人 SNX21 (NM_001042632) cDNA克隆

基本信息

Accession: NM_001042632
基因名称: SNX21
基因别名: SNX-L; PP3993; C20orf161; dJ337O18.4
基因描述: Homo sapiens sorting nexin family member 21 (SNX21), transcript variant 3, mRNA.
种属: Human
CDS区长度: 459 (查看编码区序列)
翻译后氨基酸长度: 152 (查看氨基酸序列)
Transcript Variant: This variant (3) uses an alternate splice site in the coding region, compared to variant 1, that results in a frameshift. The resulting isoform (c) has a shorter and distinct C-terminus that lacks a PX domain, compared to isoform a.

订购信息

产品编号 产品名称 载体 规格 价格
G114729 人 SNX21 (NM_001042632) 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 SNX21 (NM_033421) cDNA克隆 transcript variant 1
人 SNX21 (NM_152897) cDNA克隆 transcript variant 2
人 SNX21 (NM_001042632) cDNA克隆 transcript variant 3
人 SNX21 (NM_001042633) cDNA克隆 transcript variant 4

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. The specific function of this protein has not been determined. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

相关产品