🧬 基因注释：MT-ND6
📝 官方信息
官方名称：NADH dehydrogenase subunit 6
功能摘要：Enables NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial electron transport, NADH to ubiquinone and mitochondrial respiratory chain complex I assembly. Predicted to be located in mitochondrial inner membrane. Implicated in Leber hereditary optic neuropathy; Leigh disease; and spinal muscular atrophy with lower extremity predominante 2B. [provided by Alliance of Genome Resources, Apr 2022]
🎯 作为靶基因的剪接因子
- CELF2 置信度: 2.0
- CPSF7 置信度: 2.0
- FUBP1 置信度: 2.0
- FUBP3 置信度: 2.0
- HNRNPA1 置信度: 2.0
- HNRNPF 置信度: 2.0
- HNRNPL 置信度: 2.0
- HNRNPM 置信度: 2.0
- PABPC4 置信度: 2.0
- LUC7L2 置信度: 1.0
- MSI1 置信度: 1.0
- PRPF4 置信度: 1.0
- Ptbp2 置信度: 1.0
- Rbmx 置信度: 1.0
- SAFB 置信度: 1.0
- SF3A3 置信度: 1.0
- SMNDC1 置信度: 1.0
- Snrpa 置信度: 1.0
- Srsf4 置信度: 1.0
- TIA1 置信度: 1.0
🏥 关联疾病
该基因暂无关联疾病记录