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PPP1R2C

Gene

PPP1R2 family member C

HGNCHGNC:16324EnsemblENSG00000102055NCBI Gene80316
Locus: gene with protein productLocation: Xp11.3

Also known as

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

Also known asPPP1R2P9 · I-4
View full nomenclature history (5)
Previous symbolsPPP1R2P9
Alias symbolsI-4
Previous namesPPP1R2C family member C, protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 9, protein phosphatase 1, regulatory (inhibitor) subunit 2 pseudogene 9

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.

Graves' Disease
Turner Syndrome
Infections

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-09-20.
Open TargetsGene–disease associations from the Open Targets Platform.