DeepDNA
ai.deepdna/knowledgeVersion 1.3.1Pharmacogenomics for AI agents: cited drug–gene, gene and rsID lookups plus a medication screen.
Status
Responds157 msAnswered our handshake without sign-in.- Last checked
- Nov 14, 2026, 13:28 UTC
- Latency
- 157 ms
- Remotes responding
- 1 of 1
- Sign-in
- No sign-in
- Hosting
- Hosted outside the EU (detected)
- Registry data as of
- Nov 14, 2026, 21:12 UTC
Data from the official MCP Registry, checked by run.zero. How we check
Connect
Streamable HTTP
https://deepdna.ai/mcpResponds157 msNo sign-in
Claude Code
claude mcp add --transport http knowledge https://deepdna.ai/mcpClaude Desktop and claude.ai
Settings > Connectors > Add custom connector
Name: knowledge
Remote MCP server URL: https://deepdna.ai/mcpCursor
{
"mcpServers": {
"knowledge": {
"url": "https://deepdna.ai/mcp"
}
}
}VS Code
code --add-mcp '{"name":"knowledge","type":"http","url":"https://deepdna.ai/mcp"}'Built your own server? run.zero hosts MCP servers on European infrastructure.
Tools
5 tools
Read-only | Idempotent | Open world | ||
|---|---|---|---|---|
check_medicationsGiven a list of generic drug names, say which ones have a curated drug–gene record, with which genes and what each record rests on (a CPIC or DPWG guideline, a drug label, or the primary literature), and which are not covered. Needs no genotype. | No | Yes | Yes | No |
list_genesList the genes in the DeepDNA knowledge base, with a one-line summary and category for each. | No | Yes | Yes | No |
lookup_drug_genePharmacogenomic guidance for a gene, optionally for one drug: guideline (CPIC or DPWG, "drug label", or null when the record rests on the primary literature), summary of the recommendation, phenotypes and sources. Omit drug to list every drug curated for that gene. | No | Yes | Yes | No |
lookup_geneEverything curated about one gene: function, key variants with rsIDs, metabolizer or function phenotypes, drug interactions, what a consumer genotyping array can and cannot tell you, and sources. | No | Yes | Yes | No |
lookup_variantOne variant by dbSNP rsID: gene, star-allele or common name, alleles, functional effect, population frequency and sources. Send the rsID only, never the user's genotype. A single variant is not a phenotype or metabolizer status. | No | Yes | Yes | No |
Details
- Registry status
- Active
- Published
- Oct 29, 2026
- Updated
- Oct 29, 2026
- Categories (suggested)
- Knowledge and notesSuggested categories are assigned automatically from the registry text and may be wrong. Verified operators can correct them.
- GDPR
- Not declared