urinary system disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A disease of anatomical entity that is located_in kidney, ureter, bladder and urethra. (Human Disease Ontology, DOID_18)
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Genes

32 genes involed in the disease urinary system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
AGXT alanine-glyoxylate aminotransferase
ANKS6 ankyrin repeat and sterile alpha motif domain containing 6
AQP2 aquaporin 2 (collecting duct)
AVP arginine vasopressin
AVPR2 arginine vasopressin receptor 2
BSND barttin CLCNK-type chloride channel accessory beta subunit
CEP164 centrosomal protein 164kDa
CEP290 centrosomal protein 290kDa
CEP83 centrosomal protein 83kDa
CLCNKA chloride channel, voltage-sensitive Ka
CLCNKB chloride channel, voltage-sensitive Kb
GLIS2 GLIS family zinc finger 2
GRHPR glyoxylate reductase/hydroxypyruvate reductase
INVS inversin
IQCB1 IQ motif containing B1
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
NEK8 NIMA-related kinase 8
NPHP1 nephronophthisis 1 (juvenile)
NPHP3 nephronophthisis 3 (adolescent)
NPHP4 nephronophthisis 4
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit
SDCCAG8 serologically defined colon cancer antigen 8
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
TMEM67 transmembrane protein 67
TTC21B tetratricopeptide repeat domain 21B
UMOD uromodulin
WDR19 WD repeat domain 19
WFS1 Wolfram syndrome 1 (wolframin)
XPNPEP3 X-prolyl aminopeptidase 3, mitochondrial
ZNF423 zinc finger protein 423