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- Table of Contents
Facts about Linker for activation of T-cells family member 2.
Couples stimulation of these receptors and their associated kinases with distal intracellular events through the recruitment of GRB2. .
Human | |
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Gene Name: | LAT2 |
Uniprot: | Q9GZY6 |
Entrez: | 7462 |
Belongs to: |
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No superfamily |
LAB; LABWilliams-Beuren syndrome chromosomal region 15 protein; Linker for activation of B-cells; linker for activation of T cells family, member 2; linker for activation of T-cells family member 2; Membrane-associated adapter molecule; Non-T-cell activation linker; NTAL; NTALWilliams-Beuren syndrome chromosomal region 5 protein; WBS15; WBSCR15; WBSCR5; WBSCR5HSPC046; Williams-Beuren syndrome chromosome region 5; WSCR5
Mass (kDA):
26.55 kDA
Human | |
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Location: | 7q11.23 |
Sequence: | 7; NC_000007.14 (74210006..74229834) |
Highly expressed in spleen, peripheral blood lymphocytes, and germinal centers of lymph nodes. Also expressed in placenta, lung, pancreas and small intestine. Present in B- cells, NK cells and monocytes. Absent from T-cells (at protein level).
Cell membrane; Single-pass type III membrane protein. Present in lipid rafts.
PMID: 11124535 by Doyle J.L., et al. Divergent human and mouse orthologs of a novel gene (WBSCR15/Wbscr15) reside within the genomic interval commonly deleted in Williams syndrome.
PMID: 11003705 by Martindale D.W., et al. Comparative genomic sequence analysis of the Williams syndrome region (LIMK1-RFC2) of human chromosome 7q11.23.