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Paroxysmal central nervous system disorders v0.150 SCN11A Rebecca Foulger Marked gene: SCN11A as ready
Paroxysmal central nervous system disorders v0.150 SCN11A Rebecca Foulger Gene: scn11a has been classified as Red List (Low Evidence).
Paroxysmal central nervous system disorders v0.68 SCN11A Rebecca Foulger Classified gene: SCN11A as Red List (low evidence)
Paroxysmal central nervous system disorders v0.68 SCN11A Rebecca Foulger Added comment: Comment on list classification: Demoted SCN11A from Green to Red based on Red reviews from both London North GLH, and West Midlands, Oxford and Wessex GLH.
Paroxysmal central nervous system disorders v0.68 SCN11A Rebecca Foulger Gene: scn11a has been classified as Red List (Low Evidence).
Paroxysmal central nervous system disorders v0.27 SCN11A Rebecca Foulger Source NHS GMS was added to SCN11A.
Paroxysmal central nervous system disorders v0.26 SCN11A Rebecca Foulger commented on gene: SCN11A: Review and rating from James Polke (Neurogenetics Laboratory, Institute of Neurology, London) was collated (February 2019) on behalf of London North GLH for the GMS Neurology specialist test group.
Paroxysmal central nervous system disorders v0.25 SCN11A James Polke reviewed gene: SCN11A: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Paroxysmal central nervous system disorders v0.24 SCN11A Rebecca Foulger Source London North GLH was added to SCN11A.
Paroxysmal central nervous system disorders v0.23 SCN11A Rebecca Foulger reviewed gene: SCN11A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Paroxysmal central nervous system disorders v0.22 SCN11A Tracy Lester reviewed gene: SCN11A: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Episodic pain syndrome, familial, 3, 615552, Neuropathy, hereditary sensory and autonomic, type VII, 615548; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Paroxysmal central nervous system disorders v0.21 SCN11A Rebecca Foulger Source Wessex and West Midlands GLH was added to SCN11A.
Paroxysmal central nervous system disorders v0.3 SCN11A Ellen McDonagh Added phenotypes Familial episodic pain syndrome; Episodic pain syndrome, familial, 3, 615552; Neuropathy, hereditary sensory and autonomic, type VII, 615548; Hereditary sensory and autonomic neuropathy type VII for gene: SCN11A
Paroxysmal central nervous system disorders v0.2 SCN11A Ellen McDonagh gene: SCN11A was added
gene: SCN11A was added to Paroxysmal neurological disorders, pain disorders and sleep disorders. Sources: Expert Review Green
Mode of inheritance for gene: SCN11A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: SCN11A were set to 24776970; 24207120; 27503742; 28665811; 24813307; 24036948; 25316021; 26645915; 28298626
Phenotypes for gene: SCN11A were set to Familial episodic pain syndrome; Episodic pain syndrome, familial, 3, 615552; Neuropathy, hereditary sensory and autonomic, type VII, 615548; Hereditary sensory and autonomic neuropathy type VII