decreased myocardial infarction size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decreased size of necrotic area from normal of the myocardium resulting from a sudden insufficiency of arterial or venous blood supply due to emboli, thrombi or mechanical factors (Mammalian Phenotype Ontology, MP_0003038)
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20 gene mutations causing the decreased myocardial infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADORA3 adenosine A3 receptor
BBC3 BCL2 binding component 3
BECN1 beclin 1, autophagy related
CD44 CD44 molecule (Indian blood group)
DUSP6 dual specificity phosphatase 6
FCER1G Fc fragment of IgE, high affinity I, receptor for; gamma polypeptide
GSK3B glycogen synthase kinase 3 beta
MAPK14 mitogen-activated protein kinase 14
MAPKAPK2 mitogen-activated protein kinase-activated protein kinase 2
MASP2 mannan-binding lectin serine peptidase 2
MMP9 matrix metallopeptidase 9
NGFR nerve growth factor receptor
NPR1 natriuretic peptide receptor 1
OLR1 oxidized low density lipoprotein (lectin-like) receptor 1
PLA2G10 phospholipase A2, group X
PLA2G5 phospholipase A2, group V
PPIF peptidylprolyl isomerase F
SSTR2 somatostatin receptor 2
TSC2 tuberous sclerosis 2
VWF von Willebrand factor