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Dystonia and Chorea v1.0 SHQ1 Gene migrated from ENSG00000144736 to ENSG00000144736 (gene set migration)
Dystonia and Chorea v0.231 SHQ1 Zornitza Stark Publications for gene: SHQ1 were set to 34542157; 29178645
Dystonia and Chorea v0.230 SHQ1 Zornitza Stark Classified gene: SHQ1 as Green List (high evidence)
Dystonia and Chorea v0.230 SHQ1 Zornitza Stark Gene: shq1 has been classified as Green List (High Evidence).
Dystonia and Chorea v0.229 SHQ1 Zornitza Stark edited their review of gene: SHQ1: Added comment: Two more individuals with dystonia reported.; Changed rating: GREEN; Changed publications: 34542157, 29178645, 36847845, 37475611
Dystonia and Chorea v0.215 SHQ1 Zornitza Stark Phenotypes for gene: SHQ1 were changed from Dystonia; Neurodegeneration to Dystonia 35, childhood-onset , MIM# 619921; Neurodevelopmental disorder with dystonia and seizures, MIM# 619922
Dystonia and Chorea v0.214 SHQ1 Zornitza Stark edited their review of gene: SHQ1: Changed phenotypes: Dystonia 35, childhood-onset , MIM# 619921, Neurodevelopmental disorder with dystonia and seizures, MIM# 619922
Dystonia and Chorea v0.194 SHQ1 Zornitza Stark Marked gene: SHQ1 as ready
Dystonia and Chorea v0.194 SHQ1 Zornitza Stark Gene: shq1 has been classified as Amber List (Moderate Evidence).
Dystonia and Chorea v0.194 SHQ1 Zornitza Stark Classified gene: SHQ1 as Amber List (moderate evidence)
Dystonia and Chorea v0.194 SHQ1 Zornitza Stark Gene: shq1 has been classified as Amber List (Moderate Evidence).
Dystonia and Chorea v0.193 SHQ1 Zornitza Stark gene: SHQ1 was added
gene: SHQ1 was added to Dystonia - complex. Sources: Literature
Mode of inheritance for gene: SHQ1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SHQ1 were set to 34542157; 29178645
Phenotypes for gene: SHQ1 were set to Dystonia; Neurodegeneration
Review for gene: SHQ1 was set to AMBER
Added comment: Three unrelated families reported. Family 1: isolated dystonia only; Family 2: dystonia, and neurodegeneration; Family 3: neurodegeneration. Rated Amber as phenotypes likely represent a continuum but currently unclear what proportion will have complex dystonia.
Sources: Literature