LUCAT1
Chr 5lung cancer associated transcript 1
Also known as: SCAL1, SCAT5
30
ClinVar variants
27
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— LUCAT1
📋
ClinVar Variants
27 Pathogenic / Likely Pathogenic· 3 VUS of 30 total submissions
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
30 submitted variants in ClinVar
Classification Summary
Pathogenic22
Likely Pathogenic5
VUS3
22
Pathogenic
5
Likely Pathogenic
3
VUS
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | — | — | — | — | 22 |
Likely Pathogenic | — | — | — | — | 5 |
VUS | — | — | — | — | 3 |
Likely Benign | — | — | — | — | 0 |
Benign | — | — | — | — | 0 |
| Total | — | 30 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
LUCAT1 · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
OMIM — Genotype-Phenotype Relationships
1 OMIM entry
LUNG CANCER-ASSOCIATED TRANSCRIPT 1, NONCODING; LUCAT1
MIM #618190 · *
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
Exosome-transmitted LUCAT1 promotes stemness transformation and chemoresistance in bladder cancer by binding to IGF2BP2.
Zhan Y et al.·J Exp Clin Cancer Res
2025
High expression of long noncoding RNA LUCAT1 correlates with a poor clinical outcome in solid tumors: A systematic review and meta-analysis.
Lv P et al.·Pathol Res Pract
2020Meta-analysis
Lung cancer associated transcript 1 binds heat shock protein 90 to promote growth of hepatocellular carcinoma.
Bai Y et al.·Cell Signal
2025
LUCAT1-Mediated Competing Endogenous RNA (ceRNA) Network in Triple-Negative Breast Cancer.
Verma D et al.·Cells
2024
Clinical Value of lncRNA LUCAT1 Expression in Liver Cancer and its Potential Pathways.
Jiao Y et al.·J Gastrointestin Liver Dis
2019
Low LncRNA LUCAT1 Expression Assists in the Diagnosis of Chronic Heart Failure and Predicts Poor Prognosis.
Wang J et al.·Int Heart J
2023
Long non-coding RNA LUCAT1 modulates methotrexate resistance in osteosarcoma via miR-200c/ABCB1 axis.
Han Z et al.·Biochem Biophys Res Commun
2018
Disulfidptosis-related gene signatures as prognostic biomarkers and predictors of immunotherapy response in HNSCC.
Qin H et al.·Front Immunol
2025
Long non-coding RNA LUCAT1/miR-5582-3p/TCF7L2 axis regulates breast cancer stemness via Wnt/β-catenin pathway.
Zheng A et al.·J Exp Clin Cancer Res
2019
Long Noncoding RNAs CARMN, LUCAT1, SMILR, and MALAT1 in Thoracic Aortic Aneurysm: Validation of Biomarkers in Clinical Samples.
Patamsytė V et al.·Dis Markers
2020
Top 10 resultsSearch PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
lncRNA LUCAT1 Regulates DNA Damage Response in Glioma Stem Cells Under Hypoxia.
Huang H et al.·Neuro Oncol
2026
Hypoxia-induced exosomal LUCAT1 promotes osimertinib resistance in lung adenocarcinoma by stabilizing c-MET.
Du J et al.·Cell Death Dis
2025🔓 Open Access
RETRACTION: Downregulation of Long Noncoding RNA LUCAT1 Suppresses the Migration and Invasion of Bladder Cancer by Targeting miR-181c-5p.
Research International B.·Biomed Res Int
2025🔓 Open Access
LncRNA LUCAT1 as a prognostic biomarker in cholangiocarcinoma through targeting miR-141-3p: clinical and functional insights.
An Y et al.·Hereditas
2025🔓 Open AccessFunctional
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)