人 KCNE1 (NM_000219) cDNA克隆

基本信息

Accession: NM_000219
基因名称: KCNE1
基因别名: ISK; JLNS; LQT5; MinK; JLNS2; LQT2/5
基因描述: Homo sapiens potassium voltage-gated channel, Isk-related family, member 1 (KCNE1), transcript variant 2, mRNA.
种属: Human
CDS区长度: 390 (查看编码区序列)
翻译后氨基酸长度: 129 (查看氨基酸序列)
Transcript Variant: This variant (2) is the longest transcript. All variants encode the same protein.

订购信息

产品编号 产品名称 载体 规格 价格
G107407 人 KCNE1 (NM_000219) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 KCNE1 (NM_001127670) cDNA克隆 transcript variant 1
人 KCNE1 (NM_000219) cDNA克隆 transcript variant 2
人 KCNE1 (NM_001127668) cDNA克隆 transcript variant 3
人 KCNE1 (NM_001127669) cDNA克隆 transcript variant 4
人 KCNE1 (NM_001270402) cDNA克隆 transcript variant 5
人 KCNE1 (NM_001270403) cDNA克隆 transcript variant 6
人 KCNE1 (NM_001270404) cDNA克隆 transcript variant 7
人 KCNE1 (NM_001270405) cDNA克隆 transcript variant 8

基因简介

The product of this gene belongs to the potassium channel KCNE family. Potassium ion channels are essential to many cellular functions and show a high degree of diversity, varying in their electrophysiologic and pharmacologic properties. This gene encodes a transmembrane protein known to associate with the product of the KVLQT1 gene to form the delayed rectifier potassium channel. Mutation in this gene are associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]

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