Literature DB >> 7835902

Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism.

E M Jones1, S Menzel, R Espinosa, M M Le Beau, G I Bell, J Takeda.   

Abstract

The gene encoding a human neutral amino acid transporter-like protein (SLC1A5) was mapped to chromosome band 19q13.3 by fluorescence in situ hybridization to metaphase chromosomes. A simple sequence repeat DNA polymorphism of the form (GT)n was identified in the 3'-untranslated region of SLC1A5 mRNA. Studies in the CEPH families showed significant evidence of linkage between this DNA polymorphism and markers localized to the distal long arm of chromosome 19.

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Year:  1994        PMID: 7835902     DOI: 10.1006/geno.1994.1529

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


  3 in total

1.  Hartnup disorder: polymorphisms identified in the neutral amino acid transporter SLC1A5.

Authors:  S J Potter; A Lu; B Wilcken; K Green; J E J Rasko
Journal:  J Inherit Metab Dis       Date:  2002-10       Impact factor: 4.982

2.  The RD114/simian type D retrovirus receptor is a neutral amino acid transporter.

Authors:  J E Rasko; J L Battini; R J Gottschalk; I Mazo; A D Miller
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

3.  Localization, by linkage analysis, of the cystinuria type III gene to chromosome 19q13.1.

Authors:  L Bisceglia; M J Calonge; A Totaro; L Feliubadaló; S Melchionda; J García; X Testar; M Gallucci; A Ponzone; L Zelante; A Zorzano; X Estivill; P Gasparini; V Nunes; M Palacín
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

  3 in total

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