LAT2, linker for activation of T cells family member 2

LAT2, linker for activation of T cells family member 2

• This 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]

• Gene Synonyms (linker for activation of T-cells family member 2, Williams-Beuren syndrome chromosomal region 15 protein, Williams-Beuren syndrome chromosomal region 5 protein, linker for activation of B-cells, linker for activation of T cells, transmembrane adaptor 2, membrane-associated adapter molecule, non-T-cell activation linker, HSPC046, LAB, NTAL, WBSCR15, WBSCR5, WSCR5,)
• NCBI Gene ID: 7462
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q9GZY6
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

linker for activation of T cells family member 2 interacts with:

• decapping enzyme, scavenger
  ubiquilin 4

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.