A phenotype map of the mouse X chromosome: Models for human X-linked disease

被引:15
作者
Boyd, Y [1 ]
Blair, HJ [1 ]
Cunliffe, P [1 ]
Masson, WK [1 ]
Reed, V [1 ]
机构
[1] MRC, Mammalian Genet Unit, Harwell OX11 0RD, Oxon, England
关键词
D O I
10.1101/gr.10.3.277
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The identification of many of the transcribed genes in man-and mouse is being achieved by large scale sequencing of expressed sequence tags (ESTs). Attention is now being turned to elucidating gene function and many laboratories are looking to the mouse as a model system for this phase of the genome project. Mouse mutants have long been used as a means of investigating gene Function and disease pathogenesis, and recently, several large mutagenesis programs have been initiated to fulfill the burgeoning demand of functional genomics research. Nevertheless, there is a substantial existing mouse mutant resource that can be used immediately. This review summarizes the available information about the loci encoding X-linked phenotypic mutants and variants, including 40 classical mutants and 40 that have arisenfrom gene targeting.
引用
收藏
页码:277 / 292
页数:16
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