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All mouse models of cranial nerve disease with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | congenital nystagmus 1 | Frmd7tm1b(KOMP)Wtsi/Frmd7tm1b(KOMP)Wtsi | involves: C57BL/6 * C57BL/6N | J:299010 | View | |||
| congenital nystagmus 1 | Frmd7tm1b(KOMP)Wtsi/Y | involves: C57BL/6 * C57BL/6N | J:299010 | View | ||||
| Duane retraction syndrome |
Chn1tm1.1Ece/Chn1tm1.1Ece Tg(Hlxb9-GFP)1Tmj/0 |
involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J | J:243785 | View | ||||
| Duane retraction syndrome |
Mafbtm1.2Good/Mafb+ Tg(Isl1-EGFP*)1Slp/0 |
involves: 129S4/SvJae * BALB/c * C57BL/6 | J:237642 | View | ||||
| Duane retraction syndrome |
Mafbtm1.2Good/Mafbtm1.2Good Tg(Isl1-EGFP*)1Slp/0 |
involves: 129S4/SvJae * BALB/c * C57BL/6 | J:237642 | View | ||||
| Leber hereditary optic neuropathy | mt-Nd6m3Dwa | B6.129S-mt-Nd6m3Dwa | J:192260 | View | ||||
| optic atrophy | Opa1M1Bewi/Opa1+ | involves: C3HeB/FeJ * C57BL/6 | J:154966 | View | ||||
| optic atrophy | Opa1Q285X/Opa1+ | involves: C3HeB/FeJ * C57BL/6JCrl | J:121779, J:189276 | View | ||||
| optic atrophy | Opa1tm1.1Geno/Opa1+ | involves: 129S2/SvPas | J:237963 | View | ||||
| | congenital fibrosis of the extraocular muscles | Kif21atm1.1Ece/Kif21a+ | involves: 129S1/Sv * 129S4/SvJae | J:213171 | View | |||
| congenital fibrosis of the extraocular muscles | Kif21atm1.1Ece/Kif21atm1.1Ece | involves: 129S1/Sv * 129S4/SvJae | J:213171 | View | ||||
| congenital fibrosis of the extraocular muscles |
Kif21atm1.1Ece/Kif21atm1.1Ece Tg(Isl1-EGFP*)1Slp/0 |
involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6 | J:213171 | View | ||||
| congenital fibrosis of the extraocular muscles | Tubb3tm1.1Ece/Tubb3tm1.1Ece | involves: 129S/SvEv * C57BL/6J | J:158992 | View | ||||
| congenital nystagmus | Ahrtm1Yfk/Ahrtm1Yfk | involves: 129S/SvEv * C57BL/6J | J:195817 | View | ||||
| optic atrophy | Rpl24Bst/Rpl24+ | involves: C57BLKS | J:28035 | View | ||||
| trigeminal neuralgia | Gabrg1em1Ktka/Gabrg1em1Ktka | involves: C57BL/6N | J:299761 | View | ||||
| Transgenes and Other Mutations | Leber hereditary optic neuropathy | Tg(LONP1-mt-ND4*,-mCherry*)#Jguy | B6(D2)-Tg(LONP1-mt-ND4*,-mCherry*)#Jguy | J:224897 | View | |||
| Additional Complex Models | optic atrophy |
Fdxrm1J/Fdxrm1J Otop2m1J/Otop2m1J |
B6;129S-Fdxrm1J Otop2m1J/GrsrJ | J:247931 | View | |||