Automated description from the Alliance of Genome Resources (Release 7.5.0)
Enables actin binding activity; microtubule binding activity; and protein homodimerization activity. Involved in actin filament polymerization. Acts upstream of or within several processes, including autophagosome-lysosome fusion; cytoskeleton organization; and myeloid cell differentiation. Located in cytoplasm and nucleus. Part of ESCRT I complex and filamentous actin. Is active in several cellular components, including cleavage furrow; cytoskeleton; and stereocilia tip-link density. Is expressed in several structures, including alimentary system; brain; gonad; submandibular gland primordium; and vibrissa. Used to study autosomal dominant auditory neuropathy 1 and congenital dyserythropoietic anemia. Human ortholog(s) of this gene implicated in autosomal dominant auditory neuropathy 1. Orthologous to human DIAPH3 (diaphanous related formin 3).
This site uses cookies.
Some cookies are essential for site operations and others help us analyze use and utility of our web site.
Please refer to our
privacy policy
for more information.