HCSGD entry for PRMT5


1. General information

Official gene symbolPRMT5
Entrez ID10419
Gene full nameprotein arginine methyltransferase 5
Other gene symbolsHRMT1L5 IBP72 JBP1 SKB1 SKB1Hs
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:0000122Negative regulation of transcription from RNA polymerase II promoterIEAbiological_process
GO:0000387Spliceosomal snRNP assemblyIMP TASbiological_process
GO:0003682Chromatin bindingIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDA IEA NAScellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0005829CytosolIDA TAScellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0006479Protein methylationIEAbiological_process
GO:0007088Regulation of mitosisTASbiological_process
GO:0008168Methyltransferase activityIDA IEAmolecular_function
GO:0008283Cell proliferationTASbiological_process
GO:0008469Histone-arginine N-methyltransferase activityIEAmolecular_function
GO:0010467Gene expressionTASbiological_process
GO:0016070RNA metabolic processTASbiological_process
GO:0018216Peptidyl-arginine methylationIMPbiological_process
GO:0019918Peptidyl-arginine methylation, to symmetrical-dimethyl arginineIMPbiological_process
GO:0034660NcRNA metabolic processTASbiological_process
GO:0034709MethylosomeIDAcellular_component
GO:0035243Protein-arginine omega-N symmetric methyltransferase activityIMPmolecular_function
GO:0035246Peptidyl-arginine N-methylationIDAbiological_process
GO:0042118Endothelial cell activationIMPbiological_process
GO:0043021Ribonucleoprotein complex bindingIPImolecular_function
GO:0043234Protein complexIEAcellular_component
GO:0043985Histone H4-R3 methylationNASbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.04010167930.87403277230.44950306511.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.4962077840
GSE13712_SHEARUp0.2773535193
GSE13712_STATICUp0.2462221769
GSE19018Down-0.2449619829
GSE19899_A1Up0.6629463876
GSE19899_A2Up0.5518936842
PubMed_21979375_A1Up1.1473528988
PubMed_21979375_A2Up0.6936869526
GSE35957Down-0.4943075300
GSE36640Down-0.2177310269
GSE54402Up0.1441920904
GSE9593Down-0.2786022142
GSE43922Up0.2466408626
GSE24585Down-0.1706102712
GSE37065Up0.0447633345
GSE28863_A1Down-0.0294343130
GSE28863_A2Up0.2284231335
GSE28863_A3Down-0.4841731074
GSE28863_A4Up0.2772863496
GSE48662Down-0.0705938020

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-32-5pMIMAT0000090MIRT000982Western blotFunctional MTI18694959
hsa-miR-25-3pMIMAT0000081MIRT000983Western blotFunctional MTI18694959
hsa-miR-19a-3pMIMAT0000073MIRT004350Western blotFunctional MTI18694959
hsa-miR-92b-3pMIMAT0003218MIRT004351Western blotFunctional MTI18694959
hsa-miR-96-5pMIMAT0000095MIRT004352Western blotFunctional MTI18694959
hsa-miR-346MIMAT0000773MIRT042720CLASHFunctional MTI (Weak)23622248
hsa-miR-320aMIMAT0000510MIRT044499CLASHFunctional 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: 1 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

18676353When the expression of protein arginine methyltransferases (PRMTs), namely PRMT1, PRMT4, PRMT5 and PRMT6 was examined, a significant reduction was found in replicatively senescent cells as well as their catalytic activities against histone mixtures compared with the young cells
18676353In contrast, both up- and down-regulations of symmetrically arginine-methylated proteins (the product of type II PRMTs including PRMT5) during replicative senescence were found
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