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Date	Panel	Item	Activity
Filter activities 6 actions
07 Jun 2026	Fetal anomalies v2.0	CEP63	Gene migrated from ENSG00000182923 to ENSG00000182923 (gene set migration)
10 Dec 2021	Fetal anomalies v0.1203	CEP63	Zornitza Stark Marked gene: CEP63 as ready
10 Dec 2021	Fetal anomalies v0.1203	CEP63	Zornitza Stark Gene: cep63 has been classified as Amber List (Moderate Evidence).
10 Dec 2021	Fetal anomalies v0.1203	CEP63	Zornitza Stark Phenotypes for gene: CEP63 were changed from ?Seckel syndrome 6, OMIM:614728; Seckel syndrome 6, MONDO:0013871 to Seckel syndrome 6, OMIM:614728; Seckel syndrome 6, MONDO:0013871
10 Dec 2021	Fetal anomalies v0.1202	CEP63	Zornitza Stark Publications for gene: CEP63 were set to
24 Oct 2021	Fetal anomalies v0.0	CEP63	Zornitza Stark gene: CEP63 was added gene: CEP63 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: CEP63 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CEP63 were set to ?Seckel syndrome 6, OMIM:614728; Seckel syndrome 6, MONDO:0013871