| Human Disease |
Late-Onset Retinal Degeneration; LORD OMIM ID: 605670 |
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| Synonyms | Retinal Degeneration, Late-Onset, Autosomal Dominant | |||||||||||||||||||||
| View all models | View ALL (1) 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 |
| C1qtnf5tm1.1Itl/C1qtnf5+ |
C57BL/6-C1qtnf5tm1.1Itl | J:171089 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| C1qtnf5tm1.1Geno/C1qtnf5tm1.1Geno |
involves: 129 * C57BL/6J | J:180961 | 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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