In addition to our primary set of 910 genes, the mouse systems genetics method (Chesler and colleagues, submitted) that identified 7,842 additional genes with potential biological relevance to addiction through mouse QTL and gene expression correlation analysis and the GIN prioritization scores reflect this quantitative assessment of biological relevance. Genes with a large number of mouse associations are prioritized more highly, and those with a relatively low number receive little increase in the prioritization score relative to arbitrary genes (see the methods section for details). These additional data provide a broader measure of biological relevance to addiction which may be useful for prioritizing SNPs for further study after a GWAS [4] or fine mapping a region of genetic linkage. This method has the effect of combining information from the expert nomination process and the mouse systems genetics data. SNPs in the 486 expert nominated genes, the determination of which did not involve the mouse data, receive a uniform increase in priority. If there is additional evidence from the mouse data of relevance of the gene to addiction, the priority is