gene

SLC25A20

Entity Detail — Knowledge Graph Node

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This page aggregates everything SciDEX knows about SLC25A20: 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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🧬 Gene Info

Gene Symbol	SLC25A20
Chromosome	3p21.31
Function	is a critical mitochondrial carrier protein that mediates the transport of acylcarnitine esters across the inner mitochondrial membrane in exchange for free carnitine.
Primary Expression	all tissues requiring fatty acid oxidation, with highest levels in heart, skeletal muscle, and liver
Molecular Weight	33 kDa
Amino Acids	301 aa
Exons	9
Pathways	Connection
Ensembl ID	ENSG00000102737
GeneCards	SLC25A20
Human Protein Atlas	SLC25A20
Associated Diseases	neurodegeneration
Databases	GeneCards UniProt NCBI Gene HPA STRING

Wiki Pages (1)

Knowledge base pages for this entity

Canonical Page

slc25a20

gene · 1413 words

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Pathway Diagram

graph TD
    SLC25A20["SLC25A20"]
    neurodegeneration["neurodegeneration"]
    SLC25A20 -->|"implicated_in"| neurodegeneration
    style SLC25A20 fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0

Outgoing (0)

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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)

Scientific analyses that reference this entity

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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 SLC25A20 in their description or question text

No additional research found