nephropathy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A urinary system disease that is located_in the kidney. (Human Disease Ontology, DOID_557)
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23 genes associated with the disease nephropathy 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)
AKR1B10 aldo-keto reductase family 1, member B10 (aldose reductase)
APEX1 APEX nuclease (multifunctional DNA repair enzyme) 1
CD14 CD14 molecule
CETP cholesteryl ester transfer protein, plasma
COL4A4 collagen, type IV, alpha 4
CR1 complement component (3b/4b) receptor 1 (Knops blood group)
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
CYP3A5 cytochrome P450, family 3, subfamily A, polypeptide 5
HP haptoglobin
IFNG interferon, gamma
IL1RN interleukin 1 receptor antagonist
IL4 interleukin 4
LPL lipoprotein lipase
MMP9 matrix metallopeptidase 9
NOS3 nitric oxide synthase 3 (endothelial cell)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
PIGR polymeric immunoglobulin receptor
PON2 paraoxonase 2
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
TGFB1 transforming growth factor, beta 1
VWF von Willebrand factor