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SLC16A2 - solute carrier family 16 member 2
- Synonym(s) : MCT7, MCT8, XPCT
- Previous symbols and names : 'solute carrier family 16, member 2 (monocarboxylic acid transporter 8)', AHDS, Allan-Herndon-Dudley syndrome, DXS128, MRX22, Solute carrier family 16, member 2 (monocarboxylic acid transporter 8), mental retardation, X-linked 22, solute carrier family 16 (monocarboxylic acid transporters), member 2, solute carrier family 16 (monocarboxylic acid transporters), member 2 (putative transporter), solute carrier family 16, member 2 (thyroid hormone transporter)
- Type : gene with protein product
- Chromosomal location : Xq13.2
- OMIM: 300095
- HGNC: 10923
- UniProtKB: P36021
- Genatlas: SLC16A2
- GenCC: SLC16A2
- Ensembl: ENSG00000147100
- IUPHAR-DB: 992
- Reactome: P36021
- LOVD: SLC16A2
Diseases list
- Disease-causing germline mutation(s) in Allan-Herndon-Dudley syndrome
ORPHA:59 
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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