HNRNPK Gene

Name	heterogeneous nuclear ribonucleoprotein K
Description	This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene is located in the nucleoplasm and has three repeats of KH domains that binds to RNAs. It is distinct among other hnRNP proteins in its binding preference; it binds tenaciously to poly(C). This protein is also thought to have a role during cell cycle progession. Several alternatively spliced transcript variants have been described for this gene, however, not all of them are fully characterized. [provided by RefSeq, Jul 2008]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Heterogeneous nuclear ribonucleoprotein K (HNRNPK) is a multifunctional RNA‐binding protein that plays diverse roles in gene regulation at both transcriptional and post‐transcriptional levels. In the nucleus, HNRNPK acts as a key cofactor in p53‐mediated gene regulation by partnering with long noncoding RNAs such as lincRNA‑p21 to ensure proper promoter targeting and expression of cell cycle regulators (for example, p21), thereby influencing apoptosis and tumor suppression."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "3"}]}, {"type": "t", "text": " HNRNPK also contributes to epigenetic silencing during X chromosome inactivation by binding to Xist RNA and promoting the recruitment of Polycomb repressive complexes"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": ", and it regulates alternative 3′‑end processing of the essential NEAT1 lncRNA to favor the production of isoforms that are critical for paraspeckle formation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n In the cytoplasm, HNRNPK exerts dual functions in mRNA translation. It can mediate translational silencing—for instance, through its regulated binding to specific mRNA untranslated regions that is modulated by c‑Src phosphorylation"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": "—while also promoting cap‑independent, internal ribosome entry site (IRES)‑dependent translation of key oncogenic transcripts such as c‑myc."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "8"}]}, {"type": "t", "text": " In this context, aberrant regulation of HNRNPK has been linked to tumorigenesis across multiple cancers. For example, its targeting by miR‑21 contributes to the proproliferative and antiapoptotic phenotype in glioblastoma"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "10"}]}, {"type": "t", "text": ", and its overexpression or engagement by cancer‑associated long noncoding RNAs (such as CASC11 and MYCLo‑2) can activate pathways such as WNT/β‑catenin in colorectal cancer"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "11"}]}, {"type": "t", "text": ", while elevated levels also correlate with enhanced cell invasion in gallbladder carcinoma."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "13"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Additional roles for HNRNPK include its participation in cytoskeletal remodeling through interactions with adaptor proteins during ephrin‐mediated reverse signaling"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "14"}]}, {"type": "t", "text": "and in the autophagy‐dependent secretion pathway, where it is loaded into extracellular vesicles via the LC3‐conjugation machinery."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "15"}]}, {"type": "t", "text": " Finally, HNRNPK functions in neuron–astrocyte communication by binding to promoter regions of genes such as GLT1/EAAT2, thereby linking presynaptic signals to the transcriptional activation of critical astroglial transporters"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "16"}]}, {"type": "t", "text": ", and it is co-opted by lncRNAs like lincRNA‑p21 to engage epigenetic modifiers (for instance, SETDB1 and DNMT1) that stabilize repressive chromatin and impede cellular reprogramming."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "17"}]}, {"type": "t", "text": "\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Maite Huarte, Mitchell Guttman, David Feldser, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A large intergenic noncoding RNA induced by p53 mediates global gene repression in the p53 response."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.cell.2010.06.040"}], "href": "https://doi.org/10.1016/j.cell.2010.06.040"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20673990"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20673990"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Nadya Dimitrova, Jesse R Zamudio, Robyn M Jong, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LincRNA-p21 activates p21 in cis to promote Polycomb target gene expression and to enforce the G1/S checkpoint."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.molcel.2014.04.025"}], "href": "https://doi.org/10.1016/j.molcel.2014.04.025"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24857549"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24857549"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Martin Enge, Wenjie Bao, Elisabeth Hedström, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MDM2-dependent downregulation of p21 and hnRNP K provides a switch between apoptosis and growth arrest induced by pharmacologically activated p53."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Cell (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ccr.2009.01.019"}], "href": "https://doi.org/10.1016/j.ccr.2009.01.019"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19249676"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19249676"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Ci Chu, Qiangfeng Cliff Zhang, Simão Teixeira da Rocha, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Systematic discovery of Xist RNA binding proteins."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.cell.2015.03.025"}], "href": "https://doi.org/10.1016/j.cell.2015.03.025"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25843628"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25843628"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Greta Pintacuda, Guifeng Wei, Chloë Roustan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "hnRNPK Recruits PCGF3/5-PRC1 to the Xist RNA B-Repeat to Establish Polycomb-Mediated Chromosomal Silencing."}]}, {"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.2017.11.013"}], "href": "https://doi.org/10.1016/j.molcel.2017.11.013"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29220657"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29220657"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Takao Naganuma, Shinichi Nakagawa, Akie Tanigawa, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Alternative 3'-end processing of long noncoding RNA initiates construction of nuclear paraspeckles."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO J (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/emboj.2012.251"}], "href": "https://doi.org/10.1038/emboj.2012.251"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22960638"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22960638"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Antje Ostareck-Lederer, Dirk H Ostareck, Christophe Cans, et al. "}, {"type": "b", "children": [{"type": "t", "text": "c-Src-mediated phosphorylation of hnRNP K drives translational activation of specifically silenced mRNAs."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.22.13.4535-4543.2002"}], "href": "https://doi.org/10.1128/MCB.22.13.4535-4543.2002"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12052863"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12052863"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Joanne R Evans, Sally A Mitchell, Keith A Spriggs, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Members of the poly (rC) binding protein family stimulate the activity of the c-myc internal ribosome entry segment in vitro and in vivo."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncogene (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.onc.1206645"}], "href": "https://doi.org/10.1038/sj.onc.1206645"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12970749"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12970749"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Mario Notari, Paolo Neviani, Ramasamy Santhanam, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A MAPK/HNRPK pathway controls BCR/ABL oncogenic potential by regulating MYC mRNA translation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood-2005-09-3732"}], "href": "https://doi.org/10.1182/blood-2005-09-3732"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16293596"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16293596"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Thales Papagiannakopoulos, Alice Shapiro, Kenneth S Kosik "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-21 targets a network of key tumor-suppressive pathways in glioblastoma cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Res (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1158/0008-5472.CAN-08-1305"}], "href": "https://doi.org/10.1158/0008-5472.CAN-08-1305"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18829576"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18829576"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Zheying Zhang, Chang Zhou, Yaya Chang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Long non-coding RNA CASC11 interacts with hnRNP-K and activates the WNT/β-catenin pathway to promote growth and metastasis in colorectal cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Lett (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.canlet.2016.03.022"}], "href": "https://doi.org/10.1016/j.canlet.2016.03.022"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27012187"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27012187"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Taewan Kim, Young-Jun Jeon, Ri Cui, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "The LC3-conjugation machinery specifies the loading of RNA-binding proteins into extracellular vesicles."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Cell Biol (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41556-019-0450-y"}], "href": "https://doi.org/10.1038/s41556-019-0450-y"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31932738"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31932738"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Yongjie Yang, Oguz Gozen, Andrew Watkins, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Presynaptic regulation of astroglial excitatory neurotransmitter transporter GLT1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neuron (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.neuron.2009.02.010"}], "href": "https://doi.org/10.1016/j.neuron.2009.02.010"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19323997"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19323997"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Xichen Bao, Haitao Wu, Xihua Zhu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The p53-induced lincRNA-p21 derails somatic cell reprogramming by sustaining H3K9me3 and CpG methylation at pluripotency gene promoters."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Res (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/cr.2014.165"}], "href": "https://doi.org/10.1038/cr.2014.165"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25512341"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25512341"}]}]}]}
Synonyms	TUNP, HNRPK, AUKS
Proteins	HNRPK_HUMAN
NCBI Gene ID	3190
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

HNRNPK has 14,036 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 127 datasets.

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

If available, associations are ranked by standardized value

Harmonizome 3.0

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