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OFD1P11Y (OFD1 pseudogene 11 Y-linked) is annotated as a pseudogene on the human Y chromosome and is homologous to the OFD1 gene, whose X-linked copies are associated with oral-facial-digital syndrome type 1 and related ciliopathies in humans[3][4][1]. Unlike its functional counterpart on the X chromosome, OFD1P11Y is not believed to be transcribed or translated into a functional protein. The OFD1 gene family is important in centrosome and cilia-related cellular processes, but there is no evidence that this particular Y-linked pseudogene has any functional, diagnostic, or therapeutic significance. The annotation of OFD1P11Y as a pseudogene means it is classified as a genomic relic, lacking protein-coding capability and not implicated in disease or drug interaction[3][4].
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