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Genes search result for Homo sapiens
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3 records found for search term Lat2
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1342914LAT2linker for activation of T cells family member 2This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008]77421000674229834Human121symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
1345085SLC7A8solute carrier family 7 member 8Enables several functions, including neutral L-amino acid transmembrane transporter activity; protein heterodimerization activity; and secondary active transmembrane transporter activity. Involved in L-alanine import across plasma membrane; L-leucine import across plasma membrane; and thyroid hormon142312529523183660Human250old_gene_symbolgene, protein-coding, VALIDATED [RefSeq]
1319397SLC7A6solute carrier family 7 member 6Enables L-lysine:L-arginine antiporter activity and arginine binding activity. Involved in L-arginine transmembrane transport; L-leucine transport; and ornithine transport. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]166826452668301819Human153old_gene_symbolgene, protein-coding, VALIDATED [RefSeq]