Symbol
| LAT
| contributors: mct/npt/pgu - updated : 30-08-2017
|
HGNC name
| linker for activation of T cells
|
HGNC id
| 18874
|
corresponding disease(s)
|
IMD52
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
| --low
|  
|
lower in asthmatic patients than that in healthy people | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| T cells from mice harboring a mutation at the Plcg1 binding site of Lat (Y136F) have impaired calcium flux and Erk activation, and these T cells are highly activated, resulting in the development of a lymphoproliferative syndrome |