Activity

Filter

Cancel
Date Panel Item Activity
10 actions
Severe Paediatric Disorders v0.17 CNOT3 Louise Daugherty Mode of inheritance for gene CNOT3 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Severe Paediatric Disorders v0.12 CNOT3 Louise Daugherty reviewed gene: CNOT3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 CNOT3 Louise Daugherty Publications for gene CNOT3 were updated from to 30847515
Severe Paediatric Disorders v0.10 CNOT3 Louise Daugherty Added phenotypes CNOT3 syndrome for gene: CNOT3
Severe Paediatric Disorders v0.9 CNOT3 Louise Daugherty Added phenotypes CNOT3 syndrome for gene: CNOT3
Severe Paediatric Disorders v0.9 CNOT3 Louise Daugherty Added phenotypes CNOT3 syndrome for gene: CNOT3
Severe Paediatric Disorders v0.8 CNOT3 Louise Daugherty Added phenotypes CNOT3 syndrome for gene: CNOT3
Severe Paediatric Disorders v0.7 CNOT3 Louise Daugherty Source Next Generation Children Project was added to CNOT3.
Severe Paediatric Disorders v0.5 CNOT3 Louise Daugherty Source Expert Review Green was added to CNOT3.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 CNOT3 Louise Daugherty gene: CNOT3 was added
gene: CNOT3 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: CNOT3 was set to