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Ciliopathies v1.27 SUFU Zornitza Stark Phenotypes for gene: SUFU were changed from Joubert syndrome 32, MIM#617757 to Joubert syndrome 32, MIM#617757; SUFU-related neurodevelopmental disorder, Joubert-like
Ciliopathies v1.26 SUFU Zornitza Stark Publications for gene: SUFU were set to 28965847
Ciliopathies v1.25 SUFU Zornitza Stark Mode of inheritance for gene: SUFU was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Ciliopathies v1.24 SUFU Zornitza Stark Classified gene: SUFU as Green List (high evidence)
Ciliopathies v1.24 SUFU Zornitza Stark Gene: sufu has been classified as Green List (High Evidence).
Ciliopathies v1.23 SUFU Zornitza Stark edited their review of gene: SUFU: Added comment: Further 22 individuals reported with LoF variants in SUFU and a phenotype described as being on the mild end of JS. Clinical features included congenital oculomotor apraxia, hypotonia, ataxia and mild DD, and only a third manifested intellectual disability of variable severity. Brain MRI showed consistent findings characterised by vermis hypoplasia, superior cerebellar dysplasia and subtle-to-mild abnormalities of the superior cerebellar peduncles.; Changed rating: GREEN; Changed publications: 28965847, 34675124; Changed phenotypes: Joubert syndrome 32, MIM#617757, SUFU-related neurodevelopmental disorder, Joubert-like; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Ciliopathies v0.72 SUFU Zornitza Stark Marked gene: SUFU as ready
Ciliopathies v0.72 SUFU Zornitza Stark Gene: sufu has been classified as Amber List (Moderate Evidence).
Ciliopathies v0.72 SUFU Zornitza Stark Phenotypes for gene: SUFU were changed from to Joubert syndrome 32, MIM#617757
Ciliopathies v0.71 SUFU Zornitza Stark Publications for gene: SUFU were set to
Ciliopathies v0.70 SUFU Zornitza Stark Mode of inheritance for gene: SUFU was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Ciliopathies v0.69 SUFU Zornitza Stark Classified gene: SUFU as Amber List (moderate evidence)
Ciliopathies v0.69 SUFU Zornitza Stark Gene: sufu has been classified as Amber List (Moderate Evidence).
Ciliopathies v0.68 SUFU Zornitza Stark reviewed gene: SUFU: Rating: AMBER; Mode of pathogenicity: None; Publications: 28965847; Phenotypes: Joubert syndrome 32, MIM#617757; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ciliopathies v0.0 SUFU Zornitza Stark gene: SUFU was added
gene: SUFU was added to Ciliopathies_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: SUFU was set to Unknown