polycystic kidney disease Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An autosomal dominant disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium. (Human Disease Ontology, DOID_898)
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Genes

10 genes associated with the disease polycystic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
ACE	angiotensin I converting enzyme
ADD1	adducin 1 (alpha)
AGT	angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1	angiotensin II receptor, type 1
EGFR	epidermal growth factor receptor
NOS3	nitric oxide synthase 3 (endothelial cell)
PKD1	polycystic kidney disease 1 (autosomal dominant)
PKD2	polycystic kidney disease 2 (autosomal dominant)
PKHD1	polycystic kidney and hepatic disease 1 (autosomal recessive)
PKLR	pyruvate kinase, liver and RBC