gene

SLC39A13

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about SLC39A13: 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

SLC39A13 (ZIP13) is a zinc transporter involved in collagen biosynthesis and connective tissue development, with mutations causing spondylocheirodysplastic Ehlers-Danlos syndrome.

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🧬 Gene Info

Gene Symbol	SLC39A13
Full Name	SLC39A13 — Solute Carrier Family 39 Member 13
Aliases	ZIP13
Chromosome	11p11.2
Protein Type	Gene
Function	is a member of the solute carrier family 39 (SLC39) zinc transporter family[@liuzzi2004].
Primary Expression	various tissues, with highest levels in skin fibroblasts, cartilage, and brain
Subcellular Localization	### Transport Mechanism
Amino Acids	403 aa
NCBI Gene ID	Search NCBI
GeneCards	SLC39A13
Human Protein Atlas	SLC39A13
Associated Diseases	Alzheimer's disease, Parkinson's disease
Databases	GeneCards UniProt HPA STRING

Wiki Pages (2)

Knowledge base pages for this entity

Canonical Page

SLC39A13 — Solute Carrier Family 39 Member 13

gene · 1078 words

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Genes

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Pathway Diagram

graph TD
    SLC39A13["SLC39A13"]
    neurodegeneration["neurodegeneration"]
    SLC39A13 -->|"implicated_in"| neurodegeneration
    style SLC39A13 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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Mentioning Analyses (0)

Scientific analyses that reference this entity

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Experiments (0)

Experimental studies targeting or related to this entity

Experiment	Type	Disease	Score	Feasibility	Model	Status	Est. Cost
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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

No debates reference this entity