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SNP2NMD: A database of human SNPs (single nucleotide polymorphisms) causing NMD (nonsense-mediated mRNA decay)
Motivation
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).
Paper
Areum Han*, Woo-Yeon Kim*, and Seong-Min Park. SNP2NMD: a database of human SNPs (single nucleotide polymorphisms) causing NMD (nonsense-mediated mRNA decay). Bioinformatics 2007 23(3):397-399.
http://bioinformatics.oxfordjournals.org/cgi/content/abstract/23/3/397
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=17121775&query_hl=2&itool=pubmed_docsum
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