vascular dementia Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A dementia that involves impairments in cognitive function caused by problems in blood vessels that feed the brain. (Human Disease Ontology, DOID_8725)
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23 genes associated with the disease vascular dementia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
SYK spleen tyrosine kinase 1.5865
RASGRF2 Ras protein-specific guanine nucleotide-releasing factor 2 1.36306
USP13 ubiquitin specific peptidase 13 (isopeptidase T-3) 1.19242
AR androgen receptor 1.09769
STK32B serine/threonine kinase 32B 0.949336
GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2 0.948266
SH3PXD2A SH3 and PX domains 2A 0.927636
EPB41L3 erythrocyte membrane protein band 4.1-like 3 0.868556
C6ORF10 chromosome 6 open reading frame 10 0.859451
PAK1 p21 protein (Cdc42/Rac)-activated kinase 1 0.837718
NEGR1 neuronal growth regulator 1 0.813075
HEPH hephaestin 0.772631
AKAP10 A kinase (PRKA) anchor protein 10 0.76818
SASS6 spindle assembly 6 homolog (C. elegans) 0.748359
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit 0.747865
EFTUD1 elongation factor Tu GTP binding domain containing 1 0.743993
EPHB1 EPH receptor B1 0.742578
MGST2 microsomal glutathione S-transferase 2 0.733819
LOC643542 uncharacterized LOC643542 0.728903
LIPK lipase, family member K 0.680534
C11ORF30 chromosome 11 open reading frame 30 0.675077
TMEM132D transmembrane protein 132D 0.66924
EBF1 early B-cell factor 1 0.668936