HCSGD entry for DDIT4


1. General information

Official gene symbolDDIT4
Entrez ID54541
Gene full nameDNA-damage-inducible transcript 4
Other gene symbolsDig2 REDD-1 REDD1
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0001666Response to hypoxiaIDAbiological_process
GO:0001764Neuron migrationISSbiological_process
GO:0005622IntracellularIDAcellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0005739MitochondrionIEAcellular_component
GO:0005829CytosolIEAcellular_component
GO:0007420Brain developmentISSbiological_process
GO:0008283Cell proliferationISSbiological_process
GO:0010801Negative regulation of peptidyl-threonine phosphorylationISSbiological_process
GO:0030182Neuron differentiationISSbiological_process
GO:0032007Negative regulation of TOR signalingIMPbiological_process
GO:0033137Negative regulation of peptidyl-serine phosphorylationISSbiological_process
GO:0042771Intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorISSbiological_process
GO:0043241Protein complex disassemblyIEAbiological_process
GO:0045820Negative regulation of glycolysisIEAbiological_process
GO:0048011Neurotrophin TRK receptor signaling pathwayISSbiological_process
GO:0051607Defense response to virusIEAbiological_process
GO:007188914-3-3 protein bindingIEAmolecular_function
GO:0072593Reactive oxygen species metabolic processIEAbiological_process
GO:1901216Positive regulation of neuron deathISSbiological_process
GO:1902532Negative regulation of intracellular signal transductionISSbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.07879861710.00892678470.59099997150.1870715764

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

Data sourceUp or downLog fold change
GSE11954Down-0.5172705587
GSE13712_SHEARDown-0.4979729756
GSE13712_STATICDown-0.3677994980
GSE19018Up2.9068879785
GSE19899_A1Up0.2658405298
GSE19899_A2Down-0.9909866906
PubMed_21979375_A1Up0.0087257774
PubMed_21979375_A2Down-0.3998893363
GSE35957Down-1.6285648962
GSE36640Down-1.1937187274
GSE54402Down-0.6975915872
GSE9593Down-0.4906777410
GSE43922Up0.9067213384
GSE24585Up0.1403217976
GSE37065Down-0.5962776088
GSE28863_A1Down-0.1984496455
GSE28863_A2Down-0.3298025078
GSE28863_A3Up0.3574625314
GSE28863_A4Down-0.0460679308
GSE48662Up0.1290496855

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-221-3pMIMAT0000278MIRT003358Luciferase reporter assay//Microarray//qRT-PCR//Western blot//Reporter assay;Western blot;qRT-PCR;Microarray;OtherFunctional MTI20018759
hsa-miR-221-3pMIMAT0000278MIRT003358SequencingFunctional MTI (Weak)20371350
hsa-miR-181a-5pMIMAT0000256MIRT005575Immunoblot//Luciferase reporter assay//qRT-PCRFunctional MTI21274007
hsa-miR-124-3pMIMAT0000422MIRT022661MicroarrayFunctional MTI (Weak)18668037
hsa-miR-101-3pMIMAT0000099MIRT027381SequencingFunctional MTI (Weak)20371350
hsa-miR-615-3pMIMAT0003283MIRT040402CLASHFunctional 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-221-3pMIMAT00002781hsa-miR-221{Western blot}{overexpression by miRNA precursor transfection}20018759
hsa-miR-221-3pMIMAT00002782hsa-miR-221{Western blot}{overexpression by miRNA precursor transfection}20018759
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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

22627671Overexpression of REDD1 (Regulated in DNA Damage Response and Development), a negative regulator of TORC1, delays the onset of replicative senescence
20647331Coincident with these DNA damage markers, the level of p53 protein and genes transcriptionally activated by p53, such as p21, TP53INP1, and DDIT4, increased
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