HCSGD entry for CCND3


1. General information

Official gene symbolCCND3
Entrez ID896
Gene full namecyclin D3
Other gene symbols
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:0000307Cyclin-dependent protein kinase holoenzyme complexIDAcellular_component
GO:0001934Positive regulation of protein phosphorylationIDAbiological_process
GO:0004693Cyclin-dependent protein serine/threonine kinase activityIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIEAcellular_component
GO:0005737CytoplasmIEAcellular_component
GO:0007165Signal transductionIEAbiological_process
GO:0016020MembraneIEAcellular_component
GO:0019901Protein kinase bindingIPImolecular_function
GO:0042098T cell proliferationIEAbiological_process
GO:0045737Positive regulation of cyclin-dependent protein kinase activityIDAbiological_process
GO:0051301Cell divisionIEAbiological_process
GO:0051726Regulation of cell cycleIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.58140132590.29447337870.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.4513180445
GSE13712_SHEARUp0.1350005941
GSE13712_STATICUp0.2678649871
GSE19018Down-0.1971268143
GSE19899_A1Down-0.6309389789
GSE19899_A2Up0.0957100895
PubMed_21979375_A1Down-0.3735957900
PubMed_21979375_A2Down-0.1767557547
GSE35957Down-0.1640605236
GSE36640Up0.6631860888
GSE54402Up0.0434358550
GSE9593Down-0.1434185312
GSE43922Down-0.0927765611
GSE24585Down-0.3208656059
GSE37065Up0.0219833191
GSE28863_A1Down-0.0742603870
GSE28863_A2Up0.2359975226
GSE28863_A3Up0.0374084190
GSE28863_A4Down-0.1447462594
GSE48662Up0.1983208100

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-424-5pMIMAT0001341MIRT000937qRT-PCR//flow//Luciferase reporter assay//Western blotFunctional MTI18701644
hsa-miR-16-5pMIMAT0000069MIRT000940qRT-PCR//flow//Luciferase reporter assay//Western blotFunctional MTI18701644
hsa-miR-34a-5pMIMAT0000255MIRT001010Western blotNon-Functional MTI18406353
hsa-miR-195-5pMIMAT0000461MIRT006246Luciferase reporter assay//Western blotFunctional MTI22217655
hsa-miR-138-5pMIMAT0000430MIRT006299Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI22362728
hsa-miR-615-3pMIMAT0003283MIRT039712CLASHFunctional MTI (Weak)23622248
hsa-miR-324-5pMIMAT0000761MIRT043067CLASHFunctional MTI (Weak)23622248
hsa-miR-27b-3pMIMAT0000419MIRT046238CLASHFunctional MTI (Weak)23622248
hsa-let-7b-5pMIMAT0000063MIRT052181CLASHFunctional 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-16-5pMIMAT0000069NAhsa-miR-16{Western blot}{overexpression}18701644
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6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 4 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

23079655Ablation of cyclin D3 in mice bearing Notch1-driven T cell acute lymphoblastic leukemias (T-ALL) triggered tumor cell apoptosis
19433493PTTG1 activates cyclin D3 and represses p21 expression, indicating a role in cell cycle regulation and cell senescence
17519288In HeLa cells, RNAi-induced downregulation of BAF significantly increased the proportion of early S-phase cells that retained high levels of cyclin D3 and cyclin E expression and slowed progression through early S phase
1409718To determine if expression of human D-type cyclin genes correlates with the state of cell growth, we examined the level of mRNAs for CCND1 and a related gene, CCND3, in normal human diploid fibroblasts (HDF)
1409718Cycloheximide partially blocks the induction of CCND1 and CCND3 gene expression by serum, suggesting that both de novo protein synthesis-dependent and -independent pathways contribute to induction
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