abnormal haptoglobin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013215
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1 gene mutations causing the abnormal haptoglobin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
HPX hemopexin