TMEM126B
Gene of the species Homo sapiens / From Wikipedia, the free encyclopedia
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Transmembrane protein 126B is a protein that in humans is encoded by the TMEM126B gene.[3][4] TMEM126B is a mitochondrial transmembrane protein which is a component of the mitochondrial complex I assembly complex. The TMEM126B gene is conserved in mammals.[5] The encoded protein serves as an assembly factor that is required for formation of the membrane arm of the complex. It interacts with NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 13. Naturally occurring mutations in this gene are associated with isolated complex I deficiency. A pseudogene of this gene has been defined on chromosome 9.[3]
Quick Facts Identifiers, Aliases ...
TMEM126B | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | TMEM126B, HT007, transmembrane protein 126B | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 615533 MGI: 1915722 HomoloGene: 10222 GeneCards: TMEM126B | ||||||||||||||||||||||||||||||||||||||||||||||||||
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