potassium voltage-gated channel subfamily H member 2
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). Transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, May 2022].
Ask anything about KCNH2 — pathways, variants, literature, experimental design. Free for researchers, 30,000 AI tokens daily.
Ask AI about KCNH2 →Data source: NCBI Gene · alsesAI Gene Library