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Neurodegenerative disorders, adult onset v8.2 ABCD1 Arina Puzriakova Phenotypes for gene: ABCD1 were changed from Hereditary spastic paraplegia, MONDO:0019064; adrenal failure; VLCFA accumulation; spastic paraparesis to Adrenoleukodystrophy, adult, OMIM:300100
Neurodegenerative disorders, adult onset v2.43 ABCD1 Ivone Leong Phenotypes for gene: ABCD1 were changed from Hereditary spastic paraplegia; adrenal failure; VLCFA accumulation; spastic paraparesis to Hereditary spastic paraplegia, MONDO:0019064; adrenal failure; VLCFA accumulation; spastic paraparesis
Neurodegenerative disorders, adult onset v1.101 ABCD1 Louise Daugherty commented on gene: ABCD1: Review and rating from Tracy Lester (Oxford Medical Genetics Laboratories Oxford University Hospitals NHS Foundation Trust) on behalf of Wessex and West Midlands GLH for GMS Neurology specialist test group. All the green and amber, except for the genes with triplet repeats, were reviewed.
Neurodegenerative disorders, adult onset v1.100 ABCD1 Louise Daugherty Source Wessex and West Midlands GLH was added to ABCD1.
Neurodegenerative disorders, adult onset v1.99 ABCD1 Tracy Lester reviewed gene: ABCD1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: Hereditary spastic paraplegia, adrenal failure, VLCFA accumulation, spastic paraparesis; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Neurodegenerative disorders, adult onset v1.74 ABCD1 Louise Daugherty commented on gene: ABCD1: Review and rating submitted by Nick Beauchamp (Sheffield Diagnostic genetics Service), on behalf of Yorkshire and North East GLH for GMS Neurology specialist test group.
Neurodegenerative disorders, adult onset v1.72 ABCD1 Nick Beauchamp reviewed gene: ABCD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Hereditary spastic paraplegia, adrenal failure, VLCFA accumulation, spastic paraparesis; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males); Current diagnostic: yes
Neurodegenerative disorders, adult onset v1.67 ABCD1 Louise Daugherty Source Yorkshire and North East GLH was added to ABCD1.
Neurodegenerative disorders, adult onset v1.11 ABCD1 Louise Daugherty reviewed gene: ABCD1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Neurodegenerative disorders, adult onset v1.10 ABCD1 James Polke reviewed gene: ABCD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Neurodegenerative disorders, adult onset v1.9 ABCD1 Louise Daugherty Source NHS GMS was added to ABCD1.
Neurodegenerative disorders, adult onset v1.8 ABCD1 Louise Daugherty Source London North GLH was added to ABCD1.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Neurodegenerative disorders, adult onset v0.82 ABCD1 Rebecca Foulger Publications for gene: ABCD1 were set to 11810273; 27084228; 11739809; 26049658
Neurodegenerative disorders, adult onset v0.81 ABCD1 Rebecca Foulger Phenotypes for gene: ABCD1 were changed from Hereditary spastic paraplegia; adrenal failure; VLCFA accumulation to Hereditary spastic paraplegia; adrenal failure; VLCFA accumulation; spastic paraparesis
Neurodegenerative disorders, adult onset v0.80 ABCD1 Rebecca Foulger Classified gene: ABCD1 as Green List (high evidence)
Neurodegenerative disorders, adult onset v0.80 ABCD1 Rebecca Foulger Added comment: Comment on list classification: Updated rating from Red to Green following review on the Hereditary spastic paraplegia panel.
Neurodegenerative disorders, adult onset v0.80 ABCD1 Rebecca Foulger Gene: abcd1 has been classified as Green List (High Evidence).
Neurodegenerative disorders, adult onset v0.47 ABCD1 Rebecca Foulger Classified gene: ABCD1 as Red List (low evidence)
Neurodegenerative disorders, adult onset v0.47 ABCD1 Rebecca Foulger Added comment: Comment on list classification: Updated rating from Grey to Red, to include gene on merged panel. Gene still requires review/curator evaluation for a final rating.
Neurodegenerative disorders, adult onset v0.47 ABCD1 Rebecca Foulger Gene: abcd1 has been classified as Red List (Low Evidence).
Neurodegenerative disorders, adult onset v0.27 ABCD1 Rebecca Foulger commented on gene: ABCD1
Neurodegenerative disorders, adult onset v0.5 ABCD1 Rebecca Foulger Classified gene: ABCD1 as No list
Neurodegenerative disorders, adult onset v0.5 ABCD1 Rebecca Foulger Gene: abcd1 has been removed from the panel.
Neurodegenerative disorders, adult onset v0.4 ABCD1 Rebecca Foulger gene: ABCD1 was added
gene: ABCD1 was added to Neurodegenerative disorders - adult onset. Sources: Expert list
Mode of inheritance for gene: ABCD1 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for gene: ABCD1 were set to 11810273; 27084228; 11739809; 26049658
Phenotypes for gene: ABCD1 were set to Hereditary spastic paraplegia; adrenal failure; VLCFA accumulation