人 GRIA2 (NM_001083620) cDNA克隆

Accession: NM_001083620
基因名称: GRIA2
基因别名: GLUR2; GLURB; GluA2; HBGR2; GluR-K2
基因描述: Homo sapiens glutamate receptor, ionotropic, AMPA 2 (GRIA2), transcript variant 3, mRNA.
种属: Human
CDS区长度: 2511 (查看编码区序列)
翻译后氨基酸长度: 836 (查看氨基酸序列)
Transcript Variant: This variant (3) contains a different 5' end exon compared to transcript variant 1, resulting in translation initiation from an in-frame downstream AUG, and an isoform (3) with a shorter N-terminus compared to isoform 1. RNA editing (CAG->CGG) changes aa Gln560Arg.
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G102534 人 GRIA2 (NM_001083620) cDNA克隆 pDONR223 2ug质粒 点击询价

Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to a family of glutamate receptors that are sensitive to alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA), and function as ligand-activated cation channels. These channels are assembled from 4 related subunits, GRIA1-4. The subunit encoded by this gene (GRIA2) is subject to RNA editing (CAG->CGG; Q->R) within the second transmembrane domain, which is thought to render the channel impermeable to Ca(2+). Human and animal studies suggest that pre-mRNA editing is essential for brain function, and defective GRIA2 RNA editing at the Q/R site may be relevant to amyotrophic lateral sclerosis (ALS) etiology. Alternative splicing, resulting in transcript variants encoding different isoforms, (including the flip and flop isoforms that vary in their signal transduction properties), has been noted for this gene. [provided by RefSeq, Jul 2008]