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Fetal anomalies v0.1589 FGF3 Zornitza Stark Marked gene: FGF3 as ready
Fetal anomalies v0.1589 FGF3 Zornitza Stark Gene: fgf3 has been classified as Green List (High Evidence).
Fetal anomalies v0.1589 FGF3 Zornitza Stark Phenotypes for gene: FGF3 were changed from DEAFNESS WITH LABYRINTHINE APLASIA, MICROTIA AND MICRODONTIA to Deafness, congenital with inner ear agenesis, microtia, and microdontia, MIM#610706
Fetal anomalies v0.1588 FGF3 Zornitza Stark Publications for gene: FGF3 were set to
Fetal anomalies v0.1587 FGF3 Zornitza Stark changed review comment from: Most features would not be detectable antenatally, but micrognathia may be evident.; to: Most features would not be detectable antenatally, but micrognathia may be evident.

Over 50 affected individuals reported, functional data including animal models, expression studies and in vitro functional assays.
Fetal anomalies v0.1587 FGF3 Zornitza Stark edited their review of gene: FGF3: Changed publications: 21480479, 21306635, 18435799, 17236138, 21306635, 18701883, 8223243, 26995070, 29902227, 30504125
Fetal anomalies v0.1587 FGF3 Zornitza Stark changed review comment from: Delay in gross motor skills thought to be related to balance issues, not truly ID.; to: Most features would not be detectable antenatally, but micrognathia may be evident.
Fetal anomalies v0.1587 FGF3 Zornitza Stark edited their review of gene: FGF3: Changed rating: GREEN
Fetal anomalies v0.0 FGF3 Zornitza Stark gene: FGF3 was added
gene: FGF3 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: FGF3 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: FGF3 were set to DEAFNESS WITH LABYRINTHINE APLASIA, MICROTIA AND MICRODONTIA