OPA3

OPA3
Identifiers
Aliases	OPA3, MGA3, optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia), outer mitochondrial membrane lipid metabolism regulator, OPA3 outer mitochondrial membrane lipid metabolism regulator, outer mitochondrial membrane lipid metabolism regulator OPA3
External IDs	OMIM: 606580; MGI: 2686271; HomoloGene: 57022; GeneCards: OPA3; OMA:OPA3 - orthologs
Gene location (Human)
Chr.	Chromosome 19 (human)
End	45,602,212 bp
Gene location (Mouse)
Chr.	Chromosome 7 (mouse)
End	18,990,468 bp
RNA expression pattern
	Top expressed in
	tendon of biceps brachii; ; muscle of thigh; ; apex of heart; ; gonad; ; gastrocnemius muscle; ; left ventricle; ; gingival epithelium; ; stromal cell of endometrium; ; right auricle of heart; ; buccal mucosa cell;
	Top expressed in
	interventricular septum; ; triceps brachii muscle; ; sternocleidomastoid muscle; ; right ventricle; ; temporal muscle; ; digastric muscle; ; extraocular muscle; ; vastus lateralis muscle; ; ankle; ; epithelium of stomach;
	More reference expression data
	More reference expression data
Orthologs
	80207
	403187
	ENSG00000125741
	ENSMUSG00000052214
	Q9H6K4
	Q505D7
	NM_001017989; NM_025136
	NM_207525
	NP_001017989; NP_079412
	NP_997408
	Wikidata
View/Edit Human	View/Edit Mouse

Optic atrophy 3 protein is a protein that in humans is encoded by the OPA3 gene.