人 SLC12A3 (NM_001126107) cDNA克隆

Accession: NM_001126107
基因名称: SLC12A3
基因别名: NCC; TSC; NCCT
基因描述: Homo sapiens solute carrier family 12 (sodium/chloride transporter), member 3 (SLC12A3), transcript variant 2, mRNA.
种属: Human
CDS区长度: 3090 (查看编码区序列)
翻译后氨基酸长度: 1029 (查看氨基酸序列)
Transcript Variant: This variant (2) uses an alternate in-frame splice site in the 5' coding region, compared to variant 1, resulting in a protein (isoform 2) that is 1 aa shorter than isoform 1.
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G158500 人 SLC12A3 (NM_001126107) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a renal thiazide-sensitive sodium-chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome, a disease similar to Bartter's syndrome, that is characterized by hypokalemic alkalosis combined with hypomagnesemia, low urinary calcium, and increased renin activity associated with normal blood pressure. This cotransporter is the target for thiazide diuretics that are used for treating high blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]