🧬
GeneE

AI-powered gene search with cited answers from real research papers.

Or browse by chromosome
20,000+Genes indexed
19,000+AI summaries
2M+Papers cited
100%Cited answers
Or browse gene rankings by research, clinical impact, and variants →
New here? See how GeneE works →
How GeneE works

From seven public databases to a cited answer.

We aggregate
Seven public databases unified under a single canonical gene ID.
AI synthesizes
Claude or Gemini reads the most relevant PubMed abstracts for each gene.
Every claim cited
PMIDs are verified against PubMed before any summary publishes.
See the full architecture →
An example answer

Every numbered citation links to a real PubMed paper.

AI Summary

BRCA1 is a tumor suppressor that maintains genome stability by promoting DNA double-strand break repair through homologous recombination 1. Germline pathogenic variants in BRCA1 substantially increase lifetime risk of breast and ovarian cancer, with cumulative breast cancer risk reaching ~72% by age 80 in carriers 2. The BRCA1 protein partners with PALB2, BRCA2, and RAD51 in a complex that loads RAD51 onto resected DNA ends, a process disrupted by most clinically reported BRCA1 missense variants 3.

Sources cited
1
BRCA1 promotes DNA double-strand break repair via homologous recombination.
PMID: 12677558
2
Germline BRCA1 mutations confer high lifetime risk of breast and ovarian cancer.
PMID: 7545954
3
BRCA1, PALB2, BRCA2, and RAD51 form a complex that loads RAD51 onto resected DNA ends.
PMID: 21208872
View the full BRCA1 page →
Built on

Authoritative public data sources.

NCBI Gene
UniProt
Gene Ontology
PubTator 3.0
Open Targets
ClinVar
gnomAD
See full source attribution →