GP1BB

GP1BB is a gene in humans that encodes a protein known as platelet glycoprotein Ib beta chain. This protein is a part of the glycoprotein Ib-V-IX complex, which is a platelet surface membrane protein complex that plays a crucial role in the process of blood coagulation and platelet adhesion to the endothelium. Mutations in this gene have been associated with Bernard-Soulier syndrome, a rare disorder characterized by thrombocytopenia, giant platelets, and bleeding tendency.

Function

The GP1BB gene provides instructions for making a protein that is part of a complex known as the glycoprotein Ib-IX-V complex. This complex is found on the surface of platelets, which are blood cell fragments that play a crucial role in blood clotting. The glycoprotein Ib-IX-V complex binds to a protein called von Willebrand factor, which is necessary for platelets to adhere to the site of a blood vessel injury and form a clot, preventing excessive bleeding.

Clinical significance

Mutations in the GP1BB gene can lead to Bernard-Soulier syndrome, a rare disorder characterized by thrombocytopenia, giant platelets, and a bleeding tendency. This condition is caused by a reduced amount or absence of the glycoprotein Ib-IX-V complex on the surface of platelets, which impairs the ability of platelets to adhere to the site of a blood vessel injury and form a clot.

See also

• Bernard-Soulier syndrome
• Platelet
• Blood coagulation
• Von Willebrand factor

External links

• GP1BB at the National Center for Biotechnology Information

This article is a medical stub. You can help WikiMD by expanding it!
Most recent articles Ongoing trials	Wikipedia