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Ciliopathies v1.5 IFT122 Zornitza Stark Phenotypes for gene: IFT122 were changed from Cranioectodermal dysplasia 1, MIM# 218330; Beemer-Langer syndrome to Cranioectodermal dysplasia 1, MIM# 218330; MONDO:0021093; Beemer-Langer syndrome
Ciliopathies v0.209 IFT122 Zornitza Stark Marked gene: IFT122 as ready
Ciliopathies v0.209 IFT122 Zornitza Stark Gene: ift122 has been classified as Green List (High Evidence).
Ciliopathies v0.209 IFT122 Zornitza Stark Phenotypes for gene: IFT122 were changed from to Cranioectodermal dysplasia 1, MIM# 218330; Beemer-Langer syndrome
Ciliopathies v0.208 IFT122 Zornitza Stark Publications for gene: IFT122 were set to
Ciliopathies v0.207 IFT122 Zornitza Stark Mode of inheritance for gene: IFT122 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Ciliopathies v0.206 IFT122 Zornitza Stark reviewed gene: IFT122: Rating: GREEN; Mode of pathogenicity: None; Publications: 20493458, 23826986, 26792575, 29220510, 28370949, 27681595, 27681595; Phenotypes: Cranioectodermal dysplasia 1, MIM# 218330, Beemer-Langer syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ciliopathies v0.0 IFT122 Zornitza Stark gene: IFT122 was added
gene: IFT122 was added to Ciliopathies_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: IFT122 was set to Unknown