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Human Disease and Mouse Model Detail
Human Disease Cone-Rod Dystrophy, X-Linked, 1; CORDX1
OMIM ID: 304020
Human Phenotype Ontology associations
Synonyms Cone Dystrophy 1, X-Linked; COD1; Retinal Cone-Rod Dystrophy
View all models View ALL (2) 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
     RPGR* Rpgr* View 2 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(CMV-Rpgr)1Tili View 1 model
References Disease References using Mouse Models (2)

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