IFNLR1
Interferon lambda receptor 1
Also known as: CRF2/12, IFNLR, IL-28R1, IL28RA, INLR1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IU57
- Gene
- IFNLR1
- Ensembl
- ENSG00000185436
- Chromosome
- 1
- Canonical length
- 520 aa
- Protein class
- Human disease related genes, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Cytosol
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
The protein encoded by this gene belongs to the class II cytokine receptor family. This protein forms a receptor complex with interleukine 10 receptor, beta (IL10RB). The receptor complex has been shown to interact with three closely related cytokines, including interleukin 28A (IL28A), interleukin 28B (IL28B), and interleukin 29 (IL29). The expression of all three cytokines can be induced by viral infection. The cells overexpressing this protein have been found to have enhanced responses to IL28A and IL29, but decreased response to IL28B. Three alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
520 residues, UniProt reviewed canonical sequence.
>Q8IU57|IFNLR1
1 MAGPERWGPL LLCLLQAAPG RPRLAPPQNV TLLSQNFSVY LTWLPGLGNP QDVTYFVAYQ
61 SSPTRRRWRE VEECAGTKEL LCSMMCLKKQ DLYNKFKGRV RTVSPSSKSP WVESEYLDYL
121 FEVEPAPPVL VLTQTEEILS ANATYQLPPC MPPLDLKYEV AFWKEGAGNK TLFPVTPHGQ
181 PVQITLQPAA SEHHCLSART IYTFSVPKYS KFSKPTCFLL EVPEANWAFL VLPSLLILLL
241 VIAAGGVIWK TLMGNPWFQR AKMPRALDFS GHTHPVATFQ PSRPESVNDL FLCPQKELTR
301 GVRPTPRVRA PATQQTRWKK DLAEDEEEED EEDTEDGVSF QPYIEPPSFL GQEHQAPGHS
361 EAGGVDSGRP RAPLVPSEGS SAWDSSDRSW ASTVDSSWDR AGSSGYLAEK GPGQGPGGDG
421 HQESLPPPEF SKDSGFLEEL PEDNLSSWAT WGTLPPEPNL VPGGPPVSLQ TLTFCWESSP
481 EEEEEARESE IEDSDAGSWG AESTQRTEDR GRTLGHYMARLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IFNLR1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.55
- Highest tissue expression
- 9.1 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 9.1 nTPM
- small intestine: 8.7 nTPM
- liver: 8.1 nTPM
- lymph node: 7.3 nTPM
- skin: 6.9 nTPM
- cerebellum: 6.4 nTPM
Single-cell type
- ocular epithelial cells: 114 nCPM
- pdcs: 110 nCPM
- urothelial cells: 103 nCPM
- enterocytes: 102 nCPM
- epididymal efferent duct ciliated cells: 92 nCPM
- epididymal efferent duct absorptive cells: 73 nCPM
Immune cell
- plasmacytoid DC: 11 nTPM
- naive B-cell: 5.9 nTPM
- memory B-cell: 4.9 nTPM
- gdT-cell: 1.8 nTPM
- memory CD8 T-cell: 1.4 nTPM
- naive CD8 T-cell: 1.4 nTPM
Brain region
- cerebellum: 14 nTPM
- hypothalamus: 6.9 nTPM
- white matter: 6.9 nTPM
- medulla oblongata: 6.3 nTPM
- pons: 6.2 nTPM
- midbrain: 5.8 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)
- 0.76
- gnomAD pLI
- 0.06
- gnomAD missense Z
- 0.77
- DepMap mean gene effect
- -0.2
- 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
- cellular response to virus
- cytokine-mediated signaling pathway
- defense response to virus
- mucosal immune response
- negative regulation of cell population proliferation
- positive regulation of cellular respiration
- regulation of defense response to virus by host
- response to type III interferon
- type III interferon-mediated signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IFNLR1 as an antibody target. Whether an autoantibody or antibody against IFNLR1 could matter depends on whether native IFNLR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IFNLR1 is annotated at the cell surface, where native IFNLR1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label IFNLR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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