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重组FAM167A蛋白
交货期:1周

产品名称
Recombinant FAM167A
Recombinant family with sequence similarity 167 member A protein
产品介绍
基因名:

FAM167A


产品别名:

C8orf13; D8S265; DIORA-1; FAM167A; family with sequence similarity 167 member A; family with sequence similarity 167 member A; protein FAM167A; disordered autoimmunity 1; FAM167A蛋白;


背景信息:
Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf13 gene product has been provisionally designated C8orf13 pending further characterization.
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