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Human Disease and Mouse Model Detail
Human Disease Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a;
OMIM ID: 609260
Human Phenotype Ontology associations
Synonyms Charcot-Marie-Tooth Disease; Charcot-Marie-Tooth Disease, Axonal, Type 2A2; CMT2A2; Charcot-Marie-Tooth Disease, Neuronal, Type 2A2; Charcot-Marie-Tooth Neuropathy, Type 2A2; Cmt2a2a; Hereditary Motor and Sensory Neuropathy Iia2; HMSN2A2; HMSN IIA2
View all models View ALL (3) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     MFN2* Mfn2 View 3 models HomoloGene and HGNC
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(Eno2-MFN2*R94Q)L51Ugfm View 2 models
  Tg(Eno2-MFN2*R94Q)L87Ugfm View 1 model
References Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory