Described herein is a novel gene and its product, WIP, which associates
with WASP. The subject invention relates to the isolated WIP gene or cDNA
and transgenic mammals that have the WIP gene disrupted in their genome.
Also the subject of this invention are methods of treating conditions or
diseases in which WIP and/or WASP DNA or protein is deficient and/or
defective, for example, mutated or altered, such that an individual is
adversely affected. Also described are methods of altering or regulating
WIP and its functions in a mammal or in a cell of a mammal, for example
in a lymphocyte. A further subject of this invention is an assay to
identify drugs which alter the activity of WIP or expression of WIP DNA.