KCNN4

potassium calcium-activated channel subfamily N member 4
OMIM: 602754, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green KCNN4 in Rare anaemia


Version 3.8
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • North West GLH
  • Yorkshire and North East GLH
  • London South GLH
  • NHS GMS
  • Expert Review Green
  • Wessex and West Midlands GLH
Phenotypes
  • 616689 Dehydrated hereditary stomatocytosis 2
  • Hereditary Xerocytosis