HCSGD entry for ARHGEF1


1. General information

Official gene symbolARHGEF1
Entrez ID9138
Gene full nameRho guanine nucleotide exchange factor (GEF) 1
Other gene symbolsGEF1 LBCL2 LSC P115-RHOGEF SUB1.5
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:0005089Rho guanyl-nucleotide exchange factor activityIEAmolecular_function
GO:0005096GTPase activator activityIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005737CytoplasmIDA IEAcellular_component
GO:0005829CytosolTAScellular_component
GO:0005886Plasma membraneTAScellular_component
GO:0007266Rho protein signal transductionTASbiological_process
GO:0008283Cell proliferationTASbiological_process
GO:0032318Regulation of Ras GTPase activityTASbiological_process
GO:0032319Regulation of Rho GTPase activityTASbiological_process
GO:0038032Termination of G-protein coupled receptor signaling pathwayIEAbiological_process
GO:0043087Regulation of GTPase activityTASbiological_process
GO:0048011Neurotrophin TRK receptor signaling pathwayTASbiological_process
GO:0050770Regulation of axonogenesisTASbiological_process
GO:0050771Negative regulation of axonogenesisTASbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.47141876450.71864811750.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.0514096044
GSE13712_SHEARUp0.3391421303
GSE13712_STATICUp0.4062566609
GSE19018Up0.0950399360
GSE19899_A1Down-0.0128799017
GSE19899_A2Down-0.0442748199
PubMed_21979375_A1Down-0.5589257913
PubMed_21979375_A2Up0.2862123661
GSE35957Up0.1941074184
GSE36640Up0.0856326781
GSE54402Down-0.0265290098
GSE9593Down-0.3390037062
GSE43922--
GSE24585--
GSE37065--
GSE28863_A1--
GSE28863_A2--
GSE28863_A3--
GSE28863_A4--
GSE48662Down-0.0253337512

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-124-3pMIMAT0000422MIRT002695MicroarrayFunctional MTI (Weak)15685193
hsa-miR-124-3pMIMAT0000422MIRT002695MicroarrayFunctional MTI (Weak)18668037
hsa-miR-335-5pMIMAT0000765MIRT018227MicroarrayFunctional MTI (Weak)18185580
hsa-miR-331-3pMIMAT0000760MIRT043573CLASHFunctional MTI (Weak)23622248
hsa-miR-26a-5pMIMAT0000082MIRT050115CLASHFunctional 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: 5 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25993799The ability of LSC proliferation treated by various concentration of ASP(20-80 mg
25993799The proliferation of LSC was exhibited significantly concentration-dependent inhibited after exposure to various concentration of ASP
23296652The characteristic features of senescent cells such as their "flattened" appearance, enlarged nuclei and low saturation density at the plateau phase of cell growth, can be conveniently measured by image-assisted cytometry such as provided by a laser scanning cytometer (LSC)
23027005Laser scanning cytometer (LSC) is the microscope-based cytofluorometer that offers a plethora of unique analytical capabilities, not provided by flow cytometry (FCM)
23027005This review describes attributes of LSC and covers its numerous applications derived from plentitude of the parameters that can be measured
23027005Advantages and limitations of LSC are discussed and compared with FCM
21624810Together, these results reveal an important functional interplay between MLL/Hox and Bmi1 in regulating cellular senescence for LSC development, suggesting that a synergistic targeting of both molecules is required to eradicate a broader spectrum of LSCs
20939035The imaging analytical capabilities of laser scanning cytometer (LSC) have been used to assess morphological features considered to be typical of the senescent phenotype
20939035The saturation cell density at plateau phase of growth recorded by LSC was found to be dramatically decreased in cultures of senescent cells, thereby also serving as an additional marker
20939035The data show that morphometric analysis of cellular attributes by LSC offers an attractive tool to detect cell senescence and measure its degree particularly in assessing effects of the factors that enhance or attenuate this process
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