Activity

Filter

Cancel
Date Panel Item Activity
10 actions
Severe Paediatric Disorders v0.12 RTN2 Louise Daugherty reviewed gene: RTN2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 RTN2 Louise Daugherty Publications for gene RTN2 were updated from to 30847515
Severe Paediatric Disorders v0.10 RTN2 Louise Daugherty Added phenotypes Spastic paraplegia 12, autosomal dominant, 604805 for gene: RTN2
Severe Paediatric Disorders v0.9 RTN2 Louise Daugherty Added phenotypes Spastic paraplegia 12, autosomal dominant, 604805 for gene: RTN2
Severe Paediatric Disorders v0.9 RTN2 Louise Daugherty Added phenotypes Spastic paraplegia 12, autosomal dominant, 604805 for gene: RTN2
Severe Paediatric Disorders v0.8 RTN2 Louise Daugherty Added phenotypes Spastic paraplegia 12, autosomal dominant, 604805 for gene: RTN2
Severe Paediatric Disorders v0.8 RTN2 Louise Daugherty Mode of inheritance for gene RTN2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Spastic paraplegia 12, autosomal dominant, 604805 for gene: RTN2
Severe Paediatric Disorders v0.7 RTN2 Louise Daugherty Source Next Generation Children Project was added to RTN2.
Severe Paediatric Disorders v0.5 RTN2 Louise Daugherty Source Expert Review Green was added to RTN2.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 RTN2 Louise Daugherty gene: RTN2 was added
gene: RTN2 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: RTN2 was set to