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Adult onset dystonia, chorea or related movement disorder v1.166 ATN1_CAG Ivone Leong commented on STR: ATN1_CAG
Adult onset dystonia, chorea or related movement disorder v1.162 ATN1_CAG Arina Puzriakova Normal Number of Repeats for ATN1_CAG was changed from 35 to 36.
Adult onset dystonia, chorea or related movement disorder v1.128 ATN1_CAG Arina Puzriakova Phenotypes for STR: ATN1_CAG were changed from Dentatorubro-pallidoluysian atrophy 125370 to Dentatorubral-pallidoluysian atrophy, OMIM:125370
Adult onset dystonia, chorea or related movement disorder v1.127 ATN1 Arina Puzriakova Phenotypes for gene: ATN1 were changed from Dentatorubro-pallidoluysian atrophy 125370 to Dentatorubral-pallidoluysian atrophy, OMIM:125370
Adult onset dystonia, chorea or related movement disorder v1.126 ATN1 Arina Puzriakova Tag nucleotide-repeat-expansion tag was added to gene: ATN1.
Tag currently-ngs-unreportable tag was added to gene: ATN1.
Adult onset dystonia, chorea or related movement disorder v1.126 ATN1 Arina Puzriakova Added comment: Comment on mode of inheritance: Lack of phenotypic relevance for SNVs - nucleotide repeat expansion mechanism
Adult onset dystonia, chorea or related movement disorder v1.126 ATN1 Arina Puzriakova Mode of inheritance for gene: ATN1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to Other
Adult onset dystonia, chorea or related movement disorder v0.92 ATN1_CAG Louise Daugherty Source NHS GMS was added to STR: ATN1_CAG.
Adult onset dystonia, chorea or related movement disorder v0.91 ATN1_CAG Louise Daugherty commented on STR: ATN1_CAG: Discussed with the GMS Neurology Specialist Test Group webex call 26th July 2019: The Specialist Test Group all agreed that there is enough evidence to rate this STR Green
Adult onset dystonia, chorea or related movement disorder v0.90 ATN1 Louise Daugherty commented on gene: ATN1: As discussed with the GMS Neurology Specialist Test Group webex call 26th July 2019: The Specialist Test Group all agreed that there is only enough evidence to rate this gene Red
Adult onset dystonia, chorea or related movement disorder v0.87 ATN1 Louise Daugherty edited their review of gene: ATN1: 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) and Hereditary ataxia v1.148 - Brain channelopathy v1.46.
This gene was uploaded from the curation template sent out to the GLHs for GMS Neurology specialist test group as it is a RED gene on the Brain channelopathy panel. The GREEN review from James Polke (Neurogenetics Laboratory, Institute of Neurology, London) is likely to relate to the STR ATN1_CAG and not the gene entity, as there are no SNVs for this gene being associated to the disorder, this gene is rated RED.; Changed rating: RED
Adult onset dystonia, chorea or related movement disorder v0.54 ATN1 Louise Daugherty commented on gene: ATN1: Review and rating submitted by James Polke (North Bristol NHS Trust), unless specified in the review comment, on behalf of London North GLH for GMS Neurology specialist test group.
Adult onset dystonia, chorea or related movement disorder v0.53 ATN1 James Polke reviewed gene: ATN1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.51 ATN1 Louise Daugherty Source London North GLH was added to ATN1.
Adult onset dystonia, chorea or related movement disorder v0.50 ATN1 Louise Daugherty reviewed gene: ATN1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.49 ATN1 Emily Jones reviewed gene: ATN1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Dentatorubro-pallidoluysian atrophy 125370; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Adult onset dystonia, chorea or related movement disorder v0.48 ATN1 Louise Daugherty Added phenotypes Dentatorubro-pallidoluysian atrophy 125370 for gene: ATN1
Adult onset dystonia, chorea or related movement disorder v0.47 ATN1 Louise Daugherty Source NHS GMS was added to ATN1.
Adult onset dystonia, chorea or related movement disorder v0.46 ATN1 Louise Daugherty Source South West GLH was added to ATN1.
Adult onset dystonia, chorea or related movement disorder v0.22 ATN1_CAG Louise Daugherty Classified STR: ATN1_CAG as Green List (high evidence)
Adult onset dystonia, chorea or related movement disorder v0.22 ATN1_CAG Louise Daugherty Str: atn1_cag has been classified as Green List (High Evidence).
Adult onset dystonia, chorea or related movement disorder v0.21 ATN1_CAG Louise Daugherty Phenotypes for STR: ATN1_CAG were changed from Dentatorubro-pallidoluysian atrophy 125370 to Dentatorubro-pallidoluysian atrophy 125370
Adult onset dystonia, chorea or related movement disorder v0.20 ATN1_CAG Louise Daugherty STR: ATN1_CAG was added
STR: ATN1_CAG was added to Adult onset movement disorder. Sources: Expert list
STR tags were added to STR: ATN1_CAG.
Mode of inheritance for STR: ATN1_CAG was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for STR: ATN1_CAG were set to 20301664; 8136840; 20301664; 8136840; 8136826; 7614090
Phenotypes for STR: ATN1_CAG were set to Dentatorubro-pallidoluysian atrophy 125370
Added comment: Source PanelApp panels : Early onset dystonia v1.76, Parkinson Disease and Complex Parkinsonism v1.64, Brain channelopathy v1.48
Sources: Expert list
Adult onset dystonia, chorea or related movement disorder v0.2 ATN1 Ellen McDonagh gene: ATN1 was added
gene: ATN1 was added to Adult onset movement disorder. Sources: Expert Review Red
Mode of inheritance for gene: ATN1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: ATN1 were set to Dentatorubro-pallidoluysian atrophy 125370
Mode of pathogenicity for gene: ATN1 was set to Other - please provide details in the comments