Symbol Name ID |
Cox15
cytochrome c oxidase assembly protein 15 MGI:1920112 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased fetal movement |
Feeding difficulties |
Emotional lability |
Disease(s) Associated with COX15 | |||
Leigh disease | |||
mitochondrial complex IV deficiency nuclear type 6 |
Mouse Phenotypes | abnormal motor capabilities/coordination/movement |
|
Availability | Mouse Genotype | |
Cox15tm1.1Zev/Cox15tm1.1Zev Tg(ACTA1-cre)79Jme/0 (conditional) |
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 08/02/2024 MGI 6.24 |
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