| Human Disease |
Cleidocranial Dysplasia; CCD OMIM ID: 119600 |
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| View all models | View ALL (6) 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 |
| Runx2tm1Jals/Runx2tm1Jals |
involves: 129S7/SvEvBrd * C57BL/6 | J:143532 | View |
| Runx2tm1Kish/Runx2tm1Kish |
involves: 129P2/OlaHsd * C57BL/6 | J:40783, J:53069, J:54095 | View |
| Runx2tm1Kish/Runx2+ |
involves: 129P2/OlaHsd * C57BL/6 | J:40783 | View |
| Runx2tm1Mjo/Runx2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:40784, J:53868 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Ccd/Ccd+ |
B10Rl.101-Ccd | J:16170 | View |
| Ccd/Ccd+ |
involves: 101 * C3H | J:14006 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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