myocarditis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle. (Human Disease Ontology, DOID_820)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001856
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Genes

11 gene mutations causing the myocarditis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APEX1 APEX nuclease (multifunctional DNA repair enzyme) 1
BCL6 B-cell CLL/lymphoma 6
CHD2 chromodomain helicase DNA binding protein 2
CLU clusterin
CTLA4 cytotoxic T-lymphocyte-associated protein 4
DMD dystrophin
MMP9 matrix metallopeptidase 9
SOCS1 suppressor of cytokine signaling 1
TGFB1 transforming growth factor, beta 1
TICAM1 toll-like receptor adaptor molecule 1
TREX1 three prime repair exonuclease 1