RPS14 Gene

HGNC Family	S ribosomal proteins (RPS)
Name	ribosomal protein S14
Description	Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S11P family of ribosomal proteins. It is located in the cytoplasm. Transcript variants utilizing alternative transcription initiation sites have been described in the literature. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. In Chinese hamster ovary cells, mutations in this gene can lead to resistance to emetine, a protein synthesis inhibitor. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nRPS14 is a critical component of the small ribosomal subunit whose proper dosage is essential for normal ribosome biogenesis and erythropoiesis. Haploinsufficiency of RPS14, as observed in 5q– syndrome—a distinct subtype of myelodysplastic syndrome—and in select cases of Diamond–Blackfan anemia, leads to defective processing of precursor ribosomal RNA and impaired erythroid differentiation. In experimental systems, partial loss of RPS14 function recapitulates the anemic phenotype, while restoration of its expression rescues the defect. Moreover, detailed genomic analyses in myelodysplastic syndromes have revealed reduced RPS14 expression and small, often mosaic, deletions that underscore its role in disease pathogenesis without accompanying promoter methylation changes."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "6"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its canonical role in ribosome assembly, RPS14 modulates key signaling pathways that govern cell proliferation and survival. Depletion of RPS14 in hematopoietic progenitor cells triggers the selective accumulation of p53 through both ribosomal stress and direct mechanisms: RPS14 binds the central acidic domain of the E3 ubiquitin ligase MDM2, inhibiting p53 ubiquitination and stabilizing the tumor suppressor. In parallel, RPS14 has been shown to interfere with the oncogenic transcription factor c‐Myc by preventing the recruitment of its coactivator TRRAP and by promoting c‐Myc mRNA turnover via Argonaute 2–dependent microRNA pathways. Furthermore, the post‐translational modification of RPS14 via NEDD8—and its regulation by hCINAP—further fine‐tunes its ability to control the p53–MDM2 feedback loop."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "7", "end_ref": "11"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn addition to its central role in hematologic disorders, RPS14 exhibits context‐dependent oncogenic and prognostic properties in other malignancies. In myelodysplastic syndrome cases lacking the classical 5q deletion, reduced expression of RPS14 has been associated with distinct clinical outcomes and responses to therapeutic agents such as lenalidomide. Moreover, in transformed hematopoietic and glioma cell lines, altered levels of RPS14 affect cellular proliferation, migration, and apoptosis—underscoring its contribution to tumor progression. Recent genetic studies have also identified functional polymorphisms within the RPS14 promoter that affect transcription factor binding and modulate downstream AKT signaling in hepatocellular carcinoma, highlighting a potential oncogenic role outside of the bone marrow."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "12", "end_ref": "16"}]}, {"type": "t", "text": ""}]}]}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Benjamin L Ebert, Jennifer Pretz, Jocelyn Bosco, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Identification of RPS14 as a 5q- syndrome gene by RNA interference screen."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nature (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nature06494"}], "href": "https://doi.org/10.1038/nature06494"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18202658"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18202658"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Paola Quarello, Emanuela Garelli, Adriana Carando, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Haematologica (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3324/haematol.2009.011783"}], "href": "https://doi.org/10.3324/haematol.2009.011783"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19773262"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19773262"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Akos Czibere, Ingmar Bruns, Bärbel Junge, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Low RPS14 expression is common in myelodysplastic syndromes without 5q- aberration and defines a subgroup of patients with prolonged survival."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Haematologica (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3324/haematol.2009.008508"}], "href": "https://doi.org/10.3324/haematol.2009.008508"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19794090"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19794090"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Ioana Borze, Eeva Juvonen, Shinsuke Ninomiya, et al. "}, {"type": "b", "children": [{"type": "t", "text": "High-resolution oligonucleotide array comparative genomic hybridization study and methylation status of the RPS14 gene in de novo myelodysplastic syndromes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Genet Cytogenet (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.cancergencyto.2009.11.012"}], "href": "https://doi.org/10.1016/j.cancergencyto.2009.11.012"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20193850"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20193850"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Esther N Oliva, Maria Cuzzola, Francesco Nobile, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Changes in RPS14 expression levels during lenalidomide treatment in Low- and Intermediate-1-risk myelodysplastic syndromes with chromosome 5q deletion."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Haematol (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/j.1600-0609.2010.01473.x"}], "href": "https://doi.org/10.1111/j.1600-0609.2010.01473.x"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20491881"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20491881"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Adrianna Vlachos, Jason E Farrar, Eva Atsidaftos, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Diminutive somatic deletions in the 5q region lead to a phenotype atypical of classical 5q- syndrome."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood-2013-06-509935"}], "href": "https://doi.org/10.1182/blood-2013-06-509935"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23943650"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23943650"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Shilpee Dutt, Anupama Narla, Katherine Lin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood-2010-07-295238"}], "href": "https://doi.org/10.1182/blood-2010-07-295238"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21068437"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21068437"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Madhu S Kumar, Anupama Narla, Atsushi Nonami, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Coordinate loss of a microRNA and protein-coding gene cooperate in the pathogenesis of 5q- syndrome."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood-2010-12-324715"}], "href": "https://doi.org/10.1182/blood-2010-12-324715"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21873545"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21873545"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "X Zhou, Q Hao, J Liao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Ribosomal protein S14 unties the MDM2-p53 loop upon ribosomal stress."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncogene (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/onc.2012.63"}], "href": "https://doi.org/10.1038/onc.2012.63"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22391559"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22391559"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "J Zhang, D Bai, X Ma, et al. "}, {"type": "b", "children": [{"type": "t", "text": "hCINAP is a novel regulator of ribosomal protein-HDM2-p53 pathway by controlling NEDDylation of ribosomal protein S14."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncogene (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/onc.2012.560"}], "href": "https://doi.org/10.1038/onc.2012.560"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23246961"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23246961"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Xiang Zhou, Qian Hao, Jun-Ming Liao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Ribosomal protein S14 negatively regulates c-Myc activity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M112.445122"}], "href": "https://doi.org/10.1074/jbc.M112.445122"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23775087"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23775087"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Lingyun Wu, Xiao Li, Feng Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Low RPS14 expression in MDS without 5q - aberration confers higher apoptosis rate of nucleated erythrocytes and predicts prolonged survival and possible response to lenalidomide in lower risk non-5q- patients."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Haematol (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/ejh.12105"}], "href": "https://doi.org/10.1111/ejh.12105"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23506134"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23506134"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Li Wang, Jing Luo, Qing Nian, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Ribosomal protein S14 silencing inhibits growth of acute myeloid leukemia transformed from myelodysplastic syndromes via activating p53."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hematology (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1179/1607845413Y.0000000127"}], "href": "https://doi.org/10.1179/1607845413Y.0000000127"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24074450"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24074450"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Ismael Boussaid, Salomé Le Goff, Célia Floquet, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Integrated analyses of translatome and proteome identify the rules of translation selectivity in RPS14-deficient cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Haematologica (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3324/haematol.2019.239970"}], "href": "https://doi.org/10.3324/haematol.2019.239970"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32327500"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32327500"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Shangwei Hu, Jianhui Cai, Hua Fang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "RPS14 promotes the development and progression of glioma via p53 signaling pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Exp Cell Res (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.yexcr.2022.113451"}], "href": "https://doi.org/10.1016/j.yexcr.2022.113451"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36535509"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36535509"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Linyu Han, Yanfei Huo, Linying Huang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Genome-wide functional integration identified MAZ-controlled RPS14 dysregulation in hepatocellular carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Arch Toxicol (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s00204-023-03669-z"}], "href": "https://doi.org/10.1007/s00204-023-03669-z"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38189915"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38189915"}]}]}]}
Synonyms	EMTB
Proteins	RS14_HUMAN
NCBI Gene ID	6208
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Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

RPS14 has 17,459 functional associations with biological entities spanning 9 categories (molecular profile, organism, functional term, phrase or reference, chemical, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 126 datasets.

Click the + buttons to view associations for RPS14 from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

RPS14 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 RPS14 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 RPS14 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 RPS14 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 RPS14 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 RPS14 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 RPS14 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 RPS14 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 RPS14 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 RPS14 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 RPS14 gene relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of RPS14 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 RPS14 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with RPS14 protein from the CCLE Cell Line Proteomics dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with RPS14 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 RPS14 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of RPS14 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 RPS14 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 RPS14 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 RPS14 gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing RPS14 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing RPS14 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores	cellular components containing RPS14 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 RPS14 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 RPS14 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 RPS14 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	CORUM Protein Complexes	protein complexs containing RPS14 protein from the CORUM Protein Complexes dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with RPS14 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Chemical Interactions	chemicals interacting with RPS14 gene/protein from the curated CTD Gene-Chemical Interactions dataset.
	CTD Gene-Disease Associations	diseases associated with RPS14 gene/protein from the curated CTD Gene-Disease Associations dataset.
	DeepCoverMOA Drug Mechanisms of Action	small molecule perturbations with high or low expression of RPS14 protein relative to other small molecule perturbations from the DeepCoverMOA Drug Mechanisms of Action dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores 2025	diseases involving RPS14 gene from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores	diseases associated with RPS14 gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores	diseases co-occuring with RPS14 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 RPS14 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 RPS14 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with RPS14 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 RPS14 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 RPS14 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
	ENCODE Transcription Factor Targets	transcription factors binding the promoter of RPS14 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 RPS14 from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.