|
Symbol Name ID |
Cox15
cytochrome c oxidase assembly protein 15 MGI:1920112 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased fetal movement |
| Disease(s) Associated with COX15 | |
| mitochondrial complex IV deficiency nuclear type 6 |
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 04/30/2024 MGI 6.23 |
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