YWHAG

Gene

tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma

HGNCHGNC:12852 EnsemblENSG00000170027 NCBI Gene7532

Locus: gene with protein productLocation: 7q11.23

Also known as

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

Also known asPPP1R170 · 14-3-3GAMMA · 14-3-3γ

View full nomenclature history (6)

Alias symbolsPPP1R170, 14-3-3GAMMA, 14-3-3γ

Previous namestyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide

Alias names14-3-3 gamma, protein phosphatase 1, regulatory subunit 170

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.

Genetic developmental and epileptic encephalopathy

Genetic Diseases, Inborn

Undetermined early-onset epileptic encephalopathy

COVID-19

Severe Acute Respiratory Syndrome

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.

14-3-3 phospho-serine/phospho-threonine binding 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.