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Gene Database

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jaechang-hits
gene-database

NCBI Gene via E-utilities: curated records across 1M+ taxa. Official symbols, aliases, RefSeq IDs, summaries, coordinates, GO, interactions. Use for gene ID resolution and cross-species function queries. For sequences use Ensembl; for expression use geo-database.

Overview

Publisherjaechang-hits
RepositorySciAgent-Skills
Skill namegene-database
Stars
381
Forks
45
Bundled files
Instructions only
LicenseCC0-1.0
Links
  • Markdown instructions

    A SKILL.md file the model loads on demand, so it only costs tokens when a request actually matches.

  • Works with any LLM

    AI skills are plain Markdown, not provider-specific code, so this works with GPT, Claude, Gemini, Grok, or a local model.

  • Self-contained

    Everything the model needs lives in the instructions — no extra files to sync.

  • Open source

    Published by jaechang-hits on GitHub. Read the source before you install it.

Installation

Install the Gene Database AI skill in TypingMind to use it with any LLM, or drop it into another agent that reads SKILL.md.

1

Install in TypingMind

TypingMind installs a skill straight from its GitHub folder — it reads SKILL.md, bundles the resource files, and stores the result locally.

  1. Open the app and go to Plugins → Skills.
  2. Choose "Install from GitHub".
  3. Paste the skill folder URL below and confirm.
    https://github.com/jaechang-hits/SciAgent-Skills/tree/main/skills/genomics-bioinformatics/databases/gene-database
  4. Enable the skill in any chat where you want it available.
Plugins → Skills → Add skill → From GitHub URL, then paste the folder URL and press Continue.
2

Install in another agent

Any agent that reads the Agent Skills format can use this skill — copy the folder into that agent's skills directory.

Claude Code — .claude/skills
git clone --depth 1 https://github.com/jaechang-hits/SciAgent-Skills.git /tmp/SciAgent-Skills
mkdir -p .claude/skills
cp -r /tmp/SciAgent-Skills/skills/genomics-bioinformatics/databases/gene-database .claude/skills/gene-database
Restart Claude Code after copying so it picks up the new skill.

Use it in TypingMind

Enable Gene Database in any TypingMind chat and the model takes it from there. Its name and description sit in the system prompt, and the moment a request matches, the model loads the full instructions itself — you never invoke it by hand, and it costs no tokens until it is actually used.

The model loads Gene Database on its own as soon as a request matches it.

Works with any AI model

AI skills are plain Markdown instructions rather than provider-specific code, so Gene Database is not tied to the model it was written for. Install it once in TypingMind and use it with GPT-5, Claude, Gemini, Grok, DeepSeek, Mistral, Llama, or a local model you run yourself — all on your own API keys.

  • Loaded only when it is needed

    The system prompt carries just the name and description. The instructions are fetched on the first matching request, so an idle skill costs nothing.

  • Switch models mid-chat

    Because the skill is instructions rather than code, changing model does not break it — the next model reads the same SKILL.md.

Skill instructions

This is the SKILL.md content the model loads. Read it before installing — a skill is instructions your model will follow.

NCBI Gene Database

Overview

NCBI Gene is the authoritative curated database for gene-centric information, covering 1M+ genes across hundreds of thousands of taxa. Each gene record includes the official symbol, aliases, full name, functional summary, genomic coordinates (GRCh38/GRCh37), RefSeq accessions, GO annotations, interaction partners, and links to related databases. Access is free via E-utilities REST API (no API key required, though recommended).

When to Use

  • Resolving gene aliases and synonyms to the current official HGNC/NCBI symbol
  • Fetching the NCBI Gene ID (integer) for a gene symbol for downstream API calls (e.g., dbSNP, ClinVar, GEO)
  • Retrieving curated gene summaries and function descriptions programmatically
  • Pulling RefSeq mRNA (NM_) and protein (NP_) accessions associated with a gene
  • Querying GO functional annotations (Biological Process, Molecular Function, Cellular Component)
  • Finding orthologs across species via the NCBI Datasets v2 orthologs endpoint (legacy E-utilities gene_gene_homolog retired with HomoloGene in 2019)
  • For expression profiles across conditions use geo-database; for variant annotations use clinvar-database or ensembl-database

Prerequisites

  • Python packages: requests, xml.etree.ElementTree (stdlib), pandas (optional)
  • Data requirements: gene symbols, NCBI Gene IDs, or tax IDs
  • Environment: internet connection; NCBI email required (set email parameter)
  • Rate limits: 3 req/s unauthenticated; 10 req/s with free NCBI API key
bash
pip install requests pandas

Quick Start

python
import requests

EMAIL = "your@email.com"
BASE = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils"

def gene_search(query, retmax=5):
    r = requests.get(f"{BASE}/esearch.fcgi",
                     params={"db": "gene", "term": query,
                             "retmax": retmax, "retmode": "json", "email": EMAIL})
    r.raise_for_status()
    return r.json()["esearchresult"]["idlist"]

# Find human BRCA1 gene ID
ids = gene_search("BRCA1[sym] AND Homo sapiens[orgn]")
print(f"Gene IDs for BRCA1: {ids}")  # → ['672']

Core API

Query 1: Search by Symbol, Name, or Function

Use ESearch with field tags for precise queries.

python
import requests

EMAIL = "your@email.com"
BASE = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils"

# Exact symbol match for human gene
r = requests.get(f"{BASE}/esearch.fcgi",
                 params={"db": "gene", "email": EMAIL, "retmode": "json",
                         "term": "TP53[sym] AND Homo sapiens[orgn] AND alive[prop]"})
ids = r.json()["esearchresult"]["idlist"]
print(f"TP53 Gene ID: {ids}")  # → ['7157']
python
# Search by function keyword
r = requests.get(f"{BASE}/esearch.fcgi",
                 params={"db": "gene", "email": EMAIL, "retmode": "json",
                         "term": "CRISPR[title] AND Homo sapiens[orgn]", "retmax": 5})
ids = r.json()["esearchresult"]["idlist"]
print(f"CRISPR-related gene IDs: {ids}")

Query 2: Fetch Gene Summary (JSON/ESummary)

Retrieve key metadata fields for a list of Gene IDs.

python
import requests

EMAIL = "your@email.com"
BASE = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils"

def esummary_gene(gene_ids):
    r = requests.post(f"{BASE}/esummary.fcgi",
                      data={"db": "gene", "id": ",".join(gene_ids),
                            "retmode": "json", "email": EMAIL})
    r.raise_for_status()
    return r.json()["result"]

result = esummary_gene(["672", "675", "7157"])  # BRCA1, BRCA2, TP53

for uid in result.get("uids", []):
    g = result[uid]
    print(f"\n{g.get('name')} (ID {uid})")
    print(f"  Official symbol : {g.get('nomenclaturesymbol', g.get('name'))}")
    print(f"  Chr location    : {g.get('maplocation')}")
    print(f"  Summary (first 100): {g.get('summary', '')[:100]}...")
    print(f"  Aliases: {g.get('otheraliases', 'none')}")

Query 3: Fetch Full Gene Record (XML)

Retrieve the complete gene record in XML for RefSeq accessions, GO terms, and interaction data.

python
import requests
import xml.etree.ElementTree as ET

EMAIL = "your@email.com"
BASE = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils"

def efetch_gene_xml(gene_id):
    r = requests.get(f"{BASE}/efetch.fcgi",
                     params={"db": "gene", "id": gene_id,
                             "rettype": "gene_table", "retmode": "text", "email": EMAIL})
    r.raise_for_status()
    return r.text

# Get gene table (tab-delimited overview)
table = efetch_gene_xml("672")
print(table[:500])
python
# XML for RefSeq accession extraction
r = requests.get(f"{BASE}/efetch.fcgi",
                 params={"db": "gene", "id": "672",
                         "rettype": "xml", "retmode": "xml", "email": EMAIL})
root = ET.fromstring(r.text)

# Extract RefSeq mRNA accessions
for ref in root.iter("Gene-commentary"):
    acc = ref.find("Gene-commentary_accession")
    ver = ref.find("Gene-commentary_version")
    typ = ref.find("Gene-commentary_type")
    if acc is not None and acc.text and acc.text.startswith("NM_"):
        print(f"RefSeq mRNA: {acc.text}.{ver.text if ver is not None else ''}")

Query 4: Batch Symbol-to-ID Mapping

Map a list of gene symbols to NCBI Gene IDs efficiently.

python
import requests, time

EMAIL = "your@email.com"
BASE = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils"

def symbols_to_ids(symbols, organism="Homo sapiens"):
    """Map gene symbols to NCBI Gene IDs. Returns dict {symbol: gene_id}."""
    mapping = {}
    for sym in symbols:
        r = requests.get(f"{BASE}/esearch.fcgi",
                         params={"db": "gene", "email": EMAIL, "retmode": "json",
                                 "term": f"{sym}[sym] AND {organism}[orgn] AND alive[prop]"})
        ids = r.json()["esearchresult"]["idlist"]
        mapping[sym] = ids[0] if ids else None
        time.sleep(0.1)
    return mapping

genes = ["EGFR", "KRAS", "BRAF", "PIK3CA", "PTEN"]
id_map = symbols_to_ids(genes)
for sym, gid in id_map.items():
    print(f"{sym:10s} → Gene ID {gid}")

Query 5: GO Annotation Retrieval

Parse GO terms from the gene XML record.

python
import requests
import xml.etree.ElementTree as ET

EMAIL = "your@email.com"
BASE = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils"

r = requests.get(f"{BASE}/efetch.fcgi",
                 params={"db": "gene", "id": "7157",
                         "rettype": "xml", "retmode": "xml", "email": EMAIL})
root = ET.fromstring(r.text)

# Extract GO annotations
go_terms = []
for ref in root.iter("Gene-commentary"):
    heading = ref.find("Gene-commentary_heading")
    label = ref.find("Gene-commentary_label")
    if heading is not None and "Gene Ontology" in heading.text:
        if label is not None:
            go_terms.append(label.text)

print(f"TP53 GO terms ({len(go_terms)} found):")
for term in go_terms[:10]:
    print(f"  {term}")

Query 6: Cross-Species Orthologs (NCBI Datasets v2)

Find orthologs across species. Note: the legacy E-utilities link gene_gene_homolog was retired with HomoloGene in 2019 — the modern path is the NCBI Datasets v2 REST API, which exposes a dedicated orthologs endpoint.

python
import requests, time

DATASETS_BASE = "https://api.ncbi.nlm.nih.gov/datasets/v2"

def get_orthologs(gene_id, taxon_filter=None):
    """Return ortholog Gene reports for a given NCBI Gene ID.
    taxon_filter: optional tax_id (int) or list of tax_ids to narrow species."""
    params = {}
    if taxon_filter is not None:
        # tax_ids: human=9606, mouse=10090, rat=10116, zebrafish=7955, fly=7227
        ids = taxon_filter if isinstance(taxon_filter, (list, tuple)) else [taxon_filter]
        params["taxon_filter"] = [str(t) for t in ids]
    r = requests.get(f"{DATASETS_BASE}/gene/id/{gene_id}/orthologs",
                     params=params, timeout=30)
    r.raise_for_status()
    return r.json().get("reports", [])

# Mouse ortholog of human TP53 (Gene ID 7157)
reports = get_orthologs("7157", taxon_filter=10090)
for rep in reports[:5]:
    g = rep.get("gene", {})
    print(f"  {g.get('symbol'):8s} (tax {g.get('tax_id')}, gene_id {g.get('gene_id')}): "
          f"{g.get('description', '')[:60]}")
# Expect:  Trp53    (tax 10090, gene_id 22059): transformation related protein 53

time.sleep(0.34)
# All orthologs (every species in the orthology group)
all_orthologs = get_orthologs("7157")
print(f"\nTotal TP53 orthologs across species: {len(all_orthologs)}")

Key Concepts

NCBI Gene ID vs. HGNC ID vs. Ensembl ID

NCBI Gene IDs are integers assigned per gene per organism (e.g., human TP53 = 7157). These are distinct from HGNC IDs (e.g., HGNC:11998) and Ensembl IDs (ENSG00000141510). Many downstream NCBI databases (ClinVar, dbSNP, GEO) use NCBI Gene IDs internally.

alive[prop] Filter

NCBI Gene records for discontinued genes have status=discontinued. Always add AND alive[prop] to symbol queries to exclude retired entries and avoid retrieving stale data.

Common Workflows

Workflow 1: Build a Gene Annotation Table

Goal: For a list of gene symbols, retrieve Gene ID, official name, chromosomal location, and description.

python
import requests, time, pandas as pd

EMAIL = "your@email.com"
BASE = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils"

def search_gene(sym, organism="Homo sapiens"):
    r = requests.get(f"{BASE}/esearch.fcgi",
                     params={"db": "gene", "email": EMAIL, "retmode": "json",
                             "term": f"{sym}[sym] AND {organism}[orgn] AND alive[prop]"})
    ids = r.json()["esearchresult"]["idlist"]
    return ids[0] if ids else None

def batch_summary(gene_ids):
    r = requests.post(f"{BASE}/esummary.fcgi",
                      data={"db": "gene", "id": ",".join(gene_ids),
                            "retmode": "json", "email": EMAIL})
    return r.json()["result"]

symbols = ["BRCA1", "BRCA2", "TP53", "EGFR", "MYC", "KRAS", "PTEN"]

# Step 1: Symbol → Gene ID
id_map = {}
for sym in symbols:
    gid = search_gene(sym)
    id_map[sym] = gid
    time.sleep(0.12)

# Step 2: Batch summary
valid_ids = [v for v in id_map.values() if v]
result = batch_summary(valid_ids)

rows = []
sym_to_id = {v: k for k, v in id_map.items() if v}
for uid in result.get("uids", []):
    g = result[uid]
    rows.append({
        "symbol": sym_to_id.get(uid, g.get("name")),
        "gene_id": uid,
        "full_name": g.get("description"),
        "chr_location": g.get("maplocation"),
        "summary": g.get("summary", "")[:200],
    })

df = pd.DataFrame(rows)
df.to_csv("gene_annotations.csv", index=False)
print(df[["symbol", "gene_id", "full_name", "chr_location"]].to_string(index=False))

Workflow 2: Find All Genes in a Pathway Keyword

Goal: Retrieve all human genes associated with a biological keyword from the NCBI Gene summary field.

python
import requests, time, pandas as pd

EMAIL = "your@email.com"
BASE = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils"

keyword = "DNA mismatch repair"
r = requests.get(f"{BASE}/esearch.fcgi",
                 params={"db": "gene", "email": EMAIL, "retmode": "json",
                         "retmax": 50,
                         "term": f"{keyword}[title/abstract] AND Homo sapiens[orgn] AND alive[prop]"})
ids = r.json()["esearchresult"]["idlist"]
print(f"Found {len(ids)} genes related to '{keyword}'")

# Fetch summaries
r2 = requests.post(f"{BASE}/esummary.fcgi",
                   data={"db": "gene", "id": ",".join(ids), "retmode": "json", "email": EMAIL})
result = r2.json()["result"]

rows = []
for uid in result.get("uids", []):
    g = result[uid]
    rows.append({"gene_id": uid, "symbol": g.get("name"),
                 "description": g.get("description"),
                 "location": g.get("maplocation")})

df = pd.DataFrame(rows)
print(df.to_string(index=False))
df.to_csv(f"{keyword.replace(' ', '_')}_genes.csv", index=False)

Key Parameters

ParameterModuleDefaultRange / OptionsEffect
retmaxESearch201–10000Max records returned
retmodeESearch/ESummary"xml""json", "xml"Response format
rettypeEFetchdepends"xml", "gene_table", "text"Record format for full fetch
[sym] field tagESearch—gene symbolMatch exact official symbol only
[orgn] field tagESearch—organism name or tax IDFilter by taxonomy
alive[prop]ESearch—boolean flagExclude discontinued gene records

Best Practices

  1. Always add alive[prop]: Discontinued gene records remain in the database. Without this filter, symbol searches may return outdated records.

  2. Use Gene IDs in pipelines: Downstream NCBI databases (ClinVar, dbSNP, GEO) accept Gene IDs; avoid re-searching by symbol in each call.

  3. Use ESummary for metadata, EFetch for full records: ESummary returns JSON with all common fields; EFetch XML is needed only for RefSeq accessions, GO terms, or interaction links.

  4. Register for a free API key: Triple your rate limit (3 → 10 req/s) at https://www.ncbi.nlm.nih.gov/account/. Pass as api_key parameter.

  5. Batch with ESummary: POST up to 200 Gene IDs per call to ESummary instead of querying one at a time.

Common Recipes

Recipe: Gene ID to RefSeq NM Accession

When to use: Get the canonical mRNA accession for a protein-coding gene.

python
import requests, re

EMAIL = "your@email.com"
GENE_ID = "672"  # BRCA1

r = requests.get(
    "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi",
    params={"db": "gene", "id": GENE_ID, "rettype": "gene_table",
            "retmode": "text", "email": EMAIL}
)
nm_accessions = re.findall(r"NM_\d+\.\d+", r.text)
print(f"RefSeq mRNA accessions: {list(set(nm_accessions))}")

Recipe: Retrieve Gene Aliases

When to use: Resolve legacy/alias symbols to the current official NCBI symbol.

python
import requests

EMAIL = "your@email.com"

# P53 is an alias for TP53
r = requests.get(
    "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi",
    params={"db": "gene", "email": EMAIL, "retmode": "json",
            "term": "p53[sym] AND Homo sapiens[orgn] AND alive[prop]"}
)
ids = r.json()["esearchresult"]["idlist"]

r2 = requests.post("https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi",
                   data={"db": "gene", "id": ",".join(ids[:1]),
                         "retmode": "json", "email": EMAIL})
g = r2.json()["result"][ids[0]]
print(f"Official symbol : {g.get('nomenclaturesymbol', g.get('name'))}")
print(f"Other aliases   : {g.get('otheraliases')}")
print(f"Designations    : {g.get('otherdesignations', '')[:100]}")

Recipe: List All Genes on a Chromosome

When to use: Get all protein-coding genes on a specific human chromosome.

python
import requests

EMAIL = "your@email.com"

r = requests.get(
    "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi",
    params={"db": "gene", "email": EMAIL, "retmode": "json", "retmax": 5,
            "term": "17[chr] AND Homo sapiens[orgn] AND protein coding[filter] AND alive[prop]"}
)
result = r.json()["esearchresult"]
print(f"Protein-coding genes on chr17: {result['count']} total")
print(f"Sample IDs: {result['idlist']}")

Troubleshooting

ProblemCauseSolution
Empty idlist for known symbolSymbol is an alias, not the official termUse [gene name] or [title] field tag; check aliases via ESummary
Wrong species returnedMissing organism filterAdd AND Homo sapiens[orgn] or target tax ID (9606[taxid])
Discontinued gene returnedMissing alive[prop] filterAppend AND alive[prop] to all symbol queries
HTTP 429 rate limitToo many requestsAdd time.sleep(0.35) between calls; use NCBI API key
ESummary missing uids keyAll IDs invalid/absentCheck id values are valid integers, not empty strings
XML parse errorMalformed XML for rare genesWrap ET.fromstring in try/except; retry with rettype=text
Empty ortholog list from ELinkLegacy linkname=gene_gene_homolog retired with HomoloGene in 2019Use NCBI Datasets v2 /gene/id/{gene_id}/orthologs instead (Query 6)

Related Skills

  • geo-database — Gene Expression Omnibus for retrieving expression data linked to genes found here
  • clinvar-database — Clinical variant data indexed by NCBI Gene IDs
  • ensembl-database — Complementary gene annotations with VEP and comparative genomics
  • biopython-molecular-biology — Biopython Entrez module wraps E-utilities with typed return values

References

Frequently asked questions

What does the Gene Database AI skill do?

NCBI Gene via E-utilities: curated records across 1M+ taxa. Official symbols, aliases, RefSeq IDs, summaries, coordinates, GO, interactions. Use for gene ID resolution and cross-species function queries. For sequences use Ensembl; for expression use geo-database.

Why use Gene Database on TypingMind?

Because you install it once and use it with any model. Gene Database is plain Markdown rather than provider-specific code, so the same skill runs on GPT-5, Claude, Gemini, Grok, or a local model — and you can switch model mid-chat without it breaking. TypingMind runs on your own API keys, so you pay providers directly instead of a per-seat subscription, and your skills and chats stay in your own storage.

How do I install Gene Database in TypingMind?

Open Plugins → Skills → Install from GitHub in TypingMind and paste https://github.com/jaechang-hits/SciAgent-Skills/tree/main/skills/genomics-bioinformatics/databases/gene-database. TypingMind reads its SKILL.md and installs it as a skill you can enable per chat.

Which AI models can use Gene Database?

Any model you connect in TypingMind. AI skills are plain Markdown instructions rather than provider-specific code, so GPT, Claude, Gemini, Grok, and local models can all load this skill when a request matches it.

How many AI models can I use with Gene Database?

As many as you like. As long as a model supports skills, you can use Gene Database with it — GPT, Claude, Gemini, Grok, DeepSeek, Mistral, Llama and more — all on TypingMind with your own API keys.

Is the Gene Database AI skill free?

Yes. It is published on GitHub by jaechang-hits under the CC0-1.0 license. You only pay your own AI provider for the tokens you use.

What are AI skills?

An AI skill is a reusable instruction bundle that teaches an AI model how to do one specific task. It follows the open Agent Skills format: a SKILL.md file with a name and description, plus any scripts, templates or reference files the model may need. The model reads the instructions only when your request matches the skill, so an installed skill costs nothing until it is used.

How are AI skills different from plugins or MCP servers?

A plugin or MCP server gives a model new tools to call — code that runs somewhere and returns a result. An AI skill gives the model knowledge and process instead: how to approach a task, which steps to follow, what good output looks like. Skills are plain Markdown, so they need no server, no API key and no runtime, and they work with any model.

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