HCSGD entry for NDRG2


1. General information

Official gene symbolNDRG2
Entrez ID57447
Gene full nameNDRG family member 2
Other gene symbolsSYLD
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:0001818Negative regulation of cytokine productionIEAbiological_process
GO:0003674Molecular_functionNDmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDA IEAcellular_component
GO:0005730NucleolusIDAcellular_component
GO:0005737CytoplasmIDA IEAcellular_component
GO:0005794Golgi apparatusIDAcellular_component
GO:0005813CentrosomeIDAcellular_component
GO:0005829CytosolNAScellular_component
GO:0007165Signal transductionIEAbiological_process
GO:0007399Nervous system developmentIEAbiological_process
GO:0010574Regulation of vascular endothelial growth factor productionIEAbiological_process
GO:0016055Wnt signaling pathwayIEAbiological_process
GO:0030154Cell differentiationIEAbiological_process
GO:0030426Growth coneIEAcellular_component
GO:0048471Perinuclear region of cytoplasmIEAcellular_component
GO:0048662Negative regulation of smooth muscle cell proliferationIEAbiological_process
GO:0070373Negative regulation of ERK1 and ERK2 cascadeIEAbiological_process
GO:0090361Regulation of platelet-derived growth factor productionIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.63187065080.85993477830.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.0118570776
GSE13712_SHEARUp0.0897754070
GSE13712_STATICDown-0.1073216425
GSE19018Up0.1323773499
GSE19899_A1Up0.0246658971
GSE19899_A2Up0.0331666643
PubMed_21979375_A1Up0.3258067923
PubMed_21979375_A2Down-0.0383083699
GSE35957Up0.1685942335
GSE36640Down-0.3124684893
GSE54402Down-0.0747030364
GSE9593Up0.0700860969
GSE43922Up0.0251549077
GSE24585Up0.0736428114
GSE37065Up0.1691274850
GSE28863_A1Down-0.2821227091
GSE28863_A2Up0.1940106984
GSE28863_A3Up0.2559875593
GSE28863_A4Up0.0623041737
GSE48662Down-0.0457946500

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-145-5pMIMAT0000437MIRT021510Reporter assay;MicroarrayFunctional MTI21351259
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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: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25701873We focused on two of these proteins, NDRG2 and TRIM72, due to their putative roles in myoblast proliferation and myogenesis
25701873Follow-up analysis confirmed that both proteins were ubiquitinated by TRIM32 in vitro; however, only NDRG2 accumulated in skeletal muscle and myoblasts in the absence of TRIM32
25701873NDRG2 overexpression in myoblasts led to reduced cell proliferation and delayed cell cycle withdrawal during differentiation
25701873Thus, we identified NDRG2 as a novel target for TRIM32; these findings further corroborate the hypothesis that TRIM32 is involved in control of myogenic cells proliferation and differentiation
22043305Up-regulation of NDRG2 in senescent lens epithelial cells contributes to age-related cataract in human
22043305BACKGROUND: Human N-Myc downstream regulated gene2 (NDRG2), a novel gene has been cloned and shown to be related to a number of cellular processes, including proliferation, differentiation, stress, and apoptosis
22043305NDRG2 has also been linked to age-related Alzheimer's disease
22043305Since the role of this gene in senescence is limited, we have investigated the potential role of NDRG2 in human lens epithelial cells (HLECs), a paradigm implicated in age-related cataract
22043305Ndrg2 protein expression was also significantly increased in these senescent cells
22043305To induce overexpression of NDRG2, SRA01/04 cells were infected with the adenoviral vector of NDRG2
22043305In these cells, overexpression of NDRG2 resulted in a fibroblast-like appearance and the cell viability decreased about 20%
22043305Furthermore, the expression of NDRG2 from age-related cataracts was up-regulated 2-fold at both mRNA and protein levels compared with the clear lenses
22043305CONCLUSIONS/SIGNIFICANCE: NDRG2 is up regulated not only in the ageing process of HLECs in vitro but also in the cells from human age-related cortical cataract in vivo
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