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Date	Panel	Item	Activity
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20 Nov 2022	BabyScreen+ newborn screening v0.961	ESCO2	Zornitza Stark Marked gene: ESCO2 as ready
20 Nov 2022	BabyScreen+ newborn screening v0.961	ESCO2	Zornitza Stark Gene: esco2 has been classified as Red List (Low Evidence).
20 Nov 2022	BabyScreen+ newborn screening v0.961	ESCO2	Zornitza Stark Phenotypes for gene: ESCO2 were changed from Roberts syndrome to Juberg-Hayward syndrome, MIM# 216100; Roberts-SC phocomelia syndrome, MIM#268300
20 Nov 2022	BabyScreen+ newborn screening v0.960	ESCO2	Zornitza Stark Classified gene: ESCO2 as Red List (low evidence)
20 Nov 2022	BabyScreen+ newborn screening v0.960	ESCO2	Zornitza Stark Gene: esco2 has been classified as Red List (Low Evidence).
20 Nov 2022	BabyScreen+ newborn screening v0.959	ESCO2	Zornitza Stark reviewed gene: ESCO2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Juberg-Hayward syndrome, MIM# 216100, Roberts-SC phocomelia syndrome, MIM#268300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	BabyScreen+ newborn screening v0.0	ESCO2	Zornitza Stark gene: ESCO2 was added gene: ESCO2 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: ESCO2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ESCO2 were set to Roberts syndrome