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Homeobox protein Hox-B1 is a highly conserved sequence-specific transcription factor encoded by the HOXB1 gene in humans. It belongs to the homeobox gene family and is part of the HOXB gene cluster on chromosome 17. Hox-B1 plays a crucial role in morphogenesis by providing cells with specific positional identities along the anterior-posterior axis during development, especially in anterior body structures. Dysfunction of HOXB1 has been associated with developmental disorders affecting cranial nerve formation and facial movement. HOXB1 interacts with other regulatory proteins such as PBX1 to exert its transcriptional functions[1][2][3][6].
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