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Human Disease and Mouse Model Detail
Human Disease Retinitis Pigmentosa; RP
OMIM ID: 268000
Human Phenotype Ontology associations
Synonyms Retinitis Pigmentosa
View all models View ALL (13) 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
     PDE6G* Pde6g* View 1 model HomoloGene
     AGTPBP1 Agtpbp1* View 1 model HomoloGene and HGNC
CCDC66 Ccdc66* View 1 model HomoloGene and HGNC
CNGB1 Cngb1* View 2 models HGNC
CRB2 Crb2* View 2 models HomoloGene
PDE6A Pde6a* View 2 models HomoloGene
PDE6B Pde6b* View 1 model HomoloGene and HGNC
SLC6A6 Slc6a6* View 1 model HomoloGene and HGNC
     C8orf37* 2610301B20Rik   HomoloGene and HGNC
AIPL1* Aipl1   HomoloGene
ARL6* Arl6   HomoloGene and HGNC
CLRN1* Clrn1   HomoloGene and HGNC
CNGA1* Cnga1   HomoloGene and HGNC
CRX* Crx   HomoloGene and HGNC
LRAT* Lrat   HomoloGene and HGNC
RBP3* Rbp3   HomoloGene and HGNC
ROM1* Rom1   HomoloGene
References Disease References using Mouse Models (28)

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 6.05
The Jackson Laboratory