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10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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PGLYRP2
peptidoglycan recognition protein 2
Chromosome 19 · 19p13.12
NCBI Gene: 114770Ensembl: ENSG00000161031.14HGNC: HGNC:30013UniProt: Q96PD5
36PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
detection of bacteriumdefense response to Gram-positive bacteriumN-acetylmuramoyl-L-alanine amidase activitypeptidoglycan immune receptor activityhepatocellular carcinomaneoplasmsystemic lupus erythematosusulcerative colitis
✦AI Summary

PGLYRP2 (peptidoglycan recognition protein 2) is a liver-specific pattern recognition receptor that functions as a key innate immune regulator with N-acetylmuramoyl-L-alanine amidase activity 1. The protein serves multiple functions including degradation of bacterial peptidoglycan into inactive fragments and antiviral immunity. PGLYRP2 demonstrates age-dependent hepatocyte-intrinsic immunity against hepatitis B virus through phase separation mechanisms, recognizing and eliminating viral DNA while suppressing capsid assembly 2. In inflammatory diseases, PGLYRP2 acts through the NOD2-NFκB pathway, where its N-terminal domain binds NOD2 on macrophages, activating inflammatory cascades that promote cytokine secretion 3. Clinical significance includes its role as a biomarker for various conditions: elevated serum levels correlate with coronary artery disease severity 3, systemic lupus erythematosus activity 4, and multidrug-resistant tuberculosis diagnosis 5. In hepatocellular carcinoma, PGLYRP2 downregulation through DNA methylation correlates with poor prognosis, while overexpression enhances antitumor immunity by promoting CCL5 chemokine production 6. Additionally, genetic polymorphisms in PGLYRP2 are associated with increased Parkinson's disease risk in certain populations 7.

Sources cited
1
PGLYRP2 is liver-specific with N-acetylmuramoyl-L-alanine amidase activity and is the same protein as serum NAMLAA
PMID: 16054449
2
PGLYRP2 provides hepatocyte-intrinsic immunity against HBV through phase separation and viral DNA recognition
PMID: 39946201
3
PGLYRP2 activates NOD2-NFκB inflammatory pathway and correlates with coronary artery disease severity
PMID: 38277990
4
Serum PGLYRP2 levels correlate with SLE disease activity and lipid metabolism abnormalities
PMID: 34461924
5
PGLYRP2 serves as a potential biomarker for multidrug-resistant tuberculosis diagnosis
PMID: 32967043
6
PGLYRP2 downregulation in HCC correlates with poor prognosis and reduced antitumor immunity
PMID: 31479523
7
PGLYRP2 genetic polymorphisms are associated with increased Parkinson's disease risk
PMID: 35218888
Disease Associationsⓘ20
hepatocellular carcinomaOpen Targets
0.08Suggestive
neoplasmOpen Targets
0.08Suggestive
systemic lupus erythematosusOpen Targets
0.08Suggestive
ulcerative colitisOpen Targets
0.06Suggestive
osteoarthritisOpen Targets
0.06Suggestive
Autosomal recessive early-onset inflammatory bowel diseaseOpen Targets
0.05Suggestive
chondrocalcinosis 2Open Targets
0.05Suggestive
hepatitis B virus infectionOpen Targets
0.05Suggestive
Hirschsprung diseaseOpen Targets
0.05Suggestive
colorectal cancerOpen Targets
0.05Suggestive
Crohn's diseaseOpen Targets
0.04Suggestive
palmoplantar keratoderma-esophageal carcinoma syndromeOpen Targets
0.04Suggestive
inflammatory bowel disease 1Open Targets
0.04Suggestive
inflammatory bowel disease 30Open Targets
0.04Suggestive
inflammatory bowel disease 25Open Targets
0.04Suggestive
polyarticular juvenile idiopathic arthritis, rheumatoid factor positiveOpen Targets
0.04Suggestive
infectionOpen Targets
0.04Suggestive
visceral myopathy 2Open Targets
0.04Suggestive
NK-cell enteropathyOpen Targets
0.04Suggestive
congenital sodium diarrheaOpen Targets
0.04Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
PGLYRP1Shared pathway71%PGLYRP4Shared pathway71%PGLYRP3Shared pathway71%LYG1Shared pathway40%LYG2Shared pathway33%DEFB107AShared pathway33%
Tissue Expression6 tissues
Liver
100%
Lung
0%
Brain
0%
Heart
0%
Ovary
0%
Bone Marrow
0%
Gene Interaction Network
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PGLYRP2PGLYRP1PGLYRP4PGLYRP3LYG1LYG2DEFB107A
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q96PD5
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.14LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.86 [0.66–1.14]
RankingsWhere PGLYRP2 stands among ~20K protein-coding genes
  • #10,831of 20,598
    Most Researched36
  • #11,753of 17,882
    Most Constrained (LOEUF)1.14
Genes detectedPGLYRP2
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Association of PGLYRP2 gene polymorphism and sporadic Parkinson's disease in northern Chinese Han population.
PMID: 35218888
Neurosci Lett · 2022
1.00
2
Measurement of Organ-Specific and Acute-Phase Blood Protein Levels in Early Lyme Disease.
PMID: 31618575
J Proteome Res · 2020
0.90
3
PGLYRP2 drives hepatocyte-intrinsic innate immunity by trapping and clearing hepatitis B virus.
PMID: 39946201
J Clin Invest · 2025
0.80
4
Novel role of peptidoglycan recognition protein 2 in activating NOD2-NFκB inflammatory axis in coronary artery disease.
PMID: 38277990
Atherosclerosis · 2024
0.70
5
Identification of serum N-acetylmuramoyl-l-alanine amidase as liver peptidoglycan recognition protein 2.
PMID: 16054449
Biochim Biophys Acta · 2005
0.60