Complex Parkinsonism (includes pallido-pyramidal syndromes)
Gene: SPREnsemblGeneIds (GRCh38): ENSG00000116096
EnsemblGeneIds (GRCh37): ENSG00000116096
OMIM: 182125, Gene2Phenotype
SPR is in 16 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, 11:32 a.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Dopa-Responsive Dystonia
- Dystonia, dopa-responsive, due to sepiapterin reductase deficiency, 612716
- paediatric form of dopa responsive dystonia
- OMIM
- 182125
- Clinvar variants
- Variants in SPR
- Penetrance
- Complete
- Publications
-
- http://www.ncbi.nlm.nih.gov/books/NBK1155/
- Panels with this gene
-
- Parkinson Disease and Complex Parkinsonism
- Ataxia and cerebellar anomalies - childhood onset
- Neurodegenerative disorders, adult onset
- Early onset or syndromic epilepsy
- Dystonia, chorea or related movement disorder, childhood onset
- Likely inborn error of metabolism
- Intellectual disability
- Undiagnosed metabolic disorders
- Hereditary ataxia, adult onset
- Neurotransmitter disorders
- Early onset dystonia
- Dystonia, chorea or related movement disorder, adult onset
- Fetal anomalies
- DDG2P
- Brain channelopathy
- Paroxysmal central nervous system disorders
History Filter Activity
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)SPR was added to Complex Parkinsonism (includes pallido-pyramidal syndromes)panel. Sources: Expert list
Created
Ellen McDonagh (Genomics England Curator)SPR was created by ellenmcdonagh