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Date	Panel	Item	Activity
Filter activities 6 actions
28 Jan 2022	Fetal anomalies v0.2929	SP7	Zornitza Stark Marked gene: SP7 as ready
28 Jan 2022	Fetal anomalies v0.2929	SP7	Zornitza Stark Gene: sp7 has been classified as Red List (Low Evidence).
28 Jan 2022	Fetal anomalies v0.2929	SP7	Zornitza Stark Classified gene: SP7 as Red List (low evidence)
28 Jan 2022	Fetal anomalies v0.2929	SP7	Zornitza Stark Gene: sp7 has been classified as Red List (Low Evidence).
28 Jan 2022	Fetal anomalies v0.2928	SP7	Zornitza Stark reviewed gene: SP7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Osteogenesis imperfecta, type XII, MIM# 613849; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
24 Oct 2021	Fetal anomalies v0.0	SP7	Zornitza Stark gene: SP7 was added gene: SP7 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: SP7 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SP7 were set to Osteogenesis imperfecta type 12, MONDO:0013460; Osteogenesis imperfecta, type XII, OMIM:613849