NPPB

Gene Information
 
Gene Symbol
NPPB
 
Aliases
BNP
 
Entrez Gene ID
 
Gene Name
Natriuretic peptide B
 
Chromosomal Location
1p36.22
 
HGNC ID
 
Summary
This gene is a member of the natriuretic peptide family and encodes a secreted protein which functions as a cardiac hormone. The protein undergoes two cleavage events, one within the cell and a second after secretion into the blood. The protein's biological actions include natriuresis, diuresis, vasorelaxation, inhibition of renin and aldosterone secretion, and a key role in cardiovascular homeostasis. A high concentration of this protein in the bloodstream is indicative of heart failure. The protein also acts as an antimicrobial peptide with antibacterial and antifungal activity. Mutations in this gene have been associated with postmenopausal osteoporosis. [provided by RefSeq, Nov 2014]
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0003085 Biological process Negative regulation of systemic arterial blood pressure IBA 21873635
GO:0006182 Biological process CGMP biosynthetic process IBA 21873635
GO:0006182 Biological process CGMP biosynthetic process IDA 1672777
GO:0006457 Biological process Protein folding IDA 16870210
GO:0007166 Biological process Cell surface receptor signaling pathway NAS 12727915
Protein Information
 
Protein Name
Natriuretic peptides B, brain type natriuretic peptide, gamma-brain natriuretic peptide, natriuretic peptide precursor B, natriuretic protein
 
Function
Cardiac hormone which may function as a paracrine antifibrotic factor in the heart. Also plays a key role in cardiovascular homeostasis through natriuresis, diuresis, vasorelaxation, and inhibition of renin and aldosterone secretion. Specifically binds and stimulates the cGMP production of the NPR1 receptor. Binds the clearance receptor NPR3.
 
UniProt
 
PDB
 
Pfam
Pfam Accession Pfam ID
PF00212 ANP
Pathways
 
KEGG
 
 

cGMP-PKG signaling pathway
Vascular smooth muscle contraction
Thermogenesis

 

Interactions
 
STRING MINT IntAct
ENSP00000293288 Q07812 Q07812
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Cardiovascular Diseases
Cardiomyopathy
Heart Failure
Aortic Valve Insufficiency
Myocardial Failure
Arteriosclerosis
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
 
Cardiac risk 
N-terminal pro-B-type BNP 
Rotterdam criteria 
Related 
 
The present study demonstrated that the level of NT-proBNP was increased in PCOS subjects with asymptomatic heart disease 

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