Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

IgA nephropathy type 2

IgA nephropathy type 2 is a probably autosomal dominant disorder associated with genetic alterations at chromosome positions 4q26-q31 and 17q12-q22. The exact genes are not yet discovered.

Systematic

IgA nephropathy
CFHR1
CFHR3
CFHR5
IgA nephropathy type 1
IgA nephropathy type 2
IgA nephropathy type 3

References:

1.

Bisceglia L et al. (2006) Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci.

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2.

Paterson AD et al. (2007) Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.

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3.

OMIM.ORG article

Omim 613944 [^]
Update: April 29, 2019