Hyponatremia Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally decreased sodium concentration in the blood. (Human Phenotype Ontology, HP_0002902)
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Genes

10 genes associated with the Hyponatremia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ACE angiotensin I converting enzyme
AQP1 aquaporin 1 (Colton blood group)
AQP2 aquaporin 2 (collecting duct)
COMT catechol-O-methyltransferase
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
HCRT hypocretin (orexin) neuropeptide precursor
HCRTR1 hypocretin (orexin) receptor 1
HCRTR2 hypocretin (orexin) receptor 2
TRPV4 transient receptor potential cation channel, subfamily V, member 4