NUP93 Gene

Name	nucleoporin 93kDa
Description	The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. This gene encodes a nucleoporin protein that localizes both to the basket of the pore and to the nuclear entry of the central gated channel of the pore. The encoded protein is a target of caspase cysteine proteases that play a central role in programmed cell death by apoptosis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nNUP93 is a core structural component of the nuclear pore complex (NPC) that is essential for mediating bidirectional nucleocytoplasmic transport. Its conserved N‐terminal domain anchors the central transport channel, ensuring the proper assembly and barrier function of the NPC. Under apoptotic conditions, only select NPC constituents such as NUP93 are cleaved by caspases, which disrupts critical interactions for active transport without disassembling the overall scaffold. In addition, viral proteins (e.g., SARS coronavirus nsp1) target NUP93 to disrupt its localization, thereby perturbing the nuclear–cytoplasmic distribution of key factors. Loss of NUP93 in endothelial cells further demonstrates its importance; reduced levels compromise NPC transport, lead to the nuclear accumulation of transcriptional regulators like Yap, and trigger cellular senescence."}, {"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": "\nBeyond its structural role, genetic alterations in NUP93 are increasingly implicated in congenital human diseases. Mutations in NUP93 disrupt NPC assembly and cause aberrant signaling through pathways such as BMP7–SMAD, which contributes to steroid‐resistant nephrotic syndrome (SRNS) by impairing glomerular podocyte function. Moreover, pathogenic variants in NUP93 have been identified in patients with congenital ataxia, highlighting its central importance in nervous system development. In studies of embryonic development, knockdown of NUP93 (or its binding partner) results in defective ciliogenesis, thereby underscoring its role in proper heart formation and left–right patterning. These observations collectively emphasize that defects in NUP93 can lead to early‐onset renal, neurological, and cardiac malformations."}, {"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": "\nDysregulation of NUP93 also plays a multifaceted role in oncogenesis across a variety of cancers. In triple‐negative breast cancer, NUP93 modulates chromatin interactions that govern the expression of genes linked to actin cytoskeleton remodeling and epithelial–mesenchymal transition, thereby influencing invasive properties. Similarly, in aggressive mammary tumors, NUP93 overexpression enhances the nuclear import of key effectors such as β‐catenin and MYC and cooperates with multiple signaling pathways, including TGF‐β/SMAD and EGF/ERK, to promote tumor growth and metastasis. In cervical cancer, elevated NUP93 contributes to cell proliferation, migration, and invasion through regulation of the IL‐6/STAT3 pathway and cytoskeletal dynamics. Comparable pro‐tumorigenic functions have been observed in hepatocellular carcinoma (via β‐catenin translocation), esophageal squamous cell carcinoma (by driving AKT signaling and PD‐L1 expression), and bladder cancer, where interactions with transcription factors like YY1 further exacerbate malignancy. Collectively, these findings establish NUP93 as a context‐dependent regulator of oncogenic signaling and a promising therapeutic target."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "10", "end_ref": "15"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Monika Patre, Anja Tabbert, Daniela Hermann, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Caspases target only two architectural components within the core structure of the nuclear pore complex."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M511717200"}], "href": "https://doi.org/10.1074/jbc.M511717200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16286466"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16286466"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Garret N Gomez, Fareeha Abrar, Maya P Dodhia, et al. "}, {"type": "b", "children": [{"type": "t", "text": "SARS coronavirus protein nsp1 disrupts localization of Nup93 from the nuclear pore complex."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Cell Biol (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1139/bcb-2018-0394"}], "href": "https://doi.org/10.1139/bcb-2018-0394"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30943371"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30943371"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Parshuram J Sonawane, Pravin S Dewangan, Pankaj Kumar Madheshiya, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Molecular and structural analysis of central transport channel in complex with Nup93 of nuclear pore complex."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Protein Sci (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/pro.3983"}], "href": "https://doi.org/10.1002/pro.3983"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33085133"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33085133"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Tung D Nguyen, Mihir K Rao, Shaiva P Dhyani, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Nucleoporin93 limits Yap activity to prevent endothelial cell senescence."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Aging Cell (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/acel.14095"}], "href": "https://doi.org/10.1111/acel.14095"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38348753"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38348753"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Daniela A Braun, Carolin E Sadowski, Stefan Kohl, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Genet (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ng.3512"}], "href": "https://doi.org/10.1038/ng.3512"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26878725"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26878725"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Florencia Del Viso, Fang Huang, Jordan Myers, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Dev Cell (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.devcel.2016.08.002"}], "href": "https://doi.org/10.1016/j.devcel.2016.08.002"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27593162"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27593162"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Martin Bezdíčka, Šárka Štolbová, Tomáš Seeman, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP93."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Pediatr Nephrol (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s00467-018-3950-2"}], "href": "https://doi.org/10.1007/s00467-018-3950-2"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29869118"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29869118"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Ginevra Zanni, P De Magistris, M Nardella, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Biallelic Variants in the Nuclear Pore Complex Protein NUP93 Are Associated with Non-progressive Congenital Ataxia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cerebellum (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s12311-019-1010-5"}], "href": "https://doi.org/10.1007/s12311-019-1010-5"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30741391"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30741391"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Yanxinli Han, Hongyu Sha, Yuan Yang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutations in the NUP93, NUP107 and NUP160 genes cause steroid-resistant nephrotic syndrome in Chinese children."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Ital J Pediatr (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s13052-024-01656-3"}], "href": "https://doi.org/10.1186/s13052-024-01656-3"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38650033"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38650033"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Xiaolan Ouyang, Xiaoming Hao, Shuaibin Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Expression of Nup93 is associated with the proliferation, migration and invasion capacity of cervical cancer cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Acta Biochim Biophys Sin (Shanghai) (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/abbs/gmz131"}], "href": "https://doi.org/10.1093/abbs/gmz131"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31774908"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31774908"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Simone Bersini, Nikki K Lytle, Roberta Schulte, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Nup93 regulates breast tumor growth by modulating cell proliferation and actin cytoskeleton remodeling."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Life Sci Alliance (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.26508/lsa.201900623"}], "href": "https://doi.org/10.26508/lsa.201900623"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31959624"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31959624"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Cen-Shan Lin, Yuyi Liang, Shu-Guang Su, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Nucleoporin 93 mediates β-catenin nuclear import to promote hepatocellular carcinoma progression and metastasis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Lett (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.canlet.2021.11.001"}], "href": "https://doi.org/10.1016/j.canlet.2021.11.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34767927"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34767927"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Nishanth Belugali Nataraj, Ashish Noronha, Joo Sang Lee, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Nucleoporin-93 reveals a common feature of aggressive breast cancers: robust nucleocytoplasmic transport of transcription factors."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Rep (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.celrep.2022.110418"}], "href": "https://doi.org/10.1016/j.celrep.2022.110418"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35196484"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35196484"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Jinfeng Zhang, Yanzhong Xin, Xiaodong Ling, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Nucleoporin 93, a new substrate of the E3 ubiquitin protein ligase HECTD1, promotes esophageal squamous cell carcinoma progression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Cell (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s13577-023-01005-2"}], "href": "https://doi.org/10.1007/s13577-023-01005-2"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37993750"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37993750"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Gang Zhang, Wei Wei, Shao Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Transcription Factor yin-Yang 1 augments nucleoporin 93 oncogene activity and modulates bladder Cancer malignancy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Toxicol In Vitro (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.tiv.2024.105875"}], "href": "https://doi.org/10.1016/j.tiv.2024.105875"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38857852"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38857852"}]}]}]}
Synonyms	NIC96
Proteins	NUP93_HUMAN
NCBI Gene ID	9688
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

NUP93 has 8,766 functional associations with biological entities spanning 9 categories (molecular profile, organism, chemical, disease, phenotype or trait, functional term, phrase or reference, 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 NUP93 from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

NUP93 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 NUP93 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 NUP93 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 NUP93 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 NUP93 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 NUP93 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 NUP93 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 NUP93 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 NUP93 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 NUP93 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 NUP93 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 NUP93 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of NUP93 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 NUP93 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with NUP93 protein from the CCLE Cell Line Proteomics dataset.
	ChEA Transcription Factor Binding Site Profiles	transcription factor binding site profiles with transcription factor binding evidence at the promoter of NUP93 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of NUP93 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 NUP93 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
	ClinVar Gene-Phenotype Associations 2025	phenotypes associated with NUP93 gene from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
	CMAP Signatures of Differentially Expressed Genes for Small Molecules	small molecule perturbations changing expression of NUP93 gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing NUP93 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing NUP93 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores	cellular components co-occuring with NUP93 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 NUP93 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	CORUM Protein Complexes	protein complexs containing NUP93 protein from the CORUM Protein Complexes dataset.
	COSMIC Cell Line Gene CNV Profiles	cell lines with high or low copy number of NUP93 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with NUP93 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Chemical Interactions	chemicals interacting with NUP93 gene/protein from the curated CTD Gene-Chemical Interactions dataset.
	CTD Gene-Disease Associations	diseases associated with NUP93 gene/protein from the curated CTD Gene-Disease Associations dataset.
	dbGAP Gene-Trait Associations	traits associated with NUP93 gene in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores 2025	diseases associated with NUP93 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 NUP93 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 NUP93 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 NUP93 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with NUP93 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 NUP93 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 NUP93 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
	ENCODE Transcription Factor Targets	transcription factors binding the promoter of NUP93 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 NUP93 from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.
	GAD Gene-Disease Associations	diseases associated with NUP93 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 NUP93 gene relative to other cell lines from the GDSC Cell Line Gene Expression Profiles dataset.