HCSGD entry for LAMTOR5


1. General information

Official gene symbolLAMTOR5
Entrez ID10542
Gene full namelate endosomal/lysosomal adaptor, MAPK and MTOR activator 5
Other gene symbolsHBXIP XIP
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:0005085Guanyl-nucleotide exchange factor activityIDAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005737CytoplasmIDA IEAcellular_component
GO:0005764LysosomeIDAcellular_component
GO:0005829CytosolIDAcellular_component
GO:0008361Regulation of cell sizeIMPbiological_process
GO:0009615Response to virusTASbiological_process
GO:0019079Viral genome replicationIEAbiological_process
GO:0032008Positive regulation of TOR signalingIMPbiological_process
GO:0032947Protein complex scaffoldIDAmolecular_function
GO:0043066Negative regulation of apoptotic processIDA IEAbiological_process
GO:0043087Regulation of GTPase activityIDAbiological_process
GO:0043154Negative regulation of cysteine-type endopeptidase activity involved in apoptotic processIDA IEAbiological_process
GO:0061462Protein localization to lysosomeIMPbiological_process
GO:0071230Cellular response to amino acid stimulusIMPbiological_process
GO:0071986Ragulator complexIDAcellular_component
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.48955274880.54768333270.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.2629975950
GSE13712_SHEARDown-0.2020494396
GSE13712_STATICDown-0.0485188009
GSE19018Up0.4411682272
GSE19899_A1Up0.2192967931
GSE19899_A2Up0.1544534884
PubMed_21979375_A1Down-0.1724689106
PubMed_21979375_A2Up0.2226389294
GSE35957Down-0.1883970980
GSE36640Up0.0394563170
GSE54402Up0.2060191924
GSE9593Up0.0332534901
GSE43922Down-0.0182448453
GSE24585Down-0.2017953186
GSE37065Down-0.0675610799
GSE28863_A1Down-0.1954684971
GSE28863_A2Up0.1181961109
GSE28863_A3Down-0.3677540620
GSE28863_A4Down-0.1609149821
GSE48662Up0.1518860164

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-16-5pMIMAT0000069MIRT001458pSILAC//Proteomics;OtherFunctional MTI (Weak)18668040
hsa-miR-501-5pMIMAT0002872MIRT007340Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI23266610
hsa-miR-215-5pMIMAT0000272MIRT024286MicroarrayFunctional MTI (Weak)19074876
hsa-miR-192-5pMIMAT0000222MIRT026572MicroarrayFunctional MTI (Weak)19074876
hsa-miR-221-3pMIMAT0000278MIRT046932CLASHFunctional 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

18158869Promotion of cell proliferation by HBXIP via upregulation of human telomerase reverse transcriptase in human mesenchymal stem cells
18158869AIM: We previously found that the hepatitis B X-interacting protein (HBXIP) was able to promote the proliferation of cells
18158869To investigate the mechanism of promoting proliferation by HBXIP, the effect of HBXIP on human TERT (hTERT) was investigated in human mesenchymal stem cells (hMSC)
18158869METHODS: BMMS-03 cells and hMSC from the bone marrow of a 4-month-old elicited fetus, were transiently transfected with the pcDNA3-hbxip plasmid encoding the HBXIP gene and pSilencer-hbxip plasmid encoding RNA interference (RNAi) targeting HBXIP mRNA, followed by the examination of the hTERT promoter reporter gene by luciferase assay, and the detection of telomerase activity by telomeric repeat amplication protocol, respectively, as well as the expression levels of hTERT, c-Myc, and Bcl-2 by Western blot analysis
18158869RESULTS: The overexpression of HBXIP led to a significant upregulation of hTERT promoter activity, telomerase activity, and the expression levels of hTERT, c-Myc, and Bcl-2 in BMMS-03 cells
18158869RNAi targeting HBXIP mRNA produced the opposite results completely
18158869CONCLUSION: Our data demonstrated that HBXIP significantly stimulated the transcription and expression of hTERT and increased the activity of telomerase in BMMS-03 cells, which provides a new insight into the mechanism of promoting cell proliferation by HBXIP
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