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(AHI 1) contains an additional coiled coil domain in its N terminal region, which is entirely missing from the Ahi 1 proteins of both mouse and rat. Both murine and human Ahi 1/AHI 1 genes encode at least three isoforms and thus this gene is also subject to alternative splicing in normal cells.1 Involvement of Ahi 1 in leukemogenesis is suggested by the high frequency of Ahi 1 mutations seen in certain virus induced murine leukemias and lymphomas.1 Murine pre B and T cell leukemic cells with insertional mutations in Ahi 1 show both increased expression of Ahi 1 and expression of truncated Ahi 1/viral fused transcripts, including splice variants in which the SH3 domain is deleted.1 We have recently demonstrated that Ahi 1/AHI 1 expression is regulated at multiple stages of hematopoiesis in a manner that is highly conserved between mouse and humans.5 Ahi 1/AHI 1 is expressed at its highest level in the most primitive hematopoietic cells and is then rapidly downregulated as the cells begin to differentiate.