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ONTOLOGY REPORT - ANNOTATIONS


Term:negative regulation of cell chemotaxis to fibroblast growth factor
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Accession:GO:1904848 term browser browse the term
Definition:Any process that stops, prevents or reduces the frequency, rate or extent of cell chemotaxis to fibroblast growth factor.
Synonyms:exact_synonym: down regulation of cell chemotaxis to fibroblast growth factor;   downregulation of cell chemotaxis to fibroblast growth factor
 narrow_synonym: inhibition of cell chemotaxis to fibroblast growth factor


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negative regulation of endothelial cell chemotaxis to fibroblast growth factor term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cxcl13 C-X-C motif chemokine ligand 13 ISO (PMID:11708770) RGD PMID:11708770 NCBI chr14:15,253,146...15,258,221
Ensembl chr14:15,253,125...15,258,207
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Term paths to the root
Path 1
Term Annotations click to browse term
  biological_process 20028
    negative regulation of biological process 5686
      negative regulation of cellular process 5156
        negative regulation of cellular response to growth factor stimulus 105
          negative regulation of cell chemotaxis to fibroblast growth factor 1
            negative regulation of endothelial cell chemotaxis to fibroblast growth factor 1
Path 2
Term Annotations click to browse term
  biological_process 20028
    response to stimulus 10583
      response to chemical 6342
        response to organic substance 3865
          response to growth factor 810
            cellular response to growth factor stimulus 771
              cellular response to fibroblast growth factor stimulus 119
                cell chemotaxis to fibroblast growth factor 7
                  regulation of cell chemotaxis to fibroblast growth factor 7
                    negative regulation of cell chemotaxis to fibroblast growth factor 1
                      negative regulation of endothelial cell chemotaxis to fibroblast growth factor 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.