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All mouse models of oculopharyngeal muscular dystrophy with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
 | oculopharyngeal muscular dystrophy | Pabpn1tm1.2Gpvl/Pabpn1+ | involves: C57BL/6 * FVB/N | J:243638 | View | |||
| Transgenes and Other Mutations | oculopharyngeal muscular dystrophy | Tg(ACTA1-PABPN1*A17)1Drub/0 | involves: FVB/N | J:115642 | View | |||
| Additional Complex Models | oculopharyngeal muscular dystrophy |
Tg(CAG-GLVP)#Cath/0 Tg(GAL4-PABPN1*A16)#Cath/0 |
involves: C57BL/6 * FVB | J:178541 | View | |||