HCSGD entry for KLRG1


1. General information

Official gene symbolKLRG1
Entrez ID10219
Gene full namekiller cell lectin-like receptor subfamily G, member 1
Other gene symbols2F1 CLEC15A MAFA MAFA-2F1 MAFA-L MAFA-LIKE
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:0004872Receptor activityTASmolecular_function
GO:0005886Plasma membraneIEAcellular_component
GO:0006954Inflammatory responseTASbiological_process
GO:0006968Cellular defense responseTASbiological_process
GO:0007166Cell surface receptor signaling pathwayTASbiological_process
GO:0016021Integral component of membraneIEAcellular_component
GO:0030246Carbohydrate bindingIEAmolecular_function
GO:0045087Innate immune responseIEAbiological_process
GO:0050776Regulation of immune responseTASbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.90584888110.10695988370.99999024730.6260376028

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

Data sourceUp or downLog fold change
GSE11954Down-0.0322355674
GSE13712_SHEARDown-1.1060818451
GSE13712_STATICDown-3.4374192100
GSE19018Up0.1790547941
GSE19899_A1Up0.0604368012
GSE19899_A2Up0.0550931413
PubMed_21979375_A1Down-0.0736129480
PubMed_21979375_A2Down-0.1458749154
GSE35957Down-0.2035450955
GSE36640Up0.2752418062
GSE54402Up0.0294909942
GSE9593Down-0.2001440346
GSE43922Down-0.0484988450
GSE24585Down-0.0288758983
GSE37065Down-0.0173388412
GSE28863_A1Up0.0325881935
GSE28863_A2Up0.1416553243
GSE28863_A3Up0.0362551201
GSE28863_A4Up0.0607977225
GSE48662Up0.0975113321

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-877-3pMIMAT0004950MIRT036992CLASHFunctional 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: 4 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

22396780Instead a set of surface markers including IL-7Ralpha and KLRG1 is commonly used to predict the potential of CD8 effector T cells to differentiate into memory cells
22102004Using five-colour flow cytometry, we analyzed peripheral blood T-lymphocytes for their expression of CD28, CD57 and KLRG1 in 11 young (Y) and 11 old (O) apparently healthy human subjects
19479342The co-inhibitory receptor killer-cell lectin like receptor G1 (KLRG1) is expressed on NK cells and antigen-experienced T cells and has been postulated to be a marker of senescence
19479342Whilst KLRG1 has frequently been used as a marker of cellular differentiation, data are emerging indicating that KLRG1 plays an inhibitory role
19479342In this review we examine evidence highlighting this view of KLRG1 with emphasis on the functional defects that arise during T cell differentiation with age that may, in part, be actively maintained by inhibitory receptor signalling
17379755As a consequence of clonal expansion, some T lymphocytes acquire a senescent phenotype, fail to replicate in response to further antigenic stimulation, and express the killer cell lectin-like receptor G1 (KLRG1) and/or CD57
17379755Blood lymphocytes isolated before, immediately after, and 1 h after exercise were assessed for cell surface expression of KLRG1, CD57, CD28, CD45RA, CD45RO, CD62L, and lymphocyte subset markers (CD3, CD4, CD8, CD56) by flow cytometry
17379755The percentage of all CD3+ T lymphocytes expressing KLRG1 and CD57 increased with exercise (P < 0
17379755The change in T-lymphocyte KLRG1 expression was attributed to both CD4+ and CD8 bright T cells, with the relative change being greater for the CD8 bright population (P < 0
17379755Mobilized T-lymphocyte populations expressing KLRG1 and CD57 appeared to extravasate the peripheral blood compartment after 1 h of recovery
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