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List of intellectual disability related genes

NIPA2 - NIPA magnesium transporter 2

  • Synonym(s) : SLC57A2
  • Previous symbols and names : non imprinted in Prader-Willi/Angelman syndrome 2
  • Type : gene with protein product
  • Chromosomal location : 15q11.2
  • OMIM: 608146
  • HGNC: 17044
  • UniProtKB: Q8N8Q9
  • Genatlas: NIPA2
  • GenCC: NIPA2
  • Ensembl: ENSG00000140157
  • IUPHAR-DB: 3034
  • Reactome: Q8N8Q9
  • LOVD: NIPA2

Diseases list

  : Assessed

Additional information

Patient-centred resources for this gene

Research activities on this gene

Specialised Social Services

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