人 F9 (NM_000133) cDNA克隆

Accession: NM_000133
基因名称: F9
基因别名: FIX; P19; PTC; HEMB; THPH8
基因描述: Homo sapiens coagulation factor IX (F9), mRNA.
种属: Human
CDS区长度: 1386 (查看编码区序列)
翻译后氨基酸长度: 461 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G123495 人 F9 (NM_000133) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease. [provided by RefSeq, Jul 2008]