Early onset and familial Parkinson's Disease
Gene: TUBB4AEnsemblGeneIds (GRCh38): ENSG00000104833
EnsemblGeneIds (GRCh37): ENSG00000104833
OMIM: 602662, Gene2Phenotype
TUBB4A is in 19 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, 11:56 a.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Dystonia
- ?Dystonia 4, torsion, autosomal dominant, 128101
- hereditary whispering dysphonia
- OMIM
- 602662
- Clinvar variants
- Variants in TUBB4A
- Penetrance
- Complete
- Panels with this gene
-
- Adult onset hereditary spastic paraplegia
- Structural basal ganglia disorders
- White matter disorders and cerebral calcification - narrow panel
- Hereditary ataxia with onset in adulthood
- Adult onset leukodystrophy
- DDG2P
- Inherited white matter disorders
- Hereditary ataxia
- Fetal anomalies
- Childhood onset hereditary spastic paraplegia
- Adult onset neurodegenerative disorder
- Early onset or syndromic epilepsy
- Early onset dystonia
- Hereditary spastic paraplegia
- Intellectual disability
- Childhood onset dystonia, chorea or related movement disorder
- Parkinson Disease and Complex Parkinsonism
- Adult onset dystonia, chorea or related movement disorder
- Ataxia and cerebellar anomalies - narrow panel
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)TUBB4A was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)TUBB4A was added to Early onset and familial Parkinson's Diseasepanel. Sources: Expert list