{"symbol":"PGAM2","synonyms":["GSD10","PGAMM","PGAM-M"],"name":"phosphoglycerate mutase 2 (muscle)","description":"Phosphoglycerate mutase (PGAM) catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. The PGAM is a dimeric enzyme containing, in different tissues, different proportions of a slow-migrating muscle (MM) isozyme, a fast-migrating brain (BB) isozyme, and a hybrid form (MB). This gene encodes muscle-specific PGAM subunit. Mutations in this gene cause muscle phosphoglycerate mutase eficiency, also known as glycogen storage disease X. [provided by RefSeq, Sep 2009]","ncbiEntrezGeneId":5224,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/5224","proteins":[{"symbol":"PGAM2_HUMAN","href":"/api/1.0/protein/PGAM2_HUMAN"}],"hgncRootFamilies":[]}