这个基因编码一个大的细胞质动力蛋白,它参与纤毛的逆行运输,并在鞭毛内运输中发挥作用,这是纤毛/鞭毛组装所必需的过程。该基因的突变引起与原发性纤毛功能改变有关的异质性疾病谱,常涉及多指畸形、骨骼发生和多囊肾。选择性剪接导致编码不同蛋白质的多个转录变体。[由RefSeq提供,2010年1月]
This gene encodes a large cytoplasmic dynein protein that is involved in retrograde transport in the cilium and has a role in intraflagellar transport, a process required for ciliary/flagellar assembly. Mutations in this gene cause a heterogeneous spectrum of conditions related to altered primary cilium function and often involve polydactyly, abnormal skeletogenesis, and polycystic kidneys. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jan 2010]
基因名: | DYNC2H1 |
别名: | ATD3,DHC2,DHC1b,DNCH2,DYH1B,SRTD3,SRPS2B,hdhc11 |
基因ID: | 79659 |
Chromosome: (GRCh37) | 11 Start: 102980160 End: 103350591 Strand: |
信号通路: |