Human genome project: Current status, Keio strategy, and prospects

被引:0
|
作者
Shimizu, N [1 ]
机构
[1] Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan
来源
NEURAL DEVELOPMENT-BOOK | 1999年 / 2卷
关键词
human genome project; down syndrome; autoimmune disease; glaucoma;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Through the human genome project (HGP) at Keio University, we were able to find a number of new genes including SIM1 (single-minded), SIM2, MNB (minibrain), KNP1 (keio novel protein), KNP3, APECED/AIRE, MYOC (myocilin), RAO (retina amine oxidase), and ISLR (immunoglobulin superfamily containing LR domain). Also, we determined the genomic sequence of immunoglobulin light chain lambda (IGL) gene cluster of more than 1 megabase (Mb) and identified 69 IGLV genes, 7 IGLC genes, and 12 non-Ig genes/pseudogenes. Moreover, we established the genomic structures of previously known genes such as HCS, ETS2, TMEM1, PWP2, and PFKL. It should be noted that SIM2 and MNB are candidate genes for mental retardation in Down syndrome, that APECED/AIRE is a gene responsible for the autoimmune disease APECED, and that MYOC is identical to TIGR, which is a pathogenic gene for primary open angle glaucoma.
引用
收藏
页码:535 / 540
页数:6
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