Hypernatriuria Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An increased concentration of sodium(1+) in the urine. (Human Phenotype Ontology, HP_0012605)
External Link https://www.disgenet.org/browser/0/1/0/C3671887
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Genes

17 genes associated with the disease Hypernatriuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AVPR2 arginine vasopressin receptor 2
B2M beta-2-microglobulin
BSND barttin CLCNK-type chloride channel accessory beta subunit
CA2 carbonic anhydrase II
CLCNKA chloride channel, voltage-sensitive Ka
CLCNKB chloride channel, voltage-sensitive Kb
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
HSD3B2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MRAP melanocortin 2 receptor accessory protein
NNT nicotinamide nucleotide transhydrogenase
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit
SLC9A3 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
STAR steroidogenic acute regulatory protein
TXNRD2 thioredoxin reductase 2