The protein localizes to the cytoplasm and nucleus and may participate in p53-mediated signaling pathways. Currently, no established human diseases have been definitively linked to mutations in this gene. Clinical significance remains to be determined.

ResearchSummary from RefSeq, UniProt
Clinical SummaryTP53TG3B
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ClinVar Variants
7 unique Pathogenic / Likely Pathogenic· 3 VUS of 25 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

25 submitted variants in ClinVar

Classification Summary

Pathogenic6
Likely Pathogenic1
VUS3
Benign12
6
Pathogenic
1
Likely Pathogenic
3
VUS
12
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
6
Likely Pathogenic
1
VUS
3
Likely Benign
0
Benign
12
Total22

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

TP53TG3B · 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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