蛋白质/抗原/多肽 >> 重组蛋白
重组1号染色体开放阅读框183蛋白
产品介绍 基因名: INKA2 产品别名: C1orf183; FAM212B; INKA2; inka box actin regulator 2; inka box actin regulator 2; PAK4-inhibitor INKA2; HInca-r; family with sequence similarity 212 member B; induced in neural crest by AP2-alpha protein-related homolog; protein FAM212B; 1号染色体开放阅读框183; FAM212B蛋白; 背景信息: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf183 gene product has been provisionally designated C1orf183 pending further characterization. There are two isoforms of C1orf183 that are produced as a result of alternative splicing events. 标签:His-tag |
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