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Rare multisystem ciliopathy disorders v1.168 SUFU Arina Puzriakova Publications for gene: SUFU were set to 28965847
Rare multisystem ciliopathy disorders v1.167 SUFU Arina Puzriakova Classified gene: SUFU as Green List (high evidence)
Rare multisystem ciliopathy disorders v1.167 SUFU Arina Puzriakova Added comment: Comment on list classification: Upgraded from Amber to Green under a monoallelic MOI - sufficient unrelated cases with heterozygous variants and a comparable phenotype within the Joubert spectrum.
Rare multisystem ciliopathy disorders v1.167 SUFU Arina Puzriakova Gene: sufu has been classified as Green List (High Evidence).
Rare multisystem ciliopathy disorders v1.166 SUFU Arina Puzriakova Added comment: Comment on mode of inheritance: Following consultation with Helen Brittain (Genomics England Clinical team) it was decided that based on the current evidence the MOI should be set to 'monoallelic' only for now but with a 'watchlist' tag to monitor for additional biallelic cases relating to a Joubert-like presentation.
Rare multisystem ciliopathy disorders v1.166 SUFU Arina Puzriakova Mode of inheritance for gene: SUFU was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Rare multisystem ciliopathy disorders v1.165 SUFU Arina Puzriakova Tag watchlist was removed from gene: SUFU.
Tag watchlist_moi tag was added to gene: SUFU.
Rare multisystem ciliopathy disorders v1.165 SUFU Arina Puzriakova reviewed gene: SUFU: Rating: GREEN; Mode of pathogenicity: None; Publications: 21289193, 28965847, 33024317, 34675124; Phenotypes: Joubert syndrome 32, OMIM:617757; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Rare multisystem ciliopathy disorders v1.165 SUFU Arina Puzriakova Phenotypes for gene: SUFU were changed from Joubert syndrome 32, 617757 to Joubert syndrome 32, OMIM:617757
Rare multisystem ciliopathy disorders v1.69 SUFU Rebecca Foulger Classified gene: SUFU as Amber List (moderate evidence)
Rare multisystem ciliopathy disorders v1.69 SUFU Rebecca Foulger Added comment: Comment on list classification: Updated rating from Grey to Amber. Probable DD-G2P gene for Joubert Syndrome. 2 unrelated families from 1 paper. Biochemical assays in the paper (PMID:28965847) show that SUFU missense variants impair GLI3 binding, but further cases and/or animal model required for diagnostic rating.
Rare multisystem ciliopathy disorders v1.69 SUFU Rebecca Foulger Gene: sufu has been classified as Amber List (Moderate Evidence).
Rare multisystem ciliopathy disorders v1.67 SUFU Rebecca Foulger commented on gene: SUFU: Added 'watchlist' tag.
Rare multisystem ciliopathy disorders v1.67 SUFU Rebecca Foulger Tag watchlist tag was added to gene: SUFU.
Rare multisystem ciliopathy disorders v1.67 SUFU Rebecca Foulger commented on gene: SUFU
Rare multisystem ciliopathy disorders v1.67 SUFU Rebecca Foulger Phenotypes for gene: SUFU were changed from Joubert Syndrome 32, MIM#617757 to Joubert syndrome 32, 617757
Rare multisystem ciliopathy disorders v1.48 SUFU Andrea Nemeth reviewed gene: SUFU: Rating: GREEN; Mode of pathogenicity: None; Publications: 28965847; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Rare multisystem ciliopathy disorders SUFU Zornitza Stark Added gene to panel