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KCNN1 Gene

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gene992 wordssynced 2026-04-02

KCNN1 Gene

Introduction

<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">KCNN1 Gene</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>KCNN1</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Potassium Calcium-Activated Channel Subfamily N Member 1</td>
</tr>
<tr>
<td class="label">Aliases</td>
<td>SK1, KCa2.1, hSK1</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>1p22</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>3776</td>
</tr>
<tr>
<td class="label">OMIM</td>
<td>609921</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000105695</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q9H5Y3</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1 edges</a></td>
</tr>
</table>

KCNN1 (Potassium Calcium-Activated Channel Subfamily N Member 1), also known as SK1 (Small-Conductance Calcium-Activated Potassium Channel 1), encodes a neuronal small-conductance calcium-activated potassium channel. These channels play critical roles in regulating neuronal excitability, synaptic integration, and afterhyperpolarization. SK channels are increasingly recognized as important therapeutic targets in neurodegenerative diseases, epilepsy, and psychiatric disorders. [@stocker2004]

Overview


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