人 GP1BA (NM_000173) cDNA克隆

Accession: NM_000173
基因名称: GP1BA
基因别名: BSS; GP1B; VWDP; CD42B; GPIbA; BDPLT1; BDPLT3; DBPLT3; CD42b-alpha
基因描述: Homo sapiens glycoprotein Ib (platelet), alpha polypeptide (GP1BA), mRNA.
种属: Human
CDS区长度: 1959 (查看编码区序列)
翻译后氨基酸长度: 652 (查看氨基酸序列)
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G113621 人 GP1BA (NM_000173) cDNA克隆 pDONR223 2ug质粒 点击询价

Glycoprotein Ib (GP Ib) is a platelet surface membrane glycoprotein composed of a heterodimer, an alpha chain and a beta chain, that is linked by disulfide bonds. The Gp Ib functions as a receptor for von Willebrand factor (VWF). The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX and platelet glycoprotein V. The binding of the GP Ib-IX-V complex to VWF facilitates initial platelet adhesion to vascular subendothelium after vascular injury, and also initiates signaling events within the platelet that lead to enhanced platelet activation, thrombosis, and hemostasis. This gene encodes the alpha subunit. Mutations in this gene result in Bernard-Soulier syndromes and platelet-type von Willebrand disease. The coding region of this gene is known to contain a polymophic variable number tandem repeat (VNTR) domain that is associated with susceptibility to nonarteritic anterior ischemic optic neuropathy. [provided by RefSeq, Oct 2013]