Human Disease and Mouse Model Detail
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Human Disease
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Achromatopsia 2; ACHM2
OMIM ID: 216900
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Synonyms
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Colorblindness, Total;
Rod Monochromacy 2; RMCH2;
Rod Monochromatism 2
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View all models
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View ALL (1) mouse models for this human disease.
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Pde6c*
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PDE6C
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View 1 model
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1:1 Homology
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Cnga3
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CNGA3*
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1:1 Homology
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Mouse Models
Human Disease Modeled: Achromatopsia 2; ACHM2
Associated Mouse Gene:
Pde6c
Analysis Tools