|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||anomaly in the concentration of a pteridine derivative, which is present in body fluids and is a precursor in the biosynthesis of biopterin; elevated levels result from immune activation, malignant disease, allograft rejection, and viral infection (Mammalian Phenotype Ontology, MP_0005321)|
|Downloads & Tools|
2 gene mutations causing the abnormal neopterin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.