人 SLC6A2 (NM_001172502) cDNA克隆

基本信息

Accession: NM_001172502
基因名称: SLC6A2
基因别名: NET; NAT1; NET1; SLC6A5
基因描述: Homo sapiens solute carrier family 6 (neurotransmitter transporter), member 2 (SLC6A2), transcript variant 4, mRNA.
种属: Human
CDS区长度: 1539 (查看编码区序列)
翻译后氨基酸长度: 512 (查看氨基酸序列)
Transcript Variant: This variant (4) has alternate 5' and 3' sequences including the 5' and 3' coding regions, as compared to variant 1. The resulting isoform (3) is shorter and has different N- and C-termini, as compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G158378 人 SLC6A2 (NM_001172502) 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 SLC6A2 (NM_001172504) cDNA克隆 transcript variant 1
人 SLC6A2 (NM_001172501) cDNA克隆 transcript variant 2
人 SLC6A2 (NM_001043) cDNA克隆 transcript variant 3
人 SLC6A2 (NM_001172502) cDNA克隆 transcript variant 4

基因简介

This gene encodes a member of the sodium:neurotransmitter symporter family. This member is a multi-pass membrane protein, which is responsible for reuptake of norepinephrine into presynaptic nerve terminals and is a regulator of norepinephrine homeostasis. Mutations in this gene cause orthostatic intolerance, a syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]

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