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All mouse models of mitochondrial myopathy with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 | Tg(ACTB-Twnk*)DSuom/0 | involves: FVB/N | J:104378 | View | |||
| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 | Tg(ACTB-Twnk*A360T)HSuom/0 | involves: FVB/N | J:104378 | View | ||||
| isolated mitochondrial myopathy | Chchd10em3Dpn/Chchd10em3Dpn | C57BL/6J-Chchd10em3Dpn | J:344465 | View | ||||
| | Kearns-Sayre syndrome |
Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Ckmm-cre)1Lrsn/0 |
involves: 129S1/Sv * 129X1/SvJ | J:51964 | View | |||
| Kearns-Sayre syndrome |
Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Myhca-cre)1Lrsn/0 |
involves: 129S1/Sv * 129X1/SvJ * FVB | J:61372 | View | ||||
| MELAS syndrome | mt-Tl1m1Jiha | involves: C57BL/6NCrlj * CBA/JNCrlj | J:344247 | View | ||||
| mitochondrial myopathy | Adck2tm1(KOMP)Vlcg/Adck2+ | C57BL/6-Adck2tm1(KOMP)Vlcg | J:280282 | View | ||||
| mitochondrial myopathy |
Cox10tm1Ctm/Cox10tm1Ctm Myl1tm1(cre)Sjb/Myl1+ |
involves: 129X1/SvJ * C57BL/6 | J:101747 | View | ||||
| myopathy, lactic acidosis, and sideroblastic anemia | Pus1tm1.1Mdf/Pus1tm1.1Mdf | B6.129S7(C)-Pus1tm1.1Mdf | J:237107 | View | ||||
| Transgenes and Other Mutations | mitochondrial myopathy | Del(MTmt-Tk-mt-Nd5)1Jiha | involves: C57BL/6J * CBA | J:103743 | View | |||
| Additional Complex Models | mitochondrial myopathy |
Fdxrm1J/Fdxrm1J Otop2m1J/Otop2m1J |
B6;129S-Fdxrm1J Otop2m1J/GrsrJ | J:247931 | View | |||
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No similarity to the expected human disease phenotype was found.
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
| NOT Models | mitochondrial encephalomyopathy | Atp7aMo-vbr/Y | Not Specified | J:44695 | View | |||