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Date	Panel	Item	Activity
Filter activities 6 actions
24 Oct 2022	Genomic newborn screening: BabyScreen+ v0.613	CDT1	Zornitza Stark Marked gene: CDT1 as ready
24 Oct 2022	Genomic newborn screening: BabyScreen+ v0.613	CDT1	Zornitza Stark Gene: cdt1 has been classified as Red List (Low Evidence).
24 Oct 2022	Genomic newborn screening: BabyScreen+ v0.613	CDT1	Zornitza Stark Classified gene: CDT1 as Red List (low evidence)
24 Oct 2022	Genomic newborn screening: BabyScreen+ v0.613	CDT1	Zornitza Stark Gene: cdt1 has been classified as Red List (Low Evidence).
24 Oct 2022	Genomic newborn screening: BabyScreen+ v0.612	CDT1	Zornitza Stark reviewed gene: CDT1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Meier-Gorlin syndrome 4, MIM# 613804, MONDO:0013431; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	Genomic newborn screening: BabyScreen+ v0.0	CDT1	Zornitza Stark gene: CDT1 was added gene: CDT1 was added to gNBS. Sources: Expert Review Green,BabySeq Category C gene Mode of inheritance for gene: CDT1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CDT1 were set to 22333897; 21358632; 21358631; 33338304 Phenotypes for gene: CDT1 were set to Meier-Gorlin syndrome 4, MIM# 613804; MONDO:0013431