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FKBP10

Gene

FKBP prolyl isomerase 10

HGNCHGNC:18169EnsemblENSG00000141756NCBI Gene60681
Locus: gene with protein productLocation: 17q21.2

Also known as

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

Also known ashFKBP65 · FKBP65 · FLJ22041 · FKBP6 · FLJ20683 · FLJ23833
View full nomenclature history (9)
Alias symbolshFKBP65, FKBP65, FLJ22041, FKBP6, FLJ20683, FLJ23833
Previous namesFK506 binding protein 10, FK506 binding protein 10 (65 kDa), FK506 binding protein 10, 65 kDa

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.

Osteogenesis Imperfecta
Genetic Diseases, Inborn
Neurodegenerative 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.

EF-hand domain containingFKBP 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.