LAT2 Back

linker for activation of T cells family, member 2

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NCBI Description of LAT2

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.

Community Annotation of LAT2 Add / Edit LAT2: Annotations

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Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


LAT2 is highly significantly mutated in
LAT2 is significantly mutated in
LAT2 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for LAT2