Interestingly, distinct mutation profiles, corresponding to clusters of nonsense and frameshift mutations in the C-termini of GPCRs, GPR34, CCR6, and CCR4, have been reported in mucosa-associated lymphoid tissue (MALT) lymphoma and adult T cell leukemia/lymphoma (ATLL) as gain-of-function mutations [44–46]. This evidence concerns the gene GPR34 and adult T-cell leukemia/lymphoma.