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Human Disease and Mouse Model Detail
Human Disease Cone Dystrophy 3; COD3
OMIM ID: 602093
Human Phenotype Ontology associations
Synonyms Retinal Cone Dystrophy
View all models View ALL (5) 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
     GUCA1A* Guca1a* View 5 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(Guca1a*L151F)#Wbae View 1 model
  Tg(Guca1a*L151F/EGFP)#Wbae View 1 model
  Tg(Rho-GUCA1A*Y99C)L53Amd 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
MGI 6.07
The Jackson Laboratory