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Date	Panel	Item	Activity
Filter activities 6 actions
26 Jan 2022	Fetal anomalies v0.2818	PAX7	Zornitza Stark Marked gene: PAX7 as ready
26 Jan 2022	Fetal anomalies v0.2818	PAX7	Zornitza Stark Gene: pax7 has been classified as Red List (Low Evidence).
26 Jan 2022	Fetal anomalies v0.2818	PAX7	Zornitza Stark Classified gene: PAX7 as Red List (low evidence)
26 Jan 2022	Fetal anomalies v0.2818	PAX7	Zornitza Stark Gene: pax7 has been classified as Red List (Low Evidence).
26 Jan 2022	Fetal anomalies v0.2817	PAX7	Zornitza Stark changed review comment from: ID is not part of the phenotype.; to: Progressive disorder, onset in infancy.
24 Oct 2021	Fetal anomalies v0.0	PAX7	Zornitza Stark gene: PAX7 was added gene: PAX7 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: PAX7 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: PAX7 were set to Myopathy, congenital, progressive, with scoliosis, OMIM:618578; Myopathy, congenital, progressive, with scoliosis, MONDO:0032821