Activity

Filter

Cancel
Date Panel Item Activity
19 actions
Ciliopathies v2.0 IFT81 Gene migrated from ENSG00000122970 to ENSG00000122970 (gene set migration)
Ciliopathies v1.71 IFT81 Zornitza Stark edited their review of gene: IFT81: Changed rating: GREEN
Ciliopathies v1.71 IFT81 Zornitza Stark edited their review of gene: IFT81: Added comment: More than 5 families reported with a skeletal ciliopathy.; Changed publications: 27666822, 37427975, 32783357
Ciliopathies v0.37 IFT81 Zornitza Stark Publications for gene: IFT81 were set to 27666822; 30080953; 28460050; 26275418
Ciliopathies v0.36 IFT81 Zornitza Stark Publications for gene: IFT81 were set to 27666822; 30080953; 28460050; 26275418
Ciliopathies v0.36 IFT81 Zornitza Stark Publications for gene: IFT81 were set to 27666822
Ciliopathies v0.35 IFT81 Zornitza Stark Classified gene: IFT81 as Green List (high evidence)
Ciliopathies v0.35 IFT81 Zornitza Stark Gene: ift81 has been classified as Green List (High Evidence).
Ciliopathies v0.34 IFT81 Zornitza Stark Marked gene: IFT81 as ready
Ciliopathies v0.34 IFT81 Zornitza Stark Gene: ift81 has been classified as Amber List (Moderate Evidence).
Ciliopathies v0.34 IFT81 Zornitza Stark Classified gene: IFT81 as Amber List (moderate evidence)
Ciliopathies v0.34 IFT81 Zornitza Stark Gene: ift81 has been classified as Amber List (Moderate Evidence).
Ciliopathies v0.33 IFT81 Zornitza Stark Classified gene: IFT81 as Amber List (moderate evidence)
Ciliopathies v0.33 IFT81 Zornitza Stark Gene: ift81 has been classified as Amber List (Moderate Evidence).
Ciliopathies v0.33 IFT81 Zornitza Stark Publications for gene: IFT81 were set to
Ciliopathies v0.32 IFT81 Zornitza Stark Phenotypes for gene: IFT81 were changed from to Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895
Ciliopathies v0.31 IFT81 Zornitza Stark Mode of inheritance for gene: IFT81 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Ciliopathies v0.30 IFT81 Zornitza Stark reviewed gene: IFT81: Rating: AMBER; Mode of pathogenicity: None; Publications: 27666822; Phenotypes: Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ciliopathies v0.0 IFT81 Zornitza Stark gene: IFT81 was added
gene: IFT81 was added to Ciliopathies_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: IFT81 was set to Unknown