abnormality of urinary uric acid concentration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal concentration of urate in the urine. (Human Phenotype Ontology, HP_0012610)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012610
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Genes

6 genes associated with the abnormality of urinary uric acid concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MOCS1 molybdenum cofactor synthesis 1
MOCS2 molybdenum cofactor synthesis 2
PNP purine nucleoside phosphorylase
SLC22A12 solute carrier family 22 (organic anion/urate transporter), member 12
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9