Literature DB >> 1686020

Linkage mapping of human polymorphic proteins identified by two-dimensional electrophoresis.

D Goldman1, S J O'Brien, S Lucas-Derse, M Dean.   

Abstract

Nineteen polymorphic lymphocyte proteins were previously detected by two-dimensional protein electrophoresis (2DE). In this report, we describe the genetic linkage mapping of six of these polymorphic proteins (PNIA1-PNIA6), the identification by genetic linkage of a seventh (glyoxalase 1 on 6p21), and support for the mapping of an eighth (plastin or LCP1) to near the ESD locus on Chr 13. PNIA1-PNIA6 were assigned, respectively, to 10q26, 16p13.3, 10q, 11p15, 3q, and 19q13. These genetic linkages were achieved by classical linkage analysis of 2DE protein charge polymorphisms to the panel of RFLPs previously typed in nine pedigrees in the Centre D'Etude du Polymorphisme Humain (CEPH) collection.

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Year:  1991        PMID: 1686020     DOI: 10.1016/0888-7543(91)90010-c

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


  1 in total

1.  Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor.

Authors:  Mohammed A Junaid; Dagmar Kowal; Madhabi Barua; Premila S Pullarkat; Susan Sklower Brooks; Raju K Pullarkat
Journal:  Am J Med Genet A       Date:  2004-11-15       Impact factor: 2.802

  1 in total

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