Gene: OPA1

Alternate names for this Gene: BERHS|MGM1|MTDPS14|NPG|NTG|largeG

Gene Summary: The protein encoded by this gene is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. The encoded protein localizes to the inner mitochondrial membrane and helps regulate mitochondrial stability and energy output. This protein also sequesters cytochrome c. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness.

Gene is located in Chromosome: 3

Location in Chromosome : 3q29

Description of this Gene: OPA1 mitochondrial dynamin like GTPase

Type of Gene: protein-coding

Gene: LOC102724808

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

Type of Gene:

rs185566659 in OPA1;LOC102724808 gene and Dental caries PMID 31235808 2019 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data.

rs80356530 in OPA1;LOC102724808 gene and Mitochondrial Diseases PMID 28812649 2017 Decreased male reproductive success in association with mitochondrial dysfunction.

rs121908376 in OPA1;LOC102724808 gene and OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY PMID 16240368 2005 OPA1 R445H mutation in optic atrophy associated with sensorineural deafness.

PMID 20185555 2010 OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation.

PMID 18158317 2008 OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.

PMID 23387428 2013 Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder.

PMID 21112924 2011 Heterozygous OPA1 mutations in Behr syndrome.

PMID 15531309 2004 Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.

PMID 18065439 2008 Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.

PMID 18195150 2008 Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1.

rs1292852465 in OPA1;LOC102724808 gene and Optic Atrophy 1 PMID 11017080 2000 OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.

PMID 11440989 2001 Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy.

PMID 11440988 2001 OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance.

PMID 23401657 2013 Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy.

PMID 16617242 2006 OPA1 mutations and mitochondrial DNA haplotypes in autosomal dominant optic atrophy.

PMID 19319978 2009 Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.

PMID 15948788 2005 Dominant optic atrophy: correlation between clinical and molecular genetic studies.

PMID 12566046 2003 A novel mutation in the OPA1 gene in a Japanese patient with optic atrophy.

PMID 11017079 2000 Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy.

PMID 12036970 2002 A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy.

PMID 18204809 2008 A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.

PMID 14961560 2003 Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy.

PMID 16513463 2006 Novel mutations in the OPA1 gene and associated clinical features in Japanese patients with optic atrophy.

PMID 11810270 2001 Mutation spectrum and splicing variants in the OPA1 gene.

PMID 19325939 2009 Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect.

PMID 22857269 2012 Dominant optic atrophy in Denmark - report of 15 novel mutations in OPA1, using a strategy with a detection rate of 90%.

PMID 19969356 2010 Novel mutations of the OPA1 gene in Chinese dominant optic atrophy.

PMID 22382025 2012 A novel OPA1 mutation in a Chinese family with autosomal dominant optic atrophy.

PMID 20185555 2010 OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation.

PMID 18360822 2008 Reversible optic neuropathy with OPA1 exon 5b mutation.