| Human Disease |
Charcot-Marie-Tooth Disease, Axonal, Type 2D; CMT2D OMIM ID: 601472 |
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| Synonyms | Charcot-Marie-Tooth Disease, Neuronal, Type 2d; Charcot-Marie-Tooth Neuropathy, Type 2d | |||||||||||||||||||||
| View all models | View ALL (3) 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 |
| GarsNmf249/Gars+ |
C57BL/6J-GarsNmf249/J | J:112221 | View |
| GarsNmf249/Gars+ |
involves: C57BL/6J * CAST/Ei | J:179811 | View |
| GarsC201R/Gars+ |
involves: BALB/cAnN * C3H/HeH * C57BL/6J | J:149830, J:179811 | 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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