Symbol Name ID |
Pygm
muscle glycogen phosphorylase MGI:97830 |
Darker colors indicate more annotations |
Human Phenotypes | Hyperuricemia |
Elevated circulating creatine kinase concentration |
Highly elevated creatine kinase |
Reduced muscle glycogen phosphorylase activity |
Failure to elevate lactate upon ischemic exercise test |
Increased muscle glycogen content |
Glycogen accumulation in muscle fiber lysosomes |
Dark urine |
Myoglobinuria |
Exercise-induced myoglobinuria |
Recurrent myoglobinuria |
Exercise intolerance |
Postexertional symptom exacerbation |
Disease(s) Associated with PYGM | |||||||||||||
glycogen storage disease V |
Mouse Phenotypes | decreased aerobic running capacity |
decreased circulating calcium level |
increased circulating alkaline phosphatase level |
increased circulating aspartate transaminase level |
increased creatine kinase level |
increased skeletal muscle glycogen level |
myoglobinuria |
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Availability | Mouse Genotype | |||||||
Pygmem1(IMPC)J/Pygmem1(IMPC)J | ||||||||
Pygmtm1.1Adru/Pygmtm1.1Adru |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 05/21/2024 MGI 6.23 |
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