Target intelligence / Profile preview

Potassium inwardly-rectifying channel subfamily J member 14 (KCNJ14)

Target
KCNJ14
Molecular classification
Ion channel, Potassium channel, Inward rectifier potassium channel
01

Overview

KCNJ14 encodes Potassium inwardly-rectifying channel subfamily J member 14, an integral membrane protein forming an inward-rectifier potassium channel (Kir2.4) that allows potassium ions to enter cells more readily than they exit[1][3][6]. This channel plays a key role in controlling neuronal and motor neuron excitability and modulating membrane potential, with additional functions in heart rate and epithelial transport[1][7]. Dysregulation of KCNJ14 has been linked to the progression and prognosis of several cancers, and its expression is proposed as a biomarker for cancer patient stratification and monitoring[7]. While mechanistic understanding and therapeutic targeting are nascent, research supports its relevance to both cancer biology and neurological/cardiac physiology[7].

Other names
Kir2.4IRK4ATP-sensitive inward rectifier potassium channel 14Inward rectifier K(+) channel Kir2.4Potassium channel, inwardly rectifying subfamily J member 14Potassium voltage-gated channel subfamily J member 14
02

Mechanism of action

Potassium channel modulation affecting cell excitability (for agents modulating KCNJ channel activity in general, not KCNJ14 specifically)

03

Biological functions

Regulation of membrane potentialControl of neuronal excitabilityHeart rate modulationNeurotransmitter releaseEpithelial electrolyte transportImmunological regulation
04

Disease associations

CancerCardiovascular diseaseNeurological disorders (e.g., potential link to Kluver-Bucy syndrome, periodic paralysis)
05

Safety considerations

Potential risk of cardiac arrhythmias and neuronal excitability disturbance if modulatedLimited information; further research needed to clarify on-target toxicity[7]
06

Interacting drugs

null (no specific drugs directly targeting KCNJ14 are well-established in current literature; ion channel modulators may interact indirectly but without clinical specificity reported)
07

Biomarkers

KCNJ14 expression (prognostic biomarker for several cancers, including colorectal cancer and others)Genomic markers: associated with tumor mutation burden (TMB), microsatellite instability (MSI), neoantigen load, and PD-L1 expression in some cancers[7]

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