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Date	Panel	Item	Activity
Filter activities 7 actions
20 Jan 2022	Fetal anomalies v0.2597	SCYL1	Zornitza Stark Marked gene: SCYL1 as ready
20 Jan 2022	Fetal anomalies v0.2597	SCYL1	Zornitza Stark Gene: scyl1 has been classified as Red List (Low Evidence).
20 Jan 2022	Fetal anomalies v0.2597	SCYL1	Zornitza Stark Phenotypes for gene: SCYL1 were changed from Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia to Spinocerebellar ataxia, autosomal recessive 21, MIM# 616719
14 Jan 2022	Fetal anomalies v0.2238	SCYL1	Chirag Patel Classified gene: SCYL1 as Red List (low evidence)
14 Jan 2022	Fetal anomalies v0.2238	SCYL1	Chirag Patel Gene: scyl1 has been classified as Red List (Low Evidence).
14 Jan 2022	Fetal anomalies v0.2237	SCYL1	Chirag Patel reviewed gene: SCYL1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
24 Oct 2021	Fetal anomalies v0.0	SCYL1	Zornitza Stark gene: SCYL1 was added gene: SCYL1 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: SCYL1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SCYL1 were set to Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia