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Paroxysmal central nervous system disorders v0.150 TRPA1 Rebecca Foulger Marked gene: TRPA1 as ready
Paroxysmal central nervous system disorders v0.150 TRPA1 Rebecca Foulger Gene: trpa1 has been classified as Red List (Low Evidence).
Paroxysmal central nervous system disorders v0.78 TRPA1 Rebecca Foulger Classified gene: TRPA1 as Red List (low evidence)
Paroxysmal central nervous system disorders v0.78 TRPA1 Rebecca Foulger Added comment: Comment on list classification: Demoted TRPA1 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 v0.78 TRPA1 Rebecca Foulger Gene: trpa1 has been classified as Red List (Low Evidence).
Paroxysmal central nervous system disorders v0.77 TRPA1 Rebecca Foulger Phenotypes for gene: TRPA1 were changed from Episodic pain syndrome, familial, 615040; Familial episodic pain syndrome type I to ?Episodic pain syndrome, familial, 1, 615040; Familial episodic pain syndrome type I
Paroxysmal central nervous system disorders v0.27 TRPA1 Rebecca Foulger Source NHS GMS was added to TRPA1.
Paroxysmal central nervous system disorders v0.26 TRPA1 Rebecca Foulger commented on gene: TRPA1: 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 TRPA1 James Polke reviewed gene: TRPA1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Paroxysmal central nervous system disorders v0.24 TRPA1 Rebecca Foulger Source London North GLH was added to TRPA1.
Paroxysmal central nervous system disorders v0.23 TRPA1 Rebecca Foulger reviewed gene: TRPA1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Paroxysmal central nervous system disorders v0.22 TRPA1 Tracy Lester reviewed gene: TRPA1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Episodic pain syndrome, familial, 1, 615040; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Paroxysmal central nervous system disorders v0.21 TRPA1 Rebecca Foulger Source Wessex and West Midlands GLH was added to TRPA1.
Paroxysmal central nervous system disorders v0.3 TRPA1 Ellen McDonagh Added phenotypes Episodic pain syndrome, familial, 615040; Familial episodic pain syndrome type I for gene: TRPA1
Paroxysmal central nervous system disorders v0.2 TRPA1 Ellen McDonagh gene: TRPA1 was added
gene: TRPA1 was added to Paroxysmal neurological disorders, pain disorders and sleep disorders. Sources: Expert Review Green
Mode of inheritance for gene: TRPA1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: TRPA1 were set to 28314413; 20718100; 28436534; 24778270; 16564016; 20547126; 24564660; 21468319
Phenotypes for gene: TRPA1 were set to Episodic pain syndrome, familial, 615040; Familial episodic pain syndrome type I