Pieris rapae chromosome 19, 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\nLR990601.1.\nAssembly name: ilPieRapa1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Wellcome Sanger Institute on\n2021/01/28. The original whole-genome shotgun project has the\naccession CAJHWY000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris rapae Annotation Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
COORDINATES: polyA evidence [ECO:0006239]
solute carrier family 35 member E1 homolog
iron-sulfur clusters transporter ABCB7, mitochondrial, transcript variant X1
iron-sulfur clusters transporter ABCB7, mitochondrial, transcript variant X2
iron-sulfur clusters transporter ABCB7, mitochondrial, transcript variant X3
iron-sulfur clusters transporter ABCB7, mitochondrial isoform X1
iron-sulfur clusters transporter ABCB7, mitochondrial isoform X2
iron-sulfur clusters transporter ABCB7, mitochondrial isoform X3
iron-sulfur clusters transporter ABCB7, mitochondrial, transcript variant X4
iron-sulfur clusters transporter ABCB7, mitochondrial isoform 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 2 samples with support for all annotated introns
neuropeptide FF receptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
neuropeptide FF receptor 1, 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 11 samples with support for all annotated introns
neuropeptide FF receptor 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
neuropeptide FF receptor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
neuropeptide FF receptor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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 20% coverage of the annotated genomic feature by RNAseq alignments
phospholipase A1 VesT1.02-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phospholipase A1 VesT1.02-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ionotropic receptor 75a, 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
ionotropic receptor 75a, 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 1 sample with support for all annotated introns
uncharacterized LOC123690000, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123690000, transcript variant X4
uncharacterized LOC123690000, transcript variant X1
uncharacterized LOC123690000, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cytochrome P450 6k1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 100 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome P450 6k1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 100 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytochrome P450 6k1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC110997865, transcript variant X2
uncharacterized LOC110997865, transcript variant X1
uncharacterized protein LOC110997865 isoform X2
uncharacterized protein LOC110997865 isoform X1
protein vestigial, transcript variant X2
protein vestigial, transcript variant X1
mitotic spindle assembly checkpoint protein MAD2A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
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
netrin receptor unc-5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
netrin receptor unc-5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
netrin receptor unc-5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00007
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
netrin receptor UNC5C, transcript variant X1
netrin receptor UNC5C, 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
interferon-related developmental regulator 1
transcription factor RFX3, transcript variant X4
transcription factor RFX3, transcript variant X3
transcription factor RFX3, transcript variant X1
transcription factor RFX3, transcript variant X2
nucleoporin Nup35, 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 8 samples with support for all annotated introns
nucleoporin Nup35, 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 68 samples with support for all annotated introns
glucose-induced degradation protein 8-B homolog, transcript variant X3
glucose-induced degradation protein 8-B homolog, transcript variant X2
glucose-induced degradation protein 8-B homolog, transcript variant X1
glucose-induced degradation protein 8 homolog isoform X1
glucose-induced degradation protein 8-B homolog isoform X2
uncharacterized LOC123690016, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123690016, 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 12 samples with support for all annotated introns
eukaryotic translation initiation factor 4E1
eukaryotic translation initiation factor 4E1-like
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
X-linked retinitis pigmentosa GTPase regulator-like
four and a half LIM domains protein 2, transcript variant X2
four and a half LIM domains protein 2 isoform X2
four and a half LIM domains protein 2, transcript variant X1
prickle planar cell polarity protein 3 isoform X1
four and a half LIM domains protein 2, transcript variant X6
four and a half LIM domains protein 2, transcript variant X5
four and a half LIM domains protein 2, transcript variant X8
four and a half LIM domains protein 2, transcript variant X3
four and a half LIM domains protein 2, transcript variant X4
four and a half LIM domains protein 2 isoform X3
four and a half LIM domains protein 2 isoform X4
four and a half LIM domains protein 2 isoform X5
four and a half LIM domains protein 2, transcript variant X7
four and a half LIM domains protein 2 isoform X6
uracil phosphoribosyltransferase homolog
elongation of very long chain fatty acids protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
all trans-polyprenyl-diphosphate synthase PDSS2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
DNA N6-methyl adenine demethylase, transcript variant X4
DNA N6-methyl adenine demethylase, transcript variant X3
DNA N6-methyl adenine demethylase, transcript variant X6
DNA N6-methyl adenine demethylase, transcript variant X5
DNA N6-methyl adenine demethylase, transcript variant X2
DNA N6-methyl adenine demethylase, transcript variant X1
DNA N6-methyl adenine demethylase isoform X4
DNA N6-methyl adenine demethylase isoform X3
DNA N6-methyl adenine demethylase isoform X6
DNA N6-methyl adenine demethylase isoform X5
DNA N6-methyl adenine demethylase isoform X2
DNA N6-methyl adenine demethylase isoform X1
phosphatidate cytidylyltransferase, photoreceptor-specific
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 3 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 5 samples with support for all annotated introns
pre-rRNA-processing protein TSR1 homolog
protein transport protein Sec61 subunit alpha
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 87 samples with support for all annotated introns
ATP-binding cassette sub-family D member 3
uncharacterized LOC110993495, transcript variant X4
uncharacterized LOC110993495, transcript variant X1
uncharacterized LOC110993495, transcript variant X3
uncharacterized LOC110993495, transcript variant X5
uncharacterized LOC110993495, transcript variant X2
guanine nucleotide-binding protein-like 3 homolog
nuclear transcription factor Y subunit B-4, transcript variant X1
nuclear transcription factor Y subunit B-4, transcript variant X2
nuclear transcription factor Y subunit beta isoform X1
nuclear transcription factor Y subunit B-4 isoform X2
ATP-binding cassette sub-family G member 5
ATP-binding cassette sub-family G member 8, transcript variant X1
ATP-binding cassette sub-family G member 8, transcript variant X2
ATP-binding cassette sub-family G member 8 isoform X1
ATP-binding cassette sub-family G member 8 isoform X2
spermatogenesis associated 6-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
facilitated trehalose transporter Tret1, transcript variant X3
facilitated trehalose transporter Tret1, transcript variant X2
facilitated trehalose transporter Tret1-2 homolog isoform X2
facilitated trehalose transporter Tret1-2 homolog isoform X3
facilitated trehalose transporter Tret1, transcript variant X1
facilitated trehalose transporter Tret1 isoform X1
facilitated trehalose transporter Tret1-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
calcium uniporter protein, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 86 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
V-type proton ATPase 21 kDa proteolipid subunit, transcript variant X2
V-type proton ATPase 21 kDa proteolipid subunit, transcript variant X1
V-type proton ATPase 21 kDa proteolipid subunit
protocadherin-like wing polarity protein stan, transcript variant X5
protocadherin-like wing polarity protein stan, transcript variant X7
protocadherin-like wing polarity protein stan, transcript variant X9
protocadherin-like wing polarity protein stan, transcript variant X2
protocadherin-like wing polarity protein stan, 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 3 samples with support for all annotated introns
protocadherin-like wing polarity protein stan, transcript variant X6
protocadherin-like wing polarity protein stan isoform X5
protocadherin-like wing polarity protein stan isoform X7
protocadherin-like wing polarity protein stan isoform X2
protocadherin-like wing polarity protein stan isoform X1
protocadherin-like wing polarity protein stan isoform X9
protocadherin-like wing polarity protein stan isoform X6
protocadherin-like wing polarity protein stan, transcript variant X8
protocadherin-like wing polarity protein stan, transcript variant X4
protocadherin-like wing polarity protein stan, transcript variant X3
protocadherin-like wing polarity protein stan isoform X8
protocadherin-like wing polarity protein stan isoform X4
protocadherin-like wing polarity protein stan isoform X3
calcyphosin-like protein, transcript variant X1
calcyphosin-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
calcyphosin-like protein, transcript variant X3
calcyphosin-like protein, transcript variant X9
calcyphosin-like protein, transcript variant X6
calcyphosin-like protein, transcript variant X7
calcyphosin-like protein, transcript variant X8
calcyphosin-like protein, transcript variant X4
calcyphosin-like protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
27 kDa glycoprotein-like, transcript variant X1
27 kDa glycoprotein-like, transcript variant X2
trans-Golgi network integral membrane protein TGN38
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable ATP-dependent RNA helicase pitchoune
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
kelch repeat and BTB domain-containing protein 4, 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 50 samples with support for all annotated introns
kelch repeat and BTB domain-containing protein 4 isoform X2
kelch repeat and BTB domain-containing protein 4, transcript variant X1
kelch repeat and BTB domain-containing protein 4 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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 21 samples with support for all annotated introns
potassium voltage-gated channel unc-103-like
protein held out wings, transcript variant X3
protein held out wings, transcript variant X2
protein held out wings, transcript variant X5
protein held out wings, transcript variant X1
protein held out wings, transcript variant X4
protein held out wings, transcript variant X7
protein held out wings, transcript variant X8
protein held out wings, transcript variant X6
mitochondrial transcription rescue factor 1, transcript variant X2
mitochondrial transcription rescue factor 1, transcript variant X1
mitochondrial transcription rescue factor 1 isoform X2
mitochondrial transcription rescue factor 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
glutathione S-transferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 180 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: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
glutathione S-transferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 182 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glutathione S-transferase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 182 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glutathione S-transferase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 181 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC110998888, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC110998888, 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 4 samples with support for all annotated introns
uncharacterized protein LOC110998888 isoform X1
uncharacterized protein LOC110998888 isoform X2
protein toll-like, transcript variant X1
protein toll-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tryptophan (anticodon CCA); 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: 12 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
vacuolar protein sorting-associated protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 114 samples with support for all annotated introns
U6 snRNA-associated Sm-like protein LSm8
solute carrier family 25 member 40, 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 28 samples with support for all annotated introns
solute carrier family 25 member 40, 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 26 samples with support for all annotated introns
solute carrier family 25 member 40, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
solute carrier family 25 member 40 isoform X3
solute carrier family 25 member 40 isoform X1
solute carrier family 25 member 40 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myosin regulatory light chain, smooth muscle
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
SET domain-containing protein SmydA-8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SET domain-containing protein SmydA-8, 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 12 samples with support for all annotated introns
uncharacterized protein LOC111001641 isoform X2
SET domain-containing protein SmydA-8 isoform X1
protein lin-54 homolog, transcript variant X2
protein lin-54 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
voltage-dependent anion-selective channel
zinc finger CCHC domain-containing protein 9, 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 9 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 9, 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 71 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 9
zinc finger protein OZF, 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 13 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X2
zinc finger protein OZF, transcript variant X4
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 14 samples with support for all annotated introns
zinc finger protein OZF, 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 12 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X8
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 14 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X10
zinc finger protein OZF, transcript variant X11
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 14 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X6
zinc finger protein OZF, transcript variant X9
zinc finger protein OZF, transcript variant X7
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 14 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X13
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 7 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X15
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 11 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X12
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 14 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X14
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 16 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X16
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 18 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X17
zinc finger protein 2 homolog isoform X1
zinc finger protein 2 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC111001628, transcript variant X1
uncharacterized LOC111001628, transcript variant X2
pyrroline-5-carboxylate reductase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
pyrroline-5-carboxylate reductase, 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 21 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 9 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 15 samples with support for all annotated introns
putative inner dynein arm light chain, axonemal
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
mediator of RNA polymerase II transcription subunit 4
proton-coupled folate transporter, transcript variant X2
proton-coupled folate transporter, transcript variant X1
proton-coupled folate transporter isoform X2
proton-coupled folate transporter isoform X1
uncharacterized LOC111001624, transcript variant X2
uncharacterized LOC111001624, transcript variant X3
uncharacterized protein LOC111001624 isoform X2
uncharacterized LOC111001624, transcript variant X1
uncharacterized LOC111001624, transcript variant X4
uncharacterized LOC111001624, transcript variant X5
uncharacterized LOC111001624, transcript variant X6
uncharacterized LOC111001624, transcript variant X7
uncharacterized protein LOC111001624 isoform X1
uncharacterized protein LOC111001624 isoform X3
uncharacterized protein LOC111001624 isoform X4
uncharacterized protein LOC111001624 isoform X6
uncharacterized protein LOC111001624 isoform X5
uncharacterized LOC111001624, transcript variant X8
uncharacterized protein LOC111001624 isoform X7
microtubule-associated protein tau, transcript variant X4
microtubule-associated protein tau, transcript variant X3
microtubule-associated protein tau, transcript variant X1
microtubule-associated protein tau, transcript variant X2
microtubule-associated protein tau isoform X4
microtubule-associated protein tau isoform X1
microtubule-associated protein tau isoform X2
microtubule-associated protein tau isoform 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 90 samples with support for all annotated introns
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
myosin light chain alkali, transcript variant X1
myosin light chain alkali, transcript variant X2
uncharacterized LOC111001638, transcript variant X2
uncharacterized LOC111001638, transcript variant X1
uncharacterized protein LOC111001638 isoform X2
uncharacterized protein LOC111001638 isoform X1
protein unc-80 homolog, 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
protein unc-80 homolog, transcript variant X3
protein unc-80 homolog, transcript variant X2
protein unc-80 homolog, transcript variant X4
uncharacterized LOC110995287, transcript variant X1
uncharacterized LOC110995287, transcript variant X2
uncharacterized protein LOC110995287 isoform X2
uncharacterized protein LOC110995287 isoform X1
uncharacterized LOC110995302, transcript variant X1
uncharacterized LOC110995302, transcript variant X2
uncharacterized protein LOC110995302 isoform X1
uncharacterized protein LOC110995302 isoform X2
transmembrane emp24 domain-containing protein 3
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 39 samples with support for all annotated introns
transcription elongation factor B polypeptide 3
autophagy-related protein 16-1, transcript variant X2
autophagy-related protein 16-1, transcript variant X1
autophagy-related protein 16-1 isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
RUN and FYVE domain-containing protein 2, transcript variant X3
RUN and FYVE domain-containing protein 2 isoform X3
RUN and FYVE domain-containing protein 2, transcript variant X4
RUN and FYVE domain-containing protein 2, transcript variant X1
RUN and FYVE domain-containing protein 2, transcript variant X2
RUN and FYVE domain-containing protein 2 isoform X1
RUN and FYVE domain-containing protein 2 isoform X2
retinoid-inducible serine carboxypeptidase
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
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 CG7065, transcript variant X3
uncharacterized protein CG7065, transcript variant X1
uncharacterized protein CG7065, transcript variant X4
uncharacterized protein CG7065, transcript variant X2
uncharacterized protein CG7065, transcript variant X5
uncharacterized protein CG7065 isoform X2
uncharacterized protein CG7065 isoform X1
uncharacterized protein CG7065 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
maternal protein pumilio, transcript variant X1
maternal protein pumilio, transcript variant X2
maternal protein pumilio, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
circadian clock-controlled protein daywake
uncharacterized LOC123689996, transcript variant X2
uncharacterized LOC123689996, transcript variant X1
MFS-type transporter SLC18B1, 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 14 samples with support for all annotated introns
MFS-type transporter SLC18B1, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
zinc finger protein 37 homolog, transcript variant X2
zinc finger protein 37 homolog, transcript variant X1
zinc finger protein 37 homolog isoform X2
thiamine transporter 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
thiamine transporter 1, 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 16 samples with support for all annotated introns
thiamine transporter 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
thiamine transporter 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 7 samples with support for all annotated introns
thiamine transporter 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 37 samples with support for all annotated introns
thiamine transporter 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
single-pass membrane and coiled-coil domain-containing protein 4, 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 73 samples with support for all annotated introns
single-pass membrane and coiled-coil domain-containing protein 4, 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 117 samples with support for all annotated introns
single-pass membrane and coiled-coil domain-containing protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
28S ribosomal protein S14, mitochondrial
small G protein signaling modulator 3 homolog
uncharacterized LOC110998534, transcript variant X1
uncharacterized LOC110998534, transcript variant X2
uncharacterized protein LOC110998534 isoform X1
uncharacterized protein LOC110998534 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
gustatory receptor for sugar taste 64a-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 15 Proteins
gustatory receptor for sugar taste 64f-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123690007, transcript variant X2
uncharacterized LOC123690007, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 33 Proteins, and 26% 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 mRNA, 31 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
arylalkylamine N-acetyltransferase 1-like, transcript variant X2
arylalkylamine N-acetyltransferase 1-like, transcript variant X1
arylalkylamine N-acetyltransferase 1-like
dnaJ-like protein 60, 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 18 samples with support for all annotated introns
dnaJ-like protein 60, 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 96 samples with support for all annotated introns
fasciculation and elongation protein zeta-2
spectrin beta chain, transcript variant X1
spectrin beta chain, transcript variant X12
spectrin beta chain, transcript variant X9
spectrin beta chain, transcript variant X10
spectrin beta chain, transcript variant X6
spectrin beta chain, transcript variant X11
spectrin beta chain, transcript variant X7
spectrin beta chain, transcript variant X8
spectrin beta chain, transcript variant X4
spectrin beta chain, transcript variant X3
spectrin beta chain, transcript variant X2
spectrin beta chain, transcript variant X5
zinc finger protein 239, transcript variant X2
zinc finger protein 239, transcript variant X5
zinc finger protein 239, transcript variant X3
zinc finger protein 239, transcript variant X4
zinc finger protein 239, transcript variant X1
amyloid-beta-like protein, transcript variant X3
amyloid-beta-like protein, transcript variant X2
amyloid-beta-like protein, transcript variant X1
persulfide dioxygenase ETHE1, mitochondrial, transcript variant X2
persulfide dioxygenase ETHE1, mitochondrial, transcript variant X1
persulfide dioxygenase ETHE1, mitochondrial isoform X1
persulfide dioxygenase ETHE1, mitochondrial isoform X2
tubulin-specific chaperone cofactor E-like protein
transcriptional regulator ATRX homolog, transcript variant X5
transcriptional regulator ATRX homolog, transcript variant X4
transcriptional regulator ATRX homolog, transcript variant X3
transcriptional regulator ATRX homolog, transcript variant X2
transcriptional regulator ATRX homolog, transcript variant X1
transcriptional regulator ATRX homolog isoform X2
transcriptional regulator ATRX homolog isoform X1
transcriptional regulator ATRX homolog isoform X3
transcriptional regulator ATRX homolog isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
hypoxia up-regulated protein 1, transcript variant X1
hypoxia up-regulated protein 1, transcript variant X2
hypoxia up-regulated protein 1 isoform X2
hypoxia up-regulated protein 1 isoform X1
forkhead box protein N3, transcript variant X1
forkhead box protein N3, transcript variant X2
mitochondrial genome maintenance exonuclease 1, transcript variant X2
mitochondrial genome maintenance exonuclease 1, transcript variant X1
mitochondrial genome maintenance exonuclease 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
centrosomal protein of 164 kDa, 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 4 samples with support for all annotated introns
centrosomal protein of 164 kDa isoform X1
centrosomal protein of 164 kDa, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
centrosomal protein of 164 kDa isoform X2
26S proteasome non-ATPase regulatory subunit 8
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
insulin receptor-related protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
insulin receptor-related protein-like, transcript variant X2
insulin receptor-related protein-like, 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 10 samples with support for all annotated introns
insulin-like growth factor 1 receptor isoform X1
insulin-like growth factor 1 receptor isoform X2
insulin receptor-related protein-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ammonium transporter Rh type B-B, transcript variant X1
ammonium transporter Rh type B-B, 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 5 samples with support for all annotated introns
piggyBac transposable element-derived protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
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 8 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
uncharacterized LOC111003953, transcript variant X1
uncharacterized LOC111003953, transcript variant X2
uncharacterized protein LOC111003953 isoform X1
uncharacterized protein LOC111003953 isoform X2
acyl-CoA:lysophosphatidylglycerol acyltransferase 1, transcript variant X2
acyl-CoA:lysophosphatidylglycerol acyltransferase 1 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
acyl-CoA:lysophosphatidylglycerol acyltransferase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acyl-CoA:lysophosphatidylglycerol acyltransferase 1, transcript variant X1
fumarate hydratase, mitochondrial, transcript variant X1
fumarate hydratase, mitochondrial isoform X1
fumarate hydratase, mitochondrial, transcript variant X2
fumarate hydratase, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 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 10 samples with support for all annotated introns
uncharacterized LOC110991930, transcript variant X2
uncharacterized LOC110991930, transcript variant X3
uncharacterized LOC110991930, transcript variant X1
uncharacterized protein LOC110991930 isoform X1
uncharacterized protein LOC110991930 isoform X2
uncharacterized LOC110991930, transcript variant X4
uncharacterized protein LOC110991930 isoform X3
echinoderm microtubule-associated protein-like 2, transcript variant X2
echinoderm microtubule-associated protein-like 2 isoform X2
echinoderm microtubule-associated protein-like 2, transcript variant X1
echinoderm microtubule-associated protein-like 2 isoform X1
mitochondrial import inner membrane translocase subunit TIM44
eukaryotic translation initiation factor 5, transcript variant X10
eukaryotic translation initiation factor 5, transcript variant X9
eukaryotic translation initiation factor 5, transcript variant X2
eukaryotic translation initiation factor 5, transcript variant X5
eukaryotic translation initiation factor 5, transcript variant X8
eukaryotic translation initiation factor 5, transcript variant X4
eukaryotic translation initiation factor 5, transcript variant X1
eukaryotic translation initiation factor 5, transcript variant X3
eukaryotic translation initiation factor 5, transcript variant X6
eukaryotic translation initiation factor 5, transcript variant X11
eukaryotic translation initiation factor 5, transcript variant X7
eukaryotic translation initiation factor 5 isoform X1
eukaryotic translation initiation factor 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
thyroid adenoma-associated protein homolog
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 18 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
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 23 samples with support for all annotated introns
ribosome-recycling factor, mitochondrial
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
peroxynitrite isomerase THAP4, transcript variant X3
peroxynitrite isomerase THAP4, transcript variant X5
peroxynitrite isomerase THAP4, transcript variant X6
peroxynitrite isomerase THAP4, transcript variant X2
peroxynitrite isomerase THAP4, transcript variant X4
peroxynitrite isomerase THAP4, transcript variant X1
peroxynitrite isomerase THAP4, transcript variant X10
peroxynitrite isomerase THAP4, transcript variant X9
peroxynitrite isomerase THAP4, transcript variant X7
peroxynitrite isomerase THAP4, transcript variant X11
peroxynitrite isomerase THAP4, transcript variant X8
uncharacterized protein LOC110991901 isoform X3
uncharacterized protein LOC110991901 isoform X2
peroxynitrite isomerase THAP4 isoform X4
uncharacterized protein LOC110991901 isoform X1
uncharacterized protein LOC110991901 isoform X8
uncharacterized protein LOC110991901 isoform X6
uncharacterized protein LOC110991901 isoform X7
uncharacterized protein LOC110991901 isoform X9
interferon regulatory factor 2-binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized abhydrolase domain-containing protein DDB_G0269086
V-type proton ATPase catalytic subunit A, transcript variant X1
V-type proton ATPase catalytic subunit A, transcript variant X2
V-type proton ATPase catalytic subunit A
speckle targeted PIP5K1A-regulated poly(A) polymerase, transcript variant X2
speckle targeted PIP5K1A-regulated poly(A) polymerase, transcript variant X3
speckle targeted PIP5K1A-regulated poly(A) polymerase, transcript variant X1
speckle targeted PIP5K1A-regulated poly(A) polymerase, transcript variant X4
speckle targeted PIP5K1A-regulated poly(A) polymerase
poly(A) RNA polymerase cid13-like, transcript variant X1
poly(A) RNA polymerase cid13-like, transcript variant X2
poly(A) RNA polymerase cid11-like isoform X1
poly(A) RNA polymerase cid13-like isoform X2
acid phosphatase type 7, transcript variant X3
acid phosphatase type 7, transcript variant X2
acid phosphatase type 7, transcript variant X1
uncharacterized LOC110991928, transcript variant X2
uncharacterized LOC110991928, transcript variant X3
uncharacterized LOC110991928, transcript variant X1
visual system homeobox 2-like, transcript variant X2
visual system homeobox 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
visual system homeobox 2-like, transcript variant X1
visual system homeobox 2-like isoform X2
visual system homeobox 2-like isoform X3
visual system homeobox 2-like isoform X1
39S ribosomal protein L14, mitochondrial
calcineurin subunit B type 2, transcript variant X1
calcineurin subunit B type 2, transcript variant X2
elongation factor 1-gamma, transcript variant X1
elongation factor 1-gamma, transcript variant X2
serine/arginine repetitive matrix protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel protein eag, transcript variant X2
potassium voltage-gated channel protein eag, transcript variant X3
potassium voltage-gated channel protein eag, transcript variant X5
potassium voltage-gated channel protein eag, transcript variant X4
potassium voltage-gated channel protein eag, transcript variant X1
potassium voltage-gated channel protein eag isoform X2
potassium voltage-gated channel protein eag isoform X4
potassium voltage-gated channel protein eag isoform X3
potassium voltage-gated channel protein eag isoform X1
KAT8 regulatory NSL complex subunit 3, transcript variant X2
KAT8 regulatory NSL complex subunit 3, transcript variant X1
KAT8 regulatory NSL complex subunit 3 isoform X2
KAT8 regulatory NSL complex subunit 3 isoform X1