| Primary Identifier | MGI:6268734 | Allele Type | Chemically induced (ENU) |
| Attribute String | Not Specified | Gene | Insr |
| Inheritance Mode | Dominant | 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 3,159,475 (v38) on chromosome 8, or base pair 120,175 in the GenBank genomic region NC_000074 encoding Insr. The mutation corresponds to residue 4,096 in the mRNA sequence NM_010568 within exon 19 of 21 total exons. The mutation results in a phenylalanine to leucine substitution at position 1,203 (F1203L) in the INSR protein. |
