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WASF3
From Wikipedia, the free encyclopedia
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Wiskott–Aldrich syndrome protein family member 3 is a protein that in humans is encoded by the WASF3 gene.[5][6]
This gene encodes a member of the Wiskott–Aldrich syndrome protein family. The gene product is a protein that forms a multiprotein complex that links receptor kinases and actin. Binding to actin occurs through a C-terminal verprolin homology domain in all family members. The multiprotein complex serves to transduce signals that involve changes in cell shape, motility or function.[6]
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