Target intelligence / Profile preview

TDRD6 and SLC25A27 antisense RNA 1 (TDRD6-AS1)

Target
TDRD6-AS1
Molecular classification
Long noncoding RNA (lncRNA), Antisense RNA, Natural antisense transcript (NAT)
01

Overview

TDRD6 and SLC25A27 antisense RNA 1 (TDRD6-AS1) is a long noncoding RNA transcript that occurs antisense to protein-coding genes TDRD6 and SLC25A27. As a member of the natural antisense transcript (NAT) family, it likely modulates gene expression through complementary interactions with the mRNAs of its sense genes, impacting transcriptional, epigenetic, or RNA processing steps. While general functions of antisense RNAs include roles in cell differentiation, chromatin remodeling, and disease, currently, TDRD6-AS1’s specific biological roles and clinical relevance remain undetermined. It is not considered a classical drug target such as a receptor, enzyme, or transporter, and there are no known drugs, biomarkers of efficacy, or safety issues associated with its modulation.

Other names
TDRD6-AS1
02

Mechanism of action

Antisense oligonucleotides (ASOs): Bind target RNAs to modulate splicing, stability, or translation, often inducing RNase H-mediated degradation or blocking translational machinery. No ASO therapy specifically targets TDRD6-AS1 as of now.

03

Biological functions

Regulation of gene expression (via interaction with sense mRNAs or chromatin modulation)Epigenetic regulation (including DNA methylation and histone modification)Regulation of transcription, splicing, and mRNA stabilityPotential involvement in alternative splicing and transcript modulation
04

Disease associations

Cancer (via dysregulated NATs modulating tumor suppressors/oncogenes)Epigenetic disorders (through gene silencing/imprinting errors)Other diseases possibly linked to abnormal antisense RNA expression (e.g., alpha-thalassemia, acute lymphoblastic/myeloid leukemia via similar mechanisms)No specific evidence links TDRD6-AS1 directly to a defined disease at this time
05

Safety considerations

None reported for TDRD6-AS1; general ASO therapies can have off-target or immune effects

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