SLC22A4 and colorectal carcinoma: Proteins described as members of the gynoecium morphogenesis network [63] are also participating in other networks (Figure 4B), such as SEP3, FUL, ETT, NGA2, KNAT1/BP, or RPL regulate CRC expression, suggesting that the CRC promoter receives signals from several interconnected developmental GRNs allowing precise timing, spatial distribution, and control of transcript abundance for proper CRC expression.