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Date	Panel	Item	Activity
Filter activities 9 actions
08 Dec 2021	Fetal anomalies v0.1133	C21orf59	Zornitza Stark Tag founder tag was added to gene: C21orf59.
08 Dec 2021	Fetal anomalies v0.1133	C21orf59	Zornitza Stark Marked gene: C21orf59 as ready
08 Dec 2021	Fetal anomalies v0.1133	C21orf59	Zornitza Stark Gene: c21orf59 has been classified as Green List (High Evidence).
08 Dec 2021	Fetal anomalies v0.1133	C21orf59	Zornitza Stark Publications for gene: C21orf59 were set to
08 Dec 2021	Fetal anomalies v0.1132	C21orf59	Zornitza Stark Classified gene: C21orf59 as Green List (high evidence)
08 Dec 2021	Fetal anomalies v0.1132	C21orf59	Zornitza Stark Gene: c21orf59 has been classified as Green List (High Evidence).
08 Dec 2021	Fetal anomalies v0.1131	C21orf59	Zornitza Stark Tag new gene name tag was added to gene: C21orf59.
08 Dec 2021	Fetal anomalies v0.1131	C21orf59	Zornitza Stark changed review comment from: Comment when marking as ready: p.Tyr245* recurring in the Ashkenazi Jewish population; to: Comment when marking as ready: p.Tyr245* recurring in the Ashkenazi Jewish population. Laterality defects in about half.
24 Oct 2021	Fetal anomalies v0.0	C21orf59	Zornitza Stark gene: C21orf59 was added gene: C21orf59 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: C21orf59 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: C21orf59 were set to Primary ciliary dyskinesia 26, MONDO:0014211; Ciliary dyskinesia, primary, 26, OMIM:615500