Symbol
Name
ID

Pygm
muscle glycogen phosphorylase
MGI:97830

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes

Hyperuricemia

Elevated circulating creatine kinase activity

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
Availability	Mouse Genotype	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
	Pygm^em1(IMPC)J/Pygm^em1(IMPC)J
	Pygm^tm1.1Adru/Pygm^tm1.1Adru

Contributing Projects: 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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