Benign Paroxysmal Positional Vertigo Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0155502
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Genes

15 genes associated with the disease Benign Paroxysmal Positional Vertigo in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALB albumin
BGLAP bone gamma-carboxyglutamate (gla) protein
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
COL1A2 collagen, type I, alpha 2
DPYD dihydropyrimidine dehydrogenase
FGA fibrinogen alpha chain
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
OC90 otoconin 90
OTOL1 otolin 1
PPARG peroxisome proliferator-activated receptor gamma
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
PPARGC1B peroxisome proliferator-activated receptor gamma, coactivator 1 beta
SIRT1 sirtuin 1
SRM spermidine synthase
TP53 tumor protein p53