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Date	Panel	Item	Activity
Filter activities 7 actions
17 Jan 2022	Fetal anomalies v0.2328	DRC1	Zornitza Stark Marked gene: DRC1 as ready
17 Jan 2022	Fetal anomalies v0.2328	DRC1	Zornitza Stark Gene: drc1 has been classified as Red List (Low Evidence).
17 Jan 2022	Fetal anomalies v0.2328	DRC1	Zornitza Stark Phenotypes for gene: DRC1 were changed from PRIMARY CILARY DYSKINEASIA to Ciliary dyskinesia, primary, 21, MIM# 615294
17 Jan 2022	Fetal anomalies v0.2327	DRC1	Zornitza Stark Publications for gene: DRC1 were set to
17 Jan 2022	Fetal anomalies v0.2326	DRC1	Zornitza Stark Classified gene: DRC1 as Red List (low evidence)
17 Jan 2022	Fetal anomalies v0.2326	DRC1	Zornitza Stark Gene: drc1 has been classified as Red List (Low Evidence).
24 Oct 2021	Fetal anomalies v0.0	DRC1	Zornitza Stark gene: DRC1 was added gene: DRC1 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: DRC1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: DRC1 were set to PRIMARY CILARY DYSKINEASIA