KRT32:Ensemblv90

keratin 32
OMIM: 602760, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green KRT32 in Mendeliome


Version 1.3802

1 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 0.137

1 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

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

Green KRT32 in Palmoplantar Keratoderma and Erythrokeratoderma


Level 2: Dermatological disorders
Version 1.0

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