人 SNX12 (NM_001256187) cDNA克隆

基本信息

Accession: NM_001256187
基因名称: SNX12
基因描述: Homo sapiens sorting nexin 12 (SNX12), transcript variant 4, mRNA.
种属: Human
CDS区长度: 291 (查看编码区序列)
翻译后氨基酸长度: 96 (查看氨基酸序列)
Transcript Variant: This variant (4) lacks an exon in the coding region which results in a frameshift, compared to variant 1. The resulting protein (isoform 3) has a distinct C-terminus, compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G107841 人 SNX12 (NM_001256187) 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 SNX12 (NM_001256185) cDNA克隆 transcript variant 1
人 SNX12 (NM_013346) cDNA克隆 transcript variant 2
人 SNX12 (NM_001256186) cDNA克隆 transcript variant 3
人 SNX12 (NM_001256187) cDNA克隆 transcript variant 4
人 SNX12 (NM_001256188) cDNA克隆 transcript variant 5

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. A similar protein in mouse may be involved in regulating the neurite outgrowth. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]

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