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All mouse models of 3-methylglutaconic aciduria with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | 3-methylglutaconic aciduria type 3 | Opa3m1Votr/Opa3m1Votr | involves: C3H * C57BL/6JCrl | J:181670, J:188346 | View | |||
| 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome | Serac1em1Bcgen/Serac1em1Bcgen | C57BL/6N-Serac1em1Bcgen | J:326672 | View | ||||
| Barth syndrome | Gt(ROSA)26Sortm37(H1/tetO-RNAi:Tafazzin)Arte/? | Not Specified | J:176041 | View | ||||
| Barth syndrome | Gt(ROSA)26Sortm37(H1/tetO-RNAi:Tafazzin)Arte/Gt(ROSA)26Sor+ | involves: 129S6/SvEvTac * C57BL/6J | J:167527 | View | ||||
| Barth syndrome |
Tafazzinem1Xfa/Y Tg(myl7.L-cre)1118Tmhn/0 |
involves: C57BL/6NCrl * MF1 | J:339058 | View | ||||
| | Barth syndrome | Fkbp1atm1Zuk/Fkbp1atm1Zuk | either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J) | J:45536 | View | |||
| Barth syndrome | Mesttm1Masu/Mest+ | involves: 129S1/Sv * 129X1/SvJ | J:79223 | View | ||||