Bcs1 homolog, ubiquinol-cytochrome C reductase complex chaperone

Preferred Label : Bcs1 homolog, ubiquinol-cytochrome C reductase complex chaperone;

Symbol : BCS1L;

CISMeF acronym : BCS1L;

Type : Gene;

Alternative titles and symbols : Bcs1, s. cerevisiae, homolog-like;

Ensembl ID : ENSG00000074582;

Prefixed ID : *603647;

Details

Origin ID

603647;

UMLS CUI

C1412777;

Automatic exact mappings (from CISMeF team)
- BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone [ORDO Gene]
- BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone [HGNC gene]
- BCS1L gene [LOINC component]
HGNC gene
- BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone [HGNC gene]
ORDO concept(s)
- BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone [ORDO Gene]
Phenotypes related
- Bjornstad syndrome [OMIM Phenotype]
- Gracile syndrome [OMIM Phenotype]
- Mitochondrial complex III deficiency, nuclear type 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone [HGNC gene]
- BCS1L gene [LOINC component]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients