hypocalciuria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally decreased calcium concentration in the urine (FMA:12274). (Human Phenotype Ontology, HP_0003127)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003127
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
AP2S1 adaptor-related protein complex 2, sigma 1 subunit
CASR calcium-sensing receptor
CLCNKB chloride channel, voltage-sensitive Kb
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3