gout Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Hereditary metabolic disorder characterized by recurrent acute arthritis, hyperuricemia and deposition of sodium urate in and around the joints, sometimes with formation of uric acid calculi. (Experimental Factor Ontology, EFO_0004274)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0001997
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Genes

14 genes associated with the gout phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9 2.87876
ABCG2 ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group) 2.28874
AGBL4 ATP/GTP binding protein-like 4 1.52827
RELN reelin 1.47293
ASIC2 acid sensing (proton gated) ion channel 2 1.46501
CNTLN centlein, centrosomal protein 1.45917
TLL1 tolloid-like 1 1.42973
RPL13A ribosomal protein L13a 1.20446
MAML2 mastermind-like 2 (Drosophila) 1.18251
FGFR2 fibroblast growth factor receptor 2 1.05066
SLC17A1 solute carrier family 17 (organic anion transporter), member 1 0.974864
SLC22A11 solute carrier family 22 (organic anion/urate transporter), member 11 0.834343
GRIK2 glutamate receptor, ionotropic, kainate 2 0.740245
GCKR glucokinase (hexokinase 4) regulator 0.442937