huntington disease Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A neurodegenerative disease and an autosomal dominant disease that is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities. (Human Disease Ontology, DOID_12858)
Similar Terms
Downloads & Tools

Genes

10 genes associated with the disease huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
ADORA2A	adenosine A2a receptor
GRIK1	glutamate receptor, ionotropic, kainate 1
HAP1	huntingtin-associated protein 1
HDAC1	histone deacetylase 1
HTT	huntingtin
MAP2K6	mitogen-activated protein kinase kinase 6
MAP3K6	mitogen-activated protein kinase kinase kinase 6
PEX7	peroxisomal biogenesis factor 7
STH	saitohin
UCHL1	ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)