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Symbol
Name
ID
Pygm
muscle glycogen phosphorylase
MGI:97830
Phenotype annotations related to renal/urinary system
Darker colors indicate more annotations
Human Phenotypes
Dark urine
Myoglobinuria
Exercise-induced myoglobinuria
Recurrent myoglobinuria
Acute kidney injury
Chronic kidney disease
Disease(s) Associated with PYGM
glycogen storage disease V

Mouse Phenotypes
myoglobinuria
Availability Mouse Genotype
Pygmtm1.1Adru/Pygmtm1.1Adru

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory