{"symbol":"CNNM4","synonyms":["ACDP4"],"name":"cyclin and CBS domain divalent metal cation transport mediator 4","description":"This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta. [provided by RefSeq, Feb 2010]","ncbiEntrezGeneId":26504,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/26504","proteins":[{"symbol":"CNNM4_HUMAN","href":"/api/1.0/protein/CNNM4_HUMAN"}],"hgncRootFamilies":[]}