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LMNA - lamin A/C

  • Synonym(s) : HGPS, MADA, mandibuloacral dysplasia type A
  • Previous symbols and names : CMD1A, LGMD1B, LMN1, LMNL1, PRO1, cardiomyopathy, dilated 1A (autosomal dominant), lamin A/C-like 1, limb girdle muscular dystrophy 1B (autosomal dominant), progeria 1 (Hutchinson-Gilford type)
  • Type : gene with protein product
  • Chromosomal location : 1q22
  • OMIM: 150330
  • HGNC: 6636
  • UniProtKB: P02545
  • Genatlas: LMNA
  • GenCC: LMNA
  • Ensembl: ENSG00000160789
  • IUPHAR-DB: -
  • Reactome: P02545

Diseases list

  : Assessed

Additional information

Patient-centred resources for this gene

Specialised Social Services

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