TMEM126A
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https://rgd.mcw.edu/rgdweb/report/gene/main.html?id=1604272
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The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
该基因编码的蛋白质为一种未知功能的线粒体膜蛋白。该基因的缺陷是导致7型视神经萎缩(OPA7)的原因。针对该基因已发现两种转录变体,分别编码不同的异构体。[由RefSeq提供,2011年9月]
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