hyperuricemia Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An acquired metabolic disease that has_material_basis_in an abnormally high level of uric acid in the blood. (Human Disease Ontology, DOID_1920)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002149
Similar Terms
Downloads & Tools

Genes

14 genes associated with the hyperuricemia 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