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Paroxysmal central nervous system disorders v0.150 PRDM12 Rebecca Foulger Marked gene: PRDM12 as ready
Paroxysmal central nervous system disorders v0.150 PRDM12 Rebecca Foulger Gene: prdm12 has been classified as Red List (Low Evidence).
Paroxysmal central nervous system disorders v0.57 PRDM12 Rebecca Foulger Classified gene: PRDM12 as Red List (low evidence)
Paroxysmal central nervous system disorders v0.57 PRDM12 Rebecca Foulger Added comment: Comment on list classification: Demoted PRDM12 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 v0.57 PRDM12 Rebecca Foulger Gene: prdm12 has been classified as Red List (Low Evidence).
Paroxysmal central nervous system disorders v0.56 PRDM12 Rebecca Foulger Deleted their comment
Paroxysmal central nervous system disorders v0.56 PRDM12 Rebecca Foulger commented on gene: PRDM12: Demoted PRDM12 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 v0.27 PRDM12 Rebecca Foulger Source NHS GMS was added to PRDM12.
Paroxysmal central nervous system disorders v0.26 PRDM12 Rebecca Foulger commented on gene: PRDM12: 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 PRDM12 James Polke reviewed gene: PRDM12: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Paroxysmal central nervous system disorders v0.24 PRDM12 Rebecca Foulger Source London North GLH was added to PRDM12.
Paroxysmal central nervous system disorders v0.23 PRDM12 Rebecca Foulger reviewed gene: PRDM12: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Paroxysmal central nervous system disorders v0.22 PRDM12 Tracy Lester reviewed gene: PRDM12: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Neuropathy, hereditary sensory and autonomic, type VIII, 616488; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Paroxysmal central nervous system disorders v0.21 PRDM12 Rebecca Foulger Source Wessex and West Midlands GLH was added to PRDM12.
Paroxysmal central nervous system disorders v0.3 PRDM12 Ellen McDonagh Added phenotypes Neuropathy, hereditary sensory and autonomic, type VIII, 616488; Hereditary sensory and autonomic neuropathy type VIII; HSAN 8 for gene: PRDM12
Paroxysmal central nervous system disorders v0.2 PRDM12 Ellen McDonagh gene: PRDM12 was added
gene: PRDM12 was added to Paroxysmal neurological disorders, pain disorders and sleep disorders. Sources: Expert Review Green
Mode of inheritance for gene: PRDM12 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PRDM12 were set to 26975306; 26005867
Phenotypes for gene: PRDM12 were set to Neuropathy, hereditary sensory and autonomic, type VIII, 616488; Hereditary sensory and autonomic neuropathy type VIII; HSAN 8