CD2AP

CD2 associated protein
OMIM: 604241, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red CD2AP in Unexplained kidney failure in young people

Level 3: Disorders of function
Level 2: Renal and urinary tract disorders
Version 1.124

review Not set
Sources
  • Eligibility statement prior genetic testing
Amber CD2AP in Proteinuric renal disease


Level 2: Renal
Version 5.7
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Unexplained young onset end-stage renal disease
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • NHS GMS
    • Eligibility statement prior genetic testing
    Phenotypes
    • Glomerulosclerosis, focal segmental, 3, OMIM:607832
    • focal segmental glomerulosclerosis 3, susceptibility to, MONDO:0011917
    Tags
    • Q3_25_promote_green