KRT10

keratin 10
OMIM: 148080, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green KRT10 in Epidermolysis bullosa Level 2: Dermatological disorders Version 1.15	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Epidermolytic hyperkeratosis (MIM#113800) Ichthyosis with confetti (MIM#609165) Ichthyosis, cyclic, with epidermolytic hyperkeratosis (MIM#607602)
Green KRT10 in Ichthyosis Level 2: Dermatological disorders Version 1.11	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ichthyosis, cyclic, with epidermolytic hyperkeratosis, MIM# 607602 Ichthyosis with confetti, MIM# 609165
Green KRT10 in Mendeliome Version 1.1902	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Epidermolytic hyperkeratosis, MIM#113800 Ichthyosis with confetti, MIM#609165 Ichthyosis, cyclic, with epidermolytic hyperkeratosis, MIM#607602
Green KRT10 in Palmoplantar Keratoderma and Erythrokeratoderma Level 2: Dermatological disorders Version 0.132	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green KRT10 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Epidermolytic hyperkeratosis, 113800 (3), Autosomal recessive
Green KRT10 in Mosaic skin disorders Level 2: Dermatological disorders Version 1.12 Component of the following Super Panels: Vascular Malformations SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp NHS GMS Phenotypes Epidermolytic hyperkeratosis Pachyonychia congenita Ichythosis with confetti Palmoplantar keratoderma
Green KRT10 in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Epidermolytic hyperkeratosis, 113800 (3), Autosomal recessive