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SLC7A7


Official Full Name
solute carrier family 7 member 7
Organism
Homo sapiens
Gene ID
9056
Background
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]
Synonyms
LPI; LAT3; MOP-2; Y+LAT1; y+LAT-1

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SHH412188 shRNA set against Mouse SLC7A7 (NM_011405.4) Inquiry
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SHL012126 shRNA set against Rat Slc7a7(NM_031341.1) Inquiry
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CDCH401198 Mouse SLC7A7 ORF clone(NM_001253679.1) Inquiry
CDCH401200 Mouse SLC7A7 ORF clone(NM_001253680.1) Inquiry
CDCR250489 Mouse Slc7a7 ORF Clone(NM_011405.4) Inquiry
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