| Human Disease |
Cone-Rod Dystrophy, X-Linked, 1; CORDX1 OMIM ID: 304020 |
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| Synonyms | Cone Dystrophy 1, X-Linked; COD1 | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Rpgrtm1Tili/Rpgrtm1Tili |
involves: 129S4/SvJae * C57BL/6 | J:61371 | View |
| Rpgrtm1Tili/Rpgrtm1Tili Tg(CMV-Rpgr)1Tili/0 |
involves: 129S4/SvJae * C57BL/6 | J:87299 | 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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