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| Severe Paediatric Disorders v0.17 | KRT14 | Louise Daugherty Mode of inheritance for gene KRT14 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe Paediatric Disorders v0.12 | KRT14 | Louise Daugherty reviewed gene: KRT14: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe Paediatric Disorders v0.11 | KRT14 | Louise Daugherty Publications for gene KRT14 were updated from to 30847515 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe Paediatric Disorders v0.10 | KRT14 | Louise Daugherty Added phenotypes Epidermolysis bullosa simplex, Weber-Cockayne type, 131800; Dermatopathia pigmentosa reticularis, 125595; Epidermolysis bullosa simplex, Koebner type, 131900; Naegeli-Franceschetti-Jadassohn syndrome, 161000; Epidermolysis bullosa simplex, Dowling-Meara type, 131760; Epidermolysis bullosa simplex, recessive 1, 601001 for gene: KRT14 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe Paediatric Disorders v0.9 | KRT14 | Louise Daugherty Added phenotypes Epidermolysis bullosa simplex, Weber-Cockayne type, 131800; Dermatopathia pigmentosa reticularis, 125595; Epidermolysis bullosa simplex, Koebner type, 131900; Naegeli-Franceschetti-Jadassohn syndrome, 161000; Epidermolysis bullosa simplex, Dowling-Meara type, 131760; Epidermolysis bullosa simplex, recessive 1, 601001 for gene: KRT14 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe Paediatric Disorders v0.9 | KRT14 | Louise Daugherty Added phenotypes Epidermolysis bullosa simplex, Weber-Cockayne type, 131800; Dermatopathia pigmentosa reticularis, 125595; Epidermolysis bullosa simplex, Koebner type, 131900; Naegeli-Franceschetti-Jadassohn syndrome, 161000; Epidermolysis bullosa simplex, Dowling-Meara type, 131760; Epidermolysis bullosa simplex, recessive 1, 601001 for gene: KRT14 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe Paediatric Disorders v0.8 | KRT14 | Louise Daugherty Added phenotypes Epidermolysis bullosa simplex, Weber-Cockayne type, 131800; Naegeli-Franceschetti-Jadassohn syndrome, 161000; Dermatopathia pigmentosa reticularis, 125595; Epidermolysis bullosa simplex, recessive 1, 601001; Epidermolysis bullosa simplex, Koebner type, 131900; Epidermolysis bullosa simplex, Dowling-Meara type, 131760 for gene: KRT14 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe Paediatric Disorders v0.7 | KRT14 | Louise Daugherty Source Next Generation Children Project was added to KRT14. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe Paediatric Disorders v0.5 | KRT14 |
Louise Daugherty Source Expert Review Green was added to KRT14. Rating Changed from Red List (low evidence) to Green List (high evidence) |
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| Severe Paediatric Disorders v0.4 | KRT14 |
Louise Daugherty gene: KRT14 was added gene: KRT14 was added to Severe Paediatric Disorders. Sources: Expert list Mode of inheritance for gene: KRT14 was set to |
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