Pieris rapae chromosome 17, 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\nLR990599.1.\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.
COORDINATES: polyA evidence [ECO:0006239]
eukaryotic translation initiation factor 4 gamma 2
MOB kinase activator-like 2, transcript variant X3
MOB kinase activator-like 2, transcript variant X1
MOB kinase activator-like 2, transcript variant X4
MOB kinase activator-like 2, transcript variant X2
tyrosine-protein phosphatase 10D, transcript variant X1
tyrosine-protein phosphatase 10D, transcript variant X2
caseinolytic peptidase B protein homolog, 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 12 samples with support for all annotated introns
caseinolytic peptidase B protein homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
caseinolytic peptidase B protein homolog, 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 63 samples with support for all annotated introns
caseinolytic peptidase B protein homolog, 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 15 samples with support for all annotated introns
caseinolytic peptidase B protein homolog isoform X1
caseinolytic peptidase B protein homolog isoform X2
transient receptor potential-gamma protein
uncharacterized LOC110998346, 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 LOC110998346, 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 17 samples with support for all annotated introns
uncharacterized protein LOC110998346 isoform X1
uncharacterized protein LOC110998346 isoform X2
uncharacterized LOC110998346, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
uncharacterized protein LOC110998346 isoform X3
double-strand break repair protein MRE11
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
phosphatidylcholine:ceramide cholinephosphotransferase 2
probable phospholipid-transporting ATPase IA, transcript variant X5
probable phospholipid-transporting ATPase IA, transcript variant X8
probable phospholipid-transporting ATPase IA, transcript variant X1
probable phospholipid-transporting ATPase IA, transcript variant X3
probable phospholipid-transporting ATPase IA, transcript variant X2
probable phospholipid-transporting ATPase IA, transcript variant X7
probable phospholipid-transporting ATPase IA, transcript variant X4
probable phospholipid-transporting ATPase IA isoform X5
probable phospholipid-transporting ATPase IA isoform X8
probable phospholipid-transporting ATPase IA isoform X1
probable phospholipid-transporting ATPase IA isoform X3
probable phospholipid-transporting ATPase IA isoform X2
probable phospholipid-transporting ATPase IA isoform X7
probable phospholipid-transporting ATPase IA isoform X4
probable phospholipid-transporting ATPase IA, transcript variant X6
probable phospholipid-transporting ATPase IA isoform X6
cholinephosphotransferase 1, 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 67 samples with support for all annotated introns
cholinephosphotransferase 1, transcript variant X4
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 91 samples with support for all annotated introns
cholinephosphotransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
cholinephosphotransferase 1, 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 23 samples with support for all annotated introns
cholinephosphotransferase 1, 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 12 samples with support for all annotated introns
ankyrin repeat and BTB/POZ domain-containing protein BTBD11, transcript variant X3
ankyrin repeat and BTB/POZ domain-containing protein BTBD11, transcript variant X2
ankyrin repeat and BTB/POZ domain-containing protein BTBD11, transcript variant X1
ankyrin repeat and BTB/POZ domain-containing protein BTBD11 isoform X3
ankyrin repeat and BTB/POZ domain-containing protein 2 isoform X2
ankyrin repeat and BTB/POZ domain-containing protein BTBD11 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
balbiani ring protein 3, transcript variant X1
balbiani ring protein 3, transcript variant X2
uncharacterized protein LOC110998333 isoform X2
zinc finger protein 2, transcript variant X1
zinc finger protein 2, transcript variant X2
uncharacterized protein LOC110998345 isoform 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 59 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
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 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 11, 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 37 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 11, transcript variant X1
tyrosine-protein phosphatase non-receptor type 11 isoform X1
tyrosine-protein phosphatase non-receptor type 11, transcript variant X2
tyrosine-protein phosphatase corkscrew isoform X2
protein yippee-like 5, transcript variant X1
protein yippee-like 5, transcript variant X2
TBC1 domain family member 19, transcript variant X1
TBC1 domain family member 19, 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 1 sample with support for all annotated introns
alkylated DNA repair protein alkB homolog 8
phosphatidylinositol N-acetylglucosaminyltransferase subunit A
clathrin light chain, transcript variant X1
clathrin light chain, transcript variant X2
growth arrest and DNA damage-inducible proteins-interacting protein 1
nitric oxide synthase-interacting protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 46
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 87 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 86 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 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: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 114 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: 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, 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: 3 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: tRNAscan-SE.
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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
low-density lipoprotein receptor-related protein 6
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
dolichyl-phosphate beta-glucosyltransferase
programmed cell death protein 6, transcript variant X1
programmed cell death protein 6, transcript variant X2
programmed cell death protein 6 isoform X1
programmed cell death protein 6 isoform X2
7-methylguanosine phosphate-specific 5'-nucleotidase
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 19 samples with support for all annotated introns
protein kinase C-binding protein NELL1, 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 6 samples with support for all annotated introns
protein kinase C-binding protein NELL1, 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
protein kinase C-binding protein NELL1, 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 3 samples with support for all annotated introns
protein kinase C-binding protein NELL1, transcript variant X3
protein kinase C-binding protein NELL1 isoform X2
protein kinase C-binding protein NELL1 isoform X3
protein kinase C-binding protein NELL1 isoform X1
protein kinase C-binding protein NELL1 isoform X4
CD63 antigen-like, transcript variant X2
CD63 antigen-like, transcript variant X3
CD63 antigen-like, transcript variant X1
uncharacterized protein LOC111001744 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leukocyte surface antigen CD53 isoform X1
leukocyte surface antigen CD53 isoform X2
POC1 centriolar protein homolog A-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 35 samples with support for all annotated introns
POC1 centriolar protein homolog A-like, 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 6 samples with support for all annotated introns
POC1 centriolar protein homolog A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
POC1 centriolar protein homolog A-like isoform X1
POC1 centriolar protein homolog A-like isoform X2
POC1 centriolar protein homolog A-like 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 18 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 20 samples with support for all annotated introns
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC111001232, transcript variant X2
uncharacterized LOC111001232, transcript variant X1
rab proteins geranylgeranyltransferase component A 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
probable serine/threonine-protein kinase clkA
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 6 samples with support for all annotated introns
post-GPI attachment to proteins factor 2-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 8 samples with support for all annotated introns
transcriptional enhancer factor TEF-1, transcript variant X4
transcriptional enhancer factor TEF-1, transcript variant X2
transcriptional enhancer factor TEF-1, transcript variant X1
transcriptional enhancer factor TEF-1, transcript variant X3
transcriptional enhancer factor TEF-1 isoform X2
transcriptional enhancer factor TEF-1 isoform X1
transcriptional enhancer factor TEF-1 isoform X4
lysosomal acid glucosylceramidase, transcript variant X2
lysosomal acid glucosylceramidase, transcript variant X1
lysosomal acid glucosylceramidase isoform X1
lysosomal acid glucosylceramidase isoform X2
mitochondrial inner membrane protease subunit 1
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 117 samples with support for all annotated introns
zinc transporter 1, transcript variant X1
zinc transporter 1, transcript variant X2
zinc/cadmium resistance protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
histone deacetylase complex subunit SAP30 homolog
high mobility group protein B2, transcript variant X3
high mobility group protein B2, transcript variant X1
high mobility group protein DSP1 isoform X1
high mobility group protein B2, transcript variant X2
high mobility group protein DSP1 isoform X2
high mobility group protein B2 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 11 samples with support for all annotated introns
uncharacterized LOC111001722, transcript variant X1
uncharacterized LOC111001722, transcript variant X3
uncharacterized LOC111001722, transcript variant X2
uncharacterized protein LOC111001722 isoform X1
uncharacterized protein LOC111001722 isoform X2
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: signal peptidase complex subunit 3
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 103 samples with support for all annotated introns
uncharacterized LOC111001724, transcript variant X2
uncharacterized LOC111001724, 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 59 samples with support for all annotated introns
zinc finger protein ztf-16, transcript variant X1
zinc finger protein ztf-16, transcript variant X2
testis-specific serine/threonine-protein kinase 3
testis-specific serine/threonine-protein kinase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
testis-specific serine/threonine-protein kinase 1-like, transcript variant X1
testis-specific serine/threonine-protein kinase 1-like isoform X2
testis-specific serine/threonine-protein kinase 1-like isoform X1
testis-specific serine/threonine-protein kinase 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
testis-specific serine/threonine-protein kinase 1-like isoform X3
ER degradation-enhancing alpha-mannosidase-like protein 2, 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 14 samples with support for all annotated introns
ER degradation-enhancing alpha-mannosidase-like protein 2, 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 71 samples with support for all annotated introns
ER degradation-enhancing alpha-mannosidase-like protein 2
tumor necrosis factor receptor superfamily member wengen, transcript variant X2
tumor necrosis factor receptor superfamily member wengen, transcript variant X1
tumor necrosis factor receptor superfamily member wengen
transmembrane protein 41 homolog, transcript variant X1
transmembrane protein 41 homolog, transcript variant X2
transmembrane protein 41 homolog isoform X1
transmembrane protein 41 homolog 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 29 samples with support for all annotated introns
uncharacterized protein LOC110996109 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
flocculation protein FLO11, transcript variant X2
flocculation protein FLO11, 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 5 samples with support for all annotated introns
uncharacterized LOC110995080, transcript variant X1
uncharacterized LOC110995080, transcript variant X2
uncharacterized LOC110995073, transcript variant X2
uncharacterized LOC110995073, transcript variant X1
monocarboxylate transporter 13, 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
monocarboxylate transporter 13, 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 5 samples with support for all annotated introns
monocarboxylate transporter 1 isoform X1
monocarboxylate transporter 13 isoform X2
facilitated trehalose transporter Tret1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 107 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like isoform X1
facilitated trehalose transporter Tret1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
proton-coupled amino acid transporter-like protein pathetic
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
NADH-cytochrome b5 reductase 2, transcript variant X2
NADH-cytochrome b5 reductase 2 isoform X2
NADH-cytochrome b5 reductase 2, transcript variant X3
NADH-cytochrome b5 reductase 2 isoform X3
NADH-cytochrome b5 reductase 2, transcript variant X1
NADH-cytochrome b5 reductase 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
nuclear pore complex protein Nup50, transcript variant X1
nuclear pore complex protein Nup50, transcript variant X2
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
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
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
histidine--tRNA ligase, cytoplasmic, transcript variant X3
histidine--tRNA ligase, cytoplasmic, transcript variant X1
histidine--tRNA ligase, cytoplasmic, transcript variant X2
histidine--tRNA ligase, cytoplasmic isoform X2
histidine--tRNA ligase, cytoplasmic isoform X3
histidine--tRNA ligase, cytoplasmic isoform X1
vacuolar protein-sorting-associated protein 36, transcript variant X1
vacuolar protein-sorting-associated protein 36, transcript variant X2
vacuolar protein-sorting-associated protein 36
vacuolar ATPase assembly integral membrane protein VMA21 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 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
glutamine-dependent NAD(+) synthetase, transcript variant X1
glutamine-dependent NAD(+) synthetase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cytosolic carboxypeptidase Nna1-like
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
angiotensin-converting enzyme, transcript variant X2
angiotensin-converting enzyme, 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 5 samples with support for all annotated introns
DNA-directed RNA polymerase I subunit RPA12, transcript variant X1
DNA-directed RNA polymerase I subunit RPA12, transcript variant X3
DNA-directed RNA polymerase I subunit RPA12, transcript variant X2
DNA-directed RNA polymerase I subunit RPA12, transcript variant X4
DNA-directed RNA polymerase I subunit RPA12
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
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 21 samples with support for all annotated introns
uncharacterized LOC111003795, transcript variant X1
uncharacterized LOC111003795, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
peripheral plasma membrane protein CASK, transcript variant X1
peripheral plasma membrane protein CASK, transcript variant X2
peripheral plasma membrane protein CASK, transcript variant X5
peripheral plasma membrane protein CASK, transcript variant X3
peripheral plasma membrane protein CASK, transcript variant X4
peripheral plasma membrane protein CASK, transcript variant X7
peripheral plasma membrane protein CASK, transcript variant X6
peripheral plasma membrane protein CASK isoform X1
peripheral plasma membrane protein CASK isoform X2
peripheral plasma membrane protein CASK isoform X5
peripheral plasma membrane protein CASK isoform X3
peripheral plasma membrane protein CASK isoform X4
peripheral plasma membrane protein CASK isoform X7
peripheral plasma membrane protein CASK isoform X6
uncharacterized LOC111003804, transcript variant X3
uncharacterized LOC111003804, transcript variant X2
uncharacterized LOC111003804, transcript variant X1
uncharacterized protein LOC111003804 isoform X2
uncharacterized protein LOC111003804 isoform X1
uncharacterized protein LOC111003804 isoform X3
vacuolar protein sorting-associated protein 72 homolog
uncharacterized LOC111003803, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC111003803, 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 8 samples with support for all annotated introns
uncharacterized LOC111003803, transcript variant X1
uncharacterized protein LOC111003803 isoform X1
uncharacterized protein LOC111003803 isoform X2
C3 and PZP-like alpha-2-macroglobulin domain-containing protein 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 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 98% coverage of the annotated genomic feature by RNAseq alignments
probable 2-oxoglutarate dehydrogenase E1 component DHKTD1 homolog, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 477 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transmembrane protein 135, transcript variant X1
transmembrane protein 135, transcript variant X2
CCR4-NOT transcription complex subunit 6, transcript variant X1
CCR4-NOT transcription complex subunit 6, transcript variant X2
CCR4-NOT transcription complex subunit 6 isoform X1
CCR4-NOT transcription complex subunit 6 isoform X2
28S ribosomal protein S24, mitochondrial
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
collagen alpha-1(I) chain-like, transcript variant X2
collagen alpha-1(I) chain-like, transcript variant X1
collagen alpha-1(I) chain-like isoform X2
collagen alpha-1(I) chain-like isoform X1
soluble guanylate cyclase 89Db, transcript variant X1
soluble guanylate cyclase 89Db, transcript variant X2
soluble guanylate cyclase 89Db isoform X1
soluble guanylate cyclase 89Db isoform X2
glucose transporter type 1, transcript variant X3
glucose transporter type 1, transcript variant X2
glucose transporter type 1, transcript variant X4
glucose transporter type 1, transcript variant X1
ankyrin repeat domain-containing protein 17, transcript variant X1
ankyrin repeat domain-containing protein 17, transcript variant X4
ankyrin repeat domain-containing protein 17, transcript variant X3
ankyrin repeat domain-containing protein 17, transcript variant X2
ankyrin repeat domain-containing protein 17 isoform X1
ankyrin repeat domain-containing protein 17 isoform X4
ankyrin repeat domain-containing protein 17 isoform X3
ankyrin repeat domain-containing protein 17 isoform X2
ankyrin repeat domain-containing protein 17, transcript variant X5
ankyrin repeat domain-containing protein 17 isoform X5
alpha-2-macroglobulin receptor-associated protein, transcript variant X2
alpha-2-macroglobulin receptor-associated protein, transcript variant X1
alpha-2-macroglobulin receptor-associated protein isoform X2
alpha-2-macroglobulin receptor-associated protein isoform X1
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X1
E3 ubiquitin-protein ligase RNF19A-like isoform X1
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X2
E3 ubiquitin-protein ligase RNF19A-like isoform X2
RING finger and transmembrane domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 80 samples with support for all annotated introns
ADP-ribosylation factor-like protein 6-interacting protein 4
thioredoxin domain-containing protein 5 homolog
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 62 samples with support for all annotated introns
piggyBac transposable element-derived protein 4, transcript variant X1
piggyBac transposable element-derived protein 4, 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 19 samples with support for all annotated introns
piggyBac transposable element-derived protein 4 isoform X1
piggyBac transposable element-derived protein 4 isoform X2
piggyBac transposable element-derived protein 4, 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 13 samples with support for all annotated introns
piggyBac transposable element-derived protein 4 isoform X3
tolloid-like protein 2, transcript variant X1
tolloid-like protein 2, transcript variant X2
tolloid-like protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dorsal-ventral patterning tolloid-like protein 1 isoform X1
dorsal-ventral patterning tolloid-like protein 1 isoform X2
tolloid-like protein 2, transcript variant X4
heterogeneous nuclear ribonucleoprotein R, transcript variant X2
heterogeneous nuclear ribonucleoprotein R, transcript variant X4
heterogeneous nuclear ribonucleoprotein R, transcript variant X1
heterogeneous nuclear ribonucleoprotein R, transcript variant X5
heterogeneous nuclear ribonucleoprotein R, transcript variant X3
heterogeneous nuclear ribonucleoprotein R, transcript variant X8
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 84 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein R, transcript variant X9
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 83 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein R isoform X2
heterogeneous nuclear ribonucleoprotein R isoform X3
heterogeneous nuclear ribonucleoprotein R isoform X1
heterogeneous nuclear ribonucleoprotein R isoform X7
heterogeneous nuclear ribonucleoprotein R isoform X6
heterogeneous nuclear ribonucleoprotein R, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein R isoform X4
heterogeneous nuclear ribonucleoprotein R, transcript variant X7
heterogeneous nuclear ribonucleoprotein R isoform X5
ER membrane protein complex subunit 1, transcript variant X1
ER membrane protein complex subunit 1, transcript variant X2
ER membrane protein complex subunit 1 isoform X1
ER membrane protein complex subunit 1 isoform X2
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
BPTI/Kunitz domain-containing protein-like
transmembrane protein 135, transcript variant X3
facilitated trehalose transporter Tret1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
mitochondrial pyruvate carrier 1, 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 78 samples with support for all annotated introns
mitochondrial pyruvate carrier 1, 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 31 samples with support for all annotated introns
WD repeat-containing protein 44, transcript variant X1
WD repeat-containing protein 44, transcript variant X2
WD repeat-containing protein 44, transcript variant X5
WD repeat-containing protein 44, transcript variant X7
WD repeat-containing protein 44, transcript variant X9
WD repeat-containing protein 44, transcript variant X3
WD repeat-containing protein 44, transcript variant X8
WD repeat-containing protein 44, transcript variant X10
WD repeat-containing protein 44, transcript variant X4
WD repeat-containing protein 44, transcript variant X6
WD repeat-containing protein 44 isoform X1
WD repeat-containing protein 44 isoform X2
WD repeat-containing protein 44 isoform X5
WD repeat-containing protein 44 isoform X7
WD repeat-containing protein 44 isoform X9
WD repeat-containing protein 44 isoform X3
WD repeat-containing protein 44 isoform X8
WD repeat-containing protein 44 isoform X10
WD repeat-containing protein 44 isoform X4
WD repeat-containing protein 44 isoform X6
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
trafficking protein particle complex subunit 1
mitochondrial import inner membrane translocase subunit Tim17-B
epidermal growth factor receptor substrate 15 homolog
fragile X mental retardation syndrome-related protein 1, transcript variant X3
fragile X mental retardation syndrome-related protein 1, transcript variant X2
fragile X mental retardation syndrome-related protein 1, transcript variant X1
fragile X mental retardation syndrome-related protein 1 isoform X3
fragile X mental retardation syndrome-related protein 1 isoform X2
fragile X mental retardation syndrome-related protein 1 isoform X1
GDP-L-fucose synthase, transcript variant X2
GDP-L-fucose synthase, transcript variant X1
GDP-L-fucose synthase, transcript variant X3
glutamate dehydrogenase, mitochondrial, transcript variant X2
glutamate dehydrogenase, mitochondrial, transcript variant X1
glutamate dehydrogenase, mitochondrial isoform X2
glutamate dehydrogenase, mitochondrial isoform X1
phenylalanine--tRNA ligase alpha subunit
saccharopine dehydrogenase-like oxidoreductase, transcript variant X2
saccharopine dehydrogenase-like oxidoreductase, transcript variant X1
saccharopine dehydrogenase-like oxidoreductase isoform X1
saccharopine dehydrogenase-like oxidoreductase, 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 16 samples with support for all annotated introns
saccharopine dehydrogenase-like oxidoreductase 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 4 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 20 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 12 samples with support for all annotated introns
pyruvate dehydrogenase E1 component subunit beta, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 83% 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, including 2 samples with support for all annotated introns
collagen alpha chain CG42342, transcript variant X7
collagen alpha chain CG42342, transcript variant X8
collagen alpha chain CG42342, transcript variant X1
collagen alpha chain CG42342, transcript variant X6
collagen alpha chain CG42342, transcript variant X2
collagen alpha chain CG42342, transcript variant X3
collagen alpha chain CG42342, transcript variant X4
collagen alpha chain CG42342, 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 13 samples with support for all annotated introns
(E3-independent) E2 ubiquitin-conjugating enzyme
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like
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
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
facilitated trehalose transporter Tret1-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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like isoform X3
facilitated trehalose transporter Tret1-like, 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 4 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like isoform X4
facilitated trehalose transporter Tret1, transcript variant X3
facilitated trehalose transporter Tret1, transcript variant X2
facilitated trehalose transporter Tret1, transcript variant X1
facilitated trehalose transporter Tret1 isoform X1
facilitated trehalose transporter Tret1 isoform X2
eukaryotic translation initiation factor 3 subunit D
facilitated trehalose transporter Tret1, transcript variant X4
facilitated trehalose transporter Tret1, transcript variant X5
facilitated trehalose transporter Tret1 isoform X3
facilitated trehalose transporter Tret1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
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 LOC123689912 isoform X2
signal recognition particle subunit SRP68
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
abnormal spindle-like microcephaly-associated protein homolog
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 27 samples with support for all annotated introns
GATA-type transcription factor sreA, transcript variant X1
zinc finger transcription factor Trps1 isoform X1
GATA-type transcription factor sreA, transcript variant X2
GATA-type transcription factor sreA isoform X2
carboxypeptidase N subunit 2-like, transcript variant X2
carboxypeptidase N subunit 2-like, transcript variant X1
carboxypeptidase N subunit 2-like isoform X2
carboxypeptidase N subunit 2-like isoform X1
lethal(2) giant larvae protein, transcript variant X2
lethal(2) giant larvae protein, transcript variant X5
lethal(2) giant larvae protein, transcript variant X4
lethal(2) giant larvae protein, transcript variant X1
lethal(2) giant larvae protein, transcript variant X3
lethal(2) giant larvae protein homolog 1 isoform X1
lethal(2) giant larvae protein homolog 1 isoform X2
lethal(2) giant larvae protein isoform X5
lethal(2) giant larvae protein isoform X4
lethal(2) giant larvae protein homolog 1 isoform X3
thrombospondin type-1 domain-containing protein 7A-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
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial-like
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
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, including 4 samples with support for all annotated introns
protein shuttle craft, transcript variant X1
protein shuttle craft, transcript variant X2
uncharacterized protein C1orf194 homolog
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
serine/arginine-rich splicing factor 2, transcript variant X3
serine/arginine-rich splicing factor 2, transcript variant X1
serine/arginine-rich splicing factor 2, transcript variant X2
serine/arginine-rich splicing factor 2 isoform X1
serine/arginine-rich splicing factor 2 isoform X2
U3 small nucleolar RNA-interacting protein 2
ribosome biogenesis regulatory protein homolog
DNA fragmentation factor subunit beta, 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 24 samples with support for all annotated introns
DNA fragmentation factor subunit beta, 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 21 samples with support for all annotated introns
DNA fragmentation factor subunit beta isoform X1
DNA fragmentation factor subunit beta isoform X2
DNA fragmentation factor subunit beta, transcript variant X3
DNA fragmentation factor subunit beta, 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 9 samples with support for all annotated introns
DNA fragmentation factor subunit beta isoform X3
DNA fragmentation factor subunit beta isoform X4
dual specificity mitogen-activated protein kinase kinase 6
transmembrane protein 94, transcript variant X3
transmembrane protein 94, transcript variant X2
transmembrane protein 94, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
WASH complex subunit 1, transcript variant X1
WASH complex subunit 1, transcript variant X2
WD repeat-containing protein 13, transcript variant X2
WD repeat-containing protein 13, 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 24 samples with support for all annotated introns
WD repeat-containing protein 13 isoform X1
WD repeat-containing protein 13 isoform X2
uncharacterized LOC110992513, transcript variant X1
uncharacterized LOC110992513, transcript variant X2
uncharacterized protein LOC110992513 isoform X2
uncharacterized protein LOC110992513 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
26S proteasome non-ATPase regulatory subunit 4
putative ATP synthase subunit f, mitochondrial
mesencephalic astrocyte-derived neurotrophic factor homolog, transcript variant X2
mesencephalic astrocyte-derived neurotrophic factor homolog, transcript variant X1
mesencephalic astrocyte-derived neurotrophic factor homolog
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 30% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat and death domain-containing protein 1-like, transcript variant X3
leucine-rich repeat and death domain-containing protein 1-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 10 samples with support for all annotated introns
leucine-rich repeat and death domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
leucine-rich repeat and death domain-containing protein 1-like isoform X1
leucine-rich repeat and death domain-containing protein 1-like isoform X2
uncharacterized protein LOC110994732 isoform X3
cancer-related nucleoside-triphosphatase homolog
probable enoyl-CoA hydratase, mitochondrial, 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
probable enoyl-CoA hydratase, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
probable enoyl-CoA hydratase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 9% 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 17 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 100% coverage of the annotated genomic feature by RNAseq alignments
UPF0193 protein EVG1 homolog, transcript variant X1
UPF0193 protein EVG1 homolog, transcript variant X2
uncharacterized protein LOC110994743 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
diphthine methyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
diphthine methyltransferase, 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 20 samples with support for all annotated introns
uncharacterized protein CG5098, transcript variant X3
uncharacterized protein CG5098, transcript variant X4
uncharacterized protein CG5098, transcript variant X1
uncharacterized protein CG5098, transcript variant X2
uncharacterized protein CG5098 isoform X2
uncharacterized protein CG5098 isoform X3
uncharacterized protein CG5098 isoform 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 6 samples with support for all annotated introns
transcription factor Adf-1, 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 15 samples with support for all annotated introns
transcription factor Adf-1, 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 14 samples with support for all annotated introns
transcription factor Adf-1, transcript variant X3
transcription factor Adf-1, transcript variant X1
transcription factor Adf-1, transcript variant X2
acylamino-acid-releasing enzyme, transcript variant X2
acylamino-acid-releasing enzyme, transcript variant X1
acylamino-acid-releasing enzyme isoform X1
acylamino-acid-releasing enzyme isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
glucose dehydrogenase [FAD, quinone], transcript variant X2
glucose dehydrogenase [FAD, quinone], transcript variant X1
glucose dehydrogenase [FAD, quinone] isoform X2
glucose dehydrogenase [FAD, quinone] isoform X1
geranylgeranyl transferase type-2 subunit beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
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, including 3 samples with support for all annotated introns
uncharacterized LOC111000930, transcript variant X1
uncharacterized LOC111000930, transcript variant X2
uncharacterized protein LOC111000930 isoform X1
uncharacterized protein LOC111000930 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein subunit gamma-e
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% 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: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, non-muscle, transcript variant X1
myosin heavy chain, non-muscle isoform X1
myosin heavy chain, non-muscle, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
myosin heavy chain, non-muscle isoform X2
probable low-specificity L-threonine aldolase 2, transcript variant X1
probable low-specificity L-threonine aldolase 2, transcript variant X3
probable low-specificity L-threonine aldolase 2, transcript variant X2
probable low-specificity L-threonine aldolase 2
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 106 samples with support for all annotated introns
transmembrane channel-like protein 5, transcript variant X2
transmembrane channel-like protein 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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 2 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 9 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone], transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone] isoform X3
oxidized purine nucleoside triphosphate hydrolase
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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
peptidyl-tRNA hydrolase ICT1, mitochondrial
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 113 samples with support for all annotated introns
clusterin-associated protein 1, transcript variant X1
clusterin-associated protein 1, transcript variant X2
clusterin-associated protein 1 isoform X2
clusterin-associated protein 1 isoform X1
alcohol dehydrogenase [acceptor]-like, transcript variant X1
alcohol dehydrogenase [acceptor]-like, transcript variant X2
uncharacterized LOC111002373, transcript variant X3
uncharacterized LOC111002373, transcript variant X4
uncharacterized LOC111002373, transcript variant X1
uncharacterized LOC111002373, transcript variant X2
uncharacterized LOC111002373, transcript variant X5
uncharacterized protein LOC111002373 isoform X3
uncharacterized protein LOC111002373 isoform X1
uncharacterized protein LOC111002373 isoform X2
uncharacterized protein LOC111002373 isoform X4
beta-1,4-N-acetylgalactosaminyltransferase bre-4-like, transcript variant X2
beta-1,4-N-acetylgalactosaminyltransferase bre-4-like, transcript variant X1
beta-1,4-N-acetylgalactosaminyltransferase bre-4-like, transcript variant X3
beta-1,4-N-acetylgalactosaminyltransferase bre-4-like
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
vacuolar protein sorting-associated protein 41 homolog
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 93 samples with support for all annotated introns
enoyl-CoA hydratase domain-containing protein 2, mitochondrial
NAD-dependent protein deacetylase sirtuin-7
28S ribosomal protein S33, mitochondrial