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LRTOMT - leucine rich transmembrane and O-methyltransferase domain containing

  • Synonym(s) : CFAP111, COMT2
  • Previous symbols and names : DFNB63, LRRC51, deafness, autosomal recessive 63, leucine rich repeat containing 51
  • Type : gene with protein product
  • Chromosomal location : 11q13.4
  • OMIM: 612414
  • HGNC: 25033
  • UniProtKB: Q8WZ04
  • Genatlas: LRTOMT
  • Ensembl: ENSG00000184154
  • IUPHAR-DB: -
  • Reactome: Q8WZ04
  • LOVD: LRTOMT

Diseases list

  : Assessed

Additional information

Health care resources for this gene

Specialised Social Services

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