Symbol Name ID |
Opa1
OPA1, mitochondrial dynamin like GTPase MGI:1921393 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties |
Feeding difficulties in infancy |
Weak cry |
Fatigue |
Myalgia |
Disease(s) Associated with OPA1 | |||||
mitochondrial DNA depletion syndrome 14 | |||||
optic atrophy |
Mouse Phenotypes | abnormal response to new environment |
limb grasping |
tremors |
ataxia |
impaired coordination |
|
Availability | Mouse Genotype | |||||
Opa1M1Bewi/Opa1+ | ||||||
Opa1Q285X/Opa1+ | ||||||
Opa1tm1.1Geno/Opa1+ |
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 08/21/2024 MGI 6.24 |
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