HCSGD entry for CDKN2C


1. General information

Official gene symbolCDKN2C
Entrez ID1031
Gene full namecyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
Other gene symbolsINK4C p18 p18-INK4C
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:0000079Regulation of cyclin-dependent protein serine/threonine kinase activityIDAbiological_process
GO:0000082G1/S transition of mitotic cell cycleIDAbiological_process
GO:0000278Mitotic cell cycleTASbiological_process
GO:0004861Cyclin-dependent protein serine/threonine kinase inhibitor activityIDAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDAcellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0005829CytosolTAScellular_component
GO:0006469Negative regulation of protein kinase activityIDAbiological_process
GO:0007050Cell cycle arrestIDAbiological_process
GO:0008285Negative regulation of cell proliferationIDAbiological_process
GO:0019901Protein kinase bindingIPImolecular_function
GO:0030308Negative regulation of cell growthIDAbiological_process
GO:0042326Negative regulation of phosphorylationIDAbiological_process
GO:0043086Negative regulation of catalytic activityIDAbiological_process
GO:0048709Oligodendrocyte differentiationIEAbiological_process
GO:0071901Negative regulation of protein serine/threonine kinase activityIDAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.99750654990.00005287410.99999024730.0118779661

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

Data sourceUp or downLog fold change
GSE11954Down-1.0894602962
GSE13712_SHEARDown-1.5431740742
GSE13712_STATICDown-1.4375300633
GSE19018Down-0.0079889917
GSE19899_A1Down-1.3362046766
GSE19899_A2Down-3.3226651426
PubMed_21979375_A1Down-1.5010976104
PubMed_21979375_A2Down-4.5158534897
GSE35957Down-2.3120923891
GSE36640Down-3.4892766843
GSE54402Down-0.8652892242
GSE9593Down-1.3416836523
GSE43922Down-0.1855743861
GSE24585Down-0.0763226579
GSE37065Down-0.2467531991
GSE28863_A1Up0.1844127697
GSE28863_A2Up0.2201459256
GSE28863_A3Down-0.6357614936
GSE28863_A4Up0.1523172781
GSE48662Down-0.8872569542

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-5pMIMAT0000255MIRT025585Reporter assay;qRT-PCRFunctional MTI21128241
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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: 5 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

22548705In the absence of the Cdk4-inhibitor p18Ink4c, cell cycle exit was delayed but most cells eventually showed a senescent phenotype
22548705We found that the p53 pathway was intact in tumors arising in a p18Ink4c-/- background, indicating that the two genes represent distinct tumor suppressor pathways
22548705Upon tumor progression, both p18Ink4c-/- and p53-/- tumors showed increased Cdk2 expression
16288006Interestingly, we also found that, in the absence of p16INK4a, reexpression of hSNF5 also increased protein levels of a second cyclin-dependent kinase (CDK) inhibitor, p18INK4c
16150936Of interest, the induction of HSC senescence was associated with a prolonged elevation of p21(Cip1/Waf1), p19(Arf), and p16(Ink4a) mRNA expression, while the expression of p27(Kip1) and p18(Ink4c) mRNA was not increased following TBI
10851091Assembly and activity of the proto-oncogenic cyclin D/CDK4(6) complexes, the major driving force of G1 phase progression, is negatively regulated by a family of INK4 CDK inhibitors p16INK4a, p15INK4b, p18INK4c, and p19INK4d
9244355Both p18INK4c and p19INK4d were widely expressed during mouse embryogenesis, but p16INK4a and p15INK4b were not readily detected prenatally
9244355Although p15INK4b, p18INK4c and p19INK4d were demonstrated in many tissues by 4 weeks after birth, p16INK4a protein expression was restricted to the lung and spleen of older mice, with increased, more widespread mRNA expression during aging
9244355The levels of p16INK4a and p18INK4c, but not p15INK4b or p19INK4d, further increased as MEFs approached senescence
9244355Whereas p18INK4c and p19INK4d may regulate pre- and postnatal development, p16INK4a more likely plays a checkpoint function during cell senescence that underscores its selective role as a tumor suppressor
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