Pieris rapae chromosome 7, ilPieRapa1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Pieridae; Pierinae; Pieris.
REFSEQ INFORMATION: The reference sequence is identical to\nLR990589.1.\nAssembly name: ilPieRapa1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Wellcome Sanger Institute on\n2021/01/28. The original whole-genome shotgun project has the\naccession CAJHWY000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris rapae Annotation Release 101\nAnnotation Version :: 101\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
U4/U6 small nuclear ribonucleoprotein Prp31
COORDINATES: polyA evidence [ECO:0006239]
neurofilament medium polypeptide, transcript variant X3
neurofilament medium polypeptide 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 1 sample with support for all annotated introns
neurofilament medium polypeptide, transcript variant X2
neurofilament medium polypeptide isoform X2
neurofilament medium polypeptide, transcript variant X1
neurofilament medium polypeptide isoform X1
ATP-binding cassette sub-family F member 3
transcription factor E2F5, 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 26 samples with support for all annotated introns
transcription factor E2F5, 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 37 samples with support for all annotated introns
myelin transcription factor 1-like protein
armadillo segment polarity protein, transcript variant X1
armadillo segment polarity protein isoform X1
armadillo segment polarity protein, 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 22 samples with support for all annotated introns
armadillo segment polarity protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dynein light chain Tctex-type protein 2B
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, including 3 samples with support for all annotated introns
zinc finger protein 91, transcript variant X1
zinc finger protein 91, transcript variant X2
ras-related protein Rab-37, transcript variant X3
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 7 samples with support for all annotated introns
ras-related protein Rab-37, 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 2 samples with support for all annotated introns
ras-related protein Rab-37, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
tissue alpha-L-fucosidase, transcript variant X1
tissue alpha-L-fucosidase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tissue alpha-L-fucosidase-like isoform X3
tissue alpha-L-fucosidase, transcript variant X2
tissue alpha-L-fucosidase-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 25 samples with support for all annotated introns
tissue alpha-L-fucosidase-like, 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 12 samples with support for all annotated introns
tissue alpha-L-fucosidase-like isoform X1
tissue alpha-L-fucosidase-like isoform X2
TBC1 domain family member 9, transcript variant X2
TBC1 domain family member 9, transcript variant X1
TBC1 domain family member 9, transcript variant X3
RNA-binding protein Musashi homolog Rbp6, transcript variant X3
RNA-binding protein Musashi homolog Rbp6, transcript variant X1
RNA-binding protein Musashi homolog Rbp6, transcript variant X2
RNA-binding protein Musashi homolog Rbp6, transcript variant X5
RNA-binding protein Musashi homolog Rbp6, transcript variant X7
RNA-binding protein Musashi homolog Rbp6, transcript variant X8
RNA-binding protein Musashi homolog Rbp6, transcript variant X6
RNA-binding protein Musashi homolog Rbp6 isoform X2
RNA-binding protein Musashi homolog Rbp6 isoform X3
RNA-binding protein Musashi homolog Rbp6 isoform X1
RNA-binding protein Musashi homolog Rbp6 isoform X5
RNA-binding protein Musashi homolog Rbp6 isoform X6
RNA-binding protein Musashi homolog Rbp6, transcript variant X4
RNA-binding protein Musashi homolog Rbp6 isoform X4
uncharacterized LOC123689331, 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 7 samples with support for all annotated introns
uncharacterized LOC123689331, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
isocitrate dehydrogenase [NADP] cytoplasmic
uncharacterized LOC110994644, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC110994644, 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 7 samples with support for all annotated introns
uncharacterized protein LOC110994644 isoform X1
uncharacterized protein LOC110994644 isoform X2
uncharacterized LOC110994643, 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 3 samples with support for all annotated introns
uncharacterized LOC110994643, 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 5 samples with support for all annotated introns
GATOR complex protein Iml1, transcript variant X1
GATOR complex protein Iml1, transcript variant X2
GATOR complex protein Iml1, transcript variant X6
GATOR complex protein Iml1, transcript variant X7
GATOR complex protein Iml1, transcript variant X8
GATOR complex protein Iml1, transcript variant X9
GATOR complex protein Iml1, transcript variant X3
GATOR complex protein Iml1, transcript variant X5
GATOR complex protein Iml1, transcript variant X4
transcription factor Sp9, transcript variant X2
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 8 samples with support for all annotated introns
transcription factor Sp9, transcript variant X5
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 6 samples with support for all annotated introns
transcription factor Sp9, transcript variant X3
transcription factor Sp9, transcript variant X1
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 5 samples with support for all annotated introns
transcription factor Sp9, transcript variant X4
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 11 samples with support for all annotated introns
endoplasmic reticulum resident protein 44
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, including 24 samples with support for all annotated introns
pleckstrin homology domain-containing family A member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
BMP-binding endothelial regulator protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
BMP-binding endothelial regulator protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
BMP-binding endothelial regulator protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
BMP-binding endothelial regulator protein
putative zinc metalloproteinase C607.06c, 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 19 samples with support for all annotated introns
putative zinc metalloproteinase C607.06c, 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
putative zinc metalloproteinase C607.06c isoform X1
putative zinc metalloproteinase C607.06c isoform X2
glycolipid transfer protein, 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 14 samples with support for all annotated introns
glycolipid transfer protein, 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 29 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 22 samples with support for all annotated introns
39S ribosomal protein L16, mitochondrial
transmembrane protein 132E, transcript variant X2
transmembrane protein 132E, 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 43 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 8, transcript variant X1
potassium voltage-gated channel subfamily H member 8, 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 9 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 8, transcript variant X3
potassium voltage-gated channel subfamily H member 8, transcript variant X4
potassium voltage-gated channel subfamily H member 8, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 8, 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 4 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 8 isoform X1
potassium voltage-gated channel subfamily H member 8 isoform X2
potassium voltage-gated channel subfamily H member 8 isoform X3
potassium voltage-gated channel subfamily H member 8 isoform X4
potassium voltage-gated channel subfamily H member 8 isoform X5
potassium voltage-gated channel subfamily H member 8 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 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 41 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 33 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 18 samples with support for all annotated introns
leucine-rich repeats and immunoglobulin-like domains protein 3
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
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
trafficking kinesin-binding protein milt, transcript variant X7
trafficking kinesin-binding protein milt, transcript variant X1
trafficking kinesin-binding protein milt isoform X1
trafficking kinesin-binding protein milt, transcript variant X6
trafficking kinesin-binding protein milt, transcript variant X3
trafficking kinesin-binding protein milt, transcript variant X4
trafficking kinesin-binding protein milt, transcript variant X2
trafficking kinesin-binding protein milt, transcript variant X5
trafficking kinesin-binding protein milt isoform X2
intraflagellar transport protein 81 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 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: 3 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
receptor-type guanylate cyclase Gyc76C-like
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, including 51 samples with support for all annotated introns
ribonuclease P protein subunit p25-like protein, transcript variant X3
ribonuclease P protein subunit p25-like protein, transcript variant X2
ribonuclease P protein subunit p25-like protein, transcript variant X1
ribonuclease P protein subunit p25-like 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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable cytosolic iron-sulfur protein assembly protein Ciao1, transcript variant X1
probable cytosolic iron-sulfur protein assembly protein Ciao1, transcript variant X2
probable cytosolic iron-sulfur protein assembly protein Ciao1 isoform X1
uncharacterized LOC110996641, transcript variant X1
uncharacterized LOC110996641, transcript variant X2
uncharacterized protein LOC110996641 isoform X1
uncharacterized protein LOC110996641 isoform 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
atrial natriuretic peptide-converting enzyme
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 12 samples with support for all annotated introns
phosphatase and actin regulator 4, 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 22 samples with support for all annotated introns
phosphatase and actin regulator 4, 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 9 samples with support for all annotated introns
phosphatase and actin regulator 4, 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 27 samples with support for all annotated introns
phosphatase and actin regulator 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
phosphatase and actin regulator 4, 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 30 samples with support for all annotated introns
phosphatase and actin regulator 4 isoform X3
phosphatase and actin regulator 4 isoform X4
phosphatase and actin regulator 4 isoform X5
phosphatase and actin regulator 4 isoform X2
phosphatase and actin regulator 4 isoform X1
MLX-interacting protein, transcript variant X1
MLX-interacting protein, transcript variant X2
MLX-interacting protein, transcript variant X3
MLX-interacting protein, transcript variant X4
MLX-interacting protein, transcript variant X6
MLX-interacting protein, transcript variant X5
MLX-interacting protein, transcript variant X7
ATP-binding cassette sub-family C member Sur
cGMP-dependent protein kinase, isozyme 1
RNA binding protein fox-1 homolog 3, transcript variant X5
RNA binding protein fox-1 homolog 3, transcript variant X6
RNA binding protein fox-1 homolog 3, transcript variant X7
RNA binding protein fox-1 homolog 3, transcript variant X1
RNA binding protein fox-1 homolog 3, transcript variant X4
RNA binding protein fox-1 homolog 3, transcript variant X3
RNA binding protein fox-1 homolog 3, transcript variant X2
RNA binding protein fox-1 homolog 1-like isoform X6
RNA binding protein fox-1 homolog 3 isoform X7
RNA binding protein fox-1 homolog 1-like isoform X2
RNA binding protein fox-1 homolog 3 isoform X1
RNA binding protein fox-1 homolog 3 isoform X4
RNA binding protein fox-1 homolog 3 isoform X3
RNA binding protein fox-1 homolog 3 isoform 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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cyclin-dependent kinase 11B, transcript variant X1
cyclin-dependent kinase 11B, transcript variant X2
cyclin-dependent kinase 11B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
cyclin-dependent kinase 11B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
cyclin-dependent kinase 11B, 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 22 samples with support for all annotated introns
nuclear pore complex protein Nup154, transcript variant X1
nuclear pore complex protein Nup154, transcript variant X2
neural cell adhesion molecule 2, transcript variant X1
neural cell adhesion molecule 2, transcript variant X2
neural cell adhesion molecule 2 isoform X2
neural cell adhesion molecule 2 isoform X1
carboxypeptidase A2-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 3 samples with support for all annotated introns
carboxypeptidase A2-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 4 samples with support for all annotated introns
CKLF-like MARVEL transmembrane domain-containing protein 8, transcript variant X1
CKLF-like MARVEL transmembrane domain-containing protein 8, transcript variant X2
CKLF-like MARVEL transmembrane domain-containing protein 8 isoform X1
CKLF-like MARVEL transmembrane domain-containing protein 8 isoform 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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
nucleosome-remodeling factor subunit NURF301, transcript variant X2
nucleosome-remodeling factor subunit NURF301, transcript variant X1
nucleosome-remodeling factor subunit NURF301 isoform X2
nucleosome-remodeling factor subunit NURF301 isoform X1
uncharacterized LOC110992751, transcript variant X1
uncharacterized LOC110992751, transcript variant X2
uncharacterized protein LOC110992751 isoform X1
uncharacterized protein LOC110992751 isoform X2
uncharacterized LOC110992751, transcript variant X4
uncharacterized LOC110992751, transcript variant X3
uncharacterized protein LOC110992751 isoform X3
uncharacterized protein LOC110992751 isoform X4
UV excision repair protein RAD23 homolog A
cyclic AMP response element-binding protein B, transcript variant X6
cyclic AMP response element-binding protein B, transcript variant X5
cyclic AMP response element-binding protein B, transcript variant X4
cyclic AMP response element-binding protein B, transcript variant X3
cyclic AMP response element-binding protein B, transcript variant X2
cyclic AMP response element-binding protein B, transcript variant X1
cyclic AMP response element-binding protein B isoform X6
cyclic AMP response element-binding protein B isoform X5
cyclic AMP response element-binding protein B isoform X4
cyclic AMP response element-binding protein B isoform X3
cyclic AMP response element-binding protein B isoform X2
cyclic AMP response element-binding protein B isoform X1
actin-binding protein IPP, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
actin-binding protein IPP, 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 21 samples with support for all annotated introns
actin-binding protein IPP, 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 16 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
lys-63-specific deubiquitinase BRCC36-like
dnaJ homolog subfamily B member 6, transcript variant X1
dnaJ homolog subfamily B member 6, transcript variant X2
dnaJ homolog subfamily B member 6 isoform X2
dnaJ homolog subfamily B member 6 isoform X1
4-aminobutyrate aminotransferase, mitochondrial
sodium-coupled monocarboxylate transporter 2
pollen-specific leucine-rich repeat extensin-like protein 1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial
sodium- and chloride-dependent GABA transporter ine
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 111 samples with support for all annotated introns
neurogenic locus notch homolog protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: neurogenic locus notch homolog protein 1-like
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
transmembrane protein 11-B, mitochondrial
dehydrogenase/reductase SDR family protein 7-like
uncharacterized LOC110992771, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC110992771, transcript variant X1
uncharacterized protein LOC110992771 isoform X2
uncharacterized protein LOC110992771 isoform X1
VPS35 endosomal protein-sorting factor-like, transcript variant X1
VPS35 endosomal protein-sorting factor-like, transcript variant X2
VPS35 endosomal protein-sorting factor-like isoform X2
VPS35 endosomal protein-sorting factor-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
F-box only protein 21, 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 8 samples with support for all annotated introns
F-box only protein 21, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
F-box only protein 21, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
tectonin beta-propeller repeat-containing protein
phosphatidylinositol N-acetylglucosaminyltransferase subunit P, transcript variant X5
phosphatidylinositol N-acetylglucosaminyltransferase subunit P, transcript variant X1
phosphatidylinositol N-acetylglucosaminyltransferase subunit P, transcript variant X3
phosphatidylinositol N-acetylglucosaminyltransferase subunit P, transcript variant X4
phosphatidylinositol N-acetylglucosaminyltransferase subunit P, transcript variant X2
phosphatidylinositol N-acetylglucosaminyltransferase subunit P
serine/threonine-protein phosphatase 2B catalytic subunit 3
TOX high mobility group box family member 3, transcript variant X1
TOX high mobility group box family member 3, transcript variant X2
TOX high mobility group box family member 3, transcript variant X3
TOX high mobility group box family member 3 isoform X2
TOX high mobility group box family member 3 isoform X1
TOX high mobility group box family member 3 isoform X3
uncharacterized LOC110992689, transcript variant X3
uncharacterized LOC110992689, transcript variant X4
uncharacterized LOC110992689, transcript variant X2
uncharacterized LOC110992689, transcript variant X1
uncharacterized protein LOC110992689 isoform X2
uncharacterized protein LOC110992689 isoform X3
uncharacterized protein LOC110992689 isoform X1
U5 small nuclear ribonucleoprotein 40 kDa protein-like
protein phosphatase Slingshot, transcript variant X1
protein phosphatase Slingshot, transcript variant X2
protein phosphatase Slingshot isoform X1
protein phosphatase Slingshot isoform X2
serine/threonine-protein kinase PLK4, transcript variant X2
serine/threonine-protein kinase PLK4, transcript variant X3
serine/threonine-protein kinase PLK4, transcript variant X1
serine/threonine-protein kinase PLK4, transcript variant X4
NADPH--cytochrome P450 reductase, transcript variant X1
NADPH--cytochrome P450 reductase isoform X1
NADPH--cytochrome P450 reductase, transcript variant X2
NADPH--cytochrome P450 reductase isoform X2
A-kinase anchor protein 1, mitochondrial, transcript variant X1
A-kinase anchor protein 1, mitochondrial, transcript variant X2
A-kinase anchor protein 1, mitochondrial
eukaryotic translation initiation factor 1A, X-chromosomal
ecdysone-inducible protein E75, transcript variant X1
ecdysone-inducible protein E75 isoform X1
ecdysone-inducible protein E75, transcript variant X3
ecdysone-inducible protein E75 isoform X3
ecdysone-inducible protein E75, transcript variant X2
ecdysone-inducible protein E75 isoform X2
ecdysone-inducible protein E75, transcript variant X4
ecdysone-inducible protein E75 isoform X4
pre-rRNA 2'-O-ribose RNA methyltransferase FTSJ3
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 57 samples with support for all annotated introns
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like, transcript variant X1
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like, transcript variant X3
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like, transcript variant X2
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like isoform X1
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like isoform X2
DNA-directed RNA polymerase III subunit RPC2
mitochondrial Rho GTPase, transcript variant X1
mitochondrial Rho GTPase, transcript variant X2
mitochondrial Rho GTPase, transcript variant X3
mitochondrial Rho GTPase, transcript variant X4
RNA-binding protein cabeza, transcript variant X2
RNA-binding protein cabeza, transcript variant X3
RNA-binding protein cabeza, transcript variant X1
MICAL-like protein 1, transcript variant X2
MICAL-like protein 1, transcript variant X1
A-kinase anchor protein 10, mitochondrial
uncharacterized LOC110992757, transcript variant X2
uncharacterized LOC110992757, transcript variant X1
retinal homeobox protein Rx2-like, transcript variant X1
retinal homeobox protein Rx2-like, transcript variant X2
retinal homeobox protein Rx2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
kynurenine/alpha-aminoadipate aminotransferase, mitochondrial
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
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon CGA); 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: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
electron transfer flavoprotein beta subunit lysine methyltransferase
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
LHFPL tetraspan subfamily member 3 protein
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 25 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
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
uncharacterized LOC110993803, transcript variant X1
uncharacterized LOC110993803, transcript variant X2
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein LOC110993803 isoform X2
uncharacterized protein LOC110993803 isoform X1
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); 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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
uncharacterized LOC110993786, 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 32 samples with support for all annotated introns
uncharacterized LOC110993786, 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 4 samples with support for all annotated introns
uncharacterized LOC110993786, 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
uncharacterized LOC110993786, 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 28 samples with support for all annotated introns
uncharacterized protein LOC110993786 isoform X1
uncharacterized protein LOC110993786 isoform X2
uncharacterized protein LOC110993786 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 14 samples with support for all annotated introns
juvenile hormone epoxide hydrolase, transcript variant X2
juvenile hormone epoxide hydrolase isoform X2
juvenile hormone epoxide hydrolase, transcript variant X3
juvenile hormone epoxide hydrolase, transcript variant X1
juvenile hormone epoxide hydrolase isoform X1
juvenile hormone epoxide hydrolase isoform X3
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
facilitated trehalose transporter Tret1-like
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 2 samples with support for all annotated introns
facilitated trehalose transporter Tret1, transcript variant X1
facilitated trehalose transporter Tret1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
probable 39S ribosomal protein L24, mitochondrial
V-type proton ATPase subunit C, transcript variant X2
V-type proton ATPase subunit C, transcript variant X1
ATP synthase subunit gamma, mitochondrial
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
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
cilia- and flagella-associated protein 298
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
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
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
mediator of RNA polymerase II transcription subunit 20
putative ferric-chelate reductase 1 homolog, transcript variant X2
putative ferric-chelate reductase 1 homolog, transcript variant X1
putative ferric-chelate reductase 1 homolog isoform X2
putative ferric-chelate reductase 1 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 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 14 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 3 samples with support for all annotated introns
uncharacterized LOC110993688, transcript variant X2
uncharacterized LOC110993688, transcript variant X1
uncharacterized protein LOC110993688 isoform X1
uncharacterized protein LOC110993688 isoform X2
meiosis-specific nuclear structural protein 1-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 3 samples with support for all annotated introns
uncharacterized LOC110993487, transcript variant X1
uncharacterized LOC110993487, transcript variant X2
uncharacterized protein LOC110993487 isoform X1
uncharacterized protein LOC110993487 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments
putative odorant receptor 92a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
putative odorant receptor 92a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
putative odorant receptor 92a isoform X2
putative odorant receptor 92a isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins
ELKS/Rab6-interacting/CAST family member 1
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 6 samples with support for all annotated introns
probable 28S ribosomal protein S16, mitochondrial
receptor expression-enhancing protein 5, transcript variant X3
receptor expression-enhancing protein 5, transcript variant X2
receptor expression-enhancing protein 5, transcript variant X1
receptor expression-enhancing protein 5, transcript variant X4
receptor expression-enhancing protein 5 isoform X2
receptor expression-enhancing protein 5 isoform X3
receptor expression-enhancing protein 5 isoform X1
multiple C2 and transmembrane domain-containing protein, 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
multiple C2 and transmembrane domain-containing protein, 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 1 sample with support for all annotated introns
multiple C2 and transmembrane domain-containing protein, transcript variant X8
multiple C2 and transmembrane domain-containing protein, transcript variant X3
multiple C2 and transmembrane domain-containing protein, transcript variant X6
multiple C2 and transmembrane domain-containing protein, 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 3 samples with support for all annotated introns
multiple C2 and transmembrane domain-containing protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
multiple C2 and transmembrane domain-containing protein, transcript variant X7
multiple C2 and transmembrane domain-containing protein isoform X2
multiple C2 and transmembrane domain-containing protein isoform X1
multiple C2 and transmembrane domain-containing protein isoform X6
multiple C2 and transmembrane domain-containing protein isoform X3
multiple C2 and transmembrane domain-containing protein isoform X5
multiple C2 and transmembrane domain-containing protein isoform X4
uridine phosphorylase 1, transcript variant X1
uridine phosphorylase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44% 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 27 samples with support for all annotated introns
putative nuclease HARBI1, transcript variant X1
putative nuclease HARBI1, 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 25 samples with support for all annotated introns
uncharacterized protein LOC123689104 isoform X2
stabilizer of axonemal microtubules 2, transcript variant X2
stabilizer of axonemal microtubules 2, transcript variant X1
stabilizer of axonemal microtubules 2 isoform X1
stabilizer of axonemal microtubules 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
stabilizer of axonemal microtubules 2 isoform X2
rho guanine nucleotide exchange factor 28, transcript variant X2
rho guanine nucleotide exchange factor 28, transcript variant X8
rho guanine nucleotide exchange factor 28, transcript variant X5
rho guanine nucleotide exchange factor 28, transcript variant X4
rho guanine nucleotide exchange factor 28, transcript variant X6
rho guanine nucleotide exchange factor 28, transcript variant X3
rho guanine nucleotide exchange factor 28, transcript variant X1
rho guanine nucleotide exchange factor 28, transcript variant X7
rho guanine nucleotide exchange factor 28 isoform X7
rho guanine nucleotide exchange factor 28 isoform X4
rho guanine nucleotide exchange factor 28 isoform X3
rho guanine nucleotide exchange factor 28 isoform X5
rho guanine nucleotide exchange factor 28 isoform X2
rho guanine nucleotide exchange factor 28 isoform X1
rho guanine nucleotide exchange factor 28 isoform X6
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
homocysteine-responsive endoplasmic reticulum-resident ubiquitin-like domain member 2 protein
uncharacterized LOC110995083, transcript variant X2
uncharacterized LOC110995083, transcript variant X1
uncharacterized LOC110995130, 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 31 samples with support for all annotated introns
uncharacterized LOC110995130, transcript variant X2
uncharacterized LOC110995084, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
uncharacterized LOC110995084, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
uncharacterized LOC110995084, 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 85 samples with support for all annotated introns
uncharacterized LOC110995084, 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 112 samples with support for all annotated introns
uncharacterized LOC110995084, transcript variant X7
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 112 samples with support for all annotated introns
uncharacterized LOC110995084, 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 21 samples with support for all annotated introns
uncharacterized LOC110995084, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 114 samples with support for all annotated introns
uncharacterized LOC110995084, transcript variant X10
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 94 samples with support for all annotated introns
uncharacterized LOC110995084, transcript variant X8
uncharacterized LOC110995084, transcript variant X2
uncharacterized protein LOC110995084 isoform X5
uncharacterized protein LOC110995084 isoform X7
uncharacterized protein LOC110995084 isoform X3
uncharacterized protein LOC110995084 isoform X9
uncharacterized protein LOC110995084 isoform X6
uncharacterized protein LOC110995084 isoform X8
uncharacterized protein LOC110995084 isoform X10
uncharacterized protein LOC110995084 isoform X4
uncharacterized protein LOC110995084 isoform X1
uncharacterized protein LOC110995084 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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59% coverage of the annotated genomic feature by RNAseq alignments
tRNA (adenine(37)-N6)-methyltransferase, transcript variant X2
tRNA (adenine(37)-N6)-methyltransferase, transcript variant X1
tRNA (adenine(37)-N6)-methyltransferase isoform X1
tRNA (adenine(37)-N6)-methyltransferase isoform X2
uncharacterized LOC110995089, 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 32 samples with support for all annotated introns
uncharacterized LOC110995089, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 115 samples with support for all annotated introns
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 18 samples with support for all annotated introns
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 34 samples with support for all annotated introns
uncharacterized LOC123689339, 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 10 samples with support for all annotated introns
uncharacterized LOC123689339, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123689339, transcript variant X3
structure-specific endonuclease subunit SLX4, transcript variant X2
structure-specific endonuclease subunit SLX4, 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 23 samples with support for all annotated introns
uncharacterized protein LOC110995113 isoform X2
structure-specific endonuclease subunit SLX4 isoform X1
uncharacterized LOC110995123, transcript variant X2
uncharacterized LOC110995123, transcript variant X1
uncharacterized protein LOC110995123 isoform X1
uncharacterized protein LOC110995123 isoform X2
calcium-independent phospholipase A2-gamma
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
U6 snRNA-associated Sm-like protein LSm6
GATA zinc finger domain-containing protein 1
maternal protein exuperantia, transcript variant X2
maternal protein exuperantia, transcript variant X1
maternal protein exuperantia, transcript variant X4
maternal protein exuperantia, transcript variant X3
transcriptional repressor p66-alpha, transcript variant X5
transcriptional repressor p66-alpha, transcript variant X1
transcriptional repressor p66-alpha, transcript variant X3
transcriptional repressor p66-alpha, transcript variant X2
transcriptional repressor p66-alpha, transcript variant X4
transcriptional repressor p66-alpha, transcript variant X6
transcriptional repressor p66-alpha isoform X1
transcriptional repressor p66-alpha isoform X5
transcriptional repressor p66-alpha isoform X3
transcriptional repressor p66-alpha isoform X4
transcriptional repressor p66-alpha isoform X2
transcriptional repressor p66-alpha isoform X6
cytochrome c oxidase assembly factor 7 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 73% 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 78 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 68 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
neuronal acetylcholine receptor subunit eat-2, transcript variant X1
neuronal acetylcholine receptor subunit eat-2 isoform X1
neuronal acetylcholine receptor subunit eat-2, transcript variant X2
neuronal acetylcholine receptor subunit eat-2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
structural maintenance of chromosomes protein 4
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 95 samples with support for all annotated introns
UDP-glucosyltransferase 2, transcript variant X1
UDP-glucosyltransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 110 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% 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 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 97% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transcriptional adapter 2B, transcript variant X2
transcriptional adapter 2B, transcript variant X1
transcriptional adapter 2B, 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 20 samples with support for all annotated introns
transcriptional adapter 2B, 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 22 samples with support for all annotated introns
TNF receptor-associated factor family protein DDB_G0272098
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
probable ATP-dependent RNA helicase spindle-E
C-1-tetrahydrofolate synthase, cytoplasmic, transcript variant X2
C-1-tetrahydrofolate synthase, cytoplasmic isoform X2
C-1-tetrahydrofolate synthase, cytoplasmic, transcript variant X1
C-1-tetrahydrofolate synthase, cytoplasmic isoform X1
C-1-tetrahydrofolate synthase, cytoplasmic, transcript variant X3
C-1-tetrahydrofolate synthase, cytoplasmic isoform X3
cyclin-Y-like protein 1, transcript variant X1
cyclin-Y-like protein 1, transcript variant X2
apoptotic chromatin condensation inducer in the nucleus, transcript variant X1
apoptotic chromatin condensation inducer in the nucleus, transcript variant X2
apoptotic chromatin condensation inducer in the nucleus
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 115 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 95% 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 3 samples with support for all annotated introns
inactive dipeptidyl peptidase 10, 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 5 samples with support for all annotated introns
inactive dipeptidyl peptidase 10, 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 7 samples with support for all annotated introns
inactive dipeptidyl peptidase 10, transcript variant X2
inactive dipeptidyl peptidase 10 isoform X1
inactive dipeptidyl peptidase 10 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
RB1-inducible coiled-coil protein 1, transcript variant X2
RB1-inducible coiled-coil protein 1, transcript variant X5
RB1-inducible coiled-coil protein 1, transcript variant X4
RB1-inducible coiled-coil protein 1, transcript variant X1
RB1-inducible coiled-coil protein 1, transcript variant X3
RB1-inducible coiled-coil protein 1 isoform X3
RB1-inducible coiled-coil protein 1 isoform X2
RB1-inducible coiled-coil protein 1 isoform X1
protein ultraspiracle homolog, transcript variant X4
protein ultraspiracle homolog isoform X2
protein ultraspiracle homolog, transcript variant X2
protein ultraspiracle homolog, transcript variant X3
protein ultraspiracle homolog, transcript variant X1
protein ultraspiracle homolog isoform X1
long-chain fatty acid transport protein 4
spindle assembly abnormal protein 6 homolog, transcript variant X2
spindle assembly abnormal protein 6 homolog, transcript variant X3
spindle assembly abnormal protein 6 homolog, transcript variant X1
spindle assembly abnormal protein 6 homolog isoform X2
uncharacterized LOC111000594, transcript variant X2
uncharacterized LOC111000594, transcript variant X1
uncharacterized protein LOC111000594 isoform X2
uncharacterized protein LOC111000594 isoform X1
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
cytochrome b5-related protein, transcript variant X2
cytochrome b5-related protein, transcript variant X1
ommochrome-binding protein, transcript variant X1
ommochrome-binding protein, 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, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
disks large homolog 2-like, transcript variant X1
disks large homolog 2-like, transcript variant X2
disks large homolog 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 32% 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 12 samples with support for all annotated introns
uncharacterized LOC110996952, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC110996952, transcript variant X3
uncharacterized LOC110996952, transcript variant X1
uncharacterized protein LOC110996952 isoform X1
uncharacterized protein LOC110996952 isoform X2
ras-related and estrogen-regulated growth inhibitor-like protein
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 28 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 65 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
major facilitator superfamily domain-containing protein 9
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 94 samples with support for all annotated introns
39S ribosomal protein L32, mitochondrial
all trans-polyprenyl-diphosphate synthase PDSS1
probable serine/threonine-protein kinase mps1, transcript variant X2
golgin subfamily A member 6-like protein 1 isoform X2
probable serine/threonine-protein kinase mps1, transcript variant X1
probable serine/threonine-protein kinase mps1 isoform X1
coiled-coil domain-containing protein 12
F-box only protein 28, transcript variant X1
F-box only protein 28, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 5
dnaJ homolog subfamily C member 9, transcript variant X2
dnaJ homolog subfamily C member 9, transcript variant X1
ATP-dependent (S)-NAD(P)H-hydrate dehydratase
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 107 samples with support for all annotated introns
uncharacterized LOC110996936, transcript variant X1
uncharacterized LOC110996936, transcript variant X2
uncharacterized protein LOC110996936 isoform X1
uncharacterized protein LOC110996936 isoform X2
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit wuho
signal recognition particle 19 kDa protein
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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
alanine--glyoxylate aminotransferase 2-like, 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 38 samples with support for all annotated introns
alanine--glyoxylate aminotransferase 2-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 21 samples with support for all annotated introns
alanine--glyoxylate aminotransferase 2-like isoform X1
alanine--glyoxylate aminotransferase 2-like isoform X2
zinc finger SWIM domain-containing protein 8 homolog, transcript variant X6
zinc finger SWIM domain-containing protein 8 homolog, transcript variant X2
zinc finger SWIM domain-containing protein 8 homolog, transcript variant X3
zinc finger SWIM domain-containing protein 8 homolog, transcript variant X4
zinc finger SWIM domain-containing protein 8 homolog, transcript variant X1
zinc finger SWIM domain-containing protein 8 homolog, transcript variant X5
zinc finger SWIM domain-containing protein 8 homolog isoform X6
zinc finger SWIM domain-containing protein 8 homolog isoform X2
zinc finger SWIM domain-containing protein 8 homolog isoform X3
zinc finger SWIM domain-containing protein 8 homolog isoform X4
zinc finger SWIM domain-containing protein 8 homolog isoform X1
zinc finger SWIM domain-containing protein 8 homolog isoform X5
probable E3 ubiquitin-protein ligase HERC4, transcript variant X1
probable E3 ubiquitin-protein ligase HERC4, transcript variant X3
probable E3 ubiquitin-protein ligase HERC4, transcript variant X2
probable E3 ubiquitin-protein ligase HERC4, transcript variant X4
probable E3 ubiquitin-protein ligase HERC4 isoform X1
probable E3 ubiquitin-protein ligase HERC4 isoform X3
probable E3 ubiquitin-protein ligase HERC4 isoform X2
probable E3 ubiquitin-protein ligase HERC4 isoform X4
proline-rich extensin-like protein EPR1 isoform X2
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X4
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X3
vacuolar protein sorting-associated protein 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
vacuolar protein sorting-associated protein 13, 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 17 samples with support for all annotated introns
vacuolar protein sorting-associated protein 13 isoform X2
vacuolar protein sorting-associated protein 13 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized transporter YutK, transcript variant X3
uncharacterized transporter YutK, transcript variant X2
uncharacterized transporter YutK, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC111004170, transcript variant X1
uncharacterized LOC111004170, transcript variant X2
forkhead box protein O, transcript variant X2
forkhead box protein O, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
3-oxoacyl-[acyl-carrier-protein] reductase FabG, transcript variant X2
3-oxoacyl-[acyl-carrier-protein] reductase FabG, transcript variant X1
3-oxoacyl-[acyl-carrier-protein] reductase FabG, transcript variant X3
3-oxoacyl-[acyl-carrier-protein] reductase FabG
uncharacterized LOC111004151, transcript variant X1
uncharacterized protein LOC111004151 isoform X1
uncharacterized LOC111004151, transcript variant X2
uncharacterized LOC111004151, transcript variant X3
uncharacterized protein LOC111004151 isoform X2
uncharacterized LOC111004151, transcript variant X4
uncharacterized protein LOC111004151 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC111004161, transcript variant X1
uncharacterized LOC111004161, transcript variant X3
uncharacterized LOC111004161, transcript variant X4
uncharacterized LOC111004161, transcript variant X2
uncharacterized protein LOC111004161 isoform X1
uncharacterized protein LOC111004161 isoform X3
uncharacterized protein LOC111004161 isoform X4
uncharacterized protein LOC111004161 isoform X2
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: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
MKI67 FHA domain-interacting nucleolar phosphoprotein-like
phosphatidylinositol 4-kinase beta, transcript variant X1
phosphatidylinositol 4-kinase beta isoform X1
phosphatidylinositol 4-kinase beta, transcript variant X2
phosphatidylinositol 4-kinase beta isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 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 34 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 92% coverage of the annotated genomic feature by RNAseq alignments
tyrosine kinase receptor Cad96Ca, transcript variant X1
tyrosine kinase receptor Cad96Ca, transcript variant X2
tyrosine kinase receptor Cad96Ca isoform X1
tyrosine kinase receptor Cad96Ca isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
acid sphingomyelinase-like phosphodiesterase 3a, transcript variant X2
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, including 8 samples with support for all annotated introns
acid sphingomyelinase-like phosphodiesterase 3a, transcript variant X1
acid sphingomyelinase-like phosphodiesterase 3a
sodium- and chloride-dependent glycine transporter 2
set1/Ash2 histone methyltransferase complex subunit ASH2, transcript variant X1
set1/Ash2 histone methyltransferase complex subunit ASH2, transcript variant X2
set1/Ash2 histone methyltransferase complex subunit ASH2, transcript variant X3
set1/Ash2 histone methyltransferase complex subunit ASH2 isoform X1
set1/Ash2 histone methyltransferase complex subunit ASH2 isoform X2
set1/Ash2 histone methyltransferase complex subunit ASH2 isoform X3
uncharacterized LOC110996995, transcript variant X4
uncharacterized LOC110996995, transcript variant X2
uncharacterized LOC110996995, transcript variant X3
uncharacterized LOC110996995, transcript variant X1
uncharacterized protein LOC110996995 isoform X4
uncharacterized protein LOC110996995 isoform X2
uncharacterized protein LOC110996995 isoform X3
uncharacterized protein LOC110996995 isoform X1
myosin heavy chain 95F, transcript variant X1
myosin heavy chain 95F, transcript variant X2
nuclear envelope integral membrane protein 1, transcript variant X1
nuclear envelope integral membrane protein 1, transcript variant X2
nuclear envelope integral membrane protein 1 isoform X1
nuclear envelope integral membrane protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
katanin p60 ATPase-containing subunit A1-like, transcript variant X2
katanin p60 ATPase-containing subunit A1-like, transcript variant X1
katanin p60 ATPase-containing subunit A1-like, transcript variant X3
katanin p60 ATPase-containing subunit A1-like isoform X1
katanin p60 ATPase-containing subunit A1-like isoform X2
katanin p60 ATPase-containing subunit A1-like, transcript variant X4
katanin p60 ATPase-containing subunit A1-like isoform X3
NAD-dependent protein deacylase sirtuin-5, mitochondrial
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 102 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cytochrome P450 6k1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cytochrome P450 6k1-like, transcript variant X2
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 6 samples with support for all annotated introns
cytochrome P450 6k1-like, 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 1 sample with support for all annotated introns
cytochrome P450 6k1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cytochrome P450 6k1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 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: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 109 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 109 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 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: 1 Protein, and 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: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
WAP four-disulfide core domain protein 2
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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
TBC1 domain family member 5, 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 9 samples with support for all annotated introns
TBC1 domain family member 5, transcript variant X2
TBC1 domain family member 5, transcript variant X3
vacuolar protein sorting-associated protein 51 homolog
5-aminolevulinate synthase, erythroid-specific, mitochondrial
phosphatidylinositol-glycan biosynthesis class F protein
protein GDAP2 homolog, transcript variant X3
protein GDAP2 homolog, transcript variant X1
protein GDAP2 homolog, transcript variant X2
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
terminal nucleotidyltransferase 5C, transcript variant X1
terminal nucleotidyltransferase 5C, transcript variant X2
terminal nucleotidyltransferase 5C isoform X1
terminal nucleotidyltransferase 5C isoform X2
2-oxoisovalerate dehydrogenase subunit beta, mitochondrial
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 107 samples with support for all annotated introns
fatty-acid amide hydrolase 2-A, transcript variant X3
fatty-acid amide hydrolase 2-A, transcript variant X2
fatty-acid amide hydrolase 2-A, transcript variant X1
myc box-dependent-interacting protein 1, transcript variant X3
myc box-dependent-interacting protein 1, transcript variant X5
myc box-dependent-interacting protein 1, transcript variant X4
myc box-dependent-interacting protein 1, transcript variant X2
myc box-dependent-interacting protein 1, transcript variant X1
myc box-dependent-interacting protein 1 isoform X5
myc box-dependent-interacting protein 1 isoform X4
myc box-dependent-interacting protein 1 isoform X2
myc box-dependent-interacting protein 1 isoform X1
meiosis-specific nuclear structural protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
SH2 domain-containing protein 5, transcript variant X1
SH2 domain-containing protein 5, transcript variant X2
SH2 domain-containing protein 5 isoform X1
SH2 domain-containing protein 5 isoform X2
uncharacterized LOC123689353, transcript variant X2
uncharacterized LOC123689353, 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 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns