Mutation Databases and Maps Human Mammal

Provide information about genetic variation of the alpl gene responsible for hypophosphatasia. Includes a downloadable list of genotypes and mutations .

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• GeneDis - Features the primary sequences of genes and proteins mutation involved in mutation human genetic diseases. The mutation table mutation shows the location of mutation the mutation on the mutation cDNA, genomic DNA and protein sequence, mutation and the mutation number of exon or intron. Text partly in mutation mutation Hebrew.
• MutDB - Public initiative to annotate genomic variants with data that assists databases and maps in functional annotation. Offers tools to help determine which mutations databases and maps are the most likely to be the underlying causative agents databases and maps of disease.
• ADAbase: Mutation registry for Adenosine Deaminase Deficiency - Features an introduction, submissions, publications, and an immunodeficiency resource. Includes databases and maps a gene atlas for the ADA gene.
• RettBASE : MECP2 - Searchable database of known and novel MECP2 disease-causing human mutations and mutation polymorphisms. From the International Rett Syndrome human Association.
• X-linked Adrenoleukodystrophy Database - Catalogue and facilitate the analysis of X-ALD mutations and provide background information. Includes the structure of the ABCD1 gene and its gene sequence.
• The Tissue Nonspecific Alkaline Phosphatase Gene Mutations Database - Provide information about genetic variation of the alpl gene responsible for hypophosphatasia. Includes a downloadable list of genotypes and mutations .
• Institute of Medical Genetics in Cardiff - Database of human gene mutation data . Features human publications, newly added genes, and locus specific databases.
• Andogen Receptor Gene - A searchable mutations database. Includes a table and databases and maps human map of interacting proteins and links to related databases and maps human resources.
• Albumin - Includes a list of published albumin mutations with human references, accession numbers for nucleotide sequences, the list human of registered cases of analbuminemia with references, plus human news items of general interest .
• ADSLdb - Provide up-to-date information about genetic variation of the mutation adenylosuccinate lyase databases and maps gene. Includes cDNA sequence and gene mutation structure.
• The p53 Web Site - Features current work, a mutations analysis, and anatomy of the gene. Provided by the Institut Curie.

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