CD135
Gene Ontology | |
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Molecular function | • transmembrane receptor protein tyrosine kinase activity • cytokine receptor activity • vascular endothelial growth factor-activated receptor activity • protein binding • ATP binding • protein homodimerization activity • phosphatidylinositol 3-kinase binding |
Cellular component | • endoplasmic reticulum lumen • integral to plasma membrane • cell surface |
Biological process | • leukocyte homeostasis • myeloid progenitor cell differentiation • pro-B cell differentiation • pro-T cell differentiation • transmembrane receptor protein tyrosine kinase signaling pathway • positive regulation of cell proliferation • negative regulation of cell proliferation • positive regulation of phosphatidylinositol 3-kinase cascade • peptidyl-tyrosine phosphorylation • cytokine-mediated signaling pathway • hemopoiesis • B cell differentiation • common myeloid progenitor cell proliferation • vascular endothelial growth factor signaling pathway • positive regulation of tyrosine phosphorylation of STAT protein • regulation of apoptotic process • positive regulation of MAP kinase activity • positive regulation of MAPK cascade • positive regulation of phosphatidylinositol 3-kinase activity • negative regulation of B cell differentiation • lymphocyte proliferation • protein autophosphorylation • cellular response to cytokine stimulus • dendritic cell differentiation |
Sources: Amigo / QuickGO |
28.58 – 28.67 Mb
147.33 – 147.4 Mb
Cluster of differentiation antigen 135 (CD135) also known as Fms-like tyrosine kinase 3 (FLT-3), receptor-type tyrosine-protein kinase FLT3, or fetal liver kinase-2 (Flk2) is a protein that in humans is encoded by the FLT3 gene. Flt3 is a cytokine receptor which belongs to the receptor tryrosin kinase class III. CD135 is the receptor for the cytokine Flt3 ligand (Flt3L).
It is expressed on the surface of many hematopoietic progenitor cells. Signalling of Flt3 is important for the normal development of haematopoietic stem cells and progenitor cells.
The FLT3 gene is one of the most frequently mutated genes in acute myeloid leukemia (AML). Besides, high levels of wild-type FLT3 have been reported for blast cells of some AML patients without FLT3 mutations. These high levels may be associated with worse prognosis.
Read more about CD135: Structure, Function