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Date	Panel	Item	Activity
Filter activities 7 actions
17 Jan 2022	Fetal anomalies v0.2349	EMX2	Zornitza Stark Marked gene: EMX2 as ready
17 Jan 2022	Fetal anomalies v0.2349	EMX2	Zornitza Stark Gene: emx2 has been classified as Amber List (Moderate Evidence).
17 Jan 2022	Fetal anomalies v0.2349	EMX2	Zornitza Stark Phenotypes for gene: EMX2 were changed from Schizencephaly, 269160 to Schizencephaly, MIM# 269160
17 Jan 2022	Fetal anomalies v0.2348	EMX2	Zornitza Stark Publications for gene: EMX2 were set to
17 Jan 2022	Fetal anomalies v0.2347	EMX2	Zornitza Stark Mode of inheritance for gene: EMX2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
17 Jan 2022	Fetal anomalies v0.2346	EMX2	Zornitza Stark Tag disputed tag was added to gene: EMX2.
24 Oct 2021	Fetal anomalies v0.0	EMX2	Zornitza Stark gene: EMX2 was added gene: EMX2 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: EMX2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: EMX2 were set to Schizencephaly, 269160