HCSGD entry for CCND2


1. General information

Official gene symbolCCND2
Entrez ID894
Gene full namecyclin D2
Other gene symbolsKIAK0002
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0000307Cyclin-dependent protein kinase holoenzyme complexIDAcellular_component
GO:0000785ChromatinIDAcellular_component
GO:0001934Positive regulation of protein phosphorylationIDAbiological_process
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDAcellular_component
GO:0005730NucleolusIDAcellular_component
GO:0005829CytosolIDAcellular_component
GO:0007049Cell cycleIEAbiological_process
GO:0019901Protein kinase bindingIPImolecular_function
GO:0031965Nuclear membraneIDAcellular_component
GO:0045737Positive regulation of cyclin-dependent protein kinase activityIDAbiological_process
GO:0051301Cell divisionIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.00002100980.64279019410.01490638301.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.9265820680
GSE13712_SHEARDown-0.2890798655
GSE13712_STATICDown-0.2579621530
GSE19018Down-0.1487223449
GSE19899_A1Up0.8573231136
GSE19899_A2Up2.5026618162
PubMed_21979375_A1Up3.5947678733
PubMed_21979375_A2Up3.4501311850
GSE35957Up2.2621266987
GSE36640Up7.4299828743
GSE54402Up0.2617760397
GSE9593Up0.1729791094
GSE43922Up1.9118643823
GSE24585Down-1.5870190069
GSE37065Up0.6411269411
GSE28863_A1Up0.1828215164
GSE28863_A2Up1.7799769557
GSE28863_A3Up0.4318234165
GSE28863_A4Up0.0160112037
GSE48662Up0.8101403617

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-26a-5pMIMAT0000082MIRT000112Luciferase reporter assay//Western blotFunctional MTI19524505
hsa-miR-15a-5pMIMAT0000068MIRT000285Luciferase reporter assayFunctional MTI19549910
hsa-miR-15a-5pMIMAT0000068MIRT000285CLASHFunctional MTI (Weak)23622248
hsa-miR-16-5pMIMAT0000069MIRT003431SequencingFunctional MTI (Weak)20371350
hsa-miR-302b-3pMIMAT0000715MIRT003555Luciferase reporter assay//Western blotFunctional MTI18930031
hsa-let-7b-5pMIMAT0000063MIRT003835Luciferase reporter assayFunctional MTI17699775
hsa-let-7b-5pMIMAT0000063MIRT003835qRT-PCRFunctional MTI (Weak)17942906
hsa-let-7a-5pMIMAT0000062MIRT005478Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI20418948
hsa-miR-302d-3pMIMAT0000718MIRT005673Luciferase reporter assay//Microarray//Northern blot//Western blotFunctional MTI21062975
hsa-miR-17-5pMIMAT0000070MIRT005848Luciferase reporter assayFunctional MTI21283765
hsa-miR-17-5pMIMAT0000070MIRT005848CLASHFunctional MTI (Weak)23622248
hsa-miR-20a-5pMIMAT0000075MIRT005854Luciferase reporter assayFunctional MTI21283765
hsa-miR-106b-5pMIMAT0000680MIRT005862Luciferase reporter assayFunctional MTI21283765
hsa-miR-182-5pMIMAT0000259MIRT007064Flow//Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI22848417
hsa-miR-206MIMAT0000462MIRT007217Luciferase reporter assayFunctional MTI23348698
hsa-miR-206MIMAT0000462MIRT007217Luciferase reporter assayFunctional MTI23466356
hsa-miR-335-5pMIMAT0000765MIRT018710MicroarrayFunctional MTI (Weak)18185580
hsa-miR-196a-5pMIMAT0000226MIRT026074SequencingFunctional MTI (Weak)20371350
hsa-miR-19b-3pMIMAT0000074MIRT031274SequencingFunctional MTI (Weak)20371350
hsa-miR-877-3pMIMAT0004950MIRT036978CLASHFunctional MTI (Weak)23622248
hsa-miR-877-5pMIMAT0004949MIRT037251CLASHFunctional MTI (Weak)23622248
hsa-miR-423-5pMIMAT0004748MIRT038097CLASHFunctional MTI (Weak)23622248
hsa-miR-615-3pMIMAT0003283MIRT040184CLASHFunctional MTI (Weak)23622248
hsa-miR-324-3pMIMAT0000762MIRT042861CLASHFunctional MTI (Weak)23622248
hsa-miR-342-3pMIMAT0000753MIRT043702CLASHFunctional MTI (Weak)23622248
hsa-miR-378a-3pMIMAT0000732MIRT043920CLASHFunctional MTI (Weak)23622248
hsa-miR-301a-3pMIMAT0000688MIRT044222CLASHFunctional MTI (Weak)23622248
hsa-miR-320aMIMAT0000510MIRT044790CLASHFunctional MTI (Weak)23622248
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    • mirRecord

MicroRNA name

mirBase ID

Target site number

MiRNA mature ID

Test method inter

MiRNA regulation site

Reporter target site

Pubmed ID

hsa-miR-302b-3pMIMAT00007151hsa-miR-302b18930031
hsa-miR-302d-3pMIMAT00007181hsa-miR-302d{Western blot}{overexpression by miRNA mimics tranfection}21062975
hsa-miR-302d-3pMIMAT00007182hsa-miR-302d{Western blot}{overexpression by miRNA mimics tranfection}21062975
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6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 6 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25540416EBNA3A was at MYC, CDKN2A/B, CCND2, CXCL9/10, and BCL2, together with RUNX3, BATF, IRF4, and SPI1
21047732Paradoxically, G(1)-S phase genes such as MYC, CDK4, CDK6, CCND1, and CCND2 were strongly downregulated, in line with the observed G(1) arrest
20622962Downregulated genes included cyclin D2, keratin 8, insulin-like growth factor 2 (IGF2), natriuretic peptide precursor B (NPPB) and cellular retinoic acid binding protein 2 (CRABP2)
19693768Fifteen cell-cycle regulator genes were investigated and only three genes (APC, CCND2, and BMP2) were differentially expressed between bMSC and oMSC
10951233Cyclin D2, which is regulated by extracellular-signal-regulated kinase and functions to promote cell cycle progression, was reduced 50% in old skin compared with young skin
9584157Increased expression of cyclin D2 during multiple states of growth arrest in primary and established cells
9584157Cyclin D2 is a member of the family of D-type cyclins that is implicated in cell cycle regulation, differentiation, and oncogenic transformation
9584157To better understand the role of this cyclin in the control of cell proliferation, cyclin D2 expression was monitored under various growth conditions in primary human and established murine fibroblasts
9584157In different states of cellular growth arrest initiated by contact inhibition, serum starvation, or cellular senescence, marked increases (5- to 20-fold) were seen in the expression levels of cyclin D2 mRNA and protein
9584157Indirect immunofluorescence studies showed that cyclin D2 protein localized to the nucleus in G0, suggesting a nuclear function for cyclin D2 in quiescent cells
9584157Cyclin D2 was also found to be associated with the cyclin-dependent kinases CDK2 and CDK4 but not CDK6 during growth arrest
9584157Transient transfection and needle microinjection of cyclin D2 expression constructs demonstrated that overexpression of cyclin D2 protein efficiently inhibited cell cycle progression and DNA synthesis
9584157These data suggest that in addition to a role in promoting cell cycle progression through phosphorylation of retinoblastoma family proteins in some cell systems, cyclin D2 may contribute to the induction and/or maintenance of a nonproliferative state, possibly through sequestration of the CDK2 catalytic subunit
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