Structural highlights
Disease
NU155_HUMAN Familial atrial fibrillation. The disease is caused by mutations affecting the gene represented in this entry.
Function
NU155_HUMAN Essential component of nuclear pore complex. Could be essessential for embryogenesis. Nucleoporins may be involved both in binding and translocating proteins during nucleocytoplasmic transport.[UniProtKB:Q99P88]B7UCZ6_9RHAB
See Also