This gene encodes a protein that plays a major role in the bidirectional stimulation of T and B cells. This protein contains an SH2 domain and a short tail. It associates with the signaling lymphocyte-activation molecule, thereby acting as an inhibitor of this transmembrane protein by blocking the recruitment of the SH2-domain-containing signal-transduction molecule SHP-2 to its docking site. This protein can also bind to other related surface molecules that are expressed on activated T, B and NK cells, thereby modifying signal transduction pathways in these cells. Mutations in this gene cause lymphoproliferative syndrome X-linked type 1 or Duncan disease, a rare immunodeficiency characterized by extreme susceptibility to infection with Epstein-Barr virus, with symptoms including severe mononucleosis and malignant lymphoma. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SH2D1ABA-20-REGO | 20 (40 μL) | 200 μL |
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| SH2D1ABA-20-REGR | 20 (40 μL) | 200 μL |
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| SH2D1ABA-20-ORGR | 20 (40 μL) | 200 μL |
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| SH2D1ABA-20-GOGR | 20 (40 μL) | 200 μL |
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| SH2D1ABA-20-GRRE | 20 (40 μL) | 200 μL |
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| SH2D1ABA-20-GROR | 20 (40 μL) | 200 μL |
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| SH2D1ABA-20-GRGO | 20 (40 μL) | 200 μL |
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| SH2D1ABA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene encodes a protein that plays a major role in the bidirectional stimulation of T and B cells. This protein contains an SH2 domain and a short tail. It associates with the signaling lymphocyte-activation molecule, thereby acting as an inhibitor of this transmembrane protein by blocking the recruitment of the SH2-domain-containing signal-transduction molecule SHP-2 to its docking site. This protein can also bind to other related surface molecules that are expressed on activated T, B and NK cells, thereby modifying signal transduction pathways in these cells. Mutations in this gene cause lymphoproliferative syndrome X-linked type 1 or Duncan disease, a rare immunodeficiency characterized by extreme susceptibility to infection with Epstein-Barr virus, with symptoms including severe mononucleosis and malignant lymphoma. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Symbol : SH2D1A
Gene Name : SH2 domain containing 1A
Chromosome : CHR X: 124,346,281-124,373,159
Locus : Xq25
Alt. Genes : OPTN
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