PRKCI

protein kinase C iota
OMIM: 600539, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber PRKCI in Clefting


Level 2: Musculoskeletal
Version 6.20
Latest signed off version: v6.5 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Other
    Phenotypes
    • van der Woude syndrome, MONDO:0019508
    • orofacial cleft, MONDO:0000358
    Tags
    • Q4_25_promote_green