IL36A
Interleukin-36 alpha
Also known as: FIL1, FIL1E, IL-1F6, IL1(EPSILON), IL1F6, IL36A_HUMAN, MGC129552, MGC129553
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UHA7
- Gene
- IL36A
- Ensembl
- ENSG00000136694
- Chromosome
- 2
- Canonical length
- 158 aa
- Protein class
- Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
The protein encoded by this gene is a cytokine that can activate NF-kappa-B and MAPK signaling pathways to generate an inflammatory response. The encoded protein functions primarily in skin and demonstrates increased expression in psoriasis. In addition, decreased expression of this gene has been linked to a poor prognosis in both hepatocellular carcinoma and colorectal cancer patients. [provided by RefSeq, Nov 2015]
Canonical amino-acid sequenceUniProt
158 residues, UniProt reviewed canonical sequence.
>Q9UHA7|IL36A
1 MEKALKIDTP QQGSIQDINH RVWVLQDQTL IAVPRKDRMS PVTIALISCR HVETLEKDRG
61 NPIYLGLNGL NLCLMCAKVG DQPTLQLKEK DIMDLYNQPE PVKSFLFYHS QSGRNSTFES
121 VAFPGWFIAV SSEGGCPLIL TQELGKANTT DFGLTMLFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IL36A 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)
- 0.31
- Highest tissue expression
- 386 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 386 nTPM
- tonsil: 108 nTPM
- cervix: 29 nTPM
- vagina: 16 nTPM
- salivary gland: 16 nTPM
- thymus: 1.8 nTPM
Single-cell type
- esophageal apical cells: 215 nCPM
- suprabasal keratinocytes: 9.5 nCPM
- esophageal suprabasal cells: 1.5 nCPM
- esophageal basal cells: 0.8 nCPM
- lymphatic endothelial cells: 0.2 nCPM
- basal keratinocytes: 0.1 nCPM
Immune cell
- naive CD4 T-cell: 0.5 nTPM
- naive CD8 T-cell: 0.2 nTPM
- memory CD4 T-cell: 0.1 nTPM
- T-reg: 0.1 nTPM
- total PBMC: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 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)
- 1.3
- gnomAD pLI
- 0.03
- gnomAD missense Z
- -0.29
- DepMap mean gene effect
- -0.17
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to lipopolysaccharide
- cytokine-mediated signaling pathway
- immune response
- inflammatory response
- innate immune response
- positive regulation of interleukin-6 production
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of IL36A in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IL36A as an antibody target. Whether an autoantibody or antibody against IL36A could matter depends on whether native IL36A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IL36A is annotated as secreted, so native IL36A 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 IL36A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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