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
- Mitochondrial disorders
- Structural basal ganglia disorders
- Parkinson Disease and Complex Parkinsonism
- Intellectual disability
- Hereditary spastic paraplegia, adult onset
- Undiagnosed metabolic disorders
- Likely inborn error of metabolism
- Hereditary spastic paraplegia, childhood onset
- Early onset dystonia
- Optic neuropathy
- Dystonia, chorea or related movement disorder, childhood onset
- Dystonia, chorea or related movement disorder, adult onset
- Hereditary spastic paraplegia
- Hereditary neuropathy
- Hereditary neuropathy or pain disorder
- Neurodegenerative disorders, adult onset
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