| Human Disease |
Charcot-Marie-Tooth Disease, Axonal, Type 2E; CMT2E OMIM ID: 607684 |
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| Synonyms | Charcot-Marie-Tooth Neuropathy, Type 2E | |||||||||||||||||||||
| View all models | View ALL (2) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(NEFL*E397K)#Milg/0 |
Not Specified | J:173771 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(tetO-NEFL)173.2Jpj/0 Tg(THY1-tTA)177Jpj/0 |
involves: C3H * C57BL/6 | J:160704 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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