Gene Gene information from NCBI Gene database.
Entrez ID 1358
Gene name Carboxypeptidase A2
Gene symbol CPA2
Synonyms (NCBI Gene)
-
Chromosome 7
Chromosome location 7q32.2
Summary Three different forms of human pancreatic procarboxypeptidase A have been isolated. The encoded protein represents the A2 form, which is a monomeric protein with different biochemical properties from the A1 and A3 forms. The A2 form of pancreatic procarbo
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0004180 Function Carboxypeptidase activity IDA 2920728
GO:0004180 Function Carboxypeptidase activity IEA
GO:0004181 Function Metallocarboxypeptidase activity IBA
GO:0004181 Function Metallocarboxypeptidase activity IDA 2920728, 20385563
GO:0004181 Function Metallocarboxypeptidase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
600688 2297 ENSG00000158516
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P48052
Protein name Carboxypeptidase A2 (EC 3.4.17.15)
Protein function Carboxypeptidase that catalyzes the release of a C-terminal amino acid, with a preference for large aromatic C-terminal residues.
PDB 1AYE , 1DTD , 1O6X
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02244 Propep_M14 28 102 Carboxypeptidase activation peptide Domain
PF00246 Peptidase_M14 129 406 Zinc carboxypeptidase Domain
Sequence
Sequence length 419
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Pancreatic secretion
Protein digestion and absorption
 
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
HYPOXIA CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Aphakia, congenital primary Congenital primary aphakia BEFREE 28927587
★☆☆☆☆
Found in Text Mining only
Pancreatic Neoplasms Pancreatic neoplasm Pubtator 33099939 Associate
★☆☆☆☆
Found in Text Mining only
Pancreatitis Pancreatitis BEFREE 27114598
★☆☆☆☆
Found in Text Mining only
Pancreatitis Pancreatitis Pubtator 27114598 Associate
★☆☆☆☆
Found in Text Mining only
Pancreatitis, Chronic Pancreatitis BEFREE 26316592
★☆☆☆☆
Found in Text Mining only
Precursor Cell Lymphoblastic Leukemia Lymphoma Lymphoblastic Leukemia GWASCAT_DG 27114598
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Stomach neoplasms Pubtator 37290894 Associate
★☆☆☆☆
Found in Text Mining only