METTL14 and neoplasm: To this end, we performed immunoprecipitation (IP) assays in T47D and 293T cell lines and observed that METTL3-Δ238 had much weaker interaction with WTAP, but retained its interaction with METTL14, whereas METTL3-Δ198 could interact with both WTAP and METTL14 (Figure 4a, b), consistent with the phenotypic study showing that METTL3-Δ238, but not METTL3-Δ198, affected tumor cell proliferation.