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Date	Panel	Item	Activity
Filter activities 7 actions
14 Dec 2022	BabyScreen+ newborn screening v0.1464	RAB23	Zornitza Stark Marked gene: RAB23 as ready
14 Dec 2022	BabyScreen+ newborn screening v0.1464	RAB23	Zornitza Stark Gene: rab23 has been classified as Red List (Low Evidence).
14 Dec 2022	BabyScreen+ newborn screening v0.1464	RAB23	Zornitza Stark Phenotypes for gene: RAB23 were changed from Carpenter syndrome to Carpenter syndrome (MIM#201000)
14 Dec 2022	BabyScreen+ newborn screening v0.1463	RAB23	Zornitza Stark Classified gene: RAB23 as Red List (low evidence)
14 Dec 2022	BabyScreen+ newborn screening v0.1463	RAB23	Zornitza Stark Gene: rab23 has been classified as Red List (Low Evidence).
14 Dec 2022	BabyScreen+ newborn screening v0.1462	RAB23	Zornitza Stark reviewed gene: RAB23: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Carpenter syndrome (MIM#201000); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	BabyScreen+ newborn screening v0.0	RAB23	Zornitza Stark gene: RAB23 was added gene: RAB23 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: RAB23 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: RAB23 were set to Carpenter syndrome