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Symbol Name ID |
Cp
ceruloplasmin MGI:88476 |
| Darker colors indicate more annotations |
| Human Phenotypes | Retinal degeneration |
| Disease(s) Associated with CP | |
| aceruloplasminemia |
| Mouse Phenotypes | abnormal retina inner nuclear layer morphology |
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| Availability | Mouse Genotype | |
| Cptm1Samd/Cptm1Samd | ||
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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