EBP

GENERAL INFORMATION

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Gene name

EBP

Gene description

Emopamil binding protein (sterol isomerase)

Protein class

Disease related genes
Enzymes
Potential drug targets
Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Leydig cells of testis displayed strong cytoplasmic staining, while cells of the gastrointestinal tract were moderately positive. Remaining normal tissues were in general negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA003130
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

EBP (HGNC Symbol)

Synonyms

CDPX2, CHO2, CPX, CPXD

Description

Emopamil binding protein (sterol isomerase) (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is an integral membrane protein of the endoplasmic reticulum. It is a high affinity binding protein for the antiischemic phenylalkylamine Ca2+ antagonist [3H]emopamil and the photoaffinity label [3H]azidopamil. It is similar to sigma receptors and may be a member of a superfamily of high affinity drug-binding proteins in the endoplasmic reticulum of different tissues. This protein shares structural features with bacterial and eukaryontic drug transporting proteins. It has four putative transmembrane segments and contains two conserved glutamate residues which may be involved in the transport of cationic amphiphilics. Another prominent feature of this protein is its high content of aromatic amino acid residues (>23%) in its transmembrane segments. These aromatic amino acid residues have been suggested to be involved in the drug transport by the P-glycoprotein. Mutations in this gene cause Chondrodysplasia punctata 2 (CDPX2; also known as Conradi-Hunermann syndrome). [provided by RefSeq, Jul 2008]

Chromosome

X

Cytoband

p11.23

Chromosome location (bp)

48521158 - 48528716

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000147155 (version 78.38)

Entrez gene

10682

UniProt

Q15125 (UniProt - Evidence at protein level)

neXtProt

NX_Q15125

Antibodypedia

EBP antibodies


PROTEIN BROWSER

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ENST00000414061
 
ENST00000446158
 
ENST00000495186
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

EBP-001 ENSP00000390031
ENST00000446158
C9JJ78
Show all »
Show » Show » 160 18.3 No 3
EBP-004 ENSP00000417052
ENST00000495186
Q15125
Show all »
Show » Show » 230 26.4 No 5
EBP-005 ENSP00000405832
ENST00000414061
C9J719
Show all »
Show » Show » 146 16.7 No 3