SNORA11C
Chr Xsmall nucleolar RNA, H/ACA box 11C
SNORA11C encodes a small nucleolar RNA predicted to be involved in RNA processing within the nucleolus. Currently, no human diseases have been definitively associated with mutations in this gene, and the clinical significance of variants remains unclear. The inheritance pattern and clinical phenotype associated with SNORA11C variants have not been established.
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
0 submitted variants in ClinVar
Protein Context — Lollipop Plot
SNORA11C · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
3D Protein StructureAlphaFold
External Resources
Links to major genomics databases and tools
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →No open access results found
External Resources
Links to major genomics databases and tools