Harmonizome 3.0

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]

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term lat2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From Pathway Commons Protein-Protein Interactions

interacting proteins for LAT2 from the Pathway Commons Protein-Protein Interactions dataset.

From CORUM Protein Complexes

proteins in the CD98-LAT2-ITGB1 complex protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the LAT2-ITGB1 complex protein complex from the CORUM Protein Complexes dataset.

From Reactome Pathways 2014

proteins participating in the Role of LAT2/NTAL/LAB on calcium mobilization pathway from the Reactome Pathways dataset.

From Reactome Pathways 2024

proteins participating in the Role of LAT2/NTAL/LAB on calcium mobilization pathway from the Reactome Pathways 2024 dataset.