DIP2A Gene

Name	DIP2 disco-interacting protein 2 homolog A (Drosophila)
Description	The protein encoded by this gene may be involved in axon patterning in the central nervous system. This gene is not highly expressed. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n DIP2A is a multifunctional protein whose roles span several organ systems and cellular processes. In the nervous system, DIP2A is essential for proper dendritic spine morphogenesis and synaptic transmission by maintaining the acetylation status of key remodeling proteins such as cortactin; loss of DIP2A function leads to defects in spine structure and has been linked to autism‐like behaviors, as well as to genetic susceptibility for developmental dyslexia."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "4"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n In the cardiovascular system, DIP2A functions as a cell‐surface receptor for Follistatin‑like protein 1 (FSTL1), mediating its protective, pro‐angiogenic, and anti‐inflammatory effects through activation of signaling pathways including Akt and Smad2/3. In addition, DIP2A contributes to the regulation of histone acetylation, thereby controlling the transcription of target genes such as MGMT, which influences temozolomide sensitivity in glioblastoma and modulates tumor immunoresistance."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "5", "end_ref": "9"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Beyond serving as a receptor, DIP2A exhibits enzymatic activity related to acetyl‐coenzyme A synthesis at the mitochondria, thereby contributing to cellular metabolic regulation and antioxidative protection. Alterations in DIP2A dosage—whether by pathogenic copy number variations or through targeted mutations—have been associated with systemic developmental abnormalities, impacting not only neural differentiation and maturation"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "10"}]}, {"type": "t", "text": "but also body composition and gut microbiota homeostasis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "12", "end_ref": "14"}]}, {"type": "t", "text": " Furthermore, DIP2A is one of several genes affected by chromosomal rearrangements such as ring chromosomes or microduplications, underscoring the importance of proper genetic dosage for normal development."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "15", "end_ref": "17"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Collectively, these studies highlight DIP2A as a pivotal mediator that links extracellular cues—including those from FSTL1—to intracellular signaling, metabolic regulation, and transcriptional control. Its diverse functions in neurodevelopment, cardiovascular protection, oncologic responsiveness, and metabolic homeostasis underscore its significance in both normal physiology and disease pathogenesis.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Jun Ma, Lu-Qing Zhang, Zi-Xuan He, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Autism candidate gene DIP2A regulates spine morphogenesis via acetylation of cortactin."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS Biol (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pbio.3000461"}], "href": "https://doi.org/10.1371/journal.pbio.3000461"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31600191"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31600191"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Rui Kong, Shanshan Shao, Jia Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Med Genet B Neuropsychiatr Genet (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/ajmg.b.32392"}], "href": "https://doi.org/10.1002/ajmg.b.32392"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26452339"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26452339"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Hans Matsson, Mikael Huss, Helena Persson, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Polymorphisms in DCDC2 and S100B associate with developmental dyslexia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Hum Genet (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/jhg.2015.37"}], "href": "https://doi.org/10.1038/jhg.2015.37"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25877001"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25877001"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Gerald Egger, Katharina M Roetzer, Abdul Noor, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neurogenetics (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s10048-014-0394-0"}], "href": "https://doi.org/10.1007/s10048-014-0394-0"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24643514"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24643514"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Noriyuki Ouchi, Yasuhide Asaumi, Koji Ohashi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "DIP2A functions as a FSTL1 receptor."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M109.069468"}], "href": "https://doi.org/10.1074/jbc.M109.069468"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20054002"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20054002"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Masao Tanaka, Kosaku Murakami, Shoichi Ozaki, et al. "}, {"type": "b", "children": [{"type": "t", "text": "DIP2 disco-interacting protein 2 homolog A (Drosophila) is a candidate receptor for follistatin-related protein/follistatin-like 1--analysis of their binding with TGF-β superfamily proteins."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS J (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/j.1742-4658.2010.07816.x"}], "href": "https://doi.org/10.1111/j.1742-4658.2010.07816.x"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20860622"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20860622"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Er Nie, Faan Miao, Xin Jin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Fstl1/DIP2A/MGMT signaling pathway plays important roles in temozolomide resistance in glioblastoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncogene (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41388-018-0596-2"}], "href": "https://doi.org/10.1038/s41388-018-0596-2"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30542120"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30542120"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Chie Kudo-Saito, Akiko Ishida, Yuji Shouya, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Blocking the FSTL1-DIP2A Axis Improves Anti-tumor Immunity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Rep (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.celrep.2018.07.043"}], "href": "https://doi.org/10.1016/j.celrep.2018.07.043"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30110636"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30110636"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Yue Xi, Meili Hao, Qiaoqin Liang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Dynamic resistance exercise increases skeletal muscle-derived FSTL1 inducing cardiac angiogenesis via DIP2A-Smad2/3 in rats following myocardial infarction."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Sport Health Sci (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.jshs.2020.11.010"}], "href": "https://doi.org/10.1016/j.jshs.2020.11.010"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33246164"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33246164"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Rajiv Kumar Sah, Analn Yang, Fatoumata Binta Bah, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Transcriptome profiling of mouse brain and lung under Dip2a regulation using RNA-sequencing."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0213702"}], "href": "https://doi.org/10.1371/journal.pone.0213702"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31291246"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31291246"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Mingze Yao, Qian Yang, Mengqiao Lian, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Generation of Dip2a homozygous knockout murine ES cell line IBMSe001-A-1 via CRISPR/Cas9 technology."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Stem Cell Res (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.scr.2020.101778"}], "href": "https://doi.org/10.1016/j.scr.2020.101778"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32361465"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32361465"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Priyadarshan Kinatukara, Purnima Sailasree Subramaniyan, Gajanan S Patil, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Peri-natal growth retardation rate and fat mass accumulation in mice lacking Dip2A is dependent on the dietary composition."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Transgenic Res (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s11248-020-00219-6"}], "href": "https://doi.org/10.1007/s11248-020-00219-6"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33184751"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33184751"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Lu-Lu Bai, Lu-Qing Zhang, Jun Ma, et al. "}, {"type": "b", "children": [{"type": "t", "text": "DIP2A is involved in SOD-mediated antioxidative reactions in murine brain."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Free Radic Biol Med (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.freeradbiomed.2021.03.027"}], "href": "https://doi.org/10.1016/j.freeradbiomed.2021.03.027"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33781892"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33781892"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Yuling Zhang, Yanan Qu, Jingyuan Yang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A pilot study to investigate the alteration of gut microbial profile in Dip2a knockout mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int Microbiol (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s10123-021-00211-y"}], "href": "https://doi.org/10.1007/s10123-021-00211-y"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34562157"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34562157"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Taiwan J Obstet Gynecol (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.tjog.2020.11.024"}], "href": "https://doi.org/10.1016/j.tjog.2020.11.024"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33494993"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33494993"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Taiwan J Obstet Gynecol (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.tjog.2019.09.024"}], "href": "https://doi.org/10.1016/j.tjog.2019.09.024"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31759545"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31759545"}]}]}]}
Synonyms	C21ORF106
Proteins	DIP2A_HUMAN
NCBI Gene ID	23181
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

DIP2A has 6,051 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 114 datasets.

Click the + buttons to view associations for DIP2A from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

DIP2A 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 DIP2A 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 DIP2A 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 DIP2A gene relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles	tissue samples with high or low expression of DIP2A gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset.
	Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray	tissue samples with high or low expression of DIP2A 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 DIP2A 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 DIP2A 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 DIP2A 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 DIP2A gene relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.
	BioGPS Mouse Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of DIP2A gene relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.
	Carcinogenome Chemical Perturbation Carcinogenicity Signatures	small molecule perturbations changing expression of DIP2A gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of DIP2A 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 DIP2A gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with DIP2A protein from the CCLE Cell Line Proteomics dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with DIP2A 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 DIP2A gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of DIP2A 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 DIP2A gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
	CM4AI KOLF21J CRISPRi Gene Perturbation Atlas	gene perturbations changing expression of DIP2A gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset.
	CMAP Signatures of Differentially Expressed Genes for Small Molecules	small molecule perturbations changing expression of DIP2A gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing DIP2A protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing DIP2A protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025	cellular components co-occuring with DIP2A protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	COSMIC Cell Line Gene CNV Profiles	cell lines with high or low copy number of DIP2A gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with DIP2A gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Disease Associations	diseases associated with DIP2A gene/protein from the curated CTD Gene-Disease Associations dataset.
	dbGAP Gene-Trait Associations	traits associated with DIP2A 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 DIP2A 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 DIP2A 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 DIP2A 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 DIP2A 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 DIP2A gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with DIP2A 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 DIP2A 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 DIP2A gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
	ENCODE Transcription Factor Targets	transcription factors binding the promoter of DIP2A 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 DIP2A from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.
	GAD Gene-Disease Associations	diseases associated with DIP2A 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 DIP2A gene relative to other cell lines from the GDSC Cell Line Gene Expression Profiles dataset.
	GeneRIF Biological Term Annotations	biological terms co-occuring with DIP2A gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.