HCSGD entry for RHOA


1. General information

Official gene symbolRHOA
Entrez ID387
Gene full nameras homolog family member A
Other gene symbolsARH12 ARHA RHO12 RHOH12
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0003924GTPase activityTASmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005525GTP bindingIEAmolecular_function
GO:0005622IntracellularIEAcellular_component
GO:0005829CytosolTAScellular_component
GO:0005856CytoskeletonIEAcellular_component
GO:0005886Plasma membraneTAScellular_component
GO:0005938Cell cortexIDAcellular_component
GO:0006184GTP catabolic processTASbiological_process
GO:0007179Transforming growth factor beta receptor signaling pathwayTASbiological_process
GO:0007264Small GTPase mediated signal transductionIEA TASbiological_process
GO:0007266Rho protein signal transductionTASbiological_process
GO:0007411Axon guidanceTASbiological_process
GO:0007596Blood coagulationTASbiological_process
GO:0008152Metabolic processTASbiological_process
GO:0016020MembraneIEAcellular_component
GO:0016032Viral processIEAbiological_process
GO:0017022Myosin bindingIPImolecular_function
GO:0030027LamellipodiumISScellular_component
GO:0030036Actin cytoskeleton organizationTASbiological_process
GO:0030054Cell junctionTAScellular_component
GO:0030168Platelet activationTASbiological_process
GO:0030334Regulation of cell migrationIMPbiological_process
GO:0030496MidbodyIEAcellular_component
GO:0032154Cleavage furrowIEAcellular_component
GO:0032467Positive regulation of cytokinesisIMPbiological_process
GO:0033688Regulation of osteoblast proliferationISSbiological_process
GO:0036089Cleavage furrow formationIDAbiological_process
GO:0042346Positive regulation of NF-kappaB import into nucleusNASbiological_process
GO:0043123Positive regulation of I-kappaB kinase/NF-kappaB signalingIEPbiological_process
GO:0043296Apical junction complexIDAcellular_component
GO:0043297Apical junction assemblyIMPbiological_process
GO:0043931Ossification involved in bone maturationISSbiological_process
GO:0045666Positive regulation of neuron differentiationIMPbiological_process
GO:0048011Neurotrophin TRK receptor signaling pathwayTASbiological_process
GO:0048015Phosphatidylinositol-mediated signalingTASbiological_process
GO:0050770Regulation of axonogenesisTASbiological_process
GO:0050771Negative regulation of axonogenesisTASbiological_process
GO:0050772Positive regulation of axonogenesisTASbiological_process
GO:0051056Regulation of small GTPase mediated signal transductionTASbiological_process
GO:0051496Positive regulation of stress fiber assemblyIDAbiological_process
GO:0061383Trabecula morphogenesisISSbiological_process
GO:0090307Spindle assembly involved in mitosisIMPbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.94781697120.20657351920.99999024730.8813953206

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

Data sourceUp or downLog fold change
GSE11954Up0.0008482379
GSE13712_SHEARUp0.0167717706
GSE13712_STATICDown-0.0861842223
GSE19018Up0.2755310231
GSE19899_A1Down-0.2309398318
GSE19899_A2Down-0.1697120427
PubMed_21979375_A1Down-0.0329233953
PubMed_21979375_A2Down-0.4433746751
GSE35957Up0.0827802631
GSE36640Up0.0100960296
GSE54402Down-0.0061818421
GSE9593Up0.1590074233
GSE43922Up0.0106249011
GSE24585Up0.0718611980
GSE37065Down-0.1483106129
GSE28863_A1Down-0.1837318374
GSE28863_A2Down-0.3625707585
GSE28863_A3Down-0.0480812758
GSE28863_A4Down-0.0431165575
GSE48662Down-0.4023049734

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Name

Drug

Accession number

Guanosine-5'-DiphosphateDB04315 EXPT01573

  • MicroRNAs

    • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-31-5pMIMAT0000089MIRT000088Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI19524507
hsa-miR-31-5pMIMAT0000089MIRT000088qRT-PCR//Western blotFunctional MTI22854067
hsa-miR-122-5pMIMAT0000421MIRT000717Luciferase reporter assayFunctional MTI19617899
hsa-miR-122-5pMIMAT0000421MIRT000717Luciferase reporter assay//Functional MTI19935707
hsa-miR-155-5pMIMAT0000646MIRT001961Luciferase reporter assayFunctional MTI18794355
hsa-miR-185-5pMIMAT0000455MIRT004036Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI21186079
hsa-miR-31-3pMIMAT0004504MIRT007065qRT-PCR//Western blotFunctional MTI22854067
hsa-miR-200c-3pMIMAT0000617MIRT007345Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI23272142
hsa-miR-375MIMAT0000728MIRT019977Western blot;qRT-PCR;MicroarrayFunctional MTI20584986
hsa-miR-124-3pMIMAT0000422MIRT022883MicroarrayFunctional MTI (Weak)18668037
hsa-miR-320cMIMAT0005793MIRT036175CLASHFunctional MTI (Weak)23622248
hsa-miR-146b-5pMIMAT0002809MIRT041611CLASHFunctional MTI (Weak)23622248
hsa-miR-221-3pMIMAT0000278MIRT046885CLASHFunctional 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-155-5pMIMAT00006462hsa-miR-155{immunoblotting}{overexpression by miRNA precursor transfection}18794355
hsa-miR-155-5pMIMAT00006463hsa-miR-155{immunoblotting}{overexpression by miRNA precursor transfection}18794355
hsa-miR-155-5pMIMAT00006461hsa-miR-155{immunoblotting}{overexpression by miRNA precursor transfection}18794355
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6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 5 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

26649141Modulation of RhoA GTPase Activity Sensitizes Human Cervix Carcinoma Cells to gamma-Radiation by Attenuating DNA Repair Pathways
26649141Although RhoA GTPase overexpression/hyperactivation is observed in many malignancies, the effect of RhoA activity modulation on cancer radiosensitivity has not been previously investigated
26649141In agreement with these results, RhoA inhibition by C3 toxin expression drastically affected homologous recombination (HR) and nonhomologous end joining (NHEJ)
26649141These data suggest that modulation of RhoA GTPase activity impairs DNA damage repair, increasing HeLa cell radiosensitivity
17658517Inhibitory role of RhoA on senescence-like growth arrest by a mechanism involving modulation of phosphatase activity
17658517In this study, we showed that RhoA activation modulated phosphatase during senescence-like arrest in human prostate cancer cells
17658517Thus, we postulate that RhoA signaling may protect cells against cellular senescence by maintaining phosphatase activity and Erk dephosphorylation
16316623Lovastatin-induced RhoA modulation and its effect on senescence in prostate cancer cells
16316623We found that constitutively active RhoA (caRhoA) reversed lovastatin-induced senescence in caRhoA-transfected PC-3 cells
16316623Thus, we postulate that modulation of RhoA may be critical in lovastatin-induced senescence in PC-3 cells
11795508Perinuclear expression of Rac1 was prominent in the HDF cells and V12C40 expresser; however, in the V12S35 expresser, translocation of Rac1 from perinucleus to nucleus and strong expression of RhoA were obvious
11795508In summary, the H-ras double mutant expressers induced premature senescence through the MEK pathway, accompanied by nuclear accumulation of actin and Rac1 proteins, cytoplasmic retention of p-Erk1/2, and marked induction of RhoA expression, suggesting the translocational inefficiency of the intracellular proteins in the senescent HDF cells
11080532Perinuclear expression of Racl was prominent in the HDF cells and V12C40 expresser, while translocation of Racl from perinucleus to nucleus and strong expression of RhoA were observed in the V12S35 expresser
11080532In summary, the induced premature senescence by H-ras double mutants were accompanied by nuclear accumulation of actin and Racl proteins, cytoplasmic retention of p-Erk1/2 and marked induction of RhoA expression mainly through dysregulation of the MEK pathway
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