SNHG15
Chr 7small nucleolar RNA host gene 15
0
ClinVar variants
0
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— SNHG15
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
0 submitted variants in ClinVar
Protein Context — Lollipop Plot
SNHG15 · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
OMIM — Genotype-Phenotype
No OMIM entries found.
External Resources
Links to major genomics databases and tools
Variant Interpretation
Population Databases
Gene Resources
Expert Curation
ClinGen
Expert-curated gene-disease validity
GenCC
Gene Curation Coalition — multi-curator classifications
Orphanet
Rare disease encyclopedia and gene-disease associations
PanelApp
Gene panels for rare disease diagnostics (Genomics England)
LOVD
Leiden Open Variation Database — variant listings
GeneReviews
Expert-authored summaries of heritable conditions (NCBI)
Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
Long non-coding RNA SNHG15 in various cancers: a meta and bioinformatic analysis.
Chen C et al.·BMC Cancer
2020Meta-analysis
Clinicopathological and Prognostic Value of Long Noncoding RNA SNHG15 in Human Cancers: a Meta-Analysis and Bioinformatics.
Ge Y et al.·Clin Lab
2020Meta-analysis
Down-regulation LncRNA-SNHG15 contributes to proliferation and invasion of bladder cancer cells.
Mokhtar A et al.·BMC Urol
2021
Evaluating the diagnostic and prognostic value of long non-coding RNA SNHG15 in pancreatic ductal adenocarcinoma.
Guo XB et al.·Eur Rev Med Pharmacol Sci
2018
Increased serum exosomal long non-coding RNA SNHG15 expression predicts poor prognosis in non-small cell lung cancer.
Han P et al.·J Clin Lab Anal
2021
Long noncoding RNA SNHG15, a potential prognostic biomarker for hepatocellular carcinoma.
Zhang JH et al.·Eur Rev Med Pharmacol Sci
2016
Knockdown of SNHG15 suppresses renal cell carcinoma proliferation and EMT by regulating the NF-κB signaling pathway.
Du Y et al.·Int J Oncol
2018
Clinical and molecular relevance of genetic variants in the non-coding transcriptome of patients with cytogenetically normal acute myeloid leukemia.
Papaioannou D et al.·Haematologica
2022Cohort
Top 10 resultsSearch PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
The long non-coding RNA Snhg15 protects the heart after myocardial infarction.
Shumliakivska M et al.·J Mol Cell Cardiol
2026
Elevated SNHG15 empowers keratinocytes hyperproliferation through activation of STAT3/Cyclin D1 axis in psoriasis.
Tang L et al.·Acta Pharm Sin B
2025🔓 Open Access
LncRNA SNHG15 sponges miR-3143/FOXO3 to regulate autophagy in ovarian dysfunction induced by benzene exposure.
Ye Z et al.·Toxicol Lett
2025
LncRNA SNHG15 targets miR-200a-3p affects the proliferation, apoptosis, migration, and invasion of cervical cancer cells.
Han S et al.·BMC Cancer
2025🔓 Open Access
Top 5 resultsSearch Europe PMC ↗
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →External Resources
Links to major genomics databases and tools
Variant Interpretation
Population Databases
Gene Resources
Expert Curation
ClinGen
Expert-curated gene-disease validity
GenCC
Gene Curation Coalition — multi-curator classifications
Orphanet
Rare disease encyclopedia and gene-disease associations
PanelApp
Gene panels for rare disease diagnostics (Genomics England)
LOVD
Leiden Open Variation Database — variant listings
GeneReviews
Expert-authored summaries of heritable conditions (NCBI)