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BSND - barttin CLCNK type accessory beta subunit

  • Synonym(s) : BART
  • Previous symbols and names : Bartter syndrome, infantile, with sensorineural deafness (Barttin), DFNB73, deafness, autosomal recessive 73
  • Type : gene with protein product
  • Chromosomal location : 1p32.3
  • OMIM: 606412
  • HGNC: 16512
  • UniProtKB: Q8WZ55
  • Genatlas: BSND
  • Ensembl: ENSG00000162399
  • IUPHAR-DB: -
  • Reactome: Q8WZ55
  • LOVD: BSND

Diseases list

  : Assessed

Additional information

Health care resources for this gene

Specialised Social Services

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