| Human Disease |
Porphyria Cutanea Tarda OMIM ID: 176100 |
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| Synonyms | PCT; PCT, 'Familial' Type; Pct, Type II; Porphyria Cutanea Tarda, Type II; Porphyria, Hepatocutaneous Type; Uroporphyrinogen Decarboxylase Deficiency | |||||||||||||||||||||||||
| 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 |
| Hfetm2Nca/Hfetm2Nca Urodtm1Kush/Urod+ |
involves: C57BL/6J | J:66704 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Hfetm2Nca/Hfetm2Nca Urodtm1Kush/Urod+ |
involves: C57BL/6J | J:66704 | 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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