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Date	Panel	Item	Activity
Filter activities 7 actions
22 Sep 2022	BabyScreen+ newborn screening v0.125	ARMC4	Zornitza Stark Marked gene: ARMC4 as ready
22 Sep 2022	BabyScreen+ newborn screening v0.125	ARMC4	Zornitza Stark Gene: armc4 has been classified as Red List (Low Evidence).
22 Sep 2022	BabyScreen+ newborn screening v0.125	ARMC4	Zornitza Stark Phenotypes for gene: ARMC4 were changed from Primary ciliary dyskinesia to Ciliary dyskinesia, primary, 23, MIM# 615451
22 Sep 2022	BabyScreen+ newborn screening v0.124	ARMC4	Zornitza Stark Classified gene: ARMC4 as Red List (low evidence)
22 Sep 2022	BabyScreen+ newborn screening v0.124	ARMC4	Zornitza Stark Gene: armc4 has been classified as Red List (Low Evidence).
22 Sep 2022	BabyScreen+ newborn screening v0.123	ARMC4	Zornitza Stark reviewed gene: ARMC4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ciliary dyskinesia, primary, 23, MIM# 615451; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	BabyScreen+ newborn screening v0.0	ARMC4	Zornitza Stark gene: ARMC4 was added gene: ARMC4 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: ARMC4 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ARMC4 were set to Primary ciliary dyskinesia