Huntington's disease Gene Set

Dataset PhosphoSitePlus Phosphosite-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)
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Genes

2 proteins associated with the disease Huntington's disease from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Symbol Name
HTT huntingtin
TP53 tumor protein p53