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Human Disease and Mouse Model Detail
Human Disease Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive; CHN
OMIM ID: 605253
Synonyms Charcot-Marie-Tooth Disease, Type 4E; CMT4E; Hypomyelination, Severe Congenital
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

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Egr2* EGR2* View 2 models 1:1 Homology
     Mpz MPZ*   1:1 Homology
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(Mpz)80.2Wra View 1 model
References Disease References using Mouse Models (3)

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
12/16/2014
MGI 5.20
The Jackson Laboratory