Bos taurus Gene: EBP
Summary
InnateDB Gene IDBG-636808.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol EBP
Gene Name 3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000009287
Encoded Proteins
3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000147155:
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]
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]
Gene Information
Type Protein coding
Genomic Location Chromosome X:91735333-91739378
Strand Forward strand
Band
Transcripts
ENSBTAT00000012234 ENSBTAP00000012234
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 5 interaction(s) predicted by orthology.
Predicted by orthology
Total 5 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000247 C-8 sterol isomerase activity
GO:0016853 isomerase activity
GO:0047750 cholestenol delta-isomerase activity
Biological Process
GO:0016125 sterol metabolic process
GO:0016126 sterol biosynthetic process
GO:0030097 hemopoiesis
Cellular Component
GO:0005783 endoplasmic reticulum
GO:0016021 integral component of membrane
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Cholesterol biosynthesis pathway
Metabolism of lipids and lipoproteins pathway
Metabolism pathway
Metabolism pathway
Metabolism of lipids and lipoproteins pathway
Cholesterol biosynthesis pathway
KEGG
Steroid biosynthesis pathway
Steroid biosynthesis pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL Q3ZBT8
UniProt Splice Variant
Entrez Gene 515569
UniGene Bt.49356
RefSeq NM_001034500
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC103111 DAAA02073060
GenPept AAI03112
RNA Seq Atlas 515569