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WIPF1

Official Full Name
WAS/WASL interacting protein family member 1
Organism
Homo sapiens
GeneID
7456
Background
This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
Synonyms
WIP; WAS2; PRPL-2; WASPIP;

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