GO curators for mouse genes have assigned the following annotations to the gene product of Npr2. (This text reflects annotations as of Wednesday, January 23, 2013.) Summary from NCBI RefSeq
[Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes natriuretic peptide receptor B, one of two integral membrane receptors for natriuretic peptides. Both NPR1 and NPR2 contain five functional domains: an extracellular ligand-binding domain, a single membrane-spanning region, and intracellularly a protein kinase homology domain, a helical hinge region involved in oligomerization, and a carboxyl-terminal guanylyl cyclase catalytic domain. The protein is the primary receptor for C-type natriuretic peptide (CNP), which upon ligand binding exhibits greatly increased guanylyl cyclase activity. Mutations in this gene are the cause of acromesomelic dysplasia Maroteaux type. [provided by RefSeq, Jul 2008]Summary text based on GO annotations supported by experimental evidence in mouse
Researchers have inferred from direct assay, that the gene product of Npr2
participates in the following biological processes:
Johnson DR. (1978) The growth of femur and tibia in three genetically distinct chondrodystrophic mutants of the house mouse. J Anat, 125:267-75. (PubMed:624676)
Tamura N et al. (2003) Regulation of the guanylyl cyclase-B receptor by alternative splicing. J Biol Chem, 278:48880-9. (PubMed:14514678)