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SLC22A5 - solute carrier family 22 member 5
- Synonym(s) : OCTN2, SCD
- Previous symbols and names : CDSP, solute carrier family 22 (organic cation/carnitine transporter), member 5
- Type : gene with protein product
- Chromosomal location : 5q31.1
- OMIM: 603377
- HGNC: 10969
- UniProtKB: O76082
- Genatlas: SLC22A5
- Ensembl: ENSG00000197375
- IUPHAR-DB: -
- Reactome: O76082
- LOVD: SLC22A5
Diseases list
- Disease-causing germline mutation(s) in Systemic primary carnitine deficiency
ORPHA:158 
: AssessedGene included in a panel of genes performed as part of a diagnostic test
Additional information
Health care resources for this gene
Research activities on this gene
Specialised Social Services
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