Gene and Drug Landing Page Aggregator

ARCHS4 provides access to gene counts from HiSeq 2000, HiSeq 2500 and NextSeq 500 platforms for human and mouse experiments from GEO and SRA.

The GWAS Catalog provides a consistent, searchable, visualisable and freely available database of SNP-trait associations, which can be easily integrated with other resources.

Enrichr is an enrichment analysis tool that provides various types of visualization summaries of collective functions of gene sets.

GeneMANIA builds subnetworks around an input gene using functional association data.

The Harmonizome is a collection of knowledge about genes and proteins from 114 datasets created by processing 66 online resources to facilitate discovery via data integration.

Reactome is a free, open-source, curated and peer-reviewed pathway database that provides intuitive bioinformatics tools for the visualization, interpretation and analysis of pathway knowledge.

IDG Reactome Portal provides biologist-friendly way to visualize proteins, complexes, and reactions in high-quality Reactome pathways.

SigCom LINCS data portal serves LINCS datasets and signatures. It provides a signature similarity search to query for mimicker or reverser signatures.

CFDE Gene Partnership uses FAIR APIs from different DCCs to find and present gene-centric knowledge.

The Pharos interface provides facile access to most data types collected by the Knowledge Management Center for the IDG program.

MARRVEL enables users to search multiple public variant databases simultaneously and provides a unified interface to facilitate the search process.

The objective of MetGENE is to identify the reactions catalyzed by the given gene(s) RPE and the related metabolites.

STRING is a database of known and predicted protein-protein interactions and a functional enrichment tool covering more than 5000 genomes.

BioGPS is a free extensible and customizable gene annotation portal, a complete resource for learning about gene and protein function.

Automated Vector Quantization of Massive Co-expression RNA-seq Data Improves Gene Function Prediction (PrismEXP) is a new statistical approach for accurate gene function prediction.

The RGCSRS Appyter provides visualizations of the RNA-seq signatures induced by CRISPR knockouts and chemical perturbagens. Signatures are computed from transformed data profiles from the LINCS L1000 data.

Gene Centric GEO Reverse Search Appyter enables users to query for a gene in a species of interest; it returns an interactive volcano plot of signatures in which the gene is up- or down-regulated.

The HGNC database is a curated online repository of approved gene nomenclature, gene groups and associated resources including links to genomic, proteomic and phenotypic information.

The Knockout Mouse Programme - International Mouse Phenotyping Consortium (KOMP-IMPC) has information about the functions of protein-coding genes in the mouse genome.

KEGG is a database resource for understanding high-level functions and utilities of the biological system from molecular-level information.

The NCBI Gene Database page provides information about nomenclature, RefSeqs, maps, pathways, variations, phenotypes, and links to genome-, phenotype-, and locus-specific resources.

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.

WikiPathways was established to facilitate the contribution and maintenance of pathway information by the biology community.

PubMed comprises more than 33 million citations for biomedical literature from MEDLINE, life science journals, and online books.

PDB has information about the 3D shapes of proteins, nucleic acids, and complex assemblies that contribute to understanding everything from protein synthesis to health and disease.