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Gene
OPA1
OPA1 is a gene. This site has 85 published variants inside it, each from a published genetic study, joining it to 3 condition pages.
1
Reads by AI crawlers
Claude 0 ChatGPT 0 Google · Gemini 0 Perplexity 0 Meta AI 0 Microsoft · Copilot 0 Amazon 0 Apple 0 China (ByteDance, Huawei, Baidu…) 0 Others 1 Total 1 Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Conditions it is linked to
Variants inside OPA1 (85)
rs794727405 · Abortive cerebellar ataxia rs879255593 · Abortive cerebellar ataxia rs879255595 · Abortive cerebellar ataxia rs2474872099 · Auditory neuropathy rs886043340 · Auditory neuropathy rs104893752 · Autosomal dominant optic atrophy classic form rs104893753 · Autosomal dominant optic atrophy classic form rs1057519244 · Autosomal dominant optic atrophy classic form rs121908375 · Autosomal dominant optic atrophy classic form rs1488795500 · Autosomal dominant optic atrophy classic form rs1553876590 · Autosomal dominant optic atrophy classic form rs1577228080 · Autosomal dominant optic atrophy classic form rs1577244261 · Autosomal dominant optic atrophy classic form rs1711518217 · Autosomal dominant optic atrophy classic form rs1716524583 · Autosomal dominant optic atrophy classic form rs2109043749 · Autosomal dominant optic atrophy classic form rs2474788860 · Autosomal dominant optic atrophy classic form rs2474871913 · Autosomal dominant optic atrophy classic form rs2474922093 · Autosomal dominant optic atrophy classic form rs2475167246 · Autosomal dominant optic atrophy classic form rs28939082 · Autosomal dominant optic atrophy classic form rs398124303 · Autosomal dominant optic atrophy classic form rs754576717 · Autosomal dominant optic atrophy classic form rs761460379 · Autosomal dominant optic atrophy classic form rs761743852 · Autosomal dominant optic atrophy classic form rs772382178 · Autosomal dominant optic atrophy classic form rs863224906 · Autosomal dominant optic atrophy classic form rs879255510 · Autosomal dominant optic atrophy classic form rs921531106 · Autosomal dominant optic atrophy classic form rs9291059 · Depressive symptoms (MTAG) rs528908640 · Diastolic blood pressure rs11925699 · Educational attainment rs1553877864 · Mitochondrial disease rs869312995 · Mitochondrial DNA depletion syndrome 14B (cardioencephalomyopathic type) rs727504059 · Ocular impairment rs1553786499 · OPA1-related disorder rs1560392160 · OPA1-related disorder rs1711513392 · OPA1-related disorder rs1716527148 · OPA1-related disorder rs1732788163 · OPA1-related disorder rs2109232184 · OPA1-related disorder rs2474788771 · OPA1-related disorder rs2474922047 · OPA1-related disorder rs2475134399 · OPA1-related disorder rs2475135585 · OPA1-related disorder rs2475207285 · OPA1-related disorder rs745927258 · OPA1-related disorder rs794727069 · OPA1-related disorder rs794727392 · OPA1-related disorder rs886041318 · OPA1-related disorder rs1064797303 · Optic atrophy rs1553784985 · Optic atrophy rs1553785338 · Optic atrophy rs1560327427 · Optic atrophy rs1732086609 · Optic atrophy rs1733081846 · Optic atrophy rs1734162973 · Optic atrophy rs2109268057 · Optic atrophy rs2474395788 · Optic atrophy rs2474865823 · Optic atrophy rs2474874374 · Optic atrophy rs2474881420 · Optic atrophy rs398124299 · Optic atrophy rs727504060 · Optic atrophy rs80356528 · Optic atrophy rs863224127 · Optic atrophy rs863224131 · Optic atrophy rs863224134 · Optic atrophy rs121908376 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs1560380226 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs1577162868 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs1724946838 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs2109011385 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs2109015193 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs2109058910 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs2474584542 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs2474818291 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs387906899 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs387906900 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs387906901 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs398124298 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs80356529 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs879255592 · Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy rs983041061 · Optic neuropathy rs747454971 · Uterine corpus endometrial carcinoma
See OPA1 with everything it connects to on the Gene Knowledge Graph , or as data at /api/v1/genes/OPA1 .
Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license
OPA1 gene. MyGeneLog™. https://www.mygenelog.com/genes/OPA1
A gene page gathers published research; it is not a test result and not medical advice. If a gene matters to your health, talk to a doctor or a genetic counsellor.