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Rare multisystem ciliopathy disorders v1.171 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Joubert Syndrome and Senior-Loken Syndrome 24 gene panel to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510
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 GLI3 Andrea Nemeth reviewed gene: GLI3
Rare multisystem ciliopathy disorders GLI3 Alice Gardham marked GLI3 as ready
Rare multisystem ciliopathy disorders GLI3 Alice Gardham classified GLI3 as green
Rare multisystem ciliopathy disorders GLI3 Alice Gardham commented on GLI3