dementia Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A cognitive disorder resulting from a loss of brain function affecting memory, thinking, language, judgement and behavior. (Human Disease Ontology, DOID_1307)
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Genes

14 genes involed in the disease dementia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ADAM10 ADAM metallopeptidase domain 10
APOE apolipoprotein E
APP amyloid beta (A4) precursor protein
CTSD cathepsin D
GSK3A glycogen synthase kinase 3 alpha
GSK3B glycogen synthase kinase 3 beta
MAPT microtubule-associated protein tau
PLD3 phospholipase D family, member 3
PPP5C protein phosphatase 5, catalytic subunit
PSEN1 presenilin 1
PSEN2 presenilin 2
RALGPS2 Ral GEF with PH domain and SH3 binding motif 2
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SORL1 sortilin-related receptor, L(DLR class) A repeats containing