Activity

Filter

Cancel
Date Panel Item Activity
5 actions
Rare genetic inflammatory skin disorders v0.22 DCLRE1C Catherine Snow Source Expert Review Amber was added to DCLRE1C.
Added phenotypes Omenn syndrome for gene: DCLRE1C
Publications for gene DCLRE1C were changed from to 15731174
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Rare genetic inflammatory skin disorders v0.21 DCLRE1C Tom Cullup reviewed gene: DCLRE1C: Rating: AMBER; Mode of pathogenicity: ; Publications: 15731174; Phenotypes: Omenn syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Rare genetic inflammatory skin disorders v0.5 DCLRE1C Rebecca Foulger Source London North GLH was added to DCLRE1C.
Rare genetic inflammatory skin disorders v0.4 DCLRE1C Rebecca Foulger reviewed gene: DCLRE1C: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Rare genetic inflammatory skin disorders v0.3 DCLRE1C Rebecca Foulger gene: DCLRE1C was added
gene: DCLRE1C was added to Rare genetic inflammatory skin disorders. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: DCLRE1C was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: DCLRE1C were set to Omenn syndrome