KRT10:Ensemblv90

keratin 10
OMIM: 148080, ClinGen, DECIPHER

12 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 12 panels
Green KRT10 in Epidermolysis bullosa Level 2: Dermatological disorders Version 1.22	1 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 and Porokeratosis Level 2: Dermatological disorders Version 1.23	1 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 1.3802	1 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 0.137	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green KRT10 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.111	0 reviews	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 1.15 Component of the following Super Panels: Vascular Malformations SuperPanel	2 reviews	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 2.15	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Epidermolytic hyperkeratosis 2B, autosomal recessive MIM#620707 MONDO:0700245
Green KRT10 in Epidermolysis bullosa Level 2: Dermatological disorders Version 2.0	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Literature Expert Review Green Phenotypes Epidermolytic hyperkeratosis (MIM#113800) Ichthyosis with confetti (MIM#609165) Ichthyosis, cyclic, with epidermolytic hyperkeratosis (MIM#607602)
Green KRT10 in Ichthyosis and Porokeratosis Level 2: Dermatological disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Ichthyosis, cyclic, with epidermolytic hyperkeratosis, MIM# 607602 Ichthyosis with confetti, MIM# 609165
Green KRT10 in Palmoplantar Keratoderma and Erythrokeratoderma Level 2: Dermatological disorders Version 1.0	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services
Green KRT10 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 1.0	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Mackenzie's Mission Expert Review Green Phenotypes Epidermolytic hyperkeratosis, 113800 (3), Autosomal recessive
Green KRT10 in Prepair 1000+ Level 2: Screening Version 3.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Mackenzie's Mission Expert Review Green Phenotypes Epidermolytic hyperkeratosis 2B, autosomal recessive MIM#620707 MONDO:0700245