GeneMatcher: a matching tool for connecting investigators with an interest in the same gene.

TitleGeneMatcher: a matching tool for connecting investigators with an interest in the same gene.
Publication TypeJournal Article
Year of Publication2015
AuthorsSobreira, N, Schiettecatte, F, Valle, D, Hamosh, A
JournalHum Mutat
Date Published2015 Oct
KeywordsComputational Biology, Databases, Genetic, Genetic Predisposition to Disease, Genetic Variation, Humans, Information Dissemination, Phenotype, Rare Diseases, Software, User-Computer Interface, Web Browser

Here, we describe an overview and update on GeneMatcher (, a freely accessible Web-based tool developed as part of the Baylor-Hopkins Center for Mendelian Genomics. We created GeneMatcher with the goal of identifying additional individuals with rare phenotypes who had variants in the same candidate disease gene. We also wanted to facilitate connections to basic scientists working on orthologous genes in model systems with the goal of connecting their work to human Mendelian phenotypes. Meeting these goals will enhance the identification of novel Mendelian genes. Launched in September, 2013, GeneMatcher now has 2,178 candidate genes from 486 submitters spread across 38 countries entered in the database (June 1, 2015). GeneMatcher is also part of the Matchmaker Exchange ( with an Application Programing Interface enabling submitters to query other databases of genetic variants and phenotypes without having to create accounts and data entries in multiple systems.

Alternate JournalHum. Mutat.
PubMed ID26220891
PubMed Central IDPMC4833888
Grant ListU54 HG006542 / HG / NHGRI NIH HHS / United States
1U54HG006542 / HG / NHGRI NIH HHS / United States