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Syndromic Retinopathy v0.128 PLK4 Zornitza Stark changed review comment from: Microcephaly and chorioretinopathy, autosomal recessive, 2, MIM# 616171; to: Microcephaly and chorioretinopathy, autosomal recessive, 2, MIM# 616171, three unrelated families reported.
Syndromic Retinopathy v0.75 PLK4 Zornitza Stark Marked gene: PLK4 as ready
Syndromic Retinopathy v0.75 PLK4 Zornitza Stark Gene: plk4 has been classified as Green List (High Evidence).
Syndromic Retinopathy v0.75 PLK4 Zornitza Stark Phenotypes for gene: PLK4 were changed from to Microcephaly and chorioretinopathy, autosomal recessive, 2, MIM# 616171
Syndromic Retinopathy v0.74 PLK4 Zornitza Stark Publications for gene: PLK4 were set to
Syndromic Retinopathy v0.73 PLK4 Zornitza Stark Mode of inheritance for gene: PLK4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Syndromic Retinopathy v0.72 PLK4 Zornitza Stark reviewed gene: PLK4: Rating: GREEN; Mode of pathogenicity: None; Publications: 25344692, 25320347, 27650967; Phenotypes: Microcephaly and chorioretinopathy, autosomal recessive, 2, MIM# 616171; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Syndromic Retinopathy v0.0 PLK4 Bryony Thompson gene: PLK4 was added
gene: PLK4 was added to Syndromic Retinopathy. Sources: Expert Review Green,RetNet
Mode of inheritance for gene: PLK4 was set to Unknown