HCSGD entry for DARC


1. General information

Official gene symbolDARC
Entrez ID2532
Gene full nameDuffy blood group, chemokine receptor
Other gene symbolsCCBP1 CD234 Dfy FY GPD GpFy WBCQ1
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0004872Receptor activityTASmolecular_function
GO:0004888Transmembrane signaling receptor activityTASmolecular_function
GO:0004930G-protein coupled receptor activityIEAmolecular_function
GO:0005769Early endosomeIEAcellular_component
GO:0005886Plasma membraneTAScellular_component
GO:0006952Defense responseNASbiological_process
GO:0006954Inflammatory responseIEAbiological_process
GO:0016021Integral component of membraneIEAcellular_component
GO:0019956Chemokine bindingIEAmolecular_function
GO:0019957C-C chemokine bindingIPImolecular_function
GO:0032642Regulation of chemokine productionIEAbiological_process
GO:0055037Recycling endosomeIEAcellular_component
GO:0070098Chemokine-mediated signaling pathwayIEAbiological_process
Entries Per Page
Displaying Page of

4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.34171253370.27779031190.99999024731.0000000000

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Down-0.1815925962
GSE13712_SHEARDown-2.6986447261
GSE13712_STATICDown-0.3571446561
GSE19018Up0.0202652833
GSE19899_A1Up0.1229363931
GSE19899_A2Down-0.1576728732
PubMed_21979375_A1Up0.1437091007
PubMed_21979375_A2Down-0.3116588358
GSE35957Up0.1086313413
GSE36640Down-0.0253639465
GSE54402Up0.1414728541
GSE9593Up0.1892299318
GSE43922Up0.1512146527
GSE24585Down-0.0697591999
GSE37065Up0.0051934319
GSE28863_A1Up0.2694660529
GSE28863_A2Up0.8516190613
GSE28863_A3Up0.1348597568
GSE28863_A4Up0.2447712772
GSE48662Up0.0380973341

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

    • mirTarBase
No target information from mirTarBase
    • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

23873025Mechanistic studies showed that inducible expression of CD82 in highly metastatic melanoma cells significantly increased p21 expression upon binding of Duffy antigen receptor group (DARC), inducing tumor cell senescence and interrupting IL-8-mediated vascular endothelial (VE)-cadherin disassembly
17955335Duffy antigen/receptor for chemokines (DARC) attenuates angiogenesis by causing senescence in endothelial cells
17955335Duffy antigen/receptor for chemokines (DARC), expressed on erythrocytes and post-capillary venular endothelial cells, selectively binds both CXC and CC chemokines
17955335DARC binds ELR + angiogenic chemokines such as IL-8 (CXCL8)
17955335We show that the DARC on endothelial cells plays a direct role in regulating angiogenesis
17955335Matrigel(TM) in vivo plug assay showed that there was more capillary formation in DARC knockout mice compared to wild type mice indicating that DARC attenuated angiogenic activity
17955335In vitro angiogenic assay on Matrigel coated plates using DARC expressing stable human cerebro-microvascular endothelial cells (HCEC) showed that, although capillary formation in transfected cells started early within 4-8 h; capillary formation was attenuated within 12-24 h
17955335Preincubation of DARC-expressing HCEC with monoclonal antibody (mAb-Fy6) against the N-terminal chemokine-binding domain of DARC increased capillary formation in vitro
17955335Interestingly, after several days in the conditioned medium, DARC expressing senescent cells started to initiate capillary formation; whereas capillary formed with DARC non-expressing cells remained the same
17955335Our data evidently demonstrated that DARC on endothelial cells attenuated the angiogenic activity by causing senescence
Entries Per Page
Displaying Page of