| Primary Identifier | MGI:5632158 | Allele Type | Chemically induced (ENU) |
| Gene | Cd22 | Inheritance Mode | Recessive |
| Strain of Origin | C57BL/6J | Is Recombinase | false |
| Is Wild Type | false | Project Collection | Beutler Mutagenetix |
| molecularNote | The mutation is a G to T transversion at base pair 30,869,509 (Build 38) on Chromosome 7, or base pair 10,834 in the GenBank genomic region NC_000073, within the donor splice site of intron 9. The mutation is predicted to result in in-frame skipping of the 264-nucleotide exon 9 (out of 14 total exons), which encodes amino acids 612-699. The effect of the mutation at the cDNA and protein levels has not been tested. |
