LOC102724594 Gene

Name splicing factor U2AF 35 kDa subunit
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Despite the breadth of research summarized in these abstracts—which collectively illuminate key aspects of RNA processing, pre‐mRNA splicing, epigenetic regulation, and their perturbation in hematologic and other malignancies through mutations in factors such as CALR, U2AF1, SF3B1, SRSF2, and related regulators"}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "4"}]}, {"type": "t", "text": ",\n none of these studies provide any experimental evidence or detailed discussion regarding the locus designated LOC102724594. In other words, while these works collectively enhance our understanding of the mechanisms underlying splicing alterations, dysregulated mRNA processing, and chromatin‐mediated transcriptional control in cancer"}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "5", "end_ref": "8"}]}, {"type": "t", "text": ", they do not address or characterize LOC102724594."}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n As a result, the biological function of LOC102724594 remains uncharacterized in the context of these reports. Given the important roles played by well‐established splicing factors and epigenetic regulators in maintaining normal hematopoiesis or in driving malignant transformation, it is conceivable that LOC102724594 might warrant future investigation to determine whether it participates—and if so, how it might contribute—to these critical pathways. In this light, further studies expressly focused on LOC102724594 are needed to uncover its molecular role and possible implications in disease, which could ultimately extend our understanding of RNA regulatory networks in both normal biology and cancer."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "9"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n In summary, while the provided abstracts significantly advance the field of RNA splicing and epigenetic regulation in malignancies, they do not contain information that defines or elucidates the function of LOC102724594. Future targeted research will be necessary to determine whether LOC102724594 participates in similar regulatory mechanisms or represents a novel factor in these processes.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "J Nangalia, C E Massie, E J Baxter, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "N Engl J Med (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1056/NEJMoa1312542"}], "href": "https://doi.org/10.1056/NEJMoa1312542"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24325359"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24325359"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "R Coleman Lindsley, Brenton G Mar, Emanuele Mazzola, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Acute myeloid leukemia ontogeny is defined by distinct somatic mutations."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood-2014-11-610543"}], "href": "https://doi.org/10.1182/blood-2014-11-610543"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25550361"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25550361"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "John S Welch, Allegra A Petti, Christopher A Miller, et al. "}, {"type": "b", "children": [{"type": "t", "text": "TP53 and Decitabine in Acute Myeloid Leukemia and Myelodysplastic Syndromes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "N Engl J Med (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1056/NEJMoa1605949"}], "href": "https://doi.org/10.1056/NEJMoa1605949"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27959731"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27959731"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Timothy A Graubert, Dong Shen, Li Ding, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Genet (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ng.1031"}], "href": "https://doi.org/10.1038/ng.1031"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22158538"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22158538"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Kyle C Strickland, Brooke E Howitt, Sachet A Shukla, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Association and prognostic significance of BRCA1/2-mutation status with neoantigen load, number of tumor-infiltrating lymphocytes and expression of PD-1/PD-L1 in high grade serous ovarian cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncotarget (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.18632/oncotarget.7277"}], "href": "https://doi.org/10.18632/oncotarget.7277"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26871470"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26871470"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Eunhee Kim, Janine O Ilagan, Yang Liang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "SRSF2 Mutations Contribute to Myelodysplasia by Mutant-Specific Effects on Exon Recognition."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Cell (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ccell.2015.04.006"}], "href": "https://doi.org/10.1016/j.ccell.2015.04.006"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25965569"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25965569"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Raphaël Itzykson, Olivier Kosmider, Aline Renneville, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Prognostic score including gene mutations in chronic myelomonocytic leukemia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Clin Oncol (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1200/JCO.2012.47.3314"}], "href": "https://doi.org/10.1200/JCO.2012.47.3314"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23690417"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23690417"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "A Tefferi, T L Lasho, C M Finke, et al. "}, {"type": "b", "children": [{"type": "t", "text": "CALR vs JAK2 vs MPL-mutated or triple-negative myelofibrosis: clinical, cytogenetic and molecular comparisons."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Leukemia (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/leu.2014.3"}], "href": "https://doi.org/10.1038/leu.2014.3"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24402162"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24402162"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Sarah L Maguire, Andri Leonidou, Patty Wai, et al. "}, {"type": "b", "children": [{"type": "t", "text": "SF3B1 mutations constitute a novel therapeutic target in breast cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Pathol (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/path.4483"}], "href": "https://doi.org/10.1002/path.4483"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25424858"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25424858"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Yong Zhu, Xiuye Wang, Elmira Forouzmand, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Molecular Mechanisms for CFIm-Mediated Regulation of mRNA Alternative Polyadenylation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.molcel.2017.11.031"}], "href": "https://doi.org/10.1016/j.molcel.2017.11.031"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29276085"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29276085"}]}]}]}
Synonyms U2AF1L5
NCBI Gene ID 102724594
API
Download Associations
Predicted Functions View LOC102724594's ARCHS4 Predicted Functions.
Co-expressed Genes View LOC102724594's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View LOC102724594's ARCHS4 Predicted Functions.

Functional Associations

LOC102724594 has 227 functional associations with biological entities spanning 6 categories (chemical, functional term, phrase or reference, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA) extracted from 12 datasets.

Click the + buttons to view associations for LOC102724594 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 LOC102724594 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 LOC102724594 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 cellular components co-occuring with LOC102724594 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
DisGeNET Gene-Disease Associations diseases associated with LOC102724594 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
GTEx Tissue Gene Expression Profiles 2023 tissues with high or low expression of LOC102724594 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.
InterPro Predicted Protein Domain Annotations protein domains predicted for LOC102724594 protein from the InterPro Predicted Protein Domain Annotations dataset.
KEGG Pathways 2026 pathways involving LOC102724594 protein from the KEGG Pathways 2026 dataset.
PerturbAtlas Signatures of Differentially Expressed Genes for Gene Perturbations gene perturbations changing expression of LOC102724594 gene from the PerturbAtlas Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
ProteomicsDB Cell Type and Tissue Protein Expression Profiles cell types and tissues with high or low expression of LOC102724594 protein relative to other cell types and tissues from the ProteomicsDB Cell Type and Tissue Protein Expression Profiles dataset.
Rummagene Transcription Factor Associations 2026 transcription factors regulating expression of LOC102724594 gene from the Rummagene Transcription Factor Associations 2026 dataset.
Sci-Plex Drug Perturbation Signatures drug perturbations changing expression of LOC102724594 gene from the Sci-Plex Drug Perturbation Signatures dataset.
TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 tissues co-occuring with LOC102724594 protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.