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Symbol Name ID |
Ercc1
excision repair cross-complementing rodent repair deficiency, complementation group 1 MGI:95412 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal retinal morphology |
Retinoblastoma |
Deeply set eye |
Bilateral microphthalmos |
Nystagmus |
| Disease(s) Associated with ERCC1 | |||||
| cerebrooculofacioskeletal syndrome 4 | |||||
| osteosarcoma |
| Mouse Phenotypes | increased retina apoptosis |
thin retina outer nuclear layer |
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| Availability | Mouse Genotype | ||
| Ercc1tm1Jhjh/Ercc1tm2Jhjh | |||
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 04/16/2024 MGI 6.23 |
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