CPD, or Carboxypeptidase D, is indeed genetic. It is encoded by the CPD gene, which is located on chromosome 16 in humans. The CPD gene provides instructions for making the carboxypeptidase D protein, an enzyme that plays a role in various physiological processes.
Here's why CPD is considered genetic:
- Inherited: The CPD gene, like most genes, is inherited from parents. This means that individuals inherit two copies of the CPD gene, one from each parent.
- Genetic Variations: Variations within the CPD gene can influence the amount or activity of the carboxypeptidase D protein, potentially contributing to certain health conditions.
- Role in Disease: Studies have linked variations in the CPD gene to diseases like Hepatitis B and Hepatitis.
While CPD is primarily determined by genetics, environmental factors can also influence its expression and activity.
