IL27
Interleukin-27 subunit alpha
Also known as: IL-27, IL-27A, IL27A, IL27A_HUMAN, IL27p28, IL30, MGC71873, p28
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NEV9
- Gene
- IL27
- Ensembl
- ENSG00000197272
- Chromosome
- 16
- Canonical length
- 243 aa
- Protein class
- Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
The protein encoded by this gene is one of the subunits of a heterodimeric cytokine complex. This protein is related to interleukin 12A (IL12A). It interacts with Epstein-Barr virus induced gene 3 (EBI3), a protein similar to interleukin 12B (IL12B), and forms a complex that has been shown to drive rapid expansion of naive but not memory CD4(+) T cells. The complex is also found to synergize strongly with interleukin 12 to trigger interferon gamma (IFNG) production of naive CD4(+) T cells. The biological effects of this cytokine are mediated by the class I cytokine receptor (WSX1/TCRR). [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
243 residues, UniProt reviewed canonical sequence.
>Q8NEV9|IL27
1 MGQTAGDLGW RLSLLLLPLL LVQAGVWGFP RPPGRPQLSL QELRREFTVS LHLARKLLSE
61 VRGQAHRFAE SHLPGVNLYL LPLGEQLPDV SLTFQAWRRL SDPERLCFIS TTLQPFHALL
121 GGLGTQGRWT NMERMQLWAM RLDLRDLQRH LRFQVLAAGF NLPEEEEEEE EEEEEERKGL
181 LPGALGSALQ GPAQVSWPQL LSTYRLLHSL ELVLSRAVRE LLLLSKAGHS VWPLGFPTLS
241 PQPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IL27 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.38
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- liver: 26 nTPM
- spleen: 1.6 nTPM
- appendix: 1.1 nTPM
- bone marrow: 0.8 nTPM
- placenta: 0.6 nTPM
- testis: 0.6 nTPM
Single-cell type
- syncytiotrophoblasts: 34 nCPM
- hepatocytes: 25 nCPM
- neutrophils: 12 nCPM
- migrating cytotrophoblasts: 5 nCPM
- breast lactating cells: 3.8 nCPM
- extravillous trophoblasts: 3.6 nCPM
Immune cell
- intermediate monocyte: 3.8 nTPM
- classical monocyte: 3.6 nTPM
- neutrophil: 2.1 nTPM
- NK-cell: 1.5 nTPM
- total PBMC: 1 nTPM
- eosinophil: 0.8 nTPM
Brain region
- thalamus: 1.7 nTPM
- medulla oblongata: 1.3 nTPM
- cerebral cortex: 1.2 nTPM
- midbrain: 1.1 nTPM
- cerebellum: 1 nTPM
- hippocampal formation: 1 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.51
- gnomAD pLI
- 0.78
- gnomAD missense Z
- 1.08
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- inflammatory response
- innate immune response
- positive regulation of defense response to virus by host
- positive regulation of type II interferon production
- regulation of T cell proliferation
- response to Gram-positive bacterium
- regulation of T-helper 1 cell differentiation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Four-helical cytokine-like, core
- Interleukin-27 alpha
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IL27 as an antibody target. Whether an autoantibody or antibody against IL27 could matter depends on whether native IL27 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IL27 is annotated as secreted, so native IL27 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label IL27 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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