KCNC2

potassium voltage-gated channel subfamily C member 2
OMIM: 176256
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R59
Signed-off version 6.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
epileptic encephalopathy, spastic tetraplegia, opisthotonus attacks, intellectual disability, West syndrome