IL17B
Interleukin-17B
Also known as: IL-17B, IL-20, IL17B_HUMAN, MGC138900, MGC138901, NIRF, ZCYTO7
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UHF5
- Gene
- IL17B
- Ensembl
- ENSG00000127743
- Chromosome
- 5
- Canonical length
- 180 aa
- Protein class
- Cancer-related genes, Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
The protein encoded by this gene is a T cell-derived cytokine that shares sequence similarity with IL17. This cytokine was reported to stimulate the release of TNF alpha (TNF) and IL1 beta (IL1B) from a monocytic cell line. Immunohistochemical analysis of several nerve tissues indicated that this cytokine is primarily localized to neuronal cell bodies. Alternative splicing results in multiple splice variants. [provided by RefSeq, Dec 2015]
Canonical amino-acid sequenceUniProt
180 residues, UniProt reviewed canonical sequence.
>Q9UHF5|IL17B
1 MDWPHNLLFL LTISIFLGLG QPRSPKSKRK GQGRPGPLAP GPHQVPLDLV SRMKPYARME
61 EYERNIEEMV AQLRNSSELA QRKCEVNLQL WMSNKRSLSP WGYSINHDPS RIPVDLPEAR
121 CLCLGCVNPF TMQEDRSMVS VPVFSQVPVR RRLCPPPPRT GPCRQRAVME TIAVGCTCIFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IL17B 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)
- 0.46
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 11 nTPM
- cervix: 4.6 nTPM
- testis: 3.6 nTPM
- endometrium: 3.5 nTPM
- colon: 2.9 nTPM
- breast: 2.8 nTPM
Single-cell type
- breast myoepithelial cells: 34 nCPM
- vascular smooth muscle cells: 18 nCPM
- peritubular myoid cells: 18 nCPM
- tuft cells: 12 nCPM
- salivary myoepithelial cells: 10 nCPM
- smooth muscle cells: 9.6 nCPM
Immune cell
- basophil: 1.2 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 1.5 nTPM
- cerebral cortex: 0.8 nTPM
- pons: 0.7 nTPM
- medulla oblongata: 0.6 nTPM
- hypothalamus: 0.5 nTPM
- midbrain: 0.5 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)
- 1.24
- gnomAD pLI
- 0.03
- gnomAD missense Z
- 0.52
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell-cell signaling
- immune response
- inflammatory response
- positive regulation of cytokine production involved in inflammatory response
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IL17B as an antibody target. Whether an autoantibody or antibody against IL17B could matter depends on whether native IL17B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IL17B is annotated as secreted, so native IL17B 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 IL17B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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