C11orf91

Ideogram human chromosome 11

C11orf91

C11orf91 is a gene located on chromosome 11 in humans. It is also known as Chromosome 11 Open Reading Frame 91. The function of C11orf91 is currently not well understood and is an area of ongoing research in the field of genetics and molecular biology.

Discovery and Identification

C11orf91 was first identified through bioinformatics analysis of the human genome. The gene was predicted to encode a protein, but its specific function and role in cellular processes remain unclear. Further studies are needed to elucidate the biological significance of C11orf91.

Gene Structure

The C11orf91 gene is composed of a series of nucleotide sequences that code for a protein. It contains multiple exons and introns, which are regions of the gene involved in the process of gene expression. The exact structure of the protein encoded by C11orf91 and its interactions with other molecules are areas of interest for researchers.

Expression and Regulation

The expression of C11orf91 is regulated by various factors within the cell. It may be influenced by environmental cues, developmental stages, and other genetic elements. Understanding the regulatory mechanisms controlling C11orf91 expression is essential for determining its role in cellular functions.

Function

The precise function of C11orf91 is currently unknown. Studies suggest that it may play a role in cellular processes such as cell growth, differentiation, or signaling pathways. Further research is required to uncover the specific functions of C11orf91 and its potential implications for human health and disease.

Clinical Significance

Mutations or dysregulation of C11orf91 may be associated with certain diseases or disorders. Investigating the genetic variations in C11orf91 and their impact on cellular functions could provide insights into potential therapeutic targets for treating related conditions.