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Symbol Name ID |
Coq9
coenzyme Q9 MGI:1915164 |
| Darker colors indicate more annotations |
| Human Phenotypes | Secondary microcephaly |
Cerebral atrophy |
Cerebellar atrophy |
Hyperreflexia |
Dystonia |
Encephalopathy |
Global developmental delay |
Seizure |
| Disease(s) Associated with COQ9 | ||||||||
| primary coenzyme Q10 deficiency 5 |
| Mouse Phenotypes | increased neuron apoptosis |
brain vacuoles |
astrocytosis |
gliosis |
abnormal dendrite morphology |
spongiform encephalopathy |
demyelination |
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| Availability | Mouse Genotype | |||||||
| Coq9tm1.1Lcl/Coq9tm1.1Lcl | ||||||||
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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