| Primary Identifier | MGI:6268766 | Allele Type | Chemically induced (ENU) |
| Attribute String | Not Specified | Gene | Hcn1 |
| Inheritance Mode | Semidominant | Strain of Origin | C57BL/6J |
| Is Recombinase | false | Is Wild Type | false |
| Project Collection | Beutler Mutagenetix |
| molecularNote | ENU-induced A to T transversion at base pair 117,873,905 (v38) on chromosome 13, or base pair 271,586 in the GenBank genomic region NC_000079 encoding Hcn1. The mutation corresponds to residue 1,402 in the mRNA sequence NM_010408 within exon 4 of 8 total exons. The mutation results in substitution of lysine 340 for a premature stop codon (K340*) in the HCN1 protein. |
