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Human WIPF1 wild-type allele is located in the vicinity of 2q31.1 and is approximately 123 kb in length. This allele, which encodes WAS/WASL-interacting protein family member 1 protein, plays a role in both cytoskeletal remodeling and stabilization of Wiskott-Aldrich syndrome protein. Mutation of the gene is associated with Wiskott-Aldrich syndrome 2.
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