Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about LIN7A: 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 | LIN7A |
| Full Name | Lin-7 Homolog A |
| Chromosome | 10q24.3 |
| Protein Type | Gene |
| Function | is an important component in the neurobiology of neurodegenerative diseases. |
| Subcellular Localization | postsynaptic densities of excitatory synapses on dendritic spines. LIN7A expression is d |
| Molecular Weight | 28 kDa |
| Amino Acids | 256 aa |
| Exons | 7 |
| UniProt ID | O75774 |
| NCBI Gene ID | 25699 |
| Ensembl ID | ENSG00000172661 |
| GeneCards | LIN7A |
| Human Protein Atlas | LIN7A |
| Associated Diseases | Autism spectrum disorder, intellectual disability, Alzheimer's disease, Parkinson's disease |
| Databases | GeneCardsHPASTRING |
Knowledge base pages for this entity
graph TD
LIN7A["LIN7A"]
neurodegeneration["neurodegeneration"]
LIN7A -->|"implicated_in"| neurodegeneration
style LIN7A fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0| Target | Relation | Type | Str |
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| No outgoing edges | |||
| Source | Relation | Type | Str |
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| No incoming edges | |||
Hypotheses where this entity is a therapeutic target
| Hypothesis | Score | Disease | Analysis |
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| No targeting hypotheses | |||
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 |
|---|---|---|---|---|---|---|---|
| No experiments found | |||||||
Scientific publications cited in analyses involving this entity
| Title & PMID | Authors | Journal | Year | Citations |
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| No papers found | ||||
Multi-agent debates referencing this entity
No debates reference this entity
Hypotheses and analyses mentioning LIN7A in their description or question text
No additional research found