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Ciliopathies v0.341 CEP290 Zornitza Stark Marked gene: CEP290 as ready
Ciliopathies v0.341 CEP290 Zornitza Stark Gene: cep290 has been classified as Green List (High Evidence).
Ciliopathies v0.341 CEP290 Zornitza Stark Phenotypes for gene: CEP290 were changed from to Bardet-Biedl syndrome 14, MIM# 615991; Joubert syndrome 5 610188; Leber congenital amaurosis 10, MIM# 611755; Meckel syndrome 4, MIM# 611134; Senior-Loken syndrome 6, MIM# 610189
Ciliopathies v0.340 CEP290 Zornitza Stark Publications for gene: CEP290 were set to
Ciliopathies v0.339 CEP290 Zornitza Stark Mode of inheritance for gene: CEP290 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Ciliopathies v0.338 CEP290 Zornitza Stark changed review comment from: Variants in this gene cause a range of ciliopathies. The association with BBS is rare.; to: Variants in this gene cause a range of ciliopathies.
Ciliopathies v0.338 CEP290 Zornitza Stark edited their review of gene: CEP290: Changed publications: 18327255, 20690115, 16682973, 16682970, 17564967, 16909394, 17564974; Changed phenotypes: Bardet-Biedl syndrome 14, MIM# 615991, Joubert syndrome 5 610188, Leber congenital amaurosis 10, MIM# 611755, Meckel syndrome 4, MIM# 611134, Senior-Loken syndrome 6, MIM# 610189
Ciliopathies v0.0 CEP290 Zornitza Stark gene: CEP290 was added
gene: CEP290 was added to Ciliopathies_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CEP290 was set to Unknown