Search for a gene
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 
: AssessedAdditional information
Health care resources for this gene
Research activities on this gene
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.