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RAB38 Gene

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RAB38 — RAB38, Member RAS Oncogene Family

Overview

Rab38 Gene plays an important role in the study of neurodegenerative diseases. This page provides comprehensive information about this topic, including its mechanisms, significance in disease processes, and therapeutic implications.

Introduction

Rab38 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. [@wasmeier2004]

<div class="infobox infobox-gene"> [@gamberi2013]
<table> [@bultema2014]
<tr><th colspan="2" style="background:#e8f4f8; text-align:center; font-size:1.1em;">RAB38, Member RAS Oncogene Family</th></tr> [@wang2015]
<tr><td><strong>Gene Symbol</strong></td><td>RAB38</td></tr> [@liu2019]
<tr><td><strong>Full Name</strong></td><td>RAB38, Member RAS Oncogene Family</td></tr> [@zhou2020]
<tr><td><strong>Chromosome</strong></td><td>11q14.2</td></tr> [@kim2022]
<tr><td><strong>NCBI Gene ID</strong></td><td>[28284](https://www.ncbi.nlm.nih.gov/gene/28284)</td></tr>
<tr><td><strong>OMIM</strong></td><td>606436</td></tr>
<tr><td><strong>Ensembl ID</strong></td><td>ENSG00000123892</td></tr>
<tr><td><strong>UniProt ID</strong></td><td>[O14964](https://www.uniprot.org/uniprot/O14964)</td></tr>
<tr><td><strong>Associated Diseases</strong></td><td>Parkinson's Disease, Hermansky-Pudlak Syndrome, Cancer, Pigmentation Disorders</td></tr>
</table>
</div>

Function


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