| HGNC Family | Non-coding RNAs |
| Name | RNA, U1 small nuclear 2 |
| Description | Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nA review of the provided literature reveals a wide spectrum of cellular and molecular functions that underlie processes as diverse as osteoclast differentiation, fibrogenesis, synaptic plasticity, immune cell activation, and tumor metastasis. Notably, these studies focus on protein‐coding regulators such as c‐Fos, galectin‑3, IL‑17 receptor components, and transcription factors like Onecut and Fra‑2, which govern critical signaling cascades in bone homeostasis, inflammation, neural activity, and organ remodeling."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "9"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn contrast, there is no discussion or experimental evidence in any of these studies that directly addresses the function of RNU1-2. In general, RNU1-2 is known to encode a small nuclear RNA (snRNA) that is typically a component of the spliceosome complex, contributing to pre-mRNA processing. However, none of the abstracts examined here mention or investigate splicing factors or snRNA-mediated regulation. Instead, the reports concentrate on the dynamics of transcriptional regulation, cytokine signalling, and cell‐to‐cell interactions in various disease and developmental models."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "10", "end_ref": "19"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional studies in the set extend these themes to include regulation of inflammatory responses in the central nervous system, mechanisms of immune regulation during autoimmune or infectious challenges, and contributions to tumorigenesis and metastasis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "20", "end_ref": "27"}]}, {"type": "t", "text": " Furthermore, other reports elaborate on the roles of transcription factors and adaptor proteins in synaptic plasticity and memory formation as well as in integrin- and cytokine-mediated cell adhesion readouts."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "28", "end_ref": "32"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nCollectively, while the aggregated research underscores multifaceted mechanisms that regulate cell fate, inflammatory signalling, and tissue remodeling across diverse physiological and pathological contexts, it does not provide any insights into the function of RNU1‑2. In consequence, based on the reviewed literature the role of RNU1‑2 remains unaddressed in these studies and may be inferred only from its canonical activity—as a fundamental component of the spliceosomal machinery—in processes not examined in these reports."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "22"}, {"type": "fg_f", "ref": "33"}, {"type": "fg_f", "ref": "27"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFinally, additional studies that explore transcriptional regulators in differentiation and immune responses further reiterate that while many noncoding and coding factors contribute to the regulation of gene expression in varied contexts, the specific contributions of RNU1‑2 were not a subject of investigation in any of the provided abstracts."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "29"}, {"type": "fg_f", "ref": "22"}, {"type": "fg_f", "ref": "27"}, {"type": "fg_f", "ref": "27"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Jianhua Zhang, Dongsheng Zhang, Jill Slane McQuade, et al. 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| Synonyms | RNU1C1, U1C1, RNU1C2, U1C21 |
| NCBI Gene ID | 26870 |
| 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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RNU1-2 has 97 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 4 datasets.
Click the + buttons to view associations for RNU1-2 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| ChEA Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of RNU1-2 gene from the CHEA Transcription Factor Binding Site Profiles dataset. | |
| ChEA Transcription Factor Targets | transcription factors binding the promoter of RNU1-2 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset. | |
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of RNU1-2 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of RNU1-2 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |