人 SNX7 (NM_152238) cDNA克隆

基本信息

Accession: NM_152238
基因名称: SNX7
基因描述: Homo sapiens sorting nexin 7 (SNX7), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1191 (查看编码区序列)
翻译后氨基酸长度: 396 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks an alternate in-frame exon in the central coding region, compared to variant 1, resulting in an isoform (b) that is shorter than isoform a.

订购信息

产品编号 产品名称 载体 规格 价格
G106393 人 SNX7 (NM_152238) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 SNX7 (NM_015976) cDNA克隆 transcript variant 1
人 SNX7 (NM_152238) cDNA克隆 transcript variant 2

基因简介

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. This protein does not contain a coiled coil region like some family members, and its exact function is unknown. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 11. [provided by RefSeq, Jun 2010]

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