calcium oxalate nephrolithiasis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of calcium- and oxalate-containing calculi (stones) in the kidneys. (Human Phenotype Ontology, HP_0008672)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008672
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Genes

6 genes associated with the calcium oxalate nephrolithiasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGXT alanine-glyoxylate aminotransferase
GRHPR glyoxylate reductase/hydroxypyruvate reductase
HOGA1 4-hydroxy-2-oxoglutarate aldolase 1
SLC36A2 solute carrier family 36 (proton/amino acid symporter), member 2
SLC6A19 solute carrier family 6 (neutral amino acid transporter), member 19
SLC6A20 solute carrier family 6 (proline IMINO transporter), member 20