Search Results for: CCL21

37 interactions involving CCL21 - C-C motif chemokine ligand 21 found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Symbol Description Pathways Hide Drugs Hide Diseases Hide
CXCL13 C-X-C motif chemokine ligand 13
  • Chemokine receptors bind chemokines
  • G alpha (i) signalling events
CXCL14 C-X-C motif chemokine ligand 14
CXCL17 C-X-C motif chemokine ligand 17
CXCL2 C-X-C motif chemokine ligand 2
  • Chemokine receptors bind chemokines
  • G alpha (i) signalling events
  • Interleukin-10 signaling
CXCL9 C-X-C motif chemokine ligand 9
  • Chemokine receptors bind chemokines
  • G alpha (i) signalling events
GOT2 glutamic-oxaloacetic transaminase 2
  • Degradation of cysteine and homocysteine
  • Glyoxylate metabolism and glycine degradation
  • Aspartate and asparagine metabolism
  • Glutamate and glutamine metabolism
  • Malate-aspartate shuttle
  • Pyridoxal phosphate
  • Aspartic acid
  • Glutamic acid
  • Cysteine
  • 4'-Deoxy-4'-Acetylyamino-Pyridoxal-5'-Phosphate
IGFBP7 insulin like growth factor binding protein 7
  • Senescence-Associated Secretory Phenotype (SASP)
  • Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
  • Post-translational protein phosphorylation
  • Insulin human
LRRK1 leucine rich repeat kinase 1
OTP orthopedia homeobox
PF4 platelet factor 4
  • Platelet degranulation
  • Common Pathway of Fibrin Clot Formation
  • Cell surface interactions at the vascular wall
  • Chemokine receptors bind chemokines
  • G alpha (i) signalling events
  • RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
  • Drotrecogin alfa
  • Heparin
PF4V1 platelet factor 4 variant 1
  • Common Pathway of Fibrin Clot Formation
  • Cell surface interactions at the vascular wall
PPBP pro-platelet basic protein
  • Platelet degranulation
  • Chemokine receptors bind chemokines
  • G alpha (i) signalling events
  • Neutrophil degranulation
  • Ethanesulfonic acid
  • Copper
TMEM107 transmembrane protein 107
UBQLN4 ubiquilin 4
VCAN versican
  • Glycosaminoglycan-protein linkage region biosynthesis
  • CS-GAG biosynthesis
  • DS-GAG biosynthesis
  • CS/DS degradation
  • ECM proteoglycans
  • Defective B4GALT7 causes EDS, progeroid type
  • Defective B3GAT3 causes JDSSDHD
  • Defective CHST3 causes SEDCJD
  • Defective CHST14 causes EDS, musculocontractural type
  • Defective CHSY1 causes TPBS
  • Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
  • Defective B3GALT6 causes EDSP2 and SEMDJL1
  • Post-translational protein phosphorylation
  • Hyaluronic acid
  • Vitreoretinal degeneration, including: Stickler syndrome type I (STL1); Stickler syndrome type II (STL2); Snowflake vitreoretinal degeneration (SVD); Wagner syndrome 1 (WGN1); Knobloch syndrome (KNO); Enhanced S-cone syndrome (ESCS); Autosomal dominant vitreoretinochoroidopathy (ADVIRC)
XCL1 X-C motif chemokine ligand 1
  • Chemokine receptors bind chemokines
  • G alpha (q) signalling events
XCL2 X-C motif chemokine ligand 2
  • Chemokine receptors bind chemokines
  • G alpha (q) signalling events

Page 2 out of 2 pages