About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Retinitis Pigmentosa 3; RP3
OMIM ID: 300029
Human Phenotype Ontology associations
Synonyms Choroidoretinal Degeneration with Retinal Reflex in Heterozygous Women; Cone-Rod Degeneration, X-Linked; Retinitis Pigmentosa; Retinitis Pigmentosa 15; RP15
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
     RPGR* Rpgr* View 4 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(CAG-Rpgr)mRDefWrght View 2 models
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
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.07
The Jackson Laboratory