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Human Disease and Mouse Model Detail
Human Disease Achromatopsia 2; ACHM2
OMIM ID: 216900
Synonyms Achromatopsia; Colorblindness, Total; Rod Monochromacy 2; RMCH2; Rod Monochromatism 2
View all models View ALL (1) 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
     Pde6c* PDE6C View 1 model 1:1 Homology
     Cnga3 CNGA3*   1:1 Homology
References Disease References using Mouse Models (1)

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
12/09/2014
MGI 5.20
The Jackson Laboratory