HCSGD entry for FBN1


1. General information

Official gene symbolFBN1
Entrez ID2200
Gene full namefibrillin 1
Other gene symbolsACMICD ECTOL1 FBN GPHYSD2 MASS MFS1 OCTD SGS SSKS WMS WMS2
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:0001501Skeletal system developmentIMPbiological_process
GO:0001527MicrofibrilIDAcellular_component
GO:0001822Kidney developmentIEAbiological_process
GO:0005201Extracellular matrix structural constituentIDA IEAmolecular_function
GO:0005509Calcium ion bindingIDA IEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005576Extracellular regionTAScellular_component
GO:0005578Proteinaceous extracellular matrixIDA IEAcellular_component
GO:0005604Basement membraneIDAcellular_component
GO:0005615Extracellular spaceIDAcellular_component
GO:0007507Heart developmentIMPbiological_process
GO:0030198Extracellular matrix organizationTASbiological_process
GO:0031012Extracellular matrixIDA IEAcellular_component
GO:0035582Sequestering of BMP in extracellular matrixISSbiological_process
GO:0035583Sequestering of TGFbeta in extracellular matrixISSbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.06799606780.00193296610.56059464450.0846848435

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

Data sourceUp or downLog fold change
GSE11954Down-1.9652590045
GSE13712_SHEARDown-2.0697457298
GSE13712_STATICDown-1.2833613428
GSE19018Down-0.0892568184
GSE19899_A1Down-0.9330459799
GSE19899_A2Down-2.1832760254
PubMed_21979375_A1Down-2.2192610078
PubMed_21979375_A2Down-2.6310997474
GSE35957Up0.2812885416
GSE36640Up0.3534791517
GSE54402Down-0.6777052068
GSE9593Up0.6195822460
GSE43922Down-0.3868552130
GSE24585Up0.6941666708
GSE37065Down-0.2541105122
GSE28863_A1Up1.6532334847
GSE28863_A2Up1.6546872445
GSE28863_A3Down-0.1449232213
GSE28863_A4Up0.3537317898
GSE48662Up0.3877505640

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-29c-3pMIMAT0000681MIRT003829Luciferase reporter assay//qRT-PCRFunctional MTI18390668
hsa-miR-133a-3pMIMAT0000427MIRT021695MicroarrayFunctional MTI (Weak)21396852
hsa-miR-1MIMAT0000416MIRT023759ProteomicsFunctional MTI (Weak)18668040
hsa-miR-215-5pMIMAT0000272MIRT024378MicroarrayFunctional MTI (Weak)19074876
hsa-miR-192-5pMIMAT0000222MIRT026557MicroarrayFunctional MTI (Weak)19074876
hsa-miR-30a-5pMIMAT0000087MIRT028608ProteomicsFunctional MTI (Weak)18668040
hsa-miR-125b-5pMIMAT0000423MIRT046011CLASHFunctional 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-29c-3pMIMAT0000681NAhsa-miR-29c18390668
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6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 4 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

26569300AQFE reduced CML expression and stimulated fibrillin-1 expression in comparison to the methyglyoxal treatment
19176530Here we show that the assembly of stress granules (SGs) is part of the early events used by senescent cells to respond to certain stresses
19176530Although SGs can form in response to stress during senescence activation, their number significantly increases once the cells are fully senescent
19176530Throughout stress, p21 mRNA is stabilized and localizes to SGs, but only during late senescence does this localization interferes with its translation
11542340The purpose of this work was: a) to study the behaviour of two rat cell strains (neoplastic SGS/4A and syngeneic fibroblasts FG) in order to test whether adhesion-dependent cells are suitable for clinorotation and b) to investigate cell-cell and cell-substratum adhesion in these cells kept under simulated low-g in the fast rotating clinostat and in hypergravity at l0g in the centrifuge
10832101As the in vitro cellular system of the neoplastic cell line SGS/4A and syngeneic normal fibroblasts (FG) represents a useful tool for studies on molecular mechanisms regulating cell adhesion, neoplastic transformation and cellular ageing, we studied the changes of glycosphingolipid and of the enzymes involved in their metabolism in both cultured cells at different subculture stages
10832101On the contrary, the increasing number of SGS/4A subcultures, characterized by a specific and different glycosphingolipid composition as compared with FG cells, does not cause modifications
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