Gaa - glucosidase, alpha, acid Gene
Also Known as E430018M07Rik
Species: Mus musculus
Summary
This gene encodes a lysosomal acid glucosidase that is involved in the degradation of glycogen. The encoded preproprotein undergoes proteolytic processing to generate a mature enzyme that cleaves alpha-1-4 and alpha-1-6 glycosidic bonds of glycogen, maltose and intermediate oligosaccharides within the lysosome. Mice lacking the encoded protein exhibit symptoms similar to human Pompe syndrome such as accumulation of glycogen in cardiac and skeletal muscle lysosomes resulting in reduced mobility and strength. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2015]
Gaa Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_001159324.2 | NP_001152796.1 | lysosomal alpha-glucosidase preproprotein |
| NM_008064.4 | NP_032090.3 | lysosomal alpha-glucosidase preproprotein |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables alpha-1,4-glucosidase activity |
IDA
IDA: Inferred from direct assay
|
7323947 | MGI |
| enables alpha-1,4-glucosidase activity |
IMP
IMP: Inferred from mutant phenotype
|
9384603 | MGI |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| is active in autolysosome lumen |
IMP
IMP: Inferred from mutant phenotype
|
9668092 | MGI |
| located in lysosome |
IMP
IMP: Inferred from mutant phenotype
|
15207257 | MGI |
| located in membrane |
IMP
IMP: Inferred from mutant phenotype
|
20080761 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
lysosomal alpha-glucosidase |
|