Literature DB >> 8812428

Genomic organization of SLC3A1, a transporter gene mutated in cystinuria.

E Pras1, R Sood, N Raben, I Aksentijevich, X Chen, D L Kastner.   

Abstract

The SLC3A1 gene encodes a transport protein for cystine and the dibasic amino acids. Recently mutations in this gene have been shown to cause cystinuria. We report the genomic structure and organization of SLC3A1, which is composed of 10 exons and spans nearly 45 kb. Until now screening for mutations in SLC3A1 has been based on RT-PCR amplification of illegitimate mRNA transcripts from white blood cells. In this report we provide primers for amplification of exons from genomic DNA, thus simplifying the process of screening for SLC3A1 mutations in cystinuria.

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Year:  1996        PMID: 8812428     DOI: 10.1006/geno.1996.0437

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  5 in total

1.  Molecular analysis of cystinuria in Libyan Jews: exclusion of the SLC3A1 gene and mapping of a new locus on 19q.

Authors:  R Wartenfeld; E Golomb; G Katz; S J Bale; B Goldman; M Pras; D L Kastner; E Pras
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

2.  A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.

Authors:  R Parvari; I Brodyansky; O Elpeleg; S Moses; D Landau; E Hershkovitz
Journal:  Am J Hum Genet       Date:  2001-08-24       Impact factor: 11.025

3.  Molecular characterization of cystinuria in south-eastern European countries.

Authors:  Katerina Popovska-Jankovic; Velibor Tasic; Radovan Bogdanovic; Predrag Miljkovic; Emilija Golubovic; Alper Soylu; Marjan Saraga; Snezana Pavicevic; Esra Baskin; Ipek Akil; Alojz Gregoric; Marusia Lilova; Rezan Topaloglu; Emilija Sukarova Stefanovska; Dijana Plaseska-Karanfilska
Journal:  Urolithiasis       Date:  2012-12-27       Impact factor: 3.436

Review 4.  Cystinuria: an inborn cause of urolithiasis.

Authors:  Thomas Eggermann; Andreas Venghaus; Klaus Zerres
Journal:  Orphanet J Rare Dis       Date:  2012-04-05       Impact factor: 4.123

5.  Hypotonia-cystinuria 2p21 deletion syndrome: Intrafamilial variability of clinical expression.

Authors:  Atif Towheed; Christian L Hietanen; Vasudeva G Kamath; Larry N Singh; Angela Ho; Kristin Engelstad; Kayla Cornett; Jacqueline Montes; Darryl De Vivo
Journal:  Ann Clin Transl Neurol       Date:  2021-10-06       Impact factor: 4.511

  5 in total

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