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Genomic newborn screening: BabyScreen+ v1.98 SCNN1G Zornitza Stark Marked gene: SCNN1G as ready
Genomic newborn screening: BabyScreen+ v1.98 SCNN1G Zornitza Stark Gene: scnn1g has been classified as Green List (High Evidence).
Genomic newborn screening: BabyScreen+ v1.98 SCNN1G Zornitza Stark Phenotypes for gene: SCNN1G were changed from Pseudohypoaldosteronism, type I, MIM# 264350; Pseudohypoaldosteronism to Pseudohypoaldosteronism, type I, MIM# 264350
Genomic newborn screening: BabyScreen+ v1.97 SCNN1G Zornitza Stark Classified gene: SCNN1G as Green List (high evidence)
Genomic newborn screening: BabyScreen+ v1.97 SCNN1G Zornitza Stark Gene: scnn1g has been classified as Green List (High Evidence).
Genomic newborn screening: BabyScreen+ v1.96 SCNN1G Zornitza Stark Tag treatable tag was added to gene: SCNN1G.
Tag endocrine tag was added to gene: SCNN1G.
Genomic newborn screening: BabyScreen+ v1.96 SCNN1G Zornitza Stark reviewed gene: SCNN1G: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pseudohypoaldosteronism, type I, MIM# 264350; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.0 SCNN1G Zornitza Stark Source Expert Review Red was added to SCNN1G.
Source BabySeq Category C gene was added to SCNN1G.
Added phenotypes Pseudohypoaldosteronism for gene: SCNN1G
Rating Changed from Green List (high evidence) to Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.0 SCNN1G Zornitza Stark gene: SCNN1G was added
gene: SCNN1G was added to gNBS. Sources: BeginNGS,Expert Review Green
Mode of inheritance for gene: SCNN1G was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: SCNN1G were set to Pseudohypoaldosteronism, type I, MIM# 264350