CHUK

component of inhibitor of nuclear factor kappa B kinase complex
OMIM: 600664, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green CHUK in Mendeliome


Version 2.0

2 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Combined immunodeficiency, MONDO:0015131, CHUK-related
  • Popliteal pterygium syndrome, Bartsocas-Papas type 2, MIM# 619339
  • Cocoon syndrome, MIM# 613630
  • AEC-like syndrome

Green CHUK in Combined Immunodeficiency


Level 2: Immunological disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Combined immunodeficiency, MONDO:0015131, CHUK-related

Amber CHUK in Hand and foot malformations


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.0

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
  • Victorian Clinical Genetics Services
Phenotypes
  • ?Popliteal pterygium syndrome, Bartsocas-Papas type 2 MIM#619339
  • Cocoon syndrome MIM#613630

Amber CHUK in Fetal anomalies


Version 2.0

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Genomics England PanelApp
Phenotypes
  • Popliteal pterygium syndrome, Bartsocas-Papas type 2, MIM# 619339
  • Cocoon syndrome, MIM# 613630
  • AEC-like syndrome