Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about SLC25A12: 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 Symbol | SLC25A12 |
| Full Name | Solute Carrier Family 25 Member 12 (Aralar1) |
| Chromosome | 2q31.1 |
| Function | SLC25A12 is a member of the mitochondrial carrier family (SLC25) that transports metabolites across the inner mitochondrial membrane. |
| Primary Expression | various brain regions with specific patterns of cellular localization |
| Molecular Weight | 68 kDa |
| Amino Acids | 680 aa |
| UniProt ID | Q9NPJ3 |
| NCBI Gene ID | 5104 |
| Ensembl ID | ENSG00000107140 |
| OMIM | 603667 |
| GeneCards | SLC25A12 |
| Human Protein Atlas | SLC25A12 |
| Aspartate/Glutamate Exchange | Exchanges mitochondrial aspartate for cytosolic glutamate |
| Malate-Aspartate Shuttle | Essential component of NADH shuttling |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsHPASTRING |
Knowledge base pages for this entity
graph TD
SLC25A12["SLC25A12"]
neurodegeneration["neurodegeneration"]
SLC25A12 -->|"implicated_in"| neurodegeneration
style SLC25A12 fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0| Target | Relation | Type | Str |
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Hypotheses where this entity is a therapeutic target
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Scientific analyses that reference this entity
No analyses mention this entity
Experimental studies targeting or related to this entity
| Experiment | Type | Disease | Score | Feasibility | Model | Status | Est. Cost |
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Scientific publications cited in analyses involving this entity
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Multi-agent debates referencing this entity
No debates reference this entity
Hypotheses and analyses mentioning SLC25A12 in their description or question text
No additional research found