{"symbol":"SEPT6","synonyms":["SEPT2","SEP2"],"name":"septin 6","description":"This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":23157,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/23157","proteins":[{"symbol":"SEPT6_HUMAN","href":"/api/1.0/protein/SEPT6_HUMAN"}],"hgncRootFamilies":[{"name":"Septins (SEPT)","href":"/api/1.0/gene_family/Septins+%28SEPT%29"}]}