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FA2H - fatty acid 2-hydroxylase

  • Synonym(s) : FAAH, fatty acid hydroxylase, FLJ25287
  • Previous symbols and names : FAXDC1, SPG35, fatty acid hydroxylase domain containing 1, spastic paraplegia 35 (autosomal recessive)
  • Type : gene with protein product
  • Chromosomal location : 16q23.1
  • OMIM: 611026
  • HGNC: 21197
  • UniProtKB: Q7L5A8
  • Genatlas: FA2H
  • GenCC: FA2H
  • Ensembl: ENSG00000103089
  • IUPHAR-DB: -
  • Reactome: Q7L5A8
  • LOVD: FA2H

Diseases list

  : Assessed

Additional information

Patient-centred resources for this gene

Specialised Social Services

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