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Renal ciliopathies v1.53 IFT27 Eleanor Williams Phenotypes for gene: IFT27 were changed from ?Bardet-Biedl syndrome 19, 615996 to ?Bardet-Biedl syndrome 19, OMIM:615996
Renal ciliopathies v1.52 IFT27 Eleanor Williams Tag for-review was removed from gene: IFT27.
Renal ciliopathies v1.51 IFT27 Eleanor Williams commented on gene: IFT27: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Renal ciliopathies v1.50 IFT27 Eleanor Williams Source Expert Review Green was added to IFT27.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Renal ciliopathies v1.26 IFT27 Arina Puzriakova Tag for-review tag was added to gene: IFT27.
Renal ciliopathies v1.26 IFT27 Arina Puzriakova Classified gene: IFT27 as Amber List (moderate evidence)
Renal ciliopathies v1.26 IFT27 Arina Puzriakova Added comment: Comment on list classification: With the addition of the recent publication, there are now at least three unrelated cases reported with a renal phenotype, and therefore enough evidence for a rating upgrade from Amber to GREEN at the next major review.
Renal ciliopathies v1.26 IFT27 Arina Puzriakova Gene: ift27 has been classified as Amber List (Moderate Evidence).
Renal ciliopathies v1.25 IFT27 Arina Puzriakova reviewed gene: IFT27: Rating: GREEN; Mode of pathogenicity: None; Publications: 29588463; Phenotypes: Bardet-Biedl syndrome 19, 615996; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Renal ciliopathies v1.17 IFT27 Eleanor Williams commented on gene: IFT27
Renal ciliopathies v1.17 IFT27 Eleanor Williams Publications for gene: IFT27 were set to
Renal ciliopathies v1.0 IFT27 Zornitza Stark reviewed gene: IFT27: Rating: GREEN; Mode of pathogenicity: None; Publications: 30761183; Phenotypes: Bardet-Biedl syndrome 19, MIM# 615996; Mode of inheritance: None
Renal ciliopathies v0.1 IFT27 Eleanor Williams gene: IFT27 was added
gene: IFT27 was added to Renal ciliopathies. Sources: UKGTN,Radboud University Medical Center, Nijmegen,Expert list,Expert Review Amber
Mode of inheritance for gene: IFT27 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: IFT27 were set to ?Bardet-Biedl syndrome 19, 615996