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Date	Panel	Item	Activity
Filter activities 6 actions
23 Feb 2022	Fetal anomalies v0.4093	TBX5	Zornitza Stark Marked gene: TBX5 as ready
23 Feb 2022	Fetal anomalies v0.4093	TBX5	Zornitza Stark Gene: tbx5 has been classified as Green List (High Evidence).
23 Feb 2022	Fetal anomalies v0.4093	TBX5	Zornitza Stark Phenotypes for gene: TBX5 were changed from HOLT-ORAM SYNDROME to Holt-Oram syndrome, MIM# 142900
23 Feb 2022	Fetal anomalies v0.4092	TBX5	Zornitza Stark Publications for gene: TBX5 were set to
23 Feb 2022	Fetal anomalies v0.4091	TBX5	Zornitza Stark Mode of inheritance for gene: TBX5 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
24 Oct 2021	Fetal anomalies v0.0	TBX5	Zornitza Stark gene: TBX5 was added gene: TBX5 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp Mode of inheritance for gene: TBX5 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: TBX5 were set to HOLT-ORAM SYNDROME