蛋白质/抗原/多肽 >> 重组蛋白
重组9号染色体开放阅读框21蛋白
产品介绍 基因名: Prxl2c 产品别名: 1110018J18Rik; AI849003; Aaed1; Prxl2c; peroxiredoxin like 2C; peroxiredoxin like 2C; peroxiredoxin-like 2C; AhpC/TSA antioxidant enzyme domain containing 1; UPF0308 protein C9orf21 homolog; ahpC/TSA antioxidant enzyme domain-containing protein 1; thioredoxin-like protein AAED1; 9号染色体开放阅读框21; 背景信息: C9orf21 (chromosome 9 open reading frame 21) is a 226 amino acid protein that belongs to the UPF0308 family and is encoded by a gene that maps to human chromosome 9q22.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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. 标签:His-tag |
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