Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (362K) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (122)
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Hirakawa, M.
Right arrow Articles by Nakamura, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hirakawa, M.
Right arrow Articles by Nakamura, Y.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 2002, Vol. 30, No. 1 158-162
© 2002 Oxford University Press

JSNP: a database of common gene variations in the Japanese population

Mika Hirakawa, Toshihiro Tanaka, Yoichi Hashimoto, Masako Kuroda, Toshihisa Takagi1 and Yusuke Nakamura1,*

Bioinformatics Division, Japan Science and Technology Corporation (JST), 5-3 Yonban-cho, Chiyoda-ku, Tokyo 102-0081, Japan and 1Human Genome Center, Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan

JSNP is a repository of Japanese Single Nucleotide Polymorphism (SNP) data, begun in 2000 and developed through the Prime Minister’s Millennium Project. The aim of this undertaking is to identify and collate up to 150 000 SNPs from the Japanese population, located in genes or in adjacent regions that might influence the coding sequence of the genes. The project has been carried out by a collaboration between the Human Genome Center (HGC) in the Institute of Medical Science (IMS) at the University of Tokyo and the Japan Science and Technology Corporation (JST). JSNP serves as both a storage site for the Japanese SNPs obtained from the ongoing project and as a facility for public dissemination to allow researchers access to high quality SNP data. A primary motivation of the project is the construction of a basic data set to identify relationships between polymorphisms and common diseases or the reaction to drugs. As such, emphasis has been placed on the identification of SNPs that lie in candidate regions which may affect phenotype but which would not necessarily directly cause disease. Unrestricted access to JSNP and any associated files is available at http://snp.ims.u-tokyo.ac.jp/.

* To whom correspondence should be addressed. Tel: +81 35449 5372; Fax: +81 35449 5433; Email: yusuke{at}ims.u-tokyo.ac.jp


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Hum Mol GenetHome page
N. Kato, T. Miyata, Y. Tabara, T. Katsuya, K. Yanai, H. Hanada, K. Kamide, J. Nakura, K. Kohara, F. Takeuchi, et al.
High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project
Hum. Mol. Genet., February 14, 2008; 17(4): 617 - 627.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
I. Sato, S. Wu, M. C. A. Ibarra, Y. K. Hayashi, H. Fujita, M. Tojo, S. J. Oh, I. Nonaka, S. Noguchi, and I. Nishino
Congenital neuromuscular disease with uniform type 1 fiber and RYR1 mutation
Neurology, January 8, 2008; 70(2): 114 - 122.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
T. Yanagiya, A. Tanabe, A. Iida, S. Saito, A. Sekine, A. Takahashi, T. Tsunoda, S. Kamohara, Y. Nakata, K. Kotani, et al.
Association of single-nucleotide polymorphisms in MTMR9 gene with obesity
Hum. Mol. Genet., December 15, 2007; 16(24): 3017 - 3026.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
H. Yamada, K. Shinmura, K. Okudela, M. Goto, M. Suzuki, K. Kuriki, T. Tsuneyoshi, and H. Sugimura
Identification and characterization of a novel germ line p53 mutation in familial gastric cancer in the Japanese population
Carcinogenesis, September 1, 2007; 28(9): 2013 - 2018.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
A. Uzun, C. M. Leslin, A. Abyzov, and V. Ilyin
Structure SNP (StSNP): a web server for mapping and modeling nsSNPs on protein structures with linkage to metabolic pathways
Nucleic Acids Res., July 13, 2007; 35(suppl_2): W384 - W392.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
T. Ando, Y. Ichimaru, F. Konjiki, M. Shoji, and G. Komaki
Variations in the preproghrelin gene correlate with higher body mass index, fat mass, and body dissatisfaction in young Japanese women
Am. J. Clinical Nutrition, July 1, 2007; 86(1): 25 - 32.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
A. Tanabe, T. Yanagiya, A. Iida, S. Saito, A. Sekine, A. Takahashi, T. Nakamura, T. Tsunoda, S. Kamohara, Y. Nakata, et al.
Functional Single-Nucleotide Polymorphisms in the Secretogranin III (SCG3) Gene that Form Secretory Granules with Appetite-Related Neuropeptides Are Associated with Obesity
J. Clin. Endocrinol. Metab., March 1, 2007; 92(3): 1145 - 1154.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
M. Iemitsu, S. Maeda, T. Otsuki, J. Sugawara, T. Tanabe, S. Jesmin, S. Kuno, R. Ajisaka, T. Miyauchi, and M. Matsuda
Polymorphism in Endothelin-Related Genes Limits Exercise-Induced Decreases in Arterial Stiffness in Older Subjects
Hypertension, May 1, 2006; 47(5): 928 - 936.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
K. Yamazaki, D. McGovern, J. Ragoussis, M. Paolucci, H. Butler, D. Jewell, L. Cardon, M. Takazoe, T. Tanaka, T. Ichimori, et al.
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease
Hum. Mol. Genet., November 15, 2005; 14(22): 3499 - 3506.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
G. V Kryukov, S. Schmidt, and S. Sunyaev
Small fitness effect of mutations in highly conserved non-coding regions
Hum. Mol. Genet., August 1, 2005; 14(15): 2221 - 2229.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
T. Yahata, J. Quan, N. Tamura, H. Nagata, T. Kurabayashi, and K. Tanaka
Association between single nucleotide polymorphisms of estrogen receptor {alpha} gene and efficacy of HRT on bone mineral density in post-menopausal Japanese women
Hum. Reprod., July 1, 2005; 20(7): 1860 - 1866.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
I. Vitko, Y. Chen, J. M. Arias, Y. Shen, X.-R. Wu, and E. Perez-Reyes
Functional Characterization and Neuronal Modeling of the Effects of Childhood Absence Epilepsy Variants of CACNA1H, a T-Type Calcium Channel
J. Neurosci., May 11, 2005; 25(19): 4844 - 4855.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
H. Hiratani, D. W. Bowden, S. Ikegami, S. Shirasawa, A. Shimizu, Y. Iwatani, and T. Akamizu
Multiple SNPs in Intron 7 of Thyrotropin Receptor Are Associated with Graves' Disease
J. Clin. Endocrinol. Metab., May 1, 2005; 90(5): 2898 - 2903.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
A. Shimazaki, Y. Kawamura, A. Kanazawa, A. Sekine, S. Saito, T. Tsunoda, D. Koya, T. Babazono, Y. Tanaka, M. Matsuda, et al.
Genetic Variations in the Gene Encoding ELMO1 Are Associated With Susceptibility to Diabetic Nephropathy
Diabetes, April 1, 2005; 54(4): 1171 - 1178.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
S. Weckx, P. De Rijk, C. Van Broeckhoven, and J. Del-Favero
SNPbox: a modular software package for large-scale primer design
Bioinformatics, February 1, 2005; 21(3): 385 - 387.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
K. M. Egan, P. A. Newcomb, C. B. Ambrosone, A. Trentham-Dietz, L. Titus-Ernstoff, J. M. Hampton, M. T. Kimura, and H. Nagase
STK15 polymorphism and breast cancer risk in a population-based study
Carcinogenesis, November 1, 2004; 25(11): 2149 - 2153.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
P. D. Thomas and A. Kejariwal
Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: Evolutionary evidence for differences in molecular effects
PNAS, October 26, 2004; 101(43): 15398 - 15403.
[Abstract] [Full Text] [PDF]


Home page
J HeredHome page
K. K. Kidd, A. J. Pakstis, W. C. Speed, and J. R. Kidd
Understanding Human DNA Sequence Variation
J. Hered., September 1, 2004; 95(5): 406 - 420.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
S. Sunyaev, F. A. Kondrashov, P. Bork, and V. Ramensky
Impact of selection, mutation rate and genetic drift on human genetic variation
Hum. Mol. Genet., December 15, 2003; 12(24): 3325 - 3330.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
N. Tanaka, T. Babazono, S. Saito, A. Sekine, T. Tsunoda, M. Haneda, Y. Tanaka, T. Fujioka, K. Kaku, R. Kawamori, et al.
Association of Solute Carrier Family 12 (Sodium/Chloride) Member 3 With Diabetic Nephropathy, Identified by Genome-Wide Analyses of Single Nucleotide Polymorphisms
Diabetes, November 1, 2003; 52(11): 2848 - 2853.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
H Zhong, F J Serajee, R Nabi, and A H M M. Huq
No association between the EN2 gene and autistic disorder
J. Med. Genet., January 1, 2003; 40(1): e4 - 4.
[Full Text] [PDF]


Home page
Hum Mol GenetHome page
X. Estivill, J. Cheung, M. Angel Pujana, K. Nakabayashi, S. W. Scherer, and L.-C. Tsui
Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome
Hum. Mol. Genet., August 15, 2002; 11(17): 1987 - 1995.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
M. Hirakawa
HOWDY: an integrated database system for human genome research
Nucleic Acids Res., January 1, 2002; 30(1): 152 - 157.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.