Pieris rapae chromosome 14, 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\nLR990596.1.\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.
insulin-degrading enzyme, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
insulin-degrading enzyme, transcript variant X3
insulin-degrading enzyme, transcript variant X1
uncharacterized protein PB18E9.04c, transcript variant X1
uncharacterized protein PB18E9.04c, transcript variant X2
uncharacterized protein PB18E9.04c isoform X2
uncharacterized protein PB18E9.04c isoform X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9-like
gustatory receptor for sugar taste 43a-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
acetyl-CoA acetyltransferase A, mitochondrial
microprocessor complex subunit DGCR8, transcript variant X3
microprocessor complex subunit DGCR8, transcript variant X1
microprocessor complex subunit DGCR8, 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 2 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 1 sample with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A, transcript variant X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A isoform X2
putative tricarboxylate transport protein, mitochondrial
aldo-keto reductase AKR2E4, transcript variant X1
aldo-keto reductase AKR2E4, 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 15 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 10
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
phosphorylase b kinase gamma catalytic chain, liver/testis isoform, transcript variant X2
phosphorylase b kinase gamma catalytic chain, liver/testis isoform, transcript variant X1
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform isoform X1
phosphorylase b kinase gamma catalytic chain, liver/testis isoform isoform X2
max-binding protein MNT, transcript variant X1
max-binding protein MNT, transcript variant X2
max-binding protein MNT, transcript variant X3
hatching enzyme 1.2, 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 12 samples with support for all annotated introns
hatching enzyme 1.2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
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 1 sample with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 32, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 32, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 32, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 32, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 32 isoform X1
ubiquitin carboxyl-terminal hydrolase 32 isoform X2
ubiquitin carboxyl-terminal hydrolase 32 isoform X3
ubiquitin carboxyl-terminal hydrolase 32 isoform X4
TWiK family of potassium channels protein 18-like
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCG); 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 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 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 100 samples with support for all annotated introns
potassium channel subfamily K member 15, 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
potassium channel subfamily K member 15, 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
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00535
17-beta-hydroxysteroid dehydrogenase 14-like
alpha-tocopherol transfer protein-like, transcript variant X2
alpha-tocopherol transfer protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
PHD finger protein 12, 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 21 samples with support for all annotated introns
PHD finger protein 12, 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 21 samples with support for all annotated introns
GPN-loop GTPase 3, transcript variant X1
GPN-loop GTPase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 496 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
homeobox protein cut, transcript variant X5
homeobox protein cut, transcript variant X7
homeobox protein cut, transcript variant X6
homeobox protein cut, transcript variant X2
homeobox protein cut, transcript variant X3
homeobox protein cut, transcript variant X1
homeobox protein cut, transcript variant X4
homeobox protein cut, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 105 samples with support for all annotated introns
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
uncharacterized oxidoreductase TM_0325-like
uncharacterized oxidoreductase SSP0419-like
3-oxoacyl-[acyl-carrier-protein] reductase FabG-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
uncharacterized oxidoreductase SERP2049-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 21 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 19 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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
vacuolar protein sorting-associated protein 29
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 99 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein phosphatase alpha-2 isoform
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 42 homolog
peptidyl-tRNA hydrolase 2, mitochondrial
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 96 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 1 sample with support for all annotated introns
HIRA-interacting protein 3, transcript variant X1
HIRA-interacting protein 3, transcript variant X2
HIRA-interacting protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable 4-methylmuconolactone transporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC111002078, transcript variant X2
uncharacterized LOC111002078, transcript variant X1
uncharacterized protein LOC111002078 isoform X2
uncharacterized protein LOC111002078 isoform X1
mitochondrial import inner membrane translocase subunit Tim22
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 57 samples with support for all annotated introns
uncharacterized LOC111002079, transcript variant X3
uncharacterized LOC111002079, transcript variant X2
uncharacterized LOC111002079, transcript variant X1
uncharacterized protein LOC111002079 isoform X3
uncharacterized protein LOC111002079 isoform X2
uncharacterized protein LOC111002079 isoform X1
ectonucleoside triphosphate diphosphohydrolase 5, transcript variant X1
ectonucleoside triphosphate diphosphohydrolase 5 isoform X1
ectonucleoside triphosphate diphosphohydrolase 5, transcript variant X3
ectonucleoside triphosphate diphosphohydrolase 5 isoform X3
ectonucleoside triphosphate diphosphohydrolase 5, transcript variant X2
ectonucleoside triphosphate diphosphohydrolase 5 isoform X2
uncharacterized protein CG3556, 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 10 samples with support for all annotated introns
uncharacterized protein CG3556, transcript variant X5
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
uncharacterized protein CG3556, transcript variant X2
uncharacterized protein CG3556, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein CG3556, transcript variant X3
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 5 samples with support for all annotated introns
uncharacterized protein CG3556 isoform X2
uncharacterized protein CG3556 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phosphatidylethanolamine-binding protein 1-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 5 samples with support for all annotated introns
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
26 kDa secreted antigen-like, transcript variant X1
26 kDa secreted antigen-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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
solute carrier family 35 member G1, transcript variant X1
solute carrier family 35 member G1, transcript variant X2
mediator of RNA polymerase II transcription subunit 21
uncharacterized LOC111001731, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC111001731, transcript variant X2
uncharacterized LOC110991431, transcript variant X1
uncharacterized LOC110991431, transcript variant X2
uncharacterized protein LOC110991431 isoform X1
uncharacterized protein LOC110991431 isoform X2
leucine-rich repeat extensin-like protein 3, transcript variant X2
leucine-rich repeat extensin-like protein 3, 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 4 samples with support for all annotated introns
leucine-rich repeat extensin-like protein 3 isoform X1
vegetative cell wall protein gp1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 60% 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
T-box transcription factor TBX1, transcript variant X1
T-box transcription factor TBX1, transcript variant X2
T-box transcription factor TBX1 isoform X1
T-box transcription factor TBX1 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 28 samples with support for all annotated introns
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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein 239, 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 20 samples with support for all annotated introns
zinc finger protein 239, 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 protein 239, transcript variant X1
5'-AMP-activated protein kinase catalytic subunit alpha-2
polymerase delta-interacting protein 2, transcript variant X1
polymerase delta-interacting protein 2, transcript variant X3
polymerase delta-interacting protein 2, transcript variant X2
polymerase delta-interacting protein 2, transcript variant X4
polymerase delta-interacting protein 2 isoform X4
polymerase delta-interacting protein 2 isoform X3
polymerase delta-interacting protein 2 isoform X2
polymerase delta-interacting protein 2 isoform X1
short-chain specific acyl-CoA dehydrogenase, mitochondrial
actin-related protein 2/3 complex subunit 3
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 115 samples with support for all annotated introns
coiled-coil domain-containing protein 86
signal peptide peptidase-like 3, transcript variant X2
signal peptide peptidase-like 3, transcript variant X1
signal peptide peptidase-like 3 isoform X2
signal peptide peptidase-like 3 isoform X1
apoptosis-inducing factor 3, transcript variant X1
apoptosis-inducing factor 3, transcript variant X2
formin-like protein 5, transcript variant X4
formin-like protein 5, transcript variant X3
formin-like protein 5, transcript variant X2
formin-like protein 5, transcript variant X1
CDP-diacylglycerol--inositol 3-phosphatidyltransferase
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
MOG interacting and ectopic P-granules protein 1
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
2-(3-amino-3-carboxypropyl)histidine synthase subunit 1
protein ABHD11-like, transcript variant X1
protein ABHD11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
elongation of very long chain fatty acids protein AAEL008004, transcript variant X3
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 19 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004, transcript variant X4
elongation of very long chain fatty acids protein AAEL008004, 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 18 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004, transcript variant X2
elongation of very long chain fatty acids protein AAEL008004 isoform X1
elongation of very long chain fatty acids protein AAEL008004 isoform X2
elongation of very long chain fatty acids protein AAEL008004 isoform X3
splicing factor ESS-2 homolog, transcript variant X1
splicing factor ESS-2 homolog, 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 LOC110991432, transcript variant X1
uncharacterized LOC110991432, transcript variant X2
uncharacterized protein LOC110991432 isoform X1
uncharacterized protein LOC110991432 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 101 samples with support for all annotated introns
cell cycle checkpoint control protein RAD9A
ubiquitin-conjugating enzyme E2 G1, transcript variant X2
ubiquitin-conjugating enzyme E2 G1, transcript variant X3
ubiquitin-conjugating enzyme E2 G1, transcript variant X1
ubiquitin-conjugating enzyme E2 G1 isoform X2
ubiquitin-conjugating enzyme E2 G1 isoform X1
eukaryotic translation initiation factor 4H, transcript variant X1
eukaryotic translation initiation factor 4H, transcript variant X2
eukaryotic translation initiation factor 4H isoform X1
eukaryotic translation initiation factor 4H isoform X2
NAD-dependent protein deacylase Sirt4-like
serine/threonine-protein phosphatase 4 catalytic subunit
glucose dehydrogenase [FAD, quinone]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone], 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 11 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone], transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC110991465, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC110991465, 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 25 samples with support for all annotated introns
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X3
glucose dehydrogenase [FAD, quinone]-like isoform X1
glucose dehydrogenase [FAD, quinone]-like isoform X2
glucose dehydrogenase [FAD, quinone]-like isoform X3
glucose dehydrogenase [FAD, quinone]-like, transcript variant X4
uncharacterized protein LOC111002030 isoform X4
vanin-like protein 1, transcript variant X1
vanin-like protein 1, transcript variant X2
vanin-like protein 1, transcript variant X3
vanin-like protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
cytosolic 10-formyltetrahydrofolate dehydrogenase
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 7
bromodomain-containing protein 1, transcript variant X2
bromodomain-containing protein 1, transcript variant X1
bromodomain-containing protein 1 isoform X2
bromodomain-containing protein 1 isoform X1
uncharacterized LOC111000550, transcript variant X2
uncharacterized LOC111000550, transcript variant X1
uncharacterized LOC111000550, transcript variant X3
uncharacterized protein LOC111000550 isoform X2
uncharacterized protein LOC111000550 isoform X1
uncharacterized protein LOC111000550 isoform X3
26S proteasome non-ATPase regulatory subunit 10
methyl-CpG-binding domain protein 4, 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 31 samples with support for all annotated introns
methyl-CpG-binding domain protein 4, transcript variant X2
jmjC domain-containing histone demethylation protein 1
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 1 sample with support for all annotated introns
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
LIM/homeobox protein Lhx1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
LIM/homeobox protein Lhx1, 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 9 samples with support for all annotated introns
LIM/homeobox protein Lhx1, 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 11 samples with support for all annotated introns
LIM/homeobox protein Lhx1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
LIM/homeobox protein Lhx1, 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 7 samples with support for all annotated introns
trichoplein keratin filament-binding protein, transcript variant X3
trichoplein keratin filament-binding protein, transcript variant X2
trichoplein keratin filament-binding protein, transcript variant X1
trichoplein keratin filament-binding protein isoform X1
trichoplein keratin filament-binding protein, transcript variant X4
trichoplein keratin filament-binding protein isoform X2
39S ribosomal protein L44, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 88 samples with support for all annotated introns
piggyBac transposable element-derived protein 4-like, transcript variant X1
piggyBac transposable element-derived protein 4-like isoform X1
piggyBac transposable element-derived protein 4-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
uncharacterized protein LOC123689720 isoform X2
squamous cell carcinoma antigen recognized by T-cells 3
neurogenic locus notch homolog protein 3
vacuolar protein sorting-associated protein 33A
small G protein signaling modulator 2, 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 3 samples with support for all annotated introns
small G protein signaling modulator 2, transcript variant X2
small G protein signaling modulator 2, transcript variant X3
small G protein signaling modulator 2 isoform X1
small G protein signaling modulator 2 isoform X2
small G protein signaling modulator 2 isoform X3
serine/threonine-protein kinase Tao, transcript variant X1
serine/threonine-protein kinase Tao, transcript variant X2
serine/threonine-protein kinase Tao isoform X2
serine/threonine-protein kinase Tao isoform X1
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 15 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
chromobox protein homolog 1, transcript variant X1
chromobox protein homolog 1, transcript variant X3
chromobox protein homolog 1, transcript variant X4
chromobox protein homolog 1, transcript variant X2
uncharacterized LOC111004400, transcript variant X1
uncharacterized LOC111004400, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ABC transporter F family member 4, transcript variant X2
ABC transporter F family member 4, transcript variant X1
ABC transporter F family member 4 isoform 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 27 samples with support for all annotated introns
peptidoglycan-recognition protein LB, transcript variant X2
peptidoglycan-recognition protein LB, transcript variant X3
peptidoglycan-recognition protein LB, 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 22 samples with support for all annotated introns
uncharacterized LOC111004380, transcript variant X1
uncharacterized LOC111004380, transcript variant X2
uncharacterized LOC111004380, transcript variant X3
cytochrome b-c1 complex subunit 6, mitochondrial
histone-lysine N-methyltransferase SETD1, transcript variant X1
histone-lysine N-methyltransferase SETD1, transcript variant X3
histone-lysine N-methyltransferase SETD1, transcript variant X4
histone-lysine N-methyltransferase SETD1, transcript variant X2
histone-lysine N-methyltransferase SETD1 isoform X1
histone-lysine N-methyltransferase SETD1 isoform X2
histone-lysine N-methyltransferase SETD1 isoform X3
citron Rho-interacting kinase, transcript variant X2
citron Rho-interacting kinase, transcript variant X1
citron Rho-interacting kinase isoform X2
citron Rho-interacting kinase isoform X1
transmembrane emp24 domain-containing protein 2
ubiquitin carboxyl-terminal hydrolase isozyme L5
DNA replication ATP-dependent helicase/nuclease DNA2, transcript variant X1
DNA replication ATP-dependent helicase/nuclease DNA2, transcript variant X2
DNA replication ATP-dependent helicase/nuclease DNA2 isoform X2
DNA replication ATP-dependent helicase/nuclease DNA2 isoform X1
probable 18S rRNA (guanine-N(7))-methyltransferase
ATP synthase subunit C lysine N-methyltransferase
histone-lysine N-methyltransferase PR-Set7, transcript variant X1
histone-lysine N-methyltransferase PR-Set7, transcript variant X2
histone-lysine N-methyltransferase PR-Set7 isoform X1
histone-lysine N-methyltransferase PR-Set7 isoform X2
eukaryotic translation initiation factor 3 subunit C, transcript variant X2
eukaryotic translation initiation factor 3 subunit C, transcript variant X1
eukaryotic translation initiation factor 3 subunit C isoform X2
eukaryotic translation initiation factor 3 subunit C isoform X1
mediator of RNA polymerase II transcription subunit 31
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 90% 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 99% coverage of the annotated genomic feature by RNAseq alignments
unconventional myosin-XVIIIa, transcript variant X1
unconventional myosin-XVIIIa, transcript variant X2
fructose-bisphosphate aldolase, transcript variant X1
fructose-bisphosphate aldolase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 203 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
ras-like protein family member 10B, 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 4 samples with support for all annotated introns
ras-like protein family member 10B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ras-like protein family member 10B isoform X1
ras-like protein family member 10B isoform 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 1 sample 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 9 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 8 samples with support for all annotated introns
facilitated trehalose transporter Tret1, transcript variant X2
facilitated trehalose transporter Tret1, transcript variant X1
facilitated trehalose transporter Tret1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
ralA-binding protein 1, transcript variant X2
ralA-binding protein 1, transcript variant X1
ralA-binding protein 1, transcript variant X3
putative glutathione-specific gamma-glutamylcyclotransferase 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: putative glutathione-specific gamma-glutamylcyclotransferase 2
histone acetyltransferase type B catalytic subunit, transcript variant X2
histone acetyltransferase type B catalytic subunit, transcript variant X1
histone acetyltransferase type B catalytic subunit
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
outer dynein arm-docking complex subunit 4-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
cytochrome c oxidase subunit 5B, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cysteine-rich hydrophobic domain-containing protein 2
uncharacterized LOC111004345, transcript variant X1
uncharacterized LOC111004345, transcript variant X2
uncharacterized protein LOC111004345 isoform X1
uncharacterized protein LOC111004345 isoform X2
E3 ubiquitin-protein ligase Arkadia, transcript variant X1
E3 ubiquitin-protein ligase Arkadia, transcript variant X2
E3 ubiquitin-protein ligase Arkadia isoform X2
E3 ubiquitin-protein ligase Arkadia isoform X1
DNA-directed RNA polymerases I, II, and III subunit RPABC2
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COX assembly mitochondrial protein 2 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 116 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
pseudouridine-5'-phosphatase, 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 12 samples with support for all annotated introns
pseudouridine-5'-phosphatase, 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 69 samples with support for all annotated introns
uncharacterized LOC110995367, transcript variant X1
uncharacterized LOC110995367, transcript variant X7
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 LOC110995367, transcript variant X6
uncharacterized LOC110995367, transcript variant X4
uncharacterized LOC110995367, transcript variant X5
uncharacterized protein LOC110995367 isoform X3
uncharacterized protein LOC110995367 isoform X4
uncharacterized protein LOC110995367 isoform X5
uncharacterized protein LOC110995367 isoform X1
uncharacterized LOC110995367, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC110995367, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein LOC110995367 isoform X2
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
dopamine receptor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
dopamine receptor 2, transcript variant X1
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 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
regulator of gene activity, transcript variant X5
regulator of gene activity, transcript variant X2
regulator of gene activity, transcript variant X1
regulator of gene activity, transcript variant X3
regulator of gene activity, transcript variant X4
CCR4-NOT transcription complex subunit 2 isoform X3
CCR4-NOT transcription complex subunit 2 isoform X2
CCR4-NOT transcription complex subunit 2 isoform X1
glutamate [NMDA] receptor subunit 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glutamate [NMDA] receptor subunit 1 isoform X1
glutamate [NMDA] receptor subunit 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 1 sample with support for all annotated introns
glutamate [NMDA] receptor subunit 1 isoform X2
fibroblast growth factor 22, transcript variant X3
fibroblast growth factor 22, transcript variant X4
fibroblast growth factor 22, transcript variant X1
fibroblast growth factor 22, transcript variant X2
uncharacterized LOC110995378, transcript variant X1
uncharacterized LOC110995378, transcript variant X2
uncharacterized protein LOC110995378 isoform X1
uncharacterized protein LOC110995378 isoform X2
calcium uptake protein 3, mitochondrial, transcript variant X1
calcium uptake protein 3, mitochondrial, transcript variant X2
calcium uptake protein 3, mitochondrial, transcript variant X3
calcium uptake protein 3, mitochondrial isoform X1
calcium uptake protein 3, mitochondrial isoform X2
calcium uptake protein 3, mitochondrial isoform 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 87 samples with support for all annotated introns
uncharacterized LOC111000422, transcript variant X1
uncharacterized LOC111000422, transcript variant X2
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
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
knob-associated histidine-rich protein-like
phosphatidylinositol 4-kinase type 2-beta, transcript variant X1
phosphatidylinositol 4-kinase type 2-beta isoform X1
phosphatidylinositol 4-kinase type 2-beta, transcript variant X2
phosphatidylinositol 4-kinase type 2-beta isoform X2
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
FHF complex subunit HOOK interacting protein 2A, transcript variant X2
FHF complex subunit HOOK interacting protein 2A, transcript variant X1
FHF complex subunit HOOK interacting protein 2A isoform X1
FHF complex subunit HOOK interacting protein 2A, 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 29 samples with support for all annotated introns
FHF complex subunit HOOK interacting protein 2A isoform X2
septin-interacting protein 1, transcript variant X2
septin-interacting protein 1, 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 34 samples with support for all annotated introns
UDP-glucosyltransferase 2, 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
UDP-glucosyltransferase 2, 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 2 samples with support for all annotated introns
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 2 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 96% 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: 38 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 2% coverage of the annotated genomic feature by RNAseq alignments
atrial natriuretic peptide receptor 1, transcript variant X5
atrial natriuretic peptide receptor 1, transcript variant X3
atrial natriuretic peptide receptor 1, transcript variant X4
atrial natriuretic peptide receptor 1, transcript variant X1
atrial natriuretic peptide receptor 1, transcript variant X2
atrial natriuretic peptide receptor 1 isoform X3
atrial natriuretic peptide receptor 1 isoform X2
atrial natriuretic peptide receptor 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 10 samples with support for all annotated introns
3-hydroxyacyl-CoA dehydrogenase type-2, transcript variant X2
3-hydroxyacyl-CoA dehydrogenase type-2, transcript variant X1
3-hydroxyacyl-CoA dehydrogenase type-2 isoform X1
3-hydroxyacyl-CoA dehydrogenase type-2 isoform 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 24 samples with support for all annotated introns
mitochondrial import inner membrane translocase subunit Tim16
zinc finger CCHC domain-containing protein 10
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 20 samples with support for all annotated introns
eukaryotic translation initiation factor 2-alpha kinase, transcript variant X1
eukaryotic translation initiation factor 2-alpha kinase, transcript variant X2
eukaryotic translation initiation factor 2-alpha kinase isoform X1
eukaryotic translation initiation factor 2-alpha kinase isoform X2
biotin--protein ligase, transcript variant X2
biotin--protein ligase, transcript variant X1
biotin--protein ligase, transcript variant X3
uncharacterized LOC110993027, transcript variant X1
uncharacterized LOC110993027, transcript variant X2
uncharacterized protein LOC110993027 isoform X1
uncharacterized LOC110993027, transcript variant X3
uncharacterized protein LOC110993027 isoform X2
mediator of RNA polymerase II transcription subunit 29
uncharacterized LOC110993043, transcript variant X1
uncharacterized protein LOC110993043 isoform X1
uncharacterized LOC110993043, transcript variant X2
uncharacterized protein LOC110993043 isoform X2
putative mediator of RNA polymerase II transcription subunit 12, 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
putative mediator of RNA polymerase II transcription subunit 12, transcript variant X1
putative mediator of RNA polymerase II transcription subunit 12 isoform X1
mediator of RNA polymerase II transcription subunit 15-like isoform X2
atrial natriuretic peptide receptor 2-like
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
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 18 samples with support for all annotated introns
adenylate cyclase type 10-like, transcript variant X1
adenylate cyclase type 10-like isoform X1
adenylate cyclase type 10-like, transcript variant X2
adenylate cyclase type 10-like isoform X2
uncharacterized LOC110993011, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC110993011 isoform 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 87 samples with support for all annotated introns
uncharacterized LOC110993011, transcript variant X3
uncharacterized LOC110993011, transcript variant X1
uncharacterized protein LOC110993011 isoform X1
uncharacterized LOC110993011, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized protein LOC110993011 isoform X3
uncharacterized protein LOC110993011 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial, transcript variant X1
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial, transcript variant X2
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial isoform X2
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial isoform X1
mannose-1-phosphate guanyltransferase beta
probable DNA mismatch repair protein Msh6
palmitoyltransferase ZDHHC2, transcript variant X3
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 94 samples with support for all annotated introns
palmitoyltransferase ZDHHC2, transcript variant X1
palmitoyltransferase ZDHHC2, transcript variant X4
palmitoyltransferase ZDHHC2, transcript variant X2
protein capicua homolog, transcript variant X1
protein capicua homolog, transcript variant X4
protein capicua homolog, transcript variant X2
protein capicua homolog, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
uncharacterized protein PF11_0207, transcript variant X2
uncharacterized protein PF11_0207, transcript variant X3
uncharacterized protein PF11_0207, transcript variant X1
uncharacterized protein PF11_0207 isoform X1
mothers against decapentaplegic homolog 4, transcript variant X4
mothers against decapentaplegic homolog 4, transcript variant X3
mothers against decapentaplegic homolog 4, transcript variant X2
mothers against decapentaplegic homolog 4, transcript variant X1
mothers against decapentaplegic homolog 4 isoform X4
mothers against decapentaplegic homolog 4 isoform X3
mothers against decapentaplegic homolog 4 isoform X2
mothers against decapentaplegic homolog 4 isoform X1
trafficking protein particle complex subunit 10
katanin p60 ATPase-containing subunit A-like 1
trithorax group protein osa, transcript variant X1
trithorax group protein osa, transcript variant X12
trithorax group protein osa, transcript variant X9
trithorax group protein osa, transcript variant X3
trithorax group protein osa, transcript variant X10
trithorax group protein osa, transcript variant X4
trithorax group protein osa, transcript variant X11
trithorax group protein osa, transcript variant X5
trithorax group protein osa, transcript variant X13
trithorax group protein osa, transcript variant X2
trithorax group protein osa, transcript variant X6
trithorax group protein osa, transcript variant X7
trithorax group protein osa, transcript variant X8
trithorax group protein osa, transcript variant X14
RNA-binding protein 25, transcript variant X2
RNA-binding protein 25, 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 41 samples with support for all annotated introns
thioredoxin domain-containing protein 12-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 7 samples with support for all annotated introns
PIN2/TERF1-interacting telomerase inhibitor 1
leucine-rich repeat-containing protein 71-like
FHIP family protein AGAP011705, transcript variant X1
FHIP family protein AGAP011705, transcript variant X4
FHIP family protein AGAP011705, transcript variant X2
FHIP family protein AGAP011705, transcript variant X3
FHIP family protein AGAP011705 isoform X2
SWI/SNF complex subunit SMARCC2, transcript variant X2
SWI/SNF complex subunit SMARCC2, transcript variant X1
SWI/SNF complex subunit SMARCC2 isoform X2
SWI/SNF complex subunit SMARCC2 isoform X1
tRNA pseudouridine synthase A, transcript variant X3
tRNA pseudouridine synthase A, transcript variant X1
tRNA pseudouridine synthase A, transcript variant X4
tRNA pseudouridine synthase A, transcript variant X2
tRNA pseudouridine synthase A isoform X1
tRNA pseudouridine synthase A isoform X2
tRNA pseudouridine synthase A isoform X3
actin-interacting protein 1, transcript variant X1
actin-interacting protein 1, transcript variant X2
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: 3 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 X4
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
zinc finger and BTB domain-containing protein 17, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 17, transcript variant X2
zinc finger and BTB domain-containing protein 17 isoform X1
zinc finger and BTB domain-containing protein 17 isoform X2
B-cell receptor CD22, transcript variant X2
B-cell receptor CD22, 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 4 samples with support for all annotated introns
B-cell receptor CD22, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
B-cell receptor CD22, transcript variant X1
neural cell adhesion molecule 1 isoform X2
neural cell adhesion molecule 1 isoform X1
B-cell receptor CD22, transcript variant X5
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
probable 39S ribosomal protein L45, mitochondrial
trafficking protein particle complex subunit 2
DNA-directed RNA polymerase III subunit RPC4
probable 28S ribosomal protein S26, mitochondrial
calcineurin-binding protein cabin-1-like
proclotting enzyme-like, transcript variant X1
proclotting enzyme-like, transcript variant X2
glutamate-gated chloride channel, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
glutamate-gated chloride channel, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate-gated chloride channel, 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
glutamate-gated chloride channel, transcript variant X7
glutamate-gated chloride channel, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
glutamate-gated chloride channel, transcript variant X6
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
glutamate-gated chloride channel, transcript variant X1
glutamate-gated chloride channel, transcript variant X5
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
glutamate-gated chloride channel, transcript variant X8
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
glutamate-gated chloride channel isoform X3
glutamate-gated chloride channel isoform X6
glutamate-gated chloride channel isoform X2
glutamate-gated chloride channel isoform X5
glutamate-gated chloride channel isoform X1
glutamate-gated chloride channel isoform X4
glutamate-gated chloride channel isoform X7
glutamate-gated chloride channel, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glutamate-gated chloride channel isoform X8
ras-like protein 2, transcript variant X1
ras-like protein 2, transcript variant X2
ATP synthase subunit b, mitochondrial, transcript variant X1
ATP synthase subunit b, mitochondrial, transcript variant X2
ATP synthase subunit b, mitochondrial isoform X2
ATP synthase subunit b, mitochondrial isoform X1
small VCP/p97-interacting protein, transcript variant X2
uncharacterized protein LOC110998612 isoform X2
small VCP/p97-interacting protein, transcript variant X1
small VCP/p97-interacting protein isoform X1
solute carrier organic anion transporter family member 1B2, transcript variant X2
solute carrier organic anion transporter family member 1B2, transcript variant X1
solute carrier organic anion transporter family member 1B2
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X3
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X1
UTP--glucose-1-phosphate uridylyltransferase isoform X1
UTP--glucose-1-phosphate uridylyltransferase isoform X3
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X5
UTP--glucose-1-phosphate uridylyltransferase isoform X5
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X4
UTP--glucose-1-phosphate uridylyltransferase isoform X4
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X2
UTP--glucose-1-phosphate uridylyltransferase isoform X2
solute carrier organic anion transporter family member 74D, transcript variant X2
solute carrier organic anion transporter family member 74D, transcript variant X1
solute carrier organic anion transporter family member 74D isoform X2
solute carrier organic anion transporter family member 74D isoform 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
kinesin-like protein Klp61F, transcript variant X1
kinesin-like protein Klp61F, 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 109 samples with support for all annotated introns
uncharacterized LOC111001890, 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 14 samples with support for all annotated introns
uncharacterized LOC111001890, transcript variant X1
uncharacterized protein LOC111001890 isoform X1
uncharacterized protein LOC111001890 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 90 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 8, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 8, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 8 isoform X1
ubiquitin carboxyl-terminal hydrolase 8 isoform X2
synapse-associated protein of 47 kDa, transcript variant X3
synapse-associated protein of 47 kDa, transcript variant X1
synapse-associated protein of 47 kDa, transcript variant X2
synapse-associated protein of 47 kDa, transcript variant X4
synapse-associated protein of 47 kDa, transcript variant X5
synapse-associated protein of 47 kDa, transcript variant X6
synapse-associated protein of 47 kDa isoform X1
synapse-associated protein of 47 kDa isoform X3
synapse-associated protein of 47 kDa isoform X2
synapse-associated protein of 47 kDa isoform X4
synapse-associated protein of 47 kDa isoform X5
synapse-associated protein of 47 kDa isoform 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 21 samples with support for all annotated introns
inverted formin-2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
inverted formin-2, 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
inverted formin-2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
inverted formin-2, transcript variant X4
inverted formin-2, transcript variant X2
uncharacterized LOC111000703, 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 5 samples with support for all annotated introns
uncharacterized LOC111000703, transcript variant X3
uncharacterized protein LOC111000703 isoform X1
uncharacterized protein LOC111000703 isoform X3
uncharacterized LOC111000703, transcript variant X2
uncharacterized protein LOC111000703 isoform X2
cyclin-dependent kinases regulatory subunit-like, transcript variant X1
cyclin-dependent kinases regulatory subunit-like, transcript variant X2
cyclin-dependent kinases regulatory subunit-like
dystrophin, isoforms A/C/F/G/H, transcript variant X2
dystrophin, isoforms A/C/F/G/H, transcript variant X1
dystrophin, isoforms A/C/F/G/H, transcript variant X5
dystrophin, isoforms A/C/F/G/H, transcript variant X3
dystrophin, isoforms A/C/F/G/H isoform X5
dystrophin, isoforms A/C/F/G/H isoform X2
dystrophin, isoforms A/C/F/G/H isoform X1
dystrophin, isoforms A/C/F/G/H isoform X3
dystrophin, isoforms A/C/F/G/H, transcript variant X4
dystrophin, isoforms A/C/F/G/H isoform X4
uncharacterized PE-PGRS family protein PE_PGRS54-like, transcript variant X1
uncharacterized PE-PGRS family protein PE_PGRS54-like, transcript variant X2
uncharacterized PE-PGRS family protein PE_PGRS54-like isoform X1
uncharacterized PE-PGRS family protein PE_PGRS10-like isoform X2
uncharacterized LOC123689722, transcript variant X1
uncharacterized LOC123689722, transcript variant X2
uncharacterized LOC123689722, transcript variant X3
uncharacterized LOC123689722, transcript variant X4
uncharacterized protein LOC123689722 isoform X2
uncharacterized protein LOC123689722 isoform X1
uncharacterized protein LOC123689722 isoform X3
uncharacterized protein LOC123689722 isoform X4
uncharacterized LOC110995984, transcript variant X1
uncharacterized protein LOC110995984 isoform X1
transcription factor Adf-1, transcript variant X3
transcription factor Adf-1, transcript variant X2
transcription factor Adf-1, transcript variant X1
uncharacterized protein LOC110995985 isoform X1
uncharacterized LOC110995984, transcript variant X2
uncharacterized LOC110995984, transcript variant X3
uncharacterized protein LOC110995984 isoform X2
uncharacterized LOC110995982, transcript variant X1
uncharacterized LOC110995982, transcript variant X4
uncharacterized LOC110995982, transcript variant X3
uncharacterized LOC110995982, transcript variant X2
uncharacterized protein LOC110995982 isoform X1
uncharacterized protein LOC110995982 isoform X2
facilitated trehalose transporter Tret1 isoform X2
facilitated trehalose transporter Tret1 isoform X1
mediator of RNA polymerase II transcription subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 95% 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, 37 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
putative phospholipase B-like lamina ancestor, transcript variant X1
putative phospholipase B-like lamina ancestor, transcript variant X2
putative phospholipase B-like lamina ancestor, transcript variant X3
putative phospholipase B-like lamina ancestor
aryl hydrocarbon receptor nuclear translocator-like protein 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 23 samples with support for all annotated introns
KRR1 small subunit processome component homolog
NFX1-type zinc finger-containing protein 1, transcript variant X1
NFX1-type zinc finger-containing protein 1, transcript variant X2
NFX1-type zinc finger-containing protein 1
DNA (cytosine-5)-methyltransferase 1, transcript variant X1
DNA (cytosine-5)-methyltransferase 1, transcript variant X2
DNA (cytosine-5)-methyltransferase 1, 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 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 110 samples with support for all annotated introns
uncharacterized LOC111001906, transcript variant X1
uncharacterized LOC111001906, transcript variant X4
uncharacterized LOC111001906, transcript variant X5
uncharacterized LOC111001906, transcript variant X7
uncharacterized LOC111001906, transcript variant X2
uncharacterized LOC111001906, transcript variant X6
uncharacterized LOC111001906, transcript variant X3
uncharacterized protein LOC111001906 isoform X1
uncharacterized protein LOC111001906 isoform X4
uncharacterized protein LOC111001906 isoform X5
uncharacterized protein LOC111001906 isoform X7
uncharacterized protein LOC111001906 isoform X2
uncharacterized protein LOC111001906 isoform X3
uncharacterized protein LOC111001906 isoform X6
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2, transcript variant X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2, transcript variant X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2
transmembrane protein 19, transcript variant X2
transmembrane protein 19, transcript variant X1
signal recognition particle receptor subunit beta
pyridoxine/pyridoxamine 5'-phosphate oxidase
histidine protein methyltransferase 1 homolog, transcript variant X1
histidine protein methyltransferase 1 homolog isoform X1
histidine protein methyltransferase 1 homolog, 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 22 samples with support for all annotated introns
histidine protein methyltransferase 1 homolog isoform X2
proteasome activator complex subunit 3, transcript variant X1
proteasome activator complex subunit 3, transcript variant X2
proteasome activator complex subunit 3 isoform X1
proteasome activator complex subunit 3 isoform X2
proteasome activator complex subunit 3, transcript variant X4
proteasome activator complex subunit 3, transcript variant X3
proteasome activator complex subunit 3 isoform X3
proteasome activator complex subunit 3 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 87% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
malate dehydrogenase, mitochondrial-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 Proteins
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog, transcript variant X3
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog, transcript variant X6
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog isoform X3
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog isoform X6
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog, transcript variant X4
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog, transcript variant X1
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog, transcript variant X2
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog, transcript variant X5
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog isoform X1
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog isoform X4
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog isoform X2
interferon-inducible double-stranded RNA-dependent protein kinase activator A homolog isoform X5
probable ATP-dependent DNA helicase HFM1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
inositol polyphosphate 5-phosphatase K, transcript variant X1
inositol polyphosphate 5-phosphatase K, transcript variant X2
inositol polyphosphate 5-phosphatase K isoform X1
inositol polyphosphate 5-phosphatase K 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 12 samples with support for all annotated introns
F-box/LRR-repeat protein 4, transcript variant X1
F-box/LRR-repeat 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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 116 samples with support for all annotated introns
uncharacterized LOC110999222, transcript variant X1
uncharacterized LOC110999222, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
uncharacterized protein LOC110999222 isoform X1
uncharacterized protein LOC110999222 isoform X2
serine-enriched protein, transcript variant X3
serine-enriched protein, 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 4 samples with support for all annotated introns
serine-enriched protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine-enriched protein, transcript variant X4
putative polypeptide N-acetylgalactosaminyltransferase 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X3
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X6
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X4
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X7
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X1
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X5
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X2
putative polypeptide N-acetylgalactosaminyltransferase 9 isoform X3
putative polypeptide N-acetylgalactosaminyltransferase 9 isoform X2
putative polypeptide N-acetylgalactosaminyltransferase 9 isoform X1
uncharacterized LOC110995234, transcript variant X3
uncharacterized LOC110995234, transcript variant X2
uncharacterized LOC110995234, 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 36 samples with support for all annotated introns
uncharacterized LOC110995234, transcript variant X4
uncharacterized protein LOC110995234 isoform X1
uncharacterized protein LOC110995234 isoform X2
leucine-rich repeat and IQ domain-containing protein 4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2-like
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
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, 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 7 samples with support for all annotated introns
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X1
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, transcript variant X2
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 7% 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 98% coverage of the annotated genomic feature by RNAseq alignments
POU domain, class 6, transcription factor 2, transcript variant X2
POU domain, class 6, transcription factor 2, transcript variant X1
POU domain, class 6, transcription factor 2, transcript variant X6
POU domain, class 6, transcription factor 2, transcript variant X4
POU domain, class 6, transcription factor 2, transcript variant X7
POU domain, class 6, transcription factor 2, transcript variant X3
POU domain, class 6, transcription factor 2 isoform X1
POU domain, class 6, transcription factor 2 isoform X5
POU domain, class 6, transcription factor 2 isoform X3
POU domain, class 6, transcription factor 1 isoform X6
POU domain, class 6, transcription factor 2 isoform X2
POU domain, class 6, transcription factor 2, transcript variant X5
POU domain, class 6, transcription factor 2 isoform X4
tyrosine-protein phosphatase non-receptor type 4, transcript variant X1
tyrosine-protein phosphatase non-receptor type 4, transcript variant X2
tyrosine-protein phosphatase non-receptor type 4 isoform X1
tyrosine-protein phosphatase non-receptor type 4 isoform X2
tyrosine-protein phosphatase non-receptor type 4, transcript variant X3
tyrosine-protein phosphatase non-receptor type 4 isoform X3
glycine-rich cell wall structural protein
BMP and activin membrane-bound inhibitor homolog, transcript variant X3
BMP and activin membrane-bound inhibitor homolog, transcript variant X1
BMP and activin membrane-bound inhibitor homolog, transcript variant X2
BMP and activin membrane-bound inhibitor homolog isoform X1
BMP and activin membrane-bound inhibitor homolog isoform X2
4-hydroxyphenylpyruvate dioxygenase, transcript variant X2
4-hydroxyphenylpyruvate dioxygenase, transcript variant X1
4-hydroxyphenylpyruvate dioxygenase isoform X1
4-hydroxyphenylpyruvate dioxygenase isoform X2
translocation protein SEC62, transcript variant X1
translocation protein SEC62, 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 16 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 16 samples with support for all annotated introns
NFX1-type zinc finger-containing protein 1 isoform X1
NFX1-type zinc finger-containing protein 1 isoform X2
uncharacterized LOC110999543, transcript variant X2
uncharacterized LOC110999543, transcript variant X1
uncharacterized protein LOC110999543 isoform X2
uncharacterized protein LOC110999543 isoform X1
4-hydroxyphenylpyruvate dioxygenase-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: 4-hydroxyphenylpyruvate dioxygenase-like
rho guanine nucleotide exchange factor 10-like protein, transcript variant X3
rho guanine nucleotide exchange factor 10-like protein, transcript variant X1
rho guanine nucleotide exchange factor 10-like protein, transcript variant X2
rho guanine nucleotide exchange factor 10-like protein, transcript variant X4
rho guanine nucleotide exchange factor 10-like protein isoform X3
rho guanine nucleotide exchange factor 10-like protein isoform X1
rho guanine nucleotide exchange factor 10-like protein isoform X2
rho guanine nucleotide exchange factor 10-like protein isoform X4
uncharacterized LOC110992381, transcript variant X5
uncharacterized LOC110992381, transcript variant X4
uncharacterized LOC110992381, transcript variant X2
uncharacterized LOC110992381, transcript variant X1
uncharacterized LOC110992381, transcript variant X3
uncharacterized protein LOC110992381 isoform X2
uncharacterized protein LOC110992381 isoform X3
uncharacterized protein LOC110992381 isoform X1
serine--pyruvate aminotransferase, mitochondrial
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 15 samples with support for all annotated introns
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6
putative tRNA (cytidine(32)/guanosine(34)-2'-O)-methyltransferase
uncharacterized LOC110992356, transcript variant X1
uncharacterized LOC110992356, transcript variant X2
uncharacterized protein LOC110992356 isoform X1
uncharacterized protein LOC110992356 isoform X2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6-like, transcript variant X1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6-like, 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 15 samples with support for all annotated introns
L-dopachrome tautomerase yellow-f2-like isoform X1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6-like isoform X2
calcium-binding protein E63-1, transcript variant X1
calcium-binding protein E63-1, transcript variant X2
calcium-binding protein E63-1, transcript variant X4
calcium-binding protein E63-1, transcript variant X3
calcium-binding protein E63-1, transcript variant X5
calcium-binding protein E63-1 isoform X2
calcium-binding protein E63-1 isoform X1
calcium-binding protein E63-1 isoform X4
calcium-binding protein E63-1 isoform X3
calcium-binding protein E63-1 isoform X5
cytoplasmic phosphatidylinositol transfer protein 1
trafficking protein particle complex subunit 13
clustered mitochondria protein homolog, transcript variant X1
clustered mitochondria protein homolog isoform X1
clustered mitochondria protein homolog, transcript variant X2
clustered mitochondria protein homolog isoform X2
ubiquitin carboxyl-terminal hydrolase calypso, transcript variant X2
ubiquitin carboxyl-terminal hydrolase calypso, transcript variant X1
ubiquitin carboxyl-terminal hydrolase calypso isoform X2
ubiquitin carboxyl-terminal hydrolase calypso isoform X1
uncharacterized LOC110992382, transcript variant X4
uncharacterized LOC110992382, transcript variant X1
uncharacterized LOC110992382, transcript variant X2
uncharacterized LOC110992382, transcript variant X3
uncharacterized LOC110992382, transcript variant X6
uncharacterized LOC110992382, transcript variant X8
uncharacterized LOC110992382, transcript variant X7
uncharacterized LOC110992382, transcript variant X5
uncharacterized protein LOC110992382 isoform X4
uncharacterized protein LOC110992382 isoform X1
uncharacterized protein LOC110992382 isoform X2
uncharacterized protein LOC110992382 isoform X3
uncharacterized protein LOC110992382 isoform X6
uncharacterized protein LOC110992382 isoform X7
uncharacterized protein LOC110992382 isoform X5
uncharacterized protein LOC110992382 isoform X8
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 47 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit Rpb4
glucocorticoid-induced transcript 1 protein, transcript variant X1
glucocorticoid-induced transcript 1 protein, transcript variant X3
glucocorticoid-induced transcript 1 protein, transcript variant X2
glucocorticoid-induced transcript 1 protein, transcript variant X4
glucocorticoid-induced transcript 1 protein isoform X4
protein suppressor of sable, transcript variant X2
protein suppressor of sable, transcript variant X3
protein suppressor of sable, transcript variant X1
protein suppressor of sable, transcript variant X4
intraflagellar transport protein 22 homolog
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
biogenesis of lysosome-related organelles complex 1 subunit 1
lysophospholipid acyltransferase 7, 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 2 samples with support for all annotated introns
lysophospholipid acyltransferase 7, transcript variant X4
lysophospholipid acyltransferase 7 isoform X1
lysophospholipid acyltransferase 7 isoform X4
lysophospholipid acyltransferase 7, transcript variant X3
lysophospholipid acyltransferase 7 isoform X3
lysophospholipid acyltransferase 7, transcript variant X2
lysophospholipid acyltransferase 7 isoform X2
G protein-coupled receptor kinase 1, transcript variant X2
G protein-coupled receptor kinase 1, transcript variant X1
G protein-coupled receptor kinase 1 isoform X2
G protein-coupled receptor kinase 1 isoform X1
ATP-binding cassette sub-family B member 6, transcript variant X1
ATP-binding cassette sub-family B member 6, transcript variant X2
ATP-binding cassette sub-family B member 6
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
uncharacterized LOC110992342, transcript variant X1
uncharacterized protein LOC110992342 isoform X1
uncharacterized LOC110992342, transcript variant X2
uncharacterized protein LOC110992342 isoform X2
integrin alpha-PS1, transcript variant X1
integrin alpha-PS1, 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
dual oxidase maturation factor 2, transcript variant X1
dual oxidase maturation factor 2, transcript variant X2
EF-hand domain-containing family member C2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: EF-hand domain-containing family member C2
vacuolar fusion protein CCZ1 homolog, 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 44 samples with support for all annotated introns
vacuolar fusion protein CCZ1 homolog, transcript variant X2
vacuolar fusion protein CCZ1 homolog, 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 20 samples with support for all annotated introns
vacuolar fusion protein CCZ1 homolog isoform X1
vacuolar fusion protein CCZ1 homolog isoform X2
vacuolar fusion protein CCZ1 homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
translocon-associated protein subunit gamma
uncharacterized LOC110992358, transcript variant X3
uncharacterized LOC110992358, 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 11 samples with support for all annotated introns
uncharacterized LOC110992358, transcript variant X1
uncharacterized protein LOC110992358 isoform X2
uncharacterized protein LOC110992358 isoform 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 15 samples with support for all annotated introns
lysosomal-associated transmembrane protein 4A, transcript variant X2
lysosomal-associated transmembrane protein 4A, transcript variant X1
lysosomal-associated transmembrane protein 4A