HCSGD entry for GMNN


1. General information

Official gene symbolGMNN
Entrez ID51053
Gene full namegeminin, DNA replication inhibitor
Other gene symbolsGem
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:0000278Mitotic cell cycleTASbiological_process
GO:0003714Transcription corepressor activityIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDA IEAcellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0005829CytosolTAScellular_component
GO:0006461Protein complex assemblyIEAbiological_process
GO:0008156Negative regulation of DNA replicationIDA IEAbiological_process
GO:0009887Organ morphogenesisIEAbiological_process
GO:0042826Histone deacetylase bindingIPImolecular_function
GO:0045786Negative regulation of cell cycleIDA IEAbiological_process
GO:0045892Negative regulation of transcription, DNA-templatedIDA IEAbiological_process
GO:0070491Repressing transcription factor bindingIEAmolecular_function
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.98253905250.00006505070.99999024730.0132728682

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

Data sourceUp or downLog fold change
GSE11954Down-1.5516871083
GSE13712_SHEARUp0.1047041817
GSE13712_STATICUp0.0503835457
GSE19018Down-0.4500308526
GSE19899_A1Down-3.0281470180
GSE19899_A2Down-2.9099244575
PubMed_21979375_A1Down-2.2159295914
PubMed_21979375_A2Down-3.5611325697
GSE35957Down-3.2151426030
GSE36640Down-3.4041850271
GSE54402Down-0.6220705830
GSE9593Down-1.3558615304
GSE43922Down-1.1584295104
GSE24585Up0.0910455559
GSE37065Up0.4387969554
GSE28863_A1Down-0.1375069962
GSE28863_A2Up0.9105455806
GSE28863_A3Down-0.0997274751
GSE28863_A4Down-0.0747562649
GSE48662Down-1.1466016353

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-449b-5pMIMAT0003327MIRT006352Luciferase reporter assay//Western blotFunctional MTI21418558
hsa-miR-449aMIMAT0001541MIRT006345Luciferase reporter assay//Western blotFunctional MTI21418558
hsa-miR-193b-3pMIMAT0002819MIRT016570MicroarrayFunctional MTI (Weak)20304954
hsa-miR-26b-5pMIMAT0000083MIRT029967MicroarrayFunctional MTI (Weak)19088304
hsa-miR-324-5pMIMAT0000761MIRT043150CLASHFunctional 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: 1 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

23142824Reduced Geminin levels promote cellular senescence
23142824Cdt1 is a central regulator of DNA replication licensing acting during the G1 phase and it is negatively controlled by Geminin
23142824Here, we characterize the cell cycle expression pattern of Cdt1 and Geminin during successive passages of primary fibroblasts and compare it to tumour-derived cell lines
23142824Cdt1 and Geminin are strictly expressed in distinct subpopulations of young fibroblasts, similarly to cancer cells, with Geminin accumulating shortly after the onset of S phase
23142824Cdt1 and Geminin are down-regulated when primary human and mouse fibroblasts undergo replicative or stress-induced senescence
23142824RNAi-mediated Geminin knock-down in human cells enhances the appearance of phenotypic and molecular features of senescence
23142824Mouse embryonic fibroblasts heterozygous for Geminin exhibit accelerated senescence compared to control fibroblasts
23142824In contrast, ectopic expression of Geminin in mouse embryonic fibroblasts delays the appearance of the senescent phenotype
23142824Taken together, our data suggest that changes in Geminin expression levels affect the establishment of senescence pathways
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