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- accession：NM_001172502
- 基因别名：SLC6A2
- 基因描述：Homo sapiens solute carrier family 6 (neurotransmitter transporter), member 2 (SLC6A2), transcript variant 4, mRNA.
- 载体：现货载体
- CDS区长度：1539
- 翻译后氨基酸长度：512
- TranscriptVariant：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.
- 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]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
