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Fetal anomalies v2.0 WDR91 Gene migrated from ENSG00000105875 to ENSG00000105875 (gene set migration)
Fetal anomalies v1.377 WDR91 Bryony Thompson Phenotypes for gene: WDR91 were changed from Hydrocephaly; Hygroma to Complex neurodevelopmental disorder MONDO:0100038
Fetal anomalies v1.376 WDR91 Bryony Thompson Publications for gene: WDR91 were set to 32732226; 34028500; 28860274
Fetal anomalies v1.375 WDR91 Bryony Thompson Classified gene: WDR91 as Green List (high evidence)
Fetal anomalies v1.375 WDR91 Bryony Thompson Gene: wdr91 has been classified as Green List (High Evidence).
Fetal anomalies v1.374 WDR91 Bryony Thompson reviewed gene: WDR91: Rating: GREEN; Mode of pathogenicity: None; Publications: 32732226, 38041506, 34791078, 40550703, 28860274, 34028500, ClinVar: SCV000965687.1; Phenotypes: Complex neurodevelopmental disorder MONDO:0100038; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal anomalies v0.3984 WDR91 Zornitza Stark Marked gene: WDR91 as ready
Fetal anomalies v0.3984 WDR91 Zornitza Stark Gene: wdr91 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.3984 WDR91 Zornitza Stark Classified gene: WDR91 as Amber List (moderate evidence)
Fetal anomalies v0.3984 WDR91 Zornitza Stark Gene: wdr91 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.0 WDR91 Zornitza Stark gene: WDR91 was added
gene: WDR91 was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: WDR91 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: WDR91 were set to 32732226; 34028500; 28860274
Phenotypes for gene: WDR91 were set to Hydrocephaly; Hygroma