KCNC3 Gene

HGNC Family	Ion channels
Name	potassium channel, voltage gated Shaw related subfamily C, member 3
Description	The Shaker gene family of Drosophila encodes components of voltage-gated potassium channels and is comprised of four subfamilies. Based on sequence similarity, this gene is similar to one of these subfamilies, namely the Shaw subfamily. The protein encoded by this gene belongs to the delayed rectifier class of channel proteins and is an integral membrane protein that mediates the voltage-dependent potassium ion permeability of excitable membranes. Alternate splicing results in several transcript variants. [provided by RefSeq, Mar 2014]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n KCNC3, which encodes the Kv3.3 voltage‐gated potassium channel, is a key determinant in rapidly repolarizing neuronal membranes to enable high‐frequency firing and precise timing of action potentials in fast‐spiking neurons—most notably in cerebellar Purkinje cells. Studies show that Kv3.3 facilitates both somatic and dendritic excitability, thereby contributing to the formation and shaping of complex spikes critical for cerebellar signal processing."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "3"}]}, {"type": "t", "text": " Functional analyses using knock‐out models and rescue experiments confirm that Kv3.3 currents are essential to maintain spontaneous firing rates and regulate dendritic Ca²⁺ influx, which underpins proper synaptic integration and motor coordination."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "4", "end_ref": "6"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Mutations in KCNC3 have been directly linked to spinocerebellar ataxia type 13 (SCA13) and related ataxic phenotypes, where both dominant‐negative loss‐of‐function and altered gating properties disrupt the high-frequency firing required for neural precision. These pathogenic variants result in abnormal cerebellar output and are associated with a spectrum of neurodevelopmental and neurodegenerative deficits that include motor incoordination, cognitive impairment, and even auditory processing deficits."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}, {"type": "fg_fs", "start_ref": "7", "end_ref": "10"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n In addition, Kv3.3 channels have been implicated in non‐canonical roles such as interfacing with the actin cytoskeleton through binding partners like Hax-1, which may stabilize cortical actin networks and prevent rapid inactivation of other ion channels, further fine-tuning neuronal excitability."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "11"}]}, {"type": "t", "text": " Alterations in Kv3.3 have also been linked to deficits in auditory processing and sleep regulation, underlining the channel’s broader contributions to central nervous system function."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "12"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Finally, observations from clinical and genetic studies in patients with ataxic forms of cerebral palsy further support the role of KCNC3 mutations in disrupting cerebellar network activity and motor behavior."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "14"}]}, {"type": "t", "text": " Collectively, these findings establish KCNC3 as a critical modulator of neuronal firing dynamics and signal integration, with its dysfunction contributing to a broad range of neurological disorders.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Michael F Waters, Natali A Minassian, Giovanni Stevanin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Genet (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ng1758"}], "href": "https://doi.org/10.1038/ng1758"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16501573"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16501573"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Su Ying Chang, Edward Zagha, Elaine S Kwon, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Distribution of Kv3.3 potassium channel subunits in distinct neuronal populations of mouse brain."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Comp Neurol (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/cne.21353"}], "href": "https://doi.org/10.1002/cne.21353"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17444489"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17444489"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Yalan Zhang, Leonard K Kaczmarek "}, {"type": "b", "children": [{"type": "t", "text": "Kv3.3 potassium channels and spinocerebellar ataxia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Physiol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1113/JP271343"}], "href": "https://doi.org/10.1113/JP271343"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26442672"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26442672"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Walther Akemann, Thomas Knöpfel "}, {"type": "b", "children": [{"type": "t", "text": "Interaction of Kv3 potassium channels and resurgent sodium current influences the rate of spontaneous firing of Purkinje neurons."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurosci (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1523/JNEUROSCI.5204-05.2006"}], "href": "https://doi.org/10.1523/JNEUROSCI.5204-05.2006"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16641240"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16641240"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Edward Zagha, Eric J Lang, Bernardo Rudy "}, {"type": "b", "children": [{"type": "t", "text": "Kv3.3 channels at the Purkinje cell soma are necessary for generation of the classical complex spike waveform."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurosci (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1523/JNEUROSCI.4358-07.2008"}], "href": "https://doi.org/10.1523/JNEUROSCI.4358-07.2008"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18256249"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18256249"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Edward Zagha, Satoshi Manita, William N Ross, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Dendritic Kv3.3 potassium channels in cerebellar purkinje cells regulate generation and spatial dynamics of dendritic Ca2+ spikes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurophysiol (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1152/jn.00982.2009"}], "href": "https://doi.org/10.1152/jn.00982.2009"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20357073"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20357073"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Karla P Figueroa, Natali A Minassian, Giovanni Stevanin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Mutat (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/humu.21165"}], "href": "https://doi.org/10.1002/humu.21165"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19953606"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19953606"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Fadi A Issa, Christopher Mazzochi, Allan F Mock, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Spinocerebellar ataxia type 13 mutant potassium channel alters neuronal excitability and causes locomotor deficits in zebrafish."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurosci (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1523/JNEUROSCI.6572-10.2011"}], "href": "https://doi.org/10.1523/JNEUROSCI.6572-10.2011"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21543613"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21543613"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Natali A Minassian, Meng-Chin A Lin, Diane M Papazian "}, {"type": "b", "children": [{"type": "t", "text": "Altered Kv3.3 channel gating in early-onset spinocerebellar ataxia type 13."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Physiol (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1113/jphysiol.2012.228205"}], "href": "https://doi.org/10.1113/jphysiol.2012.228205"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22289912"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22289912"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Anna Duarri, Esther A R Nibbeling, Michiel R Fokkens, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Functional analysis helps to define KCNC3 mutational spectrum in Dutch ataxia cases."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0116599"}], "href": "https://doi.org/10.1371/journal.pone.0116599"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25756792"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25756792"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Yalan Zhang, Xiao-Feng Zhang, Matthew R Fleming, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Kv3.3 Channels Bind Hax-1 and Arp2/3 to Assemble a Stable Local Actin Network that Regulates Channel Gating."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.cell.2016.02.009"}], "href": "https://doi.org/10.1016/j.cell.2016.02.009"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26997484"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26997484"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Edward C Hurlock, Anne McMahon, Rolf H Joho "}, {"type": "b", "children": [{"type": "t", "text": "Purkinje-cell-restricted restoration of Kv3.3 function restores complex spikes and rescues motor coordination in Kcnc3 mutants."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurosci (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1523/JNEUROSCI.5486-07.2008"}], "href": "https://doi.org/10.1523/JNEUROSCI.5486-07.2008"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18448641"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18448641"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "John C Middlebrooks, Harry S Nick, S H Subramony, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutation in the kv3.3 voltage-gated potassium channel causing spinocerebellar ataxia 13 disrupts sound-localization mechanisms."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0076749"}], "href": "https://doi.org/10.1371/journal.pone.0076749"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24116147"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24116147"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Ricardo Parolin Schnekenberg, Emma M Perkins, Jack W Miller, et al. "}, {"type": "b", "children": [{"type": "t", "text": "De novo point mutations in patients diagnosed with ataxic cerebral palsy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Brain (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/brain/awv117"}], "href": "https://doi.org/10.1093/brain/awv117"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25981959"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25981959"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)."}]}, {"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.0017811"}], "href": "https://doi.org/10.1371/journal.pone.0017811"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21479265"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21479265"}]}]}]}
Synonyms	KV3.3, SCA13, KSHIIID
Proteins	KCNC3_HUMAN
NCBI Gene ID	3748
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

KCNC3 has 5,321 functional associations with biological entities spanning 9 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, sequence feature) extracted from 116 datasets.

Click the + buttons to view associations for KCNC3 from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

KCNC3 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 KCNC3 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 KCNC3 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 KCNC3 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 KCNC3 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 KCNC3 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 KCNC3 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 KCNC3 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 KCNC3 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 KCNC3 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 KCNC3 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of KCNC3 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 KCNC3 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with KCNC3 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 KCNC3 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of KCNC3 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 KCNC3 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
	ClinVar Gene-Phenotype Associations	phenotypes associated with KCNC3 gene from the curated ClinVar Gene-Phenotype Associations dataset.
	ClinVar Gene-Phenotype Associations 2025	phenotypes associated with KCNC3 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 KCNC3 gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing KCNC3 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing KCNC3 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores	cellular components co-occuring with KCNC3 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 KCNC3 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	COSMIC Cell Line Gene CNV Profiles	cell lines with high or low copy number of KCNC3 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with KCNC3 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Chemical Interactions	chemicals interacting with KCNC3 gene/protein from the curated CTD Gene-Chemical Interactions dataset.
	CTD Gene-Disease Associations	diseases associated with KCNC3 gene/protein from the curated CTD Gene-Disease Associations dataset.
	DepMap CRISPR Gene Dependency	cell lines with fitness changed by KCNC3 gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores	diseases involving KCNC3 gene from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores 2025	diseases involving KCNC3 gene from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores 2025	diseases associated with KCNC3 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 KCNC3 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 KCNC3 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 KCNC3 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with KCNC3 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Phenoptype Associations dataset.
	DrugBank Drug Targets	interacting drugs for KCNC3 protein from the curated DrugBank Drug Targets dataset.
	ENCODE Histone Modification Site Profiles	histone modification site profiles with high histone modification abundance at KCNC3 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 KCNC3 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
	ENCODE Transcription Factor Targets	transcription factors binding the promoter of KCNC3 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 KCNC3 from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.