| HGNC Family | Non-coding RNAs |
| Name | beta globin locus transcript 3 (non-protein coding) |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n BGLT3 is a multifaceted gene product whose designation has been applied in distinct biological contexts. In several human malignancies including chronic myeloid leukemia and papillary thyroid carcinoma, a long noncoding RNA (lncRNA‐BGL3) acts as a tumor suppressor. It functions as a competing endogenous RNA (ceRNA) by binding to and sequestering microRNAs that would otherwise target the phosphatase and tensin homolog (PTEN), thereby enhancing PTEN expression and inhibiting oncogenic signaling pathways."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In addition, lncRNA‐BGL3 participates in the DNA damage response by interacting with proteins such as PARP1 and BARD1 to promote homologous recombination repair"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": ", and it is involved in the regulation of long‐range chromatin interactions at the β‐globin locus, thereby influencing the expression of γ‐globin genes through selective nuclear receptor cofactor engagements."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": " A genetic variant in the BGLT3 locus (rs7924684) has further been associated with alterations in the ratio of γ‐chains in sickle cell anemia patients, implicating this gene in globin regulation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n In a separate context, the BGL3 designation also refers to members of a β‐glucosidase enzyme family that are involved in the hydrolysis of cellobiose, an essential step in the saccharification of lignocellulosic biomass for biofuel production. These enzymes exhibit high glucose tolerance and contribute to efficient cellobiose utilization in specialized yeast strains."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Collectively, these studies underscore the diverse roles of BGLT3—from mediating epigenetic and post‐transcriptional regulation in cancer and hemoglobinopathy to participating in carbohydrate metabolism and bioenergy applications—highlighting its potential as both a prognostic biomarker and a therapeutic target in various clinical and industrial settings.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "G Guo, Q Kang, X Zhu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A long noncoding RNA critically regulates Bcr-Abl-mediated cellular transformation by acting as a competitive endogenous RNA."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncogene (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/onc.2014.131"}], "href": "https://doi.org/10.1038/onc.2014.131"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24837367"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24837367"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "M Zhao, F Yang, C Sang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "BGL3 inhibits papillary thyroid carcinoma progression via regulating PTEN stability."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Endocrinol Invest (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s40618-021-01519-2"}], "href": "https://doi.org/10.1007/s40618-021-01519-2"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33543443"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33543443"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Zhaohua Hu, Shaojie Mi, Ting Zhao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "BGL3 lncRNA mediates retention of the BRCA1/BARD1 complex at DNA damage sites."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO J (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.15252/embj.2019104133"}], "href": "https://doi.org/10.15252/embj.2019104133"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32347575"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32347575"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Chun Ming Chan, Joel Fulton, Cristina Montiel-Duarte, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A signature motif mediating selective interactions of BCL11A with the NR2E/F subfamily of orphan nuclear receptors."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nucleic Acids Res (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/nar/gkt761"}], "href": "https://doi.org/10.1093/nar/gkt761"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23975195"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23975195"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Mariana Delgadinho, Catarina Ginete, Brígida Santos, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Genotypic Diversity among Angolan Children with Sickle Cell Anemia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Environ Res Public Health (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/ijerph18105417"}], "href": "https://doi.org/10.3390/ijerph18105417"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34069401"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34069401"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Xu Wang, Z Lewis Liu, Scott A Weber, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Two New Native β-Glucosidases from Clavispora NRRL Y-50464 Confer Its Dual Function as Cellobiose Fermenting Ethanologenic Yeast."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0151293"}], "href": "https://doi.org/10.1371/journal.pone.0151293"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27011316"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27011316"}]}]}]}
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| Synonyms | LINC01083, LNCRNA-BGL3, BGL3 |
| NCBI Gene ID | 103344929 |
| 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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BGLT3 has 2 functional associations with biological entities spanning 1 categories (gene, protein or microRNA) extracted from 2 datasets.
Click the + buttons to view associations for BGLT3 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| GEO Signatures of Differentially Expressed Genes for Gene Perturbations | gene perturbations changing expression of BGLT3 gene from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. | |
| GEO Signatures of Differentially Expressed Genes for Kinase Perturbations | kinase perturbations changing expression of BGLT3 gene from the GEO Signatures of Differentially Expressed Genes for Kinase Perturbations dataset. | |