蛋白质/抗原/多肽 >> 重组蛋白
重组21号染色体开放阅读框70蛋白
半岛bd体育手机客户端 介绍
基因名:
SLX9 半岛bd体育手机客户端 别名: C21orf70; FAM207A; PRED56; SLX9; SLX9 ribosome biogenesis factor; SLX9 ribosome biogenesis factor; ribosome biogenesis protein SLX9 homolog; family with sequence similarity 207 member A; protein FAM207A; 21号染色体开放阅读框70; 背景信息:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf70 gene product has been provisionally designated C21orf70 pending further characterization.
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