gene

PMP22

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about PMP22: 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.

40Connections
0Hypotheses
0Analyses
27Outgoing
13Incoming
0Experiments
0Debates

Summary

PMP22 is a gene implicated in neurodegeneration research. Key relationships include: inhibits, expressed in, causes. Associated with ALS, Als, Dementia. Connected to 23 entities in the SciDEX knowledge graph.

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🧬 Gene Info
Gene SymbolPMP22
Full NamePeripheral Myelin Protein 22
Chromosome17p12
FunctionThe PMP22 gene encodes a 22-kDa tetraspan membrane protein that is a major component of peripheral nerve myelin.
Primary ExpressionPeripheral nervous system, Schwann cells
UniProt IDP60265
NCBI Gene ID537
Ensembl IDENSG00000109099
OMIM601097
GeneCardsPMP22
Human Protein AtlasPMP22
Associated DiseasesAls, Charcot-Marie-Tooth Disease, disease, multiple sclerosis, Neuropathy
InteractionsAKT, MPZ, MTOR, NEURON, PI3K, PMP22 PROTEIN
KG Connections40 knowledge graph edges
DatabasesGeneCardsHPASTRING
🔮 Predicted Structure: PMP22 — AlphaFold P60265 Click to expand

AI-predicted structure from AlphaFold | Powered by Mol*

Wiki Pages (2)

Knowledge base pages for this entity

Canonical Page

PMP22 — Peripheral Myelin Protein 22

gene · 700 words

PMP22 Protein — Peripheral Myelin Protein 22

protein · 818 words

Pathway Diagram

graph TD
    PMP22["<b>PMP22</b>"]
    Neuropathy{"Neuropathy"}
    PMP22 -->|"associated with"| Neuropathy
    Als{"Als"}
    PMP22 -->|"associated with"| Als
    Parkinson{"Parkinson"}
    PMP22 -->|"expressed in"| Parkinson
    Dementia{"Dementia"}
    PMP22 -->|"expressed in"| Dementia
    ALS{"ALS"}
    PMP22 -->|"causes"| ALS
    PMP22 -->|"causes"| Neuropathy
    MTDNA["MTDNA"]
    PMP22 -->|"expressed in"| MTDNA
    MYELIN["MYELIN"]
    PMP22 -->|"causes"| MYELIN
    AND["AND"]
    PMP22 -->|"causes"| AND
    neurodegeneration["neurodegeneration"]
    PMP22 -->|"implicated in"| neurodegeneration
    MPZ["MPZ"]
    MPZ -->|"interacts with"| PMP22
    PARKINSON_S_DISEASE["PARKINSON'S DISEASE"]
    PARKINSON_S_DISEASE -->|"expressed in"| PMP22
    MITOCHONDRIAL_DNA["MITOCHONDRIAL DNA"]
    MITOCHONDRIAL_DNA -->|"expressed in"| PMP22
    CD9["CD9"]
    CD9 -->|"expressed in"| PMP22
    style PMP22 fill:#1a3a4a,stroke:#4fc3f7,stroke-width:3px,color:#e0e0e0

Outgoing (27)

TargetRelationTypeStr
Charcot-Marie-Tooth Diseaseimplicated_indisease0.95
Charcot-Marie-Tooth Diseasecausesdisease0.95
Myelin Maintenanceinvolved_inprocess0.85
Neuropathycausesdisease0.75
ALScausesdisease0.65

Incoming (13)

SourceRelationTypeStr
MPZinteracts_withgene0.90
PARKINSON'S DISEASEexpressed_ingene0.60
MITOCHONDRIAL DNAexpressed_ingene0.60
ANDcausesgene0.60
MYELINcausesgene0.60

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

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 (0)

Multi-agent debates referencing this entity

No debates reference this entity