蛋白质/抗原/多肽 >> 重组蛋白
重组KIAA1310蛋白
半岛bd体育手机客户端 介绍
基因名:
KANSL3 半岛bd体育手机客户端 别名: KIAA1310; NSL3; Rcd1; KANSL3; KAT8 regulatory NSL complex subunit 3; KAT8 regulatory NSL complex subunit 3; KAT8 regulatory NSL complex subunit 3; NSL complex protein NSL3; non-specific lethal 3 homolog; serum inhibited-related protein; testis development protein PRTD; KIAA1310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 FLJ10081 gene product has been provisionally designated FLJ10081 pending further characterization
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