| Human Disease |
Mitochondrial Complex IV Deficiency OMIM ID: 220110 |
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| Synonyms | COX Deficiency; Cytochrome C Oxidase Deficiency | ||||||||||||||||||||||||||||||||||||||||||||
| View all models | View ALL (2) mouse models for this human disease. | ||||||||||||||||||||||||||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Cox10tm1Ctm/Cox10tm1Ctm Tg(Camk2a-cre)#Szi/0 |
involves: 129 * C57BL/6 * C57BL/6J * CBA | J:188773 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Sco2tm1.1Easc/Sco2tm2.1Easc |
129X1/SvJ-Sco2tm1.1Easc/Sco2tm2.1Easc | J:155116 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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