Primary Identifier | MGI:3582957 | Allele Type | Spontaneous |
Gene | Hcn2 | Inheritance Mode | Recessive |
Strain of Origin | BKS.Cg-Dock7<m> +/+ Lepr<db>/J | Is Recombinase | false |
Is Wild Type | false |
molecularNote | This spontaneous mutation has a G-to-A transition at chromosome 10 position 79,724,780 (GRCm38) that causes an arginine to glutamine substitution at residue 315 (p.R315Q). |