{"symbol":"MAGT1","synonyms":["XMEN","OST3B","PRO0756","MRX95","BA217H1.1"],"name":"magnesium transporter 1","description":"This gene encodes a ubiquitously expressed magnesium cation transporter protein that localizes to the cell membrane. This protein also associates with N-oligosaccharyl transferase and therefore may have a role in N-glycosylation. Mutations in this gene cause a form of X-linked intellectual disability (XLID). This gene may have multiple in-frame translation initiation sites, one of which would encode a shorter protein with an N-terminus containing a signal peptide at amino acids 1-29. [provided by RefSeq, Jul 2017]","ncbiEntrezGeneId":84061,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/84061","proteins":[{"symbol":"MAGT1_HUMAN","href":"/api/1.0/protein/MAGT1_HUMAN"}],"hgncRootFamilies":[{"name":"X-linked mental retardation","href":"/api/1.0/gene_family/X-linked+mental+retardation"}]}