PRKCB

protein kinase C beta
OMIM: 176970, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber PRKCB in Familial Meniere Disease

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.3

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
  • Other
Phenotypes
  • Meniere disease
Tags
  • watchlist
  • multifactorial
Red PRKCB in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI