Activity

Filter

Cancel
Date Panel Item Activity
5 actions
Structural eye disease v0.76 TRIM32 Nicola Ragge reviewed gene: TRIM32: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Bardet-Biedl syndrome 11, Muscular dystrophy, limb-girdle, type 2H, 615988, 254110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Structural eye disease v0.48 TRIM32 Ivone Leong edited their review of gene: TRIM32: Changed phenotypes: Bardet-Biedl syndrome 11, 615988, Muscular dystrophy, limb-girdle, type 2H, 254110
Structural eye disease v0.38 TRIM32 Ivone Leong reviewed gene: TRIM32: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ANIRIDIA 3, 617142; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Structural eye disease v0.15 TRIM32 Ivone Leong Source NHS GMS was added to TRIM32.
Mode of inheritance for gene TRIM32 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Bardet-Biedl syndrome 11, 615988; Muscular dystrophy, limb-girdle, type 2H, 254110 for gene: TRIM32
Structural eye disease v0.2 TRIM32 Ellen McDonagh gene: TRIM32 was added
gene: TRIM32 was added to Structural eye disease. Sources: Expert Review Red
Mode of inheritance for gene: TRIM32 was set to
Phenotypes for gene: TRIM32 were set to Eye Disorders