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Fetal anomalies v0.2854 SCLT1 Zornitza Stark Marked gene: SCLT1 as ready
Fetal anomalies v0.2854 SCLT1 Zornitza Stark Gene: sclt1 has been classified as Green List (High Evidence).
Fetal anomalies v0.2854 SCLT1 Zornitza Stark Phenotypes for gene: SCLT1 were changed from Senior-L ken Syndrome; No OMIM phenotype; Oro-facio-digital syndrome type IX to Orofaciodigital syndrome type IX; Senior-Loken syndrome; Bardet-Biedl syndrome
Fetal anomalies v0.2853 SCLT1 Zornitza Stark Publications for gene: SCLT1 were set to 28486600; 30425282; 23348840; 24285566; 28005958
Fetal anomalies v0.2852 SCLT1 Zornitza Stark Classified gene: SCLT1 as Green List (high evidence)
Fetal anomalies v0.2852 SCLT1 Zornitza Stark Gene: sclt1 has been classified as Green List (High Evidence).
Fetal anomalies v0.2851 SCLT1 Zornitza Stark changed review comment from: Established ciliopathy gene but no clear association with ciliopathy/JS-type structural brain abnormalities.; to: Established ciliopathy gene.
Fetal anomalies v0.2851 SCLT1 Zornitza Stark edited their review of gene: SCLT1: Changed rating: GREEN
Fetal anomalies v0.0 SCLT1 Zornitza Stark gene: SCLT1 was added
gene: SCLT1 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: SCLT1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SCLT1 were set to 28486600; 30425282; 23348840; 24285566; 28005958
Phenotypes for gene: SCLT1 were set to Senior-L ken Syndrome; No OMIM phenotype; Oro-facio-digital syndrome type IX