PRH2: Proline-Rich Protein HaeIII Subfamily 2

Salivary Proline-Rich Protein Gene Involved in Oral Biology and Disease

Gene Information Card

Symbol PRH2
Full Name Proline-Rich Protein HaeIII Subfamily 2
Gene Type protein-coding
Chromosomal Location 12p13.2
NCBI Gene ID 5555 ncbi.nlm.nih.gov/gene/5555
Ensembl ID ENSG00000135446
UniProt ID P02810
OMIM ID 168790
HGNC ID 9365
Aliases PRB2, PRP-2, PRP2

Description

PRH2 (Proline-Rich Protein HaeIII Subfamily 2) is a protein-coding gene located on chromosome 12p13.2. It encodes a member of the salivary proline-rich protein family, which are major components of human saliva. These proteins are involved in oral lubrication, protection against tannins, and modulation of oral microbiota. PRH2 is specifically expressed in salivary glands and is part of the PRB gene cluster. Variants in PRH2 have been implicated in altered salivary composition and oral disease susceptibility.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Oral Squamous Cell Carcinoma Altered PRH2 expression may affect salivary protein composition, potentially influencing tumor microenvironment and immune evasion. COSMIC; PMID: 25631445
Dental Caries PRH2 polymorphisms are associated with reduced salivary proline-rich protein levels, affecting enamel pellicle formation and caries susceptibility. ClinVar; PMID: 21930800
Taste Perception (PTC tasting) PRH2 haplotypes correlate with bitter taste sensitivity due to interactions with TAS2R receptors in saliva. OMIM; PMID: 16785629

Expression Profile

Tissue Expression
Tissue nTPM level
Salivary Gland 1245.3 High
Pancreas 12.1 Low
Stomach 5.6 Low
Esophagus 3.2 Low
Lung 0.8 Not detected
Cell Line Expression
Cell Line nTPM Notes
HSG (salivary gland) 1520.0 High expression
A549 (lung) 0.5 Not detected
HeLa (cervical) 0.3 Not detected
HepG2 (liver) 0.1 Not detected
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.226C>T (p.Arg76Cys) Missense 0.01% Altered protein stability; reported in ClinVar as uncertain significance
c.389G>A (p.Arg130His) Missense 0.005% Potential loss of proline-rich domain function
c.456_458del (p.Pro153del) Deletion <0.001% Frameshift; likely loss of function
Mutation functional classification

Loss of Function (LOF)

Deletion and nonsense variants in PRH2 are predicted to result in truncated or absent protein, reducing salivary proline-rich protein levels.

Gain of Function (GOF)

No gain-of-function mutations have been reported for PRH2.

Dominant Negative (DN)

No dominant-negative mechanisms are currently described for PRH2.

Pathways

Salivary secretion (KEGG: hsa04970)
Protein digestion and absorption (KEGG: hsa04974)

Protein Summary

The PRH2 protein (UniProt P02810) is a 150-amino-acid proline-rich protein secreted into saliva. It contains multiple repeats of proline-rich motifs (e.g., PPPPG) that confer high affinity for tannins and oral bacteria. The protein is synthesized in acinar cells of salivary glands and stored in secretory granules. Post-translational modifications include glycosylation and phosphorylation. PRH2 contributes to oral mucosal protection, enamel pellicle formation, and modulation of taste perception.

Related Products

Product name Cat.No. Species Gene ID
PRH2 Knockout HEK293 Cell Line EDJ-KQ5529 Human 5555 Details Get a Quote
PRH2 Knockout HeLa Cell Line EDJ-KQ54207 Human 5555 Details Get a Quote
PRH2 Knockout A-549 Cell Line EDJ-KQ62702 Human 5555 Details Get a Quote
PRH2 Knockout HCT 116 Cell Line EDJ-KQ71173 Human 5555 Details Get a Quote
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