HCSGD entry for GRN


1. General information

Official gene symbolGRN
Entrez ID2896
Gene full namegranulin
Other gene symbolsCLN11 GEP GP88 PCDGF PEPI PGRN
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0001835Blastocyst hatchingIEAbiological_process
GO:0005125Cytokine activityIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005615Extracellular spaceIEAcellular_component
GO:0005739MitochondrionIEAcellular_component
GO:0007165Signal transductionNASbiological_process
GO:0007566Embryo implantationIEAbiological_process
GO:0008083Growth factor activityTASmolecular_function
GO:0008219Cell deathIEAbiological_process
GO:0043231Intracellular membrane-bounded organelleIDAcellular_component
GO:0050679Positive regulation of epithelial cell proliferationIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.00030580530.99434989930.04679709301.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.7860556669
GSE13712_SHEARDown-0.0540459836
GSE13712_STATICUp0.0588703755
GSE19018Up0.8226775545
GSE19899_A1Up0.4126286267
GSE19899_A2Up1.4494257305
PubMed_21979375_A1Up1.4009261079
PubMed_21979375_A2Up2.1325468392
GSE35957Up0.2416841572
GSE36640Up1.8704559478
GSE54402Down-0.4597742890
GSE9593Up1.2692401606
GSE43922Up0.4061622665
GSE24585Up0.7548738601
GSE37065Up0.1993980041
GSE28863_A1Up0.4801202445
GSE28863_A2Up1.0599621655
GSE28863_A3Up0.4142036725
GSE28863_A4Down-0.0915773348
GSE48662Down-0.0156591399

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-659-3pMIMAT0003337MIRT000034Luciferase reporter assay//Western blotFunctional MTI18723524
hsa-miR-107MIMAT0000104MIRT004761Microarray//Western blotFunctional MTI20884628
hsa-miR-107MIMAT0000104MIRT004761Reporter assay;Western blot;MicroarrayFunctional MTI20489155
hsa-miR-29b-3pMIMAT0000100MIRT005486ELISA//Luciferase reporter assay//qRT-PCR//Western blot//Reporter assay;Western blot;OtherFunctional MTI20479936
hsa-miR-9-5pMIMAT0000441MIRT021404Reporter assayNon-Functional MTI20479936
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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-659-3pMIMAT00033371hsa-miR-659{Western blot}{overexpression by miRNA mimics tranfection}18723524
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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

26600492Effect of progranulin (PGRN) on the proliferation and senescence of cervical cancer cells
26600492We investigated the effect of progranulin (PGRN) expression on the proliferation and senescence of cervical cancer cells
26600492PGRN small interfering RNA (siRNA) was introduced into the SiHa and HeLa cell lines of human cervical carcinoma using liposome-mediated transfection
26600492The expression levels of PGRN in each cell line after transfection of PGRN siRNA were detected by reverse transcription-polymerase chain reaction (RT-PCR)
26600492The RT-PCR assay showed that the expression of PGRN in all of the cell lines transfected with PGRN siRNA markedly decreased
26600492In the clone-forming test, compared with the control group, the colony-forming ability in all cell lines decreased significantly after transfection with PGRN siRNA
26600492The beta-galactosidase-staining experiments showed that the phenomenon of cell aging in the PGRN interference group was more obvious than in the control group
26600492This suggests that PGRN can promote the proliferation of the cervical cancer cell line; proliferation of cervical cancer cells is achieved by inhibiting their senescence
22733568Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice
22733568Loss-of-function mutations in progranulin (GRN) are associated with frontotemporal lobar degeneration with intraneuronal ubiquitinated protein accumulations composed primarily of hyperphosphorylated TDP-43 (FTLD-TDP)
22733568The mechanism by which GRN deficiency causes TDP-43 pathology or neurodegeneration remains elusive
22733568To explore the role of GRN in vivo, we established Grn knockout mice using a targeted genomic recombination approach and Cre-LoxP technology
22733568Constitutive Grn homozygous knockout (Grn(-/-) ) mice were born in an expected Mendelian pattern of inheritance and showed no phenotypic alterations compared to heterozygous (Grn(+/-) ) or wild-type (Wt) littermates until 10 months of age
22733568From then, Grn(-/-) mice showed reduced survival accompanied by significantly increased gliosis and ubiquitin-positive accumulations in the cortex, hippocampus, and subcortical regions
22733568Although phosphorylated TDP-43 could not be detected in the ubiquitinated inclusions, elevated levels of hyperphosphorylated full-length TDP-43 were recovered from detergent-insoluble brain fractions of Grn(-/-) mice
22733568Grn(-/-) mice also showed degenerative liver changes and cathepsin D-positive foamy histiocytes within sinusoids, suggesting widespread defects in lysosomal turnover
22733568An increase in insulin-like growth factor (IGF)-1 was observed in Grn(-/-) brains, and increased IGF-1 signalling has been associated with decreased longevity
22733568Our data suggest that progranulin deficiency in mice leads to reduced survival in adulthood and increased cellular ageing accompanied by hyperphosphorylation of TDP-43, and recapitulates key aspects of FTLD-TDP neuropathology
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