- accession:NM_017813
- 基因别名:IMPAD1
- 基因描述:Homo sapiens inositol monophosphatase domain containing 1 (IMPAD1), mRNA.
- 载体:现货载体
- CDS区长度:1080
- 翻译后氨基酸长度:359
- 基因简介:This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. [provided by RefSeq, Dec 2011]
- 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