solute carrier family 24 member 5

Preferred Label : solute carrier family 24 member 5;

Approved symbol HGNC : SLC24A5;

Name synonyms HGNC : Na/Ca-K exchanger 5; oculocutaneous albinism 6 (autosomal recessive);

Alias symbols HGNC : OCA6; JSX; NCKX5;

Chromosome HGNC : 15q21.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000188467;

Details

Origin ID

HGNC:20611;

UMLS CUI

C1427030;

Automatic exact mappings (from CISMeF team)
- Albinism, oculocutaneous, type VI [OMIM Phenotype]
- Sodium/Potassium/Calcium Exchanger 5 [NCIt concept]
- Solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 [OMIM gene]
- solute carrier family 24 member 5 [ORDO Gene]
NCIt concept
- SLC24A5 Gene [NCIt concept]
OMIM gene
- Solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 [OMIM gene]
Orphanet gene
- solute carrier family 24 member 5 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC24A5 Gene [NCIt concept]
- Solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 [OMIM gene]

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