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FKBP1B

Gene

FKBP prolyl isomerase 1B

HGNCHGNC:3712EnsemblENSG00000119782NCBI Gene2281
Locus: gene with protein productLocation: 2p23.3

Also known as

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

Also known asFKBP1L · OTK4 · FKBP12.6 · PPIase · FKBP9
View full nomenclature history (9)
Previous symbolsFKBP1L
Alias symbolsOTK4, FKBP12.6, PPIase, FKBP9
Previous namesFK506-binding protein 1B (12.6 kD), FK506 binding protein 1B, 12.6 kDa, FK506 binding protein 1B
Alias namescalstabin 2

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.

Enteritis
Cardiomyopathy, Hypertrophic
Rare familial disorder with hypertrophic cardiomyopathy
Familial isolated dilated cardiomyopathy
Arrhythmogenic Right Ventricular Dysplasia
Cardiomegaly
Atrial Fibrillation
Brugada 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.

FKBP 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.