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Zinc finger protein 202 (ZNF202) is a protein-coding transcription factor encoded by the human *ZNF202* gene, characterized by C2H2-type zinc finger DNA-binding motifs, a KRAB domain, and a SCAN domain[2][3]. It acts mainly as a transcriptional repressor, binding preferentially to the promoters of genes that play roles in lipid metabolism and energy homeostasis, including apolipoproteins, lipid-processing enzymes, and cholesterol/lipid transporters (e.g., ABCA1, ABCG1)[1][3]. ZNF202 was first described in the context of breast cancer[4] but is now strongly linked to cardiovascular and metabolic disorders, especially atherosclerosis and metabolic syndrome[3][4][6]. Dysfunction or genetic variation of ZNF202 can influence susceptibility to lipid disorders and related diseases. ZNF202 forms part of a broader network of transcriptional regulation through interactions mediated by its SCAN domain and is considered a potential therapeutic target in disorders of lipid metabolism and vascular disease[1].
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