| Primary Identifier | MGI:3583746 | Allele Type | Spontaneous |
| Attribute String | Not Specified | Gene | Npr2 |
| Inheritance Mode | Recessive | Strain of Origin | MRL/MpJ-Fas<lpr>/J |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | A failed complementation test of this spontaneous mutant with the Npr2cn-2J allele demonstrated that this mutation is an allele of Npr2, and a G-to-A transition was identified in chromosome 4 position 43650227 (GRCm38), which is in exon 19 and causes an alanine to threonine substitution at position 931 (p.A931T). |
