gene

SLC39A7

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about SLC39A7: 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

Page for SLC39A7 — Solute Carrier Family 39 Member 7

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🧬 Gene Info
Gene SymbolSLC39A7
Full NameSLC39A7 — Solute Carrier Family 39 Member 7
AliasesSolute Carrier Family 39 Member 7
Chromosome6p21.33
Protein TypeGene
Functionencodes a zinc transporter protein that localizes to the endoplasmic reticulum (ER) and Golgi apparatus[@huang2018].
GeneCardsSLC39A7
Human Protein AtlasSLC39A7
Amyotrophic Lateral Sclerosis (ALS)ER stress is a hallmark of motor neuron disease; ZIP7 dysfunction may exacerbate protein aggregation
Huntington's DiseaseZinc homeostasis disruption may contribute to mitochondrial dysfunction
FTD (Frontotemporal Dementia)Similar ER stress mechanisms may apply
Associated Diseasesneurodegeneration
DatabasesGeneCardsUniProtNCBI GeneHPASTRING

Wiki Pages (1)

Knowledge base pages for this entity

Canonical Page

SLC39A7 — Solute Carrier Family 39 Member 7

gene · 717 words

Pathway Diagram

graph TD
    SLC39A7["SLC39A7"]
    neurodegeneration["neurodegeneration"]
    SLC39A7 -->|"implicated_in"| neurodegeneration
    style SLC39A7 fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0

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Incoming (0)

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Targeting Hypotheses (0)

Hypotheses where this entity is a therapeutic target

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Mentioning Analyses (0)

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Experiments (0)

Experimental studies targeting or related to this entity

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Related Papers (0)

Scientific publications cited in analyses involving this entity

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Debates (0)

Multi-agent debates referencing this entity

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Related Research

Hypotheses and analyses mentioning SLC39A7 in their description or question text

No additional research found