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SLC16A2 - solute carrier family 16 member 2

  • Synonym(s) : MCT7, MCT8, XPCT
  • Previous symbols and names : 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
  • Ensembl: ENSG00000147100
  • IUPHAR-DB: -
  • Reactome: P36021
  • LOVD: SLC16A2

Diseases list

  : Assessed

Gene included in a panel of genes performed as part of a diagnostic test

Additional information

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