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PGLYRP1

Gene

peptidoglycan recognition protein 1

HGNCHGNC:8904EnsemblENSG00000008438NCBI Gene8993
Locus: gene with protein productLocation: 19q13.32

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asTNFSF3L · PGLYRP · TAG7 · PGRP · PGRP-S · PGRPS
View full nomenclature history (7)
Previous symbolsTNFSF3L, PGLYRP
Alias symbolsTAG7, PGRP, PGRP-S, PGRPS
Previous namespeptidoglycan recognition protein

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Dementia
Neurodegenerative Diseases
Colitis
Neoplasms
Arthritis, Rheumatoid
Carcinoma, Hepatocellular
Periodontitis
Infections
Dermatitis, Contact

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Peptidoglycan recognition proteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.