Summary | Mutation origin | Mutation description | Phenotypes | Disease models | Find Mice (IMSR) | References

Symbol:	Npr2pwe
Name:	natriuretic peptide receptor 2; peewee
MGI ID:	MGI:4358115
Gene:	Npr2  Location: Chr4:43631935-43651244 bp, + strand  Genetic Position: Chr4, 23.05 cM
Alliance:	Npr2pwe page

Strain of Origin:

NAW

Allele Type:    Spontaneous Mutation:    Intragenic deletion   Npr2pwe involves 1 genes/genome features (Npr2) View all   Mutation details: The peewee mutation is a 4 base pair deletion that alters codon 313 from leucine to a premature stop (L313X) in exon 3 within the ligand binding domain. The truncated protein is predicted to be nonfunctional. (J:188839) Inheritance:    Recessive

View phenotypes and curated references for all genotypes (concatenated display).

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Npr2 Mutation:	61 strains or lines available

Original:	J:105913 Moran JL, et al., Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse. Genome Res. 2006 Mar;16(3):436-40
All:	2 reference(s)