蛋白质/抗原/多肽 >> 重组蛋白
重组神经元特异性蛋白家族成员2
半岛bd体育手机客户端 介绍
基因名：
Nsg2 半岛bd体育手机客户端 别名： P19； Nsg2； neuron specific gene family member 2； neuron specific gene family member 2； neuronal vesicle trafficking-associated protein 2； neuron-specific protein family member 2； protein 8.5； protein p19； 神经元特异性蛋白家族成员2； 背景信息：
With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
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