KRT32

keratin 32
OMIM: 602760, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green KRT32 in Mendeliome


Version 1.3050

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • loose anagen syndrome MONDO:0010908
  • Pityriasis rubra pilaris MONDO:0100017

Green KRT32 in Palmoplantar Keratoderma and Erythrokeratoderma


Level 2: Dermatological disorders
Version 0.136

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Pityriasis rubra pilaris MONDO:0100017

Red KRT32 in Hair disorders


Level 2: Dermatological disorders
Version 0.81

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • loose anagen syndrome MONDO:0010908