biothings-api

name	biothings-api
description	Query gene, variant, and drug annotations via BioThings APIs
metadata	{"openclaw":{"emoji":"🧪","category":"domains","subcategory":"biomedical","keywords":["gene annotation","variant annotation","drug data","BioThings","mygene","myvariant","bioinformatics"],"source":"https://biothings.io"}}

BioThings API Suite

Overview

BioThings is a family of high-performance biomedical annotation APIs developed at the Scripps Research Institute. The suite provides unified, up-to-date access to gene, variant, and chemical/drug annotations aggregated from dozens of authoritative sources. Three primary services cover the core entities in translational research:

• MyGene.info — Gene annotations from NCBI Entrez, Ensembl, UniProt, GO, KEGG, Reactome, and 20+ sources.
• MyVariant.info — Variant annotations from dbSNP, ClinVar, gnomAD, CADD, COSMIC, and 15+ sources.
• MyChem.info — Drug and chemical annotations from NDC, DrugBank, ChEMBL, FDA, PubChem, and 10+ sources.

All three share identical query syntax, require no authentication, and return JSON. Free for academic and commercial use.

Authentication

No authentication or API keys are required. All endpoints are open-access.

# No API key needed — just query directly
curl "https://mygene.info/v3/query?q=BRCA1&size=1"

MyGene.info — Gene Annotations

Search Genes

GET https://mygene.info/v3/query?q={query}&size={n}

Query by gene symbol, name, Entrez ID, Ensembl ID, or keyword. Supports boolean operators (AND, OR, NOT) and field-specific queries like symbol:CDK2.

curl -s "https://mygene.info/v3/query?q=BRCA1&size=1"

Response:

{
  "took": 178,
  "total": 13223,
  "hits": [
    {
      "_id": "672",
      "_score": 145.6796,
      "entrezgene": "672",
      "name": "BRCA1 DNA repair associated",
      "symbol": "BRCA1",
      "taxid": 9606
    }
  ]
}

Get Gene by ID

GET https://mygene.info/v3/gene/{entrez_id}

Returns comprehensive annotations for a single gene. Use the fields parameter to select specific data sources.

# Full annotation (large response)
curl -s "https://mygene.info/v3/gene/1017"

# Selective fields
curl -s "https://mygene.info/v3/gene/1017?fields=symbol,name,summary,genomic_pos,go"

Response (key fields for CDK2, Entrez ID 1017):

{
  "_id": "1017",
  "symbol": "CDK2",
  "name": "cyclin dependent kinase 2",
  "HGNC": "1771",
  "MIM": "116953",
  "AllianceGenome": "1771",
  "taxid": 9606,
  "type_of_gene": "protein-coding"
}

The full response includes accessions, Gene Ontology terms, pathway memberships (KEGG, Reactome, WikiPathways), protein domains (InterPro, Pfam), homology data, and genomic coordinates.

MyVariant.info — Variant Annotations

Search Variants

GET https://myvariant.info/v1/query?q={query}&size={n}

Query by rsID, HGVS notation (e.g., chr7:g.140453136A>T), gene symbol, or ClinVar significance. Returns aggregated annotations from 15+ sources.

curl -s "https://myvariant.info/v1/query?q=rs58991260&size=1"

Response (truncated):

{
  "took": 20,
  "total": 1,
  "hits": [
    {
      "_id": "chr1:g.218631822G>A",
      "_score": 21.382616,
      "dbsnp": {
        "rsid": "rs58991260",
        "vartype": "snv",
        "ref": "G",
        "alt": "A",
        "chrom": "1"
      },
      "cadd": {
        "phred": 1.679,
        "consequence": "INTERGENIC",
        "chrom": 
         
      
       
                  
         
         
      
    
  

Get Variant by HGVS ID

GET https://myvariant.info/v1/variant/{hgvs_id}

curl -s "https://myvariant.info/v1/variant/chr1:g.218631822G>A?fields=dbsnp,cadd,clinvar"

MyChem.info — Drug & Chemical Annotations

Search Drugs/Chemicals

GET https://mychem.info/v1/query?q={query}&size={n}

Query by drug name, NDC code, InChIKey, or active ingredient. Aggregates data from FDA NDC, DrugBank, ChEMBL, PubChem, SIDER, and more.

curl -s "https://mychem.info/v1/query?q=aspirin&size=1"

Response (truncated):

{
  "took": 82,
  "total": 248,
  "hits": [
    {
      "_id": "0615-8613",
      "_score": 13.657401,
      "ndc": {
        "substancename": "ASPIRIN",
        "nonproprietaryname": "Aspirin",
        "proprietaryname": "Adult Low Dose Aspirin",
        "active_numerator_strength": "81",
        "active_ingred_unit": "mg/1",
        "dosageformname": "TABLET, DELAYED RELEASE",
        "routename": "ORAL",
        "producttypename": "HUMAN OTC DRUG",
         
          
          
          
          
          
        
      
    
  

Get Chemical by ID

GET https://mychem.info/v1/chem/{id}

curl -s "https://mychem.info/v1/chem/CHEMBL25?fields=drugbank,chembl,pubchem"

Query Syntax (Shared Across All Three APIs)

All BioThings APIs share the same query engine. Key features:

Feature	Syntax	Example
Field-specific	field:value	symbol:TP53
Boolean	AND, OR, NOT	BRCA1 AND cancer
Wildcard	*	CDK*
Range	[min TO max]	exac.af:[0.01 TO 0.05]
Pagination	size, from	size=20&from=40
Field selection	fields	fields=symbol,name,go
Sorting	sort	sort=_score:desc
Batch POST	POST with ids	Up to 1000 IDs per request

Rate Limits

• GET requests: 3 per second sustained; bursts up to 10/s tolerated
• POST batch requests: 1 per second; up to 1000 IDs per batch
• No daily cap for reasonable academic usage
• Best practice: Add 350ms delays between sequential requests; use batch POST for bulk queries
• User-Agent header: Set a descriptive User-Agent for priority support from the BioThings team

Python Example: Cross-API Gene-Variant-Drug Lookup

import requests, time

MYGENE = "https://mygene.info/v3"
MYVARIANT = "https://myvariant.info/v1"
MYCHEM = "https://mychem.info/v1"

def search_gene(symbol):
    resp = requests.get(f"{MYGENE}/query",
                        params={"q": f"symbol:{symbol}", "size": 1, "species": "human"})
    resp.raise_for_status()
    hits = resp.json().get("hits", [])
    return hits[0] if hits else {}

def search_variants(gene_symbol, size=5):
    resp = requests.get(f"{MYVARIANT}/query",
                        params={"q": f"clinvar.gene.symbol:{gene_symbol}",
                                "fields": "dbsnp.rsid,clinvar.rcv.clinical_significance,cadd.phred",
                                "size": size})
    resp.raise_for_status()
    return resp.json().get("hits", [])

def search_drug(name):
    resp = requests.get(f"{MYCHEM}/query",
                        params={"q": name, "size": 1,
                                "fields": "ndc.substancename,ndc.pharm_classes"})
    resp.raise_for_status()
    hits = resp.json().get(, [])
     hits[]  hits  {}


gene = search_gene()
()
time.sleep()

variants = search_variants(, size=)
 v  variants:
    rsid = v.get(, {}).get(, v.get())
    ()
time.sleep()

drug = search_drug()
()

Academic Use Cases

• GWAS follow-up: Annotate thousands of significant SNPs with allele frequencies (gnomAD), functional predictions (CADD, SIFT, PolyPhen), and clinical significance (ClinVar) via MyVariant.info batch queries.
• Drug target mapping: Link gene symbols to pathway memberships (KEGG, Reactome) via MyGene.info, then find approved drugs targeting those pathways via MyChem.info.
• Pharmacogenomics: Cross-reference variant annotations with drug metabolism data to identify clinically actionable gene-drug interactions.
• Systematic reviews: Programmatically collect gene/variant metadata across large candidate lists to populate supplementary tables in genomics publications.

References

• BioThings API Hub: https://biothings.io
• MyGene.info Documentation: https://docs.mygene.info
• MyVariant.info Documentation: https://docs.myvariant.info
• MyChem.info Documentation: https://docs.mychem.info
• Publication: Xin J et al. Genome Biology 17:91 (2016). https://doi.org/10.1186/s13059-016-0953-9