{"symbol":"GLDN","synonyms":["LCCS11","CRGL2","COLM","CLOM","CRG-L2","UNC-112"],"name":"gliomedin","description":"This gene encodes a protein that contains olfactomedin-like and collagen-like domains. The encoded protein, which exists in both transmembrane and secreted forms, promotes formation of the nodes of Ranvier in the peripheral nervous system. Mutations in this gene cause a form of lethal congenital contracture syndrome in human patients. Autoantibodies to the encoded protein have been identified in sera form patients with multifocal motor neuropathy. [provided by RefSeq, May 2017]","ncbiEntrezGeneId":342035,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/342035","proteins":[{"symbol":"GLDN_HUMAN","href":"/api/1.0/protein/GLDN_HUMAN"}],"hgncRootFamilies":[]}