IFNE
Interferon epsilon
Also known as: IFNE_HUMAN, IFNE1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86WN2
- Gene
- IFNE
- Ensembl
- ENSG00000184995
- Chromosome
- 9
- Canonical length
- 208 aa
- Protein class
- Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
Predicted to enable cytokine activity and type I interferon receptor binding activity. Predicted to be involved in several processes, including defense response to other organism; lymphocyte activation involved in immune response; and positive regulation of receptor signaling pathway via JAK-STAT. Predicted to be located in extracellular region. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
208 residues, UniProt reviewed canonical sequence.
>Q86WN2|IFNE
1 MIIKHFFGTV LVLLASTTIF SLDLKLIIFQ QRQVNQESLK LLNKLQTLSI QQCLPHRKNF
61 LLPQKSLSPQ QYQKGHTLAI LHEMLQQIFS LFRANISLDG WEENHTEKFL IQLHQQLEYL
121 EALMGLEAEK LSGTLGSDNL RLQVKMYFRR IHDYLENQDY STCAWAIVQV EISRCLFFVF
181 SLTEKLSKQG RPLNDMKQEL TTEFRSPRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IFNE 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)
- 0.33
- Highest tissue expression
- 1.4 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 1.4 nTPM
- urinary bladder: 1.4 nTPM
- cerebellum: 1.1 nTPM
- cervix: 1.1 nTPM
- vagina: 0.9 nTPM
- epididymis: 0.8 nTPM
Single-cell type
- papillary tip epithelial cells: 2.6 nCPM
- renal collecting duct principal cells: 2.1 nCPM
- renal collecting duct intercalated cells: 1.2 nCPM
- loop of henle epithelial cells: 0.8 nCPM
- proximal tubule cells: 0.3 nCPM
- renal connecting tubule cells: 0.1 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: 3.1 nTPM
- cerebral cortex: 2.1 nTPM
- thalamus: 1.5 nTPM
- pons: 1.1 nTPM
- white matter: 1.1 nTPM
- spinal cord: 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)
- 1.62
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.71
- DepMap mean gene effect
- 0.1
- 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
- adaptive immune response
- B cell activation involved in immune response
- cellular response to virus
- defense response to bacterium
- defense response to virus
- humoral immune response
- natural killer cell activation involved in immune response
- response to exogenous dsRNA
- T cell activation involved in immune response
- type I interferon-mediated signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IFNE as an antibody target. Whether an autoantibody or antibody against IFNE could matter depends on whether native IFNE is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IFNE is annotated as secreted, so native IFNE 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 IFNE as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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