HomeAboutRankingsData Sources
© 2026 GeneE
🧬
GeneE
10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
ⓘGeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
KCNIP2
potassium voltage-gated channel interacting protein 2
Chromosome 10 · 10q24.32
NCBI Gene: 30819Ensembl: ENSG00000120049.20HGNC: HGNC:15522UniProt: A0A2R8Y6D7
61PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Ion ChannelTransporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
A-type (transient outward) potassium channel activityclustering of voltage-gated potassium channelsprotein bindingpotassium channel regulator activityatrial fibrillationatrial flutterintelligenceepilepsy
✦AI Summary

KCNIP2 is a regulatory subunit of Kv4/D-type voltage-gated A-type potassium channels that modulates channel density, inactivation kinetics, and recovery rates from inactivation in a calcium-dependent manner 123456. It facilitates trafficking of KCND2 and KCND3 channels to the cell surface 7 and is essential for cardiac I(To) current expression. In cardiac electrophysiology, KCNIP2 dysregulation contributes to arrhythmias and heart failure; notably, Notch pathway activation in atrial fibrillation reduces Kcnip2 expression alongside other ion channel genes, altering action potential duration chamber-specifically 8. Beyond the heart, KCNIP2-expressing inhibitory interneurons in the spinal dorsal horn regulate cold sensitivity through modulation of nociceptive pathways 9. KCNIP2 shows tissue-specific alternative splicing patterns with distinct neuronal expression profiles 10. Clinically, KCNIP2-AS1 (an antisense lncRNA) exhibits reduced expression in breast cancer and correlates inversely with tumor grade and mitotic rates, suggesting potential tumor-suppressive function 11. Additionally, KCNIP2 undergoes DNA methylation changes in autism spectrum disorder models that correlate between brain and peripheral blood tissues 12. These diverse roles position KCNIP2 as a multifunctional regulator in cardiac and neurological physiology with emerging relevance to oncology.

Sources cited
1
KCNIP2 is a regulatory subunit of Kv4/D-type voltage-gated potassium channels
PMID: 10676964
2
KCNIP2 modulates A-type potassium channel density and inactivation kinetics
PMID: 11287421
3
KCNIP2 modulates calcium-dependent channel regulation
PMID: 11684073
4
KCNIP2 affects recovery from inactivation in potassium channels
PMID: 12297301
5
KCNIP2 provides isoform-specific modulation of potassium channels
PMID: 14623880
6
KCNIP2 regulates voltage-gated potassium channel function
PMID: 34997220
7
KCNIP2 is involved in KCND2 and KCND3 trafficking to the cell surface
PMID: 12829703
8
Kcnip2 expression is dysregulated in atrial fibrillation with heart failure through Notch signaling
PMID: 32841220
9
Kcnip2-expressing spinal interneurons regulate behavioral cold sensitivity
PMID: 36323322
10
KCNIP genes show tissue-specific alternative splicing and neuronal expression patterns
PMID: 16112838
11
KCNIP2-AS1 shows reduced expression in breast cancer with inverse correlation to tumor grade
PMID: 37820438
12
KCNIP2 undergoes differential DNA methylation in autism spectrum disorder models
PMID: 37658766
Disease Associationsⓘ20
atrial fibrillationOpen Targets
0.40Moderate
atrial flutterOpen Targets
0.27Weak
intelligenceOpen Targets
0.26Weak
epilepsyOpen Targets
0.19Weak
generalised epilepsyOpen Targets
0.15Weak
Alzheimer diseaseOpen Targets
0.14Weak
autism spectrum disorderOpen Targets
0.10Suggestive
mathematical abilityOpen Targets
0.10Suggestive
Romano-Ward syndromeOpen Targets
0.10Suggestive
Familial progressive cardiac conduction defectOpen Targets
0.10Suggestive
familial atrial fibrillationOpen Targets
0.09Suggestive
Brugada syndromeOpen Targets
0.09Suggestive
Familial short QT syndromeOpen Targets
0.09Suggestive
attention deficit hyperactivity disorderOpen Targets
0.09Suggestive
Arrhythmogenic right ventricular dysplasiaOpen Targets
0.08Suggestive
hypertrophic cardiomyopathyOpen Targets
0.08Suggestive
dilated cardiomyopathyOpen Targets
0.08Suggestive
Rare familial disorder with hypertrophic cardiomyopathyOpen Targets
0.08Suggestive
sudden cardiac arrestOpen Targets
0.08Suggestive
catecholaminergic polymorphic ventricular tachycardiaOpen Targets
0.08Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
DPP6Protein interaction99%KCNC1Protein interaction99%KCNIP4Protein interaction97%KCND1Protein interaction89%SCN5AProtein interaction84%KCNA4Protein interaction84%
Tissue Expression6 tissues
Heart
100%
Brain
9%
Ovary
7%
Liver
2%
Lung
1%
Bone Marrow
1%
Gene Interaction Network
Click a node to explore
KCNIP2DPP6KCNC1KCNIP4KCND1SCN5AKCNA4
PROTEIN STRUCTURE
Preparing viewer…
PDB7UKH · 2.33 Å · EM
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
0.77LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.52 [0.36–0.77]
RankingsWhere KCNIP2 stands among ~20K protein-coding genes
  • #7,568of 20,598
    Most Researched61
  • #6,290of 17,882
    Most Constrained (LOEUF)0.77
Genes detectedKCNIP2
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
KCNIP2: A key regulator in cardiac electrophysiology and tumorigenesis.
PMID: 40490090
Gene · 2025
1.00
2
Expression analysis of PPAR-related lncRNAs in breast cancer.
PMID: 37820438
Pathol Res Pract · 2023
0.90
3
Chamber-specific transcriptional responses in atrial fibrillation.
PMID: 32841220
JCI Insight · 2020
0.80
4
Inhibitory Kcnip2 neurons of the spinal dorsal horn control behavioral sensitivity to environmental cold.
PMID: 36323322
Neuron · 2023
0.70
5
Genetic modifiers of cardiac arrhythmias.
PMID: 12615039
Trends Mol Med · 2003
0.60