Complex Parkinsonism (includes pallido-pyramidal syndromes)
Gene: C19orf12EnsemblGeneIds (GRCh38): ENSG00000131943
EnsemblGeneIds (GRCh37): ENSG00000131943
OMIM: 614297, Gene2Phenotype
C19orf12 is in 17 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, 11:04 a.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Dystonia
- mitochondrial membrane protein-associated neurodegeneration
- OMIM
- 614297
- Clinvar variants
- Variants in C19orf12
- Penetrance
- Complete
- Panels with this gene
-
- Possible mitochondrial disorder - nuclear genes
- Adult onset hereditary spastic paraplegia
- Structural basal ganglia disorders
- Hereditary neuropathy or pain disorder
- Undiagnosed metabolic disorders
- Childhood onset dystonia, chorea or related movement disorder
- Mitochondrial disorders
- Childhood onset hereditary spastic paraplegia
- Likely inborn error of metabolism
- Intellectual disability
- Early onset dystonia
- Hereditary spastic paraplegia
- Adult onset neurodegenerative disorder
- Parkinson Disease and Complex Parkinsonism
- Optic neuropathy
- Hereditary neuropathy
- Adult onset dystonia, chorea or related movement disorder
History Filter Activity
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Created
Ellen McDonagh (Genomics England Curator)C19orf12 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)C19orf12 was added to Complex Parkinsonism (includes pallido-pyramidal syndromes)panel. Sources: Expert list