| Literature DB >> 21903995 |
Bugsu Ovunc1, Edgar A Otto, Virginia Vega-Warner, Pawaree Saisawat, Shazia Ashraf, Gokul Ramaswami, Hanan M Fathy, Dominik Schoeb, Gil Chernin, Robert H Lyons, Engin Yilmaz, Friedhelm Hildebrandt.
Abstract
In two siblings of consanguineous parents with intermittent nephrotic-range proteinuria, we identified a homozygous deleterious frameshift mutation in the gene CUBN, which encodes cubulin, using exome capture and massively parallel re-sequencing. The mutation segregated with affected members of this family and was absent from 92 healthy individuals, thereby identifying a recessive mutation in CUBN as the single-gene cause of proteinuria in this sibship. Cubulin mutations cause a hereditary form of megaloblastic anemia secondary to vitamin B(12) deficiency, and proteinuria occurs in 50% of cases since cubilin is coreceptor for both the intestinal vitamin B(12)-intrinsic factor complex and the tubular reabsorption of protein in the proximal tubule. In summary, we report successful use of exome capture and massively parallel re-sequencing to identify a rare, single-gene cause of nephropathy.Entities:
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Year: 2011 PMID: 21903995 PMCID: PMC3187182 DOI: 10.1681/ASN.2011040337
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121