SNORA77B
Chr 22small nucleolar RNA, H/ACA box 77B
SNORA77B encodes a small nucleolar RNA predicted to be involved in RNA processing within the nucleolus. Current databases do not contain established disease associations or inheritance patterns for mutations in this gene. Clinical significance of variants in SNORA77B remains to be determined.
ResearchSummary from RefSeq
Clinical Summary— SNORA77B
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
0 submitted variants in ClinVar
Protein Context — Lollipop Plot
SNORA77B · 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 →Clinical Literature
Open Research Assistant →Landmark / reviewRecent case evidence
Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
Super enhancer related gene ANP32B promotes the proliferation of acute myeloid leukemia by enhancing MYC through histone acetylation
Wan X et al.·Cancer Cell Int
2024
snoSeeker: an advanced computational package for screening of guide and orphan snoRNA genes in the human genome
Yang JH et al.·Nucleic Acids Res
2006
Top 2 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
No open access results found
Top 5 resultsSearch Europe PMC ↗
External Resources
Links to major genomics databases and tools