| Name | integrator complex subunit 15 |
| Description | Part of integrator complex. Is active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n INTS15 is a subunit of the Integrator complex that appears to contribute to the regulation of RNA processing at multiple levels. Although none of the provided abstracts discuss INTS15 explicitly, insights can be inferred from studies on splicing regulation and the cellular response to transcription‐associated stress. Two of the studies describe systematic efforts to identify splicing regulatory elements and their interacting proteins, highlighting the complex interplay between cis‑elements and trans‑acting factors that govern splice site selection in human pre‑mRNAs (see"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "and."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " In this context, several factors that associate with regulatory elements may function in coordination with larger RNA processing complexes. In a complementary proteomic and functional genomics screen, another study identified a role for the Integrator complex in the transcription‐related DNA damage response, implicating it as a contributor to the maintenance of genomic integrity under stress (see."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " \n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Taken together, although the abstracts do not address INTS15 directly, by virtue of being an Integrator subunit, INTS15 is likely involved in modulating co‑transcriptional RNA processing events—including aspects of alternative splicing—and in linking these processes to the cellular response to DNA damage. These roles position INTS15 as a potential regulator ensuring both accurate splice site selection and the integration of transcriptional regulation with genome stability mechanisms.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Yang Wang, Meng Ma, Xinshu Xiao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Intronic splicing enhancers, cognate splicing factors and context-dependent regulation rules."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Struct Mol Biol (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nsmb.2377"}], "href": "https://doi.org/10.1038/nsmb.2377"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22983564"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22983564"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Yang Wang, Zefeng Wang "}, {"type": "b", "children": [{"type": "t", "text": "Systematical identification of splicing regulatory cis-elements and cognate trans-factors."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Methods (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ymeth.2013.08.019"}], "href": "https://doi.org/10.1016/j.ymeth.2013.08.019"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23974071"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23974071"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Stefan Boeing, Laura Williamson, Vesela Encheva, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Multiomic Analysis of the UV-Induced DNA Damage Response."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Rep (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.celrep.2016.04.047"}], "href": "https://doi.org/10.1016/j.celrep.2016.04.047"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27184836"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27184836"}]}]}]}
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| NCBI Gene ID | 79034 |
| 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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INTS15 has 1,219 functional associations with biological entities spanning 6 categories (chemical, functional term, phrase or reference, disease, phenotype or trait, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 17 datasets.
Click the + buttons to view associations for INTS15 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles | tissue samples with high or low expression of INTS15 gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset. | |
| Carcinogenome Chemical Perturbation Carcinogenicity Signatures | small molecule perturbations changing expression of INTS15 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset. | |
| CM4AI KOLF21J CRISPRi Gene Perturbation Atlas | gene perturbations changing expression of INTS15 gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset. | |
| GO Cellular Component Annotations 2025 | cellular components containing INTS15 protein from the curated GO Cellular Component Annotations 2025 dataset. | |
| GTEx eQTL 2025 | SNPs regulating expression of INTS15 gene from the GTEx eQTL 2025 dataset. | |
| GTEx Tissue Gene Expression Profiles 2023 | tissues with high or low expression of INTS15 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset. | |
| GTEx Tissue-Specific Aging Signatures | tissue samples with high or low expression of INTS15 gene relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. | |
| GWAS Catalog SNP-Phenotype Associations 2025 | phenotypes associated with INTS15 gene in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. | |
| JASPAR Predicted Human Transcription Factor Targets 2025 | transcription factors regulating expression of INTS15 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Human Transcription Factor Targets dataset. | |
| JASPAR Predicted Mouse Transcription Factor Targets 2025 | transcription factors regulating expression of INTS15 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2025 dataset. | |
| LINCS L1000 CMAP Chemical Perturbation Consensus Signatures | small molecule perturbations changing expression of INTS15 gene from the LINCS L1000 CMAP Chemical Perturbations Consensus Signatures dataset. | |
| Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures | gene perturbations changing expression of INTS15 gene from the Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures dataset. | |
| Replogle et al., Cell, 2022 K562 Genome-wide Perturb-seq Gene Perturbation Signatures | gene perturbations changing expression of INTS15 gene from the Replogle et al., Cell, 2022 K562 Genome-wide Perturb-seq Gene Perturbation Signatures dataset. | |
| Rummagene Transcription Factor Associations 2026 | transcription factors regulating expression of INTS15 gene from the Rummagene Transcription Factor Associations 2026 dataset. | |
| RummaGEO Drug Perturbation Signatures | drug perturbations changing expression of INTS15 gene from the RummaGEO Drug Perturbation Signatures dataset. | |
| RummaGEO Gene Perturbation Signatures | gene perturbations changing expression of INTS15 gene from the RummaGEO Gene Perturbation Signatures dataset. | |
| Sci-Plex Drug Perturbation Signatures | drug perturbations changing expression of INTS15 gene from the Sci-Plex Drug Perturbation Signatures dataset. | |