ACSL3 Gene

HGNC Family	Acyl-CoA synthetase family (ACS)
Name	acyl-CoA synthetase long-chain family member 3
Description	The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in brain, and preferentially utilizes myristate, arachidonate, and eicosapentaenoate as substrates. The amino acid sequence of this isozyme is 92% identical to that of rat homolog. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Acyl‐CoA synthetase long‐chain family member 3 (ACSL3) is emerging as a pivotal metabolic enzyme that activates fatty acids by converting them to their corresponding acyl‐CoA esters, thereby regulating multiple aspects of cellular lipid homeostasis. ACSL3 localizes to the endoplasmic reticulum, lipid droplets, and even the inner nuclear membrane, where it facilitates rapid fatty acid uptake, esterification, and lipid droplet biogenesis, processes that underpin VLDL secretion in hepatocytes and support proper placental fatty acid metabolism ["}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "5"}]}, {"type": "t", "text": "]. In conditions of cellular stress, such as endoplasmic reticulum stress, ACSL3 expression is upregulated in a manner dependent on signaling pathways (for example, via GSK-3β), thereby contributing to lipid accumulation and altered metabolic fluxes ["}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": "]."}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n In the context of cancer, ACSL3 is co-opted by oncogenic signals to reprogram lipid metabolism. Mutant KRAS lung cancers, for instance, exploit ACSL3 to enhance fatty acid uptake, retention, and β‐oxidation, which sustain cellular ATP levels and promote tumorigenesis ["}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": "]. In prostate cancer, ACSL3 participates in oncogenic gene fusions with ETV1 and, when overexpressed, contributes to intratumoral steroidogenesis by upregulating steroidogenic enzymes and suppressing androgen catabolism, thereby fostering castration‐resistant growth ["}, {"type": "fg", "children": [{"type": "fg_f", "ref": "8"}]}, {"type": "t", "text": "]. In triple‐negative breast cancer, modulation of ACSL3 activity influences lipid droplet dynamics and fatty acid utilization, ultimately affecting cell migration and invasion ["}, {"type": "fg", "children": [{"type": "fg_f", "ref": "10"}]}, {"type": "t", "text": "]."}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Beyond its metabolic functions, ACSL3 also interfaces with signaling pathways. It physically interacts with proteins such as Lyn kinase in the Golgi apparatus, facilitating its export and thereby linking lipid metabolism with intracellular protein trafficking ["}, {"type": "fg", "children": [{"type": "fg_f", "ref": "11"}]}, {"type": "t", "text": "]. Moreover, epigenetic alterations of the ACSL3 gene have been associated with environmental exposures – for example, maternal polycyclic aromatic hydrocarbon exposure correlates with altered ACSL3 promoter methylation and gene expression, implicating ACSL3 as a potential biomarker in asthma risk ["}, {"type": "fg", "children": [{"type": "fg_f", "ref": "12"}]}, {"type": "t", "text": "]. In vascular smooth muscle cells, ACSL3 is also upregulated by saturated fatty acids, where its activation stimulates osteoblastic differentiation and calcification, processes that can be counteracted by fatty acids such as eicosapentaenoic acid ["}, {"type": "fg", "children": [{"type": "fg_f", "ref": "13"}]}, {"type": "t", "text": "]. Finally, inflammatory cytokines such as oncostatin M have been shown to induce ACSL3 (along with ACSL5) in hepatocytes, thereby channeling fatty acids into β‐oxidation and reducing triglyceride accumulation ["}, {"type": "fg", "children": [{"type": "fg_f", "ref": "14"}]}, {"type": "t", "text": "]. \n "}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Collectively, these findings highlight ACSL3 as a critical mediator of lipid metabolic reprogramming in both normal physiology and disease states. Its diverse roles in fatty acid activation, lipid droplet formation, protein trafficking, and integration of metabolic signals underscore its potential as a biomarker and therapeutic target in metabolic disorders, cancer, and inflammatory conditions.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Margarete Poppelreuther, Berenice Rudolph, Chen Du, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The N-terminal region of acyl-CoA synthetase 3 is essential for both the localization on lipid droplets and the function in fatty acid uptake."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Lipid Res (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1194/jlr.M024562"}], "href": "https://doi.org/10.1194/jlr.M024562"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22357706"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22357706"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "So Young Bu, Mara T Mashek, Douglas G Mashek "}, {"type": "b", "children": [{"type": "t", "text": "Suppression of long chain acyl-CoA synthetase 3 decreases hepatic de novo fatty acid synthesis through decreased transcriptional activity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M109.036665"}], "href": "https://doi.org/10.1074/jbc.M109.036665"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19737935"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19737935"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Kamil Sołtysik, Yuki Ohsaki, Tsuyako Tatematsu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Nuclear lipid droplets form in the inner nuclear membrane in a seipin-independent manner."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biol (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1083/jcb.202005026"}], "href": "https://doi.org/10.1083/jcb.202005026"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33315072"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33315072"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Hongbing Yao, Jin Ye "}, {"type": "b", "children": [{"type": "t", "text": "Long chain acyl-CoA synthetase 3-mediated phosphatidylcholine synthesis is required for assembly of very low density lipoproteins in human hepatoma Huh7 cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M706160200"}], "href": "https://doi.org/10.1074/jbc.M706160200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18003621"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18003621"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "M Susanne Weedon-Fekjaer, Knut Tomas Dalen, Karianne Solaas, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Activation of LXR increases acyl-CoA synthetase activity through direct regulation of ACSL3 in human placental trophoblast cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Lipid Res (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1194/jlr.M004978"}], "href": "https://doi.org/10.1194/jlr.M004978"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20219900"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20219900"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Yung-Sheng Chang, Chien-Ting Tsai, Chien-An Huangfu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "ACSL3 and GSK-3β are essential for lipid upregulation induced by endoplasmic reticulum stress in liver cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biochem (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcb.22996"}], "href": "https://doi.org/10.1002/jcb.22996"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21328461"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21328461"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Mahesh S Padanad, Georgia Konstantinidou, Niranjan Venkateswaran, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Fatty Acid Oxidation Mediated by Acyl-CoA Synthetase Long Chain 3 Is Required for Mutant KRAS Lung Tumorigenesis."}]}, {"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.2016.07.009"}], "href": "https://doi.org/10.1016/j.celrep.2016.07.009"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27477280"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27477280"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "G Attard, J Clark, L Ambroisine, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Heterogeneity and clinical significance of ETV1 translocations in human prostate cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Br J Cancer (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.bjc.6604472"}], "href": "https://doi.org/10.1038/sj.bjc.6604472"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18594527"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18594527"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Toshiro Migita, Ken-Ichi Takayama, Tomohiko Urano, et al. "}, {"type": "b", "children": [{"type": "t", "text": "ACSL3 promotes intratumoral steroidogenesis in prostate cancer cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Sci (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/cas.13339"}], "href": "https://doi.org/10.1111/cas.13339"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28771887"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28771887"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Heather J Wright, Jue Hou, Binzhi Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "CDCP1 drives triple-negative breast cancer metastasis through reduction of lipid-droplet abundance and stimulation of fatty acid oxidation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.1703791114"}], "href": "https://doi.org/10.1073/pnas.1703791114"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28739932"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28739932"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Yuuki Obata, Yasunori Fukumoto, Yuji Nakayama, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The Lyn kinase C-lobe mediates Golgi export of Lyn through conformation-dependent ACSL3 association."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Sci (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1242/jcs.066266"}], "href": "https://doi.org/10.1242/jcs.066266"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20605918"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20605918"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Frederica Perera, Wan-yee Tang, Julie Herbstman, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Relation of DNA methylation of 5'-CpG island of ACSL3 to transplacental exposure to airborne polycyclic aromatic hydrocarbons and childhood asthma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0004488"}], "href": "https://doi.org/10.1371/journal.pone.0004488"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19221603"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19221603"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Aiko Kageyama, Hiroki Matsui, Masahiko Ohta, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Palmitic acid induces osteoblastic differentiation in vascular smooth muscle cells through ACSL3 and NF-κB, novel targets of eicosapentaenoic acid."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0068197"}], "href": "https://doi.org/10.1371/journal.pone.0068197"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23840832"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23840832"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Yue Zhou, Parveen Abidi, Aekyong Kim, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Transcriptional activation of hepatic ACSL3 and ACSL5 by oncostatin m reduces hypertriglyceridemia through enhanced beta-oxidation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Arterioscler Thromb Vasc Biol (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1161/ATVBAHA.107.148429"}], "href": "https://doi.org/10.1161/ATVBAHA.107.148429"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17761945"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17761945"}]}]}]}
Synonyms	LACS3, FACL3, LACS 3, PRO2194, ACS3
Proteins	ACSL3_HUMAN
NCBI Gene ID	2181
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

ACSL3 has 9,281 functional associations with biological entities spanning 9 categories (molecular profile, organism, chemical, functional term, phrase or reference, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 119 datasets.

Click the + buttons to view associations for ACSL3 from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

ACSL3 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 ACSL3 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 ACSL3 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 ACSL3 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 ACSL3 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 ACSL3 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 ACSL3 gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
	BioGPS Cell Line Gene Expression Profiles	cell lines with high or low expression of ACSL3 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 ACSL3 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 ACSL3 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 ACSL3 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with ACSL3 protein from the CCLE Cell Line Proteomics dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with ACSL3 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 ACSL3 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of ACSL3 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 ACSL3 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 ACSL3 gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing ACSL3 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing ACSL3 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores	cellular components co-occuring with ACSL3 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 ACSL3 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with ACSL3 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Chemical Interactions	chemicals interacting with ACSL3 gene/protein from the curated CTD Gene-Chemical Interactions dataset.
	CTD Gene-Disease Associations	diseases associated with ACSL3 gene/protein from the curated CTD Gene-Disease Associations dataset.
	dbGAP Gene-Trait Associations	traits associated with ACSL3 gene in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
	DeepCoverMOA Drug Mechanisms of Action	small molecule perturbations with high or low expression of ACSL3 protein relative to other small molecule perturbations from the DeepCoverMOA Drug Mechanisms of Action dataset.
	DepMap CRISPR Gene Dependency	cell lines with fitness changed by ACSL3 gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores	diseases co-occuring with ACSL3 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 ACSL3 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 ACSL3 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with ACSL3 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Phenoptype Associations dataset.
	DrugBank Drug Targets	interacting drugs for ACSL3 protein from the curated DrugBank Drug Targets dataset.
	ENCODE Histone Modification Site Profiles	histone modification site profiles with high histone modification abundance at ACSL3 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 ACSL3 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
	ENCODE Transcription Factor Targets	transcription factors binding the promoter of ACSL3 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 ACSL3 from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.
	GAD Gene-Disease Associations	diseases associated with ACSL3 gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
	GDSC Cell Line Gene Expression Profiles	cell lines with high or low expression of ACSL3 gene relative to other cell lines from the GDSC Cell Line Gene Expression Profiles dataset.
	GeneRIF Biological Term Annotations	biological terms co-occuring with ACSL3 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
	GeneSigDB Published Gene Signatures	PubMedIDs of publications reporting gene signatures containing ACSL3 from the GeneSigDB Published Gene Signatures dataset.
	GEO Signatures of Differentially Expressed Genes for Diseases	disease perturbations changing expression of ACSL3 gene from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.