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Nat Genet. 1997 Oct;17(2):149-53.

A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1.

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  • 1University Children's Hospital, Freiburg University, Germany. hildebra@sunt.uk1.uni-freiburg.de

Abstract

Juvenile nephronophthisis (NPH), an autosomal recessive cystic kidney disease, is the primary genetic cause of chronic renal failure in children. About two thirds of patients with NPH carry a large homozygous deletion at the gene locus NPH1 on 2q13. We here identify a novel gene. NPHP1, which extends over most of this common deletion. The 4.5-kb transcript encodes a protein with an SH3 domain, which is highly conserved throughout evolution. The 11-kb interval between the 3' end of NPHP1 and an inverted repeat containing the distal deletion breakpoint was found to contain the first exon of a second gene, MALL. In patients with a hemizygous deletion of the NPH1 region, additional point mutations were found in NPHP1 but not in MALL.

PMID:
9326933
[PubMed - indexed for MEDLINE]
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