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Polydactyly v0.208 BBS9 Zornitza Stark changed review comment from: Well established gene-disease association.; to: Well established gene-disease association, polydactyly is a key feature.
Polydactyly v0.208 BBS9 Zornitza Stark Marked gene: BBS9 as ready
Polydactyly v0.208 BBS9 Zornitza Stark Gene: bbs9 has been classified as Green List (High Evidence).
Polydactyly v0.208 BBS9 Zornitza Stark Phenotypes for gene: BBS9 were changed from to Bardet-Biedl syndrome 9, MIM#615986; MONDO:0014437
Polydactyly v0.207 BBS9 Zornitza Stark Publications for gene: BBS9 were set to
Polydactyly v0.206 BBS9 Zornitza Stark edited their review of gene: BBS9: Changed phenotypes: Bardet-Biedl syndrome 9, MIM#615986, MONDO:0014437
Polydactyly v0.50 BBS9 Zornitza Stark Mode of inheritance for gene: BBS9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Polydactyly v0.36 BBS9 Anand Vasudevan reviewed gene: BBS9: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Polydactyly v0.0 BBS9 Zornitza Stark gene: BBS9 was added
gene: BBS9 was added to Polydactyly_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: BBS9 was set to Unknown