KIN Gene

Name	Kin17 DNA and RNA binding protein
Description	The protein encoded by this gene is a nuclear protein that forms intranuclear foci during proliferation and is redistributed in the nucleoplasm during the cell cycle. Short-wave ultraviolet light provokes the relocalization of the protein, suggesting its participation in the cellular response to DNA damage. Originally selected based on protein-binding with RecA antibodies, the mouse protein presents a limited similarity with a functional domain of the bacterial RecA protein, a characteristic shared by this human ortholog. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Kin17 is an evolutionarily conserved nuclear protein that performs multiple functions in the maintenance of genomic integrity and nuclear metabolism. It is subject to post‐translational modifications – for example, methylation at a specific lysine residue (K135) by protein methyltransferases influences its chromatin association and perhaps broader aspects of its activity."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Kin17 is rapidly up‐regulated in response to DNA damage – such as UVC or γ‐irradiation – and is recruited to chromosomal sites that likely represent stalled replication forks or unrepaired lesions, where it associates with key replication proteins (including RPA and PCNA) and localizes to replication factories during S phase."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "2", "end_ref": "4"}]}, {"type": "t", "text": " In addition, its appropriate expression is critical for DNA replication and repair processes; altered Kin17 levels can delay S‐phase progression or increase cellular sensitivity to genotoxic stress."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n In several cancers – including breast, cervical, thyroid, and colorectal malignancies – Kin17 is overexpressed and its high levels correlate with increased cell proliferation, metastatic potential, and chemoresistance."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "6", "end_ref": "10"}]}, {"type": "t", "text": " Such deregulation suggests that Kin17 not only plays a physiological role in preserving DNA integrity but also that its misregulation can be exploited by tumor cells to promote malignant growth."}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Insights from structural studies reveal that Kin17 is composed of several conserved domains, including a winged helix module and a C‐terminal region with tandem SH3–like subdomains. These domains likely mediate interactions with both nucleic acids and proteins, thereby contributing to its role in DNA replication, chromatin organization, and RNA processing."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "11", "end_ref": "13"}]}, {"type": "t", "text": " In a recent genetic analysis, Kin17 – together with the partnering factor PRCC – was also found to influence splice site choice, indicating a novel role in pre‐mRNA splicing and suggesting that Kin17 may “moonlight” in multiple facets of RNA metabolism."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "14"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Moreover, Kin17 is required for efficient repair of DNA double‐strand breaks, as evidenced by its critical role in class switch recombination where its reduction impairs several repair pathways – including homologous recombination and non‐homologous end–joining – thereby underlining its importance in preserving genome stability."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "15"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n In summary, Kin17 functions as a multifaceted protein that integrates signals from DNA damage, replication, and RNA processing pathways. Its dynamic regulation and interactions allow it to support proper DNA replication and repair under physiological conditions while its deregulation in cancer cells may contribute to tumor aggressiveness. These diverse roles make Kin17 an attractive target for further mechanistic studies and potential therapeutic intervention.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Philippe Cloutier, Mathieu Lavallée-Adam, Denis Faubert, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A newly uncovered group of distantly related lysine methyltransferases preferentially interact with molecular chaperones to regulate their activity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS Genet (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pgen.1003210"}], "href": "https://doi.org/10.1371/journal.pgen.1003210"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23349634"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23349634"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Denis S F Biard, Laurent Miccoli, Emmanuelle Despras, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Ionizing radiation triggers chromatin-bound kin17 complex formation in human cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M200321200"}], "href": "https://doi.org/10.1074/jbc.M200321200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "11880372"}], "href": "https://pubmed.ncbi.nlm.nih.gov/11880372"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Laurent Miccoli, Isabelle Frouin, Olivia Novac, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The human stress-activated protein kin17 belongs to the multiprotein DNA replication complex and associates in vivo with mammalian replication origins."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.25.9.3814-3830.2005"}], "href": "https://doi.org/10.1128/MCB.25.9.3814-3830.2005"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15831485"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15831485"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Denis S F Biard, Laurent Miccoli, Emmanuelle Despras, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Participation of kin17 protein in replication factories and in other DNA transactions mediated by high molecular weight nuclear complexes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cancer Res (2003)"}]}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12754299"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12754299"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "P Kannouche, J F Angulo "}, {"type": "b", "children": [{"type": "t", "text": "Overexpression of kin17 protein disrupts nuclear morphology and inhibits the growth of mammalian cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Sci (1999)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1242/jcs.112.19.3215"}], "href": "https://doi.org/10.1242/jcs.112.19.3215"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "10504327"}], "href": "https://pubmed.ncbi.nlm.nih.gov/10504327"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Tao Zeng, Hongyi Gao, Pei Yu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Up-regulation of kin17 is essential for proliferation of breast cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0025343"}], "href": "https://doi.org/10.1371/journal.pone.0025343"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21980430"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21980430"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Yuzhao Zhang, Hongyi Gao, Xiang Gao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Elevated Expression of Kin17 in Cervical Cancer and Its Association With Cancer Cell Proliferation and Invasion."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Gynecol Cancer (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1097/IGC.0000000000000928"}], "href": "https://doi.org/10.1097/IGC.0000000000000928"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28346239"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28346239"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Qiyuan Huang, Kashif Rafiq Zahid, Jinsi Chen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "KIN17 promotes tumor metastasis by activating EMT signaling in luminal-A breast cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Thorac Cancer (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/1759-7714.14004"}], "href": "https://doi.org/10.1111/1759-7714.14004"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34008927"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34008927"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Qun-Guang Jiang, Cheng-Feng Xiong, Yun-Xia Lv "}, {"type": "b", "children": [{"type": "t", "text": "Kin17 facilitates thyroid cancer cell proliferation, migration, and invasion by activating p38 MAPK signaling pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biochem (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s11010-020-03939-9"}], "href": "https://doi.org/10.1007/s11010-020-03939-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33201383"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33201383"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Miao Yu, Zhenwei Zhang, Honglan Yu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "KIN enhances stem cell-like properties to promote chemoresistance in colorectal carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2014.04.057"}], "href": "https://doi.org/10.1016/j.bbrc.2014.04.057"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24755081"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24755081"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Albane le Maire, Marc Schiltz, Enrico A Stura, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A tandem of SH3-like domains participates in RNA binding in KIN17, a human protein activated in response to genotoxics."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Mol Biol (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.jmb.2006.09.033"}], "href": "https://doi.org/10.1016/j.jmb.2006.09.033"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17045609"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17045609"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Ludovic Carlier, Joël Couprie, Albane le Maire, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Solution structure of the region 51-160 of human KIN17 reveals an atypical winged helix domain."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Protein Sci (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1110/ps.073079107"}], "href": "https://doi.org/10.1110/ps.073079107"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18029424"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18029424"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Vanessa Pinatto Gaspar, Anelise Cardoso Ramos, Philippe Cloutier, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Interactome Analysis of KIN (Kin17) Shows New Functions of This Protein."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Curr Issues Mol Biol (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/cimb43020056"}], "href": "https://doi.org/10.3390/cimb43020056"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34449532"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34449532"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Jessie M N G L Suzuki, Kenneth Osterhoudt, Catiana H Cartwright-Acar, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A genetic screen in C. elegans reveals roles for KIN17 and PRCC in maintaining 5' splice site identity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS Genet (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pgen.1010028"}], "href": "https://doi.org/10.1371/journal.pgen.1010028"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35143478"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35143478"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Michael X Le, Dania Haddad, Alexanda K Ling, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Kin17 facilitates multiple double-strand break repair pathways that govern B cell class switching."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/srep37215"}], "href": "https://doi.org/10.1038/srep37215"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27853268"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27853268"}]}]}]}
Synonyms	RTS2, BTCD, KIN17
Proteins	KIN17_HUMAN
NCBI Gene ID	22944
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

KIN has 5,198 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 KIN from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

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