人 SYN3 (NM_133633) cDNA克隆

Accession: NM_133633
基因名称: SYN3
基因描述: Homo sapiens synapsin III (SYN3), transcript variant IIIc, mRNA.
种属: Human
CDS区长度: 1335 (查看编码区序列)
翻译后氨基酸长度: 444 (查看氨基酸序列)
Transcript Variant: This variant (IIIc) lacks exon 12, which results in a frameshift and early stop codon compared to variant IIIa. The encoded isoform (IIIc) lacks domains J and E, as compared to the full-length isoform IIIa.
产品编号 产品名称 载体 规格 价格
G123397 人 SYN3 (NM_133633) cDNA克隆 pDONR223 2ug质粒 点击询价
人 SYN3 (NM_003490) cDNA克隆 transcript variant IIIa
人 SYN3 (NM_133633) cDNA克隆 transcript variant IIIc
人 SYN3 (NM_001135774) cDNA克隆 transcript variant IIIg

This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. The protein encoded by this gene shares the synapsin family domain model, with domains A, C, and E exhibiting the highest degree of conservation. The protein contains a unique domain J, located between domains C and E. Based on this gene's localization to 22q12.3, a possible schizophrenia susceptibility locus, and the established neurobiological roles of the synapsins, this family member may represent a candidate gene for schizophrenia. The TIMP3 gene is located within an intron of this gene and is transcribed in the opposite direction. Alternative splicing of this gene results in multiple splice variants that encode different isoforms. [provided by RefSeq, Oct 2008]