HCSGD entry for OLR1


1. General information

Official gene symbolOLR1
Entrez ID4973
Gene full nameoxidized low density lipoprotein (lectin-like) receptor 1
Other gene symbolsCLEC8A LOX1 LOXIN SCARE1 SLOX1
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0005041Low-density lipoprotein receptor activityIEAmolecular_function
GO:0005576Extracellular regionIEAcellular_component
GO:0005886Plasma membraneTAScellular_component
GO:0005887Integral component of plasma membraneTAScellular_component
GO:0006508ProteolysisTASbiological_process
GO:0006954Inflammatory responseIEAbiological_process
GO:0007159Leukocyte cell-cell adhesionIEAbiological_process
GO:0007596Blood coagulationTASbiological_process
GO:0008015Blood circulationTASbiological_process
GO:0008219Cell deathIEAbiological_process
GO:0016020MembraneTAScellular_component
GO:0030246Carbohydrate bindingIEAmolecular_function
GO:0042157Lipoprotein metabolic processIEAbiological_process
GO:0042542Response to hydrogen peroxideIEAbiological_process
GO:0043235Receptor complexIDAcellular_component
GO:0045121Membrane raftIEAcellular_component
GO:0050900Leukocyte migrationTASbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.72279804340.00017203370.99999024730.0242144385

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

Data sourceUp or downLog fold change
GSE11954Up0.0789096051
GSE13712_SHEARDown-0.1606079189
GSE13712_STATICDown-0.1116554314
GSE19018Down-1.0362794469
GSE19899_A1Down-0.6177408741
GSE19899_A2Down-3.1059988731
PubMed_21979375_A1Down-3.3903247876
PubMed_21979375_A2Down-3.5734403151
GSE35957Down-0.2142020831
GSE36640Up5.3217406520
GSE54402Down-1.3216545021
GSE9593Up0.3098171091
GSE43922Down-2.1184226950
GSE24585Down-0.1605680776
GSE37065Down-0.0182477174
GSE28863_A1Down-0.6342125721
GSE28863_A2Down-2.0588255960
GSE28863_A3Down-0.6786570466
GSE28863_A4Down-0.0375483062
GSE48662Down-0.0185384215

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

    • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-155-5pMIMAT0000646MIRT020773Western blotFunctional MTI21030878
hsa-miR-98-5pMIMAT0000096MIRT027749MicroarrayFunctional MTI (Weak)19088304
hsa-miR-21-5pMIMAT0000076MIRT031012MicroarrayFunctional MTI (Weak)18591254
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    • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 4 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25388834Ox-LDL receptor-1 (LOX-1) plays a central role in ox-LDL-mediated atherosclerosis via endothelial nitric oxide synthase (eNOS) uncoupling and nitric oxide reduction
25388834Therefore, we tested the hypothesis that ciglitazone, the PPARgamma agonist, protected endothelial cells against ox-LDL through regulating eNOS activity and LOX-1 signalling
25388834Ox-LDL-induced suppression of eNOS and nitric oxide synthesis were largely prevented by silencing LOX-1
22814745Strikingly, aortic explants from mice lacking lectin-like oxidized low-density lipoprotein receptor-1, a pattern-recognition receptor, were essentially unable to respond to UCMVs, whereas simultaneously treated explants from wild-type mice responded robustly by increasing monocyte recruitment
21698300Potential involvement of LOX-1 in functional consequences of endothelial senescence
21698300The analysis of a scavenger receptor LOX-1, a key molecule implicated in atherogenesis, revealed a significant decline of its message (mRNA) and protein content in senescent endothelial cells (-33%) and in aortas of 50 wk (vs
21698300These changes in senescent endothelial cells are suggestive of aberrant responses to physiological stimuli resulting in a less permissive environment for tissue remodeling and progression of diseases requiring angiogenesis and cell adhesion in elderly, possibly, mediated by LOX-1
15236625Oxidized LDL-induced EPC senescence was significantly inhibited by pretreatment with either lectin-like ox-LDL receptor-1 (LOX-1) antibody (Ab) or atorvastatin (P < 0
15236625Oxidized LDL significantly diminished telomerase activity to approximately 50%, an effect that was significantly abolished by pretreatment with either LOX-1 Ab or atorvastatin (P < 0
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