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Symbol
Name
ID
Opa1
OPA1, mitochondrial dynamin like GTPase
MGI:1921393
Phenotype annotations related to cellular
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
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)

Contributing Projects:
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
The Jackson Laboratory