IL17C
Interleukin-17C
Also known as: CX2, IL-17C, IL-21, IL17C_HUMAN, MGC126884, MGC138401
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P0M4
- Gene
- IL17C
- Ensembl
- ENSG00000124391
- Chromosome
- 16
- Canonical length
- 197 aa
- Protein class
- Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
The protein encoded by this gene is a T cell-derived cytokine that shares the sequence similarity with IL17. This cytokine was reported to stimulate the release of tumor necrosis factor alpha and interleukin 1 beta from a monocytic cell line. The expression of this cytokine was found to be restricted to activated T cells. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
197 residues, UniProt reviewed canonical sequence.
>Q9P0M4|IL17C
1 MTLLPGLLFL TWLHTCLAHH DPSLRGHPHS HGTPHCYSAE ELPLGQAPPH LLARGAKWGQ
61 ALPVALVSSL EAASHRGRHE RPSATTQCPV LRPEEVLEAD THQRSISPWR YRVDTDEDRY
121 PQKLAFAECL CRGCIDARTG RETAALNSVR LLQSLLVLRR RPCSRDGSGL PTPGAFAFHT
181 EFIHVPVGCT CVLPRSVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IL17C 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)
- 0.42
- Highest tissue expression
- 1.9 nTPM
Expression across tissuesHPA
Tissue
- endometrium: 1.9 nTPM
- urinary bladder: 1.5 nTPM
- testis: 0.4 nTPM
- gallbladder: 0.3 nTPM
- skin: 0.3 nTPM
- bone marrow: 0.2 nTPM
Single-cell type
- fallopian secretory cells: 6.6 nCPM
- cholangiocytes: 4 nCPM
- fallopian tube ciliated cells: 3.8 nCPM
- gastric progenitor cells: 3.8 nCPM
- endometrial secretory cells: 2.3 nCPM
- endometrial glandular cells: 2.2 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 0.3 nTPM
- cerebral cortex: 0.3 nTPM
- basal ganglia: 0.2 nTPM
- hippocampal formation: 0.2 nTPM
- pons: 0.2 nTPM
- amygdala: 0.1 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)
- 1.73
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.81
- DepMap mean gene effect
- -0.13
- DepMap dependency class
- selective
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IL17C as an antibody target. Whether an autoantibody or antibody against IL17C could matter depends on whether native IL17C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IL17C is annotated as secreted, so native IL17C 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 IL17C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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