| Primary Identifier | MGI:6198336 | Allele Type | Chemically induced (ENU) |
| Attribute String | Not Specified | Gene | Hr |
| Inheritance Mode | Recessive | Strain of Origin | C57BL/6J |
| Is Recombinase | false | Is Wild Type | false |
| Project Collection | Beutler Mutagenetix |
| molecularNote | ENU-induced A to G transition at base pair 70,567,833 (v38) on chromosome 14, or base pair 13,778 in the GenBank genomic region NC_000080 encoding Hr. The mutation corresponds to residue 3,708 in the mRNA sequence NM_021877 within exon 16 of 20 total exons. The mutation results in an aspartic acid to glycine substitution at position 1,005 (D1005G) in the HR protein. |
