Insufficient scRNA-seq data for expression of IL27 at single-cell level.
Insufficient scRNA-seq data for expression of IL27 at tissue level.
Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
liver | 100% | 554.23 | 225 / 226 | 88% | 11.08 | 358 / 406 |
lung | 94% | 24.48 | 542 / 578 | 14% | 0.24 | 163 / 1155 |
spleen | 99% | 82.83 | 239 / 241 | 0% | 0 | 0 / 0 |
peripheral blood | 93% | 86.82 | 867 / 929 | 0% | 0 | 0 / 0 |
adrenal gland | 69% | 9.47 | 177 / 258 | 2% | 0.03 | 4 / 230 |
adipose | 66% | 11.68 | 793 / 1204 | 0% | 0 | 0 / 0 |
breast | 42% | 5.03 | 193 / 459 | 20% | 0.35 | 219 / 1118 |
intestine | 48% | 8.07 | 464 / 966 | 9% | 0.17 | 49 / 527 |
lymph node | 0% | 0 | 0 / 0 | 55% | 6.61 | 16 / 29 |
blood vessel | 52% | 8.79 | 690 / 1335 | 0% | 0 | 0 / 0 |
bladder | 33% | 3.00 | 7 / 21 | 13% | 0.30 | 68 / 504 |
thymus | 44% | 6.34 | 286 / 653 | 2% | 0.04 | 11 / 605 |
kidney | 35% | 4.11 | 31 / 89 | 8% | 0.14 | 74 / 901 |
prostate | 39% | 8.11 | 96 / 245 | 3% | 0.05 | 15 / 502 |
brain | 31% | 4.26 | 809 / 2642 | 9% | 0.17 | 66 / 705 |
skin | 16% | 3.71 | 281 / 1809 | 24% | 0.51 | 113 / 472 |
stomach | 26% | 3.58 | 95 / 359 | 11% | 0.17 | 32 / 286 |
uterus | 18% | 3.39 | 31 / 170 | 11% | 0.21 | 49 / 459 |
esophagus | 23% | 3.73 | 337 / 1445 | 5% | 0.10 | 9 / 183 |
pancreas | 18% | 2.10 | 60 / 328 | 7% | 0.12 | 13 / 178 |
tonsil | 0% | 0 | 0 / 0 | 22% | 0.42 | 10 / 45 |
ovary | 16% | 1.87 | 28 / 180 | 6% | 0.08 | 24 / 430 |
heart | 18% | 1.95 | 153 / 861 | 0% | 0 | 0 / 0 |
muscle | 8% | 1.01 | 64 / 803 | 0% | 0 | 0 / 0 |
eye | 0% | 0 | 0 / 0 | 5% | 0.07 | 4 / 80 |
abdomen | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
bone marrow | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
diaphragm | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
gingiva | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nasal cavity | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nasopharynx | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nose | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
placenta | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
spinal column | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
ureter | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 1 |
GO_0007165 | Biological process | signal transduction |
GO_0042129 | Biological process | regulation of T cell proliferation |
GO_0032729 | Biological process | positive regulation of type II interferon production |
GO_0006954 | Biological process | inflammatory response |
GO_0140459 | Biological process | response to Gram-positive bacterium |
GO_0002230 | Biological process | positive regulation of defense response to virus by host |
GO_0045087 | Biological process | innate immune response |
GO_0045625 | Biological process | regulation of T-helper 1 cell differentiation |
GO_0005615 | Cellular component | extracellular space |
GO_0009986 | Cellular component | cell surface |
GO_0005788 | Cellular component | endoplasmic reticulum lumen |
GO_0005829 | Cellular component | cytosol |
GO_0005576 | Cellular component | extracellular region |
GO_0045523 | Molecular function | interleukin-27 receptor binding |
GO_0005102 | Molecular function | signaling receptor binding |
GO_0005515 | Molecular function | protein binding |
GO_0005125 | Molecular function | cytokine activity |
Gene name | IL27 |
Protein name | Interleukin 27 Interleukin-27 subunit alpha (IL-27 subunit alpha) (IL-27-A) (IL27-A) (Interleukin-30) (p28) |
Synonyms | IL30 IL27A |
Description | FUNCTION: Associates with EBI3 to form the IL-27 interleukin, a heterodimeric cytokine which functions in innate immunity. IL-27 has pro- and anti-inflammatory properties, that can regulate T-helper cell development, suppress T-cell proliferation, stimulate cytotoxic T-cell activity, induce isotype switching in B-cells, and that has diverse effects on innate immune cells. Among its target cells are CD4 T-helper cells which can differentiate in type 1 effector cells (TH1), type 2 effector cells (TH2) and IL17 producing helper T-cells (TH17). It drives rapid clonal expansion of naive but not memory CD4 T-cells. It also strongly synergizes with IL-12 to trigger interferon-gamma/IFN-gamma production of naive CD4 T-cells, binds to the cytokine receptor WSX-1/TCCR which appears to be required but not sufficient for IL-27-mediated signal transduction. IL-27 potentiate the early phase of TH1 response and suppress TH2 and TH17 differentiation. It induces the differentiation of TH1 cells via two distinct pathways, p38 MAPK/TBX21- and ICAM1/ITGAL/ERK-dependent pathways. It also induces STAT1, STAT3, STAT4 and STAT5 phosphorylation and activates TBX21/T-Bet via STAT1 with resulting IL12RB2 up-regulation, an event crucial to TH1 cell commitment. It suppresses the expression of GATA3, the inhibitor TH1 cells development. In CD8 T-cells, it activates STATs as well as GZMB. IL-27 reveals to be a potent inhibitor of TH17 cell development and of IL-17 production. Indeed IL27 alone is also able to inhibit the production of IL17 by CD4 and CD8 T-cells. While IL-27 suppressed the development of pro-inflammatory Th17 cells via STAT1, it inhibits the development of anti-inflammatory inducible regulatory T-cells, iTreg, independently of STAT1. IL-27 has also an effect on cytokine production, it suppresses pro-inflammatory cytokine production such as IL2, IL4, IL5 and IL6 and activates suppressors of cytokine signaling such as SOCS1 and SOCS3. Apart from suppression of cytokine production, IL-27 also antagonizes the effects of some cytokines such as IL6 through direct effects on T-cells. Another important role of IL-27 is its antitumor activity as well as its antiangiogenic activity with activation of production of antiangiogenic chemokines such as IP-10/CXCL10 and MIG/CXCL9. In vein endothelial cells, it induces IRF1/interferon regulatory factor 1 and increase the expression of MHC class II transactivator/CIITA with resulting up-regulation of major histocompatibility complex class II. IL-27 also demonstrates antiviral activity with inhibitory properties on HIV-1 replication. . |
Accessions | ENST00000568075.1 Q8NEV9 H3BQY2 ENST00000356897.1 |