| Human Disease |
Pulmonary Fibrosis, Idiopathic; IPF OMIM ID: 178500 |
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| Synonyms | Fibrosing Alveolitis, Cryptogenic; Idiopathic Pulmonary Fibrosis, Familial | |||||||||||||||||||||||||||||||||
| 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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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(H2-K-Fosl2,EGFP)13Wag/0 |
either: 129.Cg-Tg(H2-K-Fosl2,EGFP)13Wag or B6.Cg-Tg(H2-K-Fosl2,EGFP)13Wag | J:139032 | 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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