| Gene Symbol | PGAM2 |
| Entrez Gene ID | 5224 |
| Full Name | phosphoglycerate mutase 2 |
| Synonyms | GSD10,PGAM-M,PGAMM |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | 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]. |
| Disorder MIM: | |
| Disorder Html: | Glycogen storage disease X, 261670 (3) |








































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