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TFG Gene

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gene796 wordssynced 2026-04-02

TFG Gene

Introduction

<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">TFG Gene</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>TFG</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>TFG</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>3q12.2</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>10342</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000120708</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q92734</td>
</tr>
<tr>
<td class="label">Protein Size</td>
<td>400 amino acids</td>
</tr>
<tr>
<td class="label">Protein Family</td>
<td>TFG family</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1 edges</a></td>
</tr>
</table>

Tfg Gene is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.

TFG (TRK-Fused Gene) encodes a protein involved in protein secretion, endoplasmic reticulum stress response, and neurodegeneration. Mutations in TFG cause hereditary spastic paraplegia (SPG57) and Charcot-Marie-Tooth disease (CMT). [@yalcin2020]

Overview

This page provides comprehensive information about the TFG gene, its molecular function, disease associations, and therapeutic implications for neurodegenerative and peripheral neuropathy research. [@liu2017]

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