蛋白质/抗原/多肽 >> 重组蛋白
重组19号染色体开放阅读框48蛋白
半岛bd体育手机客户端 介绍
基因名:
C19orf48 半岛bd体育手机客户端 别名: CA916798; C19orf48; chromosome 19 putative open reading frame 48; multidrug resistance-related protein; uncharacterized protein C19orf48; 19号染色体开放阅读框48; 背景信息:
Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf48 gene product has been provisionally designated C19orf48 pending further characterization.
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