| Human Disease |
Xeroderma Pigmentosum, Variant Type; XPV OMIM ID: 278750 |
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| Synonyms | Photosensitivity with Defective DNA Synthesis; Xeroderma Pigmentosum with Normal DNA Repair Rates | |||||||||||||||||||||
| 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 |
| Polhtm1Crey/Polhtm1Crey |
involves: 129P2/OlaHsd * C57BL/6 | J:98037 | View |
| Polhtm1Fmh/Polhtm1Fmh |
involves: C57BL/6 | J:99721 | View |
| Polhtm1.1Rak/Polhtm1.1Rak |
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 | J:105034 | 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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