Gene Info
Workflow & Planning
View gene information by double clicking a gene name or accession on any webpage.
Users
2K
Rating
5.0
Reviews
14
7D Growth
--|--
Stable signalNo paid features detectedMedium-risk permissions
Mastermind Search Companion
The Mastermind Search Companion augments your gene and variant searches with articles citing your gene or variant from Mastermind.
Users1KCurrent public install base
Rating5.0Store average score
Reviews11Public review volume
Manifest versionV3Extension platform version
7-day growth0Net users gained this week
7-day growth rate0%Relative weekly velocity
Preview
6 assetsMastermind Search Companion Media preview
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30-day rating change
Start
5.00
Latest
5.00
30-day rating change
0.00
2026年7月7日2026年7月8日
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Version2.0
ManifestV3
Size2.36MiB
Languages1English
Published
Store updated
Last crawled
English
Overview
Product summary
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Mastermind Search Companion is used with the Mastermind Genomic Search Engine to optimize genomic variant research and interpretation by seamlessly integrating with the sites you already use. With Search Companion, you can:
Easily view helpful gene and variant information in the new sliding drawer tab with links to the evidence in Mastermind
Speed up your existing workflow without having to change it with the integrated display of Mastermind data in a variety of platforms you already use
Find more articles for your search when using ClinVar, HGMD, dbSNP, old dbSNP, OMIM, COSMIC, CIViC, UCSC Browser, Google Scholar, Google, VarSome, GeneCards, NCBI, Gnomad, SNPedia, and OncoKB by tapping into Mastermind data
Quickly compare Mastermind search results with results from the other platforms
For more information about Mastermind, visit the Mastermind Genomic Search Engine page: https://www.genomenon.com/mastermind/
Reviews
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Reviews with text2Synced review bodies
Total reviews11Chrome Web Store public rating/review count
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Allows for searching across multiple sites in parallel.
Very useful tool that overlays on ClinVar, HGMD, dbSNP, OMIM, COSMIC, CIViC, UCSC Browser, Google Scholar, VarSome, GeneCards, NCBI, Gnomad, SNPedia, & OncoKB. Quickly shows number of articles in PubMed containing the variant (no matter how the author describes it), A view of the variants published across the protein, transcripts, amino acid & CDNA positions & genomic positions.