hyperuricemia Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
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)
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Genes

30 genes co-occuring with the biological term hyperuricemia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ABCG2 ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group)
ADIPOQ adiponectin, C1Q and collagen domain containing
ADRB3 adrenoceptor beta 3
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
APOA1 apolipoprotein A-I
B2M beta-2-microglobulin
CCL2 chemokine (C-C motif) ligand 2
DECR1 2,4-dienoyl CoA reductase 1, mitochondrial
EDN1 endothelin 1
ELN elastin
FTH1 ferritin, heavy polypeptide 1
FTL ferritin, light polypeptide
GPATCH8 G patch domain containing 8
GPT glutamic-pyruvate transaminase (alanine aminotransferase)
HAVCR1 hepatitis A virus cellular receptor 1
HNF1B HNF1 homeobox B
HPRT1 hypoxanthine phosphoribosyltransferase 1
LCN2 lipocalin 2
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
OIT3 oncoprotein induced transcript 3
PPARG peroxisome proliferator-activated receptor gamma
PTH parathyroid hormone
REN renin
SAA1 serum amyloid A1
SARS seryl-tRNA synthetase
SLC22A11 solute carrier family 22 (organic anion/urate transporter), member 11
SLC22A12 solute carrier family 22 (organic anion/urate transporter), member 12
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9
UMOD uromodulin
XDH xanthine dehydrogenase