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OMIM External Links |
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Genome |
Ensembl |
Genome databases for vertebrates and other eukaryotic species. |
MITOMAP |
A curated repository of published and unpublished data on human mitochondrial DNA variation. |
NCBI Map Viewer |
Detailed views of the complete genomes of selected organisms from vertebrates to protozoa. |
UCSC |
UCSC Genome Browser; reference sequences and working draft assemblies for a large collection of genomes. |
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DNA |
Ensembl |
Transcript-based views for coding and noncoding DNA. |
NCBI RefSeq |
A collection of genome, gene, and transcript sequence data from several sources, including GenBank, RefSeq. |
UCSC |
UCSC Genome Browser; reference sequences and working draft assemblies for a large collection of genomes. |
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Protein |
UniProt |
Comprehensive protein sequence and functional information, including supporting data. |
HPRD |
The Human Protein Reference Database; manually extracted and visually depicted information on human proteins. |
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Gene Info |
BioGPS |
The Gene Portal Hub; customizable portal of gene and protein function information. |
Ensembl |
Orthologs, paralogs, regulatory regions, and splice variants. |
NCBI Gene |
Gene-specific map, sequence, expression, structure, function, citation, and homology data. |
GeneCards |
The Human Genome Compendium; web-based cards integrating automatically mined information on human genes. |
KEGG |
Kyoto Encyclopedia of Genes and Genomes; diagrams of signaling pathways. |
PharmGKB |
Pharmacogenomics Knowledge Base; curated and annotated information regarding the effects of human genetic variations on drug response. |
UCSC |
UCSC Genome Bioinformatics; gene-specific structure and function information with links to other databases. |
HGNC |
HUGO Gene Nomenclature Committee. |
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Clinical |
ClinicalTrials.gov |
A registry of federally and privately supported clinical trials conducted in the United States and around the world. |
Gene Tests |
Information on genetic testing and its use in diagnosis, management, and genetic counseling. |
Gene Reviews |
Expert-authored, peer-reviewed descriptions of inherited disorders including the uses of genetic testing in diagnosis, management, and genetic counseling. |
OrphaNet |
European reference portal for information on rare diseases and orphan drugs. |
EuroGentest |
A list of European laboratories that offer genetic testing. |
Genetic Alliance |
Network of disease-specific advocacy organizations, universities, private companies, government agencies, and public policy organizations. |
Genetics Home Reference |
Consumer-friendly information about the effects of genetic variation on human health. |
Newborn Screening |
Information and resources for newborn screening and genetics. |
POSSUM |
A dysmorphology database of multiple malformations; metabolic, teratogenic, chromosomal, and skeletal syndromes; and their images. |
DermAtlas |
Images and descriptions of lesions seen in dermatologic disorders. |
GARD |
Genetic and Rare Diseases Information Center; information on rare and/or genetic disorders including portal to clinician and patient resources. |
DECIPHER |
Database of chromosomal aberration including clinical and genomic information. |
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Variation |
Genetics Association DB |
An archive of human genetic association studies of complex diseases and disorders. |
HGMD |
Human Gene Mutation Database; published mutations causing or associated with human inherited disease; disease-associated/functional polymorphisms. |
GWAS Central |
GWAS Central; summary level genotype-to-phenotype information from genetic association studies. |
HGVS |
Human Genome Variation Society; maintains lists of and links to locus-specific mutation databases; guidelines for description of sequence variants. |
Locus Specific DBs |
A gene-specific database of variation. |
LOVD |
Colon cancer gene variant databases. |
inSIGHT |
International Society for Gastrointestinal Hereditary Tumors. |
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Animal Models |
FlyBase |
A Database of Drosophila Genes and Genomes. |
NCBI HomoloGene |
A system for automated detection of homologs among the annotated genes of several completely sequenced eukaryotic genomes. |
MGI Mouse Phenotype |
Phenotypes, alleles, and disease models from Mouse Genome Informatics. |
KOMP |
Knockout Mouse Project Repository; mouse embryonic stem cells containing null mutations in every gene in the mouse genome. |
IKMC |
International Knockout Mouse Consortium; database of mouse gene knockouts. |
MGI Mouse Gene |
Mouse Genome Informatics; international database resource for the laboratory mouse, including integrated genetic, genomic, and biological data. |
Wormbase Gene |
Database of the biology and genome of Caenorhabditis elegans and related nematodes. |
ZFin |
The Zebrafish Model Organism Database. |
OMIA |
Online Mendelian Inheritance in Animals (OMIA) is a database of genes, inherited disorders and traits in 191 animal species (other than human and mouse.) |
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Cell Lines |
Coriell |
Coriell Cell Repositories; cell cultures and DNA derived from cell cultures. |
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Pathways |
KEGG |
Kyoto Encyclopedia of Genes and Genomes; diagrams of signaling pathways. |
Reactome |
Protein-specific information in the context of relevant cellular pathways. |
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