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ACE angiotensin I converting enzyme

Gene ID: 1636, updated on 30-Apr-2024
Gene type: protein coding
Also known as: DCP; ACE1; DCP1; CD143

Summary

This gene encodes an enzyme involved in blood pressure regulation and electrolyte balance. It catalyzes the conversion of angiotensin I into a physiologically active peptide angiotensin II. Angiotensin II is a potent vasopressor and aldosterone-stimulating peptide that controls blood pressure and fluid-electrolyte balance. This angiotensin converting enzyme (ACE) also inactivates the vasodilator protein, bradykinin. Accordingly, the encoded enzyme increases blood pressure and is a drug target of ACE inhibitors, which are often prescribed to reduce blood pressure. This enzyme additionally plays a role in fertility through its ability to cleave and release GPI-anchored membrane proteins in spermatozoa. Many studies have associated the presence or absence of a 287 bp Alu repeat element in this gene with the levels of circulating enzyme. This polymorphism, as well as mutations in this gene, have been implicated in a wide variety of diseases including cardiovascular pathophysiologies, psoriasis, renal disease, stroke, and Alzheimer's disease. Regulation of the homologous ACE2 gene may be involved in progression of disease caused by several human coronaviruses, including SARS-CoV and SARS-CoV-2. Alternative splicing results in multiple transcript variants encoding both somatic (sACE) and male-specific testicular (tACE) isoforms. [provided by RefSeq, Sep 2020]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
A genome-wide assessment of variability in human serum metabolism.
GeneReviews: Not available
A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor.
GeneReviews: Not available
An atlas of genetic influences on human blood metabolites.
GeneReviews: Not available
Disorder of cardiovascular system
MedGen: C0007222GeneReviews: Not available
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Genetic determinants influencing human serum metabolome among African Americans.
GeneReviews: Not available
Genome-Wide Association Study of CSF Levels of 59 Alzheimer's Disease Candidate Proteins: Significant Associations with Proteins Involved in Amyloid Processing and Inflammation.
GeneReviews: Not available
Hemorrhage, intracerebral, susceptibility to
MedGen: C3281105OMIM: 614519GeneReviews: Not available
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Human metabolic individuality in biomedical and pharmaceutical research.
GeneReviews: Not available
Microvascular complications of diabetes, susceptibility to, 3
MedGen: C2675470OMIM: 612624GeneReviews: Not available
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Renal tubular dysgenesis of genetic origin
MedGen: C5681536OMIM: 267430GeneReviews: Not available
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Genomic context

Location:
17q23.3
Sequence:
Chromosome: 17; NC_000017.11 (63477061..63498373)
Total number of exons:
26

Links

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