蛋白质/抗原/多肽 >> 重组蛋白
重组FAM9B蛋白
半岛bd体育手机客户端 介绍
基因名:
FAM9B 半岛bd体育手机客户端 别名: TEX39B; FAM9B; family with sequence similarity 9 member B; family with sequence similarity 9 member B; protein FAM9B; testis expressed 39B; FAM9B蛋白; 背景信息:
The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The FAM9B gene product has been provisionally designated FAM9B pending further characterization.
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