SELP: Ca(2+)-dependent receptor for myeloid cells that binds to carbohydrates on neutrophils and monocytes. Mediates the interaction of activated endothelial cells or platelets with leukocytes. The ligand recognized is sialyl-Lewis X. Mediates rapid rolling of leukocyte rolling over vascular surfaces during the initial steps in inflammation through interaction with PSGL1. Defects in SELP may be a cause of susceptibility to ischemic stroke (ISCHSTR); also known as cerebrovascular accident or cerebral infarction. A stroke is an acute neurologic event leading to death of neural tissue of the brain and resulting in loss of motor, sensory and/or cognitive function. Ischemic strokes, resulting from vascular occlusion, is considered to be a highly complex disease consisting of a group of heterogeneous disorders with multiple genetic and environmental risk factors. Belongs to the selectin/LECAM family.
Protein type: Cell adhesion; Membrane protein, integral
Chromosomal Location of Human Ortholog: 1q24.2
Cellular Component: external side of plasma membrane; extracellular space; integral component of plasma membrane; plasma membrane; platelet alpha granule membrane; platelet dense granule membrane
Molecular Function: calcium-dependent protein binding; fucose binding; glycosphingolipid binding; heparin binding; lipopolysaccharide binding; protein binding; sialic acid binding
Biological Process: cell adhesion; defense response to Gram-negative bacterium; heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules; inflammatory response; leukocyte adhesion; leukocyte migration; leukocyte tethering or rolling; platelet degranulation; positive regulation of leukocyte migration; positive regulation of phosphoinositide 3-kinase cascade; positive regulation of platelet activation; regulation of integrin activation; response to lipopolysaccharide
Disease: Ige Responsiveness, Atopic
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