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GRIN3B Gene — NMDA Receptor Subunit 3B

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gene577 wordssynced 2026-04-02

GRIN3B Gene — NMDA Receptor Subunit 3B


<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">GRIN3B Gene — NMDA Receptor Subunit 3B</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td><strong>GRIN3B</strong></td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>GRIN3B — NMDA Receptor Subunit 3B</td>
</tr>
<tr>
<td class="label">Type</td>
<td>Gene</td>
</tr>
<tr>
<td class="label">NCBI</td>
<td><a href="https://www.ncbi.nlm.nih.gov/gene/?term=GRIN3B" target="_blank">Search NCBI</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1 edges</a></td>
</tr>
</table>

Introduction

Grin3B Gene — Nmda Receptor Subunit 3B is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.

GRIN3B encodes the NR3B (GluN3B) subunit of the N-methyl-D-aspartate (NMDA) receptor, a subtype of ionotropic glutamate receptor. This subunit is unique among [NMDA](/entities/nmda-receptor) receptor subunits and confers distinct pharmacological and physiological properties to the receptor complex. [@nishi2005]

Overview

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