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Severe Paediatric Disorders v0.12 TAZ Louise Daugherty reviewed gene: TAZ: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 TAZ Louise Daugherty Publications for gene TAZ were updated from to 30847515
Severe Paediatric Disorders v0.10 TAZ Louise Daugherty Added phenotypes Barth syndrome, 302060 for gene: TAZ
Severe Paediatric Disorders v0.10 SCN4A Louise Daugherty Added phenotypes Hyperkalemic periodic paralysis, type 2, 170500; Myasthenic syndrome, congenital, 16, 614198; Myotonia congenita, atypical, acetazolamide-responsive, 608390; Hypokalemic periodic paralysis, type 2, 613345; Paramyotonia congenita, 168300 for gene: SCN4A
Severe Paediatric Disorders v0.9 TAZ Louise Daugherty Added phenotypes Barth syndrome, 302060 for gene: TAZ
Severe Paediatric Disorders v0.9 SCN4A Louise Daugherty Added phenotypes Hyperkalemic periodic paralysis, type 2, 170500; Myasthenic syndrome, congenital, 16, 614198; Myotonia congenita, atypical, acetazolamide-responsive, 608390; Hypokalemic periodic paralysis, type 2, 613345; Paramyotonia congenita, 168300 for gene: SCN4A
Severe Paediatric Disorders v0.9 TAZ Louise Daugherty Added phenotypes Barth syndrome, 302060 for gene: TAZ
Severe Paediatric Disorders v0.9 SCN4A Louise Daugherty Added phenotypes Hyperkalemic periodic paralysis, type 2, 170500; Myasthenic syndrome, congenital, 16, 614198; Myotonia congenita, atypical, acetazolamide-responsive, 608390; Hypokalemic periodic paralysis, type 2, 613345; Paramyotonia congenita, 168300 for gene: SCN4A
Severe Paediatric Disorders v0.8 TAZ Louise Daugherty Added phenotypes Barth syndrome, 302060 for gene: TAZ
Severe Paediatric Disorders v0.8 SCN4A Louise Daugherty Added phenotypes Hypokalemic periodic paralysis, type 2, 613345; Myasthenic syndrome, congenital, 16, 614198; Paramyotonia congenita, 168300; Hyperkalemic periodic paralysis, type 2, 170500; Myotonia congenita, atypical, acetazolamide-responsive, 608390 for gene: SCN4A
Severe Paediatric Disorders v0.8 TAZ Louise Daugherty Mode of inheritance for gene TAZ was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Added phenotypes Barth syndrome, 302060 for gene: TAZ
Severe Paediatric Disorders v0.8 SCN4A Louise Daugherty Mode of inheritance for gene SCN4A was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes Hyperkalemic periodic paralysis, type 2, 170500; Myasthenic syndrome, congenital, 16, 614198; Myotonia congenita, atypical, acetazolamide-responsive, 608390; Hypokalemic periodic paralysis, type 2, 613345; Paramyotonia congenita, 168300 for gene: SCN4A
Severe Paediatric Disorders v0.7 TAZ Louise Daugherty Source Next Generation Children Project was added to TAZ.
Severe Paediatric Disorders v0.5 TAZ Louise Daugherty Source Expert Review Green was added to TAZ.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 TAZ Louise Daugherty gene: TAZ was added
gene: TAZ was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: TAZ was set to