人 SLC7A7 (NM_001126105) cDNA克隆

Accession: NM_001126105
基因名称: SLC7A7
基因别名: LPI; LAT3; MOP-2; Y+LAT1; y+LAT-1
基因描述: Homo sapiens solute carrier family 7 (amino acid transporter light chain, y+L system), member 7 (SLC7A7), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1536 (查看编码区序列)
翻译后氨基酸长度: 511 (查看氨基酸序列)
Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 2 and 3 encode the same protein.
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G121414 人 SLC7A7 (NM_001126105) cDNA克隆 pDONR223 2ug质粒 点击询价

The protein encoded by this gene is the light subunit of a cationic amino acid transporter. This sodium-independent transporter is formed when the light subunit encoded by this gene dimerizes with the heavy subunit transporter protein SLC3A2. This transporter is found in epithelial cell membranes where it transfers cationic and large neutral amino acids from the cell to the extracellular space. Defects in this gene are a cause of lysinuric protein intolerance (LPI). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2011]