| Primary Identifier | MGI:1856702 | Allele Type | Spontaneous |
| Attribute String | Null/knockout | Gene | Npr2 |
| Inheritance Mode | Recessive | Strain of Origin | AKR/J |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | The molecular basis of this mutation is a T-to-G transversion resulting in a leucine to arginine change in codon 885 (p.L885R). This is a missence mutation resulting in production of an inactive form of Npr2. |
