5d3a
From Proteopedia
Jump to navigationJump to search
Structural highlights
DiseaseKI21A_HUMAN Congenital fibrosis of extraocular muscles. The disease is caused by mutations affecting the gene represented in this entry. FunctionKI21A_HUMAN Microtubule-binding motor protein probably involved in neuronal axonal transport. In vitro, has a plus-end directed motor activity (By similarity). See Also | ||||||||||||||||||||
This page was last modified 11:46, 9 May 2024.