ENPEP (glutamyl aminopeptidase)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 2028 |
| Gene name | Glutamyl aminopeptidase |
| Gene symbol | ENPEP |
| Synonyms (NCBI Gene) |
APACD249gp160
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| Chromosome | 4 |
| Chromosome location | 4q25 |
| Summary | The ENPEP gene encodes glutamyl aminopeptidase, a type II integral membrane protein with an extracellular zinc-binding domain. This protein can upregulate blood pressure by cleaving the N-terminal aspartate from angiotensin II, and can regulate blood vess |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q07075 | ||||||||||||||||||||
| Protein name | Glutamyl aminopeptidase (EAP) (EC 3.4.11.7) (Aminopeptidase A) (AP-A) (Differentiation antigen gp160) (CD antigen CD249) | ||||||||||||||||||||
| Protein function | Regulates central hypertension through its calcium-modulated preference to cleave N-terminal acidic residues from peptides such as angiotensin II. | ||||||||||||||||||||
| PDB | 4KX7 , 4KX8 , 4KX9 , 4KXA , 4KXB , 4KXC , 4KXD | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in choriocarcinoma cancer cell lines (at protein level) (PubMed:10692253). Expressed by epithelial cells of the proximal tubule cells and the glomerulus of the nephron. Also found in a variety of other tissues. {ECO:0000269|P | ||||||||||||||||||||
| Sequence |
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| Sequence length | 957 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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