Literature DB >> 7835889

Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphisms.

C Heinzmann1, T L Kojis, P Gonzalez, P V Rao, J S Zigler, M H Polymeropoulos, I Klisak, R S Sparkes, T Mohandas, J B Bateman.   

Abstract

zeta-Crystallin is a lens protein that has been associated with autosomal dominant congenital cataracts in guinea pigs and thus is a candidate for human congenital cataracts. We have assigned the zeta-crystallin gene (CRYZ) to human chromosome 1 using a Southern panel of 17 human-mouse somatic cell hybrids and regionally localized it to 1p22-p31 by fluorescence in situ hybridization. Five restriction fragment length polymorphisms were identified by analyzing the DNA from 10 unrelated, unaffected individuals. Our results will permit evaluation of its role in human cataractogenesis.

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Year:  1994        PMID: 7835889     DOI: 10.1006/geno.1994.1516

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


  1 in total

1.  A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract.

Authors:  Juhua Yang; Yihua Zhu; Feng Gu; Xiang He; Zongfu Cao; Xuexi Li; Yi Tong; Xu Ma
Journal:  Mol Vis       Date:  2008-04-18       Impact factor: 2.367

  1 in total

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