| Human Disease |
Charcot-Marie-Tooth Disease, Type 4b2; CMT4B2 OMIM ID: 604563 |
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| Synonyms | Charcot-Marie-Tooth Disease, with Focally Folded Myelin Sheaths, Autosomal Recessive, Type 4B2 | |||||||||||||||||||||
| 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 |
| Sbf2Gt(RRF511)Byg/Sbf2Gt(RRF511)Byg |
involves: 129P2/OlaHsd * C57BL/6 | J:133391 | View |
| Sbf2Gt(XH212)Byg/Sbf2Gt(XH212)Byg |
involves: 129P2/OlaHsd * C57BL/6 | J:133042 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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