UTRN Gene

Name	utrophin
Description	This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described; however, the full-length nature of these variants has not yet been determined. [provided by RefSeq, Jul 2008]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nUtrophin is a large cytoskeletal protein that serves as an autosomal homolog of dystrophin, playing a critical role in linking the extracellular matrix to the intracellular actin cytoskeleton. In skeletal muscle, utrophin is normally expressed at neuromuscular junctions and in regenerating fibers, where its up‐regulation can partially compensate for the loss of dystrophin in Duchenne muscular dystrophy. Moreover, immunohistochemical and biochemical analyses have revealed that utrophin’s distribution and expression levels correlate with disease severity, while structural studies of its actin‐binding domains demonstrate that its functional integrity depends on the stability provided by its tandem calponin-homology domains."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "7"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAt the transcriptional level, multiple regulatory mechanisms modulate utrophin expression. Studies in cultured cells have demonstrated that transcription factors such as Sp1 can activate the utrophin promoter, whereas other factors—like the Ets-2 repressor factor and the homeobox protein EN1—negatively regulate utrophin transcription. These insights underline the potential for targeted therapeutic strategies aimed at enhancing utrophin expression to alleviate muscle pathology in dystrophinopathies."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "8", "end_ref": "11"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its well‐established role in skeletal muscle, utrophin is expressed in multiple tissues including the central nervous system, vascular endothelium, and even in the context of certain cancers. In the brain and other tissues, it contributes to the assembly and stabilization of the dystrophin–glycoprotein complex, which is essential not only for maintaining cellular architecture but also for proper signaling functions. Aberrant expression and altered processing of utrophin (including the generation of truncated forms) have been observed in plasma samples of cancer patients and in glioma cells, suggesting that utrophin may serve as both a biomarker and a functional player in non-muscle pathologies. Additionally, utrophin’s association with cellular membranes in immune cells further highlights its multifaceted role in human physiology."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "12", "end_ref": "18"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Federico Galvagni, Marcello Cantini, Salvatore Oliviero "}, {"type": "b", "children": [{"type": "t", "text": "The utrophin gene is transcriptionally up-regulated in regenerating muscle."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M109642200"}], "href": "https://doi.org/10.1074/jbc.M109642200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "11875058"}], "href": "https://pubmed.ncbi.nlm.nih.gov/11875058"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Kelly J Perkins, Kay E Davies "}, {"type": "b", "children": [{"type": "t", "text": "Ets, Ap-1 and GATA factor families regulate the utrophin B promoter: potential regulatory mechanisms for endothelial-specific expression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS Lett (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/s0014-5793(03)00175-3"}], "href": "https://doi.org/10.1016/s0014-5793(03"}, {"type": "t", "text": "00175-3) PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12633873"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12633873"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "C A Sewry, K J Nowak, J T Ehmsen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A and B utrophin in human muscle and sarcolemmal A-utrophin associated with tumours."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neuromuscul Disord (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.nmd.2005.08.002"}], "href": "https://doi.org/10.1016/j.nmd.2005.08.002"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16198105"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16198105"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Kleopas A Kleopa, Anthi Drousiotou, Eleni Mavrikiou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Mol Genet (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/hmg/ddl083"}], "href": "https://doi.org/10.1093/hmg/ddl083"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16595608"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16595608"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Isabelle Courdier-Fruh, Alexandre Briguet "}, {"type": "b", "children": [{"type": "t", "text": "Utrophin is a calpain substrate in muscle cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Muscle Nerve (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/mus.20549"}], "href": "https://doi.org/10.1002/mus.20549"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16598790"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16598790"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Annalisa Onori, Cinzia Pisani, Georgios Strimpakos, et al. "}, {"type": "b", "children": [{"type": "t", "text": "UtroUp is a novel six zinc finger artificial transcription factor that recognises 18 base pairs of the utrophin promoter and efficiently drives utrophin upregulation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "BMC Mol Biol (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/1471-2199-14-3"}], "href": "https://doi.org/10.1186/1471-2199-14-3"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23363418"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23363418"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Surinder M Singh, Swati Bandi, Krishna M G Mallela "}, {"type": "b", "children": [{"type": "t", "text": "The N- and C-Terminal Domains Differentially Contribute to the Structure and Function of Dystrophin and Utrophin Tandem Calponin-Homology Domains."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochemistry (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1021/acs.biochem.5b00969"}], "href": "https://doi.org/10.1021/acs.biochem.5b00969"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26516677"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26516677"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Mads Gyrd-Hansen, Thomas O B Krag, Alan G Rosmarin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Sp1 and the ets-related transcription factor complex GABP alpha/beta functionally cooperate to activate the utrophin promoter."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurol Sci (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/s0022-510x(02)00038-2"}], "href": "https://doi.org/10.1016/s0022-510x(02"}, {"type": "t", "text": "00038-2) PMID: "}, {"type": "a", "children": [{"type": "t", "text": "11997063"}], "href": "https://pubmed.ncbi.nlm.nih.gov/11997063"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Kelly J Perkins, Utpal Basu, Murat T Budak, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Ets-2 repressor factor silences extrasynaptic utrophin by N-box mediated repression in skeletal muscle."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Cell (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1091/mbc.e06-12-1069"}], "href": "https://doi.org/10.1091/mbc.e06-12-1069"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17507653"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17507653"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Qian Wang, Dong-Hua Cao, Chang-Kun Lin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "[The regulation of UTROPHIN expression by EN1]."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Yi Chuan (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3724/sp.j.1005.2011.00347"}], "href": "https://doi.org/10.3724/sp.j.1005.2011.00347"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21482524"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21482524"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Q Wang, D-H Cao, C-L Jin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A method of utrophin up-regulation through RNAi-mediated knockdown of the transcription factor EN1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Int Med Res (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1177/147323001103900117"}], "href": "https://doi.org/10.1177/147323001103900117"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21672318"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21672318"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Marta Lomnytska, Anna Dubrovska, Ulf Hellman, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Increased expression of cSHMT, Tbx3 and utrophin in plasma of ovarian and breast cancer patients."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Cancer (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/ijc.21332"}], "href": "https://doi.org/10.1002/ijc.21332"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16049973"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16049973"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "T Haenggi, J-M Fritschy "}, {"type": "b", "children": [{"type": "t", "text": "Role of dystrophin and utrophin for assembly and function of the dystrophin glycoprotein complex in non-muscle tissue."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Mol Life Sci (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s00018-005-5461-0"}], "href": "https://doi.org/10.1007/s00018-005-5461-0"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16710609"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16710609"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Kazunari Yamashita, Atsushi Suzuki, Yoshinori Satoh, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The 8th and 9th tandem spectrin-like repeats of utrophin cooperatively form a functional unit to interact with polarity-regulating kinase PAR-1b."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2009.11.144"}], "href": "https://doi.org/10.1016/j.bbrc.2009.11.144"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19945424"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19945424"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Doris Cerecedo, Bulmaro Cisneros, Pablo Gómez, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Distribution of dystrophin- and utrophin-associated protein complexes during activation of human neutrophils."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Exp Hematol (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.exphem.2010.04.010"}], "href": "https://doi.org/10.1016/j.exphem.2010.04.010"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20434517"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20434517"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Caroline Perronnet, Cyrille Vaillend "}, {"type": "b", "children": [{"type": "t", "text": "Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biomed Biotechnol (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1155/2010/849426"}], "href": "https://doi.org/10.1155/2010/849426"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20625423"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20625423"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Israel Ramírez-Sánchez, Patricia Mendoza-Lorenzo, Alejandro Zentella-Dehesa, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Caveolae and non-caveolae lipid raft microdomains of human umbilical vein endothelial cells contain utrophin-associated protein complexes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochimie (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biochi.2012.05.001"}], "href": "https://doi.org/10.1016/j.biochi.2012.05.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22609462"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22609462"}]}, {"type": "r", "ref": 18, "children": [{"type": "t", "text": "Shang-Hang Shen, Ning Yu, Hao Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Inhibition of Human Glioma Cell Proliferation Caused by Knockdown of Utrophin Using a Lentivirus-Mediated System."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Biother Radiopharm (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1089/cbr.2015.1939"}], "href": "https://doi.org/10.1089/cbr.2015.1939"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27183436"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27183436"}]}]}]}
Synonyms	DMDL, DRP
Proteins	UTRO_HUMAN
NCBI Gene ID	7402
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

UTRN has 7,361 functional associations with biological entities spanning 9 categories (molecular profile, organism, functional term, phrase or reference, chemical, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 124 datasets.

Click the + buttons to view associations for UTRN from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

UTRN Gene

Functional Associations

Please acknowledge the Harmonizome in your publications by citing the following reference(s):

	Dataset	Summary
	Achilles Cell Line Gene Essentiality Profiles	cell lines with fitness changed by UTRN gene knockdown relative to other cell lines from the Achilles Cell Line Gene Essentiality Profiles dataset.
	Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of UTRN gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles	tissues with high or low expression of UTRN gene relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray	tissue samples with high or low expression of UTRN gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
	Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq	tissue samples with high or low expression of UTRN gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
	Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of UTRN gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
	Biocarta Pathways	pathways involving UTRN protein from the Biocarta Pathways dataset.
	BioGPS Cell Line Gene Expression Profiles	cell lines with high or low expression of UTRN gene relative to other cell lines from the BioGPS Cell Line Gene Expression Profiles dataset.
	BioGPS Human Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of UTRN gene relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of UTRN 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 UTRN gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with UTRN protein from the CCLE Cell Line Proteomics dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with UTRN gene from the CellMarker Gene-Cell Type Associations dataset.
	ChEA Transcription Factor Binding Site Profiles	transcription factor binding site profiles with transcription factor binding evidence at the promoter of UTRN gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of UTRN gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset.
	ChEA Transcription Factor Targets 2022	transcription factors binding the promoter of UTRN gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
	CMAP Signatures of Differentially Expressed Genes for Small Molecules	small molecule perturbations changing expression of UTRN gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing UTRN protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing UTRN protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores	cellular components containing UTRN protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores 2025	cellular components containing UTRN protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores	cellular components co-occuring with UTRN protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025	cellular components co-occuring with UTRN protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	CORUM Protein Complexes	protein complexs containing UTRN protein from the CORUM Protein Complexes dataset.
	COSMIC Cell Line Gene CNV Profiles	cell lines with high or low copy number of UTRN gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with UTRN gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Chemical Interactions	chemicals interacting with UTRN gene/protein from the curated CTD Gene-Chemical Interactions dataset.
	CTD Gene-Disease Associations	diseases associated with UTRN gene/protein from the curated CTD Gene-Disease Associations dataset.
	dbGAP Gene-Trait Associations	traits associated with UTRN gene in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
	DepMap CRISPR Gene Dependency	cell lines with fitness changed by UTRN gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores 2025	diseases associated with UTRN gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores	diseases co-occuring with UTRN gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores 2025	diseases co-occuring with UTRN gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
	DisGeNET Gene-Disease Associations	diseases associated with UTRN gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with UTRN gene in GWAS and other genetic association datasets from the DisGeNET Gene-Phenoptype Associations dataset.
	ENCODE Histone Modification Site Profiles	histone modification site profiles with high histone modification abundance at UTRN 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 UTRN gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
	ENCODE Transcription Factor Targets	transcription factors binding the promoter of UTRN gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
	ESCAPE Omics Signatures of Genes and Proteins for Stem Cells	PubMedIDs of publications reporting gene signatures containing UTRN from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.
	GAD Gene-Disease Associations	diseases associated with UTRN gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.