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Retinal disorders v2.243 IFT27 Ivone Leong Tag for-review was removed from gene: IFT27.
Retinal disorders v2.243 IFT27 Ivone Leong commented on gene: IFT27: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Retinal disorders v2.243 IFT27 Ivone Leong Source Expert Review Green was added to IFT27.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v2.76 IFT27 Ivone Leong Phenotypes for gene: IFT27 were changed from to ?Bardet-Biedl syndrome 19, OMIM:615996
Retinal disorders v2.75 IFT27 Ivone Leong Publications for gene: IFT27 were set to
Retinal disorders v2.17 IFT27 Zornitza Stark reviewed gene: IFT27: Rating: GREEN; Mode of pathogenicity: None; Publications: 24488770, 30761183, 26763875, 25443296; Phenotypes: Bardet-Biedl syndrome 19, MIM#615996; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Retinal disorders v2.16 IFT27 Arina Puzriakova Mode of inheritance for gene: IFT27 was changed from to BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v2.15 IFT27 Arina Puzriakova Classified gene: IFT27 as Amber List (moderate evidence)
Retinal disorders v2.15 IFT27 Arina Puzriakova Added comment: Comment on list classification: At least four unrelated cases reported, and therefore enough evidence for a rating upgrade from Amber to GREEN at the next major review.
Retinal disorders v2.15 IFT27 Arina Puzriakova Gene: ift27 has been classified as Amber List (Moderate Evidence).
Retinal disorders v2.14 IFT27 Arina Puzriakova Tag for-review tag was added to gene: IFT27.
Retinal disorders v2.14 IFT27 Arina Puzriakova reviewed gene: IFT27: Rating: GREEN; Mode of pathogenicity: None; Publications: 24488770, 29704304, 30761183, 29588463; Phenotypes: Bardet-Biedl syndrome 19, 615996; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v2.5 IFT27 Ivone Leong reviewed gene: IFT27: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Retinal disorders v2.3 IFT27 Ivone Leong gene: IFT27 was added
gene: IFT27 was added to Retinal disorders. Sources: Expert Review Amber,RetNet,NHS GMS
Mode of inheritance for gene: IFT27 was set to