UTP20

Ideogram human chromosome 12

UTP20 UTP20 is a protein-coding gene located on chromosome 17 in humans. It plays a crucial role in various cellular processes, including RNA metabolism and gene expression regulation. Structure UTP20 gene consists of X exons and spans approximately Y base pairs. It encodes a protein that is involved in the assembly of the small subunit of the ribosome. Function The primary function of UTP20 is to participate in the biogenesis of ribosomes, which are essential for protein synthesis in cells. It interacts with other proteins and RNA molecules to facilitate the assembly of ribosomal subunits. Clinical Significance Mutations in the UTP20 gene have been associated with certain genetic disorders, such as ribosomopathies. These conditions can lead to abnormalities in ribosome function and protein synthesis, resulting in various developmental and growth defects. Research Studies investigating the role of UTP20 in ribosome biogenesis and its implications for human health are ongoing. Researchers are exploring potential therapeutic strategies targeting UTP20-related pathways to treat ribosomopathies and other related disorders. References 1. Author A, Author B. Title of the paper. Journal Name. Year; Volume(Issue):Page numbers. 2. Author C, Author D. Title of the book. Publisher Name. Year. Categories