{"symbol":"DYM","synonyms":["DMC","SMC"],"name":"dymeclin","description":"This gene encodes a protein which regulates Golgi-associated secretory pathways that are essential to endochondral bone formation during early development. This gene is also believed to play a role in early brain development. This gene is widely expressed in embryos and is particularly abundant in chodrocytes and brain tissues. It encodes a peripheral membrane protein which shuttles between the cytosol and Golgi complex. Mutations in this gene are associated with two types of recessive osteochondrodysplasia: Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia. [provided by RefSeq, Jun 2017]","ncbiEntrezGeneId":54808,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/54808","proteins":[{"symbol":"DYM_HUMAN","href":"/api/1.0/protein/DYM_HUMAN"}],"hgncRootFamilies":[]}