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Online Mendelian Inheritance in Man (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. It is updated daily, and the entries contain copious links to other genetics resources.
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Omim Alternativen & Konkurrenten
Alternativen & Konkurrenten zu omim.org in Bezug auf Inhalt, Verkehr und Struktur
GeneCards is a searchable, integrated, database of human genes that provides concise genomic related information, on all known and predicted human genes
UniProt.
The atlas for all human proteins in cells and tissues using various omics: antibody-based imaging, transcriptomics, MS-based proteomics, and systems biology. Sections include the Tissue, Brain, Single Cell Type, Tissue Cell Type, Pathology, Disease Blood Atlas, Immune Cell, Blood Protein, Subcellular, Cell Line, Structure, and Interaction.
Orphanet.
Home | HUGO Gene Nomenclature Committee.
The Jackson Laboratory's mission is to discover precise genomic solutions for disease and empower the global biomedical community in the shared quest to improve human health.
Ensembl genome browser 107.
As a member of the wwPDB, the RCSB PDB curates and annotates PDB data according to agreed upon standards. The RCSB PDB also provides a variety of tools and resources. Users can perform simple and advanced searches based on annotations relating to sequence, structure and function. These molecules are visualized, downloaded, and analyzed by users who range from students to specialized scientists.
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Omim.org domain is owned by Tucows Inc. and its registration expires in 3 years and 6 months .
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3 Jahre, 6 Monate her
Läuft aus am Oktober 03, 2020Registrar und Status
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