| Name | DiGeorge syndrome critical region gene 10 (non-protein coding) |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Recent investigations into the molecular underpinnings of glioma progression have identified DGCR10 as a protective factor with tumor‐suppressive activity. In particular, functional analysis within a panel of mesenchymal subtype–related long non‐coding RNAs revealed that knockdown of DGCR10 significantly enhanced the migration and invasion of glioma cells, suggesting that DGCR10 normally acts to restrain these aggressive cellular behaviors (5). This protective role implies that DGCR10 may help to stabilize cellular architecture and counteract pathways associated with mesenchymal transition—a process that, when dysregulated, contributes to tumor progression. Although studies in other biological contexts, such as the regulation of epithelial‐to‐mesenchymal transition during gastrulation (1) and the refinement of diagnostic strategies using high‐resolution genomic assays (4), underline the importance of precise molecular regulation, the specific mechanisms by which DGCR10 exerts its inhibitory effects in glioma remain to be fully elucidated. Overall, the identification of DGCR10 as a determinant of glioma invasiveness contributes to the growing evidence that distinct regulatory RNAs within mesenchymal signatures serve as valuable prognostic biomarkers and potential therapeutic targets."}]}, {"type": "t", "text": "\n\n "}, {"type": "p", "children": [{"type": "b", "children": [{"type": "t", "text": "Citations:"}]}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "5"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Yukiko Nakaya, Erike W Sukowati, Guojun Sheng "}, {"type": "b", "children": [{"type": "t", "text": "Epiblast integrity requires CLASP and Dystroglycan-mediated microtubule anchoring to the basal cortex."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biol (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1083/jcb.201302075"}], "href": "https://doi.org/10.1083/jcb.201302075"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23940118"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23940118"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Andrea Bender, Sieghard Beller "}, {"type": "b", "children": [{"type": "t", "text": "Fingers as a tool for counting - naturally fixed or culturally flexible?"}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Front Psychol (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3389/fpsyg.2011.00256"}], "href": "https://doi.org/10.3389/fpsyg.2011.00256"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22016741"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22016741"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Martin Wagenmann, Jörg Schipper "}, {"type": "b", "children": [{"type": "t", "text": "The transnasal approach to the skull base. From sinus surgery to skull base surgery."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "GMS Curr Top Otorhinolaryngol Head Neck Surg (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3205/cto000081"}], "href": "https://doi.org/10.3205/cto000081"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22558058"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22558058"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Ashutosh Halder, Manish Jain, Amanpreet Kaur Kalsi "}, {"type": "b", "children": [{"type": "t", "text": "SNP Microarray in FISH Negative Clinically Suspected 22q11.2 Microdeletion Syndrome."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Scientifica (Cairo) (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1155/2016/5826431"}], "href": "https://doi.org/10.1155/2016/5826431"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27051557"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27051557"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Kebing Huang, Xiaoyu Yue, Yinfei Zheng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Development and Validation of an Mesenchymal-Related Long Non-Coding RNA Prognostic Model in Glioma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Front Oncol (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3389/fonc.2021.726745"}], "href": "https://doi.org/10.3389/fonc.2021.726745"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34540695"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34540695"}]}]}]}
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| Synonyms | DGS-B |
| NCBI Gene ID | 26222 |
| 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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DGCR10 has 512 functional associations with biological entities spanning 5 categories (molecular profile, disease, phenotype or trait, chemical, cell line, cell type or tissue, gene, protein or microRNA) extracted from 14 datasets.
Click the + buttons to view associations for DGCR10 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 DGCR10 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| CCLE Cell Line Gene Expression Profiles | cell lines with high or low expression of DGCR10 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of DGCR10 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 DGCR10 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 DGCR10 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of DGCR10 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| GEO Signatures of Differentially Expressed Genes for Diseases | disease perturbations changing expression of DGCR10 gene from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. | |
| GEO Signatures of Differentially Expressed Genes for Kinase Perturbations | kinase perturbations changing expression of DGCR10 gene from the GEO Signatures of Differentially Expressed Genes for Kinase Perturbations dataset. | |
| GEO Signatures of Differentially Expressed Genes for Small Molecules | small molecule perturbations changing expression of DGCR10 gene from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of DGCR10 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 DGCR10 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| KnockTF Gene Expression Profiles with Transcription Factor Perturbations | transcription factor perturbations changing expression of DGCR10 gene from the KnockTF Gene Expression Profiles with Transcription Factor Perturbations dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at DGCR10 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 DGCR10 gene relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset. | |