| Human Disease |
Xeroderma Pigmentosum, Complementation Group E OMIM ID: 278740 |
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| Synonyms | Xeroderma Pigmentosum V; XP5; XP, Group E; XPE | |||||||||||||||||||||
| View all models | View ALL (4) 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 |
| Ddb2tm1Linn/Ddb2tm1Linn |
involves: 129S/SvEv * C57BL/6 | J:88125 | View |
| Ddb2tm1Pra/Ddb2tm1Pra |
involves: C57BL/6 | J:95633 | View |
| Ddb2tm1Linn/Ddb2+ |
involves: 129S/SvEv * C57BL/6 | J:88125 | View |
| Ddb2tm1Pra/Ddb2+ |
involves: C57BL/6 | J:95633 | 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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