Genomics England
GMS Panels
Panels
Genes and Entities

NFKB2

nuclear factor kappa B subunit 2
OMIM: 164012
PanelMode of inheritanceDetails
3 panels
Green
in Ectodermal dysplasia
R-numbers: R163
Signed-off version 3.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Immunodeficiency, common variable, 10 615577
Green
in Primary immunodeficiency or monogenic inflammatory bowel disease
R-numbers: R15
Signed-off version 6.12
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Immunodeficiency, common variable, 10 615577, Hypogammaglobuliaemia, immune dysregulation, central adrenal insufficiency, Common variable immunodeficiency disorders (CVID), Unclassified antibody deficiency, Recurrent sinopulmonary infections, alopecia and endorinopathies, Predominantly Antibody Deficiencies
Green
in Respiratory ciliopathies including non-CF bronchiectasis
R-numbers: R189
Signed-off version 3.10
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Immunodeficiency, common variable, 10, 615577, Bronchiectasis