| Human Disease |
Osteogenesis Imperfecta, Type III OMIM ID: 259420 |
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| Synonyms | Oi3; OI, Type III; Osteogenesis Imperfecta, Progressively Deforming, with Normal Sclerae | |||||||||||||||||||||||||
| 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 |
| Col1a1Aga2/Col1a1+ |
C3HeB/FeJ-Col1a1Aga2 | J:185988 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Col1a2oim/Col1a2oim |
B6C3Fe a/a-Col1a2oim/J | J:38013 | View |
| Col1a2oim/Col1a2oim |
involves: C3H/HeJ * C57BL/6JLe | J:4348 | 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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