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Symbol
Name
ID

Opa1
OPA1, mitochondrial dynamin like GTPase
MGI:1921393

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties	Feeding difficulties in infancy	Weak cry	Fatigue	Myalgia
Disease(s) Associated with OPA1	Feeding difficulties	Feeding difficulties in infancy	Weak cry	Fatigue	Myalgia
mitochondrial DNA depletion syndrome 14
optic atrophy

Mouse Phenotypes		abnormal response to new environment	limb grasping	tremors	ataxia	impaired coordination
Availability	Mouse Genotype	abnormal response to new environment	limb grasping	tremors	ataxia	impaired coordination
	Opa1^M1Bewi/Opa1⁺
	Opa1^Q285X/Opa1⁺
	Opa1^tm1.1Geno/Opa1⁺

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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