Primary Identifier | MGI:5056451 | Allele Type | Targeted |
Attribute String | Humanized sequence | Gene | Sqstm1 |
Transmission | Germline | Strain of Origin | 129P2/OlaHsd |
Is Recombinase | false | Is Wild Type | false |
molecularNote | Exon 8 was replaced with a modified exon with a C to T transition that results in the amino acid substitution of leucine for proline at position 394 (P394L), mimicking a mutation found in some Paget's disease of bone (PDB) patients. Cre-mediated recombination removed the neo cassette inserted upstream of the modified exon 8. |