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Date	Panel	Item	Activity
Filter activities 8 actions
05 Oct 2022	BabyScreen+ newborn screening v0.312	MCPH1	Zornitza Stark Marked gene: MCPH1 as ready
05 Oct 2022	BabyScreen+ newborn screening v0.312	MCPH1	Zornitza Stark Gene: mcph1 has been classified as Red List (Low Evidence).
05 Oct 2022	BabyScreen+ newborn screening v0.312	MCPH1	Zornitza Stark Phenotypes for gene: MCPH1 were changed from Microcephaly 1, primary, autosomal recessive to Microcephaly 1, primary, autosomal recessive, MIM# 251200
05 Oct 2022	BabyScreen+ newborn screening v0.311	MCPH1	Zornitza Stark reviewed gene: MCPH1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Microcephaly 1, primary, autosomal recessive, MIM# 251200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
05 Oct 2022	BabyScreen+ newborn screening v0.311	MCPH1	Zornitza Stark Classified gene: MCPH1 as Red List (low evidence)
05 Oct 2022	BabyScreen+ newborn screening v0.311	MCPH1	Zornitza Stark Gene: mcph1 has been classified as Red List (Low Evidence).
29 Sep 2022	BabyScreen+ newborn screening v0.270	MCPH1	David Amor reviewed gene: MCPH1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: autosomal recessive microcephaly; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	BabyScreen+ newborn screening v0.0	MCPH1	Zornitza Stark gene: MCPH1 was added gene: MCPH1 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: MCPH1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: MCPH1 were set to Microcephaly 1, primary, autosomal recessive