- accession:NM_000159
- 基因别名:GCDH
- 基因描述:Homo sapiens glutaryl-CoA dehydrogenase (GCDH), transcript variant 1, mRNA.
- 载体: 现货载体
- CDS区长度:1317
- 翻译后氨基酸长度:438
- TranscriptVariant:This variant (1) encodes the longer isoform (a, also known as the long isoform).
- 基因简介:The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family. It catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine, and L-tryptophan metabolism. It uses electron transfer flavoprotein as its electron acceptor. The enzyme exists in the mitochondrial matrix as a homotetramer of 45-kD subunits. Mutations in this gene result in the metabolic disorder glutaric aciduria type 1, which is also known as glutaric acidemia type I. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 12. [provided by RefSeq, Mar 2013]
- 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