SCARNA23

Chr X

small Cajal body-specific RNA 23

Also known as: ACA12

NCBI Gene: 677773ENSG00000251869

SCARNA23 encodes a small Cajal body-specific RNA predicted to be involved in RNA processing within Cajal bodies and the nucleolus. Currently, no human diseases have been definitively associated with mutations in this gene. The clinical significance and inheritance pattern remain to be established.

ResearchSummary from RefSeq
Clinical Summary— SCARNA23
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Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

0 submitted variants in ClinVar

ClinVar

Protein Context — Lollipop Plot

SCARNA23 · 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

ClinicalTrials.gov

No active trials found for this gene.

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Clinical Literature
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Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
PubTator3
CNV Analysis through Exome Sequencing Reveals a Large Duplication Involved in Sex Reversal, Neurodevelopmental Delay, Epilepsy and Optic Atrophy
Mehawej C et al.·Genes (Basel)
2024
Small but strong: the emerging role of small nucleolar RNA in cardiovascular diseases
Sun X et al.·Front Cell Dev Biol
2023
The Vault Complex Is Significantly Involved in Therapeutic Responsiveness of Endocrine Tumors and Linked to Autophagy under Chemotherapeutic Conditions
Bornstein S et al.·Cancers (Basel)
2023
Single-cell quantification of a broad RNA spectrum reveals unique noncoding patterns associated with cell types and states
Isakova A et al.·Proc Natl Acad Sci U S A
2021
Identification of biomarkers predictive of metastasis development in early-stage colorectal cancer using network-based regularization
Peixoto C et al.·BMC Bioinformatics
2023
Top 5 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found

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External Resources

Links to major genomics databases and tools

Franklin by Genoox
AI-powered variant curation and clinical analysis
DECIPHER
Genomic variants and phenotypes in rare disease patients