Gene Database
SkillDatabases & dataYour AI can look up genes in the NCBI Gene database by symbol or ID and pull back reference sequences, gene ontology terms, genomic locations, and associated phenotypes. Batch lookups let it annotate a whole list of genes in one pass. This is useful for resolving gene symbols to IDs or gathering functional and phenotype information for research.
Available today. Use it from your connected AI after setup.
No other account needed.
After adding it, ask your AI to look up a gene by its symbol or paste in a list of genes to annotate. Start with a single gene to see the information returned, then move on to batch lookups.
Then ask your AI: use the Gene Database skill
What your AI can do with it
- Search NCBI Gene by gene symbol or Gene ID
- Retrieve RefSeq reference sequences, gene ontology terms, genomic locations, and associated phenotypes
- Run batch lookups to annotate an entire gene list at once
- Resolve gene symbols to their NCBI Gene IDs
- Pull functional and phenotype information for genes of interest
What this skill tells your AI
The instructions your AI receives, as published by alterlab-ieu/alterlab-academic-skills in skills/databases/alterlab-gene-db/SKILL.md and read by ahel’s review.
Overview
NCBI Gene is a comprehensive database integrating gene information from diverse species. It provides nomenclature, reference sequences (RefSeqs), chromosomal maps, biological pathways, genetic variations, phenotypes, and cross-references to global genomic resources.
When to Use This Skill
This skill should be used when working with gene data including searching by gene symbol or ID, retrieving gene sequences and metadata, analyzing gene functions and pathways, or performing batch gene lookups.
Quick Start
NCBI provides two main APIs for gene data access:
- E-utilities (Traditional): Full-featured API for all Entrez databases with flexible querying
- NCBI Datasets API (Newer): Optimized for gene data retrieval with simplified workflows
Choose E-utilities for complex queries and cross-database searches. Choose the Datasets API for straightforward gene metadata retrieval (one gene report per request; transcript/protein RefSeq accessions come from the separate product_report endpoint).
Common Workflows
Search Genes by Symbol or Name
To search for genes by symbol or name across organisms:
- Use the
scripts/query_gene.pyscript with E-utilities ESearch - Specify the gene symbol and organism (e.g., "BRCA1 in human")
- The script returns matching Gene IDs
Example query patterns:
- Gene symbol:
insulin[gene name] AND human[organism] - Gene with disease:
dystrophin[gene name] AND muscular dystrophy[disease] - Chromosome location:
human[organism] AND 17q21[chromosome]
Retrieve Gene Information by ID
To fetch detailed information for known Gene IDs:
- Use
scripts/fetch_gene_data.pywith the Datasets API for comprehensive data - Alternatively, use
scripts/query_gene.pywith E-utilities EFetch for specific formats - Specify desired output format (JSON, XML, or text)
The Datasets API gene report returns:
- Gene nomenclature, aliases, and cross-references (HGNC, Ensembl, UniProt/Swiss-Prot, OMIM)
- Genomic location and assembly mapping (per assembly, e.g. GRCh38 and T2T-CHM13)
- Gene Ontology (GO) annotations
- Transcript and protein counts
For the individual transcript/protein RefSeq accessions, request the
product_report endpoint (GET /gene/id/{id}/product_report) — the base
gene report carries the counts, not the accessions.
Batch Gene Lookups
For multiple genes simultaneously:
- Use
scripts/batch_gene_lookup.pyfor efficient batch processing - Provide a list of gene symbols or IDs
- Specify the organism for symbol-based queries
- The script handles rate limiting automatically (10 requests/second with API key)
This workflow is useful for:
- Validating gene lists
- Retrieving metadata for gene panels
- Cross-referencing gene identifiers
- Building gene annotation tables
Search by Biological Context
To find genes associated with specific biological functions or phenotypes:
- Use E-utilities with Gene Ontology (GO) terms or phenotype keywords
- Query by pathway names or disease associations
- Filter by organism, chromosome, or other attributes
Example searches:
- By GO term:
GO:0006915[biological process](apoptosis) - By phenotype:
diabetes[phenotype] AND mouse[organism] - By pathway:
insulin signaling pathway[pathway]
API Access Patterns
Rate Limits:
- Without API key: 3 requests/second for E-utilities, 5 requests/second for Datasets API
- With API key: 10 requests/second for both APIs
Authentication: Register for a free NCBI API key at https://www.ncbi.nlm.nih.gov/account/ to increase rate limits.
Error Handling: Both APIs return standard HTTP status codes. Common errors include:
- 400: Malformed query or invalid parameters
- 429: Rate limit exceeded
- 404: Gene ID not found
Retry failed requests with exponential backoff.
Script Usage
query_gene.py
Query NCBI Gene using E-utilities (ESearch, ESummary, EFetch).
python scripts/query_gene.py --search "BRCA1" --organism "human"
python scripts/query_gene.py --id 672 --format json
python scripts/query_gene.py --search "insulin[gene] AND diabetes[disease]"
fetch_gene_data.py
Fetch comprehensive gene data using NCBI Datasets API.
python scripts/fetch_gene_data.py --gene-id 672
python scripts/fetch_gene_data.py --symbol BRCA1 --taxon human
python scripts/fetch_gene_data.py --symbol TP53 --taxon "Homo sapiens" --output json
batch_gene_lookup.py
Process multiple gene queries efficiently.
python scripts/batch_gene_lookup.py --file gene_list.txt --organism human
python scripts/batch_gene_lookup.py --ids 672,7157,5594 --output results.json
API References
For detailed API documentation including endpoints, parameters, response formats, and examples, refer to:
references/api_reference.md- Comprehensive API documentation for E-utilities and Datasets APIreferences/common_workflows.md- Additional examples and use case patterns
Search these references when needing specific API endpoint details, parameter options, or response structure information.
Data Formats
NCBI Gene data can be retrieved in multiple formats:
- JSON: Structured data ideal for programmatic processing
- XML: Detailed hierarchical format with full metadata
- GenBank: Sequence data with annotations
- FASTA: Sequence data only
- Text: Human-readable summaries
Choose JSON for modern applications, XML for legacy systems requiring detailed metadata, and FASTA for sequence analysis workflows.
Best Practices
- Always specify organism when searching by gene symbol to avoid ambiguity
- Use Gene IDs for precise lookups when available
- Batch requests when working with multiple genes to minimize API calls
- Cache results locally to reduce redundant queries
- Include API key in scripts for higher rate limits
- Handle errors gracefully with retry logic for transient failures
- Validate gene symbols before batch processing to catch typos
Resources
This skill includes:
scripts/
query_gene.py- Query genes using E-utilities (ESearch, ESummary, EFetch)fetch_gene_data.py- Fetch gene data using NCBI Datasets APIbatch_gene_lookup.py- Handle multiple gene queries efficiently
references/
api_reference.md- Detailed API documentation for both E-utilities and Datasets APIcommon_workflows.md- Examples of common gene queries and use cases
Signals
- GitHub stars
- 66
- Forks
- 13
- Last commit
- Sep 2026
Advanced
- Catalog kind
- skill
- Gateway key
alterlab-gene-db- Source
- github.com/alterlab-ieu/alterlab-academic-skills