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Summary Expression Phenotypes Gene Literature (0) GO Terms (13) Nucleotides (96) Proteins (44) Interactants (88) Wiki
XB-GENEPAGE-941636
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 opa3

???displayGene.name???: 
optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)

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( Nomenclature history )

???displayGene.geneFunction???
Predicted coiled-coil protein

AI Protein Function :
The opa3 gene encodes a mitochondrial membrane protein localized to the mitochondria, functioning in cellular metabolism. Expression is detected in the developing eye, brain, spinal cord, and cranial g...[+]


InterPro :
OPA3-like

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Diseases: 


Disease Ontology:
3-methylglutaconic aciduria type 3 [+]

MIM:
3-METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3 [+]

External Links:
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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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