HCSGD entry for FCGRT


1. General information

Official gene symbolFCGRT
Entrez ID2217
Gene full nameFc fragment of IgG, receptor, transporter, alpha
Other gene symbolsFCRN alpha-chain
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0002416IgG immunoglobulin transcytosis in epithelial cells mediated by FcRn immunoglobulin receptorNASbiological_process
GO:0003823Antigen bindingIBAmolecular_function
GO:0005886Plasma membraneIBAcellular_component
GO:0006955Immune responseIEAbiological_process
GO:0007165Signal transductionIBAbiological_process
GO:0016020MembraneIEAcellular_component
GO:0016021Integral component of membraneIEAcellular_component
GO:0019770IgG receptor activityIBAmolecular_function
GO:0019864IgG bindingIDAmolecular_function
GO:0019882Antigen processing and presentationIBA IEAbiological_process
GO:0030881Beta-2-microglobulin bindingIBA IEAmolecular_function
GO:0038093Fc receptor signaling pathwayIBAbiological_process
GO:0038094Fc-gamma receptor signaling pathwayIBAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.50067411570.00943712620.99999024730.1919587326

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

Data sourceUp or downLog fold change
GSE11954Down-0.2478145867
GSE13712_SHEARDown-1.0558475087
GSE13712_STATICDown-0.8166847958
GSE19018Up0.4058123789
GSE19899_A1Down-0.9696227394
GSE19899_A2Down-0.9325285310
PubMed_21979375_A1Down-1.2801690746
PubMed_21979375_A2Down-1.6529289898
GSE35957Up0.3552445578
GSE36640Up0.9830708691
GSE54402Down-0.7744494935
GSE9593Down-0.0014036365
GSE43922Down-0.8849159542
GSE24585Up0.5550900135
GSE37065Up0.1047194458
GSE28863_A1Up0.1062770292
GSE28863_A2Up0.0817234476
GSE28863_A3Down-0.0818217871
GSE28863_A4Down-0.0838436695
GSE48662Up0.4088886825

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-335-5pMIMAT0000765MIRT017375MicroarrayFunctional MTI (Weak)18185580
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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: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

8106562Age related induction of platelet-derived growth factor A-chain mRNA in normal human fibroblasts
8106562We have previously found that stimulation of normal neonatal fibroblasts with PDGF or EGF leads to a transient induction of PDGF A-chain mRNA and the synthesis of PDGF-AA proteins
8106562We have now studied the PDGF-BB mediated PDGF A-chain induction in a set of fibroblasts from young and old donors to clarify if the levels of induction are correlated to the donor age and the replicative capacity of the cells
8106562The PDGF A-chain induction was found to be reduced in cells from old donors compared with cells from embryonic and neonatal donors
8106562The PDGF A-chain mRNA induction was also decreased or absent in late passage human fibroblasts (senescent cells) when compared with early passage cells
8106562These data suggest that the PDGF A-chain mRNA induction is regulated by an age related mechanism in human fibroblasts
2166059Altered regulation of platelet-derived growth factor A-chain and c-fos gene expression in senescent progeria fibroblasts
2166059Although normal fibroblasts only express platelet-derived growth factor (PDGF) A-chain mRNA for a brief period following mitogenic stimulation, one strain of Hutchinson-Gilford (progeria) syndrome fibroblasts, AG3513, constitutively expresses PDGF A-chain mRNA and PDGF-AA homodimers
2166059The PDGF A-chain gene does not appear to be amplified or rearranged in these fibroblasts
2166059The senescent phenotype of AG3513 fibroblasts is probably unrelated to their constitutive PDGF A-chain gene expression; further studies are necessary in order to directly address this issue
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