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KCNMB3

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gene844 wordssynced 2026-04-02

KCNMB3

Gene Overview

<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">KCNMB3</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td>KCNMB3</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Potassium Calcium-Activated Channel Subfamily M Regulatory Beta Subunit 3</td>
</tr>
<tr>
<td class="label">Chromosome</td>
<td>22q12.1</td>
</tr>
<tr>
<td class="label">NCBI Gene</td>
<td>[8912](https://www.ncbi.nlm.nih.gov/gene/8912)</td>
</tr>
<tr>
<td class="label">UniProt</td>
<td>[Q9NS88](https://www.uniprot.org/uniprot/Q9NS88)</td>
</tr>
<tr>
<td class="label">Ensembl</td>
<td>[ENSG00000143001](https://www.ensembl.org/Homo_sapiens/Gene/Summary?g=ENSG00000143001)</td>
</tr>
<tr>
<td class="label">Protein Length</td>
<td>281 amino acids</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~31 kDa</td>
</tr>
<tr>
<td class="label">Condition</td>
<td>Evidence</td>
</tr>
<tr>
<td class="label">Epilepsy</td>
<td>Genetic association studies</td>
</tr>
<tr>
<td class="label">Migraine</td>
<td>GWAS signals near KCNMB3 locus</td>
</tr>
<tr>
<td class="label">Cerebellar ataxia</td>
<td>Channel dysfunction</td>
</tr>
<tr>
<td class="label">Neuropathic pain</td>
<td>Peripheral nerve involvement</td>
</tr>
<tr>
<td class="label">Partner</td>
<td>Interaction Type</td>
</tr>
<tr>
<td class="label">KCNMA1</td>
<td>Channel assembly</td>
</tr

...
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