基因名：
C21orf62
产品别名：
B37； C21orf120； PRED81； C21orf62； chromosome 21 open reading frame 62； chromosome 21 open reading frame 62； uncharacterized protein C21orf62； 21号染色体开放阅读框62；
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 C21orf62 gene product has been provisionally designated C21orf62 pending further characterization.
