Gene Gene information from NCBI Gene database.
Entrez ID 5645
Gene name Serine protease 2
Gene symbol PRSS2
Synonyms (NCBI Gene)
TRY2TRY8TRYP2
Chromosome 7
Chromosome location 7q34
Summary This gene belongs to the trypsin family of serine proteases and encodes anionic trypsinogen. It is part of a cluster of trypsinogen genes that are located within the T cell receptor beta locus. Enzymes of this family cleave peptide bonds that follow lysin
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
30
GO ID Ontology Definition Evidence Reference
GO:0004222 Function Metalloendopeptidase activity TAS
GO:0004252 Function Serine-type endopeptidase activity IBA
GO:0004252 Function Serine-type endopeptidase activity IDA 12709065, 12731883
GO:0004252 Function Serine-type endopeptidase activity IEA
GO:0004252 Function Serine-type endopeptidase activity TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601564 9483 ENSG00000275896
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P07478
Protein name Trypsin-2 (EC 3.4.21.4) (Anionic trypsinogen) (Serine protease 2) (Trypsin II)
Protein function In the ileum, may be involved in defensin processing, including DEFA5.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00089 Trypsin 24 239 Trypsin Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in Paneth cells, at the base of small intestinal crypts. {ECO:0000269|PubMed:12021776}.
Sequence
Sequence length 247
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Neuroactive ligand-receptor interaction
Pancreatic secretion
Protein digestion and absorption
Influenza A
  Collagen degradation
Alpha-defensins
Activation of Matrix Metalloproteinases
Neutrophil degranulation
Antimicrobial peptides
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Pancreatitis, chronic, protection against protective rs61734659 RCV000008536
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Anemia Aplastic Associate 35435273
Carcinogenesis Associate 37022096
Cerebral Palsy Ataxic Autosomal Recessive Associate 19096130
Colorectal Neoplasms Associate 29193645
Cystic Fibrosis Associate 36386424
Dyskinesia Drug Induced Associate 25982926
Hodgkin Disease Associate 18179710
Lewy Body Disease Associate 25982926
Lymphoma Large Cell Anaplastic Associate 18179710
Meconium Ileus Associate 36386424