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All mouse models of myotonic dystrophy type 1 with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
myotonic dystrophy type 1 | Dmpktm1Rdd/Dmpk+ | involves: 129S2/SvPas * C57BL/6J | J:53077 | View | ||||
myotonic dystrophy type 1 | Dmpktm1Rdd/Dmpktm1Rdd | involves: 129S2/SvPas * C57BL/6J | J:33714, J:53077 | View | ||||
Transgenes and Other Mutations | myotonic dystrophy type 1 |
A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ Tg(CAG-DMPK*)1323Coop/0 |
involves: FVB | J:127391 | View | |||
myotonic dystrophy type 1 |
Tg(ACTA1-cre/ERT2)97.16Mtz/0 Tg(CAG-DMPK*)1323Coop/0 |
involves: FVB | J:132154 | View | ||||
myotonic dystrophy type 1 | Tg(Ckm-CUGBP1)1039Coop/0 | FVB-Tg(Ckm-CUGBP1)1039Coop | J:99370 | View | ||||
myotonic dystrophy type 1 | Tg(DM15)26Bew/0 | involves: FVB | J:93614 | View | ||||
myotonic dystrophy type 1 | Tg(DMPK/tetO-EGFP/DMPK)5-313Masm/0 | involves: FVB/N | J:207560 | View | ||||
myotonic dystrophy type 1 | Tg(DMWD,DMPK*,SIX5)328Ggo/Tg(DMWD,DMPK*,SIX5)328Ggo | involves: C57BL/6 * DBA/2 | J:73187, J:196337 | View | ||||
myotonic dystrophy type 1 | Tg(DMWD,DMPK*,SIX5)1177Ggo/Tg(DMWD,DMPK*,SIX5)1177Ggo | involves: C57BL/6 * DBA/2 | J:73187 | View | ||||
myotonic dystrophy type 1 | Tg(HSA*LR)20aCath/? | involves: FVB/N | J:64493 | View | ||||
myotonic dystrophy type 1 | Tg(HSA*LR)20bCath/? | involves: FVB/N | J:64493 | View | ||||
myotonic dystrophy type 1 | Tg(HSA*LR)21Cath/? | involves: FVB/N | J:64493 | View | ||||
myotonic dystrophy type 1 | Tg(HSA*LR)32aCath/? | involves: FVB/N | J:64493 | View | ||||
myotonic dystrophy type 1 | Tg(HSA*LR)32bCath/? | involves: FVB/N | J:64493 | View | ||||
myotonic dystrophy type 1 | Tg(HSA*LR)41Cath/? | involves: FVB/N | J:64493 | View | ||||
myotonic dystrophy type 1 |
Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-CUGBP1)3413Coop/0 |
involves: FVB * FVB/N * FVB/NTac | J:157646 | View |