Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about SETD1B: 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.
SETD1B is a histone H3K4 methyltransferase encoding the catalytic subunit of the COMPASS complex, involved in epigenetic regulation of neuronal function and neurodegenerative disease pathogenesis.
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| Gene Symbol | SETD1B |
| Full Name | SET Domain Containing 1B, Histone Lysine Methyltransferase |
| Chromosome | 12q24.31 |
| Protein Type | Transferase |
| Function | is a human gene encoding a histone H3 lysine 4 (H3K4) methyltransferase that functions as the catalytic subunit of the COMPASS (Complex of Proteins Associated with Set1) complex. |
| Molecular Weight | 192 kDa |
| Amino Acids | 755 aa |
| UniProt ID | Q9BRL5 |
| Ensembl ID | ENSG00000146070 |
| OMIM | 612052 |
| GeneCards | SETD1B |
| Human Protein Atlas | SETD1B |
| Associated Diseases | Alzheimer's disease, Parkinson's disease |
| Databases | GeneCardsNCBI GeneHPASTRING |
Knowledge base pages for this entity
graph TD
SETD1B["SETD1B"]
neurodegeneration["neurodegeneration"]
SETD1B -->|"implicated_in"| neurodegeneration
style SETD1B 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
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Experimental studies targeting or related to this entity
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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 SETD1B in their description or question text
No additional research found