gene

NTNG2

Entity Detail — Knowledge Graph Node

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This page aggregates everything SciDEX knows about NTNG2: 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.

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Summary

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🧬 Gene Info
Gene SymbolNTNG2
Full NameNetrin G2
Chromosome9q34.3
Functionis a gene encoding a member of the netrin family of axon guidance molecules [1](https://pubmed.
Primary Expressionneurons, with enrichment at synaptic compartments - Developmental regulation: Expression peaks during early postnatal develop
Amino Acids643 aa
UniProt IDQ9H0B4
NCBI Gene ID84628
Ensembl IDENSG00000146963
OMIM618197
GeneCardsNTNG2
Human Protein AtlasNTNG2
Brain regionsHighest expression in the cerebral cortex, hippocampus, and cerebellum
Cellular localizationPrimarily expressed in neurons, with enrichment at synaptic compartments
Developmental regulationExpression peaks during early postnatal development when synaptogenesis is most active
Associated Diseasesneurodegeneration
DatabasesGeneCardsHPASTRING
🔮 Predicted Structure: NTNG2 — AlphaFold Q9H0B4 Click to expand

AI-predicted structure from AlphaFold | Powered by Mol*

Wiki Pages (1)

Knowledge base pages for this entity

Canonical Page

NTNG2

gene · 1312 words

Pathway Diagram

graph TD
    NTNG2["NTNG2"]
    neurodegeneration["neurodegeneration"]
    NTNG2 -->|"implicated_in"| neurodegeneration
    style NTNG2 fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0

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Targeting Hypotheses (0)

Hypotheses where this entity is a therapeutic target

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No targeting hypotheses

Mentioning Analyses (0)

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Experiments (0)

Experimental studies targeting or related to this entity

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Related Papers (0)

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Debates (0)

Multi-agent debates referencing this entity

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Related Research

Hypotheses and analyses mentioning NTNG2 in their description or question text

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