- accession:NM_001135774
- 基因别名:SYN3
- 基因描述:Homo sapiens synapsin III (SYN3), transcript variant IIIg, mRNA.
- 载体:现货载体
- CDS区长度:1740
- 翻译后氨基酸长度:579
- TranscriptVariant:This variant (IIIg) uses an alternate in-frame splice site in the mid coding region, compared to variant IIIa, resulting in an isoform (IIIg) that is 1 aa shorter than isoform IIIa.
- 基因简介: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]
- 规格:10ul 质粒
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