Symbol Name ID |
Opa1
OPA1, mitochondrial dynamin like GTPase MGI:1921393 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased activity of mitochondrial complex I |
Decreased activity of mitochondrial complex IV |
Disease(s) Associated with OPA1 | ||
mitochondrial DNA depletion syndrome 14 |
Mouse Phenotypes | abnormal mitochondrial morphology |
decreased muscle fiber mitochondrial DNA content |
abnormal mitochondrial crista morphology |
disorganized mitochondrial cristae |
abnormal mitochondrial shape |
decreased mitochondrial number |
increased mitochondrial number |
increased mitochondrial size |
abnormal autophagy |
abnormal mitophagy |
decreased pancreatic beta cell proliferation |
abnormal respiratory electron transport chain |
abnormal mitochondrial physiology |
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Availability | Mouse Genotype | |||||||||||||
Opa1lilr3/Opa1lilr3 | ||||||||||||||
Opa1Q285X/Opa1+ | ||||||||||||||
Opa1tm1.1Geno/Opa1+ | ||||||||||||||
Hprt1tm1(ACTB-Opa1)Lsc/Y | ||||||||||||||
Opa1tm1Lsc/Opa1tm1Lsc (conditional) | ||||||||||||||
Opa1tm1.1Hise/Opa1tm1.2Hise Tg(Ins2-cre)25Mgn/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 05/21/2024 MGI 6.23 |
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