abnormal blood uric acid level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant concentration in the blood 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_0008820)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008820
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18 gene mutations causing the abnormal blood uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CEBPD CCAAT/enhancer binding protein (C/EBP), delta
CRH corticotropin releasing hormone
DLL1 delta-like 1 (Drosophila)
EDN2 endothelin 2
G6PC glucose-6-phosphatase, catalytic subunit
JAK1 Janus kinase 1
LEPR leptin receptor
OIT3 oncoprotein induced transcript 3
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
PITX3 paired-like homeodomain 3
PXMP2 peroxisomal membrane protein 2, 22kDa
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9
SPG20 spastic paraplegia 20 (Troyer syndrome)
UMOD uromodulin
UOX urate oxidase, pseudogene
VIM vimentin
WWOX WW domain containing oxidoreductase
XDH xanthine dehydrogenase