2) insertional inactivation mutant
插入失活突变体
1.
Objective:To construct insertional inactivation mutant of the putative transporter 89k/pTP of Streptococcus suis serotype 2 and to give a correlation analysis for its virulence.
目的:构建2型猪链球菌假想转运蛋白89k/pTP的基因插入失活突变体并进行毒力相关分析。
3) insertion/deletion variation
插入/缺失变异
5) indel
插入缺失
1.
The rates and patterns of indel (insertions and deletions) and substitution in rodent (mouse and rat) and 18 mammalian genomes have been studied.
014个插入缺失;插入缺失富含碱基A和T;且在重复片段中发生的频率比较高。
6) deletion mutation
缺失突变
1.
Autosomal dominant congenital nuclear cataract caused by a deletion mutation in the βA1-crystallin gene;
晶体蛋白βA1基因缺失突变导致常染色体显性遗传核性先天性白内障
2.
Objective To search parkin gene deletion mutations at exons 1 to 6 in Chinese patients with praecox Parkinson s disease (PPD) and analyze them together with the clinical features of PPD.
方法 用 PPD患者外周血液提取 DNA,通过 PCR扩增、琼脂糖凝胶电泳鉴定 parkin基因外显子缺失突变 ,并结合临床资料分析。
3.
Objective To characterize the deletions of mitochondrial DNA (mtDNA) in Chinese patients with Kearns-Sayre syndrome (KSS) and chronic progressive external ophthalmolegia (CPEO) and identify deletion mutations of mtDNA be the etiology of these diseases.
在2例Kearns－Sayre综合征（KSS）和2例慢性进行性眼外肌麻痹（CPEO）患者的骨骼肌线粒体DNA（mtDNA）中发现存在单一的大片段缺失突变。
补充资料：插入突变(insertional mutation)
分子式：
CAS号：
性质：又称插入突变(insertional mutation)。DNA链上由于插入额外的核苷酸或DNA片段而引起的突变。
CAS号：
性质：又称插入突变(insertional mutation)。DNA链上由于插入额外的核苷酸或DNA片段而引起的突变。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条