The human obesity gene map: The 1997 update

被引:68
作者
Chagnon, YC [1 ]
Perusse, L [1 ]
Bouchard, C [1 ]
机构
[1] Univ Laval, Fac Med, Dept Social & Prevent Med, Div Kinesiol,Phys Act Sci Lab, Quebec City, PQ G1K 7P4, Canada
来源
OBESITY RESEARCH | 1998年 / 6卷 / 01期
关键词
obesity; genes; linkage; association; animal models; Mendelian disorders;
D O I
10.1002/j.1550-8528.1998.tb00318.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An update of the human obesity gene map incorporating published results up to October 1997 is presented. Evidence from Mendelian disorders exhibiting obesity as a clinical feature; single-gem mutation rodent models; quantitative trait loci uncovered in human genome-wide scans and in crossbreeding experiments with mouse, rat, and pig models; association and case-control studies with candidate genes; and linkage studies with genes and other markers is reviewed. All chromosomal locations of the animal loci are converted into human genome locations based on syntenic relationships between the genomes. A complete listing of all of these loci reveals that all but chromosome Y of the 24 human chromosomes are represented. Some chromosomes show at least three putative loci related to obesity on both arms (1, 2, 6, 8, 11, and 20) and several on one chromosome arm only (3p, 4q, 5q, 74, 12q, 13q, 15q, 15p, 22q, and Xq). Studies reporting negative association and linkage results are also listed, with the exception of the unlinked markers from genome-wide scans.
引用
收藏
页码:76 / 92
页数:17
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