| Human Disease |
Hemochromatosis, Type 3; HFE3 OMIM ID: 604250 |
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| Synonyms | Hemochromatosis Due to Defect in Transferrin Receptor 2 | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Tfr2tm1.1Anro/Tfr2tm1.1Anro |
129.Cg-Tfr2tm1.1Anro | J:160785 | View |
| Tfr2tm1Slu/Tfr2tm1Slu |
involves: 129X1/SvJ * C57BL/6J | J:78360 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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