gene

GDAP1

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about GDAP1: 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.

24Connections
0Hypotheses
0Analyses
19Outgoing
5Incoming

Summary

GDAP1 encodes a mitochondrial outer membrane protein critical for mitochondrial fission, peripheral nerve integrity, and neuronal survival. Mutations cause Charcot-Marie-Tooth disease.

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🧬 Gene Info
Gene SymbolGDAP1
Full NameGanglioside-Induced Differentiation-Associated Protein 1
Chromosome8q21.11
Protein FamilyMitochondrial fission proteins
Functionencodes a mitochondrial outer membrane protein that plays a critical role in regulating mitochondrial dynamics, particularly mitochondrial fission.
Subcellular Localizationthe mitochondrial outer membrane. The protein contains several functional domains:
Molecular Weight41 kDa
Amino Acids401 aa
Gene TypeProtein-coding
PathwaysAutophagy, Mitophagy
UniProt IDQ9UPN3
NCBI Gene ID78986
Ensembl IDENSG00000104381
OMIM607706
GeneCardsGDAP1
Human Protein AtlasGDAP1
Associated DiseasesAutosomal Recessive Ataxia, Neuropathy, Peripheral Neuropathy
InteractionsTFEB, AND, MITOPHAGY, AUTOPHAGY, BCL2, BNIP3
KG Connections24 knowledge graph edges
DatabasesGeneCardsHPASTRING
🔮 Predicted Structure: GDAP1 — AlphaFold Q9UPN3 Click to expand

AI-predicted structure from AlphaFold | Powered by Mol*

Wiki Pages (13)

Knowledge base pages for this entity

Canonical Page

GDAP1 — Ganglioside-Induced Differentiation-Associated Protein 1

gene · 1797 words

mitochondrial-dynamics

mechanism · 3276 words

Schwann Cells in Peripheral Neuropathy

cell · 3166 words

Charcot-Marie-Tooth Disease

disease · 2858 words

Schwann Cells

cell · 2252 words

AFG3L2 Gene

gene · 1120 words

Pathway Diagram

graph TD
    GDAP1["<b>GDAP1</b>"]
    Als{"Als"}
    GDAP1 -->|"regulates"| Als
    Neuropathy{"Neuropathy"}
    GDAP1 -->|"associated with"| Neuropathy
    Ms{"Ms"}
    GDAP1 -->|"contributes to"| Ms
    AUTOPHAGY["AUTOPHAGY"]
    GDAP1 -->|"contributes to"| AUTOPHAGY
    TFEB["TFEB"]
    GDAP1 -->|"activates"| TFEB
    LC3["LC3"]
    GDAP1 -->|"contributes to"| LC3
    Autophagy(["Autophagy"])
    GDAP1 -->|"contributes to"| Autophagy
    neurodegeneration["neurodegeneration"]
    GDAP1 -->|"implicated in"| neurodegeneration
    MOTOR_NEURONS["MOTOR NEURONS"]
    MOTOR_NEURONS -->|"contributes to"| GDAP1
    style GDAP1 fill:#1a3a4a,stroke:#4fc3f7,stroke-width:3px,color:#e0e0e0

Outgoing (19)

TargetRelationTypeStr
Peripheral Neuropathycausesdisease0.95
Autosomal Recessive Ataxiacausesdisease0.80
Alsregulatesdisease0.65
Neuropathyassociated_withdisease0.65
Mscontributes_todisease0.65

Incoming (5)

SourceRelationTypeStr
BCL2activatesgene0.60
BNIP3activatesgene0.60
BNIP3Lactivatesgene0.60
AFG3L2associated_withgene0.60
MOTOR NEURONScontributes_togene0.60

Targeting Hypotheses (0)

Hypotheses where this entity is a therapeutic target

HypothesisScoreDiseaseAnalysis
No targeting hypotheses

Mentioning Analyses (0)

Scientific analyses that reference this entity

No analyses mention this entity

Related Papers (0)

Scientific publications cited in analyses involving this entity

Title & PMIDAuthorsJournalYearCitations
No papers found