蛋白质/抗原/多肽 >> 重组蛋白
重组22号染色体开放阅读框23蛋白
半岛bd体育手机客户端 介绍
基因名:
C22orf23 半岛bd体育手机客户端 别名: EVG1; dJ1039K5.6; C22orf23; chromosome 22 open reading frame 23; chromosome 22 open reading frame 23; UPF0193 protein EVG1; 22号染色体开放阅读框23; 背景信息:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
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