Mar 30, 2025 · KCNJ2 (Potassium Inwardly Rectifying Channel Subfamily J Member 2) is a Protein Coding gene. Diseases associated with KCNJ2 include Andersen Cardiodysrhythmic Periodic Paralysis and Short Qt Syndrome 3 .

Mar 30, 2025 · Complete information for KCNJ2-AS1 gene (RNA Gene), KCNJ2 Antisense RNA 1, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Showing 25 of 3,979 results for KCNJ2 Search Time: 0 ms in Aliases & Descriptions Drugs & Compounds Disorders Text-Mined Disorders Domains Expression in Human Tissues Function Genomics Localization Orthologs Paralogs Pathways Phenotypes Proteins Publications Summaries Transcripts Variants in category Protein Coding RNA Gene Functional Element ...

Mar 30, 2025 · This gene encodes a component of a voltage-activated potassium channel found in cardiac muscle, nerve cells, and microglia. Four copies of this protein interact with one copy of the KCNE2 protein to form a functional potassium channel. Mutations in this gene can cause long QT syndrome type 2 (LQT2).

Mar 30, 2025 · KCNJ18 (Potassium Inwardly Rectifying Channel Subfamily J Member 18) is a Protein Coding gene. Diseases associated with KCNJ18 include Thyrotoxic Periodic Paralysis 2 and Thyrotoxic Periodic Paralysis. Gene Ontology (GO) annotations related to this gene include inward rectifier potassium channel activity. An important paralog of this gene is ...

Mar 30, 2025 · KCNJ3 (Potassium Inwardly Rectifying Channel Subfamily J Member 3) is a Protein Coding gene. Diseases associated with KCNJ3 include Familial Atrial Fibrillation and Vitreoretinal Degeneration, Snowflake Type. Among its related pathways are Inwardly rectifying K+ channels and Transmission across Chemical Synapses.

Mar 30, 2025 · KCNJ8 (Potassium Inwardly Rectifying Channel Subfamily J Member 8) is a Protein Coding gene. Diseases associated with KCNJ8 include Cantu Syndrome and Sudden Infant Death Syndrome. Among its related pathways are Inwardly rectifying K+ channels and Transmission across Chemical Synapses.

Mar 30, 2025 · 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.

Mar 30, 2025 · KCNJ1 (Potassium Inwardly Rectifying Channel Subfamily J Member 1) is a Protein Coding gene. Diseases associated with KCNJ1 include Bartter Syndrome, Type 2, Antenatal and Bartter Disease. Among its related pathways are Inwardly rectifying K+ channels and Transmission across Chemical Synapses.

Mar 30, 2025 · KCNJ4 (Potassium Inwardly Rectifying Channel Subfamily J Member 4) is a Protein Coding gene. Diseases associated with KCNJ4 include Prostate Cancer and Andersen Cardiodysrhythmic Periodic Paralysis. Among its related pathways are Inwardly rectifying K+ channels and Cardiac conduction.