MRPL20-AS1 Gene

Name MRPL20 antisense RNA 1
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nThe long non-coding RNA MRPL20‑AS1 emerges as a novel molecular player in cardiovascular health, particularly under the stress conditions associated with obstructive sleep apnea syndrome (OSAS). OSAS, known for its association with arterial hypertension, coronary artery disease, and heart failure, appears to influence cardiovascular pathology partly through mediators like MRPL20‑AS1, which is demonstrably modulated in affected patients. This observation suggests that MRPL20‑AS1 may contribute to the cellular adaptations or maladaptations induced by OSAS‐associated hypoxic stress."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n \nEmerging evidence indicates that hypoxia, a central feature of OSAS, can trigger the altered expression of specific long non‑coding RNAs. In vitro experiments further support the notion that MRPL20‑AS1 is sensitive to hypoxic conditions, underscoring its potential role as a molecular mediator in the heart’s response to reduced oxygen levels. This finding links MRPL20‑AS1 not only to the pathophysiology of OSAS but also to broader cardiovascular disease mechanisms where oxygen deprivation is a key factor."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n \nOverall, the modulation of MRPL20‑AS1 by both OSAS and direct hypoxic stimuli emphasizes its potential importance in the intricate network of genetic regulation underlying cardiovascular diseases. Further research into MRPL20‑AS1 could provide deeper insights into its mechanistic contributions and reveal novel therapeutic targets for conditions where hypoxia and cardiovascular stress are pivotal."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Andreas Zietzer, Nils Breitrück, Philip Düsing, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The lncRNA MRPL20-AS1 is associated with severe OSAS and downregulated upon hypoxic injury of endothelial cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Cardiol (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ijcard.2022.08.035"}], "href": "https://doi.org/10.1016/j.ijcard.2022.08.035"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35988669"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35988669"}]}]}]}
NCBI Gene ID 148413
API
Download Associations
Predicted Functions View MRPL20-AS1's ARCHS4 Predicted Functions.
Co-expressed Genes View MRPL20-AS1's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MRPL20-AS1's ARCHS4 Predicted Functions.

Functional Associations

MRPL20-AS1 has 3 functional associations with biological entities spanning 1 categories (cell line, cell type or tissue) extracted from 2 datasets.

Click the + buttons to view associations for MRPL20-AS1 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
GTEx Tissue-Specific Aging Signatures tissue samples with high or low expression of MRPL20-AS1 gene relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset.
HuBMAP Azimuth Cell Type Annotations cell types associated with MRPL20-AS1 gene from the HuBMAP Azimuth Cell Type Annotations dataset.