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Date	Panel	Item	Activity
Filter activities 9 actions
20 Jan 2022	Fetal anomalies v0.2571	ELMO2	Zornitza Stark Marked gene: ELMO2 as ready
20 Jan 2022	Fetal anomalies v0.2571	ELMO2	Zornitza Stark Gene: elmo2 has been classified as Red List (Low Evidence).
20 Jan 2022	Fetal anomalies v0.2571	ELMO2	Zornitza Stark Phenotypes for gene: ELMO2 were changed from Intraosseous Vascular Malformation to Vascular malformation, primary intraosseous, MIM# 606893
14 Jan 2022	Fetal anomalies v0.2202	ELMO2	Chirag Patel Classified gene: ELMO2 as Red List (low evidence)
14 Jan 2022	Fetal anomalies v0.2202	ELMO2	Chirag Patel Gene: elmo2 has been classified as Red List (Low Evidence).
14 Jan 2022	Fetal anomalies v0.2202	ELMO2	Chirag Patel Classified gene: ELMO2 as Red List (low evidence)
14 Jan 2022	Fetal anomalies v0.2202	ELMO2	Chirag Patel Gene: elmo2 has been classified as Red List (Low Evidence).
14 Jan 2022	Fetal anomalies v0.2201	ELMO2	Chirag Patel reviewed gene: ELMO2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
24 Oct 2021	Fetal anomalies v0.0	ELMO2	Zornitza Stark gene: ELMO2 was added gene: ELMO2 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: ELMO2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ELMO2 were set to Intraosseous Vascular Malformation