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Date	Panel	Item	Activity
Filter activities 8 actions
15 Jan 2022	Fetal anomalies v0.2261	DDX59	Zornitza Stark Marked gene: DDX59 as ready
15 Jan 2022	Fetal anomalies v0.2261	DDX59	Zornitza Stark Gene: ddx59 has been classified as Green List (High Evidence).
15 Jan 2022	Fetal anomalies v0.2261	DDX59	Zornitza Stark Publications for gene: DDX59 were set to
15 Jan 2022	Fetal anomalies v0.2260	DDX59	Zornitza Stark Classified gene: DDX59 as Green List (high evidence)
15 Jan 2022	Fetal anomalies v0.2260	DDX59	Zornitza Stark Gene: ddx59 has been classified as Green List (High Evidence).
15 Jan 2022	Fetal anomalies v0.2259	DDX59	Zornitza Stark changed review comment from: 5 unrelated families reported, renal involvement is not prominent.; to: 5 unrelated families reported, multiple congenital anomalies.
15 Jan 2022	Fetal anomalies v0.2259	DDX59	Zornitza Stark edited their review of gene: DDX59: Changed rating: GREEN
24 Oct 2021	Fetal anomalies v0.0	DDX59	Zornitza Stark gene: DDX59 was added gene: DDX59 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: DDX59 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: DDX59 were set to Orofaciodigital syndrome V, MONDO:0008267; Orofaciodigital syndrome V, OMIM:174300