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Interstitial Lung Disease v0.135 ASCL1 Suzanna Lindsey-Temple reviewed gene: ASCL1: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 14532329; Phenotypes: MIM# Congenital central hypoventilation syndrome, Neonatal respiratory distress syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Interstitial Lung Disease v0.119 ASCL1 Zornitza Stark Marked gene: ASCL1 as ready
Interstitial Lung Disease v0.119 ASCL1 Zornitza Stark Gene: ascl1 has been classified as Amber List (Moderate Evidence).
Interstitial Lung Disease v0.119 ASCL1 Zornitza Stark Phenotypes for gene: ASCL1 were changed from to Central hypoventilation syndrome, congenital, MIM# 209880
Interstitial Lung Disease v0.118 ASCL1 Zornitza Stark Publications for gene: ASCL1 were set to
Interstitial Lung Disease v0.117 ASCL1 Zornitza Stark Mode of inheritance for gene: ASCL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Interstitial Lung Disease v0.116 ASCL1 Zornitza Stark Classified gene: ASCL1 as Amber List (moderate evidence)
Interstitial Lung Disease v0.116 ASCL1 Zornitza Stark Gene: ascl1 has been classified as Amber List (Moderate Evidence).
Interstitial Lung Disease v0.0 ASCL1 Zornitza Stark gene: ASCL1 was added
gene: ASCL1 was added to Interstitial Lung Disease_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ASCL1 was set to Unknown