nephropathy in other diseases Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group renal (Genetic Association Database)
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Genes

26 genes associated with the disease nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
APOB apolipoprotein B
APOE apolipoprotein E
CALD1 caldesmon 1
CCL2 chemokine (C-C motif) ligand 2
CCL5 chemokine (C-C motif) ligand 5
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
CNDP1 carnosine dipeptidase 1 (metallopeptidase M20 family)
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IGHMBP2 immunoglobulin mu binding protein 2
NOS3 nitric oxide synthase 3 (endothelial cell)
NPPA natriuretic peptide A
PON1 paraoxonase 1
PON2 paraoxonase 2
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
TSC22D1 TSC22 domain family, member 1