{"symbol":"GALNT17","synonyms":[],"name":"polypeptide N-acetylgalactosaminyltransferase 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":"https://ncbi.nlm.nih.gov/gene/64409","proteins":[],"hgncRootFamilies":[]}