人 NIPA1 (NM_001142275) cDNA克隆

基本信息

Accession: NM_001142275
基因名称: NIPA1
基因别名: FSP3; SPG6
基因描述: Homo sapiens non imprinted in Prader-Willi/Angelman syndrome 1 (NIPA1), transcript variant 2, mRNA.
种属: Human
CDS区长度: 765 (查看编码区序列)
翻译后氨基酸长度: 254 (查看氨基酸序列)
Transcript Variant: This variant (2) uses an alternate 5' exon and downstream start codon, compared to variant 1. The resulting protein (isoform 2) has a shorter N-terminus, compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G100854 人 NIPA1 (NM_001142275) 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 NIPA1 (NM_144599) cDNA克隆 transcript variant 1
人 NIPA1 (NM_001142275) cDNA克隆 transcript variant 2

基因简介

This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008]

相关产品