2024年12月25日 · MT-CO3 (Mitochondrially Encoded Cytochrome C Oxidase III) is a Protein Coding gene. Diseases associated with MT-CO3 include Leber Hereditary Optic Neuropathy, …

Cytochrome c oxidase subunit III (COX3) is an enzyme that in humans is encoded by the MT-CO3 gene. [6] It is one of main transmembrane subunits of cytochrome c oxidase. It is also one of …

预计可实现电子转移活性和氧化还原驱动的活性跨膜转运蛋白活性。 参与呼吸链复合体 IV 组装。 呼吸链复合体 IV 的一部分。 与 MELAS 综合征有关。 [由基因组资源联盟提供，2022 年 4 月] …

2025年1月4日 · Title: A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness …

结果显示，包括ctnnb1、fbn1和 mt-co3在内的24个改变基因在低风险组中显着流行（图 8d），而37个改变基因，例如tp53、lrp1b和fat3在高危组中显着流行（图 8d）。

2025年1月4日 · Clinical resource with information about MT-CO3, Leber optic atrophy, MELAS syndrome, and available tests. There are links to practice guidelines and authoritative …

2005年9月9日 · Cytochrome c oxidase subunit III (COIII or MTCO3) is 1 of 3 mitochondrial DNA (mtDNA) encoded subunits (MTCO1, MTCO2, MTCO3) of respiratory Complex IV. Complex IV …

Gene target information for COX3 - cytochrome c oxidase subunit III (house mouse). Find diseases associated with this biological target and compounds tested against it in bioassay …

Analytical, diagnostic and therapeutic context of MT-CO3. Northern Blot and quantitative real-time reverse transcription-PCR analysis further demonstrated that the primary ATP6--COX3 …

Orthologous to human MT-CO3 (mitochondrially encoded cytochrome c oxidase III). [provided by Alliance of Genome Resources, Apr 2022] — Master of Bioactive Molecules