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NBPF member 17, pseudogene (NBPF17P) is a human pseudogene within the neuroblastoma breakpoint family (NBPF), located on chromosome 1. As a pseudogene, NBPF17P does not encode a functional protein and is not considered a therapeutic target such as a receptor, enzyme, or transporter. Diseases associated with this locus include neuroblastoma and microcephaly, although there is no evidence that the pseudogene has a direct, active biological function or known involvement in drug response or clinical biomarker roles[1][3][4][5][6][7][9].
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