Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about SLC6A8: 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 | SLC6A8 |
| Aliases | Creatine Transporter |
| Chromosome | Xq28 |
| Function | encodes an 11-transmembrane-domain protein of approximately 635 amino acids. |
| Primary Expression | most tissues, with particularly high expression in kidney, brain, muscle, and heart |
| Amino Acids | 635 aa |
| GeneCards | SLC6A8 |
| Human Protein Atlas | SLC6A8 |
| N-terminal intracellular domain | Contains regulatory serine residues subject to phosphorylation |
| Transmembrane core | Forms the substrate-binding site (S1) and the gate mechanism |
| Large extracellular loop 1 | Contains glycosylation sites important for surface expression |
| C-terminal intracellular tail | Contains PDZ-binding motif for scaffolding protein interaction |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
Knowledge base pages for this entity
graph TD
SLC6A8["SLC6A8"]
neurodegeneration["neurodegeneration"]
SLC6A8 -->|"implicated_in"| neurodegeneration
style SLC6A8 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 SLC6A8 in their description or question text
No additional research found