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SLC16A1 - solute carrier family 16 member 1
- Synonym(s) : MCT, MCT1
- Previous symbols and names : Solute carrier family 16, member 1 (monocarboxylic acid transporter 1), solute carrier family 16 (monocarboxylate transporter), member 1, solute carrier family 16 (monocarboxylic acid transporters), member 1
- Type : gene with protein product
- Chromosomal location : 1p13.2
- OMIM: 600682
- HGNC: 10922
- UniProtKB: P53985
- Genatlas: SLC16A1
- Ensembl: ENSG00000155380
- IUPHAR-DB: -
- Reactome: P53985
- LOVD: SLC16A1
Diseases list
- Disease-causing germline mutation(s) in Exercise-induced hyperinsulinism
ORPHA:165991 
- Disease-causing germline mutation(s) in Metabolic myopathy due to lactate transporter defect
ORPHA:171690 - Disease-causing germline mutation(s) (loss of function) in Ketoacidosis due to monocarboxylate transporter-1 deficiency
ORPHA:438075
: 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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