USP26

Gene

ubiquitin specific peptidase 26

HGNCHGNC:13485 EnsemblENSG00000134588 NCBI Gene83844

Locus: gene with protein productLocation: Xq26.2

Also known as

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

View full nomenclature history (1)

Previous namesubiquitin specific protease 26

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.

Non-syndromic male infertility due to sperm motility disorder

Infertility, Male

Carcinoma, Hepatocellular

46,XX gonadal dysgenesis

Primary Ovarian Insufficiency

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.

Ubiquitin specific peptidases

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.