gene

IL1R1

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about IL1R1: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.

67Connections
0Hypotheses
2Analyses
47Outgoing
20Incoming
0Experiments
2Debates

Summary

IL1R1 is a gene implicated in neurodegeneration research. Key relationships include: expressed in, associated with, implicated in. Associated with Als, Inflammation, Ms. Connected to 17 entities in the SciDEX knowledge graph.

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🧬 Gene Info
Gene SymbolIL1R1
Full NameInterleukin 1 Receptor Type 1
Chromosome2q12
Protein TypeReceptor
FunctionIL-1R1 mediates the potent pro-inflammatory effects of IL-1 cytokines in the central nervous system:
Subcellular Localization</b></td><td>Cell membrane (type I transmembrane)</td></tr>
Molecular Weight80 kDa
Amino Acids319 aa
PathwaysNF-κB, MAPK
UniProt ID[P01589](https://www.uniprot.org/uniprot/P01589)
Ensembl IDENSG00000115594
GeneCardsIL1R1
Human Protein AtlasIL1R1
Associated DiseasesAls, disease, Infection, Inflammation, microglial_priming, Microglial priming
InteractionsCCR2, Cytokine, IFN, Il-1, IL-1, Il-10
KG Connections67 knowledge graph edges
DatabasesGeneCardsNCBI GeneHPASTRING

Wiki Pages (2)

Knowledge base pages for this entity

Canonical Page

Interleukin-1 Receptor Type 1 Protein

protein · 1175 words

IL1R1 Gene

gene · 692 words

Pathway Diagram

graph TD
    IL1R1["IL1R1"]
    Ms{"Ms"}
    IL1R1 -->|"expressed in"| Ms
    Neuroinflammation{"Neuroinflammation"}
    IL1R1 -->|"expressed in"| Neuroinflammation
    Inflammation{"Inflammation"}
    IL1R1 -->|"expressed in"| Inflammation
    NEUROINFLAMMATION["NEUROINFLAMMATION"]
    IL1R1 -->|"expressed in"| NEUROINFLAMMATION
    SERPINA3["SERPINA3"]
    IL1R1 -->|"activates"| SERPINA3
    S100A9["S100A9"]
    IL1R1 -->|"expressed in"| S100A9
    neurodegeneration["neurodegeneration"]
    IL1R1 -->|"implicated in"| neurodegeneration
    IL1RN["IL1RN"]
    IL1RN -->|"expressed in"| IL1R1
    MICROGLIA["MICROGLIA"]
    MICROGLIA -->|"expressed in"| IL1R1
    MIRNAS["MIRNAS"]
    MIRNAS -->|"expressed in"| IL1R1
    ASTROCYTES["ASTROCYTES"]
    ASTROCYTES -->|"expressed in"| IL1R1
    MMP3["MMP3"]
    MMP3 -->|"expressed in"| IL1R1
    style IL1R1 fill:#1a3a4a,stroke:#4fc3f7,stroke-width:3px,color:#e0e0e0

Outgoing (47)

TargetRelationTypeStr
Microglial primingmediatesphenotype0.90
C1q expressionactivatesprocess0.70
Microglial primingcausesphenotype0.70
microglial_primingregulatesphenotype0.70
TNFRSF1Aassociated_withgene0.70

Incoming (20)

SourceRelationTypeStr
INFLAMMATIONassociated_withgene0.60
AMYLOIDassociated_withgene0.60
GENEScontributes_togene0.60
INFLAMMATIONactivatesgene0.60
FOSL2associated_withgene0.60

Targeting Hypotheses (0)

Hypotheses where this entity is a therapeutic target

HypothesisScoreDiseaseAnalysis
No targeting hypotheses

Mentioning Analyses (2)

Scientific analyses that reference this entity

Can circadian interventions reverse microglial priming independent of sleep disr

chronobiology | 2026-04-08 | 7 hypotheses Top: 0.455

How does sevoflurane-induced NF-κB activation specifically trigger complement ca

neuroinflammation | 2026-04-08 | 5 hypotheses Top: 0.658

Experiments (0)

Experimental studies targeting or related to this entity

ExperimentTypeDiseaseScoreFeasibilityModelStatusEst. Cost
No experiments found

Related Papers (0)

Scientific publications cited in analyses involving this entity

Title & PMIDAuthorsJournalYearCitations
No papers found

Debates (2)

Multi-agent debates referencing this entity

While the study demonstrates both NF-κB pathway activation and increased C1qa ex

closed · Rounds: 4 · Score: 0.74 · 2026-04-21

Can circadian interventions reverse microglial priming independent of sleep disr

closed · Rounds: 4 · Score: 0.95 · 2026-04-10

Related Research

Hypotheses and analyses mentioning IL1R1 in their description or question text

No additional research found