| Human Disease |
Protoporphyria, Erythropoietic; EPP OMIM ID: 177000 |
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| Synonyms | Erythrohepatic Protoporphyria; Ferrochelatase Deficiency; Heme Synthetase Deficiency | ||||||||||||||||||||||||||||
| 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 |
| Abcg2tm1Ahs/Abcg2tm1Ahs |
either: (involves: 129P2/OlaHsd * FVB) or (involves: FVB) | J:80519 | 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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