PRSS22: Serine Protease 22 – Structure, Function, and Clinical Relevance

Comprehensive genomic and proteomic overview of PRSS22 (serine protease 22) with expression, mutation, and disease association data.

Gene Information Card

Symbol PRSS22
Full Name serine protease 22
Gene Type protein coding
Chromosomal Location 16p13.3
NCBI Gene ID 64063 ncbi.nlm.nih.gov/gene/64063
Ensembl ID ENSG00000140937
UniProt ID Q9GZN4
OMIM ID 609343
HGNC ID 9476
Aliases SP001LA, TMPRSS2L, PRSS22

Description

PRSS22 (serine protease 22) is a protein-coding gene located on chromosome 16p13.3. It encodes a member of the serine protease family, characterized by a trypsin-like serine protease domain. The protein is involved in proteolytic processing and may play roles in extracellular matrix remodeling, cell signaling, and immune responses. PRSS22 is expressed in various tissues, with notable levels in the respiratory tract and gastrointestinal system. Alterations in PRSS22 expression have been implicated in certain cancers and inflammatory conditions.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Asthma PRSS22 overexpression may contribute to airway remodeling and inflammation via protease-activated receptor (PAR) signaling. PMID: 20628086
Colorectal cancer Upregulation of PRSS22 in tumor tissues suggests a role in tumor progression and metastasis. PMID: 23542379
Prostate cancer PRSS22 expression is altered in prostate cancer, potentially affecting tumor microenvironment. PMID: 24120478

Expression Profile

Tissue Expression
Tissue nTPM level
Lung 12.5 Medium
Trachea 15.2 Medium
Colon 8.3 Low
Small intestine 7.1 Low
Prostate 6.8 Low
Skin 3.2 Not detected
Cell Line Expression
Cell Line nTPM Notes
A549 (lung carcinoma) 18.4 High expression
Caco-2 (colorectal adenocarcinoma) 9.7 Moderate expression
PC-3 (prostate cancer) 7.2 Low expression
HEK 293 (embryonic kidney) 2.1 Very low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.347G>A (p.Arg116His) Missense 0.02% (gnomAD) Unknown functional impact; located in serine protease domain
c.523C>T (p.Pro175Ser) Missense 0.01% (gnomAD) May affect protein stability
c.788_789insA (p.Tyr263Ter) Frameshift Rare Predicted loss-of-function via premature stop codon
Mutation functional classification

Loss of Function (LOF)

Frameshift mutations (e.g., p.Tyr263Ter) are predicted to cause loss of protease activity.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in PRSS22.

Dominant Negative (DN)

No evidence for dominant-negative effects in PRSS22.

Gene Ontology (GO)

• serine-type endopeptidase activity (GO:0004252) • proteolysis (GO:0006508)
• extracellular region (GO:0005576) • plasma membrane (GO:0005886)
• integral component of membrane (GO:0016021)

Pathways

• Proteolysis and extracellular matrix remodeling
• PAR (protease-activated receptor) signaling pathway

Protein Summary

PRSS22 encodes a 317-amino acid serine protease with a signal peptide, a transmembrane domain, and a trypsin-like serine protease domain (S1 family). The protein is synthesized as a zymogen and activated by proteolytic cleavage. It localizes to the plasma membrane and extracellular space, where it cleaves substrates involved in cell adhesion, migration, and inflammation. PRSS22 is structurally similar to other type II transmembrane serine proteases (TTSPs) such as TMPRSS2.

Related Products

Product name Cat.No. Species Gene ID
PRSS22 Knockout HEK293 Cell Line EDJ-KQ14931 Human 64063 Details Get a Quote
PRSS22 Knockout HCT 116 Cell Line EDJ-KQ44121 Human 64063 Details Get a Quote
PRSS22 Knockout HeLa Cell Line EDJ-KQ57012 Human 64063 Details Get a Quote
PRSS22 Knockout A-549 Cell Line EDJ-KQ65518 Human 64063 Details Get a Quote
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