Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux

Phaikasame Sanyanusin, Lisa A Schimmenti, Leslie A. McNoe, Teresa A. Ward, Mary Ella M Pierpont, Michael J. Sullivan, William B. Dobyns, Michael R. Eccles

Research output: Contribution to journalArticlepeer-review

572 Scopus citations

Abstract

Paired box (PAX) genes play a critical role in human development and disease. The PAX2 gene is expressed in primitive cells of the kidney, ureter, eye, ear and central nervous system. We have conducted a mutational analysis of PAX2 in a family with optic nerve colobomas, renal hypoplasia, mild proteinuria and vesicoureteral reflux. We report a single nucleotide deletion in exon five, causing a frame–shift of the PAX2 coding region in the octapeptide domain. The phenotype resulting from the PAX2 mutation in this family was very similar to abnormalities that have been reported in Krd mutant mice. These data suggest that PAX2 is required for normal kidney and eye development.

Original languageEnglish (US)
Pages (from-to)358-364
Number of pages7
JournalNature Genetics
Volume9
Issue number4
DOIs
StatePublished - Apr 1995

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