| Human Disease |
Retinitis Pigmentosa 7; RP7 OMIM ID: 608133 |
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| View all models | View ALL (3) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Prph2tm1Nmc/Prph2tm1Nmc |
involves: 129S1/Sv * 129X1/SvJ | J:76490 | View |
| Prph2tm1Nmc/Prph2+ |
involves: 129S1/Sv * 129X1/SvJ | J:76490 | View |
| Prph2Rd2/Prph2+ |
either: (involves: BALB/c * O20/A) or (involves: GR/A * O20/A) or (involves: O20/A * STS/A) | J:25582 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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