| Human Disease |
Hemochromatosis, Type 4; HFE4 OMIM ID: 606069 |
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| Synonyms | Hemochromatosis Due to Defect in Ferroportin; Hemochromatosis, Autosomal Dominant | |||||||||||||||||||||
| 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Slc40a1ffe/Slc40a1+ |
either: (involves: 129X1/SvJ * C57BL/6J) or (involves: C3H/HeJ * C57BL/6J) | J:118592 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Slc40a1tm1Nca/Slc40a1+ |
involves: 129S4/SvJae * 129S6/SvEvTac | J:129846 | 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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