Aliases for SLC7A3 Gene
External Ids for SLC7A3 Gene
This gene encodes a member of the solute carrier family 7. The encoded protein is a sodium-independent cationic amino acid transporter. Alternate splicing results in multiple transcripts that encoded the same protein.[provided by RefSeq, May 2010]
GeneCards Summary for SLC7A3 Gene
SLC7A3 (Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 3) is a Protein Coding gene. Diseases associated with SLC7A3 include allan-herndon-dudley syndrome. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds. GO annotations related to this gene include arginine transmembrane transporter activity. An important paralog of this gene is SLC7A14.
UniProtKB/Swiss-Prot for SLC7A3 Gene
Mediates the uptake of the cationic amino acids arginine, lysine and ornithine in a sodium-independent manner.