| Primary Identifier | MGI:6285968 | Allele Type | Chemically induced (ENU) |
| Attribute String | Not Specified | Gene | Hcn2 |
| Inheritance Mode | Recessive | Strain of Origin | C57BL/6J |
| Is Recombinase | false | Is Wild Type | false |
| Project Collection | Beutler Mutagenetix |
| description | https://mutagenetix.utsouthwestern.edu/phenotypic/phenotypic_rec.cfm?pk=3750 |
| molecularNote | ENU-induced T to C transition at base pair 79,724,611 (v38) on chromosome 10, or base pair 7,978 in the GenBank genomic region NC_000076 encoding Hcn2. The mutation corresponds to residue 810 in the mRNA sequence NM_178666 within exon 2 of 8 total exons. The mutation results in a tyrosine to histidine substitution at position 259 (Y259H) in the HCN2 protein. |
