The current study aimed to investigate the role of tripartite motif containing 63 (TRIM63) in the progression of thyroid carcinomas. The results showed that TRIM63 was highly expressed in thyroid carcinomas tissues. TRIM63 knockdown inhibited the proliferation and induced the apoptosis of thyroid carcinoma cells, and overexpression of TRIM63 promoted the cell proliferation ability. These results were further confirmed by the in vivo growth of xenograft tumors. Subsequently, the underlying mechanism was explored. TRIM63 silencing repressed the AKT, p38, and ERK signaling pathways in thyroid carcinoma cells, and the contrary results were observed in TRIM63-upregulated thyroid carcinoma cells. Furthermore, we found that E26 transformation specific variant 4 (ETV4) regulated the transcription of TRIM63. The loss of TRIM63 reversed the ETV4 overexpression-induced promotion of proliferation in thyroid carcinomas cells. In conclusion, TRIM63, regulated by ETV4, activates the AKT, p38, and ERK signaling pathways and facilitates the thyroid carcinoma development.