|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||anomaly in the amount of any of haptoglobin, a protein that binds free hemoglobin (Hb) released from erythrocytes with high affinity and thereby inhibits its oxidative activity (Mammalian Phenotype Ontology, MP_0013215)|
|Downloads & Tools|
1 gene mutations causing the abnormal haptoglobin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.