Symbol Name ID |
Pygm
muscle glycogen phosphorylase MGI:97830 |
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 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/23/2024 MGI 6.23 |
|
|