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BabyScreen+ newborn screening v0.725 SFTPC Zornitza Stark Classified gene: SFTPC as Red List (low evidence)
BabyScreen+ newborn screening v0.725 SFTPC Zornitza Stark Gene: sftpc has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.724 SFTPC Zornitza Stark Tag for review was removed from gene: SFTPC.
BabyScreen+ newborn screening v0.669 SFTPC Zornitza Stark Tag for review tag was added to gene: SFTPC.
BabyScreen+ newborn screening v0.669 SFTPC Zornitza Stark reviewed gene: SFTPC: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Surfactant metabolism dysfunction, pulmonary, 2, MIM# 610913; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.651 SFTPC Seb Lunke Marked gene: SFTPC as ready
BabyScreen+ newborn screening v0.651 SFTPC Seb Lunke Gene: sftpc has been classified as Green List (High Evidence).
BabyScreen+ newborn screening v0.651 SFTPC Seb Lunke Phenotypes for gene: SFTPC were changed from Interstitial lung disease; Surfactant metabolism dysfunction, pulmonary, 2 MIM# 178620 to Surfactant metabolism dysfunction, pulmonary, 2, MIM# 610913
BabyScreen+ newborn screening v0.650 SFTPC Seb Lunke reviewed gene: SFTPC: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Surfactant metabolism dysfunction, pulmonary, 2, MIM# 610913; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.0 SFTPC Zornitza Stark gene: SFTPC was added
gene: SFTPC was added to gNBS. Sources: Expert Review Green,BabySeq Category C gene
Mode of inheritance for gene: SFTPC was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: SFTPC were set to Interstitial lung disease; Surfactant metabolism dysfunction, pulmonary, 2 MIM# 178620