人 KALRN (NM_001024660) cDNA克隆

Accession: NM_001024660
基因名称: KALRN
基因别名: DUO; CHD5; DUET; TRAD; CHDS5; HAPIP; ARHGEF24
基因描述: Homo sapiens kalirin, RhoGEF kinase (KALRN), transcript variant 1, mRNA.
种属: Human
CDS区长度: 8961 (查看编码区序列)
翻译后氨基酸长度: 2986 (查看氨基酸序列)
Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1). There are no publicly available transcripts representing the full-length splicing pattern of this variant; it is inferred from data in PMID:11891045 and from the rat homolog, NM_032062.1.
产品编号 产品名称 载体 规格 价格
G167106 人 KALRN (NM_001024660) cDNA克隆 pDONR223 2ug质粒 点击询价

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]