| Primary Identifier | MGI:6200393 | Allele Type | Chemically induced (ENU) |
| Attribute String | Not Specified | Gene | Myb |
| Inheritance Mode | Semidominant | Strain of Origin | C57BL/6J |
| Is Recombinase | false | Is Wild Type | false |
| Project Collection | Beutler Mutagenetix |
| molecularNote | ENU-induced T to C transition at base pair 21,152,617 (v38) on chromosome 10, or base pair 8,368 in the GenBank genomic region NC_000076 encoding Myb. The mutation corresponds to residue 612 in the mRNA sequence NM_010848 within exon 5 of 15 total exons. The mutation results in a serine (S) to proline (P) substitution at position 116 (S116P) in the MYB protein. |
