Supabase
MCP server for interacting with the Supabase platform
Beschreibung vom Entwickler (englisches Original)
Look up genes, sequences, variants, homologs, and cross-database xrefs from Ensembl REST.
Diese drei werden nie zu einer Punktzahl zusammengefasst: Meinungen, Messungen und Beliebtheit sind verschiedene Dinge.
Für diesen Server haben wir noch keine Zusammenfassung in einfacher Sprache geschrieben. Unten stehen die Fakten, die wir aus der Registry gelesen haben.
Wähle die KI-App, die du nutzt, und kopiere die Einstellungen.
ENSEMBL_BASE_URL, MCP_LOG_LEVELDu brauchst
Welche App nutzt du?
Wähle oben deine App. Wir merken sie uns, damit der Button beim nächsten Mal „In … installieren“ anzeigt.
Funktioniert in Claude im Web, auf dem Desktop und auf dem Handy:
https://ensembl.caseyjhand.com/mcpÖffne Claude Desktop → Settings → Developer → Edit Config und füge dies in claude_desktop_config.json ein
{
"mcpServers": {
"ensembl": {
"command": "npx",
"args": [
"-y",
"@cyanheads/ensembl-mcp-server"
],
"env": {
"ENSEMBL_BASE_URL": "your-value",
"MCP_LOG_LEVEL": "your-value"
}
}
}
}Führe das in deinem Terminal aus
claude mcp add --transport http ensembl https://ensembl.caseyjhand.com/mcpclaude mcp add ensembl --env ENSEMBL_BASE_URL=your-value --env MCP_LOG_LEVEL=your-value -- npx -y @cyanheads/ensembl-mcp-serverTrag die leeren Werte ein, bevor du ihn startest.
In .cursor/mcp.json in deinem Projekt oder in ~/.cursor/mcp.json einfügen
{
"mcpServers": {
"ensembl": {
"url": "https://ensembl.caseyjhand.com/mcp"
}
}
}In .cursor/mcp.json in deinem Projekt oder in ~/.cursor/mcp.json einfügen
{
"mcpServers": {
"ensembl": {
"command": "npx",
"args": [
"-y",
"@cyanheads/ensembl-mcp-server"
],
"env": {
"ENSEMBL_BASE_URL": "your-value",
"MCP_LOG_LEVEL": "your-value"
}
}
}
}Dein Browser fragt, ob er die App öffnen darf, dann zeigt die App die Einstellungen und bittet dich um Bestätigung. Schlüsselwerte bleiben leer, damit du sie selbst einträgst.
In .vscode/mcp.json in deinem Projekt einfügen
{
"servers": {
"ensembl": {
"type": "http",
"url": "https://ensembl.caseyjhand.com/mcp"
}
}
}In .vscode/mcp.json in deinem Projekt einfügen
{
"servers": {
"ensembl": {
"type": "stdio",
"command": "npx",
"args": [
"-y",
"@cyanheads/ensembl-mcp-server"
],
"env": {
"ENSEMBL_BASE_URL": "your-value",
"MCP_LOG_LEVEL": "your-value"
}
}
}
}Dein Browser fragt, ob er die App öffnen darf, dann zeigt die App die Einstellungen und bittet dich um Bestätigung. Schlüsselwerte bleiben leer, damit du sie selbst einträgst.
ChatGPT verbindet sich nur mit Servern im Internet:
https://ensembl.caseyjhand.com/mcpMenünamen können sich je nach Tarif und mit der Zeit leicht unterscheiden.
Deine Auswahl bleibt in einem Cookie auf diesem Gerät; kein Konto nötig.
ENSEMBL_BASE_URL envMCP_LOG_LEVEL envDiese Einstellungen werden aus dem Registry-Eintrag des Entwicklers erzeugt. Wenn in der README etwas anderes steht, folge der README.
Tool-Namen und -Beschreibungen genau so, wie der Server sie am 7. Nov. 2026 gemeldet hat. Geschrieben hat sie der Entwickler, nicht wir; wir zeigen sie als reinen Text.
ensembl_list_speciesList species supported by Ensembl with display name, common name, assembly, taxon ID, and division. Required discovery step — species names like homo_sapiens are opaque to non-biologists and are the input format every other Ensembl tool expects. Use nameContains to find a species
ensembl_lookup_geneResolve a gene by symbol + species (or by stable ID) to its Ensembl ID, genomic location (chr:start-end:strand), biotype, description, and transcript list. Entry point for most workflows — the stable ID and coordinates returned here are inputs to other tools. Accepts both symbol
ensembl_get_sequenceFetch the DNA, cDNA, CDS, or protein sequence for a gene, transcript, protein, or genomic region. Returns a window of the sequence — the first 10,000 characters by default — with its stable ID, molecule type, and full length. When more follows the window, truncated is true and ne
ensembl_query_regionFind genomic features overlapping a chromosomal region: genes, transcripts, variants, regulatory elements, or exons. Returns each feature with its stable ID, type, location, biotype, and name, plus the genome assembly the coordinates are on. Useful for "what's in this locus?" and
ensembl_predict_variantPredict the functional consequences of a sequence variant using the Ensembl Variant Effect Predictor (VEP). Accepts three input formats: HGVS notation (transcript-relative, e.g. ENST00000380152.8:c.2T>A, or genomic, e.g. 13:g.32316462T>A); region+allele (chr:start:end:strand/alle
ensembl_get_homologyFind orthologs and/or paralogs of a gene across species. Returns each homolog's stable ID, species, homology type (ortholog_one2one, ortholog_one2many, paralog_many2many, etc.), percId and percPos (percent identical and positive positions, over the target protein's length), and t
ensembl_get_xrefsRetrieve cross-database references for a gene or feature — HGNC, UniProt, EntrezGene, OMIM, RefSeq, Reactome, and others. Returns each xref with its database name, primary ID, display ID, and description, plus how Ensembl assigned it (infoType, infoText) and its evidence codes (l
Wir prüfen Informationen, die jeder sehen kann; den Code haben wir nicht gelesen. Checks, die nicht zutreffen, werden nicht mitgezählt. · Geprüft am 7. Nov. 2026
Der Registry-Name wurde mit dem GitHub-Konto cyanheads bestätigt, dem das Repo gehört
Dieses Repo haben wir noch nicht von GitHub gelesen
Dieses Repo haben wir noch nicht von GitHub gelesen
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Wir haben 7 Tool-Beschreibungen gelesen und keine versteckten Anweisungen an die KI gefunden
Verglichen mit allen aktiven Servern dieser Kategorie in der Registry. Sterne zählen nur, wenn dem Herausgeber das Repo gehört.
Er hat 3 von 3 zutreffenden Basischecks bestanden. Den Code haben wir nicht gelesen. Bevor du einen Schlüssel oder Token hinzufügst, sieh nach, welche Zugriffe der Server verlangt, und nutze einen Schlüssel, der nur die Berechtigungen hat, die du brauchst.
Die Registry nennt keinen erforderlichen Schlüssel, manche Server bitten dich aber bei der ersten Nutzung, dich anzumelden.
Beides geht: Installiere ihn auf deinem Computer oder verbinde dich mit der Cloud-Version.
Das GitHub-Repo wurde zuletzt – geändert, und die neueste Version (0.7.1) kam vor 9 Tagen in die Registry.
Apps, die MCP unterstützen, etwa Claude Desktop, Claude Code, Cursor und VS Code. Er verbindet sich per URL, also funktionieren auch Apps, die Remote-MCP-Server akzeptieren, zum Beispiel ChatGPT im Entwicklermodus.
In derselben Kategorie: Supabase, MongoDB MCP Server, Elasticsearch MCP Server
Server derselben Kategorie von anderen Entwicklern, sortiert nach Sternen.
So liest du eine Karte:★ GitHub-SterneiDrei Säulen: Bewertungen · Checks · NutzungiAktualisiert = neueste Version in der Registry veröffentlichti
MCP server for interacting with the Supabase platform
MongoDB Model Context Protocol Server
MCP server for interacting with Elasticsearch
Unverändert aus dem Repo des Entwicklers übernommen. PopNx MCP hat den Inhalt weder geprüft noch empfiehlt es ihn. HTML, Bilder und Skripte wurden entfernt. Links führen von dieser Website weg.
@cyanheads/ensembl-mcp-server Look up genes, fetch sequences, predict variant consequences, find orthologs, and retrieve cross-database xrefs from Ensembl REST via MCP. STDIO or Streamable HTTP. 7 Tools • 4 Resources • 1 Prompt
Public Hosted Server: https://ensembl.caseyjhand.com/mcp
Gene, sequence, and variant data for vertebrates and other model organisms from the Ensembl REST API. Look up genes, fetch sequences, predict variant consequences, find orthologs, and cross-reference external databases.
| Tool | Description |
|---|---|
ensembl_list_species | List species supported by Ensembl with display name, common name, assembly, taxon ID, and division |
ensembl_lookup_gene | Resolve a gene by symbol (synonyms and former symbols included) + species or by stable ID to its Ensembl ID, genomic location, biotype, and transcript list |
ensembl_get_sequence | Fetch the DNA, cDNA, CDS, or protein sequence for a gene, transcript, protein, or genomic region |
ensembl_query_region | Find genomic features (genes, transcripts, variants, regulatory elements, exons) overlapping a chromosomal region |
ensembl_predict_variant | Predict functional consequences of a sequence variant using the Ensembl Variant Effect Predictor (VEP) |
ensembl_get_homology | Find orthologs and/or paralogs of a gene across species with percent identity and taxonomy level |
ensembl_get_xrefs | Retrieve cross-database references for a gene — HGNC, UniProt, EntrezGene, OMIM, RefSeq, Reactome, and others |
| Resource | Description |
|---|---|
ensembl://gene/{id} | Gene record by stable ID (ENSG…) — location, biotype, description, and transcript list |
ensembl://transcript/{id} | Transcript record by stable ID (ENST…) — parent gene, location, biotype, canonical flag, and length |
ensembl://species | Supported Ensembl species for the endpoint default division (vertebrates on the default endpoint) |
ensembl://species/{division} | Supported species in one division (EnsemblVertebrates, EnsemblPlants, EnsemblFungi, EnsemblMetazoa, EnsemblProtists) |
The species resources return the first 50 species by internal name; the ensembl_list_species tool pages through the rest and filters by name.
| Prompt | Description |
|---|---|
ensembl_gene_dossier | Structured workflow for assembling a complete gene profile: symbol → ID + location → sequence → variants → orthologs → xrefs |
Ensembl's stable-ID endpoints answer a versioned ID (ENSG00000139618.19) as not found, so every tool and resource that takes an Ensembl stable ID drops a trailing .N from an ENS… ID before the request and returns the current version. HGVS input to ensembl_predict_variant (ENST00000380152.8:c.2T>A) keeps its version, and IDs from other sources (AT3G52430.1) are forwarded unchanged.
ensembl_list_species tooldivision (EnsemblVertebrates, EnsemblPlants, EnsemblFungi, EnsemblMetazoa, EnsemblProtists; omitted, the endpoint default — vertebrates, ~356 species on GRCh38) and nameContains, a substring match against name, display name, and common namehomo_sapiens), plus display name, common name, taxon ID, assembly, and divisionoffset (default 0) and max_results (default 50, 0 uncapped); totalCount reports every match, and nextOffset is where the next page starts when more followensembl_lookup_gene toolsymbol (+ species, default homo_sapiens), id, ids, or symbols (up to 1,000 submitted items; first 20 distinct trimmed queries processed); expand_transcripts (default false) adds the transcript list with biotype and canonical flagcanonicalTranscript identifies the canonical transcript without expansion; transcript-ID lookups also return parentGeneId. Expanded transcripts include maneSelect RefSeq accessions when available (BRCA2: ENST00000380152.8, NM_000059.4)HER2 → ERBB2), reported as matchedAlias; a name shared by several genes (MDR1) returns ambiguous with candidates to retry by idgene (or ambiguous); a batch returns ordered succeeded items carrying the submitted query, failed items with query, reason (not_found, ambiguous with candidates, or unavailable), error, and recovery, and omitted queries past the processing cap. Omitted queries are never requested or reported as failed; resubmit them separately. Errors: not_found, invalid_species, no_input, conflicting_inputensembl_get_sequence toolENSG…/ENST…/ENSP…) or a region (species:chr:start-end, or chr:start-end with species; at most 10,000,000 bases); type is genomic (default), cdna, cds, or protein — cdna and cds from a transcript ID only, protein from a transcript or protein ID; expand_5prime/expand_3prime add flanking bases:1/:-1 strand suffix (1:1000000-1000020:-1 returns the reverse complement); the mitochondrion is MT in vertebrates (mitochondrion_genome in Drosophila, MtDNA in C. elegans), and M/chrM are rejected as invalid_region where they would not resolve to itoffset (default 0) and max_length (default 10000, 0 uncapped); length is the full sequence length, and truncated/nextOffset say where to resumenot_found, type_mismatch (also a protein ID asked for genomic/cdna/cds, or a non-coding transcript asked for protein/cds), invalid_species, missing_species, invalid_region (also an id with a colon that is not a valid region)ensembl_query_region toolregion as species:chr:start-end, or chr:start-end with species (at most 5,000,000 bases; reversed coordinates are rejected; mitochondrion naming as in ensembl_get_sequence); feature defaults to ["gene"] and also accepts transcript, variation, regulatory, exon; optional case-sensitive biotype filter (protein_coding, lncRNA). An empty filtered result suggests removing the filter without inferring the locus is intergenicmax_results caps the list (default 100, 0 uncapped) while totalCount reports the true count; assemblyName names the coordinates' assembly, and exon rows carry parentId and rank. Errors: invalid_region, invalid_species, missing_speciesensembl_predict_variant toolvariant as HGVS (transcript-relative or genomic), region+allele (chr:start:end:strand/allele), or a dbSNP rsIDinvalid_notation, not_found, invalid_speciesvariantAllele, optional canonical/maneSelect, HGVS and available SIFT/PolyPhen prediction-score pairs; records retain alleleStringclinicalSignificance is aggregate, not a classification of the submitted allele. clinicalSignificanceByAllele preserves explicit per-allele terms and clinicalSignificanceReferenceAllele identifies their reference allele; absent annotations remain omittedmax_transcript_consequences and max_pubmed_ids_per_variant (default 10 each, 0 uncapped; include_all_colocated_pubmed lifts the PubMed cap) bound the result, while transcriptConsequencesTotal and pubmedTotal report the full countsensembl_get_homology toolsymbol (+ species, default homo_sapiens) or id; type is orthologues (default), paralogues, or all; optional target_species filtertarget_species outside the comparison Ensembl runs for the source species (a fly gene to homo_sapiens) is answered from Ensembl's pan-taxonomic comparison when it holds both species, with a notice saying somax_results caps the list (default 25, 0 uncapped) while totalCount reports the true count. Errors: not_found, invalid_species (unknown species or target_species), target_not_compared (a target outside the source species' comparison that the pan-taxonomic comparison cannot answer), no_input, conflicting_inputtargetProteinId for ensembl_get_sequence with type:"protein". Optional targetSymbol comes from a lookup of the returned rows' distinct gene IDs, in chunks of at most 1,000, with one five-second budget bounded by the call's remaining deadline and no retries. Missing names or failed lookups retain every primary homolog with a notice; cancellation still abortsensembl_get_xrefs toolid (ENSG…/ENST…/ENSP…) required; optional dbname filter (e.g. HGNC, Uniprot_gn, Uniprot/SWISSPROT for the reviewed UniProt accession on the translation, EntrezGene, MIM_GENE, RefSeq_mRNA, Reactome_gene for gene pathways, Reactome for translation pathways, GO)all_levels:false queries the requested object's level. Set all_levels:true to include a gene's transcript and translation references, independently of dbname; for example, gene-level RefSeq_mRNA may need this or a transcript ID. Empty lists remain successful with totalCount:0. Errors: not_foundinfoType: DIRECT, DEPENDENT, PROJECTION, …; infoText: its source, such as UniProt or the ortholog a projection came from) and its evidence codes (linkageTypes, GO evidence such as IDA or IEA) when suNur der Anfang wird gezeigt; den Rest findest du im Repo