人 KCNJ1 (NM_000220) cDNA克隆

Accession: NM_000220
基因名称: KCNJ1
基因别名: ROMK; ROMK1; KIR1.1
基因描述: Homo sapiens potassium inwardly-rectifying channel, subfamily J, member 1 (KCNJ1), transcript variant 1, mRNA.
种属: Human
CDS区长度: 1176 (查看编码区序列)
翻译后氨基酸长度: 391 (查看氨基酸序列)
Transcript Variant: This variant (1, also known as rom-k1) encodes the longest isoform (a).
产品编号 产品名称 载体 规格 价格
G151047 人 KCNJ1 (NM_000220) 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. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]