glycogenolysis
Pathways in the glycogenolysis SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | glycogenolysis | PubChem | |
| 2 | glycogen degradation II | PubChem |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | PGM2 | Phosphoglucomutase 2 | Protein Coding | 2 |
| 2 | PYGB | Glycogen Phosphorylase B | Protein Coding | 2 |
| 3 | PYGM | Glycogen Phosphorylase, Muscle Associated | Protein Coding | 2 |
| 4 | PYGL | Glycogen Phosphorylase L | Protein Coding | 2 |
| 5 | AGL | Amylo-Alpha-1,6-Glucosidase And 4-Alpha-Glucanotransferase | Protein Coding | 2 |
| 6 | PGM1 | Phosphoglucomutase 1 | Protein Coding | 2 |
| 7 | MGAM | Maltase-Glucoamylase | Protein Coding | 1 |
Disorders associated with glycogenolysis SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Glycogen storage disease | Enrichment | AGL, PYGM | 5.05 |
| 2 | Glycogen storage disease vi | Enrichment | PYGL | 3.35 |
| 3 | Glycogen storage disease v | Enrichment | PYGM | 3.35 |
| 4 | Congenital disorder of glycosylation, type it | Enrichment | PGM1 | 3.05 |
| 5 | Glycogen storage disease iii | Enrichment | AGL | 3.05 |
| 6 | Congenital disorder of glycosylation, type in | Enrichment | PGM1 | 2.13 |
