| Primary Identifier | MGI:6423595 | Allele Type | Targeted |
| Attribute String | Conditional ready | Gene | Lmna |
| Transmission | Germline | Strain of Origin | C57BL/6 |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | The most frequent mutation in Hutchinson-Gilford progeria syndrome, a C to T change, was introduced into exon 11. This mutation does not result in a protein sequence change because both encode a glycine at amino acid position 609 (G609G). In addition, a loxP flanked neomycin resistance gene was introduced upstream of exon 11. The G609G is equivalent to the human G608G mutation which activates an alternate splicing event and generates a 50-amino acid truncated form of Lamin A, referred to as progerin. |
