USP17L26

Chr 4

ubiquitin specific peptidase 17 like family member 26

This protein is a deubiquitinating enzyme that removes ubiquitin from specific proteins to regulate cell proliferation, cell cycle progression, apoptosis, and cell migration. No established Mendelian disease associations have been reported for mutations in this gene. The inheritance pattern and clinical significance remain to be determined.

Summary from RefSeq, UniProt
Research Assistant →
0
Active trials
0
Pubs (1 yr)
69
P/LP submissions
P/LP missense
LOEUF
Mechanism
Clinical SummaryUSP17L26
📋
ClinVar Variants
69 unique Pathogenic / Likely Pathogenic· 6 VUS of 78 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

78 submitted variants in ClinVar

Classification Summary

Pathogenic67
Likely Pathogenic2
VUS6
Likely Benign3
67
Pathogenic
2
Likely Pathogenic
6
VUS
3
Likely Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
67
Likely Pathogenic
2
VUS
6
Likely Benign
3
Benign
0
Total78

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

USP17L26 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

3D Protein StructureAlphaFold

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
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Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found