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PLA2G12B

Gene

phospholipase A2 group XIIB

HGNCHGNC:18555EnsemblENSG00000138308NCBI Gene84647
Locus: gene with protein productLocation: 10q22.1

Also known as

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

Also known asPLA2G13
View full nomenclature history (3)
Previous symbolsPLA2G13
Previous namesphospholipase A2, group XIII, phospholipase A2, group XIIB

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.

Familial lipoprotein lipase deficiency
Cardiomyopathy, Hypertrophic

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.

Phospholipases

Provenance

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