| Primary Identifier | MGI:6268406 | Allele Type | Chemically induced (ENU) |
| Attribute String | Hypomorph | Gene | Myo1d |
| Inheritance Mode | Recessive | 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 80,484,332 (v38) on chromosome 11 corresponding to base pair 295,724 in the GenBank genomic region NC_000077 encoding Myo1d. The mutation corresponds to residue 3,148 in the mRNA sequence NM_177390 within exon 22 of 22 total exons. The mutation results in a leucine (L) to proline (P) substitution at position 972 (L972P) in the Myo1d protein. |
