FAM89B


Description

The FAM89B (family with sequence similarity 89 member B) is a protein-coding gene located on chromosome 11.

FAM89B plays a role in regulating TGF-beta signaling, preventing the movement of SMAD2 from the nucleus to the cytoplasm. It also acts as a connector, bringing together CDC42BPA and CDC42BPB with LIMK1 at the edge of cells. This connection activates LIMK1, which then modifies CFL1, a protein crucial for the organization of the actin cytoskeleton in these cellular extensions.

FAM89B is also known as LRAP25, MTVR, MTVR1.

Associated Diseases



Disclaimer: The information provided here is not exhaustive by any means. Always consult your doctor or other qualified healthcare provider with any questions you may have regarding a medical condition, procedure, or treatment, whether it is a prescription medication, over-the-counter drug, vitamin, supplement, or herbal alternative.