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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 13/07/2006 |
Symbol | IGAN1 |
Location | 6q22-q23 |
Name | IgA nephropathy |
Other name(s) | Berger disease |
Main clinical features |
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Genetic determination | autosomal dominant |
Related entries | IGAN2, IGAN3 |
Function/system disorder | kidney and urinary tract |
Type | susceptibility factor |
Remark(s) | evidence of linkage to multiple chromosomal regions was considered consistent with both an oligo/polygenic and a multiple susceptibility gene model for familial IGAN, with small or moderate effects in determining the pathologic phenotype. |