人 SNX15 (NM_147777) cDNA克隆

Accession: NM_147777
基因名称: SNX15
基因别名: HSAF001435
基因描述: Homo sapiens sorting nexin 15 (SNX15), transcript variant B, mRNA.
种属: Human
CDS区长度: 771 (查看编码区序列)
翻译后氨基酸长度: 256 (查看氨基酸序列)
Transcript Variant: This variant (B, also known as SNX15A) lacks an alternate in-frame exon in the 3' coding region, compared to variant A, resulting in an isoform (B) that is shorter than isoform A.
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G101262 人 SNX15 (NM_147777) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Overexpression of this gene results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membrane to recycling endosomes or the trans-Golgi network. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ADP-ribosylation factor-like 2 (ARL2) gene. [provided by RefSeq, Dec 2010]