Allows the user to search across multiple NCBI databases. The Entrez system comprises 40 molecular and literature databases, including ClinVar, Gene, Genome, Nucleotide, and more.
* Registration required to access the free, public version of this resource *
The Human Gene Mutation Database (HGMD®) represents an attempt to collate known (published) gene lesions responsible for human inherited disease.
OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 15,000 genes. OMIM focuses on the relationship between phenotype and genotype.
In the upper right hand menu bar, select Browse, then Browse by subject. From there, select your area of interest to find relevant data repositories.
re3data.org is a global registry of research data repositories that covers research data repositories from different academic disciplines. It presents repositories for the permanent storage and access of data sets to researchers, funding bodies, publishers and scholarly institutions. re3data.org promotes a culture of sharing, increased access and better visibility of research data.