Npr2^cn-3J

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). (J:170669)