KRT6B

keratin 6B
OMIM: 148042, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green KRT6B in Epidermolysis bullosa


Level 2: Dermatological disorders
Version 1.24

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Pachyonychia congenita 4 MIM#615728

Green KRT6B in Mendeliome


Version 1.4216

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Pachyonychia congenita 4 (MIM#615728)

Green KRT6B in Palmoplantar Keratoderma and Erythrokeratoderma


Level 2: Dermatological disorders
Version 0.141

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Pachyonychia congenita 4 (MIM#615728)

Red KRT6B in Additional findings_Paediatric


Level 2: Screening
Version 0.280

0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Pachyonychia congenita

Red KRT6B in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 1.147

0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Pachyonychia congenita