abnormal drinking behavior Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal consumption of fluids with excessive or insufficient consumption of fluid or any other abnormal pattern of fluid consumption. (Human Phenotype Ontology, HP_0030082)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0030082
Similar Terms
Downloads & Tools

Genes

14 genes associated with the abnormal drinking behavior 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