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GP9 gene

glycoprotein IX platelet

Key facts

Official symbol
GP9
Full name
GP9
Chromosome
3
Map location
3q21.3
Organism
Homo sapiens
NCBI Gene ID
2815
Also known as
CD42a, GPIX

Function summary

This gene encodes a small membrane glycoprotein found on the surface of human platelets. It forms a 1-to-1 noncovalent complex with glycoprotein Ib, a platelet surface membrane glycoprotein complex that functions as a receptor for von Willebrand factor. The complete receptor complex includes noncovalent association of the alpha and beta subunits with the protein encoded by this gene and platelet glycoprotein V. Defects in this gene are a cause of Bernard-Soulier syndrome, also known as giant platelet disease. These patients have unusually large platelets and have a clinical bleeding tendency. [provided by RefSeq, Oct 2008].

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Data source: NCBI Gene · alsesAI Gene Library