- accession:NM_030922
- 基因别名:NIPA2
- 基因描述:Homo sapiens non imprinted in Prader-Willi/Angelman syndrome 2 (NIPA2), transcript variant 1, mRNA.
- 载体: 现货载体
- CDS区长度:1083
- 翻译后氨基酸长度:360
- TranscriptVariant:This variant (1) encodes the longer isoform (a). Variants 1, 2, 3 and 4 encode the same isoform (a).
- 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]
- 载体信息:自有图片地址
- 规格:10ul 质粒
CDS区参考序列: 点击查看序列翻译后氨基酸参数序列: 点击查看序列