基因名称：ACTB （actin beta）
别名： BRWS1,PS1TP5BP1
基因ID：60
Chromosome(GRCh37) ：7 Start: 5566779 End: 5570232 Strand:
信号通路：
靶向药：
化疗药：
简介：这个基因编码六种不同的肌动蛋白中的一种。肌动蛋白是高度保守的蛋白质，参与细胞运动、结构、完整性和细胞间信号传导。编码蛋白是收缩装置的主要组成部分，也是两种广泛表达的非肌肉细胞骨架肌动蛋白之一。该基因突变导致Baraitser-Winter综合征1，其特征是人类患者的智力残疾和独特的面部外观。在整个人类基因组中，已经鉴定出许多这种基因的假基因。[由RefSeq提供，2017年8月]This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins that are ubiquitously expressed. Mutations in this gene cause Baraitser-Winter syndrome 1, which is characterized by intellectual disability with a distinctive facial appearance in human patients. Numerous pseudogenes of this gene have been identified throughout the human genome. [provided by RefSeq, Aug 2017]
ACTB突变与药物：
