| Primary Identifier | MGI:3777551 | Allele Type | Chemically induced (ENU) |
| Gene | Lfng | Inheritance Mode | Recessive |
| Strain of Origin | C57BL/6J | Is Recombinase | false |
| Is Wild Type | false | Project Collection | Beutler Mutagenetix |
| molecularNote | The mutation is a T-to-C transition at nucleotide position 686 (Genbank Accession NM_008494), in the last of four exons, resulting in replacement of a conserved valine by alanine at amino acid position 204 (V204A) of the protein. |
