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PSAP - prosaposin

  • Synonym(s) : variant Gaucher disease and variant metachromatic leukodystrophy
  • Previous symbols and names : GLBA, SAP1, sphingolipid activator protein-1
  • Type : gene with protein product
  • Chromosomal location : 10q22.1
  • OMIM: 176801
  • HGNC: 9498
  • UniProtKB: P07602
  • Genatlas: PSAP
  • Ensembl: ENSG00000197746
  • IUPHAR-DB: -
  • Reactome: P07602
  • LOVD: PSAP

Diseases list

  : Assessed

Additional information

Health care resources for this gene

Specialised Social Services

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