protein

SARM1

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about SARM1: 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.

126Connections
2Hypotheses
1Analyses
50Outgoing
31Incoming
0Experiments
1Debates

Summary

SARM1 is a protein involved in neurodegeneration research. Key relationships include: activates, therapeutic target, regulates. Associated with Aging, Alzheimer's disease, Cancer. Connected to 29 entities in the SciDEX knowledge graph.

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🔬 Protein Info
Gene SymbolSARM1
Primary Expressionhippocampus
Molecular Weight89.5 kDa
PathwaysDisease Progression, Neuroinflammation
GeneCardsSARM1
Human Protein AtlasSARM1
Associated DiseasesAls, Alzheimer's disease, Axon Degeneration, Memory Impairment, neurodegeneration
InteractionsALZHEIMER, ALZHEIMER'S DISEASE, AND, APOPTOSIS, AUTOPHAGY, AXON
KG Connections125 knowledge graph edges
DatabasesGeneCardsUniProtNCBI GeneHPASTRING

Wiki Pages (5)

Knowledge base pages for this entity

Canonical Page

sarm1-programmed-axon-degeneration

mechanism · 1124 words

SARM1 NADase Inhibition for Axonal Preservation

idea · 2420 words

SARM1 NADase Inhibition Therapy

idea · 1497 words

SARM1 Inhibitor Therapy

therapeutic · 746 words

SARM1 Protein

protein · 623 words

Pathway Diagram

graph TD
    SARM1["SARM1"]
    axonal_degeneration(["axonal degeneration"])
    SARM1 -->|"activates"| axonal_degeneration
    neuroinflammation(["neuroinflammation"])
    SARM1 -->|"regulates"| neuroinflammation
    Alzheimer_s_disease{"Alzheimer's disease"}
    SARM1 -->|"associated with"| Alzheimer_s_disease
    hippocampal_neurons["hippocampal neurons"]
    SARM1 -->|"expressed in"| hippocampal_neurons
    Ms{"Ms"}
    SARM1 -->|"activates"| Ms
    AND["AND"]
    SARM1 -->|"activates"| AND
    DLK["DLK"]
    SARM1 -->|"activates"| DLK
    PUMA["PUMA"]
    SARM1 -->|"activates"| PUMA
    Apoptosis(["Apoptosis"])
    SARM1 -->|"activates"| Apoptosis
    Mapk(["Mapk"])
    SARM1 -->|"activates"| Mapk
    TNF["TNF"]
    TNF -->|"inhibits"| SARM1
    NAD["NAD"]
    NAD -->|"activates"| SARM1
    APOPTOSIS["APOPTOSIS"]
    APOPTOSIS -->|"activates"| SARM1
    AXON["AXON"]
    AXON -->|"activates"| SARM1
    BAX["BAX"]
    BAX -->|"activates"| SARM1
    style SARM1 fill:#1a3a4a,stroke:#4fc3f7,stroke-width:3px,color:#e0e0e0

Outgoing (95)

TargetRelationTypeStr
Jnk/Sting/Tbk1 Pathwayregulatespathway0.95
Depressive-Like Behaviorpromotesphenotype0.95
BDNFregulatesprotein0.90
Axon Degenerationcausesphenotype0.90
Axon Degenerationassociated_withphenotype0.90

Incoming (31)

SourceRelationTypeStr
31689415is the central executioner ofpaper0.90
TNFinhibitsentity0.80
NADactivatesgene0.60
APOPTOSISactivatesgene0.60
AXONactivatesgene0.60

Targeting Hypotheses (2)

Hypotheses where this entity is a therapeutic target

HypothesisScoreDiseaseAnalysis
SARM1-Mediated NAD+ Depletion as Terminal Executor of MCT1-D 0.698 neurodegeneration What is the molecular mechanism by which
NAD+/SARM1 Axis Provides Metabolic Feedback Coupling Mitopha 0.578 neurodegeneration How do different organelle-specific auto

Mentioning Analyses (1)

Scientific analyses that reference this entity

What molecular mechanisms enable functional recovery and muscle re-innervation a

neurodegeneration | 2026-04-14 | 2 hypotheses Top: 0.683

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 (1)

Multi-agent debates referencing this entity

The study shows dramatic functional recovery and muscle re-innervation after cyt

closed · Rounds: 4 · Score: 0.85 · 2026-04-15

Related Research

Hypotheses and analyses mentioning SARM1 in their description or question text

No additional research found