| Primary Identifier | MGI:3774275 | Allele Type | Spontaneous |
| Gene | Npr2 | Inheritance Mode | Recessive |
| Strain of Origin | DDY | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | A noncomplementation test with mice carrying the Npr2cn allele demonstrated that this mutation is an allele of Npr2. A 7-base deletion was identified in exon 8. The deletion caused a frameshift and the appearance of a premature termination codon at codon 513. |
