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Human Disease and Mouse Model Detail
Human Disease Achromatopsia 2; ACHM2
OMIM ID: 216900
Human Phenotype Ontology associations
Synonyms Achromatopsia; Colorblindness, Total; Rod Monochromacy 2; RMCH2; Rod Monochromatism 2
View all models View ALL (4) 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
     CNGA3* Cnga3* View 3 models HomoloGene and HGNC
     PDE6C Pde6c* View 1 model HomoloGene and HGNC
References Disease References using Mouse Models (5)

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
11/22/2016
MGI 6.06
The Jackson Laboratory