<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">RAB11A — Ras-Related Protein Rab-11A</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>RAB11A</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>RAB11A, member RAS oncogene family</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>15q21.3</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>8766</td>
</tr>
<tr>
<td class="label">OMIM</td>
<td>609758</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000103740</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>P62491</td>
</tr>
<tr>
<td class="label">Protein Class</td>
<td>Rab GTPase</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~24 kDa</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">ALS</a>, <a href="/wiki/aging" style="color:#ef9a9a">Aging</a>, <a href="/wiki/als" style="color:#ef9a9a">Als</a>, <a href="/wiki/atherosclerosis" style="color:#ef9a9a">Atherosclerosis</a>, <a href="/wiki/ftd" style="color:#ef9a9a">Ftd</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">129 edges</a></td>
</tr>
</table>
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">RAB11A — Ras-Related Protein Rab-11A</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>RAB11A</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>RAB11A, member RAS oncogene family</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>15q21.3</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>8766</td>
</tr>
<tr>
<td class="label">OMIM</td>
<td>609758</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000103740</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>P62491</td>
</tr>
<tr>
<td class="label">Protein Class</td>
<td>Rab GTPase</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~24 kDa</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">ALS</a>, <a href="/wiki/aging" style="color:#ef9a9a">Aging</a>, <a href="/wiki/als" style="color:#ef9a9a">Als</a>, <a href="/wiki/atherosclerosis" style="color:#ef9a9a">Atherosclerosis</a>, <a href="/wiki/ftd" style="color:#ef9a9a">Ftd</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">129 edges</a></td>
</tr>
</table>
RAB11A (Ras-Related Protein Rab-11A) is a member of the Rab GTPase family that functions as a master regulator of endocytic recycling. RAB11A controls the trafficking of cargo through recycling endosomes, a critical pathway for maintaining cellular homeostasis, synaptic function, and membrane receptor availability. In the nervous system, RAB11A plays essential roles in neurotransmitter release, synaptic plasticity, and the clearance of neurotoxic proteins. Emerging research has implicated RAB11A dysfunction in the pathogenesis of Parkinson's disease, Alzheimer's disease, and other neurodegenerative disorders [@rab2021][@rabmediated2021].
RAB11A is expressed throughout the body but is particularly abundant in neurons, where it localizes to recycling endosomes, synaptic vesicles, and growth cones. The protein cycles between active GTP-bound and inactive GDP-bound states, regulated by specific guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs).
RAB11A is crucial for synaptic vesicle recycling, a process that allows neurons to maintain neurotransmitter release during sustained activity. After synaptic vesicle exocytosis, membrane components must be retrieved and recycled back to the synaptic vesicle pool. RAB11A-mediated recycling endosome trafficking is essential for this process, ensuring that synaptic vesicles can be regenerated efficiently [@rab2015].
Key functions in synaptic vesicle recycling include:
In dopaminergic neurons, RAB11A plays a critical role in maintaining dopamine receptor availability at the synaptic membrane. Proper dopamine receptor recycling is essential for normal motor control and cognitive function. Dysregulation of this process contributes to the motor and non-motor symptoms of Parkinson's disease.
RAB11A participates in autophagosome maturation, a key process in the clearance of protein aggregates and damaged organelles. RAB11A coordinates the fusion of autophagosomes with lysosomes, enabling the degradation of neurotoxic proteins including alpha-synuclein and tau.
RAB11A dysfunction has emerged as a significant contributor to PD pathogenesis. Studies in patient-derived neurons and animal models have revealed multiple mechanisms by which impaired RAB11A function leads to dopaminergic neuron degeneration [@rab2021]:
In AD, RAB11A dysfunction contributes to disease pathogenesis through several mechanisms:
RAB11A dysfunction has also been implicated in:
RAB11A participates in several key cellular pathways relevant to neurodegeneration:
RAB11A represents a promising therapeutic target for neurodegenerative diseases [@wang2024]:
Research is ongoing to develop:
RAB11A has been investigated as a potential biomarker for neurodegenerative disease progression:
While RAB11A mutations are not a primary cause of familial PD, genetic variants have been associated with:
RAB11A function has been characterized in multiple experimental models:
Several RAB11A-targeted approaches are in development:
RAB11A is ubiquitously expressed with particularly high levels in:
The following diagram shows the key molecular relationships involving RAB11A — Ras-Related Protein Rab-11A discovered through SciDEX knowledge graph analysis: