Uric acid levels Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Is a quantification of uric acid, typically in blood. Uric acid is associated with gout, insulin resistance and cardivascular disease. (Experimental Factor Ontology, EFO_0004761)
External Link https://www.ebi.ac.uk/gwas/search?query=Uric acid levels
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Genes

18 genes associated with the Uric acid levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9 2.33122
ABCG2 ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group) 0.976249
SLC17A1 solute carrier family 17 (organic anion transporter), member 1 0.793579
SLC22A11 solute carrier family 22 (organic anion/urate transporter), member 11 0.77375
GCKR glucokinase (hexokinase 4) regulator 0.522843
SLC22A12 solute carrier family 22 (organic anion/urate transporter), member 12 0.499091
PDZK1 PDZ domain containing 1 0.483518
LRRC16A leucine rich repeat containing 16A 0.439318
SLC16A9 solute carrier family 16, member 9 0.434785
F5 coagulation factor V (proaccelerin, labile factor) 0.129504
ARID1B AT rich interactive domain 1B (SWI1-like) 0.129504
MYO18B myosin XVIIIB 0.104568
WDR1 WD repeat domain 1 0.085234
TENM2 teneurin transmembrane protein 2 0.085234
VSTM4 V-set and transmembrane domain containing 4 0.085234
METTL6 methyltransferase like 6 0.085234
FRAS1 Fraser extracellular matrix complex subunit 1 0.070053
ARHGAP26 Rho GTPase activating protein 26 0.048624