| HGNC Family | Non-coding RNAs |
| Name | small nucleolar RNA, H/ACA box 10 |
| 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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These findings indicate that MR1‐restricted MAIT cells play a pivotal role in immune surveillance at pathogen entry sites as well as in regulating local immune responses."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nOther reports detail the antigen‐presentation properties of MR1, emphasizing its structural similarity to classical MHC class I molecules. MR1 molecules have been shown to adopt folded conformations upon ligand binding—often via a specialized binding groove that accommodates small molecule metabolites—and to traffic through endosomal compartments. These structural and trafficking features are critical for enabling MR1 to capture both endogenous and exogenous antigens and to activate MAIT cells in a manner analogous to classical TCR–MHC interactions."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "6", "end_ref": "10"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond the local control of mucosal immunity, MR1‐mediated antigen presentation contributes to broader host defense and immunoregulatory processes. Several studies demonstrate that MR1 is involved in protection against specific bacterial infections and modulates the inflammatory milieu during systemic challenges. Moreover, the MR1/MAIT cell axis has been implicated in contexts as varied as neuroinflammation, allergic contact dermatitis, and even cardiac hypertrophy, underscoring its multifaceted role in both innate and adaptive immune responses. These observations affirm that MR1 not only governs the development and activation of a distinctive T cell subset but also plays a compensatory and sometimes pathogenic role when conventional immune mechanisms are altered."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "11", "end_ref": "21"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nNote that although the query requested a summary of the function of SNORA10, none of the provided abstracts mention SNORA10. Instead, the literature collectively focuses on MR1 and its integral role in antigen presentation to MAIT cells, thereby bridging innate and adaptive immunity.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Emmanuel Treiner, Livine Duban, Seiamak Bahram, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Antigen-loaded MR1 tetramers define T cell receptor heterogeneity in mucosal-associated invariant T cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Exp Med (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1084/jem.20130958"}], "href": "https://doi.org/10.1084/jem.20130958"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24101382"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24101382"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Shouxiong Huang, Emmanuel Martin, Sojung Kim, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MR1 antigen presentation to mucosal-associated invariant T cells was highly conserved in evolution."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.0903196106"}], "href": "https://doi.org/10.1073/pnas.0903196106"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19416870"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19416870"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Wei-Jen Chua, Sojung Kim, Nancy Myers, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Endogenous MHC-related protein 1 is transiently expressed on the plasma membrane in a conformation that activates mucosal-associated invariant T cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Immunol (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.4049/jimmunol.1003254"}], "href": "https://doi.org/10.4049/jimmunol.1003254"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21402896"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21402896"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Karmella Naidoo, Katherine Woods, Christophe Pellefigues, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MR1-dependent immune surveillance of the skin contributes to pathogenesis and is a photobiological target of UV light therapy in a mouse model of atopic dermatitis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Allergy (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/all.14994"}], "href": "https://doi.org/10.1111/all.14994"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34185885"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34185885"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Shouxiong Huang, Susan Gilfillan, Marina Cella, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Evidence for MR1 antigen presentation to mucosal-associated invariant T cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M501087200"}], "href": "https://doi.org/10.1074/jbc.M501087200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15802267"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15802267"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Shouxiong Huang, Susan Gilfillan, Sojung Kim, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MR1 uses an endocytic pathway to activate mucosal-associated invariant T cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Exp Med (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1084/jem.20072579"}], "href": "https://doi.org/10.1084/jem.20072579"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18443227"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18443227"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Michael J Miley, Steven M Truscott, Yik Yeung Lawrence Yu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Biochemical features of the MHC-related protein 1 consistent with an immunological function."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Immunol (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.4049/jimmunol.170.12.6090"}], "href": "https://doi.org/10.4049/jimmunol.170.12.6090"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12794138"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12794138"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Hisateru Yamaguchi, Keiichiro Hashimoto "}, {"type": "b", "children": [{"type": "t", "text": "Association of MR1 protein, an MHC class I-related molecule, with beta(2)-microglobulin."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1006/bbrc.2001.6277"}], "href": "https://doi.org/10.1006/bbrc.2001.6277"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "11785959"}], "href": "https://pubmed.ncbi.nlm.nih.gov/11785959"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Mary H Young, Lance U'Ren, Shouxiong Huang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MAIT cell recognition of MR1 on bacterially infected and uninfected cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0053789"}], "href": "https://doi.org/10.1371/journal.pone.0053789"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23342002"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23342002"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Philippe Georgel, Mirjana Radosavljevic, Cécile Macquin, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Major histocompatibility complex class I molecules modulate embryonic neuritogenesis and neuronal polarization."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neuroimmunol (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.jneuroim.2012.03.008"}], "href": "https://doi.org/10.1016/j.jneuroim.2012.03.008"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22503373"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22503373"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "M Selvan Joseph, Tina Bilousova, Sharon Zdunowski, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Symbiotic bacteria-dependent expansion of MR1-reactive T cells causes autoimmunity in the absence of Bcl11b."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41467-022-34802-8"}], "href": "https://doi.org/10.1038/s41467-022-34802-8"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36376329"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36376329"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Naoya Imahashi, Masashi Satoh, Emanuela Clemente, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Control of the temporal development of Alzheimer's disease pathology by the MR1/MAIT cell axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neuroinflammation (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s12974-023-02761-6"}], "href": "https://doi.org/10.1186/s12974-023-02761-6"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36944969"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36944969"}]}]}]}
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| Synonyms | SNORA10A, ACA10 |
| NCBI Gene ID | 574042 |
| 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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SNORA10 has 1,926 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 19 datasets.
Click the + buttons to view associations for SNORA10 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 SNORA10 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 SNORA10 gene from the CHEA Transcription Factor Binding Site Profiles dataset. | |
| ChEA Transcription Factor Targets | transcription factors binding the promoter of SNORA10 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 SNORA10 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 SNORA10 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 SNORA10 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of SNORA10 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| GeneSigDB Published Gene Signatures | PubMedIDs of publications reporting gene signatures containing SNORA10 from the GeneSigDB Published Gene Signatures dataset. | |
| GEO Signatures of Differentially Expressed Genes for Gene Perturbations | gene perturbations changing expression of SNORA10 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 SNORA10 gene from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. | |
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of SNORA10 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 SNORA10 gene relative to other tissue samples from the GTEx Tissue Sample Gene Expression Profiles dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of SNORA10 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 SNORA10 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 SNORA10 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 SNORA10 gene from the KnockTF Gene Expression Profiles with Transcription Factor Perturbations dataset. | |
| MotifMap Predicted Transcription Factor Targets | transcription factors regulating expression of SNORA10 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 SNORA10 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 SNORA10 gene relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset. | |