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Polydactyly v0.236 PDE6D Zornitza Stark changed review comment from: Comment on publications: Second family identified; to: Comment on publications: Second family identified.
Polydactyly v0.236 PDE6D Zornitza Stark edited their review of gene: PDE6D: Changed rating: AMBER
Polydactyly v0.236 PDE6D Zornitza Stark Deleted their comment
Polydactyly v0.36 PDE6D Anand Vasudevan reviewed gene: PDE6D: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Polydactyly v0.15 PDE6D Zornitza Stark Added comment: Comment on publications: Second family identified.
Polydactyly v0.15 PDE6D Zornitza Stark Publications for gene: PDE6D were set to 24166846; 30423442
Polydactyly v0.14 PDE6D Zornitza Stark Added comment: Comment on publications: Second family identified
Polydactyly v0.14 PDE6D Zornitza Stark Publications for gene: PDE6D were set to 24166846
Polydactyly v0.14 PDE6D Zornitza Stark Classified gene: PDE6D as Amber List (moderate evidence)
Polydactyly v0.14 PDE6D Zornitza Stark Gene: pde6d has been classified as Amber List (Moderate Evidence).
Polydactyly v0.13 PDE6D Zornitza Stark Marked gene: PDE6D as ready
Polydactyly v0.13 PDE6D Zornitza Stark Gene: pde6d has been classified as Red List (Low Evidence).
Polydactyly v0.13 PDE6D Zornitza Stark Publications for gene: PDE6D were set to 24166846
Polydactyly v0.12 PDE6D Zornitza Stark Publications for gene: PDE6D were set to
Polydactyly v0.11 PDE6D Zornitza Stark Phenotypes for gene: PDE6D were changed from to Joubert syndrome 22, OMIM #615665
Polydactyly v0.11 PDE6D Zornitza Stark Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Polydactyly v0.10 PDE6D Zornitza Stark Classified gene: PDE6D as Red List (low evidence)
Polydactyly v0.10 PDE6D Zornitza Stark Gene: pde6d has been classified as Red List (Low Evidence).
Polydactyly v0.9 PDE6D Zornitza Stark reviewed gene: PDE6D: Rating: RED; Mode of pathogenicity: None; Publications: 24166846; Phenotypes: Joubert syndrome 22, OMIM #615665; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Polydactyly v0.0 PDE6D Zornitza Stark gene: PDE6D was added
gene: PDE6D was added to Polydactyly_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: PDE6D was set to Unknown