|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||anomaly in the amount of the amino acid that is found in muscle tissue of vertebrates as phosphocreatine and supplies energy for muscle contraction when metabolized (Mammalian Phenotype Ontology, MP_0010060)|
|Downloads & Tools|
3 gene mutations causing the abnormal creatine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.