RNVU1-3

Chr 1

RNA, variant U1 small nuclear 3

Also known as: RNU1-113, RNU1-151, RNVU1-12, vU1.12, vU1.3

NCBI Gene: 101954272ENSG00000201183

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Jul 2025]

87
ClinVar variants
84
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— RNVU1-3
📋
ClinVar Variants
84 Pathogenic / Likely Pathogenic· 2 VUS of 87 total submissions

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

87 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic68
Likely Pathogenic16
VUS2
Benign1
68
Pathogenic
16
Likely Pathogenic
2
VUS
1
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————68
Likely Pathogenic
————16
VUS
————2
Likely Benign
————0
Benign
————1
Total—87

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

RNVU1-3 · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype

OMIM

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence

No publications found for RNVU1-3

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →

External Resources

Links to major genomics databases and tools