Colias croceus chromosome 7, ilColCroc2.1.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Pieridae; Coliadinae; Colias.
REFSEQ INFORMATION: The reference sequence is identical to\nHG991965.1.\nAssembly name: ilColCroc2.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/02/16.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Colias croceus Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
acetylcholine receptor subunit alpha-like
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 20 samples with support for all annotated introns
E3 ubiquitin-protein ligase listerin-like, transcript variant X2
E3 ubiquitin-protein ligase listerin-like, transcript variant X1
E3 ubiquitin-protein ligase listerin-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
cytoplasmic dynein 1 intermediate chain, transcript variant X1
cytoplasmic dynein 1 intermediate chain, transcript variant X4
cytoplasmic dynein 1 intermediate chain, transcript variant X2
cytoplasmic dynein 1 intermediate chain, transcript variant X5
cytoplasmic dynein 1 intermediate chain, transcript variant X7
cytoplasmic dynein 1 intermediate chain, transcript variant X3
cytoplasmic dynein 1 intermediate chain, transcript variant X9
cytoplasmic dynein 1 intermediate chain, transcript variant X11
cytoplasmic dynein 1 intermediate chain, transcript variant X6
cytoplasmic dynein 1 intermediate chain, transcript variant X12
cytoplasmic dynein 1 intermediate chain, transcript variant X8
cytoplasmic dynein 1 intermediate chain, transcript variant X14
cytoplasmic dynein 1 intermediate chain, transcript variant X10
cytoplasmic dynein 1 intermediate chain, transcript variant X16
cytoplasmic dynein 1 intermediate chain, transcript variant X13
cytoplasmic dynein 1 intermediate chain, transcript variant X17
cytoplasmic dynein 1 intermediate chain, transcript variant X15
cytoplasmic dynein 1 intermediate chain isoform X1
cytoplasmic dynein 1 intermediate chain isoform X4
cytoplasmic dynein 1 intermediate chain isoform X2
cytoplasmic dynein 1 intermediate chain isoform X5
cytoplasmic dynein 1 intermediate chain isoform X7
cytoplasmic dynein 1 intermediate chain isoform X3
cytoplasmic dynein 1 intermediate chain isoform X9
cytoplasmic dynein 1 intermediate chain isoform X11
cytoplasmic dynein 1 intermediate chain isoform X6
cytoplasmic dynein 1 intermediate chain isoform X12
cytoplasmic dynein 1 intermediate chain isoform X8
cytoplasmic dynein 1 intermediate chain isoform X14
cytoplasmic dynein 1 intermediate chain isoform X10
cytoplasmic dynein 1 intermediate chain isoform X16
cytoplasmic dynein 1 intermediate chain isoform X13
cytoplasmic dynein 1 intermediate chain isoform X17
cytoplasmic dynein 1 intermediate chain isoform X15
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial, transcript variant X1
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial, transcript variant X2
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial, transcript variant X3
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase PRDM9-like, transcript variant X1
histone-lysine N-methyltransferase PRDM9-like, transcript variant X2
histone-lysine N-methyltransferase PRDM9-like isoform X1
histone-lysine N-methyltransferase PRDM9-like isoform X2
histone-lysine N-methyltransferase PRDM9-like, transcript variant X3
histone-lysine N-methyltransferase PRDM9-like isoform X3
moesin/ezrin/radixin homolog 1, transcript variant X3
moesin/ezrin/radixin homolog 1, transcript variant X2
moesin/ezrin/radixin homolog 1, transcript variant X1
moesin/ezrin/radixin homolog 1 isoform X2
moesin/ezrin/radixin homolog 1 isoform 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 153 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
phospholipase B1, membrane-associated-like
V-type proton ATPase 116 kDa subunit a1, transcript variant X2
V-type proton ATPase 116 kDa subunit a1, transcript variant X1
V-type proton ATPase 116 kDa subunit a1, transcript variant X3
V-type proton ATPase 116 kDa subunit a1, transcript variant X4
V-type proton ATPase 116 kDa subunit a1 isoform X2
V-type proton ATPase 116 kDa subunit a1 isoform X1
V-type proton ATPase 116 kDa subunit a1 isoform X3
V-type proton ATPase 116 kDa subunit a1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
multiple epidermal growth factor-like domains protein 10
proteoglycan 4-like, transcript variant X1
proteoglycan 4-like, transcript variant X5
proteoglycan 4-like, transcript variant X4
proteoglycan 4-like, transcript variant X3
proteoglycan 4-like, transcript variant X2
mediator of DNA damage checkpoint protein 1-like isoform X4
mediator of DNA damage checkpoint protein 1-like isoform 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 3 samples with support for all annotated introns
uncharacterized LOC123693377, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123693377, transcript variant X1
uncharacterized protein LOC123693377 isoform X2
uncharacterized protein LOC123693377 isoform X1
uncharacterized LOC123693377, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC123693377 isoform X3
U3 small nucleolar RNA-associated protein 18 homolog
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 20 samples with support for all annotated introns
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, transcript variant X1
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, transcript variant X2
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic
methionyl-tRNA formyltransferase, mitochondrial
opsin, ultraviolet-sensitive-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 4 samples with support for all annotated introns
opsin, ultraviolet-sensitive-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
opsin, ultraviolet-sensitive-like isoform X2
opsin, ultraviolet-sensitive-like isoform X1
acetylcholine receptor subunit alpha-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 199 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like, 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 1 sample with support for all annotated introns
acetylcholine receptor subunit alpha-like isoform X1
acetylcholine receptor subunit alpha-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 2, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich melanocyte differentiation-associated protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
leucine-rich melanocyte differentiation-associated protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
leucine-rich melanocyte differentiation-associated protein-like, 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 6 samples with support for all annotated introns
leucine-rich melanocyte differentiation-associated protein-like isoform X2
leucine-rich melanocyte differentiation-associated protein-like isoform X1
leucine-rich melanocyte differentiation-associated protein-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
bifunctional purine biosynthesis protein ATIC, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
bifunctional purine biosynthesis protein ATIC, 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 10 samples with support for all annotated introns
bifunctional purine biosynthesis protein ATIC isoform X2
bifunctional purine biosynthesis protein ATIC isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein C15orf61 homolog, 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 15 samples with support for all annotated introns
uncharacterized protein C15orf61 isoform X1
uncharacterized protein C15orf61 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized protein C15orf61 homolog, 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 6 samples with support for all annotated introns
uncharacterized protein C15orf61 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 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
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
exosome complex exonuclease RRP44, transcript variant X2
exosome complex exonuclease RRP44, transcript variant X1
exosome complex exonuclease RRP44 isoform X2
exosome complex exonuclease RRP44 isoform X1
uncharacterized LOC123693420, transcript variant X2
uncharacterized LOC123693420, transcript variant X1
uncharacterized LOC123693413, transcript variant X2
uncharacterized LOC123693413, transcript variant X4
uncharacterized LOC123693413, transcript variant X3
uncharacterized LOC123693413, transcript variant X5
uncharacterized LOC123693413, transcript variant X1
uncharacterized LOC123693413, transcript variant X6
uncharacterized protein LOC123693413 isoform X3
uncharacterized protein LOC123693413 isoform X2
uncharacterized protein LOC123693413 isoform X4
uncharacterized protein LOC123693413 isoform X1
uncharacterized protein LOC123693413 isoform X5
uncharacterized LOC123693413, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tetratricopeptide repeat protein 21B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
tetratricopeptide repeat protein 21B-like, transcript variant X2
tetratricopeptide repeat protein 21B-like
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 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 8 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 8 samples with support for all annotated introns
synaptic vesicle glycoprotein 2C-like, transcript variant X2
synaptic vesicle glycoprotein 2C-like, transcript variant X1
synaptic vesicle glycoprotein 2C-like isoform X2
synaptic vesicle glycoprotein 2C-like isoform 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
A disintegrin and metalloproteinase with thrombospondin motifs 3-like
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
methylthioribose-1-phosphate isomerase, transcript variant X1
methylthioribose-1-phosphate isomerase, transcript variant X2
methylthioribose-1-phosphate isomerase isoform X1
methylthioribose-1-phosphate isomerase isoform X2
disintegrin and metalloproteinase domain-containing protein 10
Fanconi anemia group M protein, transcript variant X2
Fanconi anemia group M protein, transcript variant X1
Fanconi anemia group M protein isoform X2
Fanconi anemia group M protein isoform X1
uncharacterized LOC123693474, transcript variant X1
uncharacterized protein LOC123693474 isoform X1
uncharacterized LOC123693474, transcript variant X5
uncharacterized protein LOC123693474 isoform X3
uncharacterized LOC123693474, transcript variant X3
uncharacterized LOC123693474, transcript variant X4
uncharacterized LOC123693474, transcript variant X2
uncharacterized protein LOC123693474 isoform X2
mannosyl-oligosaccharide alpha-1,2-mannosidase IA, transcript variant X1
mannosyl-oligosaccharide alpha-1,2-mannosidase IA, transcript variant X2
mannosyl-oligosaccharide alpha-1,2-mannosidase IA
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC123693478, transcript variant X1
uncharacterized LOC123693478, transcript variant X2
CDGSH iron-sulfur domain-containing protein 2 homolog
PH and SEC7 domain-containing protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PH and SEC7 domain-containing protein, 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
PH and SEC7 domain-containing protein, transcript variant X3
PH and SEC7 domain-containing protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
PH and SEC7 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 3 samples with support for all annotated introns
PH and SEC7 domain-containing protein, 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 2 samples with support for all annotated introns
PH and SEC7 domain-containing protein isoform X1
PH and SEC7 domain-containing protein isoform X2
PH and SEC7 domain-containing protein isoform X3
PH and SEC7 domain-containing protein isoform X4
PH and SEC7 domain-containing protein isoform X5
PH and SEC7 domain-containing protein isoform X6
PH and SEC7 domain-containing protein, transcript variant X7
PH and SEC7 domain-containing protein, transcript variant X8
PH and SEC7 domain-containing protein isoform X7
tubby-related protein 4, transcript variant X3
tubby-related protein 4, transcript variant X2
tubby-related protein 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tubby-related protein 4, 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 4 samples with support for all annotated introns
fibrinogen silencer-binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
putative nuclease HARBI1, 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 3 samples with support for all annotated introns
putative nuclease HARBI1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
MICOS complex subunit MIC13 homolog QIL1-like, transcript variant X2
MICOS complex subunit MIC13 homolog QIL1-like, transcript variant X1
MICOS complex subunit MIC13 homolog QIL1-like isoform X2
MICOS complex subunit MIC13 homolog QIL1-like isoform X1
interleukin-1 receptor-associated kinase 4-like
DNA polymerase zeta catalytic subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DNA polymerase zeta catalytic subunit, transcript variant X2
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 2 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
AP2/ERF domain-containing protein PFD0985w-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123692976, transcript variant X3
uncharacterized LOC123692976, transcript variant X1
uncharacterized LOC123692976, 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
rhodanese domain-containing protein CG4456-like
histone-lysine N-methyltransferase 2C-like, transcript variant X2
histone-lysine N-methyltransferase 2C-like, transcript variant X1
histone-lysine N-methyltransferase 2C-like, transcript variant X3
histone-lysine N-methyltransferase 2C-like isoform X2
histone-lysine N-methyltransferase 2C-like isoform X1
histone-lysine N-methyltransferase 2C-like isoform X3
GTP-binding protein SAR1b, transcript variant X1
GTP-binding protein SAR1b, transcript variant X2
cytosolic carboxypeptidase-like protein 5, transcript variant X4
cytosolic carboxypeptidase-like protein 5, transcript variant X3
cytosolic carboxypeptidase-like protein 5, transcript variant X1
cytosolic carboxypeptidase-like protein 5, transcript variant X2
cytosolic carboxypeptidase-like protein 5 isoform X4
cytosolic carboxypeptidase-like protein 5 isoform X3
cytosolic carboxypeptidase-like protein 5 isoform X1
cytosolic carboxypeptidase-like protein 5 isoform X2
cytosolic carboxypeptidase-like protein 5, transcript variant X5
uncharacterized LOC123692996, 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
uncharacterized LOC123692996, transcript variant X2
uncharacterized protein LOC123692996 isoform X1
uncharacterized protein LOC123692996 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
sorting nexin-4-like, transcript variant X1
sorting nexin-4-like, transcript variant X2
tachykinin-like peptides receptor 99D, transcript variant X1
tachykinin-like peptides receptor 99D, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 1, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 1, transcript variant X1
pyruvate kinase-like, transcript variant X3
pyruvate kinase-like, transcript variant X4
pyruvate kinase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
pyruvate kinase-like, 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 9 samples with support for all annotated introns
geranylgeranyl pyrophosphate synthase-like
geranylgeranyl pyrophosphate synthase-like, transcript variant X1
geranylgeranyl pyrophosphate synthase-like, transcript variant X2
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 17 samples with support for all annotated introns
uncharacterized LOC123693068, 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 18 samples with support for all annotated introns
uncharacterized LOC123693068, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized protein LOC123693068 isoform X1
uncharacterized protein LOC123693068 isoform X2
calcium-activated potassium channel slowpoke, transcript variant X2
calcium-activated potassium channel slowpoke, transcript variant X3
calcium-activated potassium channel slowpoke, transcript variant X11
calcium-activated potassium channel slowpoke, transcript variant X10
calcium-activated potassium channel slowpoke, transcript variant X8
calcium-activated potassium channel slowpoke, transcript variant X4
calcium-activated potassium channel slowpoke, transcript variant X6
calcium-activated potassium channel slowpoke, transcript variant X7
calcium-activated potassium channel slowpoke, transcript variant X1
calcium-activated potassium channel slowpoke, transcript variant X9
calcium-activated potassium channel slowpoke, transcript variant X12
calcium-activated potassium channel slowpoke, transcript variant X5
calcium-activated potassium channel slowpoke isoform X2
calcium-activated potassium channel slowpoke isoform X3
calcium-activated potassium channel slowpoke isoform X10
calcium-activated potassium channel slowpoke isoform X8
calcium-activated potassium channel slowpoke isoform X4
calcium-activated potassium channel slowpoke isoform X6
calcium-activated potassium channel slowpoke isoform X7
calcium-activated potassium channel slowpoke isoform X1
calcium-activated potassium channel slowpoke isoform X11
calcium-activated potassium channel slowpoke isoform X9
calcium-activated potassium channel slowpoke isoform X12
calcium-activated potassium channel slowpoke isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
protein spaetzle-like, transcript variant X4
protein spaetzle-like, transcript variant X3
protein spaetzle-like, transcript variant X2
protein spaetzle-like, transcript variant X1
uncharacterized LOC123693350, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123693350, 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 11 samples with support for all annotated introns
uncharacterized protein LOC123693350 isoform X2
uncharacterized protein LOC123693350 isoform X1
uncharacterized LOC123693461, transcript variant X1
uncharacterized LOC123693461, transcript variant X2
uncharacterized protein LOC123693461 isoform X1
uncharacterized protein LOC123693461 isoform X2
methionine aminopeptidase 1, transcript variant X3
methionine aminopeptidase 1, transcript variant X2
methionine aminopeptidase 1, transcript variant X1
uncharacterized LOC123693464, transcript variant X5
uncharacterized LOC123693464, transcript variant X4
uncharacterized protein LOC123693464 isoform X4
uncharacterized LOC123693464, transcript variant X3
uncharacterized protein LOC123693464 isoform X3
uncharacterized LOC123693464, transcript variant X6
uncharacterized protein LOC123693464 isoform X5
uncharacterized LOC123693464, transcript variant X1
uncharacterized protein LOC123693464 isoform X1
uncharacterized LOC123693464, transcript variant X2
uncharacterized protein LOC123693464 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
calcium-binding mitochondrial carrier protein Aralar1, transcript variant X1
calcium-binding mitochondrial carrier protein Aralar1, transcript variant X3
calcium-binding mitochondrial carrier protein Aralar1, transcript variant X2
calcium-binding mitochondrial carrier protein Aralar1 isoform X1
calcium-binding mitochondrial carrier protein Aralar1 isoform X2
calcium-binding mitochondrial carrier protein Aralar1 isoform X3
acid sphingomyelinase-like phosphodiesterase 3a, transcript variant X2
acid sphingomyelinase-like phosphodiesterase 3a, transcript variant X1
acid sphingomyelinase-like phosphodiesterase 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
uncharacterized LOC123693282, transcript variant X2
uncharacterized LOC123693282, transcript variant X1
uncharacterized LOC123693282, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized protein LOC123693282 isoform X2
uncharacterized protein LOC123693282 isoform X1
uncharacterized LOC123693282, transcript variant X4
uncharacterized protein LOC123693282 isoform X3
NPC intracellular cholesterol transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123693409, 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 11 samples with support for all annotated introns
uncharacterized LOC123693409, 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
uncharacterized protein LOC123693409 isoform X1
uncharacterized protein LOC123693409 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
centaurin-gamma-1A, transcript variant X3
centaurin-gamma-1A, transcript variant X1
centaurin-gamma-1A, transcript variant X2
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
angiotensin-converting enzyme-like, transcript variant X2
angiotensin-converting enzyme-like, transcript variant X1
angiotensin-converting enzyme-like isoform X1
angiotensin-converting enzyme-like isoform X2
angiotensin-converting enzyme-like, transcript variant X3
angiotensin-converting enzyme-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
pollen-specific leucine-rich repeat extensin-like protein 4
cell wall protein DAN4-like, 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 5 samples with support for all annotated introns
cell wall protein DAN4-like, transcript variant X1
cell wall protein DAN4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
importin subunit alpha-7, transcript variant X2
importin subunit alpha-7, transcript variant X1
UPF0389 protein CG9231, transcript variant X2
UPF0389 protein CG9231, transcript variant X1
cytochrome P450 6k1-like, transcript variant X5
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 3 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
cytochrome P450 6k1-like, transcript variant X4
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 8 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: 13 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 2 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 7 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 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
muscarinic acetylcholine receptor gar-2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
muscarinic acetylcholine receptor gar-2, 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 2 samples with support for all annotated introns
muscarinic acetylcholine receptor gar-2 isoform X1
muscarinic acetylcholine receptor M4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
aminopeptidase N-like, transcript variant X1
aminopeptidase N-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
TBC1 domain family member 5-like, transcript variant X1
TBC1 domain family member 5-like, transcript variant X2
TBC1 domain family member 5-like isoform X1
TBC1 domain family member 5-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 4-kinase beta, transcript variant X1
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 10 samples with support for all annotated introns
phosphatidylinositol 4-kinase beta, transcript variant X2
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 5 samples with support for all annotated introns
phosphatidylinositol 4-kinase beta isoform X1
phosphatidylinositol 4-kinase beta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
phosphatidylinositol 4-kinase beta isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: peptidoglycan recognition protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
tyrosine kinase receptor Cad96Ca, transcript variant X2
tyrosine kinase receptor Cad96Ca, transcript variant X4
tyrosine kinase receptor Cad96Ca, transcript variant X1
tyrosine kinase receptor Cad96Ca, transcript variant X3
tyrosine kinase receptor Cad96Ca isoform X2
tyrosine kinase receptor Cad96Ca isoform X1
transfer RNA serine (anticodon GGA); 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 70% coverage of the annotated genomic feature by RNAseq alignments
carbonic anhydrase 13-like, transcript variant X1
carbonic anhydrase 13-like, transcript variant X2
carbonic anhydrase 13-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
sodium- and chloride-dependent glycine transporter 1-like
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: lactase-phlorizin hydrolase-like
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 LOC123692971, transcript variant X2
uncharacterized LOC123692971, transcript variant X1
uncharacterized protein LOC123692971 isoform X2
uncharacterized protein LOC123692971 isoform X1
uncharacterized LOC123692971, transcript variant X3
uncharacterized protein LOC123692971 isoform X3
myosin heavy chain 95F, transcript variant X3
myosin heavy chain 95F, transcript variant X4
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
sphingosine-1-phosphate lyase, 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 13 samples with support for all annotated introns
sphingosine-1-phosphate lyase, transcript variant X1
katanin p60 ATPase-containing subunit A1-like
V-type proton ATPase 116 kDa subunit a1-like
NAD-dependent protein deacylase sirtuin-5, mitochondrial-like
uncharacterized LOC123693075, transcript variant X1
uncharacterized LOC123693075, transcript variant X2
facilitated trehalose transporter Tret1-like
MKI67 FHA domain-interacting nucleolar phosphoprotein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123693058, transcript variant X1
uncharacterized LOC123693058, transcript variant X3
uncharacterized LOC123693058, transcript variant X6
uncharacterized LOC123693058, transcript variant X4
uncharacterized LOC123693058, transcript variant X5
uncharacterized LOC123693058, transcript variant X2
uncharacterized protein LOC123693058 isoform X1
uncharacterized protein LOC123693058 isoform X3
uncharacterized protein LOC123693058 isoform X6
uncharacterized protein LOC123693058 isoform X4
uncharacterized protein LOC123693058 isoform X5
uncharacterized protein LOC123693058 isoform X2
uncharacterized LOC123693021, transcript variant X1
uncharacterized LOC123693021, transcript variant X2
uncharacterized LOC123693021, transcript variant X3
uncharacterized protein LOC123693021 isoform X1
uncharacterized protein LOC123693021 isoform X2
uncharacterized protein LOC123693021 isoform X3
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X1
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X2
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X7
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X3
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X5
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X4
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X6
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X10
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X9
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X8
dnaJ homolog subfamily C member 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
dnaJ homolog subfamily C member 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
forkhead box protein O, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
forkhead box protein O, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
U1 small nuclear ribonucleoprotein C, transcript variant X2
U1 small nuclear ribonucleoprotein C, transcript variant X1
vacuolar protein sorting-associated protein 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB1-like isoform X1
DNA-directed RNA polymerase II subunit RPB1-like isoform X2
uncharacterized protein LOC123693062 isoform X9
DNA-directed RNA polymerase II subunit RPB1-like isoform X4
DNA-directed RNA polymerase II subunit RPB1-like isoform X5
uncharacterized protein LOC123693062 isoform X10
DNA-directed RNA polymerase II subunit RPB1-like isoform X7
DNA-directed RNA polymerase II subunit RPB1-like isoform X6
probable E3 ubiquitin-protein ligase HERC4, transcript variant X6
probable E3 ubiquitin-protein ligase HERC4, transcript variant X2
probable E3 ubiquitin-protein ligase HERC4, transcript variant X5
probable E3 ubiquitin-protein ligase HERC4, transcript variant X3
probable E3 ubiquitin-protein ligase HERC4, transcript variant X4
probable E3 ubiquitin-protein ligase HERC4, transcript variant X1
probable E3 ubiquitin-protein ligase HERC4 isoform X6
probable E3 ubiquitin-protein ligase HERC4 isoform X2
probable E3 ubiquitin-protein ligase HERC4 isoform X5
probable E3 ubiquitin-protein ligase HERC4 isoform X3
probable E3 ubiquitin-protein ligase HERC4 isoform X4
probable E3 ubiquitin-protein ligase HERC4 isoform X1
zinc finger SWIM domain-containing protein 8 homolog
alanine--glyoxylate aminotransferase 2-like
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 5 samples with support for all annotated introns
ribonuclease H1-like, transcript variant X2
ribonuclease H1-like, transcript variant X1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
signal recognition particle 19 kDa protein
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit wuho
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
mitotic checkpoint serine/threonine-protein kinase BUB1 beta-like
ATP-dependent (S)-NAD(P)H-hydrate dehydratase
26S proteasome non-ATPase regulatory subunit 5, transcript variant X2
26S proteasome non-ATPase regulatory subunit 5, transcript variant X1
26S proteasome non-ATPase regulatory subunit 5 isoform X1
26S proteasome non-ATPase regulatory subunit 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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.
F-box only protein 28, transcript variant X2
F-box only protein 28, transcript variant X3
F-box only protein 28, transcript variant X1
coiled-coil domain-containing protein 12
putative uncharacterized protein DDB_G0271606
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
all trans-polyprenyl-diphosphate synthase PDSS1
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 17 samples with support for all annotated introns
39S ribosomal protein L32, mitochondrial
major facilitator superfamily domain-containing protein 9-like
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
ras-related and estrogen-regulated growth inhibitor-like protein
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 14 samples with support for all annotated introns
disks large homolog 1-like, transcript variant X2
disks large homolog 1-like, transcript variant X1
ommochrome-binding protein-like, transcript variant X1
ommochrome-binding protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 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 97% coverage of the annotated genomic feature by RNAseq alignments
cytochrome b5-related protein-like, transcript variant X2
cytochrome b5-related protein-like, transcript variant X1
uncharacterized LOC123693114, transcript variant X1
uncharacterized LOC123693114, transcript variant X2
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1, transcript variant X1
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1, transcript variant X2
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1, transcript variant X3
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 isoform X1
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 isoform X2
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 isoform X3
U-scoloptoxin(05)-Sm1a, transcript variant X1
U-scoloptoxin(05)-Sm1a, transcript variant X2
uncharacterized LOC123693450, transcript variant X1
uncharacterized LOC123693450, transcript variant X2
uncharacterized LOC123693450, 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 12 samples with support for all annotated introns
uncharacterized protein LOC123693450 isoform X1
uncharacterized protein LOC123693450 isoform X2
zinc finger MIZ domain-containing protein 1, 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 14 samples with support for all annotated introns
zinc finger MIZ domain-containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
zinc finger MIZ domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
fatty-acid amide hydrolase 2-B-like, transcript variant X2
fatty-acid amide hydrolase 2-B-like, 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 10 samples with support for all annotated introns
fatty-acid amide hydrolase 2-B-like isoform X1
fatty-acid amide hydrolase 2-B-like isoform X2
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X7
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X8
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X1
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X6
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X5
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X4
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X3
guanine nucleotide-binding protein G(q) subunit alpha isoform X7
guanine nucleotide-binding protein G(q) subunit alpha isoform X3
guanine nucleotide-binding protein G(q) subunit alpha isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, NMDA 2C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
huntingtin-interacting protein K, transcript variant X2
huntingtin-interacting protein K, transcript variant X1
origin recognition complex subunit 2, transcript variant X1
origin recognition complex subunit 2, transcript variant X2
origin recognition complex subunit 2 isoform X1
origin recognition complex subunit 2 isoform X2
acidic leucine-rich nuclear phosphoprotein 32 family member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 80% 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 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cell division cycle and apoptosis regulator protein 1-like
putative sodium-dependent multivitamin transporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
sorbin and SH3 domain-containing protein 1, transcript variant X10
sorbin and SH3 domain-containing protein 1, transcript variant X5
sorbin and SH3 domain-containing protein 1, transcript variant X4
sorbin and SH3 domain-containing protein 1, transcript variant X1
sorbin and SH3 domain-containing protein 1, transcript variant X3
sorbin and SH3 domain-containing protein 1, transcript variant X9
sorbin and SH3 domain-containing protein 1, transcript variant X8
sorbin and SH3 domain-containing protein 1, transcript variant X7
sorbin and SH3 domain-containing protein 1, transcript variant X6
sorbin and SH3 domain-containing protein 1, transcript variant X2
sorbin and SH3 domain-containing protein 1 isoform X10
uncharacterized protein LOC123693189 isoform X5
uncharacterized protein LOC123693189 isoform X4
uncharacterized protein LOC123693189 isoform X1
uncharacterized protein LOC123693189 isoform X3
uncharacterized protein LOC123693189 isoform X9
uncharacterized protein LOC123693189 isoform X8
uncharacterized protein LOC123693189 isoform X7
uncharacterized protein LOC123693189 isoform X6
uncharacterized protein LOC123693189 isoform 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 17 samples with support for all annotated introns
molybdenum cofactor sulfurase, transcript variant X1
molybdenum cofactor sulfurase, transcript variant X2
molybdenum cofactor sulfurase isoform X1
molybdenum cofactor sulfurase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
poly(rC)-binding protein 3, transcript variant X1
poly(rC)-binding protein 3, transcript variant X3
poly(rC)-binding protein 3, transcript variant X5
poly(rC)-binding protein 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
poly(rC)-binding protein 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
poly(rC)-binding protein 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
poly(rC)-binding protein 3, transcript variant X9
poly(rC)-binding protein 3, transcript variant X10
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 6 samples with support for all annotated introns
poly(rC)-binding protein 3, transcript variant X2
poly(rC)-binding protein 3, transcript variant X4
glutamate-gated chloride channel, transcript variant X1
glutamate-gated chloride channel, transcript variant X2
glutamate-gated chloride channel, transcript variant X4
glutamate-gated chloride channel, transcript variant X7
glutamate-gated chloride channel, transcript variant X5
glutamate-gated chloride channel, transcript variant X8
glutamate-gated chloride channel, transcript variant X3
glutamate-gated chloride channel, transcript variant X10
glutamate-gated chloride channel, transcript variant X11
glutamate-gated chloride channel, transcript variant X12
glutamate-gated chloride channel, transcript variant X13
glutamate-gated chloride channel, transcript variant X16
glutamate-gated chloride channel, transcript variant X18
glutamate-gated chloride channel, transcript variant X6
glutamate-gated chloride channel, transcript variant X15
glutamate-gated chloride channel, transcript variant X19
glutamate-gated chloride channel, transcript variant X21
glutamate-gated chloride channel, transcript variant X22
glutamate-gated chloride channel, transcript variant X26
glutamate-gated chloride channel, transcript variant X28
glutamate-gated chloride channel, transcript variant X14
glutamate-gated chloride channel, transcript variant X20
glutamate-gated chloride channel, transcript variant X27
glutamate-gated chloride channel, transcript variant X9
glutamate-gated chloride channel, transcript variant X17
glutamate-gated chloride channel, transcript variant X23
glutamate-gated chloride channel, transcript variant X30
glutamate-gated chloride channel, transcript variant X25
glutamate-gated chloride channel, transcript variant X29
glutamate-gated chloride channel, transcript variant X24
glutamate-gated chloride channel subunit beta isoform X1
glycine receptor subunit alpha-3 isoform X2
glycine receptor subunit alpha-3 isoform X4
glycine receptor subunit alpha-4 isoform X7
glycine receptor subunit alpha-3 isoform X5
glycine receptor subunit alpha-3 isoform X8
glycine receptor subunit alpha-3 isoform X3
glycine receptor subunit alpha-4 isoform X10
glycine receptor subunit alpha-4 isoform X11
glutamate-gated chloride channel isoform X12
glutamate-gated chloride channel isoform X13
glutamate-gated chloride channel isoform X16
glutamate-gated chloride channel isoform X18
glutamate-gated chloride channel isoform X6
glutamate-gated chloride channel isoform X15
glutamate-gated chloride channel isoform X19
glutamate-gated chloride channel isoform X21
glutamate-gated chloride channel isoform X22
glutamate-gated chloride channel isoform X26
glutamate-gated chloride channel isoform X28
glutamate-gated chloride channel isoform X14
glutamate-gated chloride channel isoform X20
glutamate-gated chloride channel isoform X27
glycine receptor subunit alpha-4 isoform X9
glutamate-gated chloride channel isoform X17
glutamate-gated chloride channel isoform X23
glutamate-gated chloride channel isoform X30
glutamate-gated chloride channel isoform X25
glutamate-gated chloride channel isoform X29
glutamate-gated chloride channel isoform X24
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 20 samples with support for all annotated introns
uncharacterized LOC123693364, transcript variant X1
uncharacterized LOC123693364, 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 14 samples with support for all annotated introns
uncharacterized protein LOC123693364 isoform X1
uncharacterized protein LOC123693364 isoform X2
uncharacterized LOC123693366, transcript variant X4
uncharacterized LOC123693366, transcript variant X1
uncharacterized LOC123693366, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC123693366, transcript variant X7
uncharacterized LOC123693366, transcript variant X5
uncharacterized LOC123693366, transcript variant X2
uncharacterized LOC123693366, transcript variant X6
uncharacterized protein LOC123693366 isoform X4
uncharacterized protein LOC123693366 isoform X2
uncharacterized protein LOC123693366 isoform X1
uncharacterized protein LOC123693366 isoform X3
uncharacterized protein LOC123693366 isoform X5
uncharacterized protein LOC123693366 isoform X6
transcription initiation factor TFIID subunit 13, transcript variant X3
transcription initiation factor TFIID subunit 13, transcript variant X2
transcription initiation factor TFIID subunit 13, transcript variant X1
transcription initiation factor TFIID subunit 13
THAP domain-containing protein 1-like, transcript variant X1
THAP domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
arylsulfatase B-like, transcript variant X1
arylsulfatase B-like, transcript variant X2
arylsulfatase I-like, transcript variant X1
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 15 samples with support for all annotated introns
arylsulfatase I-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 15 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
uncharacterized LOC123693391, transcript variant X2
uncharacterized LOC123693391, transcript variant X1
uncharacterized protein LOC123693391 isoform X1
uncharacterized protein LOC123693391 isoform X2
PHD finger protein 14, transcript variant X1
PHD finger protein 14, transcript variant X4
PHD finger protein 14, transcript variant X2
PHD finger protein 14, transcript variant X3
calcitonin gene-related peptide type 1 receptor-like
S-adenosylmethionine synthase, transcript variant X2
S-adenosylmethionine synthase, transcript variant X1
S-adenosylmethionine synthase isoform X2
S-adenosylmethionine synthase isoform X1
protein bric-a-brac 1-like, transcript variant X2
protein bric-a-brac 1-like, transcript variant X1
protein bric-a-brac 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 228 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
corticotropin-releasing factor-binding protein
serine protease nudel, transcript variant X1
serine protease nudel, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
signal peptidase complex catalytic subunit SEC11A
NEDD8-activating enzyme E1 catalytic subunit
uncharacterized LOC123693254, transcript variant X2
uncharacterized LOC123693254, transcript variant X3
uncharacterized LOC123693254, transcript variant X1
uncharacterized LOC123693254, transcript variant X4
ATP synthase subunit beta, mitochondrial
ubiquinol-cytochrome-c reductase complex assembly factor 1
ATP synthase subunit beta, mitochondrial-like
uncharacterized LOC123693094, transcript variant X1
uncharacterized LOC123693094, transcript variant X2
vacuolar protein sorting-associated protein 51 homolog
uncharacterized LOC123692962, transcript variant X2
uncharacterized LOC123692962, transcript variant X1
uncharacterized protein LOC123692962 isoform X2
uncharacterized protein LOC123692962 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
5-aminolevulinate synthase, nonspecific, mitochondrial
phosphatidylinositol-glycan biosynthesis class F protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
putative uncharacterized protein DDB_G0293878
terminal nucleotidyltransferase 5C, transcript variant X1
terminal nucleotidyltransferase 5C, transcript variant X2
terminal nucleotidyltransferase 5C isoform X1
terminal nucleotidyltransferase 5C isoform X2
uncharacterized LOC123693107, transcript variant X1
uncharacterized LOC123693107, transcript variant X2
2-oxoisovalerate dehydrogenase subunit beta, mitochondrial
inner nuclear membrane protein Man1-like
fatty-acid amide hydrolase 2-A-like, transcript variant X2
fatty-acid amide hydrolase 2-A-like, transcript variant X1
myc box-dependent-interacting protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
myc box-dependent-interacting protein 1, transcript variant X1
myc box-dependent-interacting protein 1 isoform X2
myc box-dependent-interacting protein 1 isoform X1
meiosis-specific nuclear structural protein 1-like
IQ and AAA domain-containing protein 1-like
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% 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: 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.
delta(7)-sterol 5(6)-desaturase erg32-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123693314, transcript variant X1
uncharacterized LOC123693314, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
inorganic pyrophosphatase, transcript variant X1
inorganic pyrophosphatase, transcript variant X2
uncharacterized LOC123693455, transcript variant X2
uncharacterized LOC123693455, transcript variant X4
uncharacterized LOC123693455, transcript variant X1
uncharacterized LOC123693455, transcript variant X3
uncharacterized protein LOC123693455 isoform X1
uncharacterized protein LOC123693455 isoform X2
uncharacterized protein LOC123693455 isoform X3
uncharacterized LOC123693455, transcript variant X5
uncharacterized protein LOC123693455 isoform X4