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Severe Paediatric Disorders v0.17 | KRT5 | Louise Daugherty Mode of inheritance for gene KRT5 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.12 | KRT5 | Louise Daugherty reviewed gene: KRT5: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.11 | KRT5 | Louise Daugherty Publications for gene KRT5 were updated from to 30847515 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.10 | KRT5 | Louise Daugherty Added phenotypes Epidermolysis bullosa simplex, Weber-Cockayne type, 131800; Epidermolysis bullosa simplex, Koebner type, 131900; Dowling-Degos disease 1, 179850; Epidermolysis bullosa simplex-MCR, 609352; Epidermolysis bullosa simplex, Dowling-Meara type, 131760; Epidermolysis bullosa simplex-MP, 131960; Epidermolysis bullosa simplex, recessive 1, 601001 for gene: KRT5 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.9 | KRT5 | Louise Daugherty Added phenotypes Epidermolysis bullosa simplex, Weber-Cockayne type, 131800; Epidermolysis bullosa simplex, Koebner type, 131900; Dowling-Degos disease 1, 179850; Epidermolysis bullosa simplex-MCR, 609352; Epidermolysis bullosa simplex, Dowling-Meara type, 131760; Epidermolysis bullosa simplex-MP, 131960; Epidermolysis bullosa simplex, recessive 1, 601001 for gene: KRT5 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.9 | KRT5 | Louise Daugherty Added phenotypes Epidermolysis bullosa simplex, Weber-Cockayne type, 131800; Epidermolysis bullosa simplex, Koebner type, 131900; Dowling-Degos disease 1, 179850; Epidermolysis bullosa simplex-MCR, 609352; Epidermolysis bullosa simplex, Dowling-Meara type, 131760; Epidermolysis bullosa simplex-MP, 131960; Epidermolysis bullosa simplex, recessive 1, 601001 for gene: KRT5 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.8 | KRT5 | Louise Daugherty Added phenotypes Epidermolysis bullosa simplex-MCR, 609352; Epidermolysis bullosa simplex, Weber-Cockayne type, 131800; Epidermolysis bullosa simplex, recessive 1, 601001; Epidermolysis bullosa simplex, Koebner type, 131900; Epidermolysis bullosa simplex, Dowling-Meara type, 131760; Dowling-Degos disease 1, 179850; Epidermolysis bullosa simplex-MP, 131960 for gene: KRT5 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.7 | KRT5 | Louise Daugherty Source Next Generation Children Project was added to KRT5. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.5 | KRT5 |
Louise Daugherty Source Expert Review Green was added to KRT5. Rating Changed from Red List (low evidence) to Green List (high evidence) |
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Severe Paediatric Disorders v0.4 | KRT5 |
Louise Daugherty gene: KRT5 was added gene: KRT5 was added to Severe Paediatric Disorders. Sources: Expert list Mode of inheritance for gene: KRT5 was set to |