{"symbol":"ZNF778","synonyms":[],"name":"zinc finger protein 778","description":"The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011]","ncbiEntrezGeneId":197320,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/197320","proteins":[{"symbol":"ZN778_HUMAN","href":"/api/1.0/protein/ZN778_HUMAN"}],"hgncRootFamilies":[{"name":"Zinc fingers","href":"/api/1.0/gene_family/Zinc+fingers"}]}