Sequence based mutation analysis of GBA

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Revision as of 16:53, 21 June 2011 by Braunt (talk | contribs) (SNP Selection)

SNP Selection

The following 10 SNPs were chosen for the analysis in this task. It was tried to include SNPs all over the protein, to investigate the influence of mutations in several parts of the protein. The mutated residues forming hydrogenbonds with the active site of glucocerebrosidase are included, as these should result in either a mal- or nonfunctioning protein. Note that the positions of the SNPs listed in HGMD are different from the corresponding codon numbers, indicated in Task 5, as this position is relative to the sequence of GBA including the signal peptide (+ 39 residues).

SNP ID/Accession Number Database Position Amino Acid Change Codon Change Phenotype Description Further Remarks
CM880035 HGMD 159 Arg - Gln CGG-CAG Gaucher Disease 1 Arginin is nonpolar and positively charged. Glutamine is by contrast polar and neutral. Synonymos Mutation at this Position listed in dbSNP.
rs80205046 dbSNP Pro - Leu CCC - CTC Missense Mutation
CM993703 HGMD 350 His - Arg CAT - CGT Gaucher Disease 2 Histidin is polar and mostley neutral, whereas Arginine is nonpolar and positively charged -


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