蛋白质/抗原/多肽 >> 重组蛋白
重组5号染色体开放阅读框22蛋白
产品介绍 基因名: C5orf22 产品别名: C5orf22; chromosome 5 open reading frame 22; chromosome 5 open reading frame 22; UPF0489 protein C5orf22; 5号染色体开放阅读框22; 背景信息: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf22 gene product has been provisionally designated C5orf22 pending further characterization. 标签:His-tag |
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