蛋白质/抗原/多肽 >> 重组蛋白
重组TRMT61B蛋白
产品介绍 基因名: TRMT61B 产品别名: TRMT61B; tRNA methyltransferase 61B; tRNA methyltransferase 61B; tRNA (adenine(58)-N(1))-methyltransferase, mitochondrial; mRNA methyladenosine-N(1)-methyltransferase; potential tRNA (adenine(58)-N(1))-methyltransferase catalytic subunit TRMT61B; potential tRNA (adenine-N(1)-)-methyltransferase catalytic subunit TRMT61B; tRNA methyltransferase 61 homolog B; TRMT61B蛋白; 背景信息: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The FLJ20628 gene product has been provisionally designated FLJ20628 pending further characterization. 标签:His-tag |
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