人 SLC27A2 (NM_001159629) cDNA克隆

Accession: NM_001159629
基因名称: SLC27A2
基因别名: VLCS; FATP2; VLACS; ACSVL1; FACVL1; hFACVL1; HsT17226
基因描述: Homo sapiens solute carrier family 27 (fatty acid transporter), member 2 (SLC27A2), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1704 (查看编码区序列)
翻译后氨基酸长度: 567 (查看氨基酸序列)
Transcript Variant: This variant (2) is lacking an in-frame coding exon compared to variant 1, resulting in a shorter isoform (2) missing an internal protein segment compared to isoform 1.
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G116260 人 SLC27A2 (NM_001159629) cDNA克隆 pDONR223 2ug质粒 点击询价

The protein encoded by this gene is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes, but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009]