|
Symbol Name ID |
Cox15
cytochrome c oxidase assembly protein 15 MGI:1920112 |
| Darker colors indicate more annotations |
| Human Phenotypes | Ventricular septal defect |
Cardiomyopathy |
Hypertrophic cardiomyopathy |
Congestive heart failure |
| Disease(s) Associated with COX15 | ||||
| Leigh disease | ||||
| mitochondrial complex IV deficiency nuclear type 6 |
| Mouse Phenotypes | abnormal heart morphology |
increased heart atrium size |
increased heart weight |
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| Availability | Mouse Genotype | |||
| Cox15tm1.1(KOMP)Vlcg/Cox15+ | ||||
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 04/23/2024 MGI 6.23 |
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