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GENATLAS PHENOTYPE

last update : 24/11/06

Symbol	IGAN2
Location	4q26-31
Name	IgA nephropathy 2
Main clinical features	incomplete penetrance, most common cause of glomerulonephritis characterized by onset before the age of 40 years with hematuria and proteinuria and a progressive renal failure
Genetic determination	autosomal dominant
Function/system disorder	kidney and urinary tract
Type	susceptibility factor