| Literature DB >> 17121775 |
Areum Han1, Woo-Yeon Kim, Seong-Min Park.
Abstract
UNLABELLED: Elucidating the effects of genetic polymorphisms on genes and gene networks is an important step in disease association studies. We developed the SNP2NMD database for human SNPs (single nucleotide polymorphisms) that result in PTCs (premature termination codons) and trigger nonsense-mediated mRNA decay (NMD). The SNP2NMD Web interfaces provide extensive genetic information on and graphical views of the queried SNP, gene, and disease terms. AVAILABILITY: SNP2NMD is available from http://variome.net, or directly from http://bioportal.kobic.re.kr/SNP2NMD. SUPPLEMENTARY INFORMATION: http://bioportal.kobic.re.kr/SNP2NMD/Wiki.jsp?page=Statistics.Entities:
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Year: 2006 PMID: 17121775 DOI: 10.1093/bioinformatics/btl593
Source DB: PubMed Journal: Bioinformatics ISSN: 1367-4803 Impact factor: 6.937