基因名：
Spatc1l
产品别名：
1700022B01Rik； 1700027D21Rik； AA062323； Spatc1l； spermatogenesis and centriole associated 1 like； spermatogenesis and centriole associated 1 like； speriolin-like protein； spermatogenesis and centriole-associated protein 1-like protein； 21号染色体开放阅读框56；
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 C21orf56 gene product has been provisionally designated C21orf56 pending further characterization.
