| Human Disease |
Charcot-Marie-Tooth Disease, Type 4b1; CMT4B1 OMIM ID: 601382 |
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| Synonyms | Charcot-Marie-Tooth Disease, Autosomal Recessive, with Focally Folded Myelin Sheaths, Autosomal Recessive, Type 4B1; Charcot-Marie-Tooth Disease, Type 4b; CMT4B; Charcot-Marie-Tooth Neuropathy, Type 4B1 | |||||||||||||||||||||
| 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Mtmr2tm1.1Abol/Mtmr2tm1.1Abol |
involves: 129S2/SvPas | J:94373 | View |
| Mtmr2tm1Ueli/Mtmr2tm1Ueli |
involves: 129S6/SvEvTac * C57BL/6 | J:104120 | 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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