This Panel is marked as Internal
Early onset and familial Parkinson's Disease
Gene: TOR1A
TOR1A (torsin family 1 member A)
EnsemblGeneIds (GRCh38): ENSG00000136827
EnsemblGeneIds (GRCh37): ENSG00000136827
OMIM: 605204, Gene2Phenotype
TOR1A is in 10 panels
EnsemblGeneIds (GRCh38): ENSG00000136827
EnsemblGeneIds (GRCh37): ENSG00000136827
OMIM: 605204, Gene2Phenotype
TOR1A is in 10 panels
1 review
Ellen McDonagh (Genomics England Curator)
Comment on list classification: Is on the Complex Parkinson's Disease/Dystonia NGS Panel in the UCLH National Hospital for Neurology and Neurosurgery & Institute of Neurology (NHNN) Neurogenetics genetic testing manual.Created: 10 Jun 2016, 11:49 a.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Early-Onset Primary Dystonia
- Dystonia-1, torsion, 128100
- Autosomal dominant or sporadic dystonia (DYT1)
- OMIM
- 605204
- Clinvar variants
- Variants in TOR1A
- Penetrance
- Complete
- Publications
-
- http://www.ncbi.nlm.nih.gov/books/NBK1155/
- Panels with this gene
-
- Structural basal ganglia disorders
- Intellectual disability
- Parkinson Disease and Complex Parkinsonism
- Early onset dystonia
- Adult onset dystonia, chorea or related movement disorder
- Adult onset neurodegenerative disorder
- DDG2P
- Arthrogryposis
- Childhood onset dystonia, chorea or related movement disorder
- Fetal anomalies
History Filter Activity
10 Jun 2016, Gel status: 4
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
10 Jun 2016, Gel status: 0
Created
Ellen McDonagh (Genomics England Curator)TOR1A was created by ellenmcdonagh
10 Jun 2016, Gel status: 0
Added New Source
Ellen McDonagh (Genomics England Curator)TOR1A was added to Early onset and familial Parkinson's Diseasepanel. Sources: Expert list