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References OMIM Gene GeneReviews HGMD HGNC
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