| HGNC Family | Non-coding RNAs |
| Name | small nucleolar RNA, H/ACA box 62 |
| Description | Predicted to be involved in RNA processing. Part of box H/ACA RNP complex. [provided by Alliance of Genome Resources, Mar 2025] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nAlthough the request asks for a summary of SNORA62 function, none of the provided abstracts mention or investigate SNORA62. Instead, these studies primarily focus on a muscle‐enriched microRNA, miR‑133a (and its family members and related regulators), and its critical role in multiple tissues and disease settings. For instance, early investigations highlighted the ability of miR‑133a to modulate cardiomyocyte function and sympathetic signaling, thereby influencing heart rate, contractility, and even the electrophysiological properties via β‑adrenergic pathways."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nOther studies detailed how miR‑133a tightly regulates molecular targets such as the IP₃ receptor II, IGF‑1 receptor, and RUNX2 among others, establishing a feed‐forward mechanism in pathological cardiac remodeling, hypertrophy, and differentiation of muscle and osteoblast cells. In models of hypertrophy, reduced miR‑133a levels allow for increased pro‑hypertrophic calcium signaling, while in skeletal muscle and osteoblast contexts, miR‑133a shapes mitochondrial biogenesis, exercise tolerance, and differentiation processes."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "3", "end_ref": "7"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional work illustrated miR‑133a’s prominent involvement in translating upstream signals—whether via neurohormonal stimuli, oxidative stress in diabetic vascular tissues, or inflammatory cues in conditions such as sepsis and asthma—into downstream effects that regulate transcription factors and signaling cascades (e.g., PI3K/Akt/mTOR, nitric oxide pathways) to mediate cellular responses like airway remodeling, hypertrophy alleviation, and even bone remodeling under mechanical unloading conditions."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "8", "end_ref": "16"}]}, {"type": "t", "text": " \n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn summary, while SNORA62—a small nucleolar RNA typically implicated in rRNA modification—is not addressed in these reports, the collected abstracts comprehensively outline miR‑133a’s multifaceted regulatory functions in muscle, heart, bone, and inflammatory disease models. These findings underscore miR‑133a’s significance as a key post‑transcriptional modulator in various physiological and pathological processes.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "María Rodríguez-Muñoz, Elena de la Torre-Madrid, Pilar Sánchez-Blázquez, et al. "}, {"type": "b", "children": [{"type": "t", "text": "NMDAR-nNOS generated zinc recruits PKCgamma to the HINT1-RGS17 complex bound to the C terminus of Mu-opioid receptors."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Signal (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.cellsig.2008.06.015"}], "href": "https://doi.org/10.1016/j.cellsig.2008.06.015"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18652891"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18652891"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Yoshio Kato, Shigeru Miyaki, Shigetoshi Yokoyama, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Real-time functional imaging for monitoring miR-133 during myogenic differentiation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Biochem Cell Biol (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biocel.2009.04.018"}], "href": "https://doi.org/10.1016/j.biocel.2009.04.018"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19398036"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19398036"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Javier Garzón, María Rodríguez-Muñoz, Ana Vicente-Sánchez, et al. "}, {"type": "b", "children": [{"type": "t", "text": "RGSZ2 binds to the neural nitric oxide synthase PDZ domain to regulate mu-opioid receptor-mediated potentiation of the N-methyl-D-aspartate receptor-calmodulin-dependent protein kinase II pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Antioxid Redox Signal (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1089/ars.2010.3767"}], "href": "https://doi.org/10.1089/ars.2010.3767"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21348811"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21348811"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Javier Garzón, María Rodríguez-Muñoz, Ana Vicente-Sánchez, et al. "}, {"type": "b", "children": [{"type": "t", "text": "SUMO-SIM interactions regulate the activity of RGSZ2 proteins."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0028557"}], "href": "https://doi.org/10.1371/journal.pone.0028557"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22163035"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22163035"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Faye M Drawnel, Dagmar Wachten, Jeffery D Molkentin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutual antagonism between IP(3)RII and miRNA-133a regulates calcium signals and cardiac hypertrophy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biol (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1083/jcb.201111095"}], "href": "https://doi.org/10.1083/jcb.201111095"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23166348"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23166348"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Alessandra Castaldi, Tania Zaglia, Vittoria Di Mauro, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-133 modulates the β1-adrenergic receptor transduction cascade."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Circ Res (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1161/CIRCRESAHA.115.303252"}], "href": "https://doi.org/10.1161/CIRCRESAHA.115.303252"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24807785"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24807785"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Yueqiu Luo, Xiaoxing Wu, Zongxin Ling, et al. "}, {"type": "b", "children": [{"type": "t", "text": "microRNA133a targets Foxl2 and promotes differentiation of C2C12 into myogenic progenitor cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "DNA Cell Biol (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1089/dna.2014.2522"}], "href": "https://doi.org/10.1089/dna.2014.2522"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25317675"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25317675"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Johannes Besser, Daniela Malan, Katharina Wystub, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiRNA-1/133a clusters regulate adrenergic control of cardiac repolarization."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0113449"}], "href": "https://doi.org/10.1371/journal.pone.0113449"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25415383"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25415383"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Varun Kesherwani, Shyam Sundar Nandi, Surender K Sharawat, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Hydrogen sulfide mitigates homocysteine-mediated pathological remodeling by inducing miR-133a in cardiomyocytes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biochem (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s11010-015-2383-5"}], "href": "https://doi.org/10.1007/s11010-015-2383-5"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25763715"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25763715"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Ludivine Renaud, Lillianne G Harris, Santhosh K Mani, et al. "}, {"type": "b", "children": [{"type": "t", "text": "HDACs Regulate miR-133a Expression in Pressure Overload-Induced Cardiac Fibrosis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Circ Heart Fail (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1161/CIRCHEARTFAILURE.114.001781"}], "href": "https://doi.org/10.1161/CIRCHEARTFAILURE.114.001781"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26371176"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26371176"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Yaohui Nie, Yoriko Sato, Chao Wang, et al. 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| Synonyms | E2-1, RNE2, RNU108 |
| NCBI Gene ID | 6044 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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SNORA62 has 1,570 functional associations with biological entities spanning 5 categories (molecular profile, functional term, phrase or reference, chemical, cell line, cell type or tissue, gene, protein or microRNA) extracted from 22 datasets.
Click the + buttons to view associations for SNORA62 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 SNORA62 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| ChEA Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of SNORA62 gene from the CHEA Transcription Factor Binding Site Profiles dataset. | |
| ChEA Transcription Factor Targets | transcription factors binding the promoter of SNORA62 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of SNORA62 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 SNORA62 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 SNORA62 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of SNORA62 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| ESCAPE Omics Signatures of Genes and Proteins for Stem Cells | PubMedIDs of publications reporting gene signatures containing SNORA62 from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset. | |
| GeneSigDB Published Gene Signatures | PubMedIDs of publications reporting gene signatures containing SNORA62 from the GeneSigDB Published Gene Signatures dataset. | |
| GEO Signatures of Differentially Expressed Genes for Gene Perturbations | gene perturbations changing expression of SNORA62 gene from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. | |
| GEO Signatures of Differentially Expressed Genes for Small Molecules | small molecule perturbations changing expression of SNORA62 gene from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. | |
| GEO Signatures of Differentially Expressed Genes for Transcription Factor Perturbations | transcription factor perturbations changing expression of SNORA62 gene from the GEO Signatures of Differentially Expressed Genes for Transcription Factor Perturbations dataset. | |
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of SNORA62 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |
| GTEx Tissue Sample Gene Expression Profiles | tissue samples with high or low expression of SNORA62 gene relative to other tissue samples from the GTEx Tissue Sample Gene Expression Profiles dataset. | |
| GTEx Tissue-Specific Aging Signatures | tissue samples with high or low expression of SNORA62 gene relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of SNORA62 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles | cell lines with high or low expression of SNORA62 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles dataset. | |
| KnockTF Gene Expression Profiles with Transcription Factor Perturbations | transcription factor perturbations changing expression of SNORA62 gene from the KnockTF Gene Expression Profiles with Transcription Factor Perturbations dataset. | |
| MotifMap Predicted Transcription Factor Targets | transcription factors regulating expression of SNORA62 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 SNORA62 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |
| TCGA Signatures of Differentially Expressed Genes for Tumors | tissue samples with high or low expression of SNORA62 gene relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset. | |
| WikiPathways Pathways 2014 | pathways involving SNORA62 protein from the Wikipathways Pathways 2014 dataset. | |