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Fetal anomalies v0.3440 FGF20 Zornitza Stark Marked gene: FGF20 as ready
Fetal anomalies v0.3440 FGF20 Zornitza Stark Gene: fgf20 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.3440 FGF20 Zornitza Stark Phenotypes for gene: FGF20 were changed from ?Renal hypodysplasia/aplasia 2, 615721 to Renal hypodysplasia/aplasia 2, MIM#615721
Fetal anomalies v0.3439 FGF20 Zornitza Stark Classified gene: FGF20 as Amber List (moderate evidence)
Fetal anomalies v0.3439 FGF20 Zornitza Stark Gene: fgf20 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.3396 FGF20 Ain Roesley commented on gene: FGF20: Multiple affected fetuses in a consanguineous family; functional data.
Fetal anomalies v0.3396 FGF20 Ain Roesley reviewed gene: FGF20: Rating: AMBER; Mode of pathogenicity: None; Publications: 22698282; Phenotypes: Renal hypodysplasia/aplasia 2, MIM#615721; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Fetal anomalies v0.0 FGF20 Zornitza Stark gene: FGF20 was added
gene: FGF20 was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: FGF20 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: FGF20 were set to 22698282; 23112089
Phenotypes for gene: FGF20 were set to ?Renal hypodysplasia/aplasia 2, 615721