GUCY1B3


GCUG1B3: A Comprehensive Guide

Description

Gucy1b3 is a gene that encodes the protein guanylate cyclase 1B, beta 3 polypeptide. This protein is a member of the guanylate cyclase family, which is responsible for synthesizing cyclic guanosine monophosphate (cGMP). cGMP is a second messenger that plays a crucial role in various physiological processes, including blood pressure regulation, smooth muscle relaxation, and neurotransmission.

Associated Diseases

Mutations in the GCUG1B3 gene have been linked to several inherited diseases, including:

  • Hypertrophic cardiomyopathy (HCM): A condition characterized by the thickening of the heart muscle, leading to reduced heart function.
  • Dilated cardiomyopathy (DCM): A condition in which the heart muscle becomes enlarged and weakened, leading to heart failure.
  • Arrhythmogenic right ventricular cardiomyopathy (ARVC): A condition that affects the heart's right ventricle, causing arrhythmias and an increased risk of sudden cardiac death.
  • Congenital heart defects: Structural abnormalities of the heart present at birth, such as atrial septal defect or ventricular septal defect.

Did you Know ?

Approximately 1 in 500 people carry a mutation in the GCUG1B3 gene. However, only a small percentage of these individuals develop clinical manifestations of the associated diseases. This suggests that other genetic or environmental factors may also play a role in disease development.



Disclaimer: The information provided here is not exhaustive by any means. Always consult your doctor or other qualified healthcare provider with any questions you may have regarding a medical condition, procedure, or treatment, whether it is a prescription medication, over-the-counter drug, vitamin, supplement, or herbal alternative.