Activity

Filter

Cancel
Date Panel Item Activity
10 actions
Severe Paediatric Disorders v0.17 ACTG2 Louise Daugherty Mode of inheritance for gene ACTG2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Severe Paediatric Disorders v0.12 ACTG2 Louise Daugherty reviewed gene: ACTG2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 ACTG2 Louise Daugherty Publications for gene ACTG2 were updated from to 30847515
Severe Paediatric Disorders v0.10 ACTG2 Louise Daugherty Added phenotypes Visceral myopathy, 155310 for gene: ACTG2
Severe Paediatric Disorders v0.9 ACTG2 Louise Daugherty Added phenotypes Visceral myopathy, 155310 for gene: ACTG2
Severe Paediatric Disorders v0.9 ACTG2 Louise Daugherty Added phenotypes Visceral myopathy, 155310 for gene: ACTG2
Severe Paediatric Disorders v0.8 ACTG2 Louise Daugherty Added phenotypes Visceral myopathy, 155310 for gene: ACTG2
Severe Paediatric Disorders v0.7 ACTG2 Louise Daugherty Source Next Generation Children Project was added to ACTG2.
Severe Paediatric Disorders v0.5 ACTG2 Louise Daugherty Source Expert Review Green was added to ACTG2.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 ACTG2 Louise Daugherty gene: ACTG2 was added
gene: ACTG2 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: ACTG2 was set to