ZMYM2 Gene

HGNC Family	Zinc fingers
Name	zinc finger, MYM-type 2
Description	The protein encoded by this gene is a zinc finger protein that may act as a transcription factor. The encoded protein may be part of a BHC histone deacetylase complex. Translocation of this gene with the fibroblast growth factor receptor-1 gene (FGFR1) results in a fusion gene, which may be a cause of stem cell leukemia lymphoma syndrome (SCLL). Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nZMYM2, whose disruption through chromosomal translocations leads to fusion proteins with FGFR1 (historically also known as ZNF198‐FGFR1), plays a critical role in hematopoietic transformation and oncogenesis. Fusion events (t[8;13]) result in constitutively active tyrosine kinase activity that aberrantly activates downstream prosurvival and proliferative signaling pathways—including STAT5, AKT, and MAPK—thereby promoting leukemogenic transformation in both myeloid and lymphoid neoplasms. These fusion oncoproteins modify phosphorylation patterns on various substrates (including the ZMYM2 moiety itself), subvert normal nuclear function, and perturb the regulation of apoptosis, as evidenced by studies demonstrating altered FOXO3a and BAD handling, as well as impaired DNA damage responses."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "8"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its role in oncogenic fusions, ZMYM2 functions as a key transcriptional repressor through its integration into distinct chromatin remodeling complexes. It associates with the LSD1–CoREST–HDAC1 repressor assembly and binds multi‐SUMO platforms via its multiple MYM zinc finger motifs, a property critical for its recruitment to chromatin. Furthermore, ZMYM2 interacts with additional chromatin regulators—including components of the ADNP and TRIM28 (KAP1) complexes—to help maintain repressive chromatin states and to prevent SUMO-dependent dissociation events. In turn, these interactions facilitate precise regulation of gene expression and ensure the fidelity of cell lineage programs, particularly following DNA damage."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "9", "end_ref": "12"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nZMYM2 is also indispensable for proper embryonic development and cellular differentiation. In human embryonic stem cells, ZMYM2 is one of the most potent chromatin regulators that restrict growth and facilitate exit from pluripotency; loss of its function leads to upregulation of pluripotency genes, hyper‐acetylated promoter regions, and differentiation defects. In addition, loss-of-function mutations in ZMYM2 have been identified in patients with congenital anomalies of the kidney and urinary tract (CAKUT), a phenotype further underscored by its interaction with transcription factors such as FOXP1 and TBX18 during urinary tract development. Moreover, proper repression of germline genes and evolutionarily young, active LINE elements in early embryonic tissues depends on ZMYM2 function, underlining its broad role in establishing and maintaining epigenetic programming during development."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "13", "end_ref": "16"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFinally, post‐translational regulation further modulates ZMYM2 activity in a context‐dependent manner. In ovarian cancer cells, for example, the UBE2B/RAD18 complex promotes ZMYM2 monoubiquitination, an event that enhances its protein stability without altering its messenger RNA levels. This modification appears to be essential for the growth-promoting effect of ZMYM2 in these cancer cells, highlighting a novel regulatory axis that may offer therapeutic opportunities."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "17"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Carol Heath, Nicholas C P Cross "}, {"type": "b", "children": [{"type": "t", "text": "Critical role of STAT5 activation in transformation mediated by ZNF198-FGFR1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M308743200"}], "href": "https://doi.org/10.1074/jbc.M308743200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "14660670"}], "href": "https://pubmed.ncbi.nlm.nih.gov/14660670"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Padmaja Kunapuli, Chitta S Kasyapa, Suet-Feung Chin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "ZNF198, a zinc finger protein rearranged in myeloproliferative disease, localizes to the PML nuclear bodies and interacts with SUMO-1 and PML."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Exp Cell Res (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.yexcr.2006.06.037"}], "href": "https://doi.org/10.1016/j.yexcr.2006.06.037"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17027752"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17027752"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Shaozhong Dong, Sumin Kang, Ting-Lei Gu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "14-3-3 Integrates prosurvival signals mediated by the AKT and MAPK pathways in ZNF198-FGFR1-transformed hematopoietic cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood-2006-12-065615"}], "href": "https://doi.org/10.1182/blood-2006-12-065615"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17389761"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17389761"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Chitta S Kasyapa, Padmaja Kunapuli, John K Cowell "}, {"type": "b", "children": [{"type": "t", "text": "HSPA1A is an important regulator of the stability and function of ZNF198 and its oncogenic derivative, ZNF198-FGFR1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biochem (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcb.21362"}], "href": "https://doi.org/10.1002/jcb.21362"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17471537"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17471537"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Mingqiang Ren, Xiurong Li, John K Cowell "}, {"type": "b", "children": [{"type": "t", "text": "Genetic fingerprinting of the development and progression of T-cell lymphoma in a murine model of atypical myeloproliferative disorder initiated by the ZNF198-fibroblast growth factor receptor-1 chimeric tyrosine kinase."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood-2009-03-212704"}], "href": "https://doi.org/10.1182/blood-2009-03-212704"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19506298"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19506298"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Chitta Kasyapa, Ting-Lei Gu, Lalitha Nagarajan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Phosphorylation of the SSBP2 and ABL proteins by the ZNF198-FGFR1 fusion kinase seen in atypical myeloproliferative disorders as revealed by phosphopeptide-specific MS."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proteomics (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/pmic.200800852"}], "href": "https://doi.org/10.1002/pmic.200800852"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19658100"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19658100"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Wen-Horng Wang, Leo L Studach, Ourania M Andrisani "}, {"type": "b", "children": [{"type": "t", "text": "Proteins ZNF198 and SUZ12 are down-regulated in hepatitis B virus (HBV) X protein-mediated hepatocyte transformation and in HBV replication."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hepatology (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/hep.24163"}], "href": "https://doi.org/10.1002/hep.24163"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21480320"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21480320"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Janese Trimaldi, Estrella M Carballido, Jeremy W Bowers, et al. "}, {"type": "b", "children": [{"type": "t", "text": "B-lymphoblastic leukemia/lymphoma associated with t(8;13)(p11;q12)/ ZMYM2 (ZNF198)-FGFR1 : rare case and review of the literature."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Acta Haematol (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1159/000347030"}], "href": "https://doi.org/10.1159/000347030"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23594707"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23594707"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Christian B Gocke, Hongtao Yu "}, {"type": "b", "children": [{"type": "t", "text": "ZNF198 stabilizes the LSD1-CoREST-HDAC1 complex on chromatin through its MYM-type zinc fingers."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0003255"}], "href": "https://doi.org/10.1371/journal.pone.0003255"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18806873"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18806873"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Elisa Aguilar-Martinez, Xi Chen, Aaron Webber, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Screen for multi-SUMO-binding proteins reveals a multi-SIM-binding mechanism for recruitment of the transcriptional regulator ZMYM2 to chromatin."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.1509716112"}], "href": "https://doi.org/10.1073/pnas.1509716112"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26283374"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26283374"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Hannah Cibis, Abhiruchi Biyanee, Wolfgang Dörner, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Characterization of the zinc finger proteins ZMYM2 and ZMYM4 as novel B-MYB binding proteins."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41598-020-65443-w"}], "href": "https://doi.org/10.1038/s41598-020-65443-w"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32439918"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32439918"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Danielle J Owen, Elisa Aguilar-Martinez, Zongling Ji, et al. "}, {"type": "b", "children": [{"type": "t", "text": "ZMYM2 controls human transposable element transcription through distinct co-regulatory complexes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Elife (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.7554/eLife.86669"}], "href": "https://doi.org/10.7554/eLife.86669"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37934570"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37934570"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Elyad Lezmi, Uri Weissbein, Tamar Golan-Lev, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The Chromatin Regulator ZMYM2 Restricts Human Pluripotent Stem Cell Growth and Is Essential for Teratoma Formation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Stem Cell Reports (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.stemcr.2020.05.014"}], "href": "https://doi.org/10.1016/j.stemcr.2020.05.014"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32559458"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32559458"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Dervla M Connaughton, Rufeng Dai, Danielle J Owen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Hum Genet (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ajhg.2020.08.013"}], "href": "https://doi.org/10.1016/j.ajhg.2020.08.013"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32891193"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32891193"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Timo H-W Lüdtke, Marc-Jens Kleppa, Reginaldo Rivera-Reyes, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Proteomic analysis identifies ZMYM2 as endogenous binding partner of TBX18 protein in 293 and A549 cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem J (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1042/BCJ20210642"}], "href": "https://doi.org/10.1042/BCJ20210642"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34935912"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34935912"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Adda-Lee Graham-Paquin, Deepak Saini, Jacinthe Sirois, et al. "}, {"type": "b", "children": [{"type": "t", "text": "ZMYM2 is essential for methylation of germline genes and active transposons in embryonic development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nucleic Acids Res (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/nar/gkad540"}], "href": "https://doi.org/10.1093/nar/gkad540"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37395395"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37395395"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Xi Zeng, Wen Zheng, Yuting Sheng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "UBE2B promotes ovarian cancer growth via promoting RAD18 mediated ZMYM2 monoubiquitination and stabilization."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Bioengineered (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/21655979.2022.2048991"}], "href": "https://doi.org/10.1080/21655979.2022.2048991"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35313791"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35313791"}]}]}]}
Synonyms	RAMP, FIM, ZNF198, SCLL
Proteins	ZMYM2_HUMAN
NCBI Gene ID	7750
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

ZMYM2 has 10,190 functional associations with biological entities spanning 8 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) extracted from 129 datasets.

Click the + buttons to view associations for ZMYM2 from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

ZMYM2 Gene

Functional Associations

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

	Dataset	Summary
	Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of ZMYM2 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 ZMYM2 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 ZMYM2 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 ZMYM2 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 ZMYM2 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 ZMYM2 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 ZMYM2 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 ZMYM2 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 ZMYM2 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 ZMYM2 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of ZMYM2 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 ZMYM2 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Gene Mutation Profiles	cell lines with ZMYM2 gene mutations from the CCLE Cell Line Gene Mutation Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with ZMYM2 protein from the CCLE Cell Line Proteomics dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with ZMYM2 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 ZMYM2 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of ZMYM2 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 ZMYM2 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 ZMYM2 gene from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
	CM4AI U2OS Cell Map Protein Localization Assemblies	assemblies containing ZMYM2 protein from integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
	CMAP Signatures of Differentially Expressed Genes for Small Molecules	small molecule perturbations changing expression of ZMYM2 gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing ZMYM2 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing ZMYM2 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores	cellular components containing ZMYM2 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 ZMYM2 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 ZMYM2 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 ZMYM2 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	CORUM Protein Complexes	protein complexs containing ZMYM2 protein from the CORUM Protein Complexes dataset.
	COSMIC Cell Line Gene CNV Profiles	cell lines with high or low copy number of ZMYM2 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with ZMYM2 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Chemical Interactions	chemicals interacting with ZMYM2 gene/protein from the curated CTD Gene-Chemical Interactions dataset.
	CTD Gene-Disease Associations	diseases associated with ZMYM2 gene/protein from the curated CTD Gene-Disease Associations dataset.
	DepMap CRISPR Gene Dependency	cell lines with fitness changed by ZMYM2 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 ZMYM2 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 ZMYM2 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 ZMYM2 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 ZMYM2 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with ZMYM2 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 ZMYM2 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 ZMYM2 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.