| Human Disease |
Pulmonary Disease, Chronic Obstructive; COPD OMIM ID: 606963 |
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| View all models | View ALL (4) 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 |
| Ltbp4Gt(U3Cre)1Vmel/Ltbp4Gt(U3Cre)1Vmel |
involves: 129S2/SvPas | J:160854 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Wwtr1tm1Hku/Wwtr1tm1Hku |
involves: 129 * C57BL/6 * ICR | J:132020, J:164957 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-IL1B)KBry/0 |
involves: 129 * C57BL/6 | J:107601 | 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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