- accession:NM_001284316
- 基因别名:ACSF3
- 基因描述:Homo sapiens acyl-CoA synthetase family member 3 (ACSF3), transcript variant 3, mRNA.
- 载体:现货载体
- CDS区长度:936
- 翻译后氨基酸长度:311
- TranscriptVariant:This variant (3) lacks two exons, one of which contains a portion of the 5' UTR and the other which contains a portion of the 5' coding region including the start codon, compared to variant 1. These differences cause translation initiation at a downstream start codon and result in an isoform (2) with a shorter N-terminus, compared to isoform 1.
- 基因简介:This gene encodes a member of the acyl-CoA synthetase family of enzymes that activate fatty acids by catalyzing the formation of a thioester linkage between fatty acids and coenzyme A. The encoded protein is localized to mitochondria, has high specificity for malonate and methylmalonate and possesses malonyl-CoA synthetase activity. Mutations in this gene are a cause of combined malonic and methylmalonic aciduria. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Sep 2013]
- 规格:10ul 质粒
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