Activity

Filter

Cancel
Date Panel Item Activity
10 actions
Severe Paediatric Disorders v0.17 CNKSR2 Louise Daugherty Mode of inheritance for gene CNKSR2 was changed from to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Severe Paediatric Disorders v0.12 CNKSR2 Louise Daugherty reviewed gene: CNKSR2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 CNKSR2 Louise Daugherty Publications for gene CNKSR2 were updated from to 30847515
Severe Paediatric Disorders v0.10 CNKSR2 Louise Daugherty Added phenotypes Mental retardation, X-linked, syndromic, Houge type, 301008 for gene: CNKSR2
Severe Paediatric Disorders v0.9 CNKSR2 Louise Daugherty Added phenotypes Mental retardation, X-linked, syndromic, Houge type, 301008 for gene: CNKSR2
Severe Paediatric Disorders v0.9 CNKSR2 Louise Daugherty Added phenotypes Mental retardation, X-linked, syndromic, Houge type, 301008 for gene: CNKSR2
Severe Paediatric Disorders v0.8 CNKSR2 Louise Daugherty Added phenotypes Mental retardation, X-linked, syndromic, Houge type, 301008 for gene: CNKSR2
Severe Paediatric Disorders v0.7 CNKSR2 Louise Daugherty Source Next Generation Children Project was added to CNKSR2.
Severe Paediatric Disorders v0.5 CNKSR2 Louise Daugherty Source Expert Review Green was added to CNKSR2.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 CNKSR2 Louise Daugherty gene: CNKSR2 was added
gene: CNKSR2 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: CNKSR2 was set to