Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about ERCC9: 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.
ERCC9 (also known as FANCN) encodes a DNA repair protein essential for the Fanconi anemia pathway and transcription-coupled nucleotide excision repair. ERCC9 dysfunction leads to neurodegeneration, Cockayne syndrome, and increased cancer risk.
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| Gene Symbol | ERCC Excision Repair 9, Complementing |
| Aliases | also known as FANCN |
| Chromosome | 9q33.2 |
| Protein Type | DNA Repair Protein, Fanconi Anemia Pathway |
| Function | encodes a DNA repair protein essential for the Fanconi anemia pathway and transcription-coupled nucleotide excision repair (TC-NER)[@bogliolo2007]. |
| Amino Acids | 462 aa |
| UniProt ID | Q8IYD1 |
| NCBI Gene ID | 2075 |
| Ensembl ID | ENSG00000135821 |
| OMIM | 614721 |
| Brain | Neurons in cortex, hippocampus, and basal ganglia |
| Bone marrow | Hematopoietic stem and progenitor cells |
| Liver | Hepatocytes |
| Kidney | Tubular epithelial cells |
| Testis | Spermatogenic cells |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsHPASTRING |
Knowledge base pages for this entity
graph TD
ERCC9["ERCC9"]
neurodegeneration["neurodegeneration"]
ERCC9 -->|"implicated_in"| neurodegeneration
style ERCC9 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
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Hypotheses and analyses mentioning ERCC9 in their description or question text
No additional research found