HCSGD entry for E2F4


1. General information

Official gene symbolE2F4
Entrez ID1874
Gene full nameE2F transcription factor 4, p107/p130-binding
Other gene symbolsE2F-4
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:0000083Regulation of transcription involved in G1/S transition of mitotic cell cycleIEAbiological_process
GO:0000278Mitotic cell cycleIEA TASbiological_process
GO:0002064Epithelial cell developmentIEAbiological_process
GO:0003677DNA bindingIEA IMPmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityIDA IEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIEAcellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005667Transcription factor complexIEAcellular_component
GO:0006351Transcription, DNA-templatedIEA TASbiological_process
GO:0006367Transcription initiation from RNA polymerase II promoterTASbiological_process
GO:0006884Cell volume homeostasisIEAbiological_process
GO:0007179Transforming growth factor beta receptor signaling pathwayTASbiological_process
GO:0008015Blood circulationIEAbiological_process
GO:0008134Transcription factor bindingIPImolecular_function
GO:0008361Regulation of cell sizeIEAbiological_process
GO:0009887Organ morphogenesisIEAbiological_process
GO:0010467Gene expressionTASbiological_process
GO:0019904Protein domain specific bindingIPImolecular_function
GO:0042127Regulation of cell proliferationIEAbiological_process
GO:0042384Cilium assemblyIEAbiological_process
GO:0045944Positive regulation of transcription from RNA polymerase II promoterTASbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.40500865470.55308243230.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.0254057936
GSE13712_SHEARUp0.0524551712
GSE13712_STATICDown-0.0827385160
GSE19018Down-0.2587117303
GSE19899_A1Down-0.0664535865
GSE19899_A2Up0.2137525496
PubMed_21979375_A1Up1.0657679139
PubMed_21979375_A2Up0.4512782499
GSE35957Up0.0957061460
GSE36640Down-0.0998823989
GSE54402Up0.3010681317
GSE9593Down-0.0036439961
GSE43922Up0.1905066966
GSE24585Down-0.5388511915
GSE37065Down-0.0777073044
GSE28863_A1Down-0.0622204789
GSE28863_A2Up0.1638158551
GSE28863_A3Down-0.4692665345
GSE28863_A4Up0.0322407242
GSE48662Up0.0845428863

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-124-3pMIMAT0000422MIRT022270MicroarrayFunctional MTI (Weak)18668037
hsa-miR-615-3pMIMAT0003283MIRT039886CLASHFunctional MTI (Weak)23622248
hsa-miR-23b-3pMIMAT0000418MIRT046375CLASHFunctional MTI (Weak)23622248
hsa-miR-197-3pMIMAT0000227MIRT048137CLASHFunctional MTI (Weak)23622248
hsa-miR-98-5pMIMAT0000096MIRT048712CLASHFunctional 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: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

22002537Recruitment of PML to the TBX2 promoter is dependent on a functional p130/E2F4 repressor complex ultimately implementing a transcriptionally inactive chromatin environment at the TBX2 promoter
10585280Here we present evidence that activation of a cAMP pathway correlates with multiple cellular changes in these cells: (1) increased expression of the transcription factor microphthalmia; (2) increased melanogenesis; (3) increased association of the cyclin-dependent kinase inhibitors (CDK-Is) p27(KIP1) and p16(INK4) with CDK2 and CDK4, respectively; (4) failure to phosphorylate the retinoblastoma protein (pRB); (5) decreased expression of E2F1, E2F2, and E2F4 proteins; (6) loss of E2F DNA-binding activity; and (7) phenotypic changes characteristic of senescent cells
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