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Paroxysmal central nervous system disorders v0.125 PDE10A Rebecca Foulger Marked gene: PDE10A as ready
Paroxysmal central nervous system disorders v0.125 PDE10A Rebecca Foulger Gene: pde10a has been classified as Green List (High Evidence).
Paroxysmal central nervous system disorders v0.103 PDE10A Rebecca Foulger Classified gene: PDE10A as Green List (high evidence)
Paroxysmal central nervous system disorders v0.103 PDE10A Rebecca Foulger Added comment: Comment on list classification: Kept rating of PDE10A as Green following Green reviews from both London North GLH, and West Midlands, Oxford and Wessex GLH.
Paroxysmal central nervous system disorders v0.103 PDE10A Rebecca Foulger Gene: pde10a has been classified as Green List (High Evidence).
Paroxysmal central nervous system disorders v0.102 PDE10A Rebecca Foulger Phenotypes for gene: PDE10A were changed from to Dyskinesia, limb and orofacial, infantile-onset, 616921; Infantile-onset limb and orofacial dyskinesia
Paroxysmal central nervous system disorders v0.101 PDE10A Rebecca Foulger Added comment: Comment on mode of inheritance: Set Mode of Inheritance to BIALLELIC to match MOI suggestion from both London North GLH, and West Midlands, Oxford and Wessex GLH.
Paroxysmal central nervous system disorders v0.101 PDE10A Rebecca Foulger Mode of inheritance for gene: PDE10A was changed from to BIALLELIC, autosomal or pseudoautosomal
Paroxysmal central nervous system disorders v0.98 PDE10A Rebecca Foulger commented on gene: PDE10A: Review and rating from Robyn Labrum (University College London Hospitals) was collated (September 19th 2019) on behalf of London North GLH for the GMS Neurology specialist test group. Re-review of a subset of genes was conducted in September 2019 to reach a rating consensus for clinical indication R66: Paroxysmal central nervous system disorders. Suggested rating: Green.
Paroxysmal central nervous system disorders v0.97 PDE10A Robyn Labrum reviewed gene: PDE10A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Infantile-onset limb and orofacial dyskinesia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Paroxysmal central nervous system disorders v0.96 PDE10A Rebecca Foulger commented on gene: PDE10A: Review and rating from Penny Clouston (Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust) was collated (September 19th 2019) on behalf of West Midlands, Oxford and Wessex GLH for the GMS Neurology specialist test group. This rating is for a gene (PDE10A) previously added to the panel by London North GLH. Suggested rating: Green.
Paroxysmal central nervous system disorders v0.95 PDE10A Penny Clouston reviewed gene: PDE10A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Dyskinesia, limb and orofacial, infantile-onset (OMIM 616921); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Paroxysmal central nervous system disorders v0.27 PDE10A Rebecca Foulger Source NHS GMS was added to PDE10A.
Paroxysmal central nervous system disorders v0.26 PDE10A Rebecca Foulger reviewed gene: PDE10A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Paroxysmal central nervous system disorders v0.25 PDE10A James Polke reviewed gene: PDE10A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Paroxysmal central nervous system disorders v0.24 PDE10A Rebecca Foulger gene: PDE10A was added
gene: PDE10A was added to Paroxysmal neurological disorders, pain disorders and sleep disorders. Sources: Expert Review Green,London North GLH
Mode of inheritance for gene: PDE10A was set to