hyperuricemia Gene Set

Dataset HPO Gene-Disease 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://compbio.charite.de/hpoweb/showterm?id=HP:0002149
Similar Terms
Downloads & Tools

Genes

16 genes associated with the hyperuricemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALDOB aldolase B, fructose-bisphosphate
ALMS1 Alstrom syndrome protein 1
CLDN16 claudin 16
G6PC glucose-6-phosphatase, catalytic subunit
HNF1B HNF1 homeobox B
HPRT1 hypoxanthine phosphoribosyltransferase 1
MUC1 mucin 1, cell surface associated
PFKM phosphofructokinase, muscle
PPARG peroxisome proliferator-activated receptor gamma
PPP1R3A protein phosphatase 1, regulatory subunit 3A
PRPS1 phosphoribosyl pyrophosphate synthetase 1
REN renin
SARS2 seryl-tRNA synthetase 2, mitochondrial
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
UMOD uromodulin