| Primary Identifier | MGI:6268746 | Allele Type | Chemically induced (ENU) |
| Attribute String | Not Specified | Gene | Fgf3 |
| 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 144,840,707 (v38) on chromosome 7, or base pair 2,751 in the GenBank genomic region NC_000073 encoding Fgf3. The mutation corresponds to residue 353 in the mRNA sequence NM_008007 within exon 2 of 3 total exons. The mutation results in a valine to alanine substitution at amino acid 86 (V86A) in the FGF3 protein. |
