gene

PRKCG

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about PRKCG: 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.

34Connections
0Hypotheses
0Analyses
27Outgoing
7Incoming

Summary

PRKCG is a gene implicated in neurodegeneration research. Key relationships include: associated with, causes, expressed in. Associated with Ataxia, Neurodegeneration, Spinocerebellar Ataxia. Connected to 13 entities in the SciDEX knowledge graph.

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🧬 Gene Info
Gene SymbolPRKCG
Full NameProtein Kinase C Gamma
Chromosome19q13.42
Functionis a key mediator of the diacylglycerol (DAG) signaling pathway.
Primary ExpressionNeuron-specific
Molecular Weight89 kDa
Amino Acids697 aa
Exons17
UniProt ID[P05129](https://www.uniprot.org/uniprot/P05129)
Ensembl IDENSG00000156508
OMIM176980
GeneCardsPRKCG
Human Protein AtlasPRKCG
Associated DiseasesAtaxia, Neurodegeneration, Spinocerebellar Ataxia
InteractionsERK1
KG Connections34 knowledge graph edges
DatabasesGeneCardsNCBI GeneHPASTRING

Wiki Pages (19)

Knowledge base pages for this entity

Canonical Page

PRKCG — Protein Kinase C Gamma

gene Ā· 2761 words
→

CA8 Gene - Carbonic Anhydrase VIII

gene Ā· 2523 words
→

spinocerebellar-ataxia

disease Ā· 2304 words
→

Protein Kinase C Signaling Pathway

mechanism Ā· 2074 words
→

PRKCA Gene

gene Ā· 2014 words
→

Protein Kinase C (PKC) Signaling in Parkinson's Disease

mechanism Ā· 1953 words
→

Pathway Diagram

graph TD
    PRKCG["<b>PRKCG</b>"]
    Neurodegeneration{"Neurodegeneration"}
    PRKCG -->|"associated with"| Neurodegeneration
    Ataxia{"Ataxia"}
    PRKCG -->|"associated with"| Ataxia
    PRKCG -->|"regulates"| Neurodegeneration
    Spinocerebellar_Ataxia{"Spinocerebellar Ataxia"}
    PRKCG -->|"causes"| Spinocerebellar_Ataxia
    PRKCG -->|"causes"| Neurodegeneration
    PKC["PKC"]
    PRKCG -->|"associated with"| PKC
    NEURODEGENERATION["NEURODEGENERATION"]
    PRKCG -->|"causes"| NEURODEGENERATION
    GENES["GENES"]
    PRKCG -->|"causes"| GENES
    AND["AND"]
    PRKCG -->|"associated with"| AND
    Purkinje_Cell["Purkinje Cell"]
    PRKCG -->|"expressed in"| Purkinje_Cell
    Neuron["Neuron"]
    PRKCG -->|"expressed in"| Neuron
    neurodegeneration["neurodegeneration"]
    PRKCG -->|"implicated in"| neurodegeneration
    PKC -->|"associated with"| PRKCG
    GENES -->|"associated with"| PRKCG
    style PRKCG fill:#1a3a4a,stroke:#4fc3f7,stroke-width:3px,color:#e0e0e0

Outgoing (27)

TargetRelationTypeStr
Fragile X-Associated Tremor/Ataxia Syndromemodulatesdisease0.90
Fragile X-Associated Tremor/Ataxia Syndrometherapeutic_targetdisease0.90
Fragile X-associated tremor/ataxia syndromemodulatesdisease0.85
Cgg-Associated Neurotoxicitymodulatesmechanism0.85
Gabaergic Dysfunctionassociated_withprocess0.85

Incoming (7)

SourceRelationTypeStr
PKCassociated_withgene0.60
PKCencodesgene0.60
ERK1activatesgene0.60
MAPTregulatesgene0.60
GENESassociated_withgene0.60

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