SNORA65

Chr 9

small nucleolar RNA, H/ACA box 65

Also known as: RNU65, U65

The protein is predicted to process RNA and localize to the nucleolus. Insufficient clinical data is available to establish disease associations, inheritance patterns, or mechanisms of pathogenicity for SNORA65 mutations.

Summary from RefSeq
Research Assistant →
0
Active trials
0
Pubs (1 yr)
15
P/LP submissions
P/LP missense
LOEUF
Mechanism
Clinical SummarySNORA65
📋
ClinVar Variants
15 unique Pathogenic / Likely Pathogenic of 15 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

15 submitted variants in ClinVar

Classification Summary

Pathogenic15
15
Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
15
Likely Pathogenic
0
VUS
0
Likely Benign
0
Benign
0
Total15

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SNORA65 · protein map & ClinVar variants

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

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →
Key Publications
Landmark & review papers · by relevance
PubMed
Top 1 results · since 2015Search PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found