HCSGD entry for NEU1


1. General information

Official gene symbolNEU1
Entrez ID4758
Gene full namesialidase 1 (lysosomal sialidase)
Other gene symbolsNANH NEU SIAL1
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0004308Exo-alpha-sialidase activityIDA IEAmolecular_function
GO:0005764LysosomeIDA IEAcellular_component
GO:0005765Lysosomal membraneIEAcellular_component
GO:0005886Plasma membraneIEAcellular_component
GO:0006665Sphingolipid metabolic processTASbiological_process
GO:0006687Glycosphingolipid metabolic processTASbiological_process
GO:0009313Oligosaccharide catabolic processIMPbiological_process
GO:0016023Cytoplasmic membrane-bounded vesicleIEAcellular_component
GO:0016042Lipid catabolic processIEAbiological_process
GO:0030054Cell junctionIDAcellular_component
GO:0043202Lysosomal lumenTAScellular_component
GO:0043231Intracellular membrane-bounded organelleIDAcellular_component
GO:0044281Small molecule metabolic processTASbiological_process
GO:0052794Exo-alpha-(2->3)-sialidase activityIEAmolecular_function
GO:0052795Exo-alpha-(2->6)-sialidase activityIEAmolecular_function
GO:0052796Exo-alpha-(2->8)-sialidase activityIEAmolecular_function
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.00038288060.97868031610.05182613071.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up1.8357539058
GSE13712_SHEARUp0.0624908809
GSE13712_STATICUp0.2749859771
GSE19018Up0.1020752395
GSE19899_A1Up1.0505070166
GSE19899_A2Up1.3181310341
PubMed_21979375_A1Up1.4765247677
PubMed_21979375_A2Up1.3999428770
GSE35957Down-0.2238056735
GSE36640Up0.9400625197
GSE54402Up0.7455033044
GSE9593Up1.0127148700
GSE43922Up0.8542200164
GSE24585Up0.9526451706
GSE37065Up0.2827885067
GSE28863_A1Down-0.0481162565
GSE28863_A2Up0.9995396604
GSE28863_A3Down-0.5812424302
GSE28863_A4Down-0.3811548759
GSE48662Up0.1496495652

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Name

Drug

Accession number

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-155-5pMIMAT0000646MIRT020584ProteomicsFunctional MTI (Weak)18668040
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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: 7 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

7518456The release of the radioactivity from the anti-human IgG-bound senescent cells was enhanced by incubation with band 3 oligosaccharides but not by those digested with endo-beta-galactosidase or neuraminidase
8115995Platelets were isolated from blood of baboons and treated with neuraminidase to remove platelet membrane sialic acid, a process which artificially ages the platelets
8115995Removal of sialic acid by neuraminidase did not affect the aggregation of platelets by agonists in vitro, nor their sites of sequestration
6490404This can be mimicked by neuraminidase and protease treatment of erythrocytes in vitro
6363100Heat-eluted IgG (He-IgG) prepared from senescent red blood cells was capable of binding to either heat-treated old platelets or Vibrio cholerae neuraminidase (VCN)-treated young platelets, suggesting expression of a common age-dependent antigen on the senescent red blood cells and old platelets
7055615The decrease in sialic acid biosynthesis in differentiated erythroleukemia cells was reflected by an 83% decrease in the amount of radioactively-labeled sialic acid released by neuraminidase treatment of cells exposed to dimethylsulfoxide
7470642The efficacy of neuraminidase treatment in studies on red cell aging
29906Anomalous electrophoretic properties of neuraminidase treated human erythrocytes
29906Desialylation of human red blood cells (RBC) by Vibrio cholerae neuraminidase (VCN) was found to produce cells with electrophoretic properties which were inconsistent with the view of simple loss of N-acetylneuraminic acid (NANA) as the sole effect of VCN treatment
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