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Gene Symbol |
NPPB |
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Aliases |
BNP |
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Entrez Gene ID |
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Gene Name |
Natriuretic peptide B |
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Chromosomal Location |
1p36.22 |
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HGNC ID |
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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]
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e!Ensembl
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Protein Information |
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Protein Name |
Natriuretic peptides B, brain type natriuretic peptide, gamma-brain natriuretic peptide, natriuretic peptide precursor B, natriuretic protein |
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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. |
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UniProt |
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PDB |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000293288 |
Q07812 |
Q07812 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Cardiovascular Diseases |
Cardiomyopathy |
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Heart Failure |
19650993, 16762801, 16360360, 16333235, 15860969, 16101196, 15732037, 12628948, 16777915, 11136700, 24535859, 11279304 |
Aortic Valve Insufficiency |
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Myocardial Failure |
16360360, 16762801, 15860969, 16333235, 16101196, 16777915, 19650993, 15732037, 11136700, 24535859, 12628948, 11279304 |
Arteriosclerosis |
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Atrial Fibrillation |
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Hypertensive disease |
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Ventricular Tachycardia |
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Myocardial Diseases |
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Heart Diseases |
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Cardiovascular Abnormalities |
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
Sickle Cell Anemia |
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Endocrine System Diseases |
PCOS |
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Psychiatric/Brain disorders |
Eating Disorders |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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Cardiac risk |
N-terminal pro-B-type BNP |
Rotterdam criteria |
Related
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The present study demonstrated that the level of NT-proBNP was increased in PCOS subjects with asymptomatic heart disease |
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