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Top: Science: Biology: Genetics: Eukaryotic: Animal: Mammal: Human: Databases_and_Maps: Mutation:

Mutation (11)

See Also:
Sites:

http://www.uta.fi/imt/bioinfo/ADAbase/   » ADAbase: Mutation registry for Adenosine Deaminase Deficiency Open in a new browser window
   Features an introduction, submissions, publications, and an immunodeficiency resource. Includes a gene atlas for the ADA gene.
   http://www.uta.fi/imt/bioinfo/ADAbase/

http://www.icp.ucl.ac.be/adsldb/   » ADSLdb Open in a new browser window
   Provide up-to-date information about genetic variation of the adenylosuccinate lyase gene. Includes cDNA sequence and gene structure.
   http://www.icp.ucl.ac.be/adsldb/

http://www.albumin.org/   » Albumin Open in a new browser window
   Contains a list of published albumin mutations with references, accession numbers for nucleotide sequences, the list of registered cases of analbuminemia with references, plus news items of general interest .
   http://www.albumin.org/

http://ww2.mcgill.ca/androgendb/   » Andogen Receptor Gene Open in a new browser window
   A searchable mutations database. Includes a table and map of interacting proteins and links to related resources.
   http://ww2.mcgill.ca/androgendb/

http://life2.tau.ac.il/GeneDis/   » GeneDis Open in a new browser window
   Features the primary sequences of genes and proteins involved in human genetic diseases. The mutation table shows the location of the mutation on the cDNA, genomic DNA and protein sequence, and the number of exon or intron .
   http://life2.tau.ac.il/GeneDis/

http://archive.uwcm.ac.uk/uwcm/mg/hgmd0.html   » Institute of Medical Genetics in Cardiff Open in a new browser window
   Database of human gene mutation data . Features publications, newly added genes, and locus specific databases.
   http://archive.uwcm.ac.uk/uwcm/mg/hgmd0.html

http://mutdb.org/   » MutDB Open in a new browser window
   Public initiative to annotate genomic variants with data that assists in functional annotation. Offers tools to help determine which mutations are the most likely to be the underlying causative agents of disease.
   http://mutdb.org/

http://mecp2.chw.edu.au/   » RettBASE : MECP2 Open in a new browser window
   Searchable database of known and novel MECP2 disease-causing mutations and polymorphisms. From the International Rett Syndrome Association.
   http://mecp2.chw.edu.au/

http://www.sesep.uvsq.fr/Database.html   » The Tissue Nonspecific Alkaline Phosphatase Gene Mutations Database Open in a new browser window
   Provide information about genetic variation of the alpl gene responsible for hypophosphatasia. Includes a downloadable list of genotypes and mutations .
   http://www.sesep.uvsq.fr/Database.html

http://p53.free.fr/   » The p53 Web Site Open in a new browser window
   Features current work, a mutations analysis, and anatomy of the gene. Provided by the Institut Curie.
   http://p53.free.fr/

http://www.x-ald.nl/   » X-linked Adrenoleukodystrophy Database Open in a new browser window
   Catalogue and facilitate the analysis of X-ALD mutations and provide background information. Includes the structure of the ABCD1 gene and its gene sequence.
   http://www.x-ald.nl/


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Last Updated: 2006-09-10 04:49:09


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