polydipsia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Excessive thirst manifested by excessive fluid intake. (Human Phenotype Ontology, HP_0001959)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001959
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Genes

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

Symbol Name
AQP2 aquaporin 2 (collecting duct)
AVPR2 arginine vasopressin receptor 2
CASR calcium-sensing receptor
CLDN16 claudin 16
CTNS cystinosin, lysosomal cystine transporter
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
NPHP1 nephronophthisis 1 (juvenile)
NPHP3 nephronophthisis 3 (adolescent)
NPHP4 nephronophthisis 4
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
TMEM67 transmembrane protein 67