HCN1
Template:Short description Template:Infobox gene Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 is a protein that in humans is encoded by the HCN1 gene.[1][2][3][4]
Function
Hyperpolarization-activated cation channels of the HCN gene family, such as HCN1, contribute to spontaneous rhythmic activity in both heart and brain.[4]
Tissue distribution
HCN1 channel expression is found in the sinoatrial node,[5][6] the neocortex, hippocampus, cerebellar cortex, dorsal root ganglion, trigeminal ganglion and brainstem.[7][8][9][10][11]
Ligands
- Isoflurane and Sevoflurane inhibit HCN1.[15]
Interactions
HCN1 has been shown to interact with HCN2.[16][17]
Epilepsy
De novo mutations in HCN1 cause epilepsy.[18]
See also
References
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Further reading
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External links
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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