ATP2B2

ATPase plasma membrane Ca2+ transporting 2
OMIM: 108733
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.79
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
{Deafness, autosomal recessive 12, modifier of}, OMIM:601386, Deafness, autosomal dominant 82, OMIM:619804, hearing loss, autosomal dominant 82, MONDO:0030719