|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of a cell that is found in almost all tissues containing numerous basophilic granules and capable of releasing large amounts of histamine and heparin upon activation; progenitors leave bone marrow and mature in connective and mucosal tissue; mature mast cells are found in all tissues, except the bloodstream. (Mammalian Phenotype Ontology, MP_0011696)|
|Downloads & Tools|
1 gene mutations causing the absent mast cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|CPA3||carboxypeptidase A3 (mast cell)|