HCSGD entry for NANOG


1. General information

Official gene symbolNANOG
Entrez ID79923
Gene full nameNanog homeobox
Other gene symbols
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:0000122Negative regulation of transcription from RNA polymerase II promoterIEAbiological_process
GO:0001158Enhancer sequence-specific DNA bindingIEAmolecular_function
GO:0001710Mesodermal cell fate commitmentIEAbiological_process
GO:0001714Endodermal cell fate specificationIDAbiological_process
GO:0003677DNA bindingIDAmolecular_function
GO:0003682Chromatin bindingIEAmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityIDA IEAmolecular_function
GO:0003714Transcription corepressor activityIEA ISSmolecular_function
GO:0005634NucleusIC IDAcellular_component
GO:0005654NucleoplasmIEAcellular_component
GO:0005730NucleolusIDAcellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0006355Regulation of transcription, DNA-templatedIDAbiological_process
GO:0008283Cell proliferationIMPbiological_process
GO:0008284Positive regulation of cell proliferationIEAbiological_process
GO:0008406Gonad developmentIEAbiological_process
GO:0009790Embryo developmentIEPbiological_process
GO:0009880Embryonic pattern specificationIEAbiological_process
GO:0010454Negative regulation of cell fate commitmentIEAbiological_process
GO:0010468Regulation of gene expressionIMPbiological_process
GO:0017145Stem cell divisionIEAbiological_process
GO:0019827Stem cell maintenanceIEAbiological_process
GO:0030154Cell differentiationIEPbiological_process
GO:0030514Negative regulation of BMP signaling pathwayIEAbiological_process
GO:0032526Response to retinoic acidIEAbiological_process
GO:0035019Somatic stem cell maintenanceIMPbiological_process
GO:0045595Regulation of cell differentiationIMPbiological_process
GO:0045931Positive regulation of mitotic cell cycleIEAbiological_process
GO:0045944Positive regulation of transcription from RNA polymerase II promoterIDA IEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.73985477760.68257050260.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.0165987681
GSE13712_SHEARUp0.0176820947
GSE13712_STATICDown-0.0283563073
GSE19018Up0.1679224686
GSE19899_A1Up0.0264865636
GSE19899_A2Up0.2615832629
PubMed_21979375_A1Down-0.0321245096
PubMed_21979375_A2Up0.0045633061
GSE35957Up0.0899422003
GSE36640Up0.0566613850
GSE54402Down-0.0088745068
GSE9593Down-0.2451008822
GSE43922--
GSE24585--
GSE37065--
GSE28863_A1Down-0.1460367933
GSE28863_A2Down-0.1010727437
GSE28863_A3Up0.3524546648
GSE28863_A4Down-0.1377991047
GSE48662Down-0.1701749558

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-34a-5pMIMAT0000255MIRT006222Luciferase reporter assay//Western blotFunctional MTI22020437
hsa-miR-34b-3pMIMAT0004676MIRT006229Luciferase reporter assay//Western blotFunctional MTI22020437
hsa-miR-34c-5pMIMAT0000686MIRT006228Luciferase reporter assay//Western blotFunctional MTI22020437
hsa-miR-181a-3pMIMAT0000270MIRT007216Luciferase reporter assayFunctional MTI23344176
hsa-miR-335-5pMIMAT0000765MIRT017305MicroarrayFunctional MTI (Weak)18185580
hsa-miR-145-5pMIMAT0000437MIRT035522Luciferase reporter assayFunctional MTI23541921
hsa-miR-320aMIMAT0000510MIRT044412CLASHFunctional MTI (Weak)23622248
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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: 9 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

26860864In addition, polyploid cells were positive for markers of embryonic stemness (OCT4, SOX2, NANOG) and senescence (p16INK4a)
26514209Syndecan-1 expression diminished, whereas stem cell markers such as SOX2, NANOG, OCT4, and E2F3 increased
26102294SOX2 and NANOG expression did not change following ETO treatment suggesting a dissociation of OCT4A from its pluripotency function
26089914For each early passage BM-MSC sample (5th or 6th passages), the normalized protein expression levels of senescence-associated markers p16(INK4A), p21(WAF1), SOD2, and rpS6(S240/244); the concentration of IL6 and IL8 in cell culture supernatants; and the normalized gene expression levels of pluripotency markers OCT4, NANOG, and SOX2 were correlated with final population doubling (PD) number
25685943Magnetofection Mediated Transient NANOG Overexpression Enhances Proliferation and Myogenic Differentiation of Human Hair Follicle Derived Mesenchymal Stem Cells
25685943Then we applied the optimized MF protocol to express the pluripotency-associated transcription factor NANOG, which was previously shown to reverse the effects of organismal aging on MSC proliferation and myogenic differentiation capacity
25685943Indeed, MF-mediated NANOG delivery increased proliferation and enhanced the differentiation of hHF-MSCs into smooth muscle cells (SMCs)
25279549The BORIS-positive cells isolated using BORIS-molecular beacon, expressed higher telomerase hTERT, stem cell (NANOG, OCT4, SOX2) and cancer stem cell marker genes (CD44 and ALDH1) compared to the BORIS-negative tumor cells
21629737Further, with development of senescence and accumulation of p16inka4a and p21CIP1, NANOG is downregulated in most cells
21562774They showed alkaline phosphatase activity and expressed ESC markers, as shown by immunostaining of OCT4, SOX2, SSEA4, and TRA-1-81 as well as reverse-transcription polymerase chain reaction (RT-PCR) for OCT4 and NANOG transcripts
20457152Here, we studied the role of the pluripotency and self-renewal stem cell genes NANOG, OCT4 and SOX2 in this polyploidy-dependent survival mechanism
20457152In irradiation-resistant p53-mutated lymphoma cell-lines (Namalwa and WI-L2-NS) but not sensitive p53 wild-type counterparts (TK6), low background expression of OCT4 and NANOG was up-regulated by ionising radiation with protein accumulation evident in ETC as detected by OCT4/DNA flow cytometry and immunofluorescence (IF)
20457152IF analysis also showed that the ETC generate PML bodies that appear to concentrate OCT4, NANOG and SOX2 proteins, which extend into complex nuclear networks
20457152These polyploid tumour cells resist apoptosis, overcome cellular senescence and undergo bi- and multi-polar divisions transmitting the up-regulated OCT4, NANOG and SOX2 self-renewal cassette to their descendents
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