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Date	Panel	Item	Activity
Filter activities 8 actions
31 Jan 2022	Fetal anomalies v0.2955	NRXN2	Zornitza Stark Marked gene: NRXN2 as ready
31 Jan 2022	Fetal anomalies v0.2955	NRXN2	Zornitza Stark Gene: nrxn2 has been classified as Red List (Low Evidence).
31 Jan 2022	Fetal anomalies v0.2955	NRXN2	Zornitza Stark Phenotypes for gene: NRXN2 were changed from AUTISM to Autism
31 Jan 2022	Fetal anomalies v0.2954	NRXN2	Zornitza Stark Publications for gene: NRXN2 were set to
31 Jan 2022	Fetal anomalies v0.2953	NRXN2	Zornitza Stark Mode of inheritance for gene: NRXN2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
31 Jan 2022	Fetal anomalies v0.2952	NRXN2	Zornitza Stark Classified gene: NRXN2 as Red List (low evidence)
31 Jan 2022	Fetal anomalies v0.2952	NRXN2	Zornitza Stark Gene: nrxn2 has been classified as Red List (Low Evidence).
24 Oct 2021	Fetal anomalies v0.0	NRXN2	Zornitza Stark gene: NRXN2 was added gene: NRXN2 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: NRXN2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: NRXN2 were set to AUTISM