蛋白质/抗原/多肽 >> 重组蛋白
重组9号染色体开放阅读框57蛋白
产品介绍 基因名: C9orf57 产品别名: C9orf57; chromosome 9 open reading frame 57; chromosome 9 open reading frame 57; uncharacterized protein C9orf57; 9号染色体开放阅读框57; 背景信息: Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf57 gene product has been provisionally designated C9orf57 pending further characterization. 标签:His-tag |
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