| Human Disease |
Aceruloplasminemia OMIM ID: 604290 |
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| 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 |
| Cptm1Hrs/Cptm1Hrs |
involves: 129X1/SvJ * Black Swiss | J:57730, J:71807 | View |
| Cptm1Yos/Cptm1Yos |
C.129P2-Cptm1Yos | J:142713 | View |
| Cptm1Hrs/Cptm1Hrs Hephsla/Y |
involves: 129X1/SvJ * C57BL/6 | J:92620 | 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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