| Entrez gene ID | | 80207 |
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| Official gene symbol | | OPA3 |
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| Full name | | optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) |
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| Aliases | | ,FLJ22187,FLJ25932,MGA3,MGC75494, |
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| Gene summary | | The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq] |
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| Location | | Chromosome: 19 Locus: 19q13.32 |
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| Gene position | | 46088122 - 46031025 Map Viewer |
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| Gene orientation | | minus |
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| Gene size | | 57098 bp |
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| Gene sequence |
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| OMIM ID | | 606580 |
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