Symbol Name ID |
Chchd10
coiled-coil-helix-coiled-coil-helix domain containing 10 MGI:2143558 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Increased mitochondrial number |
Decreased activity of mitochondrial complex II |
Decreased activity of mitochondrial complex III |
Decreased activity of mitochondrial complex IV |
Disease(s) Associated with CHCHD10 | ||||
isolated mitochondrial myopathy |
Mouse Phenotypes | cellular phenotype |
decreased myocardial fiber mitochondrial DNA content |
cardiac interstitial fibrosis |
abnormal cell nucleus morphology |
abnormal mitochondrial morphology |
abnormal mitochondrial crista morphology |
abnormal mitochondrial matrix morphology |
increased mitochondrial number |
abnormal vacuole morphology |
abnormal respiratory electron transport chain |
abnormal mitochondrial physiology |
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Availability | Mouse Genotype | |||||||||||
Chchd10em3Dpn/Chchd10em3Dpn | ||||||||||||
Chchd10em5Lutzy/Chchd10em5Lutzy | * | |||||||||||
Chchd10em8Lutzy/Chchd10+ |
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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