MT-ND6 - Wikipedia
MT-ND6 is a gene of the mitochondrial genome coding for the NADH-ubiquinone oxidoreductase chain 6 protein (ND6). [5] The ND6 protein is a subunit of NADH dehydrogenase (ubiquinone), …
MT-ND6 Gene - GeneCards | NU6M Protein | NU6M Antibody
2025年3月30日 · MT-ND6 (Mitochondrially Encoded NADH:Ubiquinone Oxidoreductase Core Subunit 6) is a Protein Coding gene. Diseases associated with MT-ND6 include Leber …
MT-ND6 mitochondrially encoded NADH dehydrogenase 6
2025年2月8日 · Clinical resource with information about MT-ND6, Leber optic atrophy, MELAS syndrome, and available tests. There are links to practice guidelines and authoritative …
ND6 NADH dehydrogenase subunit 6 [ (human)] - National …
Maternally inherited non-syndromic hearing loss is linked with a novel mitochondrial ND6 gene mutation. Reduced mitochondrial-encoded NADH dehydrogenase 6 gene expression drives …
MT-ND6 gene - MedlinePlus
Each of the MT-ND6 gene variants changes a single protein building block (amino acid) in the NADH dehydrogenase 6 protein. One common MT-ND6 gene variant is responsible for about …
线粒体编码的 NADH 脱氢酶 6（MT-ND6）基因 | MCE
启用 NADH 脱氢酶 (泛醌) 活性。 参与线粒体电子传递、NADH 到泛醌和线粒体呼吸链复合体 I 的组装。 预测位于线粒体内膜。 与 Leber 遗传性视神经病变有关；利氏病；下肢为主的脊髓性 …
MT-ND6 mitochondrially encoded NADH dehydrogenase 6 …
2025年1月4日 · Circulating nicotinamide adenine dinucleotide-ubiquinone oxidoreductase chain 6 is associated with disease activity of anti-neutrophil cytoplasmic antibody-associated vasculitis.
mt-Nd6 - NADH dehydrogenase 6, mitochondrial 基因 | MCE
Enables NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial electron transport, NADH to ubiquinone and mitochondrial respiratory chain complex I assembly. Located in …
MT-ND6作为新靶点在代谢综合征诊断和治疗药物中的应用
mt-nd6作为新靶点在代谢综合征诊断和治疗药物中的应用，其机理为：mt-nd6基因能够调控线粒体功能、维持线粒体稳态，在制备改善线粒体功能失常相关疾病的药物中具有良好应用前景。
UniProt
Genetically heterogeneous disorder, characterized by episodic vomiting, seizures, and recurrent cerebral insults resembling strokes and causing hemiparesis, hemianopsia, or cortical blindness.