| Human Disease |
Charcot-Marie-Tooth Disease, Axonal, Type 2a1; CMT2A1 OMIM ID: 118210 |
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| Synonyms | Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2A1; Charcot-Marie-Tooth Disease, Neuronal, Type 2A1; Charcot-Marie-Tooth Neuropathy, Type 2A1; Hereditary Motor and Sensory Neuropathy Iia1; HMSN2A1; HMSN IIA1 | |||||||||||||||||||||
| View all models | View ALL (1) 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Kif1btm1Noh/Kif1b+ |
involves: 129S4/SvJae * C57BL/6J | J:69772 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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