{"symbol":"LAT2","synonyms":["NTAL","HSPC046","WBSCR15","LAB","WSCR5","WBSCR5"],"name":"linker for activation of T cells family, member 2","description":"This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":7462,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/7462","proteins":[{"symbol":"NTAL_HUMAN","href":"/api/1.0/protein/NTAL_HUMAN"}],"hgncRootFamilies":[]}