solute carrier family 22 member 5

Preferred Label : solute carrier family 22 member 5;

Approved symbol HGNC : SLC22A5;

Name synonyms HGNC : systemic carnitine deficiency; organic cation/carnitine transporter 2;

Alias symbols HGNC : SCD; OCTN2;

Chromosome HGNC : 5q31.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000197375;

Details

Origin ID

HGNC:10969;

UMLS CUI

C1420140;

Automatic exact mappings (from CISMeF team)
- Solute Carrier Family 22 Member 5 [MeSH Descriptor]
- Solute carrier family 22 (organic cation transporter), member 5 [OMIM gene]
- Stearoyl-coa desaturase [OMIM gene]
NCIt concept
- SLC22A5 Gene [NCIt concept]
OMIM gene
- Solute carrier family 22 (organic cation transporter), member 5 [OMIM gene]
Orphanet gene
- solute carrier family 22 member 5 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC22A5 gene [LOINC component]
- Solute carrier family 22 (organic cation transporter), member 5 [OMIM gene]

Keyword's position in hierarchy(ies) :

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