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BabyScreen+ newborn screening v1.114 KCNH2 Tommy Li Added phenotypes Long QT syndrome 2, MIM# 613688 for gene: KCNH2
BabyScreen+ newborn screening v0.1848 KCNH2 Zornitza Stark Classified gene: KCNH2 as Green List (high evidence)
BabyScreen+ newborn screening v0.1848 KCNH2 Zornitza Stark Gene: kcnh2 has been classified as Green List (High Evidence).
BabyScreen+ newborn screening v0.1847 KCNH2 Zornitza Stark Tag for review was removed from gene: KCNH2.
BabyScreen+ newborn screening v0.1847 KCNH2 Zornitza Stark edited their review of gene: KCNH2: Changed rating: GREEN
BabyScreen+ newborn screening v0.1762 KCNH2 Zornitza Stark Marked gene: KCNH2 as ready
BabyScreen+ newborn screening v0.1762 KCNH2 Zornitza Stark Gene: kcnh2 has been classified as Amber List (Moderate Evidence).
BabyScreen+ newborn screening v0.1762 KCNH2 Zornitza Stark Phenotypes for gene: KCNH2 were changed from Long QT syndrome-2 to Long QT syndrome 2, MIM# 613688
BabyScreen+ newborn screening v0.1761 KCNH2 Zornitza Stark Tag for review tag was added to gene: KCNH2.
Tag cardiac tag was added to gene: KCNH2.
Tag treatable tag was added to gene: KCNH2.
BabyScreen+ newborn screening v0.1761 KCNH2 Zornitza Stark reviewed gene: KCNH2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Long QT syndrome 2, MIM# 613688; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.0 KCNH2 Zornitza Stark gene: KCNH2 was added
gene: KCNH2 was added to gNBS. Sources: Expert Review Amber,BabySeq Category B gene
Mode of inheritance for gene: KCNH2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: KCNH2 were set to Long QT syndrome-2