iga nephropathy Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A chronic form of glomerulonephritis characterized by deposits of predominantly immunoglobulin A in the mesangial area (glomerular mesangium). Deposits of complement C3 and immunoglobulin G are also often found. Clinical features may progress from asymptomatic hematuria to end-stage kidney disease. (Experimental Factor Ontology, EFO_0004194)
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Genes

11 genes associated with the disease iga 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)
AGT	angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1	angiotensin II receptor, type 1
CYP11B2	cytochrome P450, family 11, subfamily B, polypeptide 2
EDN1	endothelin 1
IGHMBP2	immunoglobulin mu binding protein 2
IL1RN	interleukin 1 receptor antagonist
SCGB1A1	secretoglobin, family 1A, member 1 (uteroglobin)
TFRC	transferrin receptor
TRA	T cell receptor alpha locus