Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5645
Gene name Gene Name - the full gene name approved by the HGNC.
Serine protease 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PRSS2
Synonyms (NCBI Gene) Gene synonyms aliases
TRY2, TRY8, TRYP2
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q34
Summary Summary of gene provided in NCBI Entrez Gene.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004252 Function Serine-type endopeptidase activity IBA 21873635
GO:0004252 Function Serine-type endopeptidase activity IDA 12709065, 12731883
GO:0005509 Function Calcium ion binding IDA 12709065
GO:0005515 Function Protein binding IPI 16192646
GO:0005576 Component Extracellular region IDA 12731883
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601564 9483 ENSG00000275896
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Diabetes mellitus Diabetes Mellitus rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
Hereditary pancreatitis Hereditary pancreatitis, Hereditary chronic pancreatitis rs113993960, rs113993959, rs75527207, rs80034486, rs121909294, rs111033565, rs111033566, rs111033567, rs267606982, rs111033568, rs104893938, rs104893939, rs387906698, rs193922659, rs397507439
View all (24 more)
18461367, 16699518
Unknown
Disease term Disease name Evidence References Source
Pancreatitis Pancreatitis, Pancreatitis, Chronic, Autosomal Dominant Hereditary Pancreatitis, Recurrent pancreatitis 16699518, 18206817 ClinVar
Oligodendroglioma Oligodendroglioma GWAS
Associations from Text Mining
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