{"symbol":"WBSCR17","synonyms":["GALNT20","GalNAc-T5L","GALNACT17","GalNAc-T19","GALNT16","GALNTL3","GalNAc-T17"],"name":"Williams-Beuren syndrome chromosome region 17","description":"This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013]","ncbiEntrezGeneId":64409,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/64409","proteins":[{"symbol":"GLTL3_HUMAN","href":"/api/1.0/protein/GLTL3_HUMAN"}],"hgncRootFamilies":[{"name":"Glycosyltransferases","href":"/api/1.0/gene_family/Glycosyltransferases"}]}