{"symbol":"NSUN5","synonyms":["NOL1R","NSUN5A","WBSCR20","P120(NOL1)","WBSCR20A"],"name":"NOP2/Sun domain family, member 5","description":"This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","ncbiEntrezGeneId":55695,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/55695","proteins":[{"symbol":"NSUN5_HUMAN","href":"/api/1.0/protein/NSUN5_HUMAN"}],"hgncRootFamilies":[{"name":"NOP2/Sun domain containing (NSUN)","href":"/api/1.0/gene_family/NOP2%24slash%24Sun+domain+containing+%28NSUN%29"}]}