FKBP15

Gene

FKBP prolyl isomerase family member 15

HGNCHGNC:23397 EnsemblENSG00000119321 NCBI Gene23307

Locus: gene with protein productLocation: 9q32

Also known as

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

Also known asPPP1R76 · FKBP133 · WAFL

View full nomenclature history (8)

Alias symbolsPPP1R76, FKBP133, WAFL

Previous namesKIAA0674, FK506 binding protein 15, 133kDa, FK506 binding protein 15

Alias namesprotein phosphatase 1, regulatory subunit 76, WASP and FKBP-like 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.

Neurodegenerative Diseases

Wiskott-Aldrich Syndrome

Schizophrenia

Genetic Diseases, Inborn

Inflammatory Bowel Diseases

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 1 regulatory subunitsFKBP prolyl isomerase family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.