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KCNF2 Gene

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wiki page Created: 2026-04-02T07:19:19 By: crosslink-migration Quality: 50% ✓ SciDEX ID: wiki-genes-kcnf2
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KCNF2 Gene

<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">KCNF2 Gene</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>KCNF2</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Potassium Voltage-Gated Channel Modulator Subfamily F Member 2</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>5q31.1</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>58484</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000157119</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q96T59</td>
</tr>
<tr>
<td class="label">Protein Length</td>
<td>446 amino acids</td>
</tr>
<tr>
<td class="label">Expression</td>
<td>Brain (highest), heart, kidney</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1 edges</a></td>
</tr>
</table>

Introduction

KCNF2 (Potassium Voltage-Gated Channel Modulator Subfamily F Member 2) encodes the Kv5.2 protein, a modulatory subunit that influences the function of voltage-gated potassium channels, particularly Kv2.1. While KCNF2 does not form functional channels on its own, it dramatically modulates the trafficking, gating, and expression of partner potassium channels. This modulatory function has significant implications for neuronal excitability, synaptic transmission, and ultimately for neurodegenerative diseases including Alzheimer's disease (AD), Parkinson's disease (PD), and epilepsy. [@salkoff2001]

Overview


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KCNF2
Metadataorigin_type: v1_polymorphic_backfill
sluggenes-kcnf2
kg_node_idKCNF2
entity_typegene
origin_typev1_polymorphic_backfill
source_tablewiki_pages
wiki_page_idwp-624984d5743a
__merged_from{'merged_at': '2026-05-13', 'unprefixed_id': 'genes-kcnf2'}
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📊 Evidence Profile
Evidence Balance
+0%
Certainty
25%
Debates
0
Incoming
5
Outgoing
6
0 supporting 0 contradicting 0 neutral
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