Primary Identifier | MGI:6268355 | Allele Type | Chemically induced (ENU) |
Attribute String | Not Specified | Gene | Ighe |
Inheritance Mode | Semidominant | Strain of Origin | C57BL/6J |
Is Recombinase | false | Is Wild Type | false |
Project Collection | Beutler Mutagenetix |
molecularNote | ENU-induced C to T transition at base pair 113,271,374 (v38) on chromosome 12, or base pair 1,875 in the GenBank genomic region NC_000078 encoding Ighe. The mutation corresponds to residue 1,167 in the cDNA sequence ENSMUST00000137336.2 within exon 4 of 4 total exons. The mutation results in substitution of glutamine (Q) to a premature stop codon (Q389*) in the Ighe protein. |