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- accession：NM_004483
- 基因别名：GCSH
- 基因描述：Homo sapiens glycine cleavage system protein H (aminomethyl carrier) (GCSH), transcript variant 1, mRNA.
- 载体： 现货载体
- CDS区长度：522
- 翻译后氨基酸长度：173
- TranscriptVariant：This variant (1) represents the longer transcript and is the protein-coding variant.
- 基因简介：Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding,have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.[provided by RefSeq, Jan 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
