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All mouse models of congenital structural myopathy with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
centronuclear myopathy | Dnm2tm1.1Ics/Dnm2+ | involves: 129S2/SvPas * C57BL/6 | J:237196 | View | ||||
centronuclear myopathy | Klhl31em1Eno/Klhl31em1Eno | involves: C57BL/6 | J:247651 | View | ||||
centronuclear myopathy | Mtm1tm1.1Jman/Y | involves: 129T1/Sv * C57BL/6 | J:81791 | View | ||||
centronuclear myopathy | Tg(Myh7-Pln)2Egk/0 | FVB/N-Tg(Myh7-Pln)2Egk | J:224766 | View |