| Human Disease |
Cockayne Syndrome, Type B; CSB OMIM ID: 133540 |
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| Synonyms | Ckn2 | |||||||||||||||||||||
| 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 |
| Ercc6tm1Gvh/Ercc6tm1Gvh |
involves: 129P2/OlaHsd * FVB | J:40211 | View |
| Ercc6tm1Gvh/Ercc6tm1Gvh Xpatm1Hvs/Xpatm1Hvs |
B6.129P2-Xpatm1Hvs Ercc6tm1Gvh | J:122013 | View |
| Ercc6tm1Gvh/Ercc6tm1Gvh Xpatm1Hvs/Xpatm1Hvs |
involves: 129P2/OlaHsd * C57BL/6J | J:122013 | 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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