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- accession：NM_007064
- 基因别名：DUO; CHD5; DUET; TRAD; CHDS5; HAPIP; ARHGEF24
- 基因描述：Homo sapiens kalirin, RhoGEF kinase (KALRN), transcript variant 3, mRNA.
- 载体：现货载体
- CDS区长度：3870
- 翻译后氨基酸长度：1289
- TranscriptVariant：This variant (3) differs in the 5' UTR and lacks many exons in the 5' coding region, compared to variant 1. The encoded protein (isoform 3), also known as Duo, is shorter and has a distinct N-terminus, compared to isoform 1.
- 基因简介：Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
