amylo-alpha-1,6-glucosidase and 4-alpha-glucanotransferase
| UniProt | Protein Name |
|---|---|
| P35573 |
|
| A0A0S2A4E4 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| glycogen biosynthetic process | ||
| glycogen catabolic process | ||
| glycogen catabolic process | ||
| response to nutrient | ||
| response to glucocorticoid |
| GO Term | Evidence Code | PMID |
|---|---|---|
| glycogen debranching enzyme activity | ||
| 4-alpha-glucanotransferase activity | ||
| 4-alpha-glucanotransferase activity | ||
| amylo-alpha-1,6-glucosidase activity | ||
| amylo-alpha-1,6-glucosidase activity |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:2748 | glycogen storage disease III |
| HPO ID | HPO Term |
|---|---|
| HP:0003693 | Distal amyotrophy |
| HP:0004322 | Short stature |
| HP:0005280 | Depressed nasal bridge |
| HP:0011800 | Midface retrusion |
| Disease ID | Disease Name |
|---|---|
| OMIM:232400 |
|
| ORPHA:366 |
|
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026