abnormal urine uric acid level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the amount in the urine of the final oxidation product of purine catabolism in humans and primates, but which in rodents and most other mammals is normally is further oxidized by uricase to allantoin that is excreted in the urine (Mammalian Phenotype Ontology, MP_0009809)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009809
Similar Terms
Downloads & Tools

Genes

12 gene mutations causing the abnormal urine uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AHR aryl hydrocarbon receptor
APRT adenine phosphoribosyltransferase
CEBPD CCAAT/enhancer binding protein (C/EBP), delta
OIT3 oncoprotein induced transcript 3
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC22A12 solute carrier family 22 (organic anion/urate transporter), member 12
SLC22A6 solute carrier family 22 (organic anion transporter), member 6
SLC22A8 solute carrier family 22 (organic anion transporter), member 8
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9
UMOD uromodulin
UOX urate oxidase, pseudogene
UPK2 uroplakin 2