- accession:NM_172250
- 基因别名:MMAA
- 基因描述:Homo sapiens methylmalonic aciduria (cobalamin deficiency) cblA type (MMAA), mRNA.
- 载体: 现货载体
- CDS区长度:1257
- 翻译后氨基酸长度:418
- 基因简介:The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria. [provided by RefSeq, Jul 2008]
- 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