absent mast cells Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011696
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Genes

1 gene mutations causing the absent mast cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CPA3 carboxypeptidase A3 (mast cell)