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Date	Panel	Item	Activity
Filter activities 7 actions
22 Sep 2022	BabyScreen+ newborn screening v0.136	ATP2A1	Zornitza Stark Marked gene: ATP2A1 as ready
22 Sep 2022	BabyScreen+ newborn screening v0.136	ATP2A1	Zornitza Stark Gene: atp2a1 has been classified as Red List (Low Evidence).
22 Sep 2022	BabyScreen+ newborn screening v0.136	ATP2A1	Zornitza Stark Phenotypes for gene: ATP2A1 were changed from Brody myopathy to Brody myopathy, OMIM # 601003
22 Sep 2022	BabyScreen+ newborn screening v0.135	ATP2A1	Zornitza Stark Classified gene: ATP2A1 as Red List (low evidence)
22 Sep 2022	BabyScreen+ newborn screening v0.135	ATP2A1	Zornitza Stark Gene: atp2a1 has been classified as Red List (Low Evidence).
22 Sep 2022	BabyScreen+ newborn screening v0.134	ATP2A1	Zornitza Stark reviewed gene: ATP2A1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Brody myopathy, OMIM # 601003; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	BabyScreen+ newborn screening v0.0	ATP2A1	Zornitza Stark gene: ATP2A1 was added gene: ATP2A1 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: ATP2A1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ATP2A1 were set to Brody myopathy