frontotemporal lobar degeneration Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A basal ganglia disease characterized by progressive neuronal loss predominantly involving the frontal and/or temporal lobes of the brain resulting in a gradual and progressive decline in behavior or language. (Human Disease Ontology, DOID_9255)
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11 genes associated with the disease frontotemporal lobar degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
CHMP2B charged multivesicular body protein 2B
CST3 cystatin C
GRN granulin
KIF24 kinesin family member 24
MAPT microtubule-associated protein tau
SORT1 sortilin 1
TARDBP TAR DNA binding protein
TMEM106B transmembrane protein 106B
UBAP1 ubiquitin associated protein 1
UBAP2 ubiquitin associated protein 2