人 BCR (NM_021574) cDNA克隆

Accession: NM_021574
基因名称: BCR
基因别名: ALL; CML; PHL; BCR1; D22S11; D22S662
基因描述: Homo sapiens breakpoint cluster region (BCR), transcript variant 2, mRNA.
种属: Human
CDS区长度: 3684 (查看编码区序列)
翻译后氨基酸长度: 1227 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks an alternate in-frame exon compared to variant 1. The resulting isoform (2) has the same N- and C-termini but is shorter compared to isoform 1.
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G172339 人 BCR (NM_021574) cDNA克隆 pDONR223 2ug质粒 点击询价

A reciprocal translocation between chromosomes 22 and 9 produces the Philadelphia chromosome, which is often found in patients with chronic myelogenous leukemia. The chromosome 22 breakpoint for this translocation is located within the BCR gene. The translocation produces a fusion protein which is encoded by sequence from both BCR and ABL, the gene at the chromosome 9 breakpoint. Although the BCR-ABL fusion protein has been extensively studied, the function of the normal BCR gene product is not clear. The protein has serine/threonine kinase activity and is a GTPase-activating protein for p21rac. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]