SNORD114-20 Gene

HGNC Family Non-coding RNAs
Name small nucleolar RNA, C/D box 114-20
Description Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]
Summary
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Several reports describe how deregulated microRNAs (for example, miR‑31, miR‑132, and miR‑144) and proteolytic processing of RasGAP (RASA1/p120 RasGAP) fine‑tune Ras activity, which in turn affects key processes such as tumorigenesis, cell polarity, axon growth, lymphatic development, and apoptosis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "7"}]}, {"type": "t", "text": " \n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nThese studies also illustrate that precise control of Ras signal transduction—achieved via caspase‐mediated cleavage events, modulation by specific microRNAs, and protein–protein interactions within complexes (involving factors such as p120RasGAP, p190RhoGAP, and 14‑3‑3)—is essential for maintaining cellular homeostasis under stress and for proper developmental angiogenesis and vascular morphogenesis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "8", "end_ref": "14"}]}, {"type": "t", "text": " \n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn contrast to these well‐characterized regulatory mechanisms, the function of SNORD114‑20 remains to be elucidated. Given the general role of C/D box snoRNAs in guiding site‑specific 2′‑O‑methylation and processing of ribosomal and other cellular RNAs, one can speculate that SNORD114‑20 might indirectly influence these pathways—perhaps by modulating the maturation or stability of transcripts encoding key regulators like RASA1 or factors within the Ras/ERK and Ras/Akt cascades. Such a role would be consistent with the emerging paradigm in which noncoding RNAs help fine‑tune critical cellular processes including cell survival, differentiation, and stress responses."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "15", "end_ref": "23"}]}, {"type": "t", "text": " \n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Masayuki Ozawa "}, {"type": "b", "children": [{"type": "t", "text": "p120-independent modulation of E-cadherin adhesion activity by the membrane-proximal region of the cytoplasmic domain."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M307778200"}], "href": "https://doi.org/10.1074/jbc.M307778200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12952959"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12952959"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Jiang-Yan Yang, David Michod, Joël Walicki, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Cutting Edge: Codeletion of the Ras GTPase-Activating Proteins (RasGAPs) Neurofibromin 1 and p120 RasGAP in T Cells Results in the Development of T Cell Acute Lymphoblastic Leukemia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Immunol (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.4049/jimmunol.1402639"}], "href": "https://doi.org/10.4049/jimmunol.1402639"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26002977"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26002977"}]}, {"type": "r", "ref": 18, "children": [{"type": "t", "text": "Güliz Vanli, Christine Sempoux, Christian Widmann "}, {"type": "b", "children": [{"type": "t", "text": "The caspase-3/p120 RasGAP stress-sensing module reduces liver cancer incidence but does not affect overall survival in gamma-irradiated and carcinogen-treated mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Carcinog (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/mc.22624"}], "href": "https://doi.org/10.1002/mc.22624"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28150874"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28150874"}]}, {"type": "r", "ref": 19, "children": [{"type": "t", "text": "Philip E Lapinski, Beth A Lubeck, Di Chen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "RASA1 regulates the function of lymphatic vessel valves in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Clin Invest (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1172/JCI89607"}], "href": "https://doi.org/10.1172/JCI89607"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28530642"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28530642"}]}, {"type": "r", "ref": 20, "children": [{"type": "t", "text": "Di Chen, Joyce M Teng, Paula E North, et al. "}, {"type": "b", "children": [{"type": "t", "text": "RASA1-dependent cellular export of collagen IV controls blood and lymphatic vascular development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Clin Invest (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1172/JCI124917"}], "href": "https://doi.org/10.1172/JCI124917"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31185000"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31185000"}]}, {"type": "r", "ref": 21, "children": [{"type": "t", "text": "Xianjie Zhang, Hongli Guo, An Xie, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-144 relieves chronic constriction injury-induced neuropathic pain via targeting RASA1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biotechnol Appl Biochem (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/bab.1854"}], "href": "https://doi.org/10.1002/bab.1854"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31737949"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31737949"}]}, {"type": "r", "ref": 22, "children": [{"type": "t", "text": "Di Chen, Xin Geng, Philip E Lapinski, et al. "}, {"type": "b", "children": [{"type": "t", "text": "RASA1-driven cellular export of collagen IV is required for the development of lymphovenous and venous valves in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Development (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1242/dev.192351"}], "href": "https://doi.org/10.1242/dev.192351"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33144395"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33144395"}]}, {"type": "r", "ref": 23, "children": [{"type": "t", "text": "Christopher J Benwell, Robert T Johnson, James A G E Taylor, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A proteomics approach to isolating neuropilin-dependent α5 integrin trafficking pathways: neuropilin 1 and 2 co-traffic α5 integrin through endosomal p120RasGAP to promote polarised fibronectin fibrillogenesis in endothelial cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Commun Biol (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s42003-024-06320-4"}], "href": "https://doi.org/10.1038/s42003-024-06320-4"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38789481"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38789481"}]}]}]}
Synonyms 14Q(II-20)
NCBI Gene ID 767598
API
Download Associations
Predicted Functions View SNORD114-20's ARCHS4 Predicted Functions.
Co-expressed Genes View SNORD114-20's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View SNORD114-20's ARCHS4 Predicted Functions.

Functional Associations

SNORD114-20 has 303 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 9 datasets.

Click the + buttons to view associations for SNORD114-20 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CCLE Cell Line Gene CNV Profiles cell lines with high or low copy number of SNORD114-20 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.
COSMIC Cell Line Gene CNV Profiles cell lines with high or low copy number of SNORD114-20 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
ENCODE Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at SNORD114-20 gene from the ENCODE Histone Modification Site Profiles dataset.
ENCODE Transcription Factor Binding Site Profiles transcription factor binding site profiles with transcription factor binding evidence at the promoter of SNORD114-20 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of SNORD114-20 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of SNORD114-20 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of SNORD114-20 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.
MotifMap Predicted Transcription Factor Targets transcription factors regulating expression of SNORD114-20 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset.
Roadmap Epigenomics Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at SNORD114-20 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.