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PPP2R5C

Gene

protein phosphatase 2 regulatory subunit B'gamma

HGNCHGNC:9311EnsemblENSG00000078304NCBI Gene5527
Locus: gene with protein productLocation: 14q32.31

Also known as

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

Also known asB56G · PR61G · B56gamma
View full nomenclature history (5)
Alias symbolsB56G, PR61G, B56gamma
Previous namesprotein phosphatase 2, regulatory subunit B (B56), gamma isoform
Alias namesserine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform

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.

Neoplasms
Neurodegenerative Diseases
Complex neurodevelopmental disorder
chronic myelogenous leukemia, BCR-ABL1 positive
Restless Legs Syndrome
Alzheimer's Disease
Ischemic Attack, Transient

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.

Protein phosphatase 2 regulatory subunitsArmadillo like helical domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-10-10.
Open TargetsGene–disease associations from the Open Targets Platform.