基因名称:FBN2 (fibrillin 2)
别名: CCA,DA9,EOMD
基因ID:2201
Chromosome(GRCh37) :5 Start: 127593601 End: 127873735 Strand:
信号通路:
靶向药:
化疗药:
简介:该基因编码的蛋白是结缔组织微纤维的组成部分,可能参与弹性纤维的组装。该基因突变导致先天性蛛网膜挛缩[由RefSeq提供,2008年7月]The protein encoded by this gene is a component of connective tissue microfibrils and may be involved in elastic fiber assembly. Mutations in this gene cause congenital contractural arachnodactyly. [provided by RefSeq, Jul 2008]
FBN2突变与药物: