Pieris rapae chromosome 23, 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\nLR990605.1.\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]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 60% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: histone H1, gonadal-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC110997126, 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 4 samples with support for all annotated introns
uncharacterized LOC110997126, 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 3 samples with support for all annotated introns
division abnormally delayed protein, 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 14 samples with support for all annotated introns
division abnormally delayed protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
division abnormally delayed protein isoform X1
division abnormally delayed protein isoform X2
serine/threonine-protein phosphatase 2A activator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC110997125, 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 3 samples with support for all annotated introns
uncharacterized LOC110997125, 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 15 samples with support for all annotated introns
uncharacterized protein LOC110997125 isoform X2
uncharacterized protein LOC110997125 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ATP-binding cassette sub-family C member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC123690246, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123690246, 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 8 samples with support for all annotated introns
uncharacterized LOC123690246, 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
growth hormone-regulated TBC protein 1-A
mitochondrial import inner membrane translocase subunit TIM14
choline-phosphate cytidylyltransferase B, transcript variant X2
choline-phosphate cytidylyltransferase B, transcript variant X1
choline-phosphate cytidylyltransferase B isoform X1
choline-phosphate cytidylyltransferase B isoform X2
uncharacterized LOC110997855, 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 16 samples with support for all annotated introns
uncharacterized LOC110997855, 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
uncharacterized LOC110997855, 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 19 samples with support for all annotated introns
uncharacterized LOC110997855, 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 4 samples with support for all annotated introns
uncharacterized protein LOC110997855 isoform X2
uncharacterized protein LOC110997855 isoform X1
uncharacterized protein LOC110997855 isoform X3
uncharacterized LOC110997856, transcript variant X1
uncharacterized LOC110997856, transcript variant X2
prostatic acid phosphatase, transcript variant X2
prostatic acid phosphatase, transcript variant X1
venom acid phosphatase Acph-1 isoform 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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51, 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 57 samples with support for all annotated introns
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51, 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 34 samples with support for all annotated introns
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51, 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 23 samples with support for all annotated introns
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51, 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 17 samples with support for all annotated introns
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51, transcript variant X7
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
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51, 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 68 samples with support for all annotated introns
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51 isoform X1
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51 isoform X2
serine/threonine-protein kinase polo, transcript variant X2
serine/threonine-protein kinase polo, transcript variant X1
serine/threonine-protein kinase polo isoform X2
serine/threonine-protein kinase polo isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transient receptor potential cation channel subfamily V member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 81% 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:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 2 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit beta, transcript variant X1
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized protein LOC110993447 isoform X1
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit beta 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 5 samples with support for all annotated introns
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit beta, transcript variant X3
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit beta isoform X3
protein kinase C-binding protein 1, transcript variant X3
protein kinase C-binding protein 1, transcript variant X4
protein kinase C-binding protein 1, transcript variant X1
protein kinase C-binding protein 1, transcript variant X2
protein kinase C-binding protein 1 isoform X2
protein kinase C-binding protein 1 isoform X1
YTH domain-containing family protein 3, transcript variant X1
YTH domain-containing family protein 3, transcript variant X2
YTH domain-containing family protein 3, transcript variant X4
YTH domain-containing family protein 3, transcript variant X5
YTH domain-containing family protein 1 isoform X1
YTH domain-containing family protein 3 isoform X2
YTH domain-containing family protein 1 isoform X4
YTH domain-containing family protein 1 isoform X5
YTH domain-containing family protein 3, transcript variant X3
YTH domain-containing family protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
peptidyl-prolyl cis-trans isomerase NIMA-interacting 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
transmembrane protein 43 homolog, transcript variant X2
transmembrane protein 43 homolog, transcript variant X1
transcription termination factor 5, mitochondrial, transcript variant X1
transcription termination factor 5, mitochondrial, transcript variant X2
transcription termination factor 5, mitochondrial, transcript variant X3
transcription termination factor 5, mitochondrial isoform X1
transcription termination factor 5, mitochondrial isoform X2
transcription termination factor 5, mitochondrial isoform 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 14 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 90% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC111003143, 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 28 samples with support for all annotated introns
uncharacterized LOC111003143, 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 4 samples with support for all annotated introns
uncharacterized LOC111003143, transcript variant X5
uncharacterized LOC111003143, transcript variant X3
uncharacterized LOC111003143, transcript variant X4
uncharacterized protein LOC111003143 isoform X1
uncharacterized protein LOC111003143 isoform X2
zinc finger protein MSN2, 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
zinc finger protein MSN2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine/threonine-protein kinase mig-15, 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 43 samples with support for all annotated introns
serine/threonine-protein kinase mig-15, 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 29 samples with support for all annotated introns
serine/threonine-protein kinase mig-15, 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 18 samples with support for all annotated introns
serine/threonine-protein kinase mig-15, 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 49 samples with support for all annotated introns
serine/threonine-protein kinase mig-15, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
serine/threonine-protein kinase mig-15 isoform X1
serine/threonine-protein kinase mig-15 isoform X3
serine/threonine-protein kinase mig-15 isoform X4
serine/threonine-protein kinase mig-15 isoform X5
serine/threonine-protein kinase mig-15 isoform X2
basic salivary proline-rich protein 2, transcript variant X2
basic salivary proline-rich protein 2, transcript variant X1
basic salivary proline-rich protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
basic salivary proline-rich protein 2 isoform X1
basic salivary proline-rich protein 2 isoform X2
uncharacterized LOC111002303, 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 6 samples with support for all annotated introns
uncharacterized LOC111002303, transcript variant X2
uncharacterized protein LOC111002303 isoform X1
uncharacterized protein LOC111002303 isoform X2
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase hpo-8
potassium voltage-gated channel unc-103, 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 2 samples with support for all annotated introns
potassium voltage-gated channel unc-103, 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 1 sample with support for all annotated introns
potassium voltage-gated channel unc-103 isoform X2
potassium voltage-gated channel unc-103 isoform X1
ATP-binding cassette sub-family C member 4-like
ATP-binding cassette sub-family C member 4, transcript variant X1
ATP-binding cassette sub-family C member 4, transcript variant X2
ATP-binding cassette sub-family C member 4 isoform X1
ATP-binding cassette sub-family C member 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 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: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
DNA replication complex GINS protein SLD5
succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial
transcription termination factor 5, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
pseudouridine-metabolizing bifunctional protein C1861.05
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
microsomal glutathione S-transferase 1-like
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
probable Golgi SNAP receptor complex member 2
multiple C2 and transmembrane domain-containing protein
RE1-silencing transcription factor, transcript variant X1
RE1-silencing transcription factor, transcript variant X2
RE1-silencing transcription factor isoform X1
RE1-silencing transcription factor 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 15 samples with support for all annotated introns
putative ATP-dependent RNA helicase Pl10, transcript variant X1
putative ATP-dependent RNA helicase Pl10, transcript variant X2
putative ATP-dependent RNA helicase Pl10, transcript variant X3
putative ATP-dependent RNA helicase Pl10 isoform X1
putative ATP-dependent RNA helicase Pl10 isoform X2
ATP-dependent RNA helicase DDX3X 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 81 samples with support for all annotated introns
transport and Golgi organization protein 11, transcript variant X1
transport and Golgi organization protein 11, transcript variant X2
transport and Golgi organization protein 11
UDP-glucose:glycoprotein glucosyltransferase, transcript variant X1
UDP-glucose:glycoprotein glucosyltransferase, transcript variant X2
UDP-glucose:glycoprotein glucosyltransferase isoform X1
UDP-glucose:glycoprotein glucosyltransferase 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
transcription initiation factor TFIID subunit 6-like, transcript variant X2
transcription initiation factor TFIID subunit 6-like, transcript variant X1
transcription initiation factor TFIID subunit 6-like isoform X2
transcription initiation factor TFIID subunit 6-like isoform 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 15 samples with support for all annotated introns
extended synaptotagmin-2-B, transcript variant X1
extended synaptotagmin-2-B, transcript variant X2
extended synaptotagmin-2-B, transcript variant X3
NAD(P) transhydrogenase, mitochondrial-like, transcript variant X3
NAD(P) transhydrogenase, mitochondrial-like, transcript variant X1
NAD(P) transhydrogenase, mitochondrial-like, transcript variant X2
NAD(P) transhydrogenase, mitochondrial-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 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized protein LOC123690253 isoform X2
isocitrate dehydrogenase [NADP] cytoplasmic
probable serine incorporator, transcript variant X2
probable serine incorporator, transcript variant X1
probable serine incorporator, transcript variant X3
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial
cyclic nucleotide-gated cation channel alpha-3
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
zinc finger protein Xfin, transcript variant X3
zinc finger protein Xfin, transcript variant X2
transcription initiation factor TFIID subunit 11 isoform X3
uncharacterized protein LOC111000537 isoform X2
zinc finger protein Xfin, 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 62 samples with support for all annotated introns
zinc finger protein Xfin, transcript variant X4
uncharacterized protein LOC111000537 isoform X4
zinc finger protein Xfin, transcript variant X5
uncharacterized protein LOC111000537 isoform X5
zinc finger protein Xfin, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC111000539, transcript variant X1
uncharacterized protein LOC111000539 isoform X1
uncharacterized LOC111000539, transcript variant X2
uncharacterized protein LOC111000539 isoform X2
uncharacterized LOC111000542, 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 10 samples with support for all annotated introns
uncharacterized LOC111000542, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized protein LOC111000542 isoform X1
uncharacterized protein LOC111000542 isoform X2
uncharacterized LOC111000542, 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 15 samples with support for all annotated introns
uncharacterized protein LOC111000542 isoform X3
uncharacterized LOC111000543, transcript variant X1
uncharacterized LOC111000543, transcript variant X2
uncharacterized protein LOC111000543 isoform X1
uncharacterized protein LOC111000543 isoform 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 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, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
diuretic hormone 45, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
diuretic hormone 45, 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
diuretic hormone 45, transcript variant X3
dynein regulatory complex protein 9-like
ATP-binding cassette subfamily C member 4-like, transcript variant X2
ATP-binding cassette subfamily C member 4-like, transcript variant X1
ATP-binding cassette subfamily C member 4-like isoform X2
probable multidrug resistance-associated protein lethal(2)03659 isoform X1
beta-1,3-galactosyltransferase 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
beta-1,3-galactosyltransferase 6, 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 25 samples with support for all annotated introns
beta-1,3-galactosyltransferase 6 isoform X1
beta-1,3-galactosyltransferase 6 isoform X2
UDP-glucuronic acid decarboxylase 1, transcript variant X2
UDP-glucuronic acid decarboxylase 1, transcript variant X1
UDP-glucuronic acid decarboxylase 1 isoform X2
UDP-glucuronic acid decarboxylase 1 isoform X1
glycerophosphodiester phosphodiesterase GDPD6-like
glycerophosphodiester phosphodiesterase GDPD6, transcript variant X2
glycerophosphodiester phosphodiesterase GDPD6, transcript variant X1
glycerophosphodiester phosphodiesterase GDPD6 isoform X2
glycerophosphodiester phosphodiesterase GDPD6 isoform X1
transfer RNA serine (anticodon GCU); 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
glutamate--cysteine ligase catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 52% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
probable ubiquitin carboxyl-terminal hydrolase FAF
tRNA-uridine aminocarboxypropyltransferase 1
F-box-like/WD repeat-containing protein TBL1X
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 95 samples with support for all annotated introns
methionine-R-sulfoxide reductase B1, transcript variant X1
methionine-R-sulfoxide reductase B1, transcript variant X2
methionine-R-sulfoxide reductase B1 isoform X1
methionine-R-sulfoxide reductase B1 isoform X2
serine/threonine-protein kinase Pak, transcript variant X3
serine/threonine-protein kinase Pak, transcript variant X2
serine/threonine-protein kinase Pak, transcript variant X1
serine/threonine-protein kinase Pak isoform X3
serine/threonine-protein kinase Pak isoform X2
serine/threonine-protein kinase Pak isoform X1
GRIP and coiled-coil 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 21 samples with support for all annotated introns
elongation factor 1-alpha, transcript variant X1
elongation factor 1-alpha, transcript variant X2
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1
TAR DNA-binding protein 43-like, transcript variant X1
TAR DNA-binding protein 43-like, transcript variant X2
E3 ubiquitin-protein ligase RNF168, 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
E3 ubiquitin-protein ligase RNF168, transcript variant X1
E3 ubiquitin-protein ligase RNF168 isoform X2
E3 ubiquitin-protein ligase RNF169 isoform X1
E3 ubiquitin-protein ligase hyd, transcript variant X1
E3 ubiquitin-protein ligase hyd, transcript variant X2
E3 ubiquitin-protein ligase hyd, transcript variant X4
E3 ubiquitin-protein ligase hyd, transcript variant X7
E3 ubiquitin-protein ligase hyd, transcript variant X6
E3 ubiquitin-protein ligase hyd, transcript variant X9
E3 ubiquitin-protein ligase hyd, transcript variant X3
E3 ubiquitin-protein ligase hyd, transcript variant X5
E3 ubiquitin-protein ligase hyd, transcript variant X11
E3 ubiquitin-protein ligase hyd, transcript variant X12
E3 ubiquitin-protein ligase hyd, transcript variant X8
E3 ubiquitin-protein ligase hyd, transcript variant X10
E3 ubiquitin-protein ligase hyd isoform X1
E3 ubiquitin-protein ligase hyd isoform X2
E3 ubiquitin-protein ligase hyd isoform X4
E3 ubiquitin-protein ligase hyd isoform X7
E3 ubiquitin-protein ligase hyd isoform X6
E3 ubiquitin-protein ligase hyd isoform X9
E3 ubiquitin-protein ligase hyd isoform X3
E3 ubiquitin-protein ligase hyd isoform X5
E3 ubiquitin-protein ligase hyd isoform X11
E3 ubiquitin-protein ligase hyd isoform X12
E3 ubiquitin-protein ligase hyd isoform X8
E3 ubiquitin-protein ligase hyd isoform X10
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 44% coverage of the annotated genomic feature by RNAseq alignments
GAS2-like protein 3, transcript variant X2
GAS2-like protein 3, transcript variant X3
GAS2-like protein 3, transcript variant X4
GAS2-like protein 3, transcript variant X1
eukaryotic translation initiation factor 2D
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
kinesin-like protein Klp68D, transcript variant X2
kinesin-like protein Klp68D, transcript variant X1
vacuolar protein sorting-associated protein 26C, 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 25 samples with support for all annotated introns
vacuolar protein sorting-associated protein 26C, 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 25 samples with support for all annotated introns
vacuolar protein sorting-associated protein 26C isoform X1
vacuolar protein sorting-associated protein 26C isoform X2
transmembrane protein 131 homolog, 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 2 samples with support for all annotated introns
transmembrane protein 131 homolog, 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 16 samples with support for all annotated introns
transmembrane protein 131 homolog isoform X1
transmembrane protein 131 homolog isoform X2
lutropin-choriogonadotropic hormone receptor, 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 5 samples with support for all annotated introns
lutropin-choriogonadotropic hormone receptor, 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 6 samples with support for all annotated introns
lutropin-choriogonadotropic hormone receptor isoform X2
lutropin-choriogonadotropic hormone receptor isoform X1
Krueppel homolog 2, transcript variant X1
Krueppel homolog 2, transcript variant X2
probable asparagine--tRNA ligase, mitochondrial
pre-mRNA cleavage complex 2 protein Pcf11, transcript variant X2
pre-mRNA cleavage complex 2 protein Pcf11, 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 17 samples with support for all annotated introns
pre-mRNA cleavage complex 2 protein Pcf11 isoform X2
pre-mRNA cleavage complex 2 protein Pcf11 isoform X1
putative oxidoreductase GLYR1 homolog, transcript variant X1
putative oxidoreductase GLYR1 homolog, transcript variant X2
putative oxidoreductase GLYR1 homolog isoform X1
putative oxidoreductase GLYR1 homolog isoform X2
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3, transcript variant X3
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3, transcript variant X2
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3, transcript variant X1
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3, transcript variant X4
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3 isoform X2
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
rho GTPase-activating protein 6, transcript variant X2
rho GTPase-activating protein 6 isoform X2
rho GTPase-activating protein 6, transcript variant X1
uncharacterized protein LOC110998258 isoform X1
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
endoplasmic reticulum-Golgi intermediate compartment protein 2
uncharacterized LOC110998267, transcript variant X1
uncharacterized protein LOC110998267 isoform X1
uncharacterized LOC110998267, transcript variant X3
uncharacterized LOC110998267, transcript variant X2
uncharacterized LOC110998267, transcript variant X4
uncharacterized protein LOC110998267 isoform X2
uncharacterized LOC110998267, transcript variant X5
uncharacterized protein LOC110998267 isoform X3
protein Fe65 homolog, transcript variant X1
protein Fe65 homolog, transcript variant X3
protein Fe65 homolog, transcript variant X2
protein Fe65 homolog, transcript variant X4
protein Fe65 homolog, transcript variant X7
protein Fe65 homolog, transcript variant X5
protein Fe65 homolog, transcript variant X6
protein Fe65 homolog, transcript variant X8
protein Fe65 homolog, transcript variant X9
leucine-rich repeat-containing protein 24
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 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC123690305, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123690305, transcript variant X4
uncharacterized LOC123690305, transcript variant X1
uncharacterized LOC123690305, transcript variant X2
uncharacterized LOC123690305, transcript variant X5