| Primary Identifier | MGI:6268730 | Allele Type | Chemically induced (ENU) |
| Attribute String | Not Specified | Gene | Insr |
| 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 3,161,770 (v38) on chromosome 8, or base pair 117,880 in the GenBank genomic region NC_000074 encoding Insr. The mutation corresponds to residue 3,739 in the mRNA sequence NM_010568 within exon 17 of 21 total exons. The mutation results in a serine (S) to proline (P) substitution at position 1,084 (S1084P) in the InsR protein. |
