gene

CLDN5

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about CLDN5: 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.

381Connections
1Hypotheses
2Analyses
50Outgoing
50Incoming

Summary

CLDN5 is a gene implicated in neurodegeneration research. Key relationships include: activates, inhibits, co discussed. Associated with ALS, Als, Brain Arteriovenous Malformations. Connected to 121 entities in the SciDEX knowledge graph.

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🧬 Gene Info
Gene SymbolCLDN5
Full NameClaudin-5
Chromosome22q11.21
Protein TypeStructural Protein
Target ClassStructural Protein
FunctionTight junction protein modulation - no established druggable mechanisms
Mechanism of ActionTight junction protein modulation - no established druggable mechanisms
Primary ExpressionBrain endothelial cells, Tight junctions of blood-brain barrier
DruggabilityUndruggable (0.20)
Clinical StageApproved
Amino Acids218 aa
Exons4
PathwaysCerebrovascular
UniProt IDO00511
NCBI Gene ID9079
Ensembl IDENSG00000184113
OMIM602507
GeneCardsCLDN5
Human Protein AtlasCLDN5
Associated DiseasesALS, Brain Edema, Stroke, blood-retinal barrier integrity, neurodegeneration
Known Drugs/Compoundscurcumin, resveratrol
InteractionsOCLN, CAV1, HIF1A, IL23A, BECN1, IL6
SciDEX TargetView Target Profile (5 clinical trials)
SciDEX HypothesesVascular-Glial Interface Restoration
KG Connections381 knowledge graph edges
DatabasesGeneCardsHPASTRING
🔮 Predicted Structure: CLDN5 — AlphaFold O00511 Click to expand

AI-predicted structure from AlphaFold | Powered by Mol*

Wiki Pages (21)

Knowledge base pages for this entity

Canonical Page

CLDN5 — Claudin-5

gene · 699 words

Blood-Brain Barrier Dysfunction in Neurodegeneration

mechanism · 4726 words

Blood-Brain Barrier Biology and Crossing Strategies

mechanism · 4474 words

bbb-transport-mechanisms

mechanism · 3506 words

Blood-Brain Barrier Breakdown in Neurodegeneration

mechanism · 3474 words

blood-brain-barrier-endothelial-cells

cell_type · 3383 words

Pathway Diagram

graph TD
    CLDN5["CLDN5"]
    CLDN5 -->|"encodes"| CLAUDIN5["CLAUDIN5"]
    CLDN5 -->|"encodes"| Claudin_5["Claudin-5"]
    CLDN5 -->|"activates"| Stroke["Stroke"]
    CLDN5 -->|"inhibits"| Als["Als"]
    CLDN5 -->|"target for"| Ms["Ms"]
    CLDN5 -->|"inhibits"| ALS["ALS"]
    h_7a8d7379["h-7a8d7379"] -->|"target for"| CLDN5
    H3K27me3["H3K27me3"] -->|"inhibits"| CLDN5
    AUTOPHAGY["AUTOPHAGY"] -->|"regulates"| CLDN5
    OCLN["OCLN"] -->|"activates"| CLDN5
    BECN1["BECN1"] -->|"activates"| CLDN5
    CXCL2["CXCL2"] -->|"inhibits"| CLDN5
    IL6["IL6"] -->|"inhibits"| CLDN5
    ATF4["ATF4"] -->|"target for"| CLDN5
    PPP1R15A["PPP1R15A"] -->|"target for"| CLDN5

Outgoing (249)

TargetRelationTypeStr
ds-f2c28aed24a7provides_data_fordataset1.00
Blood-Brain Barrier Integritycomponent_ofphenotype0.95
TIGHT JUNCTIONinvolved_inentity0.95
Blood-Brain Barrier Integrityregulatesphenotype0.95
Blood-Retinal Barrier Integritypromotesphenotype0.95

Incoming (132)

SourceRelationTypeStr
ds-f2c28aed24a7data_indataset1.00
Brain Arteriovenous Malformationsdownregulatesdisease0.95
Autophagyregulatesprocess0.95
DTGdownregulatesentity0.95
BRAIN ARTERIOVENOUS MALFORMATIONSdownregulatesentity0.95

Targeting Hypotheses (1)

Hypotheses where this entity is a therapeutic target

HypothesisScoreDiseaseAnalysis
Vascular-Glial Interface Restoration 0.544 neurodegeneration Cell type vulnerability in Alzheimers Di

Mentioning Analyses (2)

Scientific analyses that reference this entity

Cell type vulnerability in Alzheimers Disease (SEA-AD transcriptomic data)

neurodegeneration | 2026-04-03 | 17 hypotheses Top: 0.662

Blood-brain barrier transport mechanisms for antibody therapeutics

neurodegeneration | 2026-04-01 | 7 hypotheses Top: 0.566

Related Papers (0)

Scientific publications cited in analyses involving this entity

Title & PMIDAuthorsJournalYearCitations
No papers found