人 KCNJ2 (NM_000891) cDNA克隆

Accession: NM_000891
基因名称: KCNJ2
基因别名: IRK1; LQT7; SQT3; ATFB9; HHIRK1; KIR2.1; HHBIRK1
基因描述: Homo sapiens potassium inwardly-rectifying channel, subfamily J, member 2 (KCNJ2), mRNA.
种属: Human
CDS区长度: 1284 (查看编码区序列)
翻译后氨基酸长度: 427 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G151052 人 KCNJ2 (NM_000891) cDNA克隆 pDONR223 2ug质粒 点击询价

Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features. [provided by RefSeq, Jul 2008]