HCSGD entry for KHDRBS1


1. General information

Official gene symbolKHDRBS1
Entrez ID10657
Gene full nameKH domain containing, RNA binding, signal transduction associated 1
Other gene symbolsSam68 p62 p68
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:0000086G2/M transition of mitotic cell cycleISSbiological_process
GO:0003677DNA bindingTASmolecular_function
GO:0003723RNA bindingIDAmolecular_function
GO:0005070SH3/SH2 adaptor activityIPImolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDAcellular_component
GO:0005737CytoplasmIEAcellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0006397MRNA processingTASbiological_process
GO:0007050Cell cycle arrestTASbiological_process
GO:0007165Signal transductionTASbiological_process
GO:0007166Cell surface receptor signaling pathwayIDAbiological_process
GO:0008143Poly(A) bindingIDAmolecular_function
GO:0008266Poly(U) RNA bindingIDAmolecular_function
GO:0008283Cell proliferationTASbiological_process
GO:0009967Positive regulation of signal transductionIPIbiological_process
GO:0016020MembraneIDAcellular_component
GO:0017124SH3 domain bindingIEAmolecular_function
GO:0031647Regulation of protein stabilityIDAbiological_process
GO:0032403Protein complex bindingIEAmolecular_function
GO:0045892Negative regulation of transcription, DNA-templatedISSbiological_process
GO:0045948Positive regulation of translational initiationIDAbiological_process
GO:0046831Regulation of RNA export from nucleusISSbiological_process
GO:0046833Positive regulation of RNA export from nucleusIDAbiological_process
GO:0070618Grb2-Sos complexIEAcellular_component
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.97322420120.03516783940.99999024730.3549281825

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

Data sourceUp or downLog fold change
GSE11954Down-0.0462591000
GSE13712_SHEARDown-0.2014596177
GSE13712_STATICDown-0.1746459234
GSE19018Down-0.2309161940
GSE19899_A1Down-0.4111328842
GSE19899_A2Down-0.3304829868
PubMed_21979375_A1Down-0.3569473453
PubMed_21979375_A2Down-0.3091810206
GSE35957Down-0.7094447469
GSE36640Down-0.9456690739
GSE54402Up0.2094164878
GSE9593Down-0.3034078739
GSE43922Down-0.3663043839
GSE24585Up0.0117532694
GSE37065Down-0.1024549296
GSE28863_A1Up0.3538931862
GSE28863_A2Up0.4353673969
GSE28863_A3Down-0.0965544368
GSE28863_A4Down-0.0278707302
GSE48662Down-0.5680703786

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-877-3pMIMAT0004950MIRT037105CLASHFunctional MTI (Weak)23622248
hsa-miR-615-3pMIMAT0003283MIRT040001CLASHFunctional MTI (Weak)23622248
hsa-miR-18a-3pMIMAT0002891MIRT040829CLASHFunctional MTI (Weak)23622248
hsa-miR-27b-3pMIMAT0000419MIRT046222CLASHFunctional MTI (Weak)23622248
hsa-miR-34a-5pMIMAT0000255MIRT047357CLASHFunctional MTI (Weak)23622248
hsa-miR-92a-3pMIMAT0000092MIRT049690CLASHFunctional 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

17726370Therefore, the aims of the present study were to refine the feedback regulation of protein arginine methylation using one of the heavily methylated proteins, an RNA-binding protein Sam68, as a prototype, to elucidate the relations between Sam68 methylation and tyrosine phosphorylation and the role of methylation in RNA binding and subcellular distribution, as well as the cellular consequences of reduced protein methylation
17726370Screening pro-atherogenic substances known to induce endothelial dysfunction showed that ADMA did not affect the level of arginine methylation of Sam68, whereas peroxynitrite was a strong inhibitor of methylation
17726370Advanced glycation-modified collagen I, which accumulates in diabetes and induces formation of peroxynitrite and premature endothelial cell senescence, also inhibited arginine methylation of Sam68
17726370When the level of arginine methylation of Sam68 was pharmacologically reduced, this did not affect its RNA binding or degree of tyrosine phosphorylation, but resulted in the predominantly nuclear hypomethylation pattern
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