Pieris rapae chromosome 16, 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\nLR990598.1.\nAssembly name: ilPieRapa1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Wellcome Sanger Institute on\n2021/01/28. The original whole-genome shotgun project has the\naccession CAJHWY000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris rapae Annotation Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
glycogen debranching enzyme, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
glycogen debranching enzyme, transcript variant X1
uncharacterized LOC111002320, transcript variant X2
uncharacterized LOC111002320, transcript variant X1
uncharacterized protein LOC111002320 isoform X1
uncharacterized protein LOC111002320 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 2 samples with support for all annotated introns
radial spoke head protein 3 homolog, transcript variant X2
radial spoke head protein 3 homolog, transcript variant X3
radial spoke head protein 3 homolog, transcript variant X1
radial spoke head protein 3 homolog isoform X2
radial spoke head protein 3 homolog B isoform X1
radial spoke head protein 3 homolog isoform X3
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 86% 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: 46 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
MATH and LRR domain-containing protein PFE0570w-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
basic helix-loop-helix neural transcription factor TAP
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
tubulin alpha-8 chain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
tubulin alpha-8 chain, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein ZK1073.1, 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 12 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X5
uncharacterized protein ZK1073.1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein ZK1073.1, 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 10 samples with support for all annotated introns
uncharacterized protein ZK1073.1 isoform X7
uncharacterized protein ZK1073.1 isoform X4
uncharacterized protein ZK1073.1 isoform X3
uncharacterized protein ZK1073.1 isoform X1
uncharacterized protein ZK1073.1 isoform X6
uncharacterized protein ZK1073.1 isoform X5
uncharacterized protein ZK1073.1 isoform X2
uncharacterized protein ZK1073.1 isoform X8
rap1 GTPase-GDP dissociation stimulator 1-B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC110991760, transcript variant X1
uncharacterized LOC110991760, transcript variant X2
uncharacterized protein LOC110991760 isoform X1
uncharacterized protein LOC110991760 isoform X2
uncharacterized LOC110991757, transcript variant X2
uncharacterized protein LOC110991757 isoform X2
uncharacterized LOC110991757, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein LOC110991757 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glutamate receptor-interacting protein 2, 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 8 samples with support for all annotated introns
glutamate receptor-interacting protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glutamate receptor-interacting protein 2 isoform X1
glutamate receptor-interacting protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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 LOC111001211, 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 1 sample with support for all annotated introns
uncharacterized LOC111001211, transcript variant X3
uncharacterized LOC111001211, transcript variant X2
uncharacterized protein LOC111001211 isoform X1
uncharacterized protein LOC111001211 isoform X3
uncharacterized protein LOC111001211 isoform X2
elongation of very long chain fatty acids protein 4
elongation of very long chain fatty acids protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
elongation of very long chain fatty acids protein 7-like
elongation of very long chain fatty acids protein-like, transcript variant X1
elongation of very long chain fatty acids protein-like, transcript variant X2
elongation of very long chain fatty acids protein AAEL008004-like isoform X1
elongation of very long chain fatty acids protein-like isoform X2
nose resistant to fluoxetine protein 6-like
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
elongation of very long chain fatty acids protein AAEL008004-like
inducible metalloproteinase inhibitor protein-like
probable RNA-binding protein 46, transcript variant X1
probable RNA-binding protein 46, transcript variant X2
probable RNA-binding protein 46 isoform X2
probable RNA-binding protein 46 isoform X1
vesicular glutamate transporter 1, transcript variant X2
vesicular glutamate transporter 1, transcript variant X1
vesicular glutamate transporter 1 isoform X2
vesicular glutamate transporter 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cardioacceleratory peptide receptor
cardioacceleratory peptide receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cardioacceleratory peptide receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC110991963, transcript variant X2
uncharacterized LOC110991963, transcript variant X1
uncharacterized protein LOC110991963 isoform X1
uncharacterized protein LOC110991963 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 3 samples with support for all annotated introns
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
uncharacterized LOC110991972, transcript variant X2
uncharacterized LOC110991972, 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 2 samples with support for all annotated introns
uncharacterized protein LOC110991972 isoform X2
uncharacterized protein LOC110991972 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 2 homolog, transcript variant X1
activating signal cointegrator 1 complex subunit 2 homolog, transcript variant X2
activating signal cointegrator 1 complex subunit 2 homolog 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 11 samples with support for all annotated introns
uncharacterized LOC110991946, transcript variant X2
uncharacterized LOC110991946, transcript variant X1
uncharacterized protein LOC110991946 isoform X1
uncharacterized protein LOC110991946 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 110 samples with support for all annotated introns
antichymotrypsin-2, 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 4 samples with support for all annotated introns
antichymotrypsin-2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 117 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
MAP kinase-interacting serine/threonine-protein kinase 1
E3 ubiquitin-protein ligase Hakai, transcript variant X2
E3 ubiquitin-protein ligase Hakai, transcript variant X1
E3 ubiquitin-protein ligase Hakai isoform X1
E3 ubiquitin-protein ligase Hakai isoform X2
NAD(P)H-hydrate epimerase, transcript variant X2
NAD(P)H-hydrate epimerase, transcript variant X4
NAD(P)H-hydrate epimerase, transcript variant X1
NAD(P)H-hydrate epimerase, transcript variant X3
protein tramtrack, beta isoform, 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 1 sample with support for all annotated introns
protein tramtrack, beta isoform, transcript variant X1
protein tramtrack, beta isoform, 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 18 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 14 isoform X1
zinc finger and BTB domain-containing protein 14 isoform X2
protein tramtrack, beta isoform isoform X3
zinc finger and BTB domain-containing protein 17, transcript variant X7
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
zinc finger and BTB domain-containing protein 17, transcript variant X9
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
zinc finger and BTB domain-containing protein 17, 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 10 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 17, transcript variant X2
zinc finger and BTB domain-containing protein 17, transcript variant X5
zinc finger and BTB domain-containing protein 17, transcript variant X3
zinc finger and BTB domain-containing protein 17, transcript variant X4
zinc finger and BTB domain-containing protein 17, transcript variant X6
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
zinc finger and BTB domain-containing protein 17, transcript variant X8
zinc finger and BTB domain-containing protein 17 isoform X5
zinc finger and BTB domain-containing protein 14 isoform X4
zinc finger and BTB domain-containing protein 17 isoform X2
zinc finger and BTB domain-containing protein 17 isoform X3
zinc finger and BTB domain-containing protein 17 isoform X1
zinc finger and BTB domain-containing protein 17 isoform X6
zinc finger and BTB domain-containing protein 17 isoform X7
zinc finger and BTB domain-containing protein 17 isoform X8
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
leucine-rich repeat-containing protein 74A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
kinesin-like protein KIF18A, 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 9 samples with support for all annotated introns
kinesin-like protein KIF18A, 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins
signal recognition particle subunit SRP72
probable rRNA-processing protein EBP2 homolog
uncharacterized LOC111003219, transcript variant X2
uncharacterized LOC111003219, transcript variant X1
uncharacterized LOC111003219, transcript variant X3
uncharacterized protein LOC111003219 isoform X1
uncharacterized protein LOC111003219 isoform X2
transcription factor cwo, transcript variant X2
transcription factor cwo, transcript variant X1
transcription factor cwo, transcript variant X3
uncharacterized LOC111003142, transcript variant X4
uncharacterized LOC111003142, transcript variant X2
uncharacterized LOC111003142, transcript variant X1
uncharacterized LOC111003142, transcript variant X3
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC110998393, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC110998393, transcript variant X2
uncharacterized LOC110998393, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC110998393, 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 5 samples with support for all annotated introns
uncharacterized protein LOC110998393 isoform X2
uncharacterized protein LOC110998393 isoform X1
elongation of very long chain fatty acids protein 7, transcript variant X2
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 4 samples with support for all annotated introns
elongation of very long chain fatty acids protein 7, transcript variant X6
elongation of very long chain fatty acids protein 7, transcript variant X4
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 5 samples with support for all annotated introns
elongation of very long chain fatty acids protein 7, transcript variant X5
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 3 samples with support for all annotated introns
elongation of very long chain fatty acids protein 7, transcript variant X3
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 14 samples with support for all annotated introns
elongation of very long chain fatty acids protein 7, transcript variant X1
elongation of very long chain fatty acids protein 7
elongation of very long chain fatty acids protein 5-like, transcript variant X2
elongation of very long chain fatty acids protein 5-like, transcript variant X1
elongation of very long chain fatty acids protein 7-like isoform X2
elongation of very long chain fatty acids protein 5-like isoform X1
LMBR1 domain-containing protein 2 homolog, transcript variant X1
LMBR1 domain-containing protein 2 homolog, transcript variant X2
LMBR1 domain-containing protein 2 homolog isoform X1
LMBR1 domain-containing protein 2 homolog isoform X2
proteasome-associated protein ECM29 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
E3 ubiquitin-protein ligase NRDP1, transcript variant X1
E3 ubiquitin-protein ligase NRDP1, transcript variant X2
E3 ubiquitin-protein ligase NRDP1 isoform X2
E3 ubiquitin-protein ligase NRDP1 isoform X1
cyclin-G-associated kinase, 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 18 samples with support for all annotated introns
cyclin-G-associated kinase, transcript variant X1
uncharacterized LOC123689862, 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
uncharacterized LOC123689862, 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 16 samples with support for all annotated introns
uncharacterized protein LOC123689862 isoform X2
uncharacterized protein LOC123689862 isoform X1
homeobox protein unc-4-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 6 samples with support for all annotated introns
homeobox protein unc-4-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 10 samples with support for all annotated introns
homeobox protein unc-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC110998394, 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 19 samples with support for all annotated introns
uncharacterized LOC110998394, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
uncharacterized protein LOC110998394 isoform X1
uncharacterized protein LOC110998394 isoform X2
zinc-type alcohol dehydrogenase-like protein SERP1785
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
breast cancer anti-estrogen resistance protein 1, transcript variant X2
breast cancer anti-estrogen resistance protein 1 isoform X2
breast cancer anti-estrogen resistance protein 1, transcript variant X3
breast cancer anti-estrogen resistance protein 1 isoform X3
breast cancer anti-estrogen resistance protein 1, transcript variant X4
breast cancer anti-estrogen resistance protein 1, transcript variant X1
breast cancer anti-estrogen resistance protein 1 isoform X1
breast cancer anti-estrogen resistance protein 1 isoform X4
uncharacterized LOC110998101, transcript variant X1
uncharacterized LOC110998101, transcript variant X2
uncharacterized LOC110998101, transcript variant X3
N-alpha-acetyltransferase 11, transcript variant X1
N-alpha-acetyltransferase 11, transcript variant X3
N-alpha-acetyltransferase 11, transcript variant X2
uncharacterized LOC110998069, transcript variant X2
uncharacterized LOC110998069, 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
dual specificity protein phosphatase 22, 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 6 samples with support for all annotated introns
dual specificity protein phosphatase 22, 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 6 samples with support for all annotated introns
dual specificity protein phosphatase 22 isoform X2
dual specificity protein phosphatase 22 isoform X1
transmembrane protein 184B, transcript variant X1
transmembrane protein 184B, transcript variant X2
transmembrane protein 184B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC110998063, 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 2 samples with support for all annotated introns
uncharacterized LOC110998063, transcript variant X2
uncharacterized protein LOC110998063 isoform X1
uncharacterized protein LOC110998063 isoform X2
sodium/hydrogen exchanger 3, transcript variant X3
sodium/hydrogen exchanger 3, transcript variant X1
sodium/hydrogen exchanger 3, transcript variant X8
sodium/hydrogen exchanger 3, transcript variant X6
sodium/hydrogen exchanger 3, transcript variant X5
sodium/hydrogen exchanger 3, transcript variant X7
sodium/hydrogen exchanger 3, transcript variant X9
sodium/hydrogen exchanger 3, transcript variant X2
sodium/hydrogen exchanger 3, 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
protein phosphatase 1 regulatory subunit 16A, transcript variant X1
protein phosphatase 1 regulatory subunit 16A, transcript variant X2
protein phosphatase 1 regulatory subunit 16A isoform X1
protein phosphatase 1 regulatory subunit 16A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 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 17 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X2
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X1
chitooligosaccharidolytic beta-N-acetylglucosaminidase
MAPK regulated corepressor interacting protein 2, transcript variant X1
MAPK regulated corepressor interacting protein 2, transcript variant X2
MAPK regulated corepressor interacting protein 2 isoform X1
MAPK regulated corepressor interacting protein 2 isoform X2
2-oxoglutarate and iron-dependent oxygenase JMJD4
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 66 samples with support for all annotated introns
mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase
repressor of RNA polymerase III transcription MAF1 homolog
ATP synthase mitochondrial F1 complex assembly factor 2
uncharacterized LOC110998073, transcript variant X2
uncharacterized LOC110998073, transcript variant X1
uncharacterized LOC110998073, transcript variant X3
growth hormone-inducible transmembrane protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 58% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase lubel, transcript variant X2
E3 ubiquitin-protein ligase lubel, transcript variant X1
E3 ubiquitin-protein ligase lubel, transcript variant X3
E3 ubiquitin-protein ligase lubel, transcript variant X4
E3 ubiquitin-protein ligase lubel isoform X1
E3 ubiquitin-protein ligase lubel isoform X3
E3 ubiquitin-protein ligase lubel isoform 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 62 samples with support for all annotated introns
small nuclear ribonucleoprotein-associated protein B
TBC1 domain family member 25, 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 20 samples with support for all annotated introns
uncharacterized protein LOC110998057 isoform X1
TBC1 domain family member 25, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
general transcription factor IIF subunit 2, transcript variant X3
general transcription factor IIF subunit 2, transcript variant X2
general transcription factor IIF subunit 2, transcript variant X1
general transcription factor IIF subunit 2
transport and Golgi organization protein 6
ubiquitin-conjugating enzyme E2Q-like protein 1, transcript variant X1
ubiquitin-conjugating enzyme E2Q-like protein 1, transcript variant X2
ubiquitin-conjugating enzyme E2Q-like protein 1
solute carrier family 66 member 2, transcript variant X1
solute carrier family 66 member 2, transcript variant X2
solute carrier family 66 member 2, transcript variant X3
solute carrier family 66 member 2 isoform X3
solute carrier family 66 member 2 isoform X2
solute carrier family 66 member 2 isoform X1
solute carrier family 66 member 2, transcript variant X4
solute carrier family 66 member 2, 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
solute carrier family 66 member 2 isoform X5
solute carrier family 66 member 2 isoform X4
mitochondrial import inner membrane translocase subunit Tim21
transmembrane protein 231, transcript variant X1
transmembrane protein 231, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
hemocyte protein-glutamine gamma-glutamyltransferase-like
T-box transcription factor TBX20-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
T-box transcription factor TBX20-like, 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 9 samples with support for all annotated introns
T-box transcription factor TBX20-like isoform X2
T-box transcription factor TBX20-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 5 samples with support for all annotated introns
NADH-ubiquinone oxidoreductase 49 kDa subunit-like
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
large neutral amino acids transporter small subunit 2
39S ribosomal protein L10, mitochondrial
large neutral amino acids transporter small subunit 1
uncharacterized LOC111000355, transcript variant X3
uncharacterized LOC111000355, transcript variant X1
uncharacterized LOC111000355, transcript variant X2
tyrosine aminotransferase, transcript variant X2
tyrosine aminotransferase, transcript variant X1
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6, transcript variant X2
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6, transcript variant X1
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 isoform X1
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 isoform X2
platelet-activating factor acetylhydrolase IB subunit beta homolog
lysine--tRNA ligase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
lysine--tRNA ligase, 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 51 samples with support for all annotated introns
uncharacterized LOC111000340, 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 19 samples with support for all annotated introns
uncharacterized LOC111000340, transcript variant X1
uncharacterized protein LOC111000340 isoform X2
uncharacterized protein LOC111000340 isoform X1
uncharacterized LOC110999663, transcript variant X1
uncharacterized LOC110999663, transcript variant X2
eukaryotic initiation factor 4A, transcript variant X1
eukaryotic initiation factor 4A, transcript variant X3
eukaryotic initiation factor 4A, transcript variant X2
eukaryotic initiation factor 4A, transcript variant X4
uncharacterized LOC110999672, transcript variant X1
uncharacterized LOC110999672, transcript variant X2
uncharacterized LOC110999672, transcript variant X4
uncharacterized LOC110999672, transcript variant X5
uncharacterized LOC110999672, transcript variant X3
uncharacterized protein LOC110999672 isoform X1
uncharacterized protein LOC110999672 isoform X2
uncharacterized protein LOC110999672 isoform X3
activating signal cointegrator 1 complex subunit 1
schwannomin-interacting protein 1, transcript variant X2
schwannomin-interacting protein 1, transcript variant X1
schwannomin-interacting protein 1, transcript variant X3
schwannomin-interacting protein 1 homolog isoform X1
schwannomin-interacting protein 1 homolog isoform X2
schwannomin-interacting protein 1, transcript variant X4
schwannomin-interacting protein 1 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CDK5 and ABL1 enzyme substrate 2, transcript variant X2
CDK5 and ABL1 enzyme substrate 2, transcript variant X3
CDK5 and ABL1 enzyme substrate 2, transcript variant X1
CDK5 and ABL1 enzyme substrate 2 isoform X2
CDK5 and ABL1 enzyme substrate 2 isoform X3
CDK5 and ABL1 enzyme substrate 2 isoform X1
WW domain-containing oxidoreductase-like
pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16
succinate dehydrogenase assembly factor 4, mitochondrial
conserved oligomeric Golgi complex subunit 6
39S ribosomal protein L15, mitochondrial
adenosylhomocysteinase, transcript variant X1
adenosylhomocysteinase, transcript variant X3
adenosylhomocysteinase, transcript variant X2
importin subunit beta-1, transcript variant X2
importin subunit beta-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 1
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
uncharacterized protein LOC110999640 isoform X2
probable palmitoyltransferase ZDHHC24, transcript variant X1
probable palmitoyltransferase ZDHHC24, transcript variant X2
probable palmitoyltransferase ZDHHC24 isoform X1
probable palmitoyltransferase ZDHHC24 isoform X2
trifunctional enzyme subunit alpha, mitochondrial
aromatic-L-amino-acid decarboxylase, transcript variant X1
aromatic-L-amino-acid decarboxylase isoform X1
aromatic-L-amino-acid decarboxylase, transcript variant X2
aromatic-L-amino-acid decarboxylase isoform X2
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-like, transcript variant X1
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-like isoform X1
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-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
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-like isoform X2
uncharacterized LOC110999665, transcript variant X1
uncharacterized LOC110999665, transcript variant X2
uncharacterized protein LOC110999665 isoform X1
uncharacterized protein LOC110999665 isoform X2
vacuolar protein sorting-associated protein 52 homolog
5'-AMP-activated protein kinase subunit gamma-2, transcript variant X2
5'-AMP-activated protein kinase subunit gamma-2, transcript variant X1
5'-AMP-activated protein kinase subunit gamma-2, transcript variant X4
5'-AMP-activated protein kinase subunit gamma-2, transcript variant X3
5'-AMP-activated protein kinase subunit gamma-2
chitin synthase chs-2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
chitin synthase chs-2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
suppressor APC domain-containing protein 2
28S ribosomal protein S18b, mitochondrial
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 7 samples with support for all annotated introns
U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 2
transcription termination factor, mitochondrial, transcript variant X1
transcription termination factor, mitochondrial, transcript variant X2
transcription termination factor, mitochondrial isoform X1
transcription termination factor, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
dnaJ homolog subfamily C member 7, transcript variant X1
dnaJ homolog subfamily C member 7, transcript variant X2
dnaJ homolog subfamily C member 7 isoform X1
dnaJ homolog subfamily C member 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 25
uncharacterized LOC111002239, transcript variant X1
uncharacterized LOC111002239, transcript variant X2
uncharacterized protein LOC111002239 isoform X1
uncharacterized protein LOC111002239 isoform X2
uncharacterized LOC111002239, transcript variant X3
uncharacterized protein LOC111002239 isoform X3
cAMP-dependent protein kinase catalytic subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 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 21 samples with support for all annotated introns
triple functional domain protein, transcript variant X2
triple functional domain protein, transcript variant X1
triple functional domain protein isoform X1
triple functional domain protein isoform X2
protein muscleblind, transcript variant X3
protein muscleblind, transcript variant X2
protein muscleblind, transcript variant X1
protein muscleblind, transcript variant X6
protein muscleblind, transcript variant X5
protein muscleblind, transcript variant X8
protein muscleblind, transcript variant X7
protein muscleblind, transcript variant X11
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 18 samples with support for all annotated introns
protein muscleblind, transcript variant X10
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 28 samples with support for all annotated introns
protein muscleblind, transcript variant X12
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 29 samples with support for all annotated introns
protein muscleblind, transcript variant X4
protein muscleblind, transcript variant X9
ras-associated and pleckstrin homology domains-containing protein 1 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-prolyl cis-trans isomerase, rhodopsin-specific isozyme
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 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
enhancer of yellow 2 transcription factor-like
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 116 samples with support for all annotated introns
multiple epidermal growth factor-like domains protein 8
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 13 samples with support for all annotated introns
neural retina-specific leucine zipper protein-like
diacylglycerol O-acyltransferase 1, 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 26 samples with support for all annotated introns
diacylglycerol O-acyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
diacylglycerol O-acyltransferase 1, 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 100 samples with support for all annotated introns
diacylglycerol O-acyltransferase 1 isoform X2
diacylglycerol O-acyltransferase 1 isoform X1
mediator of RNA polymerase II transcription subunit 11
COORDINATES: nucleotide motif:Rfam:12.0:RF01174
nuclear fragile X mental retardation-interacting protein 1
RNA 5'-monophosphate methyltransferase, 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
RNA 5'-monophosphate methyltransferase isoform X2
RNA 5'-monophosphate methyltransferase, 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 8 samples with support for all annotated introns
RNA 5'-monophosphate methyltransferase isoform X1
chromatin complexes subunit BAP18, 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 75 samples with support for all annotated introns
chromatin complexes subunit BAP18, 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 80 samples with support for all annotated introns
uncharacterized protein LOC110991416 isoform X1
chromatin complexes subunit BAP18 isoform X2
sal-like protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
sal-like protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sal-like protein 3, transcript variant X3
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 8 samples with support for all annotated introns
sal-like protein 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sal-like protein 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 6, transcript variant X1
26S proteasome non-ATPase regulatory subunit 6, transcript variant X2
26S proteasome non-ATPase regulatory subunit 6
geranylgeranyl transferase type-2 subunit alpha, 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 30 samples with support for all annotated introns
geranylgeranyl transferase type-2 subunit alpha, 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 16 samples with support for all annotated introns
geranylgeranyl transferase type-2 subunit alpha isoform X1
geranylgeranyl transferase type-2 subunit alpha isoform X2
broad-complex core protein isoforms 1/2/3/4/5
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leucine-rich repeat extensin-like protein 5
probable 26S proteasome non-ATPase regulatory subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein phosphatase PHLPP-like protein, transcript variant X1
protein phosphatase PHLPP-like protein isoform X1
protein phosphatase PHLPP-like protein, transcript variant X2
protein phosphatase PHLPP-like protein isoform X2
protein phosphatase PHLPP-like protein, transcript variant X3
protein phosphatase PHLPP-like protein isoform X3
LIM/homeobox protein Lhx3, 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 4 samples with support for all annotated introns
LIM/homeobox protein Lhx3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LIM/homeobox protein Lhx3, transcript variant X3
LIM/homeobox protein Lhx3, transcript variant X4
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
LIM/homeobox protein Lhx3, transcript variant X5
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
LIM/homeobox protein Lhx3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aromatic-L-amino-acid decarboxylase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
cysteine desulfurase, mitochondrial, 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 60 samples with support for all annotated introns
cysteine desulfurase, mitochondrial, transcript variant X2
cysteine desulfurase, mitochondrial isoform X1
cysteine desulfurase, mitochondrial isoform X2
transmembrane protein 268, transcript variant X2
transmembrane protein 268, 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 23 samples with support for all annotated introns
uncharacterized protein LOC110999104 isoform X1
glycerophosphocholine phosphodiesterase GPCPD1, transcript variant X2
glycerophosphocholine phosphodiesterase GPCPD1, transcript variant X1
glycerophosphocholine phosphodiesterase GPCPD1, transcript variant X3
glycerophosphocholine phosphodiesterase GPCPD1 isoform X1
glycerophosphocholine phosphodiesterase GPCPD1 isoform X2
glycerophosphocholine phosphodiesterase GPCPD1 isoform X3
serine/threonine-protein phosphatase 1 regulatory subunit 10
FAD-dependent oxidoreductase domain-containing protein 1, 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 7 samples with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 1
sodium/hydrogen exchanger 9B2, transcript variant X2
sodium/hydrogen exchanger 9B2, transcript variant X4
sodium/hydrogen exchanger 9B2, transcript variant X1
sodium/hydrogen exchanger 9B2, 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 2 samples with support for all annotated introns
sodium/hydrogen exchanger 9B2 isoform X1
sodium/hydrogen exchanger 9B2 isoform X2
sodium/hydrogen exchanger 9B2 isoform X3
sodium/hydrogen exchanger 9B1, transcript variant X1
sodium/hydrogen exchanger 9B1 isoform X1
sodium/hydrogen exchanger 9B1, transcript variant X2
sodium/hydrogen exchanger 9B1 isoform X2
sodium/hydrogen exchanger 9B2, transcript variant X5
sodium/hydrogen exchanger 9B2, transcript variant X6
sodium/hydrogen exchanger 9B2 isoform X4
G-protein coupled receptor Mth2, transcript variant X1
G-protein coupled receptor Mth2, transcript variant X2
G-protein coupled receptor Mth2 isoform X2
G-protein coupled receptor Mth2 isoform X1
uncharacterized LOC110995849, transcript variant X1
uncharacterized LOC110995849, transcript variant X2
uncharacterized protein LOC110995849 isoform X1
uncharacterized protein LOC110995849 isoform X2
uncharacterized LOC110995848, transcript variant X2
uncharacterized LOC110995848, transcript variant X1
protein transport protein Sec61 subunit beta
anaphase-promoting complex subunit 5, transcript variant X1
anaphase-promoting complex subunit 5 isoform X1
anaphase-promoting complex subunit 5, transcript variant X2
anaphase-promoting complex subunit 5 isoform X2
adenylate cyclase type 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
adenylate cyclase type 3, 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 2 samples with support for all annotated introns
chitin deacetylase 1, transcript variant X2
chitin deacetylase 1, transcript variant X1
kinesin-associated protein 3, transcript variant X2
kinesin-associated protein 3, transcript variant X1
E3 ubiquitin-protein ligase Su(dx), transcript variant X2
E3 ubiquitin-protein ligase Su(dx), transcript variant X1
alanine--tRNA ligase, cytoplasmic, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 384 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 101 samples with support for all annotated introns
alanine--tRNA ligase, cytoplasmic, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 384 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
alanine--tRNA ligase, cytoplasmic isoform X1
alanine--tRNA ligase, cytoplasmic isoform X2
transcription termination factor 3, mitochondrial
endoplasmic reticulum-Golgi intermediate compartment protein 3
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 116 samples with support for all annotated introns
carnitine O-acetyltransferase, transcript variant X3
carnitine O-acetyltransferase, transcript variant X2
carnitine O-acetyltransferase, transcript variant X1
carnitine O-acetyltransferase isoform X1
carnitine O-acetyltransferase isoform X2
UPF0184 protein AAEL002161, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
UPF0184 protein AAEL002161, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
UPF0184 protein AAEL002161, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
UPF0184 protein AAEL002161, 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 109 samples with support for all annotated introns
probable NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial
chromodomain-helicase-DNA-binding protein 7, transcript variant X2
chromodomain-helicase-DNA-binding protein 7, transcript variant X1
chromodomain-helicase-DNA-binding protein 7 isoform X2
chromodomain-helicase-DNA-binding protein 7 isoform X1
phosphatidylserine synthase, transcript variant X1
phosphatidylserine synthase, transcript variant X2
uncharacterized LOC110998671, 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 9 samples with support for all annotated introns
uncharacterized LOC110998671, transcript variant X2
N-terminal Xaa-Pro-Lys N-methyltransferase 1-A
GDP-fucose protein O-fucosyltransferase 1
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 75 samples with support for all annotated introns
WD repeat-containing protein 55 homolog, transcript variant X2
WD repeat-containing protein 55 homolog, transcript variant X3
WD repeat-containing protein 55 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
actin-related protein 2/3 complex subunit 5-B
programmed cell death protein 10, 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 84 samples with support for all annotated introns
programmed cell death protein 10, 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 115 samples with support for all annotated introns
programmed cell death protein 10, 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 35 samples with support for all annotated introns
programmed cell death protein 10, transcript variant X4
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
transfer RNA isoleucine (anticodon UAU); 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
EGF domain-specific O-linked N-acetylglucosamine transferase, transcript variant X1
EGF domain-specific O-linked N-acetylglucosamine transferase, transcript variant X2
EGF domain-specific O-linked N-acetylglucosamine transferase isoform X1
EGF domain-specific O-linked N-acetylglucosamine transferase isoform X2
EGF domain-specific O-linked N-acetylglucosamine transferase, transcript variant X3
EGF domain-specific O-linked N-acetylglucosamine transferase isoform X3
transcription factor Dp-1, transcript variant X3
transcription factor Dp-1, transcript variant X1
transcription factor Dp-1, transcript variant X2
transcription factor Dp-1, transcript variant X4
transcription factor Dp-1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 92 samples with support for all annotated introns
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like
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 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
katanin p80 WD40 repeat-containing subunit B1, transcript variant X1
katanin p80 WD40 repeat-containing subunit B1, transcript variant X3
katanin p80 WD40 repeat-containing subunit B1, transcript variant X2
katanin p80 WD40 repeat-containing subunit B1 isoform X1
katanin p80 WD40 repeat-containing subunit B1 isoform X3
katanin p80 WD40 repeat-containing subunit B1 isoform X2
uncharacterized LOC111004272, transcript variant X3
uncharacterized LOC111004272, transcript variant X2
uncharacterized LOC111004272, transcript variant X1
uncharacterized protein LOC111004272 isoform X2
uncharacterized protein LOC111004272 isoform X1
uncharacterized protein LOC111004272 isoform X3
sodium leak channel non-selective protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium leak channel non-selective protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium leak channel non-selective protein, transcript variant X1
sodium leak channel non-selective protein, transcript variant X3
sodium leak channel non-selective protein isoform X2
sodium leak channel non-selective protein isoform X1
thioredoxin reductase-like selenoprotein T homolog CG3887
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 29 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
B9 domain-containing protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
B9 domain-containing protein 2 isoform X4
B9 domain-containing protein 2, 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 7 samples with support for all annotated introns
B9 domain-containing protein 2, transcript variant X2
B9 domain-containing protein 2, transcript variant X3
uncharacterized protein LOC110999839 isoform X3
anti-apoptotic protein NR13, transcript variant X2
anti-apoptotic protein NR13, transcript variant X1
bcl-2-related ovarian killer protein homolog A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
ankyrin repeat domain-containing protein 39
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 115 samples with support for all annotated introns
rho guanine nucleotide exchange factor 7, transcript variant X1
rho guanine nucleotide exchange factor 7, 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 6 samples with support for all annotated introns
rho guanine nucleotide exchange factor 7, transcript variant X4
rho guanine nucleotide exchange factor 7, transcript variant X5
rho guanine nucleotide exchange factor 7, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
rho guanine nucleotide exchange factor 7, transcript variant X3
rho guanine nucleotide exchange factor 7 isoform X2
rho guanine nucleotide exchange factor 7 isoform X3
uncharacterized protein LOC110997278 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
transcription initiation factor TFIID subunit 5
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
uncharacterized LOC110997282, transcript variant X6
uncharacterized LOC110997282, transcript variant X8
uncharacterized LOC110997282, transcript variant X7
uncharacterized protein LOC110997282 isoform X6
uncharacterized protein LOC110997282 isoform X7
uncharacterized LOC110997282, transcript variant X1
uncharacterized LOC110997282, transcript variant X3
uncharacterized LOC110997282, transcript variant X2
uncharacterized LOC110997282, transcript variant X9
uncharacterized LOC110997282, transcript variant X5
uncharacterized LOC110997282, transcript variant X4
uncharacterized protein LOC110997282 isoform X1
uncharacterized protein LOC110997282 isoform X3
uncharacterized protein LOC110997282 isoform X2
uncharacterized protein LOC110997282 isoform X5
uncharacterized protein LOC110997282 isoform X4
uncharacterized protein LOC110997282 isoform X8
stromal interaction molecule homolog, transcript variant X1
stromal interaction molecule homolog, transcript variant X2
stromal interaction molecule homolog isoform X1
stromal interaction molecule homolog isoform X2
nucleosome assembly protein 1-like 1, transcript variant X1
nucleosome assembly protein 1-like 1 isoform X1
nucleosome assembly protein 1-like 1, transcript variant X2
nucleosome assembly protein 1-like 1 isoform X2
RNA polymerase II-associated factor 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% 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 14% coverage of the annotated genomic feature by RNAseq alignments
carbonic anhydrase-related protein 10, transcript variant X3
carbonic anhydrase-related protein 10, transcript variant X4
carbonic anhydrase-related protein 10, transcript variant X1
carbonic anhydrase-related protein 10, transcript variant X2
carbonic anhydrase-related protein 10 isoform X2
carbonic anhydrase-related protein 10 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 77% 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
alpha-(1,3)-fucosyltransferase C, transcript variant X4
alpha-(1,3)-fucosyltransferase C, transcript variant X2
alpha-(1,3)-fucosyltransferase C, transcript variant X5
alpha-(1,3)-fucosyltransferase C, transcript variant X7
alpha-(1,3)-fucosyltransferase C, transcript variant X6
alpha-(1,3)-fucosyltransferase C, transcript variant X3
alpha-(1,3)-fucosyltransferase C, transcript variant X1
alpha-(1,3)-fucosyltransferase C isoform X4
alpha-(1,3)-fucosyltransferase C isoform X3
alpha-(1,3)-fucosyltransferase C isoform X2
alpha-(1,3)-fucosyltransferase C isoform X1
glucose dehydrogenase [FAD, quinone]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
N-alpha-acetyltransferase 15, NatA auxiliary subunit, transcript variant X2
N-alpha-acetyltransferase 15, NatA auxiliary subunit, transcript variant X1
N-alpha-acetyltransferase 15, NatA auxiliary subunit
nuclear transcription factor Y subunit alpha, transcript variant X2
nuclear transcription factor Y subunit alpha, transcript variant X1
nuclear transcription factor Y subunit alpha, 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 31 samples with support for all annotated introns
nuclear transcription factor Y subunit alpha isoform X1
nuclear transcription factor Y subunit alpha isoform X2
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
homeodomain-interacting protein kinase 2, transcript variant X1
homeodomain-interacting protein kinase 2, transcript variant X3
homeodomain-interacting protein kinase 2, transcript variant X5
homeodomain-interacting protein kinase 2, transcript variant X4
homeodomain-interacting protein kinase 2, transcript variant X2
homeodomain-interacting protein kinase 2 isoform X1
homeodomain-interacting protein kinase 2 isoform X2
uncharacterized protein LOC110994037 isoform X4
homeodomain-interacting protein kinase 2 isoform X3
cyclin-dependent kinase inhibitor 1, transcript variant X2
cyclin-dependent kinase inhibitor 1, transcript variant X1
cyclin-dependent kinase inhibitor 1 isoform X1
cyclin-dependent kinase inhibitor 1 isoform X2
ras association domain-containing protein 10, transcript variant X1
ras association domain-containing protein 10, transcript variant X2
ras association domain-containing protein 10, transcript variant X3
ras association domain-containing protein 10
proteasome subunit alpha type-1, transcript variant X2
proteasome subunit alpha type-1, transcript variant X1
proteasome subunit alpha type-1 isoform X2
proteasome subunit alpha type-1 isoform X1
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transient receptor potential protein, transcript variant X2
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 3 samples with support for all annotated introns
transient receptor potential protein, transcript variant X1
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 1 sample with support for all annotated introns
transient receptor potential protein, transcript variant X3
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 1 sample with support for all annotated introns
transient receptor potential protein isoform X1
transient receptor potential protein isoform X3
transient receptor potential protein isoform X2
transient-receptor-potential-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transient-receptor-potential-like protein, transcript variant X2
transient-receptor-potential-like protein isoform X1
transient-receptor-potential-like protein isoform 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
probable protein phosphatase 2C T23F11.1, 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 5 samples with support for all annotated introns
probable protein phosphatase 2C T23F11.1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
probable protein phosphatase 2C T23F11.1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
probable protein phosphatase 2C T23F11.1 isoform X1
probable protein phosphatase 2C T23F11.1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable protein phosphatase 2C T23F11.1 isoform X2
probable protein phosphatase 2C T23F11.1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
probable protein phosphatase 2C T23F11.1 isoform X3
galactose mutarotase, transcript variant X3
galactose mutarotase, transcript variant X1
galactose mutarotase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1, transcript variant X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1, transcript variant X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1, transcript variant X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X2
uncharacterized LOC110993110, transcript variant X1
uncharacterized LOC110993110, transcript variant X2
UHRF1-binding protein 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
UHRF1-binding protein 1-like, transcript variant X1
UHRF1-binding protein 1-like, transcript variant X3
UHRF1-binding protein 1-like, transcript variant X4
UHRF1-binding protein 1-like, transcript variant X2
protein kinase C and casein kinase substrate in neurons protein 1, transcript variant X2
protein kinase C and casein kinase substrate in neurons protein 1, transcript variant X3
protein kinase C and casein kinase substrate in neurons protein 1, transcript variant X1
protein kinase C and casein kinase substrate in neurons protein 1 isoform X1
protein kinase C and casein kinase substrate in neurons protein 1 isoform X3
protein kinase C and casein kinase substrate in neurons protein 1 isoform X2
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
myotubularin-related protein 13, transcript variant X2
myotubularin-related protein 13, 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 18 samples with support for all annotated introns
myotubularin-related protein 13 isoform X2
myotubularin-related protein 13 isoform X1
uncharacterized LOC123689858, transcript variant X1
uncharacterized LOC123689858, transcript variant X2
uncharacterized protein LOC123689858 isoform X1
uncharacterized protein LOC123689858 isoform X2
E3 ubiquitin-protein ligase UBR1, transcript variant X2
E3 ubiquitin-protein ligase UBR1, transcript variant X1
E3 ubiquitin-protein ligase UBR1 isoform X2
E3 ubiquitin-protein ligase UBR1 isoform X1
protein arginine methyltransferase NDUFAF7 homolog, mitochondrial
probable ATP-dependent RNA helicase Dbp45A
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 40 samples with support for all annotated introns
myotubularin-related protein 8, transcript variant X2
myotubularin-related protein 8 isoform X2
myotubularin-related protein 8, transcript variant X1
myotubularin-related protein 8 isoform 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 2
transfer RNA glutamic acid (anticodon UUC); 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00007
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: 6 Proteins, and 76% 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 29 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, including 109 samples with support for all annotated introns
apoptosis-inducing factor 1, 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase
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 115 samples with support for all annotated introns
uncharacterized LOC111000060, transcript variant X1
uncharacterized LOC111000060, transcript variant X2
uncharacterized protein LOC111000060 isoform X1
uncharacterized protein LOC111000060 isoform X2
chymotrypsin-1-like, transcript variant X1
chymotrypsin-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
neuropeptides capa receptor, 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 4 samples with support for all annotated introns
neuropeptides capa receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
neuropeptides capa receptor-like, transcript variant X1
neuropeptides capa receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
neuropeptides capa receptor-like isoform X1
neuropeptides capa receptor-like 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 30 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 12 samples with support for all annotated introns
prothoracicostatic peptides, 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 8 samples with support for all annotated introns
prothoracicostatic peptides, transcript variant X4
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 10 samples with support for all annotated introns
prothoracicostatic peptides, transcript variant X3
prothoracicostatic peptides, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
prolyl 3-hydroxylase sudestada1, transcript variant X1
prolyl 3-hydroxylase sudestada1 isoform X1
prolyl 3-hydroxylase sudestada1, transcript variant X2
prolyl 3-hydroxylase sudestada1 isoform X2
tRNA:m(4)X modification enzyme TRM13 homolog, transcript variant X1
tRNA:m(4)X modification enzyme TRM13 homolog, transcript variant X2
tRNA:m(4)X modification enzyme TRM13 homolog, transcript variant X3
tRNA:m(4)X modification enzyme TRM13 homolog isoform X1
tRNA:m(4)X modification enzyme TRM13 homolog, transcript variant X4
tRNA:m(4)X modification enzyme TRM13 homolog isoform X2
ADP-ribosylation factor GTPase-activating protein 3, transcript variant X3
ADP-ribosylation factor GTPase-activating protein 3, transcript variant X2
ADP-ribosylation factor GTPase-activating protein 3, transcript variant X4
ADP-ribosylation factor GTPase-activating protein 3, transcript variant X1
ADP-ribosylation factor GTPase-activating protein 2 isoform X3
ADP-ribosylation factor GTPase-activating protein 3 isoform X2
ADP-ribosylation factor GTPase-activating protein 3 isoform X4
ADP-ribosylation factor GTPase-activating protein 3 isoform X1
glucosamine-6-phosphate isomerase 2, transcript variant X3
glucosamine-6-phosphate isomerase 2, transcript variant X2
glucosamine-6-phosphate isomerase 2, transcript variant X4
glucosamine-6-phosphate isomerase 2, transcript variant X1
glucosamine-6-phosphate isomerase 2 isoform X2
glucosamine-6-phosphate isomerase isoform X1
charged multivesicular body protein 2a, transcript variant X1
charged multivesicular body protein 2a, transcript variant X3
charged multivesicular body protein 2a, transcript variant X2
fibril-forming collagen alpha chain isoform X1
apoptosis-inducing factor 1, mitochondrial