PRKCZ

protein kinase C zeta
OMIM: 176982, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list PRKCZ in Retinal disorders


Level 2: Ophthalmology
Version 9.19
Latest signed off version: v9.14 (12 Aug 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • retinal dystrophy
  • retinitis pigmentosa