| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Fetal anomalies v0.2344 | EMG1 | Zornitza Stark Marked gene: EMG1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.2344 | EMG1 | Zornitza Stark Gene: emg1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.2344 | EMG1 | Zornitza Stark Phenotypes for gene: EMG1 were changed from Bowen-Conradi syndrome, 211180; Bowen-Conradi syndrome to Bowen-Conradi syndrome, MIM#211180 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.2343 | EMG1 | Zornitza Stark Tag founder tag was added to gene: EMG1. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.2343 | EMG1 |
Zornitza Stark changed review comment from: Founder mutation in Hutterite, D86G. Sources: Expert list; to: Founder mutation in Hutterite, D86G. SGA, contractures. Sources: Expert list |
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| Fetal anomalies v0.0 | EMG1 |
Zornitza Stark gene: EMG1 was added gene: EMG1 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: EMG1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: EMG1 were set to 19463982 Phenotypes for gene: EMG1 were set to Bowen-Conradi syndrome, 211180; Bowen-Conradi syndrome Mode of pathogenicity for gene: EMG1 was set to Other |
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