Health Conditions Related to Genetic Changes
Bernard-Soulier syndrome
At least 32 GP1BB gene mutations have been found to cause Bernard-Soulier syndrome, a condition characterized by a reduced number of platelets that are larger than normal (macrothrombocytopenia) and excessive bleeding. These mutations lead to production of an altered GPIbβ subunit that is likely broken down too soon or that cannot get to the platelet surface. Lack of this subunit on the surface of platelets prevents formation of the GPIb-IX-V complex. Without GPIb-IX-V, platelets cannot come together at the site of an injury to form a clot, leading to the bleeding problems associated with Bernard-Soulier syndrome.
More About This Health ConditionOther Names for This Gene
- antigen CD42b-beta
- BDPLT1
- BS
- CD42C
- glycoprotein Ib (platelet), beta polypeptide
- glycoprotein Ib platelet beta subunit
- GP-Ib beta
- GPIBB
- GPIbbeta
- nuclear localization signal deleted in velocardiofacial syndrome
- platelet glycoprotein Ib beta chain precursor
- platelet membrane glycoprotein Ib beta
- truncated platelet membrane glycoprotein Ib beta
Additional Information & Resources
Tests Listed in the Genetic Testing Registry
Scientific Articles on PubMed
Catalog of Genes and Diseases from OMIM
References
- Geng H, Xu G, Ran Y, Lopez JA, Peng Y. Platelet glycoprotein Ib beta/IX mediates glycoprotein Ib alpha localization to membrane lipid domain critical for von Willebrand factor interaction at high shear. J Biol Chem. 2011 Jun 17;286(24):21315-23. doi: 10.1074/jbc.M110.202549. Epub 2011 Apr 20. Citation on PubMed or Free article on PubMed Central
- Li R, Emsley J. The organizing principle of the platelet glycoprotein Ib-IX-V complex. J Thromb Haemost. 2013 Apr;11(4):605-14. doi: 10.1111/jth.12144. Citation on PubMed or Free article on PubMed Central
- McEwan PA, Yang W, Carr KH, Mo X, Zheng X, Li R, Emsley J. Quaternary organization of GPIb-IX complex and insights into Bernard-Soulier syndrome revealed by the structures of GPIbbeta and a GPIbbeta/GPIX chimera. Blood. 2011 Nov 10;118(19):5292-301. doi: 10.1182/blood-2011-05-356253. Epub 2011 Sep 8. Citation on PubMed or Free article on PubMed Central
- Savoia A, Kunishima S, De Rocco D, Zieger B, Rand ML, Pujol-Moix N, Caliskan U, Tokgoz H, Pecci A, Noris P, Srivastava A, Ward C, Morel-Kopp MC, Alessi MC, Bellucci S, Beurrier P, de Maistre E, Favier R, Hezard N, Hurtaud-Roux MF, Latger-Cannard V, Lavenu-Bombled C, Proulle V, Meunier S, Negrier C, Nurden A, Randrianaivo H, Fabris F, Platokouki H, Rosenberg N, HadjKacem B, Heller PG, Karimi M, Balduini CL, Pastore A, Lanza F. Spectrum of the mutations in Bernard-Soulier syndrome. Hum Mutat. 2014 Sep;35(9):1033-45. doi: 10.1002/humu.22607. Epub 2014 Jul 15. Citation on PubMed
- Xu G, Shang D, Zhang Z, Shaw TS, Ran Y, Lopez JA, Peng Y. The Transmembrane Domains of beta and IX Subunits Mediate the Localization of the Platelet Glycoprotein Ib-IX Complex to the Glycosphingolipid-enriched Membrane Domain. J Biol Chem. 2015 Sep 4;290(36):22155-62. doi: 10.1074/jbc.M115.668145. Epub 2015 Jul 22. Citation on PubMed or Free article on PubMed Central
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