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Symbol Name ID |
Ercc6
excision repair cross-complementing rodent repair deficiency, complementation group 6 MGI:1100494 |
| Darker colors indicate more annotations |
| Human Phenotypes | Retinal hemorrhage |
Splenomegaly |
| Disease(s) Associated with ERCC6 | ||
| Cockayne syndrome | ||
| Cockayne syndrome B |
| Mouse Phenotypes | microgliosis |
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| Availability | Mouse Genotype | |
| Ercc6tm1Gvh/Ercc6tm1Gvh | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 05/14/2024 MGI 6.23 |
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