| Primary Identifier | MGI:5640788 | Allele Type | Chemically induced (ENU) |
| Gene | Malt1 | 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-A transversion at base pair 65,475,260 (GRCm38) on chromosome 18, or base pair 44,325 in the GenBank genomic region NC_000084. The mutation corresponds to nucleotide two within the donor splice site of intron 15. The effect of the mutation at the cDNA and protein level has not been tested, but the mutation is predicted to result in skipping of the 126-base pair exon 15 (out of 16 total exons). Skipping of exon 15 would cause an in-frame deletion of amino acids 635-676. |
