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Adult onset dystonia, chorea or related movement disorder v0.88 MCOLN1 Louise Daugherty edited their review of gene: MCOLN1: Added comment: This panel was initially created as a merge of genomic entities from the following Rare Disease 100K panels - Early onset dystonia (v1.76, code 192) - Parkinson Disease and Complex Parkinsonism (v1.64, code 39) - Brain channelopathy (v1.48, code 90) - Structural basal ganglia disorders (v1.10, code 180). This gene was RED and external expert review from South West GLH for GMS Neurology specialist test group for R56 agrees this gene should remain RED; Changed rating: RED
Adult onset dystonia, chorea or related movement disorder v0.50 MCOLN1 Louise Daugherty reviewed gene: MCOLN1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.49 MCOLN1 Emily Jones reviewed gene: MCOLN1: Rating: RED; Mode of pathogenicity: ; Publications: 29449188; Phenotypes: Mucolipidosis IV, 252650; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.48 MCOLN1 Louise Daugherty Added phenotypes Mucolipidosis IV, 252650 for gene: MCOLN1
Publications for gene MCOLN1 were changed from to 29449188
Adult onset dystonia, chorea or related movement disorder v0.47 MCOLN1 Louise Daugherty Source NHS GMS was added to MCOLN1.
Adult onset dystonia, chorea or related movement disorder v0.46 MCOLN1 Louise Daugherty Source South West GLH was added to MCOLN1.
Adult onset dystonia, chorea or related movement disorder v0.2 MCOLN1 Ellen McDonagh gene: MCOLN1 was added
gene: MCOLN1 was added to Adult onset movement disorder. Sources: Expert Review Red
Mode of inheritance for gene: MCOLN1 was set to
Phenotypes for gene: MCOLN1 were set to Dystonia