ACE angiotensin I converting enzyme
Gene ID: 1636, updated on 4-Jan-2025Gene type: protein coding
Also known as: DCP; ACE1; DCP1; CD143
- See all available tests in GTR for this gene
- Go to complete Gene record for ACE
- Go to Variation Viewer for ACE variants
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
Description | Tests |
---|---|
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 | See labs |
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 | See labs |
Human metabolic individuality in biomedical and pharmaceutical research. GeneReviews: Not available | |
Microvascular complications of diabetes, susceptibility to, 3 | See labs |
Renal tubular dysgenesis of genetic origin | See labs |
Genomic context
- Location:
- 17q23.3
- Sequence:
- Chromosome: 17; NC_000017.11 (63477061..63498373)
- Total number of exons:
- 26
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for ACE variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ACE database
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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