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USP31

Gene

ubiquitin specific peptidase 31

HGNCHGNC:20060EnsemblENSG00000103404NCBI Gene57478
Locus: gene with protein productLocation: 16p12.2

Also known as

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

Also known asKIAA1203
View full nomenclature history (2)
Alias symbolsKIAA1203
Previous namesubiquitin specific protease 31

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.

Temporomandibular Joint Disorders
Alcohol drinking
Sleep Disorders, Circadian Rhythm
Stroke
Barrett Esophagus
Bilateral striopallidodentate calcinosis
Genetic developmental and epileptic encephalopathy

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.