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Often these common and rare diseases show phenotypic overlap, though monogenic diseases generally have a more extreme symptomatology.\n                    <jats:italic>ABCC6<\/jats:italic>\n                    , the gene responsible for pseudoxanthoma elasticum, an autosomal recessive ectopic mineralization disorder, can be considered a paradigm gene with relevance that reaches far beyond this enigmatic orphan disease. Indeed, common traits such as chronic kidney disease or cardiovascular disorders have been linked to the\n                    <jats:italic>ABCC6<\/jats:italic>\n                    gene. While during the last decade the awareness of the wide ramifications of\n                    <jats:italic>ABCC6<\/jats:italic>\n                    has increased significantly, the gene itself and the transmembrane transporter it encodes have not unveiled all of the mysteries that surround them. To gain more insights, multiple approaches are being used including next-generation sequencing, computational methods, and various \u201comics\u201d technologies. Much effort is made to place the vast amount of data that is gathered in an integrated system-biological network; the involvement of\n                    <jats:italic>ABCC6<\/jats:italic>\n                    in common disorders provides a good view on the wide implications and potential of such a network. In this review, we summarize the network approaches used to study\n                    <jats:italic>ABCC6<\/jats:italic>\n                    and the role of this gene in several complex diseases.\n                  <\/jats:p>","DOI":"10.1155\/2015\/648569","type":"journal-article","created":{"date-parts":[[2015,8,18]],"date-time":"2015-08-18T17:03:58Z","timestamp":1439917438000},"page":"1-18","source":"Crossref","is-referenced-by-count":3,"title":["The ABCC6 Transporter as a Paradigm for Networking from an Orphan Disease to Complex Disorders"],"prefix":"10.1155","volume":"2015","author":[{"given":"Eva Y. 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