CDYL Gene

Name	chromodomain protein, Y-like
Description	Chromodomain Y is a primate-specific Y-chromosomal gene family expressed exclusively in the testis and implicated in infertility. Although the Y-linked genes are testis-specific, this autosomal gene is ubiquitously expressed. The Y-linked genes arose by retrotransposition of an mRNA from this gene, followed by amplification of the retroposed gene. Proteins encoded by this gene superfamily possess a chromodomain, a motif implicated in chromatin binding and gene suppression, and a catalytic domain believed to be involved in histone acetylation. Multiple proteins are encoded by transcript variants of this gene. [provided by RefSeq, Jul 2008]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Chromodomain Y‐like (CDYL) is a multifunctional epigenetic regulator that acts primarily as a transcriptional corepressor by bridging chromatin‐modifying enzymes with target loci. Its crotonyl–coenzyme A hydratase activity enables CDYL to negatively regulate histone crotonylation, thereby linking metabolic cues with chromatin structure and gene repression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " CDYL also participates in repressor complexes; for example, it physically connects the neuronal repressor REST with the histone methyltransferase G9a to help silence gene expression and prevent oncogenic transformation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n During mouse spermiogenesis, CDYL is highly expressed and contributes to chromatin remodeling events necessary for germ cell development, acting as a corepressor that coordinates the activities of histone deacetylases and other chromatin modifiers."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " In addition, CDYL specifically recognizes repressive histone marks such as H3K27me2/3 through its chromodomain and directly interacts with EZH2, the catalytic subunit of Polycomb Repressive Complex 2, thereby enhancing PRC2 activity and ensuring efficient deposition and propagation of these marks."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": " This function extends to the regulation of X chromosome inactivation, where CDYL cooperates with H3K9me2 and H3K27me3 marks and associates with factors like G9a to help maintain the silent state."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Multiple isoforms of CDYL have been described, and studies indicate that efficient heterochromatin binding requires not only the intact chromodomain but also protein multimerization through its enoyl-CoA hydratase–like domain."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": " Beyond its role in normal development, CDYL is implicated in various disease processes. Upregulation of CDYL has been linked to stress‐induced depression through its repression of neurotrophic factors via combined effects on histone crotonylation and H3K27 trimethylation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": " Moreover, CDYL is rapidly recruited to sites of DNA double‐strand breaks, where it facilitates the recruitment of EZH2 and the deposition of repressive marks that promote homology‐directed repair, thereby contributing to genomic stability."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "8"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n In models of stem cell differentiation, CDYL appears to restrict neuronal fate, as its deficiency in induced pluripotent stem cells leads to enhanced spontaneous neuronal differentiation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "9"}]}, {"type": "t", "text": " In the context of reproduction, genetic studies in mice implicate CDYL in proper spermatogenesis and male fertility."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "10"}]}, {"type": "t", "text": " CDYL is also involved in the transmission and restoration of repressive histone modifications during DNA replication by bridging chromatin assembly factors with replicative helicases and histone methyltransferases, ensuring the faithful propagation of epigenetic states."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "11"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Finally, CDYL regulates neuronal migration by repressing genes such as RhoA, and its dysregulation can lead to aberrant neuronal positioning and increased seizure susceptibility, highlighting its importance in normal brain development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "12"}]}, {"type": "t", "text": " Altered expression of CDYL has also been observed in disorders of the enteric nervous system, including Hirschsprung disease, suggesting a broader role for CDYL in neural development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "13"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Collectively, these findings establish CDYL as a versatile chromatin regulator that integrates metabolic signals and chromatin modifications to control gene expression programs critical for spermatogenesis, neuronal differentiation and migration, stress responses, and DNA repair.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Shumeng Liu, Huajing Yu, Yongqing Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Chromodomain Protein CDYL Acts as a Crotonyl-CoA Hydratase to Regulate Histone Crotonylation and Spermatogenesis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.molcel.2017.07.011"}], "href": "https://doi.org/10.1016/j.molcel.2017.07.011"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28803779"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28803779"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Peter Mulligan, Thomas F Westbrook, Matthias Ottinger, et al. "}, {"type": "b", "children": [{"type": "t", "text": "CDYL bridges REST and histone methyltransferases for gene repression and suppression of cellular transformation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.molcel.2008.10.025"}], "href": "https://doi.org/10.1016/j.molcel.2008.10.025"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19061646"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19061646"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Cécile Caron, Christophe Pivot-Pajot, Leo A van Grunsven, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Cdyl: a new transcriptional co-repressor."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO Rep (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.embor.embor917"}], "href": "https://doi.org/10.1038/sj.embor.embor917"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12947414"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12947414"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Yu Zhang, Xiaohan Yang, Bin Gui, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Corepressor protein CDYL functions as a molecular bridge between polycomb repressor complex 2 and repressive chromatin mark trimethylated histone lysine 27."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M111.271064"}], "href": "https://doi.org/10.1074/jbc.M111.271064"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22009739"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22009739"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "M Escamilla-Del-Arenal, S T da Rocha, C G Spruijt, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Cdyl, a new partner of the inactive X chromosome and potential reader of H3K27me3 and H3K9me2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.00866-13"}], "href": "https://doi.org/10.1128/MCB.00866-13"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24144980"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24144980"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Henriette Franz, Kerstin Mosch, Szabolcs Soeroes, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Multimerization and H3K9me3 binding are required for CDYL1b heterochromatin association."}]}, {"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.M109.052332"}], "href": "https://doi.org/10.1074/jbc.M109.052332"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19808672"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19808672"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Yongqing Liu, Minghua Li, Minghua Fan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Chromodomain Y-like Protein-Mediated Histone Crotonylation Regulates Stress-Induced Depressive Behaviors."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biol Psychiatry (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biopsych.2018.11.025"}], "href": "https://doi.org/10.1016/j.biopsych.2018.11.025"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30665597"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30665597"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Enas R Abu-Zhayia, Samah W Awwad, Bella M Ben-Oz, et al. "}, {"type": "b", "children": [{"type": "t", "text": "CDYL1 fosters double-strand break-induced transcription silencing and promotes homology-directed repair."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Mol Cell Biol (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/jmcb/mjx050"}], "href": "https://doi.org/10.1093/jmcb/mjx050"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29177481"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29177481"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Li Wan, Xiao-Jun Hu, Sun-Xing Yan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Generation and neuronal differentiation of induced pluripotent stem cells in Cdyl-/- mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neuroreport (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1097/WNR.0b013e32835cf179"}], "href": "https://doi.org/10.1097/WNR.0b013e32835cf179"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23282990"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23282990"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Xiaoyu Xia, Xiaowei Zhou, Yanmei Quan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Germline deletion of Cdyl causes teratozoospermia and progressive infertility in male mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Death Dis (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41419-019-1455-y"}], "href": "https://doi.org/10.1038/s41419-019-1455-y"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30850578"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30850578"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Yongqing Liu, Shumeng Liu, Shuai Yuan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Chromodomain protein CDYL is required for transmission/restoration of repressive histone marks."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Mol Cell Biol (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/jmcb/mjx013"}], "href": "https://doi.org/10.1093/jmcb/mjx013"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28402439"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28402439"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Rui Qin, Shuai Cao, Tianjie Lyu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "CDYL Deficiency Disrupts Neuronal Migration and Increases Susceptibility to Epilepsy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Rep (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.celrep.2016.12.043"}], "href": "https://doi.org/10.1016/j.celrep.2016.12.043"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28076783"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28076783"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "María Valle Enguix-Riego, Ana Torroglosa, Raquel María Fernández, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Identification of different mechanisms leading to PAX6 down-regulation as potential events contributing to the onset of Hirschsprung disease."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/srep21160"}], "href": "https://doi.org/10.1038/srep21160"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26879676"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26879676"}]}]}]}
Synonyms	CDYL1
Proteins	CDYL1_HUMAN
NCBI Gene ID	9425
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

CDYL has 5,708 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 122 datasets.

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

If available, associations are ranked by standardized value

Harmonizome 3.0

CDYL 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 CDYL 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 CDYL 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 CDYL 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 CDYL 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 CDYL 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 CDYL 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 CDYL 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 CDYL 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 CDYL 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 CDYL gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of CDYL 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 CDYL gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with CDYL protein from the CCLE Cell Line Proteomics dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with CDYL 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 CDYL gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of CDYL 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 CDYL gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
	CM4AI U2OS Cell Map Protein Localization Assemblies	assemblies containing CDYL 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 CDYL gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing CDYL protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing CDYL protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores	cellular components co-occuring with CDYL 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 CDYL protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	CORUM Protein Complexes	protein complexs containing CDYL protein from the CORUM Protein Complexes dataset.
	COSMIC Cell Line Gene CNV Profiles	cell lines with high or low copy number of CDYL gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with CDYL gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Chemical Interactions	chemicals interacting with CDYL gene/protein from the curated CTD Gene-Chemical Interactions dataset.
	CTD Gene-Disease Associations	diseases associated with CDYL gene/protein from the curated CTD Gene-Disease Associations dataset.
	dbGAP Gene-Trait Associations	traits associated with CDYL 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 CDYL gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores	diseases associated with CDYL gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores 2025	diseases associated with CDYL 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 CDYL 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 CDYL 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 CDYL gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with CDYL 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 CDYL 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 CDYL gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
	ENCODE Transcription Factor Targets	transcription factors binding the promoter of CDYL 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 CDYL from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.