|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||anomaly in the amount per unit of blood of an amino acid that is found in muscle tissue of vertebrates as phosphocreatine and supplies energy for muscle contraction when metabolized (Mammalian Phenotype Ontology, MP_0010063)|
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2 gene mutations causing the abnormal circulating creatine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.