Progressive supranuclear palsy Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A movement disease characterized by serious and progressive problems with control of gait and balance, along with complex eye movement and thinking problems. It involves gradual deterioration and death of specific volumes of the brain. (Human Disease Ontology, DOID_678)
External Link supranuclear palsy
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7 genes associated with the Progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
MAPT microtubule-associated protein tau 1.99506
MOBP myelin-associated oligodendrocyte basic protein 0.923741
IRF4 interferon regulatory factor 4 0.827738
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3 0.734471
STX6 syntaxin 6 0.618573
CD8B CD8b molecule 0.434785
SLCO1A2 solute carrier organic anion transporter family, member 1A2 0.356403