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Human genetic and genomic disorders linked to homeodomain proteins

Information on human genetic and genomic disorders linked to homeodomain proteins has been compiled from both Online Mendelian Inheritance in Man (OMIM) and the Human Gene Mutation Database (HGMD). The data contained here result from manual searches of both OMIM and HGMD, with all data being inspected for accuracy and redundancy. Any false positives resulting from the OMIM and HGMD searches were manually removed from the data set.

Two search options are provided here:

Searches performed using the Protein Names and Gene Symbols option below returns the OMIM accession number, protein name, gene symbol, and chromosomal map location for each entry.

Searches performed using the Disease Names and Mutations option below returns a table containing gene symbols, map locations, OMIM accession number, disease name, nucleotide- and protein-level mutations, HGMD accession number, and the number of mutations documented in HGMD.

Leaving the text field in either of the search forms below empty will return the entire set of data related to human genetic and genomic disorders linked to homeodomain proteins.

• Protein Names and Gene Symbols

  All Fields OMIM Protein Name Gene Symbol Map Location Nucleotide Mutation Protein Mutation in the Homeodomain Resource for

• Disease Names and Mutations

  All Fields OMIM Disease/Disorder Gene Symbol Map Location Nucleotide Mutation Protein Mutation in the Homeodomain Resource for

Comments, suggestions and problems to bioinformatics@nhgri.nih.gov