gout Gene Set

Dataset HPO Gene-Disease 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://compbio.charite.de/hpoweb/showterm?id=HP:0001997
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Genes

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

Symbol Name
G6PC glucose-6-phosphatase, catalytic subunit
HNF1B HNF1 homeobox B
HPRT1 hypoxanthine phosphoribosyltransferase 1
MUC1 mucin 1, cell surface associated
PFKM phosphofructokinase, muscle
PRPS1 phosphoribosyl pyrophosphate synthetase 1
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
UMOD uromodulin