamine transporter SLC35F3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
putative thiamine transporter SLC35F3 isoform X1
putative thiamine transporter SLC35F3 isoform X2
putative thiamine transporter SLC35F3 isoform X3
glucose transporter type 1-like, transcript variant X2
glucose transporter type 1-like, transcript variant X1
glucose transporter type 1-like, transcript variant X4
glucose transporter type 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
28S ribosomal protein S24, mitochondrial
CCR4-NOT transcription complex subunit 6, transcript variant X3
CCR4-NOT transcription complex subunit 6, transcript variant X1
CCR4-NOT transcription complex subunit 6, transcript variant X2
CCR4-NOT transcription complex subunit 6, transcript variant X4
CCR4-NOT transcription complex subunit 6 isoform X2
CCR4-NOT transcription complex subunit 6 isoform X1
CCR4-NOT transcription complex subunit 6-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 495 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: 6 Proteins, and 100% 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC124535457, 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 12 samples with support for all annotated introns
uncharacterized LOC124535457, 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 31 samples with support for all annotated introns
uncharacterized protein LOC124535457 isoform X1
uncharacterized protein LOC124535457 isoform X2
sodium/potassium-transporting ATPase subunit beta-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
neuropeptide F-like, transcript variant X1
neuropeptide F-like, transcript variant X2
uncharacterized protein LOC124535208 isoform X1
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, 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 2 samples with support for all annotated introns
uncharacterized LOC124535039, transcript variant X3
uncharacterized LOC124535039, transcript variant X2
uncharacterized LOC124535039, transcript variant X1
uncharacterized protein LOC124535039 isoform X1
uncharacterized protein LOC124535039 isoform X2
vacuolar protein sorting-associated protein 72 homolog
peripheral plasma membrane protein CASK, transcript variant X3
peripheral plasma membrane protein CASK, transcript variant X2
peripheral plasma membrane protein CASK, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
peripheral plasma membrane protein CASK, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
peripheral plasma membrane protein CASK, transcript variant X5
peripheral plasma membrane protein CASK, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
peripheral plasma membrane protein CASK, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
peripheral plasma membrane protein CASK, transcript variant X1
peripheral plasma membrane protein CASK isoform X6
peripheral plasma membrane protein CASK isoform X4
peripheral plasma membrane protein CASK isoform X3
peripheral plasma membrane protein CASK isoform X5
peripheral plasma membrane protein CASK isoform X2
peripheral plasma membrane protein CASK 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 10 samples with support for all annotated introns
DNA-directed RNA polymerase I subunit RPA12
chromobox protein homolog 1-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 77 samples with support for all annotated introns
chromobox protein homolog 1-like, 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 86 samples with support for all annotated introns
chromobox protein homolog 1-like isoform X1
chromobox protein homolog 1-like isoform X2
eclosion hormone-like, transcript variant X2
eclosion hormone-like, transcript variant X1
eclosion hormone-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
angiotensin-converting enzyme-like, transcript variant X1
angiotensin-converting enzyme-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 40% 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
angiotensin-converting enzyme-like, transcript variant X2
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 74 samples with support for all annotated introns
myosin regulatory light chain, smooth muscle
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable mitochondrial glutathione transporter SLC25A40, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
probable mitochondrial glutathione transporter SLC25A40, 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 65 samples with support for all annotated introns
probable mitochondrial glutathione transporter SLC25A40, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
probable mitochondrial glutathione transporter SLC25A40 isoform X1
probable mitochondrial glutathione transporter SLC25A40 isoform X2
U6 snRNA-associated Sm-like protein LSm8
putative peptidyl-tRNA hydrolase PTRHD1, transcript variant X2
putative peptidyl-tRNA hydrolase PTRHD1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 86 samples with support for all annotated introns
vacuolar protein sorting-associated protein 4
protein toll-like, 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 3 samples with support for all annotated introns
protein toll-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 66% 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 81 samples with support for all annotated introns
angiotensin-converting enzyme-like isoform X2
angiotensin-converting enzyme-like isoform X1
glutathione S-transferase 1-like, transcript variant X2
glutathione S-transferase 1-like, transcript variant X1
glutathione S-transferase 1-like, transcript variant X4
glutathione S-transferase 1-like, transcript variant X3
glutathione S-transferase 1-like, transcript variant X5
glutathione S-transferase 1-like isoform X2
glutathione S-transferase 1-like isoform X1
glutathione S-transferase 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 14% 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 8 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 86 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
immunoglobulin superfamily DCC subclass member 3-like, 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 7 samples with support for all annotated introns
immunoglobulin superfamily DCC subclass member 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
immunoglobulin superfamily DCC subclass member 3-like
protein held out wings, transcript variant X2
protein held out wings, transcript variant X6
protein held out wings, transcript variant X3
protein held out wings, transcript variant X4
protein held out wings, transcript variant X1
protein held out wings, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 6-like, transcript variant X1
zinc finger and BTB domain-containing protein 6-like isoform X2
zinc finger and BTB domain-containing protein 6-like isoform X1
probable ATP-dependent RNA helicase pitchoune
splicing factor 3A subunit 3, transcript variant X2
splicing factor 3A subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 50% coverage of the annotated genomic feature by RNAseq alignments
trans-Golgi network integral membrane protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
mediator of RNA polymerase II transcription subunit 4, transcript variant X2
mediator of RNA polymerase II transcription subunit 4, transcript variant X1
mediator of RNA polymerase II transcription subunit 4
putative inner dynein arm light chain, axonemal
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pyrroline-5-carboxylate reductase 3-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 86 samples with support for all annotated introns
uncharacterized LOC124535162, transcript variant X2
uncharacterized LOC124535162, transcript variant X1
uncharacterized LOC124535367, transcript variant X2
uncharacterized LOC124535367, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
uncharacterized LOC124535069, transcript variant X7
uncharacterized LOC124535069, transcript variant X6
uncharacterized protein LOC124535069 isoform X5
uncharacterized LOC124535069, transcript variant X1
uncharacterized LOC124535069, transcript variant X4
uncharacterized LOC124535069, transcript variant X5
uncharacterized LOC124535069, transcript variant X9
uncharacterized LOC124535069, transcript variant X8
uncharacterized protein LOC124535069 isoform X1
uncharacterized protein LOC124535069 isoform X3
uncharacterized protein LOC124535069 isoform X7
uncharacterized protein LOC124535069 isoform X6
uncharacterized protein LOC124535069 isoform X4
uncharacterized LOC124535069, transcript variant X2
uncharacterized LOC124535069, transcript variant X3
uncharacterized protein LOC124535069 isoform X2
uncharacterized LOC124535069, transcript variant X10
uncharacterized protein LOC124535069 isoform X8
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
myosin light chain alkali, transcript variant X1
myosin light chain alkali, transcript variant X2
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
transmembrane emp24 domain-containing protein 7
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 71 samples with support for all annotated introns
transcription elongation factor B polypeptide 3, transcript variant X2
transcription elongation factor B polypeptide 3, transcript variant X1
transcription elongation factor B polypeptide 3 isoform X2
transcription elongation factor B polypeptide 3 isoform X1
autophagy-related protein 16-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
autophagy-related protein 16-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
autophagy-related protein 16-1 isoform X2
autophagy-related protein 16-1 isoform X1
uncharacterized LOC124535308, transcript variant X4
uncharacterized LOC124535308, transcript variant X3
uncharacterized LOC124535308, transcript variant X2
uncharacterized LOC124535308, transcript variant X1
uncharacterized protein LOC124535308 isoform X4
uncharacterized protein LOC124535308 isoform X3
uncharacterized protein LOC124535308 isoform X2
uncharacterized protein LOC124535308 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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: 1 Protein, and 55% 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 isoform X2
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 7 samples with support for all annotated introns
RUN and FYVE domain-containing protein 2, transcript variant X3
RUN and FYVE domain-containing protein 2, transcript variant X1
RUN and FYVE domain-containing protein 2 isoform X1
uncharacterized LOC124535105, 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 33 samples with support for all annotated introns
uncharacterized LOC124535105, 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 LOC124535105, 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 41 samples with support for all annotated introns
uncharacterized protein LOC124535105 isoform X2
uncharacterized protein LOC124535105 isoform X1
uncharacterized protein LOC124535105 isoform X3
protein N-lysine methyltransferase METTL21D-like, transcript variant X2
protein N-lysine methyltransferase METTL21D-like, transcript variant X1
protein N-lysine methyltransferase METTL21D-like isoform X2
protein N-lysine methyltransferase METTL21D-like isoform X1
ATPase H(+)-transporting accessory protein 2
52 kDa repressor of the inhibitor of the protein kinase-like
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L
LIM and senescent cell antigen-like-containing domain protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
LIM and senescent cell antigen-like-containing domain protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 77 samples with support for all annotated introns
LIM and senescent cell antigen-like-containing domain protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
LIM and senescent cell antigen-like-containing domain protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
LIM and senescent cell antigen-like-containing domain protein 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 82 samples with support for all annotated introns
LIM and senescent cell antigen-like-containing domain protein 2, transcript variant X6
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
LIM and senescent cell antigen-like-containing domain protein 1 isoform X1
LIM and senescent cell antigen-like-containing domain protein 2 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 8 samples with support for all annotated introns
sex determination protein fruitless, transcript variant X7
sex determination protein fruitless isoform X4
sex determination protein fruitless, transcript variant X2
sex determination protein fruitless, transcript variant X3
sex determination protein fruitless, transcript variant X5
sex determination protein fruitless, transcript variant X4
sex determination protein fruitless, transcript variant X6
sex determination protein fruitless, transcript variant X1
sex determination protein fruitless isoform X1
IQ and ubiquitin-like domain-containing protein
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 23 samples with support for all annotated introns
homeobox protein abdominal-A homolog, transcript variant X1
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 24 samples with support for all annotated introns
homeobox protein abdominal-A homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
homeobox protein abdominal-A homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
homeobox protein abdominal-A homolog, transcript variant X4
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 6 samples with support for all annotated introns
homeobox protein abdominal-A homolog isoform X1
homeobox protein abdominal-A homolog isoform X2
homeobox protein abdominal-A homolog isoform X3
homeobox protein abdominal-A homolog isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
uncharacterized LOC124535068, transcript variant X2
uncharacterized LOC124535068, transcript variant X1
homeotic protein antennapedia-like, transcript variant X2
homeotic protein antennapedia-like, transcript variant X3
homeotic protein antennapedia-like, transcript variant X4
homeotic protein antennapedia-like, transcript variant X5
homeotic protein antennapedia-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 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: 25 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cleavage stimulation factor subunit 2 tau variant
leucine-rich repeat protein soc-2 homolog
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
ras-related C3 botulinum toxin substrate 1
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 61 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 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 43% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein A1-like isoform X2
heterogeneous nuclear ribonucleoprotein A1-like isoform X1
heterogeneous nuclear ribonucleoprotein 87F-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein 87F-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein 87F-like isoform X1
heterogeneous nuclear ribonucleoprotein 87F-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 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: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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: 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: 1 Protein, and 19% coverage of the annotated genomic feature by RNAseq alignments
vacuolar protein sorting-associated protein 16 homolog
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 46 samples with support for all annotated introns
juxtaposed with another zinc finger protein 1
ATP synthase lipid-binding protein, mitochondrial, transcript variant X1
ATP synthase lipid-binding protein, mitochondrial, transcript variant X2
ATP synthase lipid-binding protein, mitochondrial
zinc finger BED domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
double-strand-break repair protein rad21 homolog, transcript variant X2
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
transmembrane and ubiquitin-like domain-containing protein 1, transcript variant X1
transmembrane and ubiquitin-like domain-containing protein 1, transcript variant X2
transmembrane and ubiquitin-like domain-containing protein 1, transcript variant X3
transmembrane and ubiquitin-like domain-containing protein 1 isoform X2
transmembrane and ubiquitin-like domain-containing protein 1 isoform X1
uncharacterized LOC124535055, transcript variant X4
uncharacterized LOC124535055, transcript variant X2
uncharacterized LOC124535055, transcript variant X1
uncharacterized LOC124535055, transcript variant X3
uncharacterized protein LOC124535055 isoform X1
uncharacterized protein LOC124535055 isoform X2
eukaryotic translation initiation factor 4B
tyrosine-protein kinase Fer, transcript variant X1
tyrosine-protein kinase Fer, transcript variant X2
tyrosine-protein kinase Fer, transcript variant X3
tyrosine-protein kinase Fer, transcript variant X4
translation initiation factor eIF-2B subunit alpha
NADP-dependent malic enzyme-like, transcript variant X2
NADP-dependent malic enzyme-like isoform X2
NADP-dependent malic enzyme-like, transcript variant X3
NADP-dependent malic enzyme-like, transcript variant X1
NADP-dependent malic enzyme-like isoform X1
NADP-dependent malic enzyme-like isoform X3
serine/threonine-protein kinase Doa, transcript variant X1
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 37 samples with support for all annotated introns
serine/threonine-protein kinase Doa, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
serine/threonine-protein kinase Doa, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
serine/threonine-protein kinase Doa, transcript variant X4
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 28 samples with support for all annotated introns
serine/threonine-protein kinase Doa, transcript variant X5
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
serine/threonine-protein kinase Doa, transcript variant X6
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 17 samples with support for all annotated introns
serine/threonine-protein kinase Doa, transcript variant X7
serine/threonine-protein kinase Doa, transcript variant X9
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 37 samples with support for all annotated introns
serine/threonine-protein kinase Doa, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
dual specificity protein kinase CLK2 isoform X5
dual specificity protein kinase CLK2 isoform X7
dual specificity protein kinase CLK2 isoform X4
serine/threonine-protein kinase Doa isoform X6
dual specificity protein kinase lkh1 isoform X1
serine/threonine-protein kinase Doa isoform X8
dual specificity tyrosine-phosphorylation-regulated kinase 4 isoform X3
dual specificity protein kinase lkh1 isoform X2
progestin and adipoQ receptor family member 4
AN1-type zinc finger protein 6, transcript variant X2
AN1-type zinc finger protein 6, transcript variant X4
AN1-type zinc finger protein 6, transcript variant X3
AN1-type zinc finger protein 6, transcript variant X6
AN1-type zinc finger protein 6, transcript variant X5
AN1-type zinc finger protein 6, transcript variant X1
AN1-type zinc finger protein 6 isoform X2
AN1-type zinc finger protein 6 isoform X1
secreted protein C-like, transcript variant X2
secreted protein C-like, 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
uncharacterized transmembrane protein DDB_G0289901-like isoform X2
modifier of mdg4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
modifier of mdg4-like, transcript variant X2
modifier of mdg4-like, transcript variant X3
modifier of mdg4-like, transcript variant X4
modifier of mdg4-like, transcript variant X5
modifier of mdg4-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
uncharacterized protein LOC124535174 isoform X2
uncharacterized protein LOC124535174 isoform X3
protein tramtrack, beta isoform-like isoform X4
broad-complex core protein isoforms 1/2/3/4/5-like isoform X1
protein tramtrack, beta isoform-like isoform X6
uncharacterized LOC124535175, transcript variant X1
uncharacterized LOC124535175, 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 21 samples with support for all annotated introns
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: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
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 8 samples with support for all annotated introns
transfer RNA glutamine (anticodon CUG); 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: 8 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CDK5 regulatory subunit-associated protein 3
leucine-rich melanocyte differentiation-associated protein-like, 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 80 samples with support for all annotated introns
leucine-rich melanocyte differentiation-associated protein-like, 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 83 samples with support for all annotated introns
leucine-rich melanocyte differentiation-associated protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
dihydroceramide fatty acyl 2-hydroxylase FAH2
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 55 samples with support for all annotated introns
eukaryotic translation initiation factor 4E type 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 30 samples with support for all annotated introns
cytoplasmic polyadenylation element-binding protein 1-B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
nonsense-mediated mRNA decay factor SMG8
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: 1 Protein, 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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
lipid storage droplets surface-binding protein 2, transcript variant X2
lipid storage droplets surface-binding protein 2, transcript variant X1
lipid storage droplets surface-binding protein 2, transcript variant X3
lipid storage droplets surface-binding protein 2 isoform X1
lipid storage droplets surface-binding protein 2 isoform X2
AP-1 complex subunit sigma-2, transcript variant X1
AP-1 complex subunit sigma-2, transcript variant X3
AP-1 complex subunit sigma-2, transcript variant X2
diacylglycerol kinase theta, transcript variant X1
diacylglycerol kinase theta, transcript variant X2
diacylglycerol kinase theta, transcript variant X5
diacylglycerol kinase theta, transcript variant X6
diacylglycerol kinase theta, transcript variant X3
diacylglycerol kinase theta, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
lipid storage droplets surface-binding protein 1, transcript variant X10
lipid storage droplets surface-binding protein 1, transcript variant X5
lipid storage droplets surface-binding protein 1, transcript variant X9
lipid storage droplets surface-binding protein 1, transcript variant X8
lipid storage droplets surface-binding protein 1, transcript variant X4
lipid storage droplets surface-binding protein 1, transcript variant X3
lipid storage droplets surface-binding protein 1, transcript variant X7
lipid storage droplets surface-binding protein 1, transcript variant X6
lipid storage droplets surface-binding protein 1, transcript variant X2
lipid storage droplets surface-binding protein 1, transcript variant X1
lipid storage droplets surface-binding protein 1 isoform X10
lipid storage droplets surface-binding protein 1 isoform X5
lipid storage droplets surface-binding protein 1 isoform X9
lipid storage droplets surface-binding protein 1 isoform X8
lipid storage droplets surface-binding protein 1 isoform X4
lipid storage droplets surface-binding protein 1 isoform X3
lipid storage droplets surface-binding protein 1 isoform X7
lipid storage droplets surface-binding protein 1 isoform X6
lipid storage droplets surface-binding protein 1 isoform X2
lipid storage droplets surface-binding protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 109 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 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 18 samples with support for all annotated introns
zinc finger protein 91, 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 12 samples with support for all annotated introns
zinc finger protein 91, 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 12 samples with support for all annotated introns
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 79 samples with support for all annotated introns
ER membrane protein complex subunit 2-A-like
phosphopantothenate--cysteine ligase, 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 37 samples with support for all annotated introns
phosphopantothenate--cysteine ligase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
organic cation/carnitine transporter 7-like, 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 26 samples with support for all annotated introns
organic cation/carnitine transporter 7-like, 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 28 samples with support for all annotated introns
organic cation/carnitine transporter 7-like isoform X1
organic cation/carnitine transporter 7-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
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 14 samples with support for all annotated introns
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
FAST kinase domain-containing protein 4, transcript variant X1
FAST kinase domain-containing protein 4 isoform X1
FAST kinase domain-containing protein 4, transcript variant X2
FAST kinase domain-containing protein 4, transcript variant X3
FAST kinase domain-containing protein 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
mothers against decapentaplegic homolog 6
heterogeneous nuclear ribonucleoprotein F-like, 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 40 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein F-like, 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 69 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein F-like isoform X2
heterogeneous nuclear ribonucleoprotein H2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
iodotyrosine deiodinase 1, 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 18 samples with support for all annotated introns
iodotyrosine deiodinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
transmembrane protease serine 13-like, 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 1 sample with support for all annotated introns
transmembrane protease serine 13-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
transfer RNA isoleucine (anticodon AAU); 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: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124535460, transcript variant X2
uncharacterized LOC124535460, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
scavenger receptor class B member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 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 53% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase kinase kinase 4
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124535217, transcript variant X1
uncharacterized LOC124535217, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RNA-binding protein squid, transcript variant X8
RNA-binding protein squid, transcript variant X10
RNA-binding protein squid, transcript variant X6
RNA-binding protein squid, transcript variant X9
RNA-binding protein squid, transcript variant X4
RNA-binding protein squid, transcript variant X3
RNA-binding protein squid, transcript variant X7
RNA-binding protein squid, transcript variant X2
RNA-binding protein squid, transcript variant X5
RNA-binding protein squid, transcript variant X1
RNA-binding protein squid, transcript variant X11
RNA-binding protein squid, transcript variant X12
COORDINATES: nucleotide motif:Rfam:12.0:RF00476
ras GTPase-activating protein-binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ras GTPase-activating protein-binding protein 2, transcript variant X1
ras GTPase-activating protein-binding protein 2
splicing factor 1, transcript variant X1
splicing factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 86 samples with support for all annotated introns
programmed cell death 6-interacting protein
cilia- and flagella-associated protein 91, transcript variant X1
cilia- and flagella-associated protein 91, transcript variant X2
cilia- and flagella-associated protein 91 isoform X2
cilia- and flagella-associated protein 91 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
ATP synthase mitochondrial F1 complex assembly factor 1