Catalog of human genes and genetic disorders Online version of the book Mendelian Inheritence in Man maintained by Johns Hopkins University and located at –Contains same information as the book, only more up to date –16532 entries for genes or suspected Mendelian traits as of February 1 st, 2006 Used primarily by genetics researchers and those interested in genetic diseases One of the oldest non-relational databases still available ONLINE MENDELIAN INHERITANCE IN MAN

Only a few aspects of OMIM are stored as a relational database; it is primarily store as formatted text Each entry in OMIM is given: –A unique six-number ID (In this case, the ID is “176730”) that can be used to identify it –A symbol used to classify the type of entry (in this case a plus) –The locus of the gene (if applicable) –A lists of alias the entry can be described by All of these are used to identify an entry that contains large sections of text and references relevant to the entry A heavily abbreviated entry is shown at the right Mim-entry ::= { mimNumber "176730", mimType plus, title "INSULIN; INS", copyright "Copyright (c) Johns Hopkins University", symbol "INS", locus "11p15.5", aliases { "PROINSULIN" }, included { "HYPERPROINSULINEMIA, INCLUDED" } … text { { label "TEXT", text "Insulin, synthesized by the beta cells of the islets of Langerhans, consists of 2 dissimilar polypeptide chains, A and B, which are linked by 2 disulfide bonds. However, unlike many other proteins, e.g., hemoglobin, made up of structurally distinct subunits, insulin is under the control of a single genetic locus; chains A and B are derived from a one-chain precursor, proinsulin, which was discovered by {72:Steiner and Oyer (1967)}. Proinsulin is converted to insulin by the enzymatic removal of a segment that connects the amino end of the A chain to the carboxyl end of the B chain. This segment is called the C (for 'connecting') peptide. The insulin gene contains 3 exons and 2 introns; exon 2 encodes the signal peptide, the B chain, and part of the C peptide, while exon 3 encodes the remainder of the C peptide and the A chain."} } OMIM DATABASE

Example: Tay-Sachs Disease Suppose a user wished to find information on Tay-Sachs disease The OMIM entry contains the following for Tay-Sachs disease: –Alternative Titles –Description –Clinical Features –Biochemical Features (chemical changes in the body caused by the disease) –Pathogenesis (the origination and development of a disease) –Mapping (what area of a chromosome causes the disease) –Molecular Genetics –Diagnosis (techniques for finding the disease) –Population Genetics (which genetic groups are susceptible to the disease) –History –Animal Model (efforts to replicate and study the disease in animals) –References

Tay-Sachs continued An entry in OMIM typically contains extensive information both for individuals who may have a personal stake in the disease in question and professionals and students studying the disease OMIM is constantly updated to reflect the most current knowledge and research on genes and genetic diseases