Renal Corticomedullary Cysts Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The presence of multiple cysts at the border between the renal cortex and medulla. (Human Phenotype Ontology, HP_0000108)
External Link https://www.disgenet.org/browser/0/1/0/C1968619
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Genes

8 genes associated with the disease Renal Corticomedullary Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CRB2 crumbs family member 2
MUC1 mucin 1, cell surface associated
NPHP1 nephronophthisis 1 (juvenile)
NPHP3 nephronophthisis 3 (adolescent)
NPHP4 nephronophthisis 4
TMEM67 transmembrane protein 67
UMOD uromodulin
XPNPEP3 X-prolyl aminopeptidase 3, mitochondrial