FAM49B
Description
The FAM49B gene, located on chromosome 17, encodes a protein with a complex and still evolving role in human biology. Its function is not fully understood, but studies suggest involvement in various cellular processes, including cell growth, differentiation, and apoptosis. While FAM49B is known to interact with other proteins involved in these pathways, its exact mechanism of action remains a topic of active research. Mutations in the FAM49B gene have been linked to several diseases, highlighting its significance in maintaining cellular homeostasis. Understanding the intricacies of FAM49B‘s function is crucial for developing potential therapeutic strategies for associated diseases.
Associated Diseases
Did you know?
FAM49B is a relatively newly discovered gene, and its full functional repertoire is still under investigation.
