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Symbol Name ID |
Cox10
heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 MGI:1917633 |
| Darker colors indicate more annotations |
| Human Phenotypes | Generalized hypotonia |
Cytochrome C oxidase-negative muscle fibers |
Muscle weakness |
| Disease(s) Associated with COX10 | |||
| mitochondrial complex IV deficiency nuclear type 3 |
| Mouse Phenotypes | increased variability of skeletal muscle fiber size |
abnormal skeletal muscle morphology |
decreased skeletal muscle mass |
increased muscle fatigability |
myopathy |
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| Availability | Mouse Genotype | |||||
| Cox10tm1Ctm/Cox10tm1Ctm Myl1tm1(cre)Sjb/Myl1+ (conditional) |
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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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