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Genomic newborn screening: BabyScreen+ v1.119 KCNE2 Zornitza Stark Marked gene: KCNE2 as ready
Genomic newborn screening: BabyScreen+ v1.119 KCNE2 Zornitza Stark Gene: kcne2 has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v1.119 KCNE2 Zornitza Stark Phenotypes for gene: KCNE2 were changed from Long QT syndrome-6 to Long QT syndrome 6, MIM# 613693
Genomic newborn screening: BabyScreen+ v1.118 KCNE2 Zornitza Stark Classified gene: KCNE2 as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v1.118 KCNE2 Zornitza Stark Gene: kcne2 has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v1.117 KCNE2 Zornitza Stark edited their review of gene: KCNE2: Changed phenotypes: Long QT syndrome 6, MIM# 613693
Genomic newborn screening: BabyScreen+ v1.117 KCNE2 Zornitza Stark reviewed gene: KCNE2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genomic newborn screening: BabyScreen+ v0.0 KCNE2 Zornitza Stark gene: KCNE2 was added
gene: KCNE2 was added to gNBS. Sources: Expert Review Amber,BabySeq Category B gene
Mode of inheritance for gene: KCNE2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: KCNE2 were set to Long QT syndrome-6