Term: Myocardial Infarction, Susceptibility to
OMIM ID: 608446

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene	Human Gene		Characteristics of this human disease are associated with mutations in...
Esr1 ESR1 F13a1 F13A1 F7 F7 Gclc GCLC Gclm GCLM Itgb3 ITGB3 Lgals2 LGALS2 Lrp8 LRP8 Lta LTA Miat MIAT Olr1 OLR1 Psma6 PSMA6 Tnfsf4 TNFSF4			...the human gene.      MGI data currently do not associate this disease with mutations in the orthologous mouse gene.