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Gene
SOX11
SOX11 is a gene. This site has 37 published variants inside it and 2 near it, each from a published genetic study, joining it to 2 condition pages.
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1
1
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Reads by AI crawlers
Claude 0
ChatGPT 0
Google · Gemini 0
Perplexity 0
Meta AI 0
Microsoft · Copilot 1
Amazon 0
Apple 0
China (ByteDance, Huawei, Baidu…) 0
Others 0
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 SOX11 (37)
rs11887646 · Age at first birth rs2103276364 · Craniosynostosis syndrome rs11894081 · Crohn's disease rs114244809 · Educational attainment rs141874683 · Educational attainment rs1252447458 · Hypogonadotropic hypogonadism rs2465087457 · Hypogonadotropic hypogonadism rs2465087534 · Hypogonadotropic hypogonadism rs1553327954 · Inborn genetic diseases rs2103276445 · Inborn genetic diseases rs2465087461 · Inborn genetic diseases rs2465087545 · Inborn genetic diseases rs1057518672 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs1064794628 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs1064794702 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs1558373293 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs1572216329 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs1665661372 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs1665662335 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2103276330 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2103276337 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2103276338 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2103276340 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2465087380 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2465087392 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2465087401 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2465087402 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2465087455 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2465087460 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2465087515 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2465087527 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2465088378 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs2465088961 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs587777480 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs780122780 · Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism rs1215459755 · SOX11-related disorder rs2465087382 · SOX11-related disorder
Variants near SOX11 (2)
Positions outside the gene, filed under it because it is the closest. A variant near a gene does not always act through it.
See SOX11 with everything it connects to on the Gene Knowledge Graph , or as data at /api/v1/genes/SOX11 .
Quoting this page
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
SOX11 gene. MyGeneLog™. https://www.mygenelog.com/genes/SOX11
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.