Mutations in the SLC3A1 transporter gene in cystinuria

E. Pras, N. Raben, E. Golomb, N. Arber, I. Aksentijevich, J. M. Schapiro, D. Harel, G. Katz, U. Liberman, M. Pras, D. L. Kastner

Research output: Contribution to journalArticlepeer-review

Abstract

Cystinuria is an autosomal recessive disease characterized by the development of kidney stones. Guided by the identification of the SLC3A1 amino acid-transport gene on chromosome 2, we recently established genetic linkage of cystinuria to chromosome 2p in 17 families, without evidence for locus heterogeneity. Other authors have independently identified missense mutations in SLC3A1 in cystinuria patients. In this report we describe four additional cystinuria-associated mutations in this gene: a frameshift, a deletion, a transversion inducing a critical amino acid change, and a nonsense mutation. The latter stop codon was found in all of eight Ashkenazi Jewish carrier chromosomes examined. This report brings the number of disease-associated mutations in this gene to 10. We also assess the frequency of these mutations in our 17 cystinuria families.

Original languageEnglish
Pages (from-to)1297-1303
Number of pages7
JournalAmerican Journal of Human Genetics
Volume56
Issue number6
StatePublished - 1995
Externally publishedYes

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