HCSGD entry for TBL1XR1


1. General information

Official gene symbolTBL1XR1
Entrez ID79718
Gene full nametransducin (beta)-like 1 X-linked receptor 1
Other gene symbolsC21 DC42 IRA1 TBLR1
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:0000118Histone deacetylase complexIDAcellular_component
GO:0000122Negative regulation of transcription from RNA polymerase II promoterIDAbiological_process
GO:0003714Transcription corepressor activityIDA IEA IGImolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDAcellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005730NucleolusIDAcellular_component
GO:0005876Spindle microtubuleIDAcellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0007219Notch signaling pathwayTASbiological_process
GO:0008013Beta-catenin bindingIPImolecular_function
GO:0016568Chromatin modificationIEAbiological_process
GO:0017053Transcriptional repressor complexIDAcellular_component
GO:0042393Histone bindingIDAmolecular_function
GO:0043161Proteasome-mediated ubiquitin-dependent protein catabolic processIEA ISSbiological_process
GO:0044212Transcription regulatory region DNA bindingIDA IEA ISSmolecular_function
GO:0044255Cellular lipid metabolic processTASbiological_process
GO:0044281Small molecule metabolic processTASbiological_process
GO:0045892Negative regulation of transcription, DNA-templatedIEAbiological_process
GO:0045893Positive regulation of transcription, DNA-templatedIDAbiological_process
GO:0045944Positive regulation of transcription from RNA polymerase II promoterIDA IEAbiological_process
GO:0047485Protein N-terminus bindingIPImolecular_function
GO:0060070Canonical Wnt signaling pathwayIMPbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.99154143080.00399002700.99999024730.1281476829

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

Data sourceUp or downLog fold change
GSE11954Down-0.4560064728
GSE13712_SHEARUp0.0150518913
GSE13712_STATICUp0.0783169474
GSE19018Up0.0532847822
GSE19899_A1Down-0.2850603706
GSE19899_A2Down-0.6778581731
PubMed_21979375_A1Down-0.7420103873
PubMed_21979375_A2Down-0.4315905820
GSE35957Up0.2571891515
GSE36640Down-0.4995973326
GSE54402Down-0.2312827012
GSE9593Down-0.2474759925
GSE43922Down-0.3361085855
GSE24585Down-0.4238918415
GSE37065Down-0.1289660283
GSE28863_A1Down-0.6145723561
GSE28863_A2Down-0.3805468276
GSE28863_A3Down-0.6681016946
GSE28863_A4Down-0.5057527858
GSE48662Up0.3712141360

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-148b-3pMIMAT0000759MIRT019306MicroarrayFunctional MTI (Weak)17612493
hsa-miR-122-5pMIMAT0000421MIRT023246MicroarrayFunctional MTI (Weak)17612493
hsa-miR-21-5pMIMAT0000076MIRT030705MicroarrayFunctional MTI (Weak)18591254
hsa-miR-30c-5pMIMAT0000244MIRT047851CLASHFunctional 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: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25487516We demonstrate for the first time that the high-affinity, non-peptide AT(2) receptor agonist, Compound 21 (C21), penetrates the cell membrane of quiescent SK-UT-1 cells, activates intracellular AT(2) receptors and induces rapid cell death; approximately 70% of cells died within 24 h
25487516All quiescent SK-UT-1 cells died within 5 days after treatment with a single dose of C21
25487516C21 was devoid of cytotoxic effects in proliferating SK-UT-1 cells and in quiescent HutSMC
15561193The formation of these compounds is attributed to the involvement of enzymatic processes acting specifically on the C-21 or C-22 allylic carbon and the omega15 double bond of methyl and ethyl alkenones respectively
15561193The structures of these compounds indicate that they are derivatives of methyl and ethyl alkenones with an additional carbonyl group on the C-21 or C-22 carbon respectively and without the omega15 double bond
15561193We propose that these compounds are formed by an initial regiospecific lipoxygenase-catalyzed peroxidation of methyl and ethyl alkenones on their C-21 or C-22 allylic carbon, respectively
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