人 NIPA2 (NM_030922) cDNA克隆

基本信息

Accession: NM_030922
基因名称: NIPA2
基因描述: Homo sapiens non imprinted in Prader-Willi/Angelman syndrome 2 (NIPA2), transcript variant 1, mRNA.
种属: Human
CDS区长度: 1083 (查看编码区序列)
翻译后氨基酸长度: 360 (查看氨基酸序列)
Transcript Variant: This variant (1) encodes the longer isoform (a). Variants 1, 2, 3 and 4 encode the same isoform (a).

订购信息

产品编号 产品名称 载体 规格 价格
G106174 人 NIPA2 (NM_030922) 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 NIPA2 (NM_030922) cDNA克隆 transcript variant 1
人 NIPA2 (NM_001008860) cDNA克隆 transcript variant 2
人 NIPA2 (NM_001008892) cDNA克隆 transcript variant 3
人 NIPA2 (NM_001008894) cDNA克隆 transcript variant 4
人 NIPA2 (NM_001184889) cDNA克隆 transcript variant 5
人 NIPA2 (NM_001184888) cDNA克隆 transcript variant 6

基因简介

This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]

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