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USPL1

Gene

ubiquitin specific peptidase like 1

HGNCHGNC:20294EnsemblENSG00000132952NCBI Gene10208
Locus: gene with protein productLocation: 13q12.3

Also known as

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

Also known asC13orf22 · bA121O19.1 · D13S106E
View full nomenclature history (4)
Previous symbolsC13orf22
Alias symbolsbA121O19.1, D13S106E
Previous nameschromosome 13 open reading frame 22

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
Alcohol drinking
Stroke
Pre-Eclampsia
Spondylitis, Ankylosing
Proximal spinal muscular atrophy
Colorectal Neoplasms
Breast Neoplasms

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 peptidasesUbiquitin specific peptidase like

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.