HCSGD entry for ZMYND11


1. General information

Official gene symbolZMYND11
Entrez ID10771
Gene full namezinc finger, MYND-type containing 11
Other gene symbolsBRAM1 BS69
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:0000122Negative regulation of transcription from RNA polymerase II promoterTASbiological_process
GO:0003677DNA bindingIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDAcellular_component
GO:0005694ChromosomeIEAcellular_component
GO:0005730NucleolusIDAcellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0007049Cell cycleIEAbiological_process
GO:0008270Zinc ion bindingIEAmolecular_function
GO:0008283Cell proliferationTASbiological_process
GO:0016032Viral processIEAbiological_process
GO:0016568Chromatin modificationIEAbiological_process
GO:0043124Negative regulation of I-kappaB kinase/NF-kappaB signalingIMPbiological_process
GO:0046329Negative regulation of JNK cascadeIMPbiological_process
GO:2001237Negative regulation of extrinsic apoptotic signaling pathwayIMPbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.71335832990.47190442610.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.0138377526
GSE13712_SHEARDown-0.1456886238
GSE13712_STATICDown-0.2826357665
GSE19018Up0.0001367168
GSE19899_A1Down-0.2579608944
GSE19899_A2Down-0.2462796316
PubMed_21979375_A1Up0.0444403227
PubMed_21979375_A2Down-0.1868223166
GSE35957Up0.2009073586
GSE36640Down-0.0343812058
GSE54402Up0.0622909721
GSE9593Up0.2587006136
GSE43922Down-0.1816772478
GSE24585Up0.0803021291
GSE37065Down-0.0236852918
GSE28863_A1Up0.2889293650
GSE28863_A2Down-0.0062833877
GSE28863_A3Down-0.2631809544
GSE28863_A4Up0.0963455397
GSE48662Up0.3634481915

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-361-5pMIMAT0000703MIRT020086SequencingFunctional MTI (Weak)20371350
hsa-miR-215-5pMIMAT0000272MIRT024469MicroarrayFunctional MTI (Weak)19074876
hsa-miR-192-5pMIMAT0000222MIRT026851MicroarrayFunctional MTI (Weak)19074876
hsa-miR-324-5pMIMAT0000761MIRT043022CLASHFunctional MTI (Weak)23622248
hsa-miR-125b-5pMIMAT0000423MIRT045941CLASHFunctional MTI (Weak)23622248
hsa-miR-27b-3pMIMAT0000419MIRT046219CLASHFunctional MTI (Weak)23622248
hsa-miR-222-3pMIMAT0000279MIRT046758CLASHFunctional 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

19944017We found that the chromatin modifier-encoding genes Eu-HMTase1, ZMYND11, and RASA3 were overexpressed in adults
17721438BS69 is involved in cellular senescence through the p53-p21Cip1 pathway
17721438The multidomain-containing cellular protein BS69 interacts with adenovirus E1A and several other viral and cellular factors, and acts as a transcription repressor
17721438Here, we show that BS69 is involved in the p53-p21Cip1-mediated senescence pathway
17721438Knockdown of BS69 by RNA interference in human primary fibroblasts results in elevated levels of p21Cip1 and the appearance of several senescent markers, including enhanced senescence-associated beta-galactosidase activity and formation of senescence-associated heterochromatin foci
17721438Importantly, knockdown of either p53 or p21Cip1, but not p16(INK4a) or Rb, allows cells to bypass premature senescence that is induced by BS69 knockdown
17721438Furthermore, we show that BS69 forms complexes with both p53 and p400, and that BS69 associates with the p21Cip1 promoter through p53
17721438Together, our data indicate that BS69 is involved in cellular senescence mainly through the p53-p21Cip1 pathway
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