Nocturia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormally increased production of urine during the night leading to an unusually frequent need to urinate. (Human Phenotype Ontology, HP_0000017)
External Link https://www.disgenet.org/browser/0/1/0/C0028734
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Genes

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

Symbol Name
AMBP alpha-1-microglobulin/bikunin precursor
ARIH1 ariadne RBR E3 ubiquitin protein ligase 1
ARNT aryl hydrocarbon receptor nuclear translocator
AVP arginine vasopressin
CENPJ centromere protein J
CLCNKB chloride channel, voltage-sensitive Kb
CLOCK clock circadian regulator
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
GJA5 gap junction protein, alpha 5, 40kDa
GJB2 gap junction protein, beta 2, 26kDa
KLK3 kallikrein-related peptidase 3
MIA3 melanoma inhibitory activity family, member 3
NPEPPS aminopeptidase puromycin sensitive
PDSS2 prenyl (decaprenyl) diphosphate synthase, subunit 2
PLAG1 pleiomorphic adenoma gene 1
POLG polymerase (DNA directed), gamma
POLG2 polymerase (DNA directed), gamma 2, accessory subunit
PROS1 protein S (alpha)
PSAT1 phosphoserine aminotransferase 1
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
TGFB1 transforming growth factor, beta 1
TLR4 toll-like receptor 4
TNS1 tensin 1
TWNK twinkle mtDNA helicase
WIPF1 WAS/WASL interacting protein family, member 1