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GRIN2A Protein (NMDA Receptor Subunit 2A)

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GRIN2A Protein (NMDA Receptor Subunit 2A)


<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">GRIN2A Protein (NMDA Receptor Subunit 2A)</th>
</tr>
<tr>
<td class="label">Drug</td>
<td>Target</td>
</tr>
<tr>
<td class="label">Memantine</td>
<td>NMDAR (all subunits)</td>
</tr>
<tr>
<td class="label">Amantadine</td>
<td>NMDAR</td>
</tr>
<tr>
<td class="label">Compound</td>
<td>Mechanism</td>
</tr>
<tr>
<td class="label">D-serine</td>
<td>NMDAR co-agonist</td>
</tr>
<tr>
<td class="label">Rapastinel</td>
<td>NMDAR (GluN2B) modulator</td>
</tr>
<tr>
<td class="label">AV-101</td>
<td>D-serine synthesis</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">10 edges</a></td>
</tr>
</table>

Introduction

Grin2A Protein (Nmda Receptor Subunit 2A) is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.

Overview

The GRIN2A (NR2A) protein is a subunit of the NMDA (N-methyl-D-aspartate) glutamate receptor, a ligand-gated ion channel critical for synaptic plasticity, learning, and memory. NMDA receptors containing the NR2A subunit are involved in [long-term potentiation](/mechanisms/long-term-potentiation) and depression. GRIN2A mutations cause epilepsy-aphasia spectrum disorders. [@liu2017]

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Related Entities
GRIN2APROTEIN
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slugproteins-grin2a-protein
kg_node_idGRIN2APROTEIN
entity_typeprotein
origin_typev1_polymorphic_backfill
source_tablewiki_pages
wiki_page_idwp-5a11938cfd8b
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📊 Evidence Profile Foundational
Evidence Balance
+0%
Certainty
70%
Debates
0
Incoming
14
Outgoing
15
0 supporting 0 contradicting 0 neutral
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