| Human Disease |
Fanconi Anemia, Complementation Group A; FANCA OMIM ID: 227650 |
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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 |
| Fancatm1Faw/Fancatm1Faw |
involves: 129P2/OlaHsd * FVB | J:63742 | View |
| Fancatm1.1Wong/Fancatm1.1Wong |
involves: C57BL/6 | J:85108 | View |
| Fancatm1Wong/Fancatm1Wong |
involves: C57BL/6 | J:85108 | 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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