Activity

Filter

Cancel
Date Panel Item Activity
8 actions
Congenital diaphragmatic hernia v0.74 SMC1A Zornitza Stark Marked gene: SMC1A as ready
Congenital diaphragmatic hernia v0.74 SMC1A Zornitza Stark Gene: smc1a has been classified as Amber List (Moderate Evidence).
Congenital diaphragmatic hernia v0.74 SMC1A Zornitza Stark Phenotypes for gene: SMC1A were changed from to Cornelia de Lange syndrome 2, MIM# 300590
Congenital diaphragmatic hernia v0.73 SMC1A Zornitza Stark Mode of inheritance for gene: SMC1A was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Congenital diaphragmatic hernia v0.72 SMC1A Zornitza Stark Classified gene: SMC1A as Amber List (moderate evidence)
Congenital diaphragmatic hernia v0.72 SMC1A Zornitza Stark Gene: smc1a has been classified as Amber List (Moderate Evidence).
Congenital diaphragmatic hernia v0.71 SMC1A Zornitza Stark reviewed gene: SMC1A: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Cornelia de Lange syndrome 2, MIM# 300590; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Congenital diaphragmatic hernia v0.0 SMC1A Zornitza Stark gene: SMC1A was added
gene: SMC1A was added to Congenital diaphragmatic hernia, CDH_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: SMC1A was set to Unknown