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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
angiotensin I converting enzyme
Summary
- Gene Symbol
-
- ACE
- Aliases
-
- ACE1
- CD143
- peptidyl-dipeptidase A
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative promoter usage
- Alternative splicing
- Calmodulin-binding
- Carboxypeptidase
- Cell membrane
- Cytoplasm
- Direct protein sequencing
- Disulfide bond
- Glycoprotein
- Metal-binding
- Metalloprotease
- Phosphoprotein
- Reference proteome
- Repeat
- Secreted
- Signal
- Transmembrane helix
- Zinc
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| negative regulation of glucose import | ||
| hormone catabolic process | ||
| regulation of heart rate by cardiac conduction | ||
| regulation of vasoconstriction | ||
| positive regulation of peptidyl-cysteine S-nitrosylation |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
developmental process [inference]
response to stimulus [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of localization [inference]
negative regulation of biological process [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| endosome | ||
| extracellular region |
|
|
| external side of plasma membrane | ||
| basal plasma membrane | ||
| plasma membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| heterocyclic compound binding | ||
| metalloendopeptidase activity | ||
| peptidyl-dipeptidase activity | ||
| chloride ion binding | ||
| zinc ion binding |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:13579 | kwashiorkor | |
| DOID:0002116 | pterygium | |
| DOID:0014667 | disease of metabolism | |
| DOID:0040085 | bacterial sepsis | |
| DOID:0050083 | Keshan disease | |
| DOID:0050152 | aspiration pneumonia | |
| DOID:0050156 | idiopathic pulmonary fibrosis | |
| DOID:0050328 | congenital hypothyroidism | |
| DOID:0050387 | nonpapillary renal cell carcinoma | |
| DOID:0050430 | multiple endocrine neoplasia type 2A |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000079 | Abnormality of the urinary system |
| HP:0000252 | Microcephaly |
| HP:0001562 | Oligohydramnios |
| HP:0002009 | Potter facies |
| HP:0002089 | Pulmonary hypoplasia |
| HP:0002093 | Respiratory insufficiency |
| HP:0002615 | Hypotension |
| HP:0004492 | Widely patent fontanelles and sutures |
| HP:0008660 | Renotubular dysgenesis |
| Disease ID | Disease Name |
|---|---|
| OMIM:267430 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 101819593 | FICAL13746 | ||
| 114581443 | PODMU00436 | ||
| 115059877 | ECHNA46481 | ||
| 115393331 | SALFA42463 | ||
| 113489137 | ATHCN20156 | ||
| 109060366 | CYPCA113140 | ||
| 109099167 | CYPCA105584 | ||
| 116435326 | CORMO12859 |
