HomeAboutRankingsData Sources
© 2026 GeneE
🧬
GeneE
4 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
ⓘGeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
DUS4L-BCAP29
DUS4L-BCAP29 readthrough
Chromosome 7 · 7q22.3
NCBI Gene: 115253422Ensembl: ENSG00000288558.3HGNC: HGNC:54422UniProt: A0A669KAY5
1PubMed Papers
0Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Swiss-Prot Reviewed
✦AI Summary

DUS4L-BCAP29 is a readthrough fusion transcript generated through cis-splicing between adjacent genes on chromosome 7 1. Originally identified as a cancer-associated fusion in gastric and prostate cancers 2, subsequent research revealed that DUS4L-BCAP29 is not cancer-specific but rather a normal physiological transcript present across diverse tissues and non-neoplastic cell lines at comparable expression levels to cancer cells 13. The fusion transcript demonstrates context-dependent biological functions: in neural development, DUS4L-BCAP29 dramatically increases during neural differentiation of human umbilical mesenchymal stem cells and effectively promotes neural differentiation 4. In cellular contexts, gain-of-function studies show that DUS4L-BCAP29 overexpression promotes cell growth and motility in both cancer and non-cancer cells 13. Notably, loss-of-function approaches (siRNA knockdown) inhibited gastric cancer cell proliferation in soft agar assays, suggesting tumorigenic potential 2. However, the pro-growth effects are not uniquely oncogenic 13. DUS4L-BCAP29 cannot serve as a cancer biomarker due to its ubiquitous normal expression, but represents a functional chimeric RNA with roles in both development and cellular proliferation.

Sources cited
1
DUS4L-BCAP29 fusion transcript identified in gastric cancer cell lines and tissues; siRNA knockdown inhibits cell proliferation; soft agar assay confirms tumorigenic potential
PMID: 24240688
2
DUS4L-BCAP29 dramatically increases during neural differentiation of stem cells and promotes neural differentiation when overexpressed
PMID: 30959201
3
DUS4L-BCAP29 exists in normal tissues and non-cancer cell lines at comparable expression levels to cancer cells; generated by cis-splicing between adjacent genes; overexpression promotes cell growth and motility; not suitable as cancer biomarker
PMID: 28415823
4
Confirms DUS4L-BCAP29 presence in normal physiology with similar expression in noncancerous tissues as cancer tissues; gain-of-function shows promotion of cell growth and motility; not cancer-specific
PMID: 31728976
⚠Limited data available — This gene has 4 indexed publications. Summary and analysis may be incomplete.
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
DUS4LCo-mentioned in literature100%BCAP29Protein interaction93%
Tissue Expression4 tissues
Bone Marrow
0%
Lung
0%
Ovary
0%
Liver
0%
Gene Interaction Network
Click a node to explore
DUS4L-BCAP29DUS4LBCAP29
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt A0A669KAY5
View on AlphaFold ↗
RankingsWhere DUS4L-BCAP29 stands among ~20K protein-coding genes
  • #19,297of 20,598
    Most Researched1
Genes detectedDUS4L-BCAP29
Sources retrieved4 papers
Response time—
📄 Sources
4
1
Novel fusion transcripts in human gastric cancer revealed by transcriptome analysis.
PMID: 24240688
Oncogene · 2014
1.00
2
Identification of chimeric RNAs in human infant brains and their implications in neural differentiation.
PMID: 30959201
Int J Biochem Cell Biol · 2019
0.75
3
Recurrent fusion RNA DUS4L-BCAP29 in non-cancer human tissues and cells.
PMID: 28415823
Oncotarget · 2017
0.50
4
Case Study: The Recurrent Fusion RNA DUS4L-BCAP29 in Noncancer Human Tissues and Cells.
PMID: 31728976
Methods Mol Biol · 2020
0.25