Table 4 |
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In silico analysis of all induced or spontaneous alleles (4,984) with phenotypes reported in the Mouse Genomes Database [1] |
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|
Mutation |
Number of alleles |
|
|
|
|
Unknown or uncharacterized |
3,105 |
|
Introns, UTRs, regulatory regions (including instances where the lesion is not known but coding sequence has been sequenced), cryptic splice sites, inversions |
150 |
|
Exons (single nucleotide substitutions, deletions, insertions) |
1,581 |
|
Conserved splice acceptor or donor |
148 |
|
|
|
|
This analysis shows that the vast majority of induced or spontaneous alleles that have been characterized at the molecular level (1,879) are mutations in coding sequence or conserved splice acceptor/splice donor sites. |
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Fairfield et al. Genome Biology 2011 12:R86 doi:10.1186/gb-2011-12-9-r86 |
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