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Mammalian Phenotype Browser
Term Detail
MP term:abnormal mitochondrial ATP synthesis coupled electron transport
MP id: MP:0010956
Definition: anomaly in the transfer of electrons through a series of electron donors and acceptors, generating energy that is ultimately used for synthesis of ATP, as it occurs in the mitochondrial inner membrane and mediated by multisubunit enzyme complexes known as complex I-IV
Number of paths to term: 3

is-adenotes an 'is-a' relationship
part-ofdenotes a 'part-of' relationship


mammalian phenotype
        is-acellular phenotype
                is-aabnormal cell physiology
                        is-aabnormal cellular respiration
                                is-aabnormal respiratory electron transport chain
                                        is-aabnormal mitochondrial ATP synthesis coupled electron transport [MP:0010956] (42 genotypes, 42 annotations)


mammalian phenotype
        is-acellular phenotype
                is-aabnormal cell physiology
                        is-aabnormal mitochondrial physiology
                                is-aabnormal oxidative phosphorylation
                                        is-aabnormal mitochondrial ATP synthesis coupled electron transport [MP:0010956] (42 genotypes, 42 annotations)


mammalian phenotype
        is-acellular phenotype
                is-aabnormal cell physiology
                        is-aabnormal mitochondrial physiology
                                is-aabnormal respiratory electron transport chain
                                        is-aabnormal mitochondrial ATP synthesis coupled electron transport [MP:0010956] (42 genotypes, 42 annotations)

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last database update
10/08/2014
MGI 5.20
The Jackson Laboratory