SCARNA8

Chr 9

small Cajal body-specific RNA 8

Also known as: U92

This gene encodes a small Cajal body-specific RNA (scaRNA) that is predicted to be involved in RNA processing within Cajal bodies and the nucleolus. Currently, no human diseases have been definitively associated with mutations in SCARNA8. The clinical significance of variants in this gene remains to be established.

OMIMResearchSummary from RefSeq
Clinical SummarySCARNA8
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ClinVar Variants
36 unique Pathogenic / Likely Pathogenic· 1 VUS of 37 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

37 submitted variants in ClinVar

Classification Summary

Pathogenic34
Likely Pathogenic2
VUS1
34
Pathogenic
2
Likely Pathogenic
1
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
34
Likely Pathogenic
2
VUS
1
Likely Benign
0
Benign
0
Total37

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SCARNA8 · 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
Open Research Assistant →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found